Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I)
The reaction of (bromoethynyl)benzene with κ2-acetylacetonatobis(trimethylphosphine)rhodium(I), [Rh(acac)(PMe3)2] 1, was followed by in situ1H and 31P NMR spectroscopy. The kinetic product is that of cis-oxidative addition of the C–Br bond to Rh, and this species rearranges to the thermodynamically...
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my.unimas.ir.74032015-06-24T02:05:44Z http://ir.unimas.my/id/eprint/7403/ Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) Marie-Hélèn, Thibault Meng Guan, Tay Andrei S, Batsanov Judith AK, Howard Todd B, Marder Q Science (General) QD Chemistry The reaction of (bromoethynyl)benzene with κ2-acetylacetonatobis(trimethylphosphine)rhodium(I), [Rh(acac)(PMe3)2] 1, was followed by in situ1H and 31P NMR spectroscopy. The kinetic product is that of cis-oxidative addition of the C–Br bond to Rh, and this species rearranges to the thermodynamically more stable trans-oxidative addition product trans-[Rh(acac)(Br)(CCPh)(PMe3)2] 3. The structures of both 1 and 3 have been determined by single-crystal X-ray diffraction. Elsevier 2013 E-Article PeerReviewed Marie-Hélèn, Thibault and Meng Guan, Tay and Andrei S, Batsanov and Judith AK, Howard and Todd B, Marder (2013) Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I). Journal of Organometallic Chemistry, 730. pp. 104-107. ISSN 0022-328X http://www.sciencedirect.com/science/article/pii/S0022328X12006778 doi:10.1016/j.jorganchem.2012.11.019 |
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Q Science (General) QD Chemistry Marie-Hélèn, Thibault Meng Guan, Tay Andrei S, Batsanov Judith AK, Howard Todd B, Marder Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) |
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The reaction of (bromoethynyl)benzene with κ2-acetylacetonatobis(trimethylphosphine)rhodium(I), [Rh(acac)(PMe3)2] 1, was followed by in situ1H and 31P NMR spectroscopy. The kinetic product is that of cis-oxidative addition of the C–Br bond to Rh, and this species rearranges to the thermodynamically more stable trans-oxidative addition product trans-[Rh(acac)(Br)(CCPh)(PMe3)2] 3. The structures of both 1 and 3 have been determined by single-crystal X-ray diffraction. |
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E-Article |
author |
Marie-Hélèn, Thibault Meng Guan, Tay Andrei S, Batsanov Judith AK, Howard Todd B, Marder |
author_facet |
Marie-Hélèn, Thibault Meng Guan, Tay Andrei S, Batsanov Judith AK, Howard Todd B, Marder |
author_sort |
Marie-Hélèn, Thibault |
title |
Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) |
title_short |
Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) |
title_full |
Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) |
title_fullStr |
Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) |
title_full_unstemmed |
Oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (I) |
title_sort |
oxidative addition of (bromoethynyl) benzene to κ 2-acetylacetonatobis (trimethylphosphine) rhodium (i) |
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Elsevier |
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2013 |
url |
http://ir.unimas.my/id/eprint/7403/ http://www.sciencedirect.com/science/article/pii/S0022328X12006778 |
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1644510276193615872 |
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13.160551 |