Literature DB >> 17033704

The reaction of tertiary phosphines with (Ph2Se2I2)2--the influence of steric and electronic effects.

Nicholas A Barnes1, Stephen M Godfrey, Ruth T A Halton, Imrana Mushtaq, Robin G Pritchard.   

Abstract

The reaction of (Ph(2)Se(2)I(2))(2) with a wide variety of tertiary phosphines possessing different steric and electronic properties has been studied, leading in most cases to R(3)PSe(Ph)I adducts; [R(3)P = (p-CH(3)C(6)H(4))(3)P (1), (m-CH(3)C(6)H(4))(3)P (2), (o-OCH(3)C(6)H(4))(3)P (4), Ph(2)MeP (6), Me(2)PhP (7), Me(3)P (8), Cy(3)P (9)]. All of the products formed were characterised by elemental analysis, Raman and multinuclear NMR spectroscopy. Both steric and electronic factors are important in determining the structural motif (CT vs. ionic) observed in the solid-state. In general, highly basic phosphines result in a lengthening of the Se-I interaction, and a preference for an ionic structure. The reaction with (o-CH(3)C(6)H(4))(3)P does not yield a stable R(3)PSe(Ph)I adduct, and instead (o-CH(3)C(6)H(4))(3)PI(2) (3) is formed. The unusually long P-I bond, [2.5523(12) A], and short I-I bond, [3.0724(4) A], exhibited by is a result of the high steric requirements of this phosphine. The similarly bulky (o-SCH(3)C(6)H(4))(3)P yields a mixture of (o-SCH(3)C(6)H(4))(3)PSe(Ph)I (5a) and [(o-SCH(3)C(6)H(4))(3)PSePh]I(3) (5b). The crystal structures of (m-CH(3)C(6)H(4))(3)PSe(Ph)I, 2, (o-CH(3)C(6)H(4))(3)PI(2), 3, [(o-OCH(3)C(6)H(4))(3)PSePh]I.CH(2)Cl(2), 4, [(o-SCH(3)C(6)H(4))(3)PSePh]I(3), 5b, two pseudo-polymorphs of Ph(2)MePSe(Ph)I, 6a/6b, and [Me(3)PSe(Ph)I](2).CH(2)Cl(2), 8, are reported. The R(3)PSe(Ph)I adducts formed exhibit one of four types of behaviour. Type I products, (such as 2) are CT in the solid-state and display fluxionality in solution. Type II products (such as 6a/6b) lie close to the CT/ionic structural borderline, displaying long Se-I bonds, and are more appropriately classified as [R(3)PSePh] (acceptor)/I(-) (donor) CT complexes. Type II complexes ionise in solution to [R(3)PSePh]I. Type III products, such as 8, are ionic in solution, but frequently show cation-anion, or cation-solvent interactions in the solid-state, although these interactions are weak and the linear P-Se-I motif is lost. Type IV products (such as 4) are ionic and feature bulky phosphines. They display no short cation-anion interactions in the solid-state.

Entities:  

Year:  2006        PMID: 17033704     DOI: 10.1039/b608453b

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  2 in total

1.  Tris(2-methoxy-phen-yl)phosphine.

Authors:  Omar Bin Shawkataly; Mohd Aslam A Pankhi; Imthyaz Ahmed Khan; Chin Sing Yeap; Hoong-Kun Fun
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-06-06

2.  A family of cis-macrocyclic diphosphines: modular, stereoselective synthesis and application in catalytic CO2/ethylene coupling.

Authors:  Ioana Knopf; Daniel Tofan; Dirk Beetstra; Abdulaziz Al-Nezari; Khalid Al-Bahily; Christopher C Cummins
Journal:  Chem Sci       Date:  2016-10-11       Impact factor: 9.825

  2 in total

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