Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:

Thesis advisor: Jeffery A. Byers === Thesis advisor: Chia-Kuang Tsung === Homogeneous catalysts are advantageous in selective catalysis due to the well-defined active site at the molecular level. The poor recyclability, bimolecular aggregation, and undesired poison resistance of homogeneous catalyst...

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Main Author: Li, Zhehui
Format: Others
Language:English
Published: Boston College 2019
Subjects:
Online Access:http://hdl.handle.net/2345/bc-ir:108707
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spelling ndltd-BOSTON-oai-dlib.bc.edu-bc-ir_1087072020-09-11T05:01:12Z Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework: Li, Zhehui Thesis advisor: Jeffery A. Byers Thesis advisor: Chia-Kuang Tsung Text thesis 2019 Boston College English electronic application/pdf Homogeneous catalysts are advantageous in selective catalysis due to the well-defined active site at the molecular level. The poor recyclability, bimolecular aggregation, and undesired poison resistance of homogeneous catalysts hinder further industrial application despite the controlled reaction pathway due to the homogeneous environment. On the other hand, heterogeneous catalysts are preferred in industry due to their high recyclability and high activity. Yet, poor selectivity due to undefined active sites is a drawback. The construction of a host-guest system where a molecular level catalyst is incorporated into the Metal-Organic Framework (MOF) provides a promising solution to bridge those two fields. This composite maintains the advantages of homogeneous and heterogeneous catalysts and overcomes the disadvantages. However, finding an incorporation method that is versatile with minimum synthetic modification of the host and guest remains one of the challenges. In the first part of this dissertation, a new concept called “aperture-opening encapsulation’’ is introduced for incorporating large and diverse guest molecules into MOFs without changing the identity of either the guest or MOF. The approach capitalizes on the existence of linker exchange reactions, which, as our kinetic studies show, proceed via competition between associative and dissociative exchange mechanisms. The second part describes how this method is applied to incorporate a molecular catalyst into the cavity of UiO-66 for the hydrogenation of carbon dioxide to formate, which is a useful application for energy related industry. The developed hybrid composite showed the ability to be recycled, showed no evidence of bimolecular catalyst decomposition, and was less prone to catalyst poisoning. These results demonstrate for the first time how the aperture-opening process resulting from linker dissociation in MOFs can be utilized as a strategy to synthesize host-guest materials useful for chemical catalysis. After the establishment of the hybrid catalyst, the last part of the dissertation describes our efforts into the investigation of mass transport in catalysis. The understanding of the interaction between the host-guest is beneficial for the development of biological analogs in the future. Host-guest system Copyright is held by the author, with all rights reserved, unless otherwise noted. Thesis (PhD) — Boston College, 2019. Submitted to: Boston College. Graduate School of Arts and Sciences. Discipline: Chemistry. Catalysis Metal-Organic Framework http://hdl.handle.net/2345/bc-ir:108707
collection NDLTD
language English
format Others
sources NDLTD
topic Host-guest system
Catalysis
Metal-Organic Framework
spellingShingle Host-guest system
Catalysis
Metal-Organic Framework
Li, Zhehui
Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:
description Thesis advisor: Jeffery A. Byers === Thesis advisor: Chia-Kuang Tsung === Homogeneous catalysts are advantageous in selective catalysis due to the well-defined active site at the molecular level. The poor recyclability, bimolecular aggregation, and undesired poison resistance of homogeneous catalysts hinder further industrial application despite the controlled reaction pathway due to the homogeneous environment. On the other hand, heterogeneous catalysts are preferred in industry due to their high recyclability and high activity. Yet, poor selectivity due to undefined active sites is a drawback. The construction of a host-guest system where a molecular level catalyst is incorporated into the Metal-Organic Framework (MOF) provides a promising solution to bridge those two fields. This composite maintains the advantages of homogeneous and heterogeneous catalysts and overcomes the disadvantages. However, finding an incorporation method that is versatile with minimum synthetic modification of the host and guest remains one of the challenges. In the first part of this dissertation, a new concept called “aperture-opening encapsulation’’ is introduced for incorporating large and diverse guest molecules into MOFs without changing the identity of either the guest or MOF. The approach capitalizes on the existence of linker exchange reactions, which, as our kinetic studies show, proceed via competition between associative and dissociative exchange mechanisms. The second part describes how this method is applied to incorporate a molecular catalyst into the cavity of UiO-66 for the hydrogenation of carbon dioxide to formate, which is a useful application for energy related industry. The developed hybrid composite showed the ability to be recycled, showed no evidence of bimolecular catalyst decomposition, and was less prone to catalyst poisoning. These results demonstrate for the first time how the aperture-opening process resulting from linker dissociation in MOFs can be utilized as a strategy to synthesize host-guest materials useful for chemical catalysis. After the establishment of the hybrid catalyst, the last part of the dissertation describes our efforts into the investigation of mass transport in catalysis. The understanding of the interaction between the host-guest is beneficial for the development of biological analogs in the future. === Thesis (PhD) — Boston College, 2019. === Submitted to: Boston College. Graduate School of Arts and Sciences. === Discipline: Chemistry.
author Li, Zhehui
author_facet Li, Zhehui
author_sort Li, Zhehui
title Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:
title_short Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:
title_full Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:
title_fullStr Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:
title_full_unstemmed Design of a Host-guest Hybrid Catalytic System Through Aperture-opening Encapsulation Using Metal-organic Framework:
title_sort design of a host-guest hybrid catalytic system through aperture-opening encapsulation using metal-organic framework:
publisher Boston College
publishDate 2019
url http://hdl.handle.net/2345/bc-ir:108707
work_keys_str_mv AT lizhehui designofahostguesthybridcatalyticsystemthroughapertureopeningencapsulationusingmetalorganicframework
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