Issue 27, 2008

Csp3–F bond activation by nucleophilic attack of the {Pt2S2} core assisted by non-covalent interactions

Abstract

The high nucleophilicity of the sulfur atoms in [Pt2(dppp)2(μ-S)2] triggers a C–F activation process in 1,3-difluoro-2-propanol that leads to the [Pt2(dppp)2(μ-S)(μ-SCH2CH(OH)CH2F]F product through a SN2 mechanism, where the O–H⋯F hydrogen bond established from the alcohol group of the organic substrate is essential for assisting the departure of the fluoride anion.

Graphical abstract: Csp3–F bond activation by nucleophilic attack of the {Pt2S2} core assisted by non-covalent interactions

Supplementary files

Article information

Article type
Communication
Submitted
01 Feb 2008
Accepted
27 Mar 2008
First published
29 Apr 2008

Chem. Commun., 2008, 3130-3132

Csp3–F bond activation by nucleophilic attack of the {Pt2S2} core assisted by non-covalent interactions

A. Nova, R. Mas-Ballesté, G. Ujaque, P. González-Duarte and A. Lledós, Chem. Commun., 2008, 3130 DOI: 10.1039/B801889H

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