Please use this identifier to cite or link to this item: https://doi.org/10.1021/om800356k
Title: Regioselective double cycloplatination of 9,10-bis(diphenylphosphino) anthracene
Authors: Jian, H. 
Yip, J.H.K. 
Issue Date: 23-Feb-2009
Citation: Jian, H., Yip, J.H.K. (2009-02-23). Regioselective double cycloplatination of 9,10-bis(diphenylphosphino) anthracene. Organometallics 28 (4) : 1093-1100. ScholarBank@NUS Repository. https://doi.org/10.1021/om800356k
Abstract: Double eyclometalation of 9,10-bis(diphenylphosphino)anthracene (PAnP) by Pt(L)(OTf)2 (L = diphosphines, OTf = CF3SO3) gives rise to the geometrical isomers syn- and anti-[Pt2(L) 2(PAnP-H2)](OTf)2 (Pt2). The reaction is regioselective, with the syn-isomer being the kinetic product. The cyclomelation is reversible, and thermodynamic product distribution is obtained after prolonged standing. The ratio of the isomers is subject to the influence of solvents and ancillary diphosphines. Protonolysis of the Pt-C leads to a monocyclometalated intermediate. A mechanistic postulate that invokes a preferential electrophilic attack of the Pt ions at the C-H bonds of the anthracenyl ring is proposed to explain the regioselectivity. © 2009 American Chemical Society.
Source Title: Organometallics
URI: http://scholarbank.nus.edu.sg/handle/10635/94712
ISSN: 02767333
DOI: 10.1021/om800356k
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