Synthesis, structure and isomerism of the [Fe3Pt(mu(4)-Q)(CO)(9)(dppm)] clusters (Q = Se, Te; dppm = Ph2PCH2PPh2)

Pushkarevsky, Nikolay A. and Konchenko, Sergey N. and Scheer, Manfred (2007) Synthesis, structure and isomerism of the [Fe3Pt(mu(4)-Q)(CO)(9)(dppm)] clusters (Q = Se, Te; dppm = Ph2PCH2PPh2). JOURNAL OF CLUSTER SCIENCE, 18 (3). pp. 606-617. ISSN 1040-7278,

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Abstract

The reaction of K-2[Fe-3(mu(3)-Q)(CO)(9)] (Q = Se (K-2[1a]), Te (K-2[1b])) with [(dppm)PtCl2] leads to the addition of a [(dppm)Pt](2+) unit to a Fe(2)Q face of the initial cluster. By this way new heteronuclear clusters [Fe3Pt(mu(3)-Q)(CO)(9)(dppm)] were obtained possessing a butterfly-shaped cluster core bridged by a mu(4)-Q unit. It has been found that the resulting Fe-Pt clusters exist as equilibrium mixtures of two isomeric forms in solution differing by the dppm coordination mode: as a chelate ligand coordinated to Pt or as a bridging ligand coordinated to Pt and Fe atoms. The mixtures of isomers can be separated by chromatography and the pure isomers can be isolated as stable crystalline phases. Solutions of both isomers attain equilibrium at normal conditions in about 1 month as found by NMR.

Item Type: Article
Uncontrolled Keywords: HETEROMETALLIC CARBONYL CLUSTERS; PLATINUM; LIGANDS; ANIONS; REACTIVITY; COMPLEXES; CHEMISTRY; SULFIDE; BONDS; cluster; carbonyl complexes; iron; platinum; selenium; tellurium
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 01 Dec 2020 13:06
Last Modified: 01 Dec 2020 13:06
URI: https://pred.uni-regensburg.de/id/eprint/32291

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