Research Article: Bis[dicyclo­hexyl­(phenyl)­phosphane-κP]silver(I) perchlorate dichloro­methane monosolvate

Date Published: April 01, 2011

Publisher: International Union of Crystallography

Author(s): Apollinaire Munyaneza, Reinout Meijboom, Bernard Omondi.

http://doi.org/10.1107/S1600536811009822

Abstract

In the title compound, [Ag{P(C6H11)2(C6H5)}2]ClO4·CH2Cl2, the AgI atom in the mononuclear complex cation is coordinated by two P atoms of the phosphane ligands [Ag—P = 2.3993 (4) and 2.4011 (4) Å; P—Ag—P = 177.473 (18)°] and the perchlorate anion acts as the counter-anion. There is an Ag⋯Operchlorate inter­action of 2.873 (2) Å, which contributes to the slightly non-linear bond angle about the AgI atom. Weak inter­molecular C—H⋯O hydrogen-bonding inter­actions involving phenyl, cyclo­hexyl and dichloro­methane H-atom donors and perchlorate O-atom acceptors contribute to the stabilization of the crystal structure.

Partial Text

For a review of the chemistry of silver(I) complexes, see: Meijboom et al. (2009 ▶). For the coordination chemistry of AgX salts (X = F−, Cl−, Br−, I−, BF4−, PF6−, NO3−) with group 15 donor ligands, with the main focus on tertiary phosphanes and in their context as potential anti­tumor agents, see: Berners-Price et al. (1998 ▶); Liu et al. (2008 ▶). For two- and three-coordinate AgX (X = NO3−) complexes/salts with bulky phosphane ligands, see: Bowmaker et al. (1996 ▶); Camalli & Caruso (1988 ▶); Fenske et al. (2007 ▶); for X = NO2, see: Cingolani et al. (2002 ▶); for X = Cl−, Br−, I−, CN−, SCN− and NCO−, see: Bowmaker et al. (1996 ▶); Bayler et al. (1996 ▶); for two-coord­inate X = ClO4−, see: Alyea et al. (1982 ▶, 2002 ▶); Baiada et al. (1990 ▶); Burgoyne et al. (2010 ▶). For the solution behavior of [LnAgX] complexes, see: Muetterties & Alegranti (1972 ▶). For atomic radii, see: Pauling (1960 ▶).

 

Source:

http://doi.org/10.1107/S1600536811009822

 

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