THE EFFECT OF N2-MONOMETHYLATION AND DIMETHYLATION ON THE CRYSTAL-STRUCTURES OF BIS[(S)-PHENYLALANINAMIDATO]COPPER(II) COMPLEXES

Citation
R. Corradini et al., THE EFFECT OF N2-MONOMETHYLATION AND DIMETHYLATION ON THE CRYSTAL-STRUCTURES OF BIS[(S)-PHENYLALANINAMIDATO]COPPER(II) COMPLEXES, Tetrahedron : asymmetry, 3(3), 1992, pp. 387-400
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
09574166
Volume
3
Issue
3
Year of publication
1992
Pages
387 - 400
Database
ISI
SICI code
0957-4166(1992)3:3<387:TEONAD>2.0.ZU;2-7
Abstract
(S)-phenylalaninamide, N2-methyl-(S)-phenylalaninamide, and N2,N2-dime thyl-(S)-phenylalaninamide co-ordinate to copper(II) as amidates, givi ng rise to trans bis(phenylalaninamidato) copper(II) complexes CuL2H-2 respectively (1), (2), and (3). Their crystal structures were determi ned by X-ray crystallography. The striking feature is that in bis[N2-m ethyl-(S)-phenylalaninamidato]copper(II) complex (2), both methyl grou ps are on the axial positions and on the same side of the co-ordinatio n plane. The knowledge of the crystal structures of complexes (1), (2) , and (3) which are used successfully as chiral selectors in HPLC (rev ersed phase), provides very useful information on the stereochemical f eatures of enantioselective species.