Show simple item record

dc.contributor.advisorMircea Dincă.en_US
dc.contributor.authorMetzger, Eric Danielen_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemistry.en_US
dc.date.accessioned2018-09-28T20:59:38Z
dc.date.available2018-09-28T20:59:38Z
dc.date.copyright2018en_US
dc.date.issued2018en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/118271
dc.descriptionThesis: Ph. D. in Inorganic Chemistry, Massachusetts Institute of Technology, Department of Chemistry, 2018.en_US
dc.descriptionCataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 195-207).en_US
dc.description.abstractThe benefits of heterogeneous catalysis for industry and the society at large cannot be overstated, with approximately 90% of all industrial catalysis being performed with heterogeneous catalysts. Despite the undeniable operational advantages of heterogeneous catalysts, several large volume industrial processes involved in the production of commodity chemicals remain impenetrable to solid catalysts. Among them are the selective dimerization of ethylene and the selective trimerization of ethylene, which require fine steric and electronic tuning to optimize the production of the desired olefin. In this thesis, I describe the development of new heterogeneous catalysts to address the lack of activity and selectivity found among heterogeneous catalysts for selective ethylene oligomerizations, with an emphasis on developing new metal-organic framework (MOF) catalysts for the selective dimerization of ethylene to 1-butene. The ability to tune the catalytically active site of a solid at the molecular level places MOFs in prime position to answer challenges in heterogeneous catalysis that no other class of solids has been able to address. Chapter 2 of this thesis describes the development of Ni-MFU-4/, a nickel-substituted MOF with excellent activity and selectivity for the dimerization of ethylene to 1-butene. Although the active sites in the MOF are designed to mimic homogeneous Nitrispyrazolylborate dimerization catalysts, the selectivity observed for the solid catalyst is considerably higher than that of the homogeneous system, highlighting the importance of active site isolation in the porous solid. Chapter 3 details a combination of studies utilizing isotopic labeling and mechanistic probes to demonstrate that Ni-MFU-4/ dimerizes ethylene via the Cossee-Arlman mechanism. Chapter 4 reports the preparation of Ni-CFA-1, a related heterogeneous ethylene dimerization catalyst that is far more synthetically accessible than Ni- MFU-4/. Lastly, chapter 5 relays initial results towards the development of MOF-based ethylene trimerization catalysts.en_US
dc.description.statementofresponsibilityby Eric Daniel Metzger.en_US
dc.format.extent208 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemistry.en_US
dc.titleThe selective oligomerization of ethylene with metal-organic frameworksen_US
dc.typeThesisen_US
dc.description.degreePh. D. in Inorganic Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.identifier.oclc1054187190en_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record