The reaction of the unsaturated cluster anion [Re3(μ-H)4(CO)10]- with tertiary phosphines at room temperature results in the substitution of two hydride ligands (eliminated as H2) by two PR3 ligands, leading to saturated [Re3(μ-H)2(CO)10-(PR3)2]- compounds. A single crystal X-ray diffraction study of the PPh3 derivative revealed that the two phosphines occupy non-equivalent equatorial coordination sites on the triangular cluster. The rate of the reaction greatly increases with increase of the basicity of the phosphine.

REACTIONS OF THE UNSATURATED ANION {[RE3(MU-H)4(CO)10]- WITH PHOSPHINES - SYNTHESIS OF THE ANIONS [RE3(MU-H)2(CO)10(PR3)2]-, AND CRYSTAL-STRUCTURE OF [NET4][RE3(MU-H)2(CO)10(PPH3)2]} / T. BERINGHELLI, G. CIANI, G. DALFONSO, M. FRENI. - In: JOURNAL OF ORGANOMETALLIC CHEMISTRY. - ISSN 0022-328X. - 311:3(1986), pp. C51-C51-C54.

REACTIONS OF THE UNSATURATED ANION {[RE3(MU-H)4(CO)10]- WITH PHOSPHINES - SYNTHESIS OF THE ANIONS [RE3(MU-H)2(CO)10(PR3)2]-, AND CRYSTAL-STRUCTURE OF [NET4][RE3(MU-H)2(CO)10(PPH3)2]}

T. BERINGHELLI
Primo
;
G. CIANI
Secondo
;
G. DALFONSO
Penultimo
;
1986

Abstract

The reaction of the unsaturated cluster anion [Re3(μ-H)4(CO)10]- with tertiary phosphines at room temperature results in the substitution of two hydride ligands (eliminated as H2) by two PR3 ligands, leading to saturated [Re3(μ-H)2(CO)10-(PR3)2]- compounds. A single crystal X-ray diffraction study of the PPh3 derivative revealed that the two phosphines occupy non-equivalent equatorial coordination sites on the triangular cluster. The rate of the reaction greatly increases with increase of the basicity of the phosphine.
Settore CHIM/03 - Chimica Generale e Inorganica
1986
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/187849
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