Artikel,

Bis(homoleptic) vs. heteroleptic copper(I) complexes: Electrosynthesis, spectroscopy, and crystal structure of [Cu(BIK)2]+2[Cu4(SR)6]2-·3(CH3CN)·(RSH); BIK = bis(2-methylimidazol-2-yl)ketone, R = o-tolyl

, und .
Zeitschrift fuer Anorganische und Allgemeine Chemie, 622 (7): 1118--1124 (1996)
DOI: 10.1002/zaac.19966220703

Zusammenfassung

Anodic oxidn. of Cu in MeCN/2mM Bu4NClO4 and in the presence of bis(N-methylimidazol-2-yl)ketone (BIK) and excess o-thiocresol RSH yields the title compd. as the main product. Whereas the dianionic cluster [Cu4(SR)6]2- is similar to such previously reported species with R = Ph or Me, the purple cations [Cu(BIK)2]+ exhibit spectroscopic and structural effects of p back bonding between electron-rich Cu(I) and the p acceptor ligand BIK. In contrast to the formally related [Zn(BIK)2]2+, the Cu(I) complex cations exhibit distorted tetrahedral structures with almost coplanar BIK chelate arrangements which ensures max. metal-ligand p interaction. [on SciFinder(R)]

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