Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103103
Title: Mechanism of phosphinidene complex arylation by arylboronic acids
Authors: Ng, Yong Xiang
Mathey, Francois
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2014
Source: Ng, Y. X., & Mathey, F. (2014). Mechanism of phosphinidene complex arylation by arylboronic acids. Organometallics, 33(5), 1322-1324.
Series/Report no.: Organometallics
Abstract: The arylation reaction of terminal phosphinidene complexes [RP-W(CO)5] by arylboronic acids is very sensitive to steric hindrance and the electronic properties of the substituents on the aryl ring. On the basis of DFT calculations and additional experiments, it seems that the mechanism involves first an insertion of the phosphinidene into one of the B–O bonds, followed by an intramolecular nucleophilic attack of the aryl group onto the P–OH bond promoted by the potassium phosphate. The [1,2]-aryl shift from B to P cannot be reproduced with an alkyl group.
URI: https://hdl.handle.net/10356/103103
http://hdl.handle.net/10220/24380
DOI: 10.1021/om5001138
Rights: © 2014 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Organometallics, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1021/om5001138].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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