The Crystal and Molecular Structures of Gold(I) Complexes Containing the Electron-Rich P-Donor Ligand Ph3PNPPh2†

The reaction of [AuCl(tht)] (tht = tetrahydrothiophene) with an equimolar amount of the electron-rich ligand N-diphenylphosphino-triphenylphosphinimine, Ph3PNPPh2, in THF afforded the new complex [AuCl(Ph3PNPPh2)] (1) in good yield. Furthermore, the reaction of [AuHCl4] with Ph3PNPPh2 in a molar ratio of 1:3 in dichloromethane at room temperature yielded the complex salt [Au(Ph3PNPPh2)2]Cl (2) as the dichloromethane solvate beside Ph3PNPPh2Cl2 as the side-product of oxidation. The molecular structures of metal complexes 1 and 2 were determined by single-crystal X-ray diffraction. Because of the bulkiness of the ligand Ph3PNPPh2 no short intermolecular gold–gold interactions (aurophilic aggregation) could be observed in the solid-state structures.

[1]  S. Nolan,et al.  Solution calorimetric study of ligand exchange reactions in the [Au(L)Cl] system (L = phosphine and phosphite) , 2010 .

[2]  E. Tiekink,et al.  Luminescence properties of phosphinegold(I) halides and thiolates , 2009 .

[3]  C. Incarvito,et al.  Surveying the {AuCl} adducts of bulky phosphines bearing the 2,6-dimesitylphenyl group , 2009 .

[4]  G. Hutchings,et al.  Gold--an introductory perspective. , 2008, Chemical Society reviews.

[5]  M. Taillefer,et al.  Reactivity of Ph3PNLi towards PIII and PV electrophiles , 2008 .

[6]  U. Monkowius,et al.  Unprecedented coordination chemistry of a chloro(phosphine)gold(I) complex: [(Ad2BnP)2Au][AuCl2] , 2008 .

[7]  A Stephen K Hashmi,et al.  Gold-catalyzed organic reactions. , 2007, Chemical reviews.

[8]  C. Friend,et al.  Heterogeneous gold-based catalysis for green chemistry: low-temperature CO oxidation and propene oxidation. , 2007, Chemical reviews.

[9]  N. Shapiro,et al.  Rearrangement of alkynyl sulfoxides catalyzed by gold(I) complexes. , 2007, Journal of the American Chemical Society.

[10]  A. Echavarren,et al.  Molecular diversity through gold catalysis with alkynes. , 2007, Chemical communications.

[11]  G. Bowmaker,et al.  Gold Is Smaller than Silver. Crystal Structures of (Bis(trimesitylphosphine)gold(I)) and (Bis(trimesitylphosphine)silver(I)) Tetrafluoroborate , 1996 .

[12]  J.-C. Wang [Au(PPh3)2]+[BF4]− , 1996 .

[13]  D. N. Kravtsov,et al.  Synthesis and crystal structure of bis(triphenylphosphine)gold tricyanomethanide, [(PPh3)2Au]+[C(CN)3]− , 1989 .

[14]  P. Healy,et al.  Lewis-Base Adducts of Group 11 Metal(I) Compounds. XXVI : Solid-state cross-polarization magic-angle-spinning 31P N.M.R. and structural studies on 1:1 adducts of triphenylphosphine with gold(I) salts , 1987 .

[15]  D. G. Tuck,et al.  The direct electrochemical synthesis of triphenylphosphine adducts of Group IB monohalides , 1981 .

[16]  A. Laguna,et al.  Novel anionic gold(I) and gold(III) organocomplexes , 1977 .

[17]  W. Bennett,et al.  Chloro(triphenylphosphine)gold(I) , 1976 .

[18]  L. Meinel,et al.  Aminophosphane. IX. N-Diphenylphosphino-triphenylphosphazen , 1969 .