Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:

Thesis advisor: Jeffery A. Byers === Thesis advisor: Chia-Kuang (Frank) Tsung === Biological systems have evolved over time to favor structures beneficial for the efficient transformation of simple feedstocks to sophisticated products. In particular, enzymes have evolved such that cooperative and ge...

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Main Author: Rayder, Thomas M.
Format: Others
Language:English
Published: Boston College 2020
Subjects:
Online Access:http://hdl.handle.net/2345/bc-ir:108930
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spelling ndltd-BOSTON-oai-dlib.bc.edu-bc-ir_1089302021-08-04T05:01:04Z Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes: Rayder, Thomas M. Thesis advisor: Jeffery A. Byers Thesis advisor: Chia-Kuang (Frank) Tsung Text thesis 2020 Boston College English electronic application/pdf Biological systems have evolved over time to favor structures beneficial for the efficient transformation of simple feedstocks to sophisticated products. In particular, enzymes have evolved such that cooperative and geometrically controlled interactions between active sites and substrates enhance catalytic activity and selectivity. Separation of these active sites from other incompatible catalytic components allows for chemical transformation in a stepwise fashion, circumventing the inherent limitations to performing reactions in a single step. This dissertation describes the use of porous crystalline materials called metal-organic frameworks (MOFs) as hosts to mimic the component separation and precise active site control observed in nature. The first phase of these efforts explores the use of dissociative “aperture-opening” linker exchange pathways in a MOF to encapsulate transition metal complexes for carbon dioxide hydrogenation to formate. This strategy is then used to separate two incompatible complexes and perform the cascade conversion of carbon dioxide to methanol, resulting in unique and previously unobserved network autocatalytic behavior. Finally, the modularity of the MOF host is leveraged to install beneficial functionality in close proximity to the encapsulated transition metal complex, leading to activity exceeding that of any reported homogeneous system for carbon dioxide reduction. The insights gained through these studies can inform the development of composites for other reactions, allowing for access to new and unique reaction manifolds. Alternative Fuel Autocatalysis Carbon Dioxide Catalysis Metal-Organic Framework Porous Copyright is held by the author, with all rights reserved, unless otherwise noted. Thesis (PhD) — Boston College, 2020. Submitted to: Boston College. Graduate School of Arts and Sciences. Discipline: Chemistry. http://hdl.handle.net/2345/bc-ir:108930
collection NDLTD
language English
format Others
sources NDLTD
topic Alternative Fuel
Autocatalysis
Carbon Dioxide
Catalysis
Metal-Organic Framework
Porous
spellingShingle Alternative Fuel
Autocatalysis
Carbon Dioxide
Catalysis
Metal-Organic Framework
Porous
Rayder, Thomas M.
Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:
description Thesis advisor: Jeffery A. Byers === Thesis advisor: Chia-Kuang (Frank) Tsung === Biological systems have evolved over time to favor structures beneficial for the efficient transformation of simple feedstocks to sophisticated products. In particular, enzymes have evolved such that cooperative and geometrically controlled interactions between active sites and substrates enhance catalytic activity and selectivity. Separation of these active sites from other incompatible catalytic components allows for chemical transformation in a stepwise fashion, circumventing the inherent limitations to performing reactions in a single step. This dissertation describes the use of porous crystalline materials called metal-organic frameworks (MOFs) as hosts to mimic the component separation and precise active site control observed in nature. The first phase of these efforts explores the use of dissociative “aperture-opening” linker exchange pathways in a MOF to encapsulate transition metal complexes for carbon dioxide hydrogenation to formate. This strategy is then used to separate two incompatible complexes and perform the cascade conversion of carbon dioxide to methanol, resulting in unique and previously unobserved network autocatalytic behavior. Finally, the modularity of the MOF host is leveraged to install beneficial functionality in close proximity to the encapsulated transition metal complex, leading to activity exceeding that of any reported homogeneous system for carbon dioxide reduction. The insights gained through these studies can inform the development of composites for other reactions, allowing for access to new and unique reaction manifolds. === Thesis (PhD) — Boston College, 2020. === Submitted to: Boston College. Graduate School of Arts and Sciences. === Discipline: Chemistry.
author Rayder, Thomas M.
author_facet Rayder, Thomas M.
author_sort Rayder, Thomas M.
title Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:
title_short Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:
title_full Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:
title_fullStr Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:
title_full_unstemmed Modulation of Catalyst@MOF Host-Guest Composites in Pursuit of Synthetic Artificial Enzymes:
title_sort modulation of catalyst@mof host-guest composites in pursuit of synthetic artificial enzymes:
publisher Boston College
publishDate 2020
url http://hdl.handle.net/2345/bc-ir:108930
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