ELECTROCHEMICAL SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF BIS(TRIPHENYLPHOSPHINE)COPPER(I) FLUOROACETATES

Citation
Rd. Hart et al., ELECTROCHEMICAL SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF BIS(TRIPHENYLPHOSPHINE)COPPER(I) FLUOROACETATES, Journal of the Chemical Society. Dalton transactions, (5), 1994, pp. 773-779
Citations number
21
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
03009246
Issue
5
Year of publication
1994
Pages
773 - 779
Database
ISI
SICI code
0300-9246(1994):5<773:ESASCO>2.0.ZU;2-I
Abstract
Bis(triphenylphosphine)copper(I) fluoroacetate complexes have been pre pared by the electrochemical oxidation of copper metal in acetonitrile solutions of triphenylphosphine and mono-, di- and tri-fluoroacetic a cid respectively. Recrystallization from toluene yields unsolvated mon onuclear complexes [Cu(PPh3)2(O2CCH3-nFn)], n = 1-3, which have been c haracterized by single-crystal X-ray crystallographic determinations. Crystals of the three complexes are isomorphous with the acetate compl ex (n = 0), crystallizing in the monoclinic space group P2(1)/a with c ell dimensions a almost-equal-to 18.0, b almost-equal-to 11.0 and c al most-equal-to 19.3 angstrom and beta almost-equal-to 120-degrees. Resi duals for the complexes with n = 1, 2 and 3 were R = 0.077, 0.045 and 0.048 for 3677, 2789 and 3527 'observed' [I > 3sigma(I)] reflections r espectively. The bond distances Cu-P are 2.232(3), 2.222(3); 2.234(2), 2.219(2); and 2.235(2) 2.228(2) angstrom with the corresponding P-Cu- P angles increasing from 135.0(1) to 135.8(1) to 1 36.7(1)-degrees, th is latter value being the largest recorded for [Cu(PPh3)2]+. The asymm etry of the co-ordination of the carboxylate group increases along the series with Cu-0 distances of 2.144(6) and 2.363(7); 2.118(4), 2.465( 6); and 2.113(4), 2.545(5) angstrom for n = 1, 2 and 3 respectively. C rystallization of the difluoro- and trifluoro-acetate complexes from e thanol results in isomorphous orthorhombic Pb2(1)a crystals (a almost- equal-to 22.2, b almost-equal-to 18.5, c almost-equal-to 9.0 angstrom) with monodentate carboxylate and co-ordinated ethanol; the monofluoro acetate is unsolvated. For [Cu(PPh3)2(O2CCHF2)(EtOH)] R was 0.052 for 2090 'observed' reflections with Cu-P 2.248(3), 2.236(3) angstrom and P-Cu-P 120.5(1)-degrees; Cu-O(carboxylate) is 2.074(8) angstrom and Cu -O(ethanol) is 2.169(8) angstrom. For [Cu(PPh3)2(O2CCF3)(EtOH)] R was 0.043 for 2350 'observed' reflections, Cu-P being 2.248(2), 2.240(2) a ngstrom and P-Cu-P 120.8(1)-degrees; Cu-O(carboxylate) is 2.104(6) ang strom and Cu-O(ethanol) is 2.160(6) angstrom.