subject:(porphyrin)

Queensland University of Technology

1. Harper, Shannon R. Diporphyrins linked by two-atom bridges synthestic, structural and theoretical studies.

Degree: 2014, Queensland University of Technology

► The syntheses, properties and electronic structures of a series of porphyrin dimers connected by two-atom bridges were compared. The study found that an azo linker… (more)

Subjects/Keywords: Porphyrin; Porphyrin Dimer; Ethanediyl Porphyrin; Ethenediyl Porphyrin; Ethynediyl Porphyrin; Imine Porphyrin; Azoporphyrin; Synthesis; Spectroscopy; Dimer

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APA (6^th Edition):

Harper, S. R. (2014). Diporphyrins linked by two-atom bridges synthestic, structural and theoretical studies. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/68643/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Harper, Shannon R. “Diporphyrins linked by two-atom bridges synthestic, structural and theoretical studies.” 2014. Thesis, Queensland University of Technology. Accessed April 15, 2021. https://eprints.qut.edu.au/68643/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Harper, Shannon R. “Diporphyrins linked by two-atom bridges synthestic, structural and theoretical studies.” 2014. Web. 15 Apr 2021.

Vancouver:

Harper SR. Diporphyrins linked by two-atom bridges synthestic, structural and theoretical studies. [Internet] [Thesis]. Queensland University of Technology; 2014. [cited 2021 Apr 15]. Available from: https://eprints.qut.edu.au/68643/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Harper SR. Diporphyrins linked by two-atom bridges synthestic, structural and theoretical studies. [Thesis]. Queensland University of Technology; 2014. Available from: https://eprints.qut.edu.au/68643/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

2. Inaba, Yusuke. Studies of special pair and hemoglobin models consisting of imidazolyl-substituted metalloporphyrin dimer : イミダゾリル置換金属ポルフィリン二量体を用いたスペシャルペア及びヘモグロビンモデル化合物の研究; イミダゾリルチカンキンゾクポルフィリンニリョウタイオモチイタスペシャルペアオヨビヘモグロビンモデルカゴウブツノケンキュウ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

URL: http://hdl.handle.net/10061/4016

Subjects/Keywords: Porphyrin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Inaba, Y. (n.d.). Studies of special pair and hemoglobin models consisting of imidazolyl-substituted metalloporphyrin dimer : イミダゾリル置換金属ポルフィリン二量体を用いたスペシャルペア及びヘモグロビンモデル化合物の研究; イミダゾリルチカンキンゾクポルフィリンニリョウタイオモチイタスペシャルペアオヨビヘモグロビンモデルカゴウブツノケンキュウ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/4016

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Inaba, Yusuke. “Studies of special pair and hemoglobin models consisting of imidazolyl-substituted metalloporphyrin dimer : イミダゾリル置換金属ポルフィリン二量体を用いたスペシャルペア及びヘモグロビンモデル化合物の研究; イミダゾリルチカンキンゾクポルフィリンニリョウタイオモチイタスペシャルペアオヨビヘモグロビンモデルカゴウブツノケンキュウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 15, 2021. http://hdl.handle.net/10061/4016.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Inaba, Yusuke. “Studies of special pair and hemoglobin models consisting of imidazolyl-substituted metalloporphyrin dimer : イミダゾリル置換金属ポルフィリン二量体を用いたスペシャルペア及びヘモグロビンモデル化合物の研究; イミダゾリルチカンキンゾクポルフィリンニリョウタイオモチイタスペシャルペアオヨビヘモグロビンモデルカゴウブツノケンキュウ.” Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Inaba Y. Studies of special pair and hemoglobin models consisting of imidazolyl-substituted metalloporphyrin dimer : イミダゾリル置換金属ポルフィリン二量体を用いたスペシャルペア及びヘモグロビンモデル化合物の研究; イミダゾリルチカンキンゾクポルフィリンニリョウタイオモチイタスペシャルペアオヨビヘモグロビンモデルカゴウブツノケンキュウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10061/4016.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Inaba Y. Studies of special pair and hemoglobin models consisting of imidazolyl-substituted metalloporphyrin dimer : イミダゾリル置換金属ポルフィリン二量体を用いたスペシャルペア及びヘモグロビンモデル化合物の研究; イミダゾリルチカンキンゾクポルフィリンニリョウタイオモチイタスペシャルペアオヨビヘモグロビンモデルカゴウブツノケンキュウ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/4016

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

3. Uyar, Zafer. Stable Complexation of Light-Harvesting Porphyrin Supramolecular Nanoring and Multidendate Ligands:Elucidation of Mechanism by Thermodynamic Insight : 光捕集機能を有する超分子ポルフィリンナノリングと多座リガンドの安定複合体形成：熱力学的解析による機構解明; ヒカリホシュウキノウオユウスルチョウブンシポルフィリンナノリングトタザリガンドノアンテイフクゴウタイケイセイネツリキガクテキカイセキニヨルキコウカイメイ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

URL: http://hdl.handle.net/10061/4709

Subjects/Keywords: Porphyrin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Uyar, Z. (n.d.). Stable Complexation of Light-Harvesting Porphyrin Supramolecular Nanoring and Multidendate Ligands:Elucidation of Mechanism by Thermodynamic Insight : 光捕集機能を有する超分子ポルフィリンナノリングと多座リガンドの安定複合体形成：熱力学的解析による機構解明; ヒカリホシュウキノウオユウスルチョウブンシポルフィリンナノリングトタザリガンドノアンテイフクゴウタイケイセイネツリキガクテキカイセキニヨルキコウカイメイ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/4709

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Uyar, Zafer. “Stable Complexation of Light-Harvesting Porphyrin Supramolecular Nanoring and Multidendate Ligands:Elucidation of Mechanism by Thermodynamic Insight : 光捕集機能を有する超分子ポルフィリンナノリングと多座リガンドの安定複合体形成：熱力学的解析による機構解明; ヒカリホシュウキノウオユウスルチョウブンシポルフィリンナノリングトタザリガンドノアンテイフクゴウタイケイセイネツリキガクテキカイセキニヨルキコウカイメイ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 15, 2021. http://hdl.handle.net/10061/4709.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Uyar, Zafer. “Stable Complexation of Light-Harvesting Porphyrin Supramolecular Nanoring and Multidendate Ligands:Elucidation of Mechanism by Thermodynamic Insight : 光捕集機能を有する超分子ポルフィリンナノリングと多座リガンドの安定複合体形成：熱力学的解析による機構解明; ヒカリホシュウキノウオユウスルチョウブンシポルフィリンナノリングトタザリガンドノアンテイフクゴウタイケイセイネツリキガクテキカイセキニヨルキコウカイメイ.” Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Uyar Z. Stable Complexation of Light-Harvesting Porphyrin Supramolecular Nanoring and Multidendate Ligands:Elucidation of Mechanism by Thermodynamic Insight : 光捕集機能を有する超分子ポルフィリンナノリングと多座リガンドの安定複合体形成：熱力学的解析による機構解明; ヒカリホシュウキノウオユウスルチョウブンシポルフィリンナノリングトタザリガンドノアンテイフクゴウタイケイセイネツリキガクテキカイセキニヨルキコウカイメイ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10061/4709.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Uyar Z. Stable Complexation of Light-Harvesting Porphyrin Supramolecular Nanoring and Multidendate Ligands:Elucidation of Mechanism by Thermodynamic Insight : 光捕集機能を有する超分子ポルフィリンナノリングと多座リガンドの安定複合体形成：熱力学的解析による機構解明; ヒカリホシュウキノウオユウスルチョウブンシポルフィリンナノリングトタザリガンドノアンテイフクゴウタイケイセイネツリキガクテキカイセキニヨルキコウカイメイ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/4709

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

4. Fujisawa, Kaori. Construction of Giant Porphyrin Macrorings for Light-Harvesting Antennae : 光捕集アンテナを目指した巨大ポルフィリン環状体の構築; ヒカリホシュウアンテナオメザシタキョダイポルフィリンカンジョウタイノコウチク.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

URL: http://hdl.handle.net/10061/5228

Subjects/Keywords: porphyrin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Fujisawa, K. (n.d.). Construction of Giant Porphyrin Macrorings for Light-Harvesting Antennae : 光捕集アンテナを目指した巨大ポルフィリン環状体の構築; ヒカリホシュウアンテナオメザシタキョダイポルフィリンカンジョウタイノコウチク. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/5228

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Fujisawa, Kaori. “Construction of Giant Porphyrin Macrorings for Light-Harvesting Antennae : 光捕集アンテナを目指した巨大ポルフィリン環状体の構築; ヒカリホシュウアンテナオメザシタキョダイポルフィリンカンジョウタイノコウチク.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 15, 2021. http://hdl.handle.net/10061/5228.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Fujisawa, Kaori. “Construction of Giant Porphyrin Macrorings for Light-Harvesting Antennae : 光捕集アンテナを目指した巨大ポルフィリン環状体の構築; ヒカリホシュウアンテナオメザシタキョダイポルフィリンカンジョウタイノコウチク.” Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Fujisawa K. Construction of Giant Porphyrin Macrorings for Light-Harvesting Antennae : 光捕集アンテナを目指した巨大ポルフィリン環状体の構築; ヒカリホシュウアンテナオメザシタキョダイポルフィリンカンジョウタイノコウチク. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10061/5228.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Fujisawa K. Construction of Giant Porphyrin Macrorings for Light-Harvesting Antennae : 光捕集アンテナを目指した巨大ポルフィリン環状体の構築; ヒカリホシュウアンテナオメザシタキョダイポルフィリンカンジョウタイノコウチク. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/5228

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

University of Wollongong

5. Roach, Nicholas. Synthesis of Amphiphilic Porphyrins and Porphyrin Arrays.

Degree: PhD, 2016, University of Wollongong

URL: ; https://ro.uow.edu.au/theses/4941

► The natural photosynthetic systems utilise protein scaffolds to hold their components, which self assemble to form complex structures. Artificial protein maquettes offer the possibility… (more)

Subjects/Keywords: Porphyrin; Porphyrin array; }\mphiphilic; Maquette; Photosynthesis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Roach, N. (2016). Synthesis of Amphiphilic Porphyrins and Porphyrin Arrays. (Doctoral Dissertation). University of Wollongong. Retrieved from ; https://ro.uow.edu.au/theses/4941

Chicago Manual of Style (16^th Edition):

Roach, Nicholas. “Synthesis of Amphiphilic Porphyrins and Porphyrin Arrays.” 2016. Doctoral Dissertation, University of Wollongong. Accessed April 15, 2021. ; https://ro.uow.edu.au/theses/4941.

MLA Handbook (7^th Edition):

Roach, Nicholas. “Synthesis of Amphiphilic Porphyrins and Porphyrin Arrays.” 2016. Web. 15 Apr 2021.

Vancouver:

Roach N. Synthesis of Amphiphilic Porphyrins and Porphyrin Arrays. [Internet] [Doctoral dissertation]. University of Wollongong; 2016. [cited 2021 Apr 15]. Available from: ; https://ro.uow.edu.au/theses/4941.

Council of Science Editors:

Roach N. Synthesis of Amphiphilic Porphyrins and Porphyrin Arrays. [Doctoral Dissertation]. University of Wollongong; 2016. Available from: ; https://ro.uow.edu.au/theses/4941

North Carolina State University

6. Meneely, Kelly Rose. Synthesis of Substituted Bacteriochlorins.

Degree: MS, Chemistry, 2010, North Carolina State University

URL: http://www.lib.ncsu.edu/resolver/1840.16/6351

► The objective of this work is two-fold: first, to find new conditions to improve the condensation reactions leading to the macrocycles 3,13-dibromo-5-methoxybacteriochlorin (BC-Br3OMe5Br13) and 3,13-dibromobacteriochlorin… (more)

Subjects/Keywords: porphyrin; bacteriochlorin; chlorin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Meneely, K. R. (2010). Synthesis of Substituted Bacteriochlorins. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/6351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Meneely, Kelly Rose. “Synthesis of Substituted Bacteriochlorins.” 2010. Thesis, North Carolina State University. Accessed April 15, 2021. http://www.lib.ncsu.edu/resolver/1840.16/6351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Meneely, Kelly Rose. “Synthesis of Substituted Bacteriochlorins.” 2010. Web. 15 Apr 2021.

Vancouver:

Meneely KR. Synthesis of Substituted Bacteriochlorins. [Internet] [Thesis]. North Carolina State University; 2010. [cited 2021 Apr 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Meneely KR. Synthesis of Substituted Bacteriochlorins. [Thesis]. North Carolina State University; 2010. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

North Carolina State University

7. Gauger, Kelly Ann. Synthesis of Novel Chlorins and Carotenoid-Porphyrin Dyads.

Degree: MS, Chemistry, 2010, North Carolina State University

URL: http://www.lib.ncsu.edu/resolver/1840.16/6303

► The first part of this thesis discusses the synthesis of chlorins bearing electron donating groups in the 3-position. A 3-dimethylaminochlorin ZnC-(NMe2)3M10 was synthesized in 49%… (more)

Subjects/Keywords: porphyrin; carotenoid; chlorin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Gauger, K. A. (2010). Synthesis of Novel Chlorins and Carotenoid-Porphyrin Dyads. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/6303

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Gauger, Kelly Ann. “Synthesis of Novel Chlorins and Carotenoid-Porphyrin Dyads.” 2010. Thesis, North Carolina State University. Accessed April 15, 2021. http://www.lib.ncsu.edu/resolver/1840.16/6303.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Gauger, Kelly Ann. “Synthesis of Novel Chlorins and Carotenoid-Porphyrin Dyads.” 2010. Web. 15 Apr 2021.

Vancouver:

Gauger KA. Synthesis of Novel Chlorins and Carotenoid-Porphyrin Dyads. [Internet] [Thesis]. North Carolina State University; 2010. [cited 2021 Apr 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6303.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gauger KA. Synthesis of Novel Chlorins and Carotenoid-Porphyrin Dyads. [Thesis]. North Carolina State University; 2010. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6303

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Wollongong

8. Mitchell, Rhys Thomas. Synthesis of water soluble porphyrins and their applications.

Degree: PhD, 2016, University of Wollongong

URL: 0305 ORGANIC CHEMISTRY ; https://ro.uow.edu.au/theses/4798

► This thesis is focused on the generation of water soluble amphiphilic porphyrins for the creation of an artificial photosynthesis model. The development of functionalised… (more)

Subjects/Keywords: Porphyrin; Maquette; photosynthesis

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APA (6^th Edition):

Mitchell, R. T. (2016). Synthesis of water soluble porphyrins and their applications. (Doctoral Dissertation). University of Wollongong. Retrieved from 0305 ORGANIC CHEMISTRY ; https://ro.uow.edu.au/theses/4798

Chicago Manual of Style (16^th Edition):

Mitchell, Rhys Thomas. “Synthesis of water soluble porphyrins and their applications.” 2016. Doctoral Dissertation, University of Wollongong. Accessed April 15, 2021. 0305 ORGANIC CHEMISTRY ; https://ro.uow.edu.au/theses/4798.

MLA Handbook (7^th Edition):

Mitchell, Rhys Thomas. “Synthesis of water soluble porphyrins and their applications.” 2016. Web. 15 Apr 2021.

Vancouver:

Mitchell RT. Synthesis of water soluble porphyrins and their applications. [Internet] [Doctoral dissertation]. University of Wollongong; 2016. [cited 2021 Apr 15]. Available from: 0305 ORGANIC CHEMISTRY ; https://ro.uow.edu.au/theses/4798.

Council of Science Editors:

Mitchell RT. Synthesis of water soluble porphyrins and their applications. [Doctoral Dissertation]. University of Wollongong; 2016. Available from: 0305 ORGANIC CHEMISTRY ; https://ro.uow.edu.au/theses/4798

University of Minnesota

9. Fathi Rasekh, Mahtab. Synthesis and characterization of ruthenium (II) tetraphenylporphyrin with redox active axial ligands for molecular wires.

Degree: MS, Chemistry, 2016, University of Minnesota

URL: http://hdl.handle.net/11299/181831

► Four new ruthenium(II) tetraphenylporphyrin with redox active axially coordinated ligands including two new heterotrinuclear Fe-Ru-Fe complexes of the ruthenium(II) tetraphenylporphyrin axially coordinated with a pair… (more)

▼ Four new ruthenium(II) tetraphenylporphyrin with redox active axially coordinated ligands including two new heterotrinuclear Fe-Ru-Fe complexes of the ruthenium(II) tetraphenylporphyrin axially coordinated with a pair of isocyanoferrocene ((FcNC)2RuTPP) or 1,1'-diisocyanoferrocene (([C5H4NC]2Fe)2RuTPP) ligands [Fc = ferrocenyl, TPP = 5,10,15,20-tetraphenylporphyrinato(2-) anion], and two new isocyanoazulene containing complexes (2-CNAz)2RuTPP ( 2-CNAz = 2-isocyanoazulene) and (6-CNAz)2RuTPP ( 6-CNAz = 6-isocyanoazulene) were synthesized and characterized by UV-vis, MCD, NMR, and FTIR spectroscopies as well as by electrospray ionization mass spectrometry and single crystal X-ray diffraction. Isolation of insoluble polymeric {([C5H4NC]2Fe)RuTPP}n molecular wires was also achieved for the first time. The redox properties of the new trinuclear (FcNC)2RuTPP and ([C5H4NC]2Fe)2RuTPP complexes were probed using electrochemical (CV and DPV), spectroelectrochemical, and chemical oxidation methods and correlated to those of the bis(tert-butylisocyano)ruthenium(II) tetraphenylporphyrin reference compound, (t-BuNC)2RuTPP, as well as (2-CNAz)2RuTPP and (6-CNAz)2RuTPP complexes. In all cases, the first oxidation process was attributed to the reversible oxidation of the RuII center. The second and third reversible oxidation processes in (FcNC)2RuTPP are separated by ~100 mV and were assigned to two single-electron FeII/FeIII couples suggesting a weak long-range iron-iron coupling in this complex. Electrochemical data acquired for ([C5H4NC]2Fe)2RuTPP complex are complicated by the interaction between the axial 1-1,1'-diisocyanoferrocene ligand and the electrode surface as well as by axial ligand dissociation in solution. Spectroelectrochemical and chemical oxidation methods were used to elucidate spectroscopic signatures of the [(RCN)2RuTPP]n+ species in solution. In both (2-CNAz)2RuTPP and (6-CNAz)2RuTPP complexes, the first oxidation process was attributed to the reversible oxidation of RuII center and the second oxidation process was assigned to the reversible oxidation of porphyrin core. The third and fourth irreversible processes were assigned to the oxidation of two isocyanoazulene axially coordinated ligands. DFT and TDDFT calculations aided in correlating spectroscopic and redox properties of complexes with their electronic structures.

Subjects/Keywords: Porphyrin; Ruthenium; tetraphenylporphyrin

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APA (6^th Edition):

Fathi Rasekh, M. (2016). Synthesis and characterization of ruthenium (II) tetraphenylporphyrin with redox active axial ligands for molecular wires. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/181831

Chicago Manual of Style (16^th Edition):

Fathi Rasekh, Mahtab. “Synthesis and characterization of ruthenium (II) tetraphenylporphyrin with redox active axial ligands for molecular wires.” 2016. Masters Thesis, University of Minnesota. Accessed April 15, 2021. http://hdl.handle.net/11299/181831.

MLA Handbook (7^th Edition):

Fathi Rasekh, Mahtab. “Synthesis and characterization of ruthenium (II) tetraphenylporphyrin with redox active axial ligands for molecular wires.” 2016. Web. 15 Apr 2021.

Vancouver:

Fathi Rasekh M. Synthesis and characterization of ruthenium (II) tetraphenylporphyrin with redox active axial ligands for molecular wires. [Internet] [Masters thesis]. University of Minnesota; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11299/181831.

Council of Science Editors:

Fathi Rasekh M. Synthesis and characterization of ruthenium (II) tetraphenylporphyrin with redox active axial ligands for molecular wires. [Masters Thesis]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/181831

University of North Texas

10. Lin, Chunyu. Studies on the Porphyrin and Phthalocyanine Modified on Sno2 Photoelectrochemical Cells.

Degree: 2013, University of North Texas

URL: https://digital.library.unt.edu/ark:/67531/metadc407761/

► The world is facing a tough challenge regarding fulfilling human energy needs. Scientists are motivated to find alternative ways to the fossil fuel at a… (more)

Subjects/Keywords: DSSCs; porphyrin; pthalocyanine

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APA (6^th Edition):

Lin, C. (2013). Studies on the Porphyrin and Phthalocyanine Modified on Sno2 Photoelectrochemical Cells. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc407761/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Lin, Chunyu. “Studies on the Porphyrin and Phthalocyanine Modified on Sno2 Photoelectrochemical Cells.” 2013. Thesis, University of North Texas. Accessed April 15, 2021. https://digital.library.unt.edu/ark:/67531/metadc407761/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Lin, Chunyu. “Studies on the Porphyrin and Phthalocyanine Modified on Sno2 Photoelectrochemical Cells.” 2013. Web. 15 Apr 2021.

Vancouver:

Lin C. Studies on the Porphyrin and Phthalocyanine Modified on Sno2 Photoelectrochemical Cells. [Internet] [Thesis]. University of North Texas; 2013. [cited 2021 Apr 15]. Available from: https://digital.library.unt.edu/ark:/67531/metadc407761/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lin C. Studies on the Porphyrin and Phthalocyanine Modified on Sno2 Photoelectrochemical Cells. [Thesis]. University of North Texas; 2013. Available from: https://digital.library.unt.edu/ark:/67531/metadc407761/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

11. 永田, 直人. イミダゾリルポルフィリン組織体を用いた光合成アンテナシステムの構築と機能 : Construction and function of supramolecular assemblies formed from imidazolyl-substituted porphyrin toward photosynthetic antenna systems; イミダゾリルポルフィリンソシキタイオモチイタコウゴウセイアンテナシステムノコウチクトキノウ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

URL: http://hdl.handle.net/10061/4021

Subjects/Keywords: ポルフィリン (porphyrin)

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APA (6^th Edition):

永田, �. (n.d.). イミダゾリルポルフィリン組織体を用いた光合成アンテナシステムの構築と機能 : Construction and function of supramolecular assemblies formed from imidazolyl-substituted porphyrin toward photosynthetic antenna systems; イミダゾリルポルフィリンソシキタイオモチイタコウゴウセイアンテナシステムノコウチクトキノウ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/4021

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

永田, 直人. “イミダゾリルポルフィリン組織体を用いた光合成アンテナシステムの構築と機能 : Construction and function of supramolecular assemblies formed from imidazolyl-substituted porphyrin toward photosynthetic antenna systems; イミダゾリルポルフィリンソシキタイオモチイタコウゴウセイアンテナシステムノコウチクトキノウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 15, 2021. http://hdl.handle.net/10061/4021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

永田, 直人. “イミダゾリルポルフィリン組織体を用いた光合成アンテナシステムの構築と機能 : Construction and function of supramolecular assemblies formed from imidazolyl-substituted porphyrin toward photosynthetic antenna systems; イミダゾリルポルフィリンソシキタイオモチイタコウゴウセイアンテナシステムノコウチクトキノウ.” Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

永田 �. イミダゾリルポルフィリン組織体を用いた光合成アンテナシステムの構築と機能 : Construction and function of supramolecular assemblies formed from imidazolyl-substituted porphyrin toward photosynthetic antenna systems; イミダゾリルポルフィリンソシキタイオモチイタコウゴウセイアンテナシステムノコウチクトキノウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10061/4021.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

永田 �. イミダゾリルポルフィリン組織体を用いた光合成アンテナシステムの構築と機能 : Construction and function of supramolecular assemblies formed from imidazolyl-substituted porphyrin toward photosynthetic antenna systems; イミダゾリルポルフィリンソシキタイオモチイタコウゴウセイアンテナシステムノコウチクトキノウ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/4021

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

University of Minnesota

12. Purchel, Anatolii. Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins.

Degree: MS, Chemistry, 2013, University of Minnesota

URL: http://purl.umn.edu/160259

►

University of Minnesota M.S. thesis. August 2013. Major: Chemistry. Advisor: Dr. Victor Nemykin. 1 computer file (PDF); viii, 107 pages.

Nano-sized molecular-based platforms provide a… (more)

Subjects/Keywords: DFT; Porphyrin; Spectroelectrochemistry; Tetraazaporphyrin

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APA (6^th Edition):

Purchel, A. (2013). Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/160259

Chicago Manual of Style (16^th Edition):

Purchel, Anatolii. “Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins.” 2013. Masters Thesis, University of Minnesota. Accessed April 15, 2021. http://purl.umn.edu/160259.

MLA Handbook (7^th Edition):

Purchel, Anatolii. “Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins.” 2013. Web. 15 Apr 2021.

Vancouver:

Purchel A. Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2021 Apr 15]. Available from: http://purl.umn.edu/160259.

Council of Science Editors:

Purchel A. Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/160259

13. Mishra Bhupendra Ashok. Synthesis and Photocytotoxicity Studies of Some Novel Porphyrin Heterocycles;.

Degree: 2014, INFLIBNET

URL: http://shodhganga.inflibnet.ac.in/handle/10603/25703

►

Porphyrinoids have found promising applications as photosensitizers in photodynamic therapy and newlinephotodynamic imaging due to their unique absorption and emission properties in visible region 400800… (more)

▼

Porphyrinoids have found promising applications as photosensitizers in photodynamic therapy and newlinephotodynamic imaging due to their unique absorption and emission properties in visible region 400800 nm newlineAlso their ability to absorb light and transfer its energy to molecular oxygen to produce reactive oxygen newlinespecies ROS such as singlet oxygen and superoxide radicals which initiate a series of complex chemical and newlinebiological events that ultimately leads to cell death Porphyrins and metalloporphyrins are also ideal model newlinecompounds for studying light harvesting energy and electron transfer and redox catalysis This thesis newlinedescribes the synthesis absorptionemission and photocytotoxicity properties of some novel porphyrin newlineconjugates and porphyrinbased heterocycles newlineThe thesis entitled Synthesis and biological Studies of some novel porphyrins and their conjugates is divided newlineinto four chapters The first chapter Introduction provides some insight about natural occurrence of newlineporphyrins their nomenclature and photophysical properties A detailed review of classical synthetic routes to newlinethe most recent improvements to achieve simple as well as complex porphyrin systems has been provided newlineParticularly porphyrinbased photosensitizers currently in market and several others in clinical trials have also newlinebeen elaborated along with their mechanism of action newlineThe second chapter unveils design synthesis and photocytotoxicity studies of some cationic porphyrin newlineconjugates The work embodied in this chapter has been divided into four parts Part A Part B Part C and Part newlineD Part A reports an iodineIIImediated facile synthesis of 4and#8242;cyanophenylporphyrins from readily newlineavailable porphyrin thioamides Two novel cationic cyanoporphyrins displayed efficient photonuclease activity newline1 and#956;M and their absorption and emission studies

Advisors/Committee Members: Dalip Kumar.

Subjects/Keywords: Photocytotoxicity; Porphyrin Heterocycles; Synthesis

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APA (6^th Edition):

Ashok, M. B. (2014). Synthesis and Photocytotoxicity Studies of Some Novel Porphyrin Heterocycles;. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/25703

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Ashok, Mishra Bhupendra. “Synthesis and Photocytotoxicity Studies of Some Novel Porphyrin Heterocycles;.” 2014. Thesis, INFLIBNET. Accessed April 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/25703.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Ashok, Mishra Bhupendra. “Synthesis and Photocytotoxicity Studies of Some Novel Porphyrin Heterocycles;.” 2014. Web. 15 Apr 2021.

Vancouver:

Ashok MB. Synthesis and Photocytotoxicity Studies of Some Novel Porphyrin Heterocycles;. [Internet] [Thesis]. INFLIBNET; 2014. [cited 2021 Apr 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25703.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ashok MB. Synthesis and Photocytotoxicity Studies of Some Novel Porphyrin Heterocycles;. [Thesis]. INFLIBNET; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25703

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Texas A&M University

14. Wang, Kecheng. Synthesis of Porphyrinic Metal Organic Frameworks with High Robustness and Catalytic Activity.

Degree: PhD, Chemistry, 2017, Texas A&M University

URL: http://hdl.handle.net/1969.1/166070

► MOFs are ideal platforms to immobilize porphyrins and their derivatives. MOF’s high surface areas and rigid structures not only make porphyrin moieties approachable substrates but… (more)

▼ MOFs are ideal platforms to immobilize porphyrins and their derivatives. MOF’s high surface areas and rigid structures not only make porphyrin moieties approachable substrates but also prevent the dimerization of their active centers. These advantages effectively enhance the reactivity and optical performance of porphyrins. Extensive study has been done to synthesize porphyrinic MOFs, however, many of the previously reported porphyrinic MOFs suffer from weak chemical stabilities, which severely hinders their wide utilization. My study is focused on the design and syntheses of porphyrinic MOFs with high robustness in various chemical environments. Three porphyrinic MOFs with excellent chemical stability, namely PCN-600, PCN-601 and PCN-602, were obtained, and their performances as catalysts in different reactions were explored. PCN-600, a Fe-based mesoporous porphyrinic MOF was successfully synthesized through rational topological design and KTDA method. It exhibits high chemical stability in aqueous solutions with pH values ranging from 2 to 11. The catalytic activity of PCN-600(Fe) (with Fe³⁺ at the porphyrin center) was confirmed by its excellent performance in the co-oxidation of phenol and 4-aminoantipyrine (4-AAP) by H₂O₂. Most of the reported stable porphyrinic MOFs, including PCN-22Xs (X = 2, 3, 4, 5) and PCN-600, are constructed by high-valent metal ions and carboxylate-based porphyrinic ligands. Though these materials have very high robustness in acidic solutions, they are relatively vulnerable in aqueous solutions containing some coordinating anions, such as OH⁻, F⁻, CO₃²⁻ and PO₄³⁻. To address these problems, two iso-structural porphyrinic MOFs constructed by pyrazolate-terminated ligands were synthesized, namely PCN-601 and PCN-602. These materials exhibit extraordinary stability in the solutions of NaOH, KF, Na₂CO₃ and K₃PO₄. Their chemical stabilities were rationalized from both thermodynamic and kinetic perspectives. The catalytic performance of PCN-601(Mn) and PCN-602(Mn) (with Mn³⁺ at the coordination centers of the porphyrinic ligands) in C-H halogenation reactions was explored. Compared with PCN-601(Mn), PCN-602(Mn) has a higher porosity and displays a better activity as a recyclable hetergeneous catalyst. Advisors/Committee Members: Zhou, Hongcai (advisor), Dunbar, Kim (committee member), Lindahl, Paul (committee member), Jeong, Hae-Kwon (committee member).

Subjects/Keywords: MOFs; Porphyrin; Stability; Catalysts

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APA (6^th Edition):

Wang, K. (2017). Synthesis of Porphyrinic Metal Organic Frameworks with High Robustness and Catalytic Activity. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/166070

Chicago Manual of Style (16^th Edition):

Wang, Kecheng. “Synthesis of Porphyrinic Metal Organic Frameworks with High Robustness and Catalytic Activity.” 2017. Doctoral Dissertation, Texas A&M University. Accessed April 15, 2021. http://hdl.handle.net/1969.1/166070.

MLA Handbook (7^th Edition):

Wang, Kecheng. “Synthesis of Porphyrinic Metal Organic Frameworks with High Robustness and Catalytic Activity.” 2017. Web. 15 Apr 2021.

Vancouver:

Wang K. Synthesis of Porphyrinic Metal Organic Frameworks with High Robustness and Catalytic Activity. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1969.1/166070.

Council of Science Editors:

Wang K. Synthesis of Porphyrinic Metal Organic Frameworks with High Robustness and Catalytic Activity. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/166070

University of North Texas

15. Hu, Yi. Synthesis and Characterization of β-Functionalized π-Extended Porphyrins.

Degree: 2019, University of North Texas

URL: https://digital.library.unt.edu/ark:/67531/metadc1609167/

► Porphyrins with extended π-electronic networks are promising candidates for a wide range of applications from medicine to nanotechnology owing to their unique optical and electronic… (more)

Subjects/Keywords: β-Functionalized porphyrin; Synthesis

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APA (6^th Edition):

Hu, Y. (2019). Synthesis and Characterization of β-Functionalized π-Extended Porphyrins. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc1609167/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Hu, Yi. “Synthesis and Characterization of β-Functionalized π-Extended Porphyrins.” 2019. Thesis, University of North Texas. Accessed April 15, 2021. https://digital.library.unt.edu/ark:/67531/metadc1609167/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Hu, Yi. “Synthesis and Characterization of β-Functionalized π-Extended Porphyrins.” 2019. Web. 15 Apr 2021.

Vancouver:

Hu Y. Synthesis and Characterization of β-Functionalized π-Extended Porphyrins. [Internet] [Thesis]. University of North Texas; 2019. [cited 2021 Apr 15]. Available from: https://digital.library.unt.edu/ark:/67531/metadc1609167/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hu Y. Synthesis and Characterization of β-Functionalized π-Extended Porphyrins. [Thesis]. University of North Texas; 2019. Available from: https://digital.library.unt.edu/ark:/67531/metadc1609167/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Houston

16. Fang, Yuanyuan 1984-. Electrochemisty, Spectroelectrochemistry And/Or Electrosynthesis of Pi-Extended Porphyrins in Nonaqueous Media.

Degree: PhD, Chemistry, 2014, University of Houston

URL: http://hdl.handle.net/10657/5356

► This dissertation presents the electrochemistry, spectroelectrochemistry and electrosynthesis of pi-extended porphyrins. The electrochemistry and UV-vis spectral properties of neutral and protonated Au(III) quinoxalinoporphyrins containing one… (more)

Subjects/Keywords: Electrochemistry; Spectroelectrochemistry; Extended porphyrin

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APA (6^th Edition):

Fang, Y. 1. (2014). Electrochemisty, Spectroelectrochemistry And/Or Electrosynthesis of Pi-Extended Porphyrins in Nonaqueous Media. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/5356

Chicago Manual of Style (16^th Edition):

Fang, Yuanyuan 1984-. “Electrochemisty, Spectroelectrochemistry And/Or Electrosynthesis of Pi-Extended Porphyrins in Nonaqueous Media.” 2014. Doctoral Dissertation, University of Houston. Accessed April 15, 2021. http://hdl.handle.net/10657/5356.

MLA Handbook (7^th Edition):

Fang, Yuanyuan 1984-. “Electrochemisty, Spectroelectrochemistry And/Or Electrosynthesis of Pi-Extended Porphyrins in Nonaqueous Media.” 2014. Web. 15 Apr 2021.

Vancouver:

Fang Y1. Electrochemisty, Spectroelectrochemistry And/Or Electrosynthesis of Pi-Extended Porphyrins in Nonaqueous Media. [Internet] [Doctoral dissertation]. University of Houston; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10657/5356.

Council of Science Editors:

Fang Y1. Electrochemisty, Spectroelectrochemistry And/Or Electrosynthesis of Pi-Extended Porphyrins in Nonaqueous Media. [Doctoral Dissertation]. University of Houston; 2014. Available from: http://hdl.handle.net/10657/5356

University of Illinois – Urbana-Champaign

17. Kemling, Jonathan W. Artificial and mammalian olfaction and low-coordinate metalloporphyrin complexes.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

URL: http://hdl.handle.net/2142/26291

► Part 1 A low-cost yet highly sensitive colorimetric sensor array for the detection and identification of toxic industrial chemicals (TICs) has been developed. The sensor… (more)

▼ Part 1 A low-cost yet highly sensitive colorimetric sensor array for the detection and identification of toxic industrial chemicals (TICs) has been developed. The sensor consists of a disposable array of cross-responsive nanoporous pigments whose colors are changed by diverse chemical interactions with analytes. Clear differentiation among 20 different TICs has been easily achieved at both their IDLH (immediately dangerous to life or health) concentration within two minutes of exposure, and PEL (permissible exposure limits) concentration within five minutes of exposure with no errors or misclassifications. Detection limits are generally well below the PEL (in most cases below 5% of PEL) and are typically in the low ppb range for the analytes tested. The colorimetric sensor array is not responsive to changes in humidity or temperature over a substantial range and shows excellent batch to batch reproducibility and long shelf-life (greater than 3 months). Part 2 The sense of smell is arguably the least understood of our senses, and the activation mechanism for olfactory receptors is still unclear. Previous work has suggested that vertebrate olfactory receptors are metalloproteins, utilizing metal ion ligation in an extracellular loop as a primary interaction with odorants. A highly conserved metal ion binding motif, HXXC[D,E], has been found to be present in 62-77% of all mammalian olfactory receptors and an alternative sequence, QXXC[D,E], is present in 76-91% of birds, while neither is found in other G protein-coupled receptors. This suggests an important role for odorant binding to metal ions in olfactory signaling. Part 3 Highly sterically hindered bis-pocket siloxy porphyrins were synthesized to isolate the four-coordinate porphyrin species for the first time. Previous work in the Suslick group has focused on four-coordinate Iron(III) species, however, these porphyrins showed no unique chemical reactivities for small molecule or C-H activation. A number of different four-coordinate species (Manganeese(III), Chromium(III) and Cobalt(III)) with varying electronic properties were synthesized and characterized in an effort to explore the reactivities of these coordinatively-unsaturated compounds. Advisors/Committee Members: Suslick, Kenneth S. (advisor), Kenneth S. Suslick (Committee Chair), Bailey, Ryan C. (committee member), Lu, Yi (committee member), Luthey-Schulten, Zaida A. (committee member).

Subjects/Keywords: colorimetric; sensors; olfaction; porphyrin

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APA (6^th Edition):

Kemling, J. W. (2011). Artificial and mammalian olfaction and low-coordinate metalloporphyrin complexes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26291

Chicago Manual of Style (16^th Edition):

Kemling, Jonathan W. “Artificial and mammalian olfaction and low-coordinate metalloporphyrin complexes.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 15, 2021. http://hdl.handle.net/2142/26291.

MLA Handbook (7^th Edition):

Kemling, Jonathan W. “Artificial and mammalian olfaction and low-coordinate metalloporphyrin complexes.” 2011. Web. 15 Apr 2021.

Vancouver:

Kemling JW. Artificial and mammalian olfaction and low-coordinate metalloporphyrin complexes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2142/26291.

Council of Science Editors:

Kemling JW. Artificial and mammalian olfaction and low-coordinate metalloporphyrin complexes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26291

University of Minnesota

18. Purchel, Anatolii. Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins.

Degree: MS, Chemistry, 2013, University of Minnesota

URL: http://purl.umn.edu/160259

► Nano-sized molecular-based platforms provide a promising approach to materials which can be used in optoelectronics, switchable redox-driven devices, and dye-sensitized solar cells (DSSC), as well… (more)

Subjects/Keywords: DFT; Porphyrin; Spectroelectrochemistry; Tetraazaporphyrin

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APA (6^th Edition):

Purchel, A. (2013). Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/160259

Chicago Manual of Style (16^th Edition):

Purchel, Anatolii. “Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins.” 2013. Masters Thesis, University of Minnesota. Accessed April 15, 2021. http://purl.umn.edu/160259.

MLA Handbook (7^th Edition):

Purchel, Anatolii. “Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins.” 2013. Web. 15 Apr 2021.

Vancouver:

Purchel A. Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2021 Apr 15]. Available from: http://purl.umn.edu/160259.

Council of Science Editors:

Purchel A. Synthesis and characterization of ferrocenyl-containing porphyrins and tetraazaporphyrins. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/160259

University of Minnesota

19. Hinke, Jonathan Arthur. Excited state dynamics of metalloporphyrins utilized in optoelectronic devices.

Degree: PhD, Chemical Physics, 2013, University of Minnesota

URL: http://purl.umn.edu/158327

► Energy consumption in the world is currently dominated by fossil fuels (85%) which include coal, gas, and oil while photovoltaics constitute a small portion (0.1%).… (more)

▼ Energy consumption in the world is currently dominated by fossil fuels (85%) which include coal, gas, and oil while photovoltaics constitute a small portion (0.1%). The hotovoltaic market is primarily comprised of silicon based photovoltaics which are currently unable to compete with fossil fuels in cost per kilowatt hour. However, emerging organic photovoltaics (OPVs) have shown potential to be surpass silicon based photovoltaics and be cost competitive with fossil fuels. One of the limitations in OPVs is the short diffusion length (10 nm) relative to the absorbing layer thickness (100-200 nm). Porphyrins, of which chlorophylls are derivatives, remain at the forefront of OPV investigation due to their success in natural photosynthesis and potential in photovoltaic devices. Furthermore, platinum octaethyl porphyrin (PtOEP) has been estimated to have a diusion length between 18-30 nm and long triplet lifetime (100 microsecondss). This long diffusion length indicates that platinum porphyrins are able to efficiently funnel excitons to the interface, showing promise as suitable donor materials. Other porphyrins, such as nickel, palladium, tin, and indium show similar properties including strong absorption, enhanced excited state lifetimes, and charge separated states. This thesis investigates the excited state properties of porphyrin materials. Ultrafast pump probe spectroscopy allows for investigation of excited state dynamics including intramolecular energy transfer observed in nickel porphyrins. Femtosecond dynamics of palladium and platinum porphyrins are explored as well as triplet fusion in PtOEP neat films, providing a unique way to study energy transfer and amorphous films. Finally, pump probe studies aim to explain photoluminescent quenching behavior in tin and indium porphyrins through observation of charge separated states. Investigation of these porphyrins is crucial to improving device efficiency through fundamental understanding of the excited state dynamics in films and neat films.

Subjects/Keywords: Dynamics; Excited; Porphyrin; Sectroscopy; Ultrafast

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APA (6^th Edition):

Hinke, J. A. (2013). Excited state dynamics of metalloporphyrins utilized in optoelectronic devices. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/158327

Chicago Manual of Style (16^th Edition):

Hinke, Jonathan Arthur. “Excited state dynamics of metalloporphyrins utilized in optoelectronic devices.” 2013. Doctoral Dissertation, University of Minnesota. Accessed April 15, 2021. http://purl.umn.edu/158327.

MLA Handbook (7^th Edition):

Hinke, Jonathan Arthur. “Excited state dynamics of metalloporphyrins utilized in optoelectronic devices.” 2013. Web. 15 Apr 2021.

Vancouver:

Hinke JA. Excited state dynamics of metalloporphyrins utilized in optoelectronic devices. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2021 Apr 15]. Available from: http://purl.umn.edu/158327.

Council of Science Editors:

Hinke JA. Excited state dynamics of metalloporphyrins utilized in optoelectronic devices. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://purl.umn.edu/158327

University of Georgia

20. Butler, Angil. The synthesis of meso-substituted porphyrins: reaction conditions and substituent effects.

Degree: 2014, University of Georgia

URL: http://hdl.handle.net/10724/20295

► The purpose of this study is to gain a better understanding of the parameters governing the synthesis of meso-substituted porphyrins. As a result of doing… (more)

Subjects/Keywords: Porphyrin; Synthesis; BF3-Aldehyde Complex

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APA (6^th Edition):

Butler, A. (2014). The synthesis of meso-substituted porphyrins: reaction conditions and substituent effects. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/20295

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Butler, Angil. “The synthesis of meso-substituted porphyrins: reaction conditions and substituent effects.” 2014. Thesis, University of Georgia. Accessed April 15, 2021. http://hdl.handle.net/10724/20295.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Butler, Angil. “The synthesis of meso-substituted porphyrins: reaction conditions and substituent effects.” 2014. Web. 15 Apr 2021.

Vancouver:

Butler A. The synthesis of meso-substituted porphyrins: reaction conditions and substituent effects. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10724/20295.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Butler A. The synthesis of meso-substituted porphyrins: reaction conditions and substituent effects. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/20295

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Texas – Austin

21. -8140-8646. Synthesis and anticancer activity of water soluble porphyrin.

Degree: MA, Chemistry, 2015, University of Texas – Austin

URL: http://hdl.handle.net/2152/34059

► As resistance to traditional chemotherapies increases, there is a concurrent need for novel therapies. Much work has been devoted the development of gold(III) treatments, however… (more)

Subjects/Keywords: Gold; Porphyrin; Water-soluble

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APA (6^th Edition):

-8140-8646. (2015). Synthesis and anticancer activity of water soluble porphyrin. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/34059

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16^th Edition):

-8140-8646. “Synthesis and anticancer activity of water soluble porphyrin.” 2015. Masters Thesis, University of Texas – Austin. Accessed April 15, 2021. http://hdl.handle.net/2152/34059.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7^th Edition):

-8140-8646. “Synthesis and anticancer activity of water soluble porphyrin.” 2015. Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8140-8646. Synthesis and anticancer activity of water soluble porphyrin. [Internet] [Masters thesis]. University of Texas – Austin; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152/34059.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8140-8646. Synthesis and anticancer activity of water soluble porphyrin. [Masters Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/34059

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Texas A&M University

22. Sun, Yujia. Construction of Highly Stable Metal-Organic Frameworks with Multiple Functionalities.

Degree: PhD, Chemistry, 2018, Texas A&M University

URL: http://hdl.handle.net/1969.1/174404

► Metal-organic frameworks (MOFs) are a class of newly emerged crystalline porous materials consisting of metal ions or clusters and organic linkers. Through judicious choice of… (more)

▼ Metal-organic frameworks (MOFs) are a class of newly emerged crystalline porous materials consisting of metal ions or clusters and organic linkers. Through judicious choice of inorganic joints and organic struts, the structure, porosity and functionality of MOFs can be tuned. However, the lack of high stability of most of the reported MOFs as well as limited methods to introduce multiple functionalities into the framework hinders the exploration of MOFs towards a wide variety of potential applications. The main goal of this research is to develop synthetic strategies to construct MOFs with high stability and multiple functionalities. Firstly, a brief introduction of MOFs was provided, focusing on strategies to increase their stability and introduce functionalities. Secondly, a facile one-pot synthetic strategy was developed to introduce porphyrin into highly stable UiO-66 homogeneously. The crystal structure, morphology, and ultrahigh chemical stability of UiO-66 were well maintained in the functionalized MOFs. In addition, the amount of integrated porphyrin can be gradually tuned. Thirdly, a general in situ secondary ligand incorporation (ISLI) strategy was investigated to synthesize multivariate UiO series of MOFs. Both experimental and computational studies were carried out to understand the chemistry behind this strategy. Fourthly, ISLI strategy was further applied in highly stable Zr-MOFs constructed from multitopic ligands to incorporate multiple functionalities. Fifthly, a porphyrin and pyrene-based mixed-ligand MOF with high stability and novel topology was synthesized. This MOF provides an ideal platform for further functionalization and exploration of new structures. In summary, different strategies were investigated to construct highly stable MOFs with the incorporation of multiple functionalities. These studies provide useful tools to explore stable MOFs with desired multifunctionality for potential applications. Advisors/Committee Members: Zhou, Hongcai (advisor), Clearfield, Abraham (advisor), Lindahl, Paul (committee member), Grunlan, Jaime (committee member).

Subjects/Keywords: Metal-Organic Frameworks; Porphyrin; Multifunctionality

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APA (6^th Edition):

Sun, Y. (2018). Construction of Highly Stable Metal-Organic Frameworks with Multiple Functionalities. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174404

Chicago Manual of Style (16^th Edition):

Sun, Yujia. “Construction of Highly Stable Metal-Organic Frameworks with Multiple Functionalities.” 2018. Doctoral Dissertation, Texas A&M University. Accessed April 15, 2021. http://hdl.handle.net/1969.1/174404.

MLA Handbook (7^th Edition):

Sun, Yujia. “Construction of Highly Stable Metal-Organic Frameworks with Multiple Functionalities.” 2018. Web. 15 Apr 2021.

Vancouver:

Sun Y. Construction of Highly Stable Metal-Organic Frameworks with Multiple Functionalities. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1969.1/174404.

Council of Science Editors:

Sun Y. Construction of Highly Stable Metal-Organic Frameworks with Multiple Functionalities. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/174404

RMIT University

23. La, D. Porphyrin-based nanomaterials and their applications for photocatalysis.

Degree: 2017, RMIT University

URL: http://researchbank.rmit.edu.au/view/rmit:162278

► The design and fabrication of organic-based supramolecular nanoassemblies is a powerful method for the fabrication of nanostructured materials with tunable morphologies. The resulting materials often… (more)

▼ The design and fabrication of organic-based supramolecular nanoassemblies is a powerful method for the fabrication of nanostructured materials with tunable morphologies. The resulting materials often have unique optical and electronic properties, which can be used for potential applications including but not limited to, optoelectronic nanodevices, energy storage, catalysis, sensors, and photonics. Among the numerous organic-based supramolecular nanoassemblies described in the literature, -conjugated porphyrins have attracted great attention as organic building blocks for the construction of soft materials. Porphyrin-based nanomaterials in particular have been extensively studied for visible-light photocatalysis due to their intrinsic optical properties. This thesis describes the synthesis of Porphyrin derived nanostructures, and reports on their properties, using a variety of methods. A particular focus is the design and fabrication of composite materials, which combine the properties of self assembled porphyrins with other materials. Firstly, a facile synthetic protocol to grow thin films of Cu(II) tetrakis(4-carboxyphenyl)porphyrin (CuTCPP) metal-organic frameworks (MOF) from a tetrakis(4-carboxyphenyl)porphyrin (H2TCPP) solution and a Cu(OH)2 nanoneedle array formed on a Cu substrate at room temperature is described. The formation of Cu-centered TCPP ligands and crystalline platelet-like Cu MOFs were characterised by SEM, XRD, FTIR, UV-vis, and XPS. The formation process from Cu(OH)2 was monitored by using SEM images obtained at different reaction times during the first 24 h, allowing the proposal of a possible reaction pathway involving Cu(OH)2 dissolution followed by the reprecipitation of CuTCPP MOFs at the near surface. By using self-assembly with the assistance of Arginine porphyrin, (TCPP)-based supramolecular nanobelts are produced that show enhanced photocatalytic activity for the photodegradation of pollutant Rhodamine B under simulated visible-light. Graphene has received considerable attention as a platform for studies concerning photocatalytic activity due to favorable properties imparted by its 2D geometry and large surface area. Graphene-based materials have shown excellent charge transfer properties, and have also been used as a scaffold for enhancement the photocatalytic activity of semiconductors. Hence, in this thesis, graphene is used as a substrate for porphyrin nanomaterials for enhanced photocatalytic performance. An industrial-scale method of mass production of graphene nanoplatelets is developed by chemical exfoliation of natural graphite flakes in a single step using sodium persulfate and sulphuric acid at room temperature followed by washing with dry acetone. The produced GNPs (~100%) are tens of microns in diameter with a thickness of around 10-20 nm. The structure of the so-formed GNPs was confirmed by SEM, TEM, and AFM microscopy. Using these good quality graphene nanoplates, well-dispersed porphyrin nanorods were assembled of the GNPs by surfactant-assisted self-assembly of tetrakis…

Subjects/Keywords: Fields of Research; porphyrin-based nanomaterials; porphyrin; graphene; hybrid nanomaterials; Photocatalysis

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APA (6^th Edition):

La, D. (2017). Porphyrin-based nanomaterials and their applications for photocatalysis. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:162278

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

La, D. “Porphyrin-based nanomaterials and their applications for photocatalysis.” 2017. Thesis, RMIT University. Accessed April 15, 2021. http://researchbank.rmit.edu.au/view/rmit:162278.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

La, D. “Porphyrin-based nanomaterials and their applications for photocatalysis.” 2017. Web. 15 Apr 2021.

Vancouver:

La D. Porphyrin-based nanomaterials and their applications for photocatalysis. [Internet] [Thesis]. RMIT University; 2017. [cited 2021 Apr 15]. Available from: http://researchbank.rmit.edu.au/view/rmit:162278.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

La D. Porphyrin-based nanomaterials and their applications for photocatalysis. [Thesis]. RMIT University; 2017. Available from: http://researchbank.rmit.edu.au/view/rmit:162278

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Anna University

24. Sujatha V. Studies on metal tolerant bacteria and applications of porphyrin derivatives;.

Degree: 2013, Anna University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/11502

►

Metal resistant property of an isolate from Brassica oleracea var. capitata (Cabbage) was studied for the first time. Among the isolates, the strain PGSV4207 showed… (more)

▼

Metal resistant property of an isolate from Brassica oleracea var. capitata (Cabbage) was studied for the first time. Among the isolates, the strain PGSV4207 showed heavy metal tolerance at high concentrations. This potent isolate was identified as Pseudomonas aeruginosa by morphological observation, biochemical and physiological characterization and was further confirmed by 16S rDNA sequence analysis (NCBI Accession no. EU732606). The uptake of heavy metals like cadmium, lead, nickel and zinc was confirmed by atomic absorption spectroscopic studies (AAS). We have analysed the isolate PGSV4207 for lipase production and the protein was purified by ammonium sulphate precipitation followed by hydrophobic interaction chromatography. We have used tetrakis-(4-sulphanato)-phenyl porphyrin (TPPS) to study the aggregation of Candida rugosa lipase and P.aeruginosa lipase in Native gel. This method overcomes protein aggregation that occurs when native PAGE is used to study these proteins. We have developed a method for in-gel staining of proteins using tetrakis (4-sulphonato phenyl) porphyrin (TPPS). This method is inexpensive, easy to perform and also aids in efficient recovery of protein from Native-PAGE for further analysis. Advantage of TPPS in protein identification is that it does not involve the problem of post-electrophoretic techniques. The substrate triacetin is broken down into acetic acid by the lipolytic activity and the drop in pH brings changes TPPS from green to red. This change can be visualized by naked eye as well as by spectrophotometric analysis. Live-cell imaging requires the use of non-cytotoxic dyes at low concentrations at non-harmful visible wavelengths. TPPS was used as a stain to visualize Pseudomonas aeruginosa and Bacillus cereus using fluorescent microscopy. TPPS was effectively used to analyse two strains of bacteria. The variation of brightness with varying concentrations of TPPS was studied and Bacillus was found to have consistently higher brightness. newline newline newline

None

Advisors/Committee Members: Gautam, P..

Subjects/Keywords: Metal; bacteria; porphyrin derivatives; cabage; tetrakis porphyrin (TPPS)

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APA (6^th Edition):

V, S. (2013). Studies on metal tolerant bacteria and applications of porphyrin derivatives;. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/11502

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

V, Sujatha. “Studies on metal tolerant bacteria and applications of porphyrin derivatives;.” 2013. Thesis, Anna University. Accessed April 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/11502.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

V, Sujatha. “Studies on metal tolerant bacteria and applications of porphyrin derivatives;.” 2013. Web. 15 Apr 2021.

Vancouver:

V S. Studies on metal tolerant bacteria and applications of porphyrin derivatives;. [Internet] [Thesis]. Anna University; 2013. [cited 2021 Apr 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/11502.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

V S. Studies on metal tolerant bacteria and applications of porphyrin derivatives;. [Thesis]. Anna University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/11502

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Houston

25. Jiang, Xiaoqin 1989-. Electrochemistry of Porphyrinoids and Tetrapyrrole Triple-Decker Complexes.

Degree: PhD, Chemistry, 2016, University of Houston

URL: http://hdl.handle.net/10657/4861

► This dissertation describes the electrochemistry and spectroelectrochemistry of porphyrinoids and tetrapyrrole triple-decker complexes, which were examined in nonaqueous media using electrochemical techniques in combination with… (more)

▼ This dissertation describes the electrochemistry and spectroelectrochemistry of porphyrinoids and tetrapyrrole triple-decker complexes, which were examined in nonaqueous media using electrochemical techniques in combination with spectroelectrochemical analysis as a function of the central metal ions, the axial ligands, the π-conjugated macrocycles, the peripheral substituents as well as solution conditions. Examined macrocyclic compounds in this dissertation are (i) meso-nitrophenyl metalloporphyrins; (ii) meso-diphosphorylated metalloporphyrins; (iii) unsymmetrical mono-benzoporphyrins; (iv) push-pull opp-dibenzoporphyrins; (v) phthalocyanine-corrole and phthalocyanine-porphyrin triple-decker complexes. In addition to two ring-centered reductions and two ring-centered oxidations, the meso-nitrophenyl metalloporphyrins exhibit reductions of the electroactive NO2Ph groups with a first reversible one-electron-addition followed by one or more irreversible reductions at more negative potentials. The meso-diphosphrylated porphyrins exhibit a slow chemical reaction after the second ring-centered reduction, forming a redox-active phlorin anion which can either be re-oxidized back to the initial porphyrin or be further reduced to form the phlorin dianion. The β, β’-fused mono-benzoporphyrin and opp-dibenzoporphyrin possess smaller HOMO-LUMO gaps and red-shifted and broadened absorption bands compared to those of the corresponding non-benzo porphyrin derivatives, due to the extension of the π-system. The Pc-M-Cor-M-Pc triple-decker complexes bearing nitrophenyl groups on the corrole unit exhibit 5 oxidations and 3-5 reductions depending on the number of the redox-active NO2Ph groups. However, the Pc-M-Pc-M-Por triple-deckers exhibit 4 oxidations and 3 reductions with the first oxidation and the first reduction both being assigned as a one-electron-transfer process on the Pc macrocycle. Advisors/Committee Members: Kadish, Karl M. (advisor), Czernuszewicz, Roman S. (committee member), Baldelli, Steven (committee member), Guloy, Arnold M. (committee member), Briggs, James M. (committee member).

Subjects/Keywords: Electrochemistry; Spectroelectrochemistry; Porphyrinoids; Tetrapyrrole triple-decker complexes; Nitrophenyl porphyrin; Phosphorylate porphyrin; Benzoporphyrin; Phthalocyanine/porphyrin triple-deckers; Phthalocyanine/corrole triple-deckers

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APA (6^th Edition):

Jiang, X. 1. (2016). Electrochemistry of Porphyrinoids and Tetrapyrrole Triple-Decker Complexes. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/4861

Chicago Manual of Style (16^th Edition):

Jiang, Xiaoqin 1989-. “Electrochemistry of Porphyrinoids and Tetrapyrrole Triple-Decker Complexes.” 2016. Doctoral Dissertation, University of Houston. Accessed April 15, 2021. http://hdl.handle.net/10657/4861.

MLA Handbook (7^th Edition):

Jiang, Xiaoqin 1989-. “Electrochemistry of Porphyrinoids and Tetrapyrrole Triple-Decker Complexes.” 2016. Web. 15 Apr 2021.

Vancouver:

Jiang X1. Electrochemistry of Porphyrinoids and Tetrapyrrole Triple-Decker Complexes. [Internet] [Doctoral dissertation]. University of Houston; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10657/4861.

Council of Science Editors:

Jiang X1. Electrochemistry of Porphyrinoids and Tetrapyrrole Triple-Decker Complexes. [Doctoral Dissertation]. University of Houston; 2016. Available from: http://hdl.handle.net/10657/4861

26. Thomas, Ajesh P. N confused porphyrin derivatives: syntheses tautomeric existence exchange, aggregation properties and photodynamic therapy; -.

Degree: Chemical science, 2014, INFLIBNET

URL: http://shodhganga.inflibnet.ac.in/handle/10603/37482

None

Reference p.186 - 200

Advisors/Committee Members: Srinivasan, A.

Subjects/Keywords: confused; derivatives; porphyrin

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APA (6^th Edition):

Thomas, A. P. (2014). N confused porphyrin derivatives: syntheses tautomeric existence exchange, aggregation properties and photodynamic therapy; -. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/37482

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Thomas, Ajesh P. “N confused porphyrin derivatives: syntheses tautomeric existence exchange, aggregation properties and photodynamic therapy; -.” 2014. Thesis, INFLIBNET. Accessed April 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/37482.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Thomas, Ajesh P. “N confused porphyrin derivatives: syntheses tautomeric existence exchange, aggregation properties and photodynamic therapy; -.” 2014. Web. 15 Apr 2021.

Vancouver:

Thomas AP. N confused porphyrin derivatives: syntheses tautomeric existence exchange, aggregation properties and photodynamic therapy; -. [Internet] [Thesis]. INFLIBNET; 2014. [cited 2021 Apr 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37482.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Thomas AP. N confused porphyrin derivatives: syntheses tautomeric existence exchange, aggregation properties and photodynamic therapy; -. [Thesis]. INFLIBNET; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37482

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Universidade do Estado do Rio de Janeiro

27. Gabriela Batista Alves. Produção de porfirinas por corynebacterium diphtheriae.

Degree: Master, 2009, Universidade do Estado do Rio de Janeiro

URL: http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=3052 ;

►

A produção de porfirinas por Corynebacterium diphtheriae é um objeto de estudo antigo, porém pouco explorado em Química e Ciências Médicas. O presente trabalho teve… (more)

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A produção de porfirinas por Corynebacterium diphtheriae é um objeto de estudo antigo, porém pouco explorado em Química e Ciências Médicas. O presente trabalho teve como objetivos comparar a influência de diferentes meios de cultura na produção de porfirinas por Corynebacterium diphtheriae, determinar a influencia da concentração do ferro na produção de porfirina, comparar quantitativamente a produção de porfirinas por diferentes amostras de bacilo diftérico e caracterizar químicamente os tipos de porfirinas produzidas. As técnicas utilizadas para isso foram a espectroscopia de absorção UV-visível e de fluorescência. O meio de cultura descrito por Mueller (1939), para a produção de toxina, se mostrou mais eficiente que o meio B de king, utilizado no diagnóstico laboratorial da difteria. A concentração de ferro no cultivo de Corynebacterium diphtheriae influencia a produção de porfirina. Altas concentrações de ferro inibem a produção de porfirina. A concentração de ferro onde a produção de porfirinas é máxima é de 0,20g/mL. Dentre as 11 amostras de bacilo diftérico estudadas, a amostra HC03, fermentadora de sacarose e toxinogênica, isolada de um caso de endocardite, foi a maior produtora de porfirina. A amostra ATCC de Corynebacterium ulcerans, não fermentadora de sacarose e toxinogênica, foi a amostra que produziu menos porfirina. Todas as 11 amostras apresentaram o mesmo perfil de espectro de fluorescência, sugerindo que a porfirina produzida seja a mesma nas amostras pesquisadas. As análises feitas para a caracterização do tipo de porfirina produzida levam a crer que esta seja uma coproporfirina. Os espectros de absorção e fluorescência não permitem porém determinar o(s) isômero(s) presente(s).

Porphyrin production by Corynebacterium diphtheriae is an old research interest but less attention has been given to the subject in the areas of chemistry and medical sciences. The object of this study is to compare the influence of different culture media in the production of porphyrins by Corynebacterium diphtheriae, to determine the iron concentration influence, to compare quantitatively the production of porphyrins by different samples of diphtheria bacilli and to characterize the porphyrins identities. UV-visible absorption and fluorescence spectroscopies were chosen as analytical tools. The culture medium described by Mueller (1939), for the production of toxin, was more efficient than the medium B of King, used in the laboratory diagnosis of diphtheria. The iron concentration in the cultivation of Corynebacterium diphtheriae influence the production of porphyrin. High concentrations inhibit their production. The iron concentration for maximum production of porphyrins is 0.20  g / mL. Among the 11 studied diphtheria bacillus, the sample HC03, fermented sucrose and toxinogenic, isolated from a case of endocarditis, was the largest producer of porphyrin. The sample of Corynebacterium ulcerans ATCC, unfermented sucrose and toxinogenic was the sample that produced less. All 11 samples showed the same…

Advisors/Committee Members: Raphael Hirata Júnior, Ana Luiza de Mattos Guaraldi, André Luiz Barboza Formiga, Juliano Alves Bonacin.

Subjects/Keywords: QUIMICA; porfirinas, Corynebacterium diphtheriae; porphyrin; Corynebacterium diphtheriae

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APA (6^th Edition):

Alves, G. B. (2009). Produção de porfirinas por corynebacterium diphtheriae. (Masters Thesis). Universidade do Estado do Rio de Janeiro. Retrieved from http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=3052 ;

Chicago Manual of Style (16^th Edition):

Alves, Gabriela Batista. “Produção de porfirinas por corynebacterium diphtheriae.” 2009. Masters Thesis, Universidade do Estado do Rio de Janeiro. Accessed April 15, 2021. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=3052 ;.

MLA Handbook (7^th Edition):

Alves, Gabriela Batista. “Produção de porfirinas por corynebacterium diphtheriae.” 2009. Web. 15 Apr 2021.

Vancouver:

Alves GB. Produção de porfirinas por corynebacterium diphtheriae. [Internet] [Masters thesis]. Universidade do Estado do Rio de Janeiro; 2009. [cited 2021 Apr 15]. Available from: http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=3052 ;.

Council of Science Editors:

Alves GB. Produção de porfirinas por corynebacterium diphtheriae. [Masters Thesis]. Universidade do Estado do Rio de Janeiro; 2009. Available from: http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=3052 ;

Stellenbosch University

28. Mongwaketsi, Nametso Precious. Studies on porphyrin-based nanorods for artificial light harvesting applications.

Degree: PhD, Chemistry and Polymer Science, 2014, Stellenbosch University

URL: http://hdl.handle.net/10019.1/86772

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ENGLISH ABSTRACT: The work presented in this thesis throws light on the supramolecular approach in exploration of bi-porphyrin nanorods system wherein self-assembly plays an important… (more)

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ENGLISH ABSTRACT: The work presented in this thesis throws light on the supramolecular approach in exploration of bi-porphyrin nanorods system wherein self-assembly plays an important role. Porphyrin based nanorods were synthesized via self-assembly of meso-tetrakis (4-phenylsulfonicacid) porphyrin dihydrochloride and Sn (IV) tetrakis (4-pyridyl) porphyrin. Understanding the sizes and growth mechanism of the porphyrin nanorods by self-assembly and molecular recognition is essential for their successful implementation in nanodevices. Spectroscopic and microscopic studies were carried out to investigate the effect that time, concentration and solvents have on the fabrication of the porphyrin nanorods by ionic self- assembly. This study demonstrated that aggregates of the di- acid form of meso-tetrakis (4-phenylsulfonic acid) porphyrin dihydrochloride and Sn (IV) tetrakis (4-pyridyl) porphyrin resulted in porphyrin nanorods with diameters between 20 nm and 60 nm, and μm in lengths. Enhanced optical properties illustrated the potential for slightly modifying the method of synthesis to influence the physical and optical properties of porphyrin nanorods. The porphyrin nanorods reflectance data demonstrated that these structures are good absorbers of light and therefore could potentially be used to harvest light. The nonlinear optical (NLO) properties of the porphyrin nanorods were investigated for the first time in this study by second and third harmonic generation techniques. Such study was influenced by the fact that porphyrins have great thermal stability and extended -conjugated macro cyclic ring which give them large nonlinear optical effects. The NLO results showed that the porphyrin nanorods may have many potential uses in photonic applications due to larger third order nonlinear susceptibility. Single molecule spectroscopy was also used to investigate the dynamics of intermolecular and intramolecular processes. Porphyrin nanorods were incorporated into polymer matrices to achieve an arrangement where they can be directly used as a device. The assembly of porphyrin nanorods on track-etched membranes was achieved through altering the surface charge of the respective membranes. Porphyrin nanorods-polymer composites were produced using latex technology and electrospinning techniques. The fibres were characterized with respect to morphology and optical properties.

AFRIKAANSE OPSOMMING: Die werk wat in hierdie tesis beskryf word werp lig op die supramolekulêre benadering in die ondersoek van bi-porfirien nano-silinders waarin self-versameling ‘n belangrike rol speel. Porifirien nano-silinders was voorberei via self-versameling van meso-tetrakis(4-feniel sulfoonsuur) porfirien dihidrochloried en Sn (IV) terakis (4-piridiel) porfirien. Dit is belangrik om die meganismes wat verband hou met die groei en grootte van die nano-silinder struktuur te ondersoek. Dit het ‘n invloed op die self-versameling asook die uiteindelike toepassing. Spectroskopiese en mikroskopiese studies was uitgevoer om…

Advisors/Committee Members: Maaza, Malik, Klumperman, Bert, Sparrow, Raymond, Stellenbosch University. Faculty of Science. Dept. of Chemistry and Polymer Science..

Subjects/Keywords: Latex; Electrospinning; Photosynthesis; Biomimicry; Porphyrin nanorods; UCTD

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Mongwaketsi, N. P. (2014). Studies on porphyrin-based nanorods for artificial light harvesting applications. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/86772

Chicago Manual of Style (16^th Edition):

Mongwaketsi, Nametso Precious. “Studies on porphyrin-based nanorods for artificial light harvesting applications.” 2014. Doctoral Dissertation, Stellenbosch University. Accessed April 15, 2021. http://hdl.handle.net/10019.1/86772.

MLA Handbook (7^th Edition):

Mongwaketsi, Nametso Precious. “Studies on porphyrin-based nanorods for artificial light harvesting applications.” 2014. Web. 15 Apr 2021.

Vancouver:

Mongwaketsi NP. Studies on porphyrin-based nanorods for artificial light harvesting applications. [Internet] [Doctoral dissertation]. Stellenbosch University; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10019.1/86772.

Council of Science Editors:

Mongwaketsi NP. Studies on porphyrin-based nanorods for artificial light harvesting applications. [Doctoral Dissertation]. Stellenbosch University; 2014. Available from: http://hdl.handle.net/10019.1/86772

University of Newcastle

29. Cooling, Nathan. Ternary porphyrinoid:polymer:fullerene bulk heterojunction organic solar cells.

Degree: PhD, 2013, University of Newcastle

URL: http://hdl.handle.net/1959.13/1037406

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Research Doctorate - Doctor of Philosophy (PhD)

This thesis will investigate how porphyrinic materials may be successfully incorporated into polymer/fullerene organic solar cells to broaden… (more)

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Research Doctorate - Doctor of Philosophy (PhD)

This thesis will investigate how porphyrinic materials may be successfully incorporated into polymer/fullerene organic solar cells to broaden light absorption, enhance power conversion efficiency, and to further probe and broaden the understanding of the chemistry and physics of both binary and ternary blended organic solar cells. This thesis will begin with a discussion of bulk heterojunction organic solar cells, and how porphyrinic materials can be incorporated into these devices to form ternary blends, including a review of the ternary polymer:porphyrinoid:fullerene literature published to date. The performance of standard MEH-PPV:PCBM organic solar cells manufactured at the University of Newcastle during the course of this PhD will be examined to show how device efficiency has steadily improved over the course of the project (2007-2011). Furthermore, it will show that the incremental improvements made to the standard binary devices over time are directly transferable to ternary blend devices. The effect of systematically changing the steric bulk of a porphyrin on the performance of ternary blend devices is then investigated, as is the effect of changing the electronic states of the core while maintaining a constant steric profile. The effect on device performance of varying the para-phenyl substituents of a series of tetraphenylporphyrin derivatives is also examined. Finally, the effect of altering the central metal cation in a series of metalloporphyrins with octaethylporphyrins and tetraphenylporphyrins ligands is investigated. This thesis as a whole provides an insight into the chemistry and physics of ternary blend organic solar cells, detailing not only the interaction of porphyrin with polymer and fullerene, but also the effects of porphyrin-porphyrin interactions and how these may be controlled. Steric, electronic, and morphological effects are investigated, to provide a comprehensive study of ternary blend organic solar cells.

Advisors/Committee Members: University of Newcastle. Faculty of Science & Information Technology, School of Environmental and Life Sciences.

Subjects/Keywords: porphyrin; organic solar cell; organic photovoltaic

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Cooling, N. (2013). Ternary porphyrinoid:polymer:fullerene bulk heterojunction organic solar cells. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1037406

Chicago Manual of Style (16^th Edition):

Cooling, Nathan. “Ternary porphyrinoid:polymer:fullerene bulk heterojunction organic solar cells.” 2013. Doctoral Dissertation, University of Newcastle. Accessed April 15, 2021. http://hdl.handle.net/1959.13/1037406.

MLA Handbook (7^th Edition):

Cooling, Nathan. “Ternary porphyrinoid:polymer:fullerene bulk heterojunction organic solar cells.” 2013. Web. 15 Apr 2021.

Vancouver:

Cooling N. Ternary porphyrinoid:polymer:fullerene bulk heterojunction organic solar cells. [Internet] [Doctoral dissertation]. University of Newcastle; 2013. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1959.13/1037406.

Council of Science Editors:

Cooling N. Ternary porphyrinoid:polymer:fullerene bulk heterojunction organic solar cells. [Doctoral Dissertation]. University of Newcastle; 2013. Available from: http://hdl.handle.net/1959.13/1037406

University of Wollongong

30. Zhao, Long. Di-chromophoric porphyrins: exploring new strategies for enhanced light harvesting and increased photovoltage of dye-sensitized solar cells.

Degree: PhD, 2016, University of Wollongong

URL: 020504 Photonics, Optoelectronics and Optical Communications, 030206 Solid State Chemistry, 030302 Nanochemistry and Supramolecular Chemistry, 0306 PHYSICAL CHEMISTRY (INCL. STRUCTURAL) ; https://ro.uow.edu.au/theses/4630

► Although numerous improvements have been achieved in the field of dye-sensitized solar cells (DSSCs), there are still some potential strategies for further development in… (more)

▼ Although numerous improvements have been achieved in the field of dye-sensitized solar cells (DSSCs), there are still some potential strategies for further development in this technology. In that regard, the most straightforward strategy is to enhance the dye light harvesting properties, in particular, by using low band gap dyes. While such approach would in principle increase the photocurrent, low band gap sensitizers typically yield relatively low photovoltage. This phenomenon is caused by strong intermolecular forces, inherent of low band gap materials. Therefore, to simultaneously increase the photocurrent and photovoltage, new concept of the dye design is required. For instance, a multi-chromophoric dye structure, which is basically a single molecule containing several independent light absorbing units. Thus, the present thesis concerns with the investigation of different di-chromophoric dyes in DSSCs. As will be shown, these novel dyes can overcome the typical limitations of low band gap dyes in photovoltage, while increasing the photocurrent as a result of the increased light absorption. They not only enhance light absorption and overcome dispersion forces, but also feature other benefits owing to the tri-dimensionality. This is for instance the addition of bulky groups, which can hinder non desired processes such as recombination. The electron lifetimes and consequently the photovoltage of DSSCs increase as a result. Aspects related to the arrangement of the dyes on the photoanode are also benefited from such groups, which enhance the electron injection efficiency and photocurrent. Therefore, in some cases, co-adsorbers such as chenodeoxycholic acid are no longer needed in the di-chromophoric dye sensitization process. The utilization of the cobalt-based electrolyte in DSSCs using di-chromophoric dyes is also investigated in this thesis in terms of photovoltaic performance and dye regeneration. In a specific case, a microsecond component of partial intramolecular hole transfer is observed in a di-chromophoric dye for the first time, and dye regeneration kinetics in this dichromophoric dye is favoured in respect with the single chromophore of similar driving force. Attaching an organic chromophore with tuned band gap to extend light absorption of the dyad towards the red may introduce competing electron injection pathways, probing a limitation of di-chromophoric dye using low band gap chromophore. Although the latter effect reduces the photocurrent of DSSCs, the electron lifetimes and photovoltage are increased. A comparison between di-chromophoric dye and co-sensitization approaches has been carried out. Utilizing intermolecular forces to enhance the electron lifetimes in DSSCs using di-chromophoric dye will be reported for the first time. Although the power conversion efficiencies of DSSCs using the di-chromophoric dyes still lag behind compared to that of traditional dyes, this thesis provides new prospects in electron transfer mechanisms at the dye-sensitized interfaces. Thus, some…

Subjects/Keywords: Porphyrin; electron lifetime; di-chromophoric; recombination

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Zhao, L. (2016). Di-chromophoric porphyrins: exploring new strategies for enhanced light harvesting and increased photovoltage of dye-sensitized solar cells. (Doctoral Dissertation). University of Wollongong. Retrieved from 020504 Photonics, Optoelectronics and Optical Communications, 030206 Solid State Chemistry, 030302 Nanochemistry and Supramolecular Chemistry, 0306 PHYSICAL CHEMISTRY (INCL. STRUCTURAL) ; https://ro.uow.edu.au/theses/4630

Chicago Manual of Style (16^th Edition):

Zhao, Long. “Di-chromophoric porphyrins: exploring new strategies for enhanced light harvesting and increased photovoltage of dye-sensitized solar cells.” 2016. Doctoral Dissertation, University of Wollongong. Accessed April 15, 2021. 020504 Photonics, Optoelectronics and Optical Communications, 030206 Solid State Chemistry, 030302 Nanochemistry and Supramolecular Chemistry, 0306 PHYSICAL CHEMISTRY (INCL. STRUCTURAL) ; https://ro.uow.edu.au/theses/4630.

MLA Handbook (7^th Edition):

Zhao, Long. “Di-chromophoric porphyrins: exploring new strategies for enhanced light harvesting and increased photovoltage of dye-sensitized solar cells.” 2016. Web. 15 Apr 2021.

Vancouver:

Zhao L. Di-chromophoric porphyrins: exploring new strategies for enhanced light harvesting and increased photovoltage of dye-sensitized solar cells. [Internet] [Doctoral dissertation]. University of Wollongong; 2016. [cited 2021 Apr 15]. Available from: 020504 Photonics, Optoelectronics and Optical Communications, 030206 Solid State Chemistry, 030302 Nanochemistry and Supramolecular Chemistry, 0306 PHYSICAL CHEMISTRY (INCL. STRUCTURAL) ; https://ro.uow.edu.au/theses/4630.

Council of Science Editors:

Zhao L. Di-chromophoric porphyrins: exploring new strategies for enhanced light harvesting and increased photovoltage of dye-sensitized solar cells. [Doctoral Dissertation]. University of Wollongong; 2016. Available from: 020504 Photonics, Optoelectronics and Optical Communications, 030206 Solid State Chemistry, 030302 Nanochemistry and Supramolecular Chemistry, 0306 PHYSICAL CHEMISTRY (INCL. STRUCTURAL) ; https://ro.uow.edu.au/theses/4630

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