Volume 19, Issue 33
Organoelement Compounds
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ChemInform Abstract: Reorientation of the Alkyne Moiety in the Heterometallic Cluster (FeCo2(CO)9(EtC2Et)), Induced by Phosphine, Phosphite, or Isonitrile Substitution for CO. Crystal Structure of (FeCo2(CO)8(PPh3)(EtC2Et)).

D. BOCCARDO

D. BOCCARDO

Ist. Chim. Gen. Inorg., Univ. Torino, 10125 Torino, Italy

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M. BOTTA

M. BOTTA

Ist. Chim. Gen. Inorg., Univ. Torino, 10125 Torino, Italy

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R. GOBETTO

R. GOBETTO

Ist. Chim. Gen. Inorg., Univ. Torino, 10125 Torino, Italy

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D. OSELLA

D. OSELLA

Ist. Chim. Gen. Inorg., Univ. Torino, 10125 Torino, Italy

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A. TIRIPICCHIO

A. TIRIPICCHIO

Ist. Chim. Gen. Inorg., Univ. Torino, 10125 Torino, Italy

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M. TIRIPICCHIO-CAMELLINI

M. TIRIPICCHIO-CAMELLINI

Ist. Chim. Gen. Inorg., Univ. Torino, 10125 Torino, Italy

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First published: August 16, 1988

Abstract

The spectroscopic and structural data of the parent cluster (I) are compared with those of its monosubstitution derivatives (III) which are formed as shown in the scheme.

ChemInform Abstract

The spectroscopic and structural data of the parent cluster (I) are compared with those of its monosubstitution derivatives (III) which are formed as shown in the scheme. Their structure is confirmed by X-ray structure analysis of the title compound (IIIa) (space group P1, Z=2). The substitution of a CO ligand has caused the reorientation of the alkyne moiety in the ground state. In similar way, the diphosphine-bridged dimers (IV) are obtained. The products are characterized by elemental analysis, IR, 31P(1H), 1H, and 13C(1H) NMR spectral data.

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