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You searched for +publisher:"University of Michigan" +contributor:("Sanford, Melanie"). Showing records 1 – 30 of 68 total matches.

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University of Michigan

1. Todd, David. Development of Nickel-Catalyzed Methods for Deoxygenation Processes.

Degree: PhD, Chemistry, 2017, University of Michigan

 A new method for the reductive coupling of enals or enones and alkynes has been developed. The method results in a unique net four-electron reduction… (more)

Subjects/Keywords: Nickel-Catalyzed Methods; Deoxygenation Processes; Chemistry; Science

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APA (6th Edition):

Todd, D. (2017). Development of Nickel-Catalyzed Methods for Deoxygenation Processes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/137174

Chicago Manual of Style (16th Edition):

Todd, David. “Development of Nickel-Catalyzed Methods for Deoxygenation Processes.” 2017. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/137174.

MLA Handbook (7th Edition):

Todd, David. “Development of Nickel-Catalyzed Methods for Deoxygenation Processes.” 2017. Web. 04 Apr 2020.

Vancouver:

Todd D. Development of Nickel-Catalyzed Methods for Deoxygenation Processes. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/137174.

Council of Science Editors:

Todd D. Development of Nickel-Catalyzed Methods for Deoxygenation Processes. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/137174

2. Wagner, Anna M. Controlling Site-Selectivity in Palladium and Platinum-Catalyzed C-H Arylation Reactions And A Novel Method to Prepare Aryl Sulfides from Thioethers.

Degree: PhD, Chemistry, 2014, University of Michigan

 In recent years, there has been an increased focus on developing transition-metal catalyzed reactions to directly functionalize carbon-hydrogen bonds. Specifically, efficient C-H arylation reactions to… (more)

Subjects/Keywords: C-H Functionalization; Preparation of Aryl Thioethers; Chemistry; Science

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APA (6th Edition):

Wagner, A. M. (2014). Controlling Site-Selectivity in Palladium and Platinum-Catalyzed C-H Arylation Reactions And A Novel Method to Prepare Aryl Sulfides from Thioethers. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/108897

Chicago Manual of Style (16th Edition):

Wagner, Anna M. “Controlling Site-Selectivity in Palladium and Platinum-Catalyzed C-H Arylation Reactions And A Novel Method to Prepare Aryl Sulfides from Thioethers.” 2014. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/108897.

MLA Handbook (7th Edition):

Wagner, Anna M. “Controlling Site-Selectivity in Palladium and Platinum-Catalyzed C-H Arylation Reactions And A Novel Method to Prepare Aryl Sulfides from Thioethers.” 2014. Web. 04 Apr 2020.

Vancouver:

Wagner AM. Controlling Site-Selectivity in Palladium and Platinum-Catalyzed C-H Arylation Reactions And A Novel Method to Prepare Aryl Sulfides from Thioethers. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/108897.

Council of Science Editors:

Wagner AM. Controlling Site-Selectivity in Palladium and Platinum-Catalyzed C-H Arylation Reactions And A Novel Method to Prepare Aryl Sulfides from Thioethers. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/108897


University of Michigan

3. Carter, Tyler Joseph. Metal Mediated Reduction of Borazines for the Regeneration of Boron-Nitrogen Hydrogen Storage Materials.

Degree: PhD, Chemistry, 2014, University of Michigan

 Boron-nitrogen materials such as ammonia borane and cyclotriborazane are promising candidates for hydrogen storage due to their high gravimetric and volumetric hydrogen capacities. Though many… (more)

Subjects/Keywords: hydrogen storage; ammonia borane; borazine; Chemistry; Science

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APA (6th Edition):

Carter, T. J. (2014). Metal Mediated Reduction of Borazines for the Regeneration of Boron-Nitrogen Hydrogen Storage Materials. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/110495

Chicago Manual of Style (16th Edition):

Carter, Tyler Joseph. “Metal Mediated Reduction of Borazines for the Regeneration of Boron-Nitrogen Hydrogen Storage Materials.” 2014. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/110495.

MLA Handbook (7th Edition):

Carter, Tyler Joseph. “Metal Mediated Reduction of Borazines for the Regeneration of Boron-Nitrogen Hydrogen Storage Materials.” 2014. Web. 04 Apr 2020.

Vancouver:

Carter TJ. Metal Mediated Reduction of Borazines for the Regeneration of Boron-Nitrogen Hydrogen Storage Materials. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/110495.

Council of Science Editors:

Carter TJ. Metal Mediated Reduction of Borazines for the Regeneration of Boron-Nitrogen Hydrogen Storage Materials. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/110495

4. Furgal, Joseph C. Synthesis and Structure-Photophysical Property Relationships of T8, T10, T12 and Oligomeric Organic Functionalized Silsesquioxanes.

Degree: PhD, Chemistry, 2015, University of Michigan

 Silsesquioxanes with conjugated organic tethers (chromophores) offer high orders of functionality (> 8 tethers), unusual enhanced absorption, emission and charge separation over free chromophores, excited… (more)

Subjects/Keywords: Silsesquioxanes; Photophysical Properties; Fluoride Rearrangement; Organosilicon Chemistry; Energy; Chemistry; Science

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APA (6th Edition):

Furgal, J. C. (2015). Synthesis and Structure-Photophysical Property Relationships of T8, T10, T12 and Oligomeric Organic Functionalized Silsesquioxanes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111393

Chicago Manual of Style (16th Edition):

Furgal, Joseph C. “Synthesis and Structure-Photophysical Property Relationships of T8, T10, T12 and Oligomeric Organic Functionalized Silsesquioxanes.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/111393.

MLA Handbook (7th Edition):

Furgal, Joseph C. “Synthesis and Structure-Photophysical Property Relationships of T8, T10, T12 and Oligomeric Organic Functionalized Silsesquioxanes.” 2015. Web. 04 Apr 2020.

Vancouver:

Furgal JC. Synthesis and Structure-Photophysical Property Relationships of T8, T10, T12 and Oligomeric Organic Functionalized Silsesquioxanes. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/111393.

Council of Science Editors:

Furgal JC. Synthesis and Structure-Photophysical Property Relationships of T8, T10, T12 and Oligomeric Organic Functionalized Silsesquioxanes. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111393


University of Michigan

5. Thompson, Benjamin Bristol. The Reductive Couplings of Enones and Alkynes and Application to Heterocycle Synthesis.

Degree: PhD, Chemistry, 2012, University of Michigan

 A new method for the reductive coupling of alkynes to enones has been developed. This method provides an alternative to more traditional methods of conjugate… (more)

Subjects/Keywords: Nickel-Catalyzed Reductive Coupling of Enones and Alkynes; Heterocycle Synthesis; Chemistry; Science

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APA (6th Edition):

Thompson, B. B. (2012). The Reductive Couplings of Enones and Alkynes and Application to Heterocycle Synthesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/91615

Chicago Manual of Style (16th Edition):

Thompson, Benjamin Bristol. “The Reductive Couplings of Enones and Alkynes and Application to Heterocycle Synthesis.” 2012. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/91615.

MLA Handbook (7th Edition):

Thompson, Benjamin Bristol. “The Reductive Couplings of Enones and Alkynes and Application to Heterocycle Synthesis.” 2012. Web. 04 Apr 2020.

Vancouver:

Thompson BB. The Reductive Couplings of Enones and Alkynes and Application to Heterocycle Synthesis. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/91615.

Council of Science Editors:

Thompson BB. The Reductive Couplings of Enones and Alkynes and Application to Heterocycle Synthesis. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/91615

6. Klepser, Benjamin M. Solar Activation of Molecular Water Oxidation Catalysts Using Semiconductors.

Degree: PhD, Chemistry, 2015, University of Michigan

 Water splitting has been proposed as a viable route toward the renewable production of hydrogen. However, this approach is limited by the water oxidation half-reaction… (more)

Subjects/Keywords: Solar Energy; Photoelectrochemical Water Splitting; Semiconductor Photocatalysis; Molecular Photocatalysis; Water Oxidation; Chemistry; Science

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APA (6th Edition):

Klepser, B. M. (2015). Solar Activation of Molecular Water Oxidation Catalysts Using Semiconductors. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111517

Chicago Manual of Style (16th Edition):

Klepser, Benjamin M. “Solar Activation of Molecular Water Oxidation Catalysts Using Semiconductors.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/111517.

MLA Handbook (7th Edition):

Klepser, Benjamin M. “Solar Activation of Molecular Water Oxidation Catalysts Using Semiconductors.” 2015. Web. 04 Apr 2020.

Vancouver:

Klepser BM. Solar Activation of Molecular Water Oxidation Catalysts Using Semiconductors. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/111517.

Council of Science Editors:

Klepser BM. Solar Activation of Molecular Water Oxidation Catalysts Using Semiconductors. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111517


University of Michigan

7. Miller, Zachary D. New Strategies for Stereo- and Regiocontrol in Allene Hydrosilylation.

Degree: PhD, Chemistry, 2015, University of Michigan

 Controlling the regiochemistry in additions of silanes across units of unsaturation is a significant challenge in route to important stereo- and regiodefined alkenyl- and allylsilane… (more)

Subjects/Keywords: regioreversals; Chemistry; Science

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APA (6th Edition):

Miller, Z. D. (2015). New Strategies for Stereo- and Regiocontrol in Allene Hydrosilylation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111587

Chicago Manual of Style (16th Edition):

Miller, Zachary D. “New Strategies for Stereo- and Regiocontrol in Allene Hydrosilylation.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/111587.

MLA Handbook (7th Edition):

Miller, Zachary D. “New Strategies for Stereo- and Regiocontrol in Allene Hydrosilylation.” 2015. Web. 04 Apr 2020.

Vancouver:

Miller ZD. New Strategies for Stereo- and Regiocontrol in Allene Hydrosilylation. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/111587.

Council of Science Editors:

Miller ZD. New Strategies for Stereo- and Regiocontrol in Allene Hydrosilylation. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111587

8. Bryan, Zachary Jacob. Developing New Catalysts and Methods for Catalyst-transfer Polycondensations (CTP).

Degree: PhD, Chemistry, 2015, University of Michigan

 Chapter 1 provides a general introduction and brief history of the controlled synthesis of pi-conjugated polymers via catalyst-transfer polycondensation (CTP). We focus on the mechanistic… (more)

Subjects/Keywords: Catalyst-transfer Polycondensation; Pi-conjugated Polymer Synthesis; Nickely-catalyzed Chain-growth Polymerization; Conjugated Copolymers; Mechanism; Catalysis; Chemistry; Science

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APA (6th Edition):

Bryan, Z. J. (2015). Developing New Catalysts and Methods for Catalyst-transfer Polycondensations (CTP). (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113350

Chicago Manual of Style (16th Edition):

Bryan, Zachary Jacob. “Developing New Catalysts and Methods for Catalyst-transfer Polycondensations (CTP).” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113350.

MLA Handbook (7th Edition):

Bryan, Zachary Jacob. “Developing New Catalysts and Methods for Catalyst-transfer Polycondensations (CTP).” 2015. Web. 04 Apr 2020.

Vancouver:

Bryan ZJ. Developing New Catalysts and Methods for Catalyst-transfer Polycondensations (CTP). [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113350.

Council of Science Editors:

Bryan ZJ. Developing New Catalysts and Methods for Catalyst-transfer Polycondensations (CTP). [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113350


University of Michigan

9. Hopkins, Brett A. Enantioselective Synthesis of Heterocycles via Palladium Catalyzed Alkene Difunctionalization Reactions.

Degree: PhD, Chemistry, 2015, University of Michigan

 Enantiopure nitrogen and oxygen containing heterocycles are prominently displayed in a variety of important pharmaceuticals and biologically active products. As such accessing these scaffolds in… (more)

Subjects/Keywords: Enantioselective; Heterocycles; Chemistry; Science

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APA (6th Edition):

Hopkins, B. A. (2015). Enantioselective Synthesis of Heterocycles via Palladium Catalyzed Alkene Difunctionalization Reactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113418

Chicago Manual of Style (16th Edition):

Hopkins, Brett A. “Enantioselective Synthesis of Heterocycles via Palladium Catalyzed Alkene Difunctionalization Reactions.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113418.

MLA Handbook (7th Edition):

Hopkins, Brett A. “Enantioselective Synthesis of Heterocycles via Palladium Catalyzed Alkene Difunctionalization Reactions.” 2015. Web. 04 Apr 2020.

Vancouver:

Hopkins BA. Enantioselective Synthesis of Heterocycles via Palladium Catalyzed Alkene Difunctionalization Reactions. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113418.

Council of Science Editors:

Hopkins BA. Enantioselective Synthesis of Heterocycles via Palladium Catalyzed Alkene Difunctionalization Reactions. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113418


University of Michigan

10. Dutta, Ananya. Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers.

Degree: PhD, Chemistry, 2015, University of Michigan

 Microporous coordination polymers (MCPs), materials built from metal clusters bridged with organic linkers, constitute a rapidly growing class of porous solids. The conventional synthetic strategies… (more)

Subjects/Keywords: Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers; Chemistry; Science

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APA (6th Edition):

Dutta, A. (2015). Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113422

Chicago Manual of Style (16th Edition):

Dutta, Ananya. “Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113422.

MLA Handbook (7th Edition):

Dutta, Ananya. “Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers.” 2015. Web. 04 Apr 2020.

Vancouver:

Dutta A. Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113422.

Council of Science Editors:

Dutta A. Multicomponent Approaches for the Generation of Structurally Diverse Microporous Coordination Polymers. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113422


University of Michigan

11. Jackson, Evan P. Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes.

Degree: PhD, Chemistry, 2015, University of Michigan

 Advances in nickel catalyzed reactions have been achieved that allow for alteration and control of the rate- and regioselectivity determining step in nickel-catalyzed aldehyde-alkyne reductive… (more)

Subjects/Keywords: Ni-Catalyzed Reductive Couplings; Chemistry; Science

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APA (6th Edition):

Jackson, E. P. (2015). Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113425

Chicago Manual of Style (16th Edition):

Jackson, Evan P. “Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113425.

MLA Handbook (7th Edition):

Jackson, Evan P. “Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes.” 2015. Web. 04 Apr 2020.

Vancouver:

Jackson EP. Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113425.

Council of Science Editors:

Jackson EP. Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113425

12. Borovika, Alina. Advances in Bronsted Acid Catalysis: Reactions of Oxocarbenium Ions.

Degree: PhD, Chemistry, 2015, University of Michigan

 Oxocarbenium ions are common intermedates or transition states for a variety of biological and synthetic transformations. Due to the fact that oxocarbenium ions are typically… (more)

Subjects/Keywords: chiral Bronsted acids; hydrogen bond donors; oxocarbenium ions; [4+2] cycloaddition; glycosylation; 2-deoxystreptamine; Chemistry; Science

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APA (6th Edition):

Borovika, A. (2015). Advances in Bronsted Acid Catalysis: Reactions of Oxocarbenium Ions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113511

Chicago Manual of Style (16th Edition):

Borovika, Alina. “Advances in Bronsted Acid Catalysis: Reactions of Oxocarbenium Ions.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113511.

MLA Handbook (7th Edition):

Borovika, Alina. “Advances in Bronsted Acid Catalysis: Reactions of Oxocarbenium Ions.” 2015. Web. 04 Apr 2020.

Vancouver:

Borovika A. Advances in Bronsted Acid Catalysis: Reactions of Oxocarbenium Ions. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113511.

Council of Science Editors:

Borovika A. Advances in Bronsted Acid Catalysis: Reactions of Oxocarbenium Ions. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113511


University of Michigan

13. Lotz, Monica D. Mechanistic Insights with Homogeneous Pd and Pt Complexes for the Oxidative Coupling of Methane.

Degree: PhD, Chemistry, 2015, University of Michigan

 As a result of the increasing production of natural gas in the U.S., there is a demand to utilize its main component, methane, as a… (more)

Subjects/Keywords: methane functionalization; organometallic chemistry; palladium; Chemistry; Science

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APA (6th Edition):

Lotz, M. D. (2015). Mechanistic Insights with Homogeneous Pd and Pt Complexes for the Oxidative Coupling of Methane. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113556

Chicago Manual of Style (16th Edition):

Lotz, Monica D. “Mechanistic Insights with Homogeneous Pd and Pt Complexes for the Oxidative Coupling of Methane.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113556.

MLA Handbook (7th Edition):

Lotz, Monica D. “Mechanistic Insights with Homogeneous Pd and Pt Complexes for the Oxidative Coupling of Methane.” 2015. Web. 04 Apr 2020.

Vancouver:

Lotz MD. Mechanistic Insights with Homogeneous Pd and Pt Complexes for the Oxidative Coupling of Methane. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113556.

Council of Science Editors:

Lotz MD. Mechanistic Insights with Homogeneous Pd and Pt Complexes for the Oxidative Coupling of Methane. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113556


University of Michigan

14. Moore, Cameron M. Secondary Coordination Sphere Contributions to Primary Sphere Structure, Bonding and Reactivity.

Degree: PhD, Chemistry, 2015, University of Michigan

 Metalloenzymes are unique in their ability to mediate the transformations of relatively inert substrates with impressive selectivity and speed. Secondary interactions such as hydrogen bonding… (more)

Subjects/Keywords: Inorganic chemistry; Secondary coordination sphere; Hydrogen bonding; Ligand design; Chemistry; Science

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APA (6th Edition):

Moore, C. M. (2015). Secondary Coordination Sphere Contributions to Primary Sphere Structure, Bonding and Reactivity. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113626

Chicago Manual of Style (16th Edition):

Moore, Cameron M. “Secondary Coordination Sphere Contributions to Primary Sphere Structure, Bonding and Reactivity.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/113626.

MLA Handbook (7th Edition):

Moore, Cameron M. “Secondary Coordination Sphere Contributions to Primary Sphere Structure, Bonding and Reactivity.” 2015. Web. 04 Apr 2020.

Vancouver:

Moore CM. Secondary Coordination Sphere Contributions to Primary Sphere Structure, Bonding and Reactivity. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/113626.

Council of Science Editors:

Moore CM. Secondary Coordination Sphere Contributions to Primary Sphere Structure, Bonding and Reactivity. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113626


University of Michigan

15. Cook-Sneathen, Amanda Karena. Transition Metal-Catalyzed Non-Directed C-H Functionalization of Arenes and Alkanes.

Degree: PhD, Chemistry, 2015, University of Michigan

 The development of novel methods to convert chemical feedstocks is desirable, as it holds the potential for valorization. These chemicals are primarily hydrocarbons and therefore,… (more)

Subjects/Keywords: C-H activation; Catalysis; Alkane; Arene; Chemistry; Science

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APA (6th Edition):

Cook-Sneathen, A. K. (2015). Transition Metal-Catalyzed Non-Directed C-H Functionalization of Arenes and Alkanes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/116781

Chicago Manual of Style (16th Edition):

Cook-Sneathen, Amanda Karena. “Transition Metal-Catalyzed Non-Directed C-H Functionalization of Arenes and Alkanes.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/116781.

MLA Handbook (7th Edition):

Cook-Sneathen, Amanda Karena. “Transition Metal-Catalyzed Non-Directed C-H Functionalization of Arenes and Alkanes.” 2015. Web. 04 Apr 2020.

Vancouver:

Cook-Sneathen AK. Transition Metal-Catalyzed Non-Directed C-H Functionalization of Arenes and Alkanes. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/116781.

Council of Science Editors:

Cook-Sneathen AK. Transition Metal-Catalyzed Non-Directed C-H Functionalization of Arenes and Alkanes. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/116781


University of Michigan

16. Tseng, Kuei-Nin T. Structure and Reactivity Studies of Bis(pyridylimino)isoindolate Transition Metal Complexes.

Degree: PhD, Chemistry, 2016, University of Michigan

 In this dissertation, transition metal complexes supported by bpi-type (bpi = 1,3-bis(2’-pyridylimino)isoindolate) ligands were designed and synthesized to study their activity, selectivity, and stability in… (more)

Subjects/Keywords: Organometallic Chemistry; Homogeneous Catalysis; Acceptorless Alcohol Dehydrogenation; Alkene Hydroboration Catalyzed by Iron; Upgrading Ethanol to Butanol; Metal Ligand Cooperativity; Chemistry; Science

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APA (6th Edition):

Tseng, K. T. (2016). Structure and Reactivity Studies of Bis(pyridylimino)isoindolate Transition Metal Complexes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120813

Chicago Manual of Style (16th Edition):

Tseng, Kuei-Nin T. “Structure and Reactivity Studies of Bis(pyridylimino)isoindolate Transition Metal Complexes.” 2016. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/120813.

MLA Handbook (7th Edition):

Tseng, Kuei-Nin T. “Structure and Reactivity Studies of Bis(pyridylimino)isoindolate Transition Metal Complexes.” 2016. Web. 04 Apr 2020.

Vancouver:

Tseng KT. Structure and Reactivity Studies of Bis(pyridylimino)isoindolate Transition Metal Complexes. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/120813.

Council of Science Editors:

Tseng KT. Structure and Reactivity Studies of Bis(pyridylimino)isoindolate Transition Metal Complexes. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120813


University of Michigan

17. Keylor, Mitchell Henry. A Unified Approach to Resveratrol-Derived Natural Products: Harnessing the Reactivity of Persistent Radical and Quinone Methide Intermediates for Complex Molecule Synthesis.

Degree: PhD, Chemistry, 2016, University of Michigan

 Numerous reports of therapeutically relevant biological activities of resveratrol (3,4ʹ,5-trihydroxy-trans-stilbene) and oligomers derived therefrom have stimulated widespread interest in these natural products. In spite of… (more)

Subjects/Keywords: Resveratrol; Oligomer; Quinone Methide; Persistent Radical; Antioxidant; Biomimetic Total Synthesis; Chemistry; Science

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APA (6th Edition):

Keylor, M. H. (2016). A Unified Approach to Resveratrol-Derived Natural Products: Harnessing the Reactivity of Persistent Radical and Quinone Methide Intermediates for Complex Molecule Synthesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/133498

Chicago Manual of Style (16th Edition):

Keylor, Mitchell Henry. “A Unified Approach to Resveratrol-Derived Natural Products: Harnessing the Reactivity of Persistent Radical and Quinone Methide Intermediates for Complex Molecule Synthesis.” 2016. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/133498.

MLA Handbook (7th Edition):

Keylor, Mitchell Henry. “A Unified Approach to Resveratrol-Derived Natural Products: Harnessing the Reactivity of Persistent Radical and Quinone Methide Intermediates for Complex Molecule Synthesis.” 2016. Web. 04 Apr 2020.

Vancouver:

Keylor MH. A Unified Approach to Resveratrol-Derived Natural Products: Harnessing the Reactivity of Persistent Radical and Quinone Methide Intermediates for Complex Molecule Synthesis. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/133498.

Council of Science Editors:

Keylor MH. A Unified Approach to Resveratrol-Derived Natural Products: Harnessing the Reactivity of Persistent Radical and Quinone Methide Intermediates for Complex Molecule Synthesis. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/133498


University of Michigan

18. Kubota, Asako. Pd-Catalyzed Oxidative Functionalizations.

Degree: PhD, Chemistry, 2012, University of Michigan

 A traditional Pd(0/II) mechanism is commonly evoked for a number of well-known cross-coupling reactions (i.e. Heck, Suzuki, Negishi, etc). In recent years, there has been… (more)

Subjects/Keywords: Pd-catalyzed Olefin Difunctionalization; Chemistry; Science

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APA (6th Edition):

Kubota, A. (2012). Pd-Catalyzed Oxidative Functionalizations. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/94086

Chicago Manual of Style (16th Edition):

Kubota, Asako. “Pd-Catalyzed Oxidative Functionalizations.” 2012. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/94086.

MLA Handbook (7th Edition):

Kubota, Asako. “Pd-Catalyzed Oxidative Functionalizations.” 2012. Web. 04 Apr 2020.

Vancouver:

Kubota A. Pd-Catalyzed Oxidative Functionalizations. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/94086.

Council of Science Editors:

Kubota A. Pd-Catalyzed Oxidative Functionalizations. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/94086


University of Michigan

19. Neufeldt, Sharon Rose. Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization.

Degree: PhD, Chemistry, 2013, University of Michigan

 Because of their abundance, C-H bonds are highly attractive starting materials for the elaboration of complex molecules. Transition metal catalysis can enable these typically inert… (more)

Subjects/Keywords: Palladium; C-H Activation; Radicals; Chemistry; Science

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APA (6th Edition):

Neufeldt, S. R. (2013). Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/98061

Chicago Manual of Style (16th Edition):

Neufeldt, Sharon Rose. “Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization.” 2013. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/98061.

MLA Handbook (7th Edition):

Neufeldt, Sharon Rose. “Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization.” 2013. Web. 04 Apr 2020.

Vancouver:

Neufeldt SR. Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/98061.

Council of Science Editors:

Neufeldt SR. Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/98061


University of Michigan

20. Baxter, Ryan David. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.

Degree: PhD, Chemistry, 2010, University of Michigan

 Many classes of standard organic transformations involve the coupling or cycloaddition of two different π-components to assemble a more functionalized product. Many such processes are… (more)

Subjects/Keywords: Nickel Catalyzed Reductive Coupling; Chemistry; Science

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APA (6th Edition):

Baxter, R. D. (2010). Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/78979

Chicago Manual of Style (16th Edition):

Baxter, Ryan David. “Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.” 2010. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/78979.

MLA Handbook (7th Edition):

Baxter, Ryan David. “Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.” 2010. Web. 04 Apr 2020.

Vancouver:

Baxter RD. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/78979.

Council of Science Editors:

Baxter RD. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/78979


University of Michigan

21. Mai, Duy N. Asymmetric Palladium-Catalyzed Reactions for the Synthesis of Pyrrolidines and Other Heterocycles.

Degree: PhD, Chemistry, 2011, University of Michigan

 The synthesis of nitrogen-containing heterocycles is important due to the fact that many biologically active molecules contain these motifs. Over the past 10 years, the… (more)

Subjects/Keywords: Asymmetric; Palladium-Catalyzed; Carboamination; Enantioselective; Pyrrolidines; Chemistry; Science

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APA (6th Edition):

Mai, D. N. (2011). Asymmetric Palladium-Catalyzed Reactions for the Synthesis of Pyrrolidines and Other Heterocycles. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86278

Chicago Manual of Style (16th Edition):

Mai, Duy N. “Asymmetric Palladium-Catalyzed Reactions for the Synthesis of Pyrrolidines and Other Heterocycles.” 2011. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/86278.

MLA Handbook (7th Edition):

Mai, Duy N. “Asymmetric Palladium-Catalyzed Reactions for the Synthesis of Pyrrolidines and Other Heterocycles.” 2011. Web. 04 Apr 2020.

Vancouver:

Mai DN. Asymmetric Palladium-Catalyzed Reactions for the Synthesis of Pyrrolidines and Other Heterocycles. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/86278.

Council of Science Editors:

Mai DN. Asymmetric Palladium-Catalyzed Reactions for the Synthesis of Pyrrolidines and Other Heterocycles. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86278


University of Michigan

22. Schaidle, Joshua A. Carbide and Nitride Based Catalysts for Synthesis Gas Conversion.

Degree: PhD, Chemical Engineering, 2011, University of Michigan

 The production of fuels and chemicals from syngas (H2 and CO) plays a critical role in our economy and will play an even greater role… (more)

Subjects/Keywords: Fischer-Tropsch; Catalyst; Water Gas Shift; Early Transition Metal Carbide; X-ray Absorption Spectroscopy; Synthesis Gas; Chemical Engineering; Engineering

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APA (6th Edition):

Schaidle, J. A. (2011). Carbide and Nitride Based Catalysts for Synthesis Gas Conversion. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/89768

Chicago Manual of Style (16th Edition):

Schaidle, Joshua A. “Carbide and Nitride Based Catalysts for Synthesis Gas Conversion.” 2011. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/89768.

MLA Handbook (7th Edition):

Schaidle, Joshua A. “Carbide and Nitride Based Catalysts for Synthesis Gas Conversion.” 2011. Web. 04 Apr 2020.

Vancouver:

Schaidle JA. Carbide and Nitride Based Catalysts for Synthesis Gas Conversion. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/89768.

Council of Science Editors:

Schaidle JA. Carbide and Nitride Based Catalysts for Synthesis Gas Conversion. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/89768


University of Michigan

23. Wiensch, Eric. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis.

Degree: PhD, Chemistry, 2018, University of Michigan

 Silane protecting groups are traditionally only viewed as inert protecting groups to mask an alcohol functionality, allowing for orthogonal reactivity compared with other protecting groups… (more)

Subjects/Keywords: Silyloxyarene; C-O Bond Coupling; Nickel Catalysis; Chemistry; Science

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APA (6th Edition):

Wiensch, E. (2018). Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/146110

Chicago Manual of Style (16th Edition):

Wiensch, Eric. “Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis.” 2018. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/146110.

MLA Handbook (7th Edition):

Wiensch, Eric. “Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis.” 2018. Web. 04 Apr 2020.

Vancouver:

Wiensch E. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/146110.

Council of Science Editors:

Wiensch E. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/146110


University of Michigan

24. James, Bryant. Applications of Metal-Organic Frameworks in Catalysis and Separations.

Degree: PhD, Chemistry, 2018, University of Michigan

 Metal-organic frameworks (MOFs) are a class of porous coordination polymers that has been the subject of intense investigation since there discovery almost 30 years ago.… (more)

Subjects/Keywords: Metal-Organic Framework; Chemistry; Science

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APA (6th Edition):

James, B. (2018). Applications of Metal-Organic Frameworks in Catalysis and Separations. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/146126

Chicago Manual of Style (16th Edition):

James, Bryant. “Applications of Metal-Organic Frameworks in Catalysis and Separations.” 2018. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/146126.

MLA Handbook (7th Edition):

James, Bryant. “Applications of Metal-Organic Frameworks in Catalysis and Separations.” 2018. Web. 04 Apr 2020.

Vancouver:

James B. Applications of Metal-Organic Frameworks in Catalysis and Separations. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/146126.

Council of Science Editors:

James B. Applications of Metal-Organic Frameworks in Catalysis and Separations. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/146126


University of Michigan

25. Nett, Alex. Development and Mechanistic Implications of Nickel Pre-Catalysts for Organic Synthesis.

Degree: PhD, Chemistry, 2018, University of Michigan

 Nickel catalysis is a versatile tool for constructing complex molecules, but a variety of operational challenges limit the wide spread use of these methods outside… (more)

Subjects/Keywords: Nickel Catalysis; Air-stable Nickel Pre-catalysts; Computational and Experimental Mechanistic Studies of Nickel-catalyzed C-H Functionalization; Chemistry; Science

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APA (6th Edition):

Nett, A. (2018). Development and Mechanistic Implications of Nickel Pre-Catalysts for Organic Synthesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/146127

Chicago Manual of Style (16th Edition):

Nett, Alex. “Development and Mechanistic Implications of Nickel Pre-Catalysts for Organic Synthesis.” 2018. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/146127.

MLA Handbook (7th Edition):

Nett, Alex. “Development and Mechanistic Implications of Nickel Pre-Catalysts for Organic Synthesis.” 2018. Web. 04 Apr 2020.

Vancouver:

Nett A. Development and Mechanistic Implications of Nickel Pre-Catalysts for Organic Synthesis. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/146127.

Council of Science Editors:

Nett A. Development and Mechanistic Implications of Nickel Pre-Catalysts for Organic Synthesis. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/146127


University of Michigan

26. Meucci, Elizabeth. Development of High-Valent Nickel Complexes for Carbon-Carbon and Carbon-Heteroatom Bond Formation.

Degree: PhD, Chemistry, 2019, University of Michigan

 Nickel has served as a valuable transition metal catalyst for over a century, helping to forge key chemical disconnections under mild reaction conditions. The unique… (more)

Subjects/Keywords: High-Valent Nickel Chemistry; Chemistry; Science

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APA (6th Edition):

Meucci, E. (2019). Development of High-Valent Nickel Complexes for Carbon-Carbon and Carbon-Heteroatom Bond Formation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/151526

Chicago Manual of Style (16th Edition):

Meucci, Elizabeth. “Development of High-Valent Nickel Complexes for Carbon-Carbon and Carbon-Heteroatom Bond Formation.” 2019. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/151526.

MLA Handbook (7th Edition):

Meucci, Elizabeth. “Development of High-Valent Nickel Complexes for Carbon-Carbon and Carbon-Heteroatom Bond Formation.” 2019. Web. 04 Apr 2020.

Vancouver:

Meucci E. Development of High-Valent Nickel Complexes for Carbon-Carbon and Carbon-Heteroatom Bond Formation. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/151526.

Council of Science Editors:

Meucci E. Development of High-Valent Nickel Complexes for Carbon-Carbon and Carbon-Heteroatom Bond Formation. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/151526


University of Michigan

27. Dewyer, Amanda. Automated Reaction Discovery Tools and their Application to Understanding Organometallic Reactions.

Degree: PhD, Chemistry, 2019, University of Michigan

 Using computational simulations to model reaction mechanisms has been a common way to garner kinetic and thermodynamic information of a chemical system that can help… (more)

Subjects/Keywords: Computational Chemistry; Polymerization; C-H Activation; Density Functional Theory; Chemistry; Science

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APA (6th Edition):

Dewyer, A. (2019). Automated Reaction Discovery Tools and their Application to Understanding Organometallic Reactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/151527

Chicago Manual of Style (16th Edition):

Dewyer, Amanda. “Automated Reaction Discovery Tools and their Application to Understanding Organometallic Reactions.” 2019. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/151527.

MLA Handbook (7th Edition):

Dewyer, Amanda. “Automated Reaction Discovery Tools and their Application to Understanding Organometallic Reactions.” 2019. Web. 04 Apr 2020.

Vancouver:

Dewyer A. Automated Reaction Discovery Tools and their Application to Understanding Organometallic Reactions. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/151527.

Council of Science Editors:

Dewyer A. Automated Reaction Discovery Tools and their Application to Understanding Organometallic Reactions. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/151527


University of Michigan

28. Fisher, Sydney. Non-Aqueous Redox Flow Batteries: Active Species Stability and Cost Saving Design Concepts.

Degree: PhD, Chemical Engineering, 2017, University of Michigan

 Non-aqueous redox flow batteries (NAqRFBs) have recently received considerable attention as promising high energy density grid-level energy storage devices. Despite many attractive features, NAqRFBs are… (more)

Subjects/Keywords: Redox flow batteries; Nonaqueous; Metal coordination complex; Common ion exchange; Chemical Engineering; Engineering

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APA (6th Edition):

Fisher, S. (2017). Non-Aqueous Redox Flow Batteries: Active Species Stability and Cost Saving Design Concepts. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/140904

Chicago Manual of Style (16th Edition):

Fisher, Sydney. “Non-Aqueous Redox Flow Batteries: Active Species Stability and Cost Saving Design Concepts.” 2017. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/140904.

MLA Handbook (7th Edition):

Fisher, Sydney. “Non-Aqueous Redox Flow Batteries: Active Species Stability and Cost Saving Design Concepts.” 2017. Web. 04 Apr 2020.

Vancouver:

Fisher S. Non-Aqueous Redox Flow Batteries: Active Species Stability and Cost Saving Design Concepts. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/140904.

Council of Science Editors:

Fisher S. Non-Aqueous Redox Flow Batteries: Active Species Stability and Cost Saving Design Concepts. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/140904


University of Michigan

29. Rezayee, Nomaan. Strategies Towards the Hydrogenation of CO2 and Carboxylic Acid Derivatives.

Degree: PhD, Chemistry, 2017, University of Michigan

 Increasing energy demands have been met with added combustion of fossil fuels. The massive quantities of carbon dioxide (CO2) given off as a byproduct of… (more)

Subjects/Keywords: Carbon Dioxide Hydrogenation; Catalysis; Amide Hydrogenation; Ester Hydrogenation; Chemistry; Science

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APA (6th Edition):

Rezayee, N. (2017). Strategies Towards the Hydrogenation of CO2 and Carboxylic Acid Derivatives. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/140933

Chicago Manual of Style (16th Edition):

Rezayee, Nomaan. “Strategies Towards the Hydrogenation of CO2 and Carboxylic Acid Derivatives.” 2017. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/140933.

MLA Handbook (7th Edition):

Rezayee, Nomaan. “Strategies Towards the Hydrogenation of CO2 and Carboxylic Acid Derivatives.” 2017. Web. 04 Apr 2020.

Vancouver:

Rezayee N. Strategies Towards the Hydrogenation of CO2 and Carboxylic Acid Derivatives. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/140933.

Council of Science Editors:

Rezayee N. Strategies Towards the Hydrogenation of CO2 and Carboxylic Acid Derivatives. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/140933


University of Michigan

30. Ichiishi, Naoko. Transition Metal-Catalyzed Fluorination/ [18]fluorination and Decarbonylative Carbon Heteroatom Bond Formation.

Degree: PhD, Chemistry, 2016, University of Michigan

 The development of novel methods to incorporate fluorine and fluoroalkyl groups into organic molecules is highly desirable, as these substituents can impart unique stability, reactivity… (more)

Subjects/Keywords: fluorination; copper; PET; Chemistry; Science

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APA (6th Edition):

Ichiishi, N. (2016). Transition Metal-Catalyzed Fluorination/ [18]fluorination and Decarbonylative Carbon Heteroatom Bond Formation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/133480

Chicago Manual of Style (16th Edition):

Ichiishi, Naoko. “Transition Metal-Catalyzed Fluorination/ [18]fluorination and Decarbonylative Carbon Heteroatom Bond Formation.” 2016. Doctoral Dissertation, University of Michigan. Accessed April 04, 2020. http://hdl.handle.net/2027.42/133480.

MLA Handbook (7th Edition):

Ichiishi, Naoko. “Transition Metal-Catalyzed Fluorination/ [18]fluorination and Decarbonylative Carbon Heteroatom Bond Formation.” 2016. Web. 04 Apr 2020.

Vancouver:

Ichiishi N. Transition Metal-Catalyzed Fluorination/ [18]fluorination and Decarbonylative Carbon Heteroatom Bond Formation. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Apr 04]. Available from: http://hdl.handle.net/2027.42/133480.

Council of Science Editors:

Ichiishi N. Transition Metal-Catalyzed Fluorination/ [18]fluorination and Decarbonylative Carbon Heteroatom Bond Formation. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/133480

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