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dc.identifier.urihttp://hdl.handle.net/1951/55631
dc.identifier.urihttp://hdl.handle.net/11401/72674
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeThesis
dcterms.abstractHydrogenases are a class of enzyme with the unique ability to catalytically reduce or oxidize hydrogen. Due to this ability they have received much attention from chemists who want to harness this power in a controlled setting. This power will allow not only for the mass production of hydrogen but also the potential for the production of cheaper catalysts to be used in fuel cells. The focus of this research is to create different models for the active site of hydrogenase based around the nickel center of the [NiFe] class of hydrogenase. It is believed that this nickel center is responsible for catalytically producing dihydrogen from two protons and two electrons. Currently no model has the ability to perform this at an efficient rate.This work primarily uses the potentially tridentate bis(2-thiophenyl)phenylphosphine ligand, or H2[PS2], for short. This ligand represents the sulfur rich environment of the nickel with its two thiol functional groups, and has shown prior success in making stable metal complexes at a few different oxidation states. Metal complexes of vanadium, chromium, and manganese containing this ligand were successfully synthesized and characterized using single crystal X-ray diffraction, cyclic voltammetry, and ultraviolet-visible spectroscopy.
dcterms.available2012-05-15T18:06:54Z
dcterms.available2015-04-24T14:53:11Z
dcterms.contributorMillar, Michelleen_US
dcterms.contributorAndreas Mayren_US
dcterms.contributorRobert Kerber.en_US
dcterms.creatorSpritzer, David
dcterms.dateAccepted2012-05-15T18:06:54Z
dcterms.dateAccepted2015-04-24T14:53:11Z
dcterms.dateSubmitted2012-05-15T18:06:54Z
dcterms.dateSubmitted2015-04-24T14:53:11Z
dcterms.descriptionDepartment of Chemistryen_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/1951/55631
dcterms.identifierSpritzer_grad.sunysb_0771M_10091.pdfen_US
dcterms.identifierhttp://hdl.handle.net/11401/72674
dcterms.issued2010-05-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2012-05-15T18:06:54Z (GMT). No. of bitstreams: 1 Spritzer_grad.sunysb_0771M_10091.pdf: 1625176 bytes, checksum: 12dcda74e1500f8e9ecc0a5025f7960c (MD5) Previous issue date: 1en
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dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectChemistry, Inorganic
dcterms.titleNew Transition Metal Chemistry With Phosphino-Thiol Ligands
dcterms.typeThesis


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