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https://scholarbank.nus.edu.sg/handle/10635/27523
DC Field | Value | |
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dc.title | RU(II) AND NI(II) N, S-HETEROCYCLIC CARBENE COMPLEXES AND THEIR CATALYTIC PROPERTIES | |
dc.contributor.author | DING NINI | |
dc.date.accessioned | 2011-10-05T18:00:12Z | |
dc.date.available | 2011-10-05T18:00:12Z | |
dc.date.issued | 2011-01-07 | |
dc.identifier.citation | DING NINI (2011-01-07). RU(II) AND NI(II) N, S-HETEROCYCLIC CARBENE COMPLEXES AND THEIR CATALYTIC PROPERTIES. ScholarBank@NUS Repository. | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/27523 | |
dc.description.abstract | This thesis describes the synthetic, structural and catalytic studies of Ru(II) and Ni(II) N,S-heterocyclic (NSHC) carbene complexes. It includes: 1) A series of Ru(II) and Ni(II) N,S-heterocyclic carbene complexes have been synthesized and characterized. They represent the first isolation of Ru/Ni-NHC complexes of benzothiazol-2-ylidene kind. Their catalytic activities towards transfer hydrogenation of ketones, Ullmann-type coupling and hydrosilylation of terminal alkynes have been examined and discussed. 2) The reactivity of Ru(II)-NSHC complexes RuBr(RCOO)(3-R¿BzTh)(PPh3)2 (R = Me, Et; 3-R¿BzTh = 3-benzylbenzothiazol-2-ylidene) have also been examined. Specifically, phosphine substitution of RuIIBr(MeCOO)(3-RBzTh)(PPh3)2 with diphosphine ligands gives complexes of two structural types depending on the relative dispositions of the ligands; a simple way to prepare solvato (CH3CN) Ru(II)-NSHC complexes is provided which avoids the use of silver source; intramolecular sp2 and sp3 C-H bond activation at carbene ligands is studied. | |
dc.language.iso | en | |
dc.subject | N,S-heterocyclic, carbene, Ruthenium, nickel, catalytic properties, N-heterocyclic | |
dc.type | Thesis | |
dc.contributor.department | CHEMISTRY | |
dc.contributor.supervisor | HOR TZI SUM, ANDY | |
dc.description.degree | Ph.D | |
dc.description.degreeconferred | DOCTOR OF PHILOSOPHY | |
dc.identifier.isiut | NOT_IN_WOS | |
Appears in Collections: | Ph.D Theses (Open) |
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Ding Nini Thesis.pdf | 2.27 MB | Adobe PDF | OPEN | None | View/Download |
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