The beta-thiophosphinoyl carbene PhCCH2P(S)Ph-2 (5) has been prepared by irradiation of the corresponding diazo compound. The relative rates for insertion into the OH bond of methanol and for addition to the double bond of 2-methyl-2-butene indicate enhanced nucleophilic properties of the carbene, comparable to those of PhCCH2CH3 The unusual effect of increased nucleophilicity by an electron-withdrawing substituent probably results from hyperconjugative electron donation by the C-P bond, as recently documented for the same group in a carbocation. (C) 1997 Elsevier Science Ltd.
Photothermographic materials containing silver halide sensitized with combination of compounds
申请人:Simpson M. Sharon
公开号:US20060078833A1
公开(公告)日:2006-04-13
Photothermographic materials are designed with increased photospeed by chemical sensitizing the photosensitive silver halide grains with a combination of compounds. A first chemical sensitizer is a specific gold(III)-containing compound and a second chemical sensitizer is a sulfur-containing compound that is a diphenylphosphine sulfide. The molar ratio of the gold (III)-containing compound to the sulfur-containing compound is at least 1:1.
La reduction-complexation des sulfures de phosphines par le fer pentacarbonyle: un outil original pour la synthese des phosphines
作者:François Mercier、François Mathey、Jacques Angenault、Jean-Claude Couturier、Yves Mary
DOI:10.1016/s0022-328x(00)92891-2
日期:1982.5
DIVISIA A., TETRAHEDRON, 1979, 35, NO 2, 181-187
作者:DIVISIA A.
DOI:——
日期:——
BARLUENGA, J.;LOPEZ, F.;PALACIOS, F., J. CHEM. RES. SYNOP., 1985, N 7, 211
作者:BARLUENGA, J.、LOPEZ, F.、PALACIOS, F.
DOI:——
日期:——
The β-Heteroatom Effect on Carbenes
作者:Joseph B Lambert、Xiaoyang Liu
DOI:10.1016/s0040-4020(97)00341-4
日期:1997.7
The beta-thiophosphinoyl carbene PhCCH2P(S)Ph-2 (5) has been prepared by irradiation of the corresponding diazo compound. The relative rates for insertion into the OH bond of methanol and for addition to the double bond of 2-methyl-2-butene indicate enhanced nucleophilic properties of the carbene, comparable to those of PhCCH2CH3 The unusual effect of increased nucleophilicity by an electron-withdrawing substituent probably results from hyperconjugative electron donation by the C-P bond, as recently documented for the same group in a carbocation. (C) 1997 Elsevier Science Ltd.