Komplexchemischer Aufbau cyclischer 1,2‐Dithiolato‐Liganden mit dem nido ‐Cluster [(CO) 3 FeS] 2 . — Molekülstruktur und partielle S ‐Oxidation von Hexacarbonyl(μ 2 ‐ cis ‐1,2‐cyclohexandithiolato‐ S,S )dieisen

Autor: Regine Lingnau, Hermann A. Mayer, Ingo-Peter Lorenz, Anja Kramer
Rok vydání: 1990
Předmět:
Zdroj: Chemische Berichte. 123:1821-1826
ISSN: 0009-2940
DOI: 10.1002/cber.19901230911
Popis: Complex-Chemical Synthesis of Cyclic 1.2-Dithiolato Ligands with the nido Cluster [(CO)3,FeS]2. — Molecular Structure and Partial S-Oxidation of Hexacarbonyl(μ2,-cis-1,2-cyclohexanedithiolato-S,S)diiron The cyclic alkenes, dienes, and trienes C6H10, C8C14, C5H6, C8C12 and C7H8 are inserted into the S-S bond of the nido cluster [(CO)3FeS]2 (1) by photochemically induced [2+2] cycloaddition reactions to give the complexes 2–6; thus, saturated and unsaturated cyclic 1,2-dithiolato ligands can be selectively built onto the complex in a μ2-bridging fashion. According to an X-ray structure analysis, the μ2-1,2-cyclohexanedithiolato-S,S complex 2a with the pseudotetrahedral skeleton [(CO)3FeS]2 crystallizes in the monoclinic space group P21/c; the S2 moiety is bridged by cyclohexane with 1,2-cis configuration. As an example, the partial S oxidation of 2a was carried out, leading to 2b by selective transformation of one thiolato into a sulfenato function.
Databáze: OpenAIRE