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dc.contributor.advisorRichard R. Shrock.en_US
dc.contributor.authorO'Donoghue, Myra Brigid, 1966-en_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Chemistry.en_US
dc.date.accessioned2010-01-07T20:51:16Z
dc.date.available2010-01-07T20:51:16Z
dc.date.copyright1999en_US
dc.date.issued1999en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/50544
dc.descriptionThesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstract{ [N 3N]Mo-N=N} 2Mg(THF)2, isolated from the reduction of [N3N]MoCl by magnesium powder under dinitrogen, serves as an entry into the dinitrogen chemistry of molybdenum complexes containing the TMS-TREN ligand. ... Five coordinate tungsten oxo alkylidene complexes of the general type (ArO)2W(O)(CHtBu)(PR 3 ) (Ar = 2,6-Ph2C6H3 ) are synthesized by reaction of Ta(CHtBu)(PR 3)2X3 (X = Cl, Br) with W(O)(OtBu) 4. 1H NMR spectroscopy reveals that only the syn rotamer is present in solution and PPh2Me is labile on the NMR time scale.en_US
dc.description.statementofresponsibilityby Myra Brigid O'Donoghue.en_US
dc.format.extent178 leavesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemistry.en_US
dc.titleDinitrogen and organometallic chemistry of trimethylsilyl-substituted triamidoamine complexes of molybdenumen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.identifier.oclc43852050en_US


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