Oxidative addition of (bromoethynyl)benzene to κ2- acetylacetonatobis(trimethylphosphine)rhodium(I)

Marie-Hélène, Thibault and Tay, Meng Guan and Andrei S, Batsanov and Judith AK, Howard and Todd B, Marder (2013) Oxidative addition of (bromoethynyl)benzene to κ2- acetylacetonatobis(trimethylphosphine)rhodium(I). Journal of Organometallic Chemistry, 730. pp. 104-107. ISSN 0022-328X

Oxidative addition of (bromoethynyl)benzene to 2-acetylacetonato bis(trimethylphosphine) rhodium(I) - (abstract).pdf

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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.

Item Type: Article
Uncontrolled Keywords: Oxidative addition; Acetylide; In situ NMR spectroscopy; X-ray crystal structure ,unimas, university, universiti, Borneo, Malaysia, Sarawak, Kuching, Samarahan, ipta, education , research, Universiti Malaysia Sarawak.
Subjects: Q Science > QC Physics
Q Science > QD Chemistry
Divisions: Academic Faculties, Institutes and Centres > Faculty of Resource Science and Technology
Faculties, Institutes, Centres > Faculty of Resource Science and Technology
Depositing User: Karen Kornalius
Date Deposited: 24 Jun 2015 02:07
Last Modified: 03 Sep 2018 01:30
URI: http://ir.unimas.my/id/eprint/7404

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