Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0dt00562b
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dc.titleRuthenium(II) N,S-heterocyclic carbene complexes and transfer hydrogenation of ketones
dc.contributor.authorDing, N.
dc.contributor.authorHor, T.S.A.
dc.date.accessioned2014-10-16T08:39:36Z
dc.date.available2014-10-16T08:39:36Z
dc.date.issued2010-11-14
dc.identifier.citationDing, N., Hor, T.S.A. (2010-11-14). Ruthenium(II) N,S-heterocyclic carbene complexes and transfer hydrogenation of ketones. Dalton Transactions 39 (42) : 10179-10185. ScholarBank@NUS Repository. https://doi.org/10.1039/c0dt00562b
dc.identifier.issn14779226
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94746
dc.description.abstractA series of ruthenium(II) N,S-heterocyclic carbene (NSHC) complexes Ru IIX(RCOO)(PPh3)2(3-R′BzTh) (BzTh = benzothiazol-2-ylidene; R = Me, R′/X = Bz/Br (4), Pri/I (6), Bui/I (8); R = Et, R′/X = Bz/Br (5), Pri/I (7), Bui/I (9)) have been synthesized and characterized. Single-crystal X-ray structural analysis revealed that in each case the Ru(II) center adopts an essentially octahedral geometry, coordinated by two trans-oriented PPh 3 completed by an NSHC, chelating carboxylate and halide X (X = Br (4-5), X = I (6-9)) ligands. Although thiazol-2-ylidiene Ru(II) complexes are established and applied in metathesis, these benzothiazol-2-ylidene complexes (4-9) are the first of its kind. Their catalytic activities towards transfer hydrogenation of ketones have been examined and discussed. © The Royal Society of Chemistry 2010.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0dt00562b
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c0dt00562b
dc.description.sourcetitleDalton Transactions
dc.description.volume39
dc.description.issue42
dc.description.page10179-10185
dc.identifier.isiut000283147300021
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