subject:(Thiophenes Synthesis)

Michigan State University

1. Mueller, Albert Joseph. Synthesis of thienyl and thianaphthenyl dioxolanes and thienyl dicarbonyls.

Degree: PhD, Department of Chemistry, 1968, Michigan State University

URL: http://etd.lib.msu.edu/islandora/object/etd:35142

Subjects/Keywords: Thiophenes – Synthesis; Thianaphthenes – Synthesis

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APA (6^th Edition):

Mueller, A. J. (1968). Synthesis of thienyl and thianaphthenyl dioxolanes and thienyl dicarbonyls. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35142

Chicago Manual of Style (16^th Edition):

Mueller, Albert Joseph. “Synthesis of thienyl and thianaphthenyl dioxolanes and thienyl dicarbonyls.” 1968. Doctoral Dissertation, Michigan State University. Accessed March 06, 2021. http://etd.lib.msu.edu/islandora/object/etd:35142.

MLA Handbook (7^th Edition):

Mueller, Albert Joseph. “Synthesis of thienyl and thianaphthenyl dioxolanes and thienyl dicarbonyls.” 1968. Web. 06 Mar 2021.

Vancouver:

Mueller AJ. Synthesis of thienyl and thianaphthenyl dioxolanes and thienyl dicarbonyls. [Internet] [Doctoral dissertation]. Michigan State University; 1968. [cited 2021 Mar 06]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35142.

Council of Science Editors:

Mueller AJ. Synthesis of thienyl and thianaphthenyl dioxolanes and thienyl dicarbonyls. [Doctoral Dissertation]. Michigan State University; 1968. Available from: http://etd.lib.msu.edu/islandora/object/etd:35142

2. Sharma, Jayesh Anilkumar. Design Synthesis And Pharmacological Evaluation Of New Thiophenes; Design Synthesis And Pharmacological Evaluation Of New Thiophenes.

Degree: Department, 2015, Maharaja Krishnakumarsinhji Bhavnagar University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/54925

none

References Not Given

Advisors/Committee Members: Vasu, Dr Kamala K.

Subjects/Keywords: Design; Evaluation; Pharmacological; Synthesis; Thiophenes

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APA (6^th Edition):

Sharma, J. A. (2015). Design Synthesis And Pharmacological Evaluation Of New Thiophenes; Design Synthesis And Pharmacological Evaluation Of New Thiophenes. (Thesis). Maharaja Krishnakumarsinhji Bhavnagar University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54925

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):

Sharma, Jayesh Anilkumar. “Design Synthesis And Pharmacological Evaluation Of New Thiophenes; Design Synthesis And Pharmacological Evaluation Of New Thiophenes.” 2015. Thesis, Maharaja Krishnakumarsinhji Bhavnagar University. Accessed March 06, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/54925.

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

MLA Handbook (7^th Edition):

Sharma, Jayesh Anilkumar. “Design Synthesis And Pharmacological Evaluation Of New Thiophenes; Design Synthesis And Pharmacological Evaluation Of New Thiophenes.” 2015. Web. 06 Mar 2021.

Vancouver:

Sharma JA. Design Synthesis And Pharmacological Evaluation Of New Thiophenes; Design Synthesis And Pharmacological Evaluation Of New Thiophenes. [Internet] [Thesis]. Maharaja Krishnakumarsinhji Bhavnagar University; 2015. [cited 2021 Mar 06]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54925.

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

Council of Science Editors:

Sharma JA. Design Synthesis And Pharmacological Evaluation Of New Thiophenes; Design Synthesis And Pharmacological Evaluation Of New Thiophenes. [Thesis]. Maharaja Krishnakumarsinhji Bhavnagar University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54925

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

Ryerson University

3. Abdinejad, Maryam. Synthesis and structure-property studies of organic dyes possessing unique fused thiophene π-spacers.

Degree: 2014, Ryerson University

URL: https://digital.library.ryerson.ca/islandora/object/RULA%3A3304

► This thesis examines the synthesis of metal-free organic dyes for light-harvesting applications within the DSSC manifold. All DSSC organic dyes possess a similar donor-π-spacer-acceptor (D-π-A)… (more)

Subjects/Keywords: Dye-sensitized solar cells; Thiophenes.; Dyes and dyeing – Synthesis; Photosynthetic reaction centers

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APA (6^th Edition):

Abdinejad, M. (2014). Synthesis and structure-property studies of organic dyes possessing unique fused thiophene π-spacers. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A3304

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):

Abdinejad, Maryam. “Synthesis and structure-property studies of organic dyes possessing unique fused thiophene π-spacers.” 2014. Thesis, Ryerson University. Accessed March 06, 2021. https://digital.library.ryerson.ca/islandora/object/RULA%3A3304.

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

MLA Handbook (7^th Edition):

Abdinejad, Maryam. “Synthesis and structure-property studies of organic dyes possessing unique fused thiophene π-spacers.” 2014. Web. 06 Mar 2021.

Vancouver:

Abdinejad M. Synthesis and structure-property studies of organic dyes possessing unique fused thiophene π-spacers. [Internet] [Thesis]. Ryerson University; 2014. [cited 2021 Mar 06]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A3304.

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

Council of Science Editors:

Abdinejad M. Synthesis and structure-property studies of organic dyes possessing unique fused thiophene π-spacers. [Thesis]. Ryerson University; 2014. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A3304

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

Hong Kong University of Science and Technology

4. Zhang, Renwei CHEM. Construction of five-membered heterocycles by intramolecular oxetane ring opening.

Degree: 2018, Hong Kong University of Science and Technology

URL: http://repository.ust.hk/ir/Record/1783.1-97833 ; https://doi.org/10.14711/thesis-991012662567203412 ; http://repository.ust.hk/ir/bitstream/1783.1-97833/1/th_redirect.html

► Heterocycles form the largest group of organic compounds by far. They are widely found in natural products, drug molecules and organic materials. Extensive efforts have… (more)

▼ Heterocycles form the largest group of organic compounds by far. They are widely found in natural products, drug molecules and organic materials. Extensive efforts have been devoted to develop new and efficient approaches for their synthesis. This thesis mainly describes the synthesis of several five-membered heterocycles via intramolecular oxetane ring opening. Chapter 1 is an introduction to oxetane ring, mainly including structure features, applications and reported ring-opening reactions of oxetanes. In Chapter 2, an In-catalyzed intramolecular oxetane ring opening employing Ellman’s N-tert-butanesulfinamides as a chiral auxiliary is disclosed. A range of pyrrolidines bearing an all-carbon quaternary stereocenter at the 3-position was obtained. And finally, the tert-butanesulfinyl auxiliary group could be easily removed. In Chapter 3, a new asymmetric synthesis of tetrahydrothiophenes has been developed by means of organocatalytic enantioselective desymmetrization of oxetanes accompanied by an acyl transfer. This mild process proceeds with high efficiency and enantioselectivity to establish the quaternary stereocenters. Also, this method can be extended to the synthesis of chiral tetrahydroselenophenes and tetrahydrothiopyrans, which are also highly useful structural units which are difficult to acess due to lacking efficient synthetic methods previously. In Chapter 4, the first base-promoted oxetane ring opening by secondary phosphine oxide intramolecularly is described. A variety of phospholane oxides bearing an all-carbon quaternary carbon center at the 3-position was obtained. Other than phospholane oxides, six-membered ring phosphinanes and seven-membered ring phosphepanes could also be obtained using this method with excellent diastereoselectivity. Moreover, the phospholane oxides could be easily reduced to phospholanes, which are potential ligands and organocatalysis. In Chapter 5, the first organobase-catalyzed reaction between CO₂ and oxetane bearing a secondary amino group is developed. Various highly useful oxazolidin-2-ones were obtained with high yields. In comparison with most other reactions involved using CO₂, this method is user friendly with CO₂ used at atmospheric pressure.

Subjects/Keywords: Propylene oxide ; Ring formation (Chemistry) ; Organic compounds ; Synthesis ; Enantioselective catalysis ; Pyrrolizidines ; Thiophenes

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APA (6^th Edition):

Zhang, R. C. (2018). Construction of five-membered heterocycles by intramolecular oxetane ring opening. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-97833 ; https://doi.org/10.14711/thesis-991012662567203412 ; http://repository.ust.hk/ir/bitstream/1783.1-97833/1/th_redirect.html

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):

Zhang, Renwei CHEM. “Construction of five-membered heterocycles by intramolecular oxetane ring opening.” 2018. Thesis, Hong Kong University of Science and Technology. Accessed March 06, 2021. http://repository.ust.hk/ir/Record/1783.1-97833 ; https://doi.org/10.14711/thesis-991012662567203412 ; http://repository.ust.hk/ir/bitstream/1783.1-97833/1/th_redirect.html.

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

MLA Handbook (7^th Edition):

Zhang, Renwei CHEM. “Construction of five-membered heterocycles by intramolecular oxetane ring opening.” 2018. Web. 06 Mar 2021.

Vancouver:

Zhang RC. Construction of five-membered heterocycles by intramolecular oxetane ring opening. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2018. [cited 2021 Mar 06]. Available from: http://repository.ust.hk/ir/Record/1783.1-97833 ; https://doi.org/10.14711/thesis-991012662567203412 ; http://repository.ust.hk/ir/bitstream/1783.1-97833/1/th_redirect.html.

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

Council of Science Editors:

Zhang RC. Construction of five-membered heterocycles by intramolecular oxetane ring opening. [Thesis]. Hong Kong University of Science and Technology; 2018. Available from: http://repository.ust.hk/ir/Record/1783.1-97833 ; https://doi.org/10.14711/thesis-991012662567203412 ; http://repository.ust.hk/ir/bitstream/1783.1-97833/1/th_redirect.html

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

Michigan State University

5. Teot, Arthur Stafford. The syntheses of some omega-tertiary amine salts of substituted acyl-3-aminothiophenes.

Degree: MS, 1961, Michigan State University

URL: http://etd.lib.msu.edu/islandora/object/etd:13116

Subjects/Keywords: Organic compounds – Synthesis; Thiophenes; Local anesthesia

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APA (6^th Edition):

Teot, A. S. (1961). The syntheses of some omega-tertiary amine salts of substituted acyl-3-aminothiophenes. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:13116

Chicago Manual of Style (16^th Edition):

Teot, Arthur Stafford. “The syntheses of some omega-tertiary amine salts of substituted acyl-3-aminothiophenes.” 1961. Masters Thesis, Michigan State University. Accessed March 06, 2021. http://etd.lib.msu.edu/islandora/object/etd:13116.

MLA Handbook (7^th Edition):

Teot, Arthur Stafford. “The syntheses of some omega-tertiary amine salts of substituted acyl-3-aminothiophenes.” 1961. Web. 06 Mar 2021.

Vancouver:

Teot AS. The syntheses of some omega-tertiary amine salts of substituted acyl-3-aminothiophenes. [Internet] [Masters thesis]. Michigan State University; 1961. [cited 2021 Mar 06]. Available from: http://etd.lib.msu.edu/islandora/object/etd:13116.

Council of Science Editors:

Teot AS. The syntheses of some omega-tertiary amine salts of substituted acyl-3-aminothiophenes. [Masters Thesis]. Michigan State University; 1961. Available from: http://etd.lib.msu.edu/islandora/object/etd:13116

6. Freeman, Jason Lee. Synthesis and optical characterization of molecular and polymeric phosphonate-substituted bithiophene derivatives.

Degree: PhD, 2011, University of Alabama – Birmingham

URL: http://contentdm.mhsl.uab.edu/u?/etd,1050

►

The synthesis and optical characterization of a series of novel molecular and polymeric phosphonate-substituted bithiophenes are reported. Many of the compounds reported herein exhibit good… (more)

▼

The synthesis and optical characterization of a series of novel molecular and polymeric phosphonate-substituted bithiophenes are reported. Many of the compounds reported herein exhibit good nonlinear optical absorption and emission properties in the violet-blue spectral region. The first chapter investigates a series of molecular phosphonate bithiophenes derived from 2,2!-biphenol, BpP(X)(C4H2S)2H and BpP(X)(C4H2S)2P(X)Bp (Bp = 2,2!- C12H8O2; X = O, S , Se). Their syntheses have been optimized, and solid-state structures of two of these compounds are reported. The linear absorption spectra, emission spectra, and emission quantum yields show distinct trends with respect to the chalcogen attached to the phosphorus and the number of phosphorus substituents attached to the 2,2!- bithiophene ring. Nonlinear transmission measurements indicate that solutions of the compounds show nonlinear absorption at 430 nm with 27-ps laser pulses in spite of their low solubilities in organic solvents. In the second chapter, the synthesis, linear absorption and emission spectra, and nonlinear absorptions at 430 nm of two new series of molecular phosphonate-substituted bithiophenes, pdP(X)(C4H2S)2H and pdP(X)(C4H2S)2P(X)pd (pd = OCH2C(CH3)2CH2O; X = O, S, Se), are reported. The X-ray crystal structures of four of these compounds have also been determined. Similar structure-optical property relationships are observed to those reported from Chapter 1. The nonlinear optical absorption of saturated solutions of two of these compounds is significantly improved relative to those of the phosphonates reported in the first chapter and rivals the best violet-blue nonlinear absorbers reported in the literature. In the last chapter, a method of incorporating phosphonate-functionalized 2,2!- bithiophenes into a polymer system was developed. The number average molecular weights of these polymers range from 1.1 to 4.3 x 10 4 Da. Thermal characterization indicates that all of the polymers are in the rubbery state at room temperature and have thermally stabilities as high as 290 ºC. The linear optical properties of the polyphosphonates are similar to those of previously reported nonlinear optical molecular phosphonates, yet are more soluble in organic solvents making them excellent candidates for violet-blue optical power limiting applications.

1 online resource (xiv, 168 p.) : ill.

Chemistry

College of Arts and Sciences

UNRESTRICTED

Advisors/Committee Members: Gray, Gary M., Byrd, Houston <br>, Lawson, Christopher M. <br>, Velu, Sadanandan E. <br>, Watkins, Charles L..

Subjects/Keywords: Thiophenes – Derivatives – Synthesis <; br>; Thiophenes – Derivatives – Optical properties <; br>; Thiophenes – Derivatives – Structure <; br>; Phosphonates – Thermal properties <; br>; Phosphonates – Optical properties <; br>; Polymerization

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APA (6^th Edition):

Freeman, J. L. (2011). Synthesis and optical characterization of molecular and polymeric phosphonate-substituted bithiophene derivatives. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1050

Chicago Manual of Style (16^th Edition):

Freeman, Jason Lee. “Synthesis and optical characterization of molecular and polymeric phosphonate-substituted bithiophene derivatives.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 06, 2021. http://contentdm.mhsl.uab.edu/u?/etd,1050.

MLA Handbook (7^th Edition):

Freeman, Jason Lee. “Synthesis and optical characterization of molecular and polymeric phosphonate-substituted bithiophene derivatives.” 2011. Web. 06 Mar 2021.

Vancouver:

Freeman JL. Synthesis and optical characterization of molecular and polymeric phosphonate-substituted bithiophene derivatives. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2021 Mar 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1050.

Council of Science Editors:

Freeman JL. Synthesis and optical characterization of molecular and polymeric phosphonate-substituted bithiophene derivatives. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1050

Indian Institute of Science

7. Gopinath, P. Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes.

Degree: PhD, Faculty of Science, 2013, Indian Institute of Science

URL: http://etd.iisc.ac.in/handle/2005/2157

► The thesis entitled "Synthesis of Novel Chalcogenides using Acyloxyphosphonium Intermediates and Doubly Activated Cyclopropanes" is divided into six chapters. Chapter 1: Part 1: Synthesis of… (more)

▼ The thesis entitled "Synthesis of Novel Chalcogenides using Acyloxyphosphonium Intermediates and Doubly Activated Cyclopropanes" is divided into six chapters. Chapter 1: Part 1: Synthesis of thioesters from carboxylic acids and alkyl halides using benzyltriethylammonium tetrathiomolybdate In this chapter, we describe the synthesis of thioesters from carboxylic acids and alkyl halides. Aryl carboxylic acids are first activated using PPh3 and NBS to form the corresponding acyloxy phosphonium intermediates which then on further reaction with reagent, 1generate thioaroylate ions in situ. These thioaroylates on further reaction with various electrophiles such as alkyl halides / dihalides in the same pot gives the corresponding functionalized thioesters. This methodology was then extended to carbohydrate based thioesters as they are important synthetic intermediates in various transformations and also they could be deprotected later to synthetically more valuable thiols. For this study, we took 1,2,3,4tetra-O-acetyl-β-D-glucopyranuronic acid which on treatment with PPh3,NBS, reagent, 1 and I-bromo propane (CHCl3, 28°C, 2h) afforded the corresponding thioester in 55% yield. An intramolecular version of the reaction was then performed on a compound containing both anomeric bromide and carboxylic acid functionality. This was achieved by treating tetra acetyl glucuronic acid, with HBr/AcOH to form α-D-bromo-glucopyranuronic acid which on further treatment with PPh3, NBS and reagent, 1 gave the corresponding bicyclic thiolactone in 55% yield. Chapter 1: Part 2: Synthesis of Thioesters by Simultaneous Activation of Carboxylic Acids and Alcohols using PPh3/NBS In this chapter, we have shown the synthesis of thioester from carboxylic acids and alcohols. Both carboxylic acids and alcohols are first activated using PPh3 and NBS to form the corresponding phosphonium salts. Reagent, 1 then reacts selectively with acyloxyphosphonium intermediates to generate thioaroylate ions in situ which then react either with alkoxy phosphonium salts or the corresponding alkyl bromide to give thioesters in good yield. The same methodology was then used for a one pot conversion of N-Boc serine ester to s-protected cysteine using reagent 1 as the key sulfur transfer reagent. Chapter 2: Part 1: Tetrathiomolybdate mediated Michael addition of thioaroylates generated from acyloxyphosphonium salts In this chapter, we have reported an easy and alternative protocol for the Michael addition of thioacids to various Michael acceptors. Acyloxyphosphonium salts and tetrathiomolybdate reacts to generate thioaroylate ions which then undergo Michael additionto givethe corresponding Michael adducts. This methodology was then extended for the synthesis carbohydrate based thiolactone by an intramolecular Michael addition reaction to show the applicability of the methodology. Chapter 2: Part 2: Regioselective and chemoselective ring opening of aziridines and epoxides using thioaroylate ions In this chapter, we have demonstrated nucleophilic ring… Advisors/Committee Members: Chandrasekaran, S (advisor).

Subjects/Keywords: Cyclopropanes; Chalcogenides - Synthesis; Acyloxyphosphonium; Thioesters; Bromo Esters; Bromo Thioesters; Benzyltriethylammonium Tetrathiomolybdate; Dihydrothiophenes; Thiophenes; Selenolates; Aziridines; Epoxides; Thioaroylate; Organic Chemistry

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APA (6^th Edition):

Gopinath, P. (2013). Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2157

Chicago Manual of Style (16^th Edition):

Gopinath, P. “Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes.” 2013. Doctoral Dissertation, Indian Institute of Science. Accessed March 06, 2021. http://etd.iisc.ac.in/handle/2005/2157.

MLA Handbook (7^th Edition):

Gopinath, P. “Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes.” 2013. Web. 06 Mar 2021.

Vancouver:

Gopinath P. Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2013. [cited 2021 Mar 06]. Available from: http://etd.iisc.ac.in/handle/2005/2157.

Council of Science Editors:

Gopinath P. Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes. [Doctoral Dissertation]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ac.in/handle/2005/2157

University of Florida

8. Stalder, Romain. Organic Semiconducting Molecules and Polymers for Solution Processed Organic Electronics.

Degree: PhD, Chemistry, 2012, University of Florida

URL: https://ufdc.ufl.edu/UFE0043948

► In the field of organic electronics, each material differs in its ability to balance hole (p-type) and electron (n-type) carrier creation and transport in devices,… (more)

Subjects/Keywords: Absorption spectra; Electrons; Flasks; Molecules; Oligomers; Photovoltaic cells; Polymers; Room temperature; Solvents; Thiophenes; materials – organic – semiconducting – synthesis

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APA (6^th Edition):

Stalder, R. (2012). Organic Semiconducting Molecules and Polymers for Solution Processed Organic Electronics. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0043948

Chicago Manual of Style (16^th Edition):

Stalder, Romain. “Organic Semiconducting Molecules and Polymers for Solution Processed Organic Electronics.” 2012. Doctoral Dissertation, University of Florida. Accessed March 06, 2021. https://ufdc.ufl.edu/UFE0043948.

MLA Handbook (7^th Edition):

Stalder, Romain. “Organic Semiconducting Molecules and Polymers for Solution Processed Organic Electronics.” 2012. Web. 06 Mar 2021.

Vancouver:

Stalder R. Organic Semiconducting Molecules and Polymers for Solution Processed Organic Electronics. [Internet] [Doctoral dissertation]. University of Florida; 2012. [cited 2021 Mar 06]. Available from: https://ufdc.ufl.edu/UFE0043948.

Council of Science Editors:

Stalder R. Organic Semiconducting Molecules and Polymers for Solution Processed Organic Electronics. [Doctoral Dissertation]. University of Florida; 2012. Available from: https://ufdc.ufl.edu/UFE0043948

Georgia Tech

9. Shotwell, Sandra Leigh. Synthesis and Characterization of ortho-Phenyleneethynylenes and Diphenylamine Polymers.

Degree: PhD, Chemistry and Biochemistry, 2006, Georgia Tech

URL: http://hdl.handle.net/1853/10449

► In the first part of this thesis, the synthesis, characterization and investigation of ortho-phenyleneethynylenes containing heterocycles, are presented. These compounds display changes in absorption and… (more)

Subjects/Keywords: Polymers; Thiophenes Synthesis; Pyridinium compounds Synthesis; Ligands; Diphenylamine Synthesis; Oligomers

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APA (6^th Edition):

Shotwell, S. L. (2006). Synthesis and Characterization of ortho-Phenyleneethynylenes and Diphenylamine Polymers. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/10449

Chicago Manual of Style (16^th Edition):

Shotwell, Sandra Leigh. “Synthesis and Characterization of ortho-Phenyleneethynylenes and Diphenylamine Polymers.” 2006. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/10449.

MLA Handbook (7^th Edition):

Shotwell, Sandra Leigh. “Synthesis and Characterization of ortho-Phenyleneethynylenes and Diphenylamine Polymers.” 2006. Web. 06 Mar 2021.

Vancouver:

Shotwell SL. Synthesis and Characterization of ortho-Phenyleneethynylenes and Diphenylamine Polymers. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/10449.

Council of Science Editors:

Shotwell SL. Synthesis and Characterization of ortho-Phenyleneethynylenes and Diphenylamine Polymers. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/10449

University of Florida

10. Xie, Linghong, 1963-. Benzotriazole mediated heteroalkylation and arylalkylation in organic synthesis.

Degree: 1994, University of Florida

URL: https://ufdc.ufl.edu/AA00003231

Subjects/Keywords: Carbazoles; Chlorides; Chromatography; Cyanides; Furans; Indoles; Phenyls; Solvents; Sulfides; Thiophenes; Heterocyclic compounds – Synthesis

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APA (6^th Edition):

Xie, Linghong, 1. (1994). Benzotriazole mediated heteroalkylation and arylalkylation in organic synthesis. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00003231

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):

Xie, Linghong, 1963-. “Benzotriazole mediated heteroalkylation and arylalkylation in organic synthesis.” 1994. Thesis, University of Florida. Accessed March 06, 2021. https://ufdc.ufl.edu/AA00003231.

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

MLA Handbook (7^th Edition):

Xie, Linghong, 1963-. “Benzotriazole mediated heteroalkylation and arylalkylation in organic synthesis.” 1994. Web. 06 Mar 2021.

Vancouver:

Xie, Linghong 1. Benzotriazole mediated heteroalkylation and arylalkylation in organic synthesis. [Internet] [Thesis]. University of Florida; 1994. [cited 2021 Mar 06]. Available from: https://ufdc.ufl.edu/AA00003231.

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

Council of Science Editors:

Xie, Linghong 1. Benzotriazole mediated heteroalkylation and arylalkylation in organic synthesis. [Thesis]. University of Florida; 1994. Available from: https://ufdc.ufl.edu/AA00003231

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

11. Myrex, Ronald Dustan. Synthesis and characterization of phosphorus-containing inorganic polymers.

Degree: PhD, 2007, University of Alabama – Birmingham

URL: http://contentdm.mhsl.uab.edu/u?/etd,314

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This research project involves the synthesis of novel phosphorus-containing inorganic polymers. These materials share similar structures to their organic counterparts but are not comprised entirely… (more)

Subjects/Keywords: Inorganic polymers – Synthesis <; br>; Inorganic polymers – Optical properties <; br>; Esters – Reactivity <; br>; Phosphonates – Reactivity <; br>; Thiophenes – Reactivity <; br>; Phosphine – Reactivity <; br>; Oligomers

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

APA (6^th Edition):

Myrex, R. D. (2007). Synthesis and characterization of phosphorus-containing inorganic polymers. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,314

Chicago Manual of Style (16^th Edition):

Myrex, Ronald Dustan. “Synthesis and characterization of phosphorus-containing inorganic polymers.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 06, 2021. http://contentdm.mhsl.uab.edu/u?/etd,314.

MLA Handbook (7^th Edition):

Myrex, Ronald Dustan. “Synthesis and characterization of phosphorus-containing inorganic polymers.” 2007. Web. 06 Mar 2021.

Vancouver:

Myrex RD. Synthesis and characterization of phosphorus-containing inorganic polymers. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2021 Mar 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,314.

Council of Science Editors:

Myrex RD. Synthesis and characterization of phosphorus-containing inorganic polymers. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,314

University of Florida

12. Welsh, Dean M., 1973-. High-Contrast and three-color electrochromic polymers.

Degree: PhD, Chemistry, 2001, University of Florida

URL: https://ufdc.ufl.edu/AA00038471

Subjects/Keywords: Carbazoles; Conducting polymers; Electrodes; Electrons; Molecular weight; Monomers; Oxidation; Polymerization; Polymers; Thiophenes; Electrochromic devices; Polymers – Synthesis

Record Details Similar Records Cite « Share

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

APA (6^th Edition):

Welsh, Dean M., 1. (2001). High-Contrast and three-color electrochromic polymers. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00038471

Chicago Manual of Style (16^th Edition):

Welsh, Dean M., 1973-. “High-Contrast and three-color electrochromic polymers.” 2001. Doctoral Dissertation, University of Florida. Accessed March 06, 2021. https://ufdc.ufl.edu/AA00038471.

MLA Handbook (7^th Edition):

Welsh, Dean M., 1973-. “High-Contrast and three-color electrochromic polymers.” 2001. Web. 06 Mar 2021.

Vancouver:

Welsh, Dean M. 1. High-Contrast and three-color electrochromic polymers. [Internet] [Doctoral dissertation]. University of Florida; 2001. [cited 2021 Mar 06]. Available from: https://ufdc.ufl.edu/AA00038471.

Council of Science Editors:

Welsh, Dean M. 1. High-Contrast and three-color electrochromic polymers. [Doctoral Dissertation]. University of Florida; 2001. Available from: https://ufdc.ufl.edu/AA00038471

Open Access Theses and Dissertations