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You searched for +publisher:"Dalhousie University" +contributor:("Dr. Norman P. Schepp"). Showing records 1 – 6 of 6 total matches.

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Dalhousie University

1. Hesp, Kevin. Late Transition Metal Complexes for E-H Bond Activation and Additions to Multiple Bonds.

Degree: PhD, Department of Chemistry, 2010, Dalhousie University

 The study of organometallic chemistry in the context of catalysis can be approached from a stoichiometric perspective, in which PGM complexes are examined in the… (more)

Subjects/Keywords: Orgnaometallic; Catalysis; Hydroamination; Bifunctional Ligands

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

APA (6th Edition):

Hesp, K. (2010). Late Transition Metal Complexes for E-H Bond Activation and Additions to Multiple Bonds. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13104

Chicago Manual of Style (16th Edition):

Hesp, Kevin. “Late Transition Metal Complexes for E-H Bond Activation and Additions to Multiple Bonds.” 2010. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/13104.

MLA Handbook (7th Edition):

Hesp, Kevin. “Late Transition Metal Complexes for E-H Bond Activation and Additions to Multiple Bonds.” 2010. Web. 29 May 2020.

Vancouver:

Hesp K. Late Transition Metal Complexes for E-H Bond Activation and Additions to Multiple Bonds. [Internet] [Doctoral dissertation]. Dalhousie University; 2010. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/13104.

Council of Science Editors:

Hesp K. Late Transition Metal Complexes for E-H Bond Activation and Additions to Multiple Bonds. [Doctoral Dissertation]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13104


Dalhousie University

2. Morgan, Erin. Rhodium and Iridium Pincer Complexes Supported by Bis(phosphino)silyl Ligation: Applications in Bond Cleavage Chemistry.

Degree: PhD, Department of Chemistry, 2013, Dalhousie University

 Group 9 transition metal pincer complexes have shown tremendous utility in a variety of E-H (E = main group element) bond activation reactions. In an… (more)

Subjects/Keywords: Rhodium; iridium; N-H bonds; bond activation; oxidative addition

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APA (6th Edition):

Morgan, E. (2013). Rhodium and Iridium Pincer Complexes Supported by Bis(phosphino)silyl Ligation: Applications in Bond Cleavage Chemistry. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/27968

Chicago Manual of Style (16th Edition):

Morgan, Erin. “Rhodium and Iridium Pincer Complexes Supported by Bis(phosphino)silyl Ligation: Applications in Bond Cleavage Chemistry.” 2013. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/27968.

MLA Handbook (7th Edition):

Morgan, Erin. “Rhodium and Iridium Pincer Complexes Supported by Bis(phosphino)silyl Ligation: Applications in Bond Cleavage Chemistry.” 2013. Web. 29 May 2020.

Vancouver:

Morgan E. Rhodium and Iridium Pincer Complexes Supported by Bis(phosphino)silyl Ligation: Applications in Bond Cleavage Chemistry. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/27968.

Council of Science Editors:

Morgan E. Rhodium and Iridium Pincer Complexes Supported by Bis(phosphino)silyl Ligation: Applications in Bond Cleavage Chemistry. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/27968


Dalhousie University

3. MacDonald, Elizabeth. Cationic and Dicationic Phosphine Complexes of Tin and Germanium.

Degree: PhD, Department of Chemistry, 2013, Dalhousie University

 This dissertation explores the synthesis and characterization of phosphine stabilized tetrel (group 14) cations. Tetrel cations are readily generated by reacting a halogermane or halostannane… (more)

Subjects/Keywords: Phosphorus; Germanium; Tin; Salts

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APA (6th Edition):

MacDonald, E. (2013). Cationic and Dicationic Phosphine Complexes of Tin and Germanium. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/35413

Chicago Manual of Style (16th Edition):

MacDonald, Elizabeth. “Cationic and Dicationic Phosphine Complexes of Tin and Germanium.” 2013. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/35413.

MLA Handbook (7th Edition):

MacDonald, Elizabeth. “Cationic and Dicationic Phosphine Complexes of Tin and Germanium.” 2013. Web. 29 May 2020.

Vancouver:

MacDonald E. Cationic and Dicationic Phosphine Complexes of Tin and Germanium. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/35413.

Council of Science Editors:

MacDonald E. Cationic and Dicationic Phosphine Complexes of Tin and Germanium. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/35413


Dalhousie University

4. Alsabeh, Pamela G. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.

Degree: PhD, Department of Chemistry, 2013, Dalhousie University

 The use of homogeneous organometallic catalysis for otherwise challenging chemical transformations is a concept that has gained significant interest in recent decades, providing access to… (more)

Subjects/Keywords: catalysis; cross-coupling; palladium; ammonia; amination; carbonylation; indole synthesis

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APA (6th Edition):

Alsabeh, P. G. (2013). The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/39740

Chicago Manual of Style (16th Edition):

Alsabeh, Pamela G. “The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.” 2013. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/39740.

MLA Handbook (7th Edition):

Alsabeh, Pamela G. “The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.” 2013. Web. 29 May 2020.

Vancouver:

Alsabeh PG. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/39740.

Council of Science Editors:

Alsabeh PG. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/39740


Dalhousie University

5. Ruddy, Adam. Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation.

Degree: PhD, Department of Chemistry, 2014, Dalhousie University

 Pincer complexes of the platinum group metals have been the subject of intense research in recent years, owing to the remarkable stoichiometric and catalytic reactivity… (more)

Subjects/Keywords: organometallic; inorganic; ligands; catalysis; bond activation

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APA (6th Edition):

Ruddy, A. (2014). Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/54005

Chicago Manual of Style (16th Edition):

Ruddy, Adam. “Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation.” 2014. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/54005.

MLA Handbook (7th Edition):

Ruddy, Adam. “Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation.” 2014. Web. 29 May 2020.

Vancouver:

Ruddy A. Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation. [Internet] [Doctoral dissertation]. Dalhousie University; 2014. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/54005.

Council of Science Editors:

Ruddy A. Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation. [Doctoral Dissertation]. Dalhousie University; 2014. Available from: http://hdl.handle.net/10222/54005

6. Ruzic-Gauthier, Michael. Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones.

Degree: MS, Department of Chemistry, 2013, Dalhousie University

 DNA photocleaving reagents are a unique class of molecules that display the ability to cleave DNA, causing strand breaks, upon exposure to an irradiation source.… (more)

Subjects/Keywords: two-photon excitation; DNA cleavage

…of my master’s degree. Firstly, I would like to thank my research supervisor Dr. Norman P… …Schepp for providing me this wonderful opportunity and allowing me to participate in his unique… 

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

APA (6th Edition):

Ruzic-Gauthier, M. (2013). Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/36323

Chicago Manual of Style (16th Edition):

Ruzic-Gauthier, Michael. “Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones.” 2013. Masters Thesis, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/36323.

MLA Handbook (7th Edition):

Ruzic-Gauthier, Michael. “Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones.” 2013. Web. 29 May 2020.

Vancouver:

Ruzic-Gauthier M. Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/36323.

Council of Science Editors:

Ruzic-Gauthier M. Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/36323

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