STEREOSELECTIVE SYNTHESIS OF OCTAHEDRAL COMPLEXES WITH PREDETERMINED HELICAL CHIRALITY

Citation
P. Hayoz et al., STEREOSELECTIVE SYNTHESIS OF OCTAHEDRAL COMPLEXES WITH PREDETERMINED HELICAL CHIRALITY, Journal of the American Chemical Society, 115(12), 1993, pp. 5111-5114
Citations number
18
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
115
Issue
12
Year of publication
1993
Pages
5111 - 5114
Database
ISI
SICI code
0002-7863(1993)115:12<5111:SSOOCW>2.0.ZU;2-U
Abstract
Facile stereoselective synthesis of an enantiomerically pure DELTA-Ru- trisbipyridine type complex is accomplished by using a new chiral and conformationally rigid ligand, which completely predetermines the heli cal chirality of the metal, yielding exclusively DELTA-configuration i n the present case. The ligand, abbreviated chiragen[6] is a bisbipyri dine compound, where two pinene substituted bipyridine units are linke d through an aliphatic C6-chain. The two remaining coordination sites of the complex are occupied by 4,4'-dimethylbipyridine. The structure of the u(chiragen-[6])(4,4'-dimethylbipyridine)](CF3SO3)2 complex has been determined by X-ray crystallography. Metal complexes formed by ch iragen ligands have potential applications in enantioselective catalys is and as chiral building blocks for polynuclear species.