Chromium(III) chloro-complexes with L(+)-cysteine, dl-penicillamine and l(-)-cystine were isolated and characterized by their vibrational, electronic and spectromagnetic properties. The coordination of sulphur containing amino acids involves amino and/or carboxylato groups; only in the case of penicillamine the mercapto group shows bonding with metal. The difference in the relative strength of binding sites, in the compounds here reported, is related to the σ -donor and π -acceptor properties of sulphur containing amino acids; specifically coordination of mercapto group becomes possible if amino and carboxylato groups supply to chromium the electronic charge required for the back-donation to dπ sulphur orbitals.

Chromium(III) complexes of L(+)-cysteine, DL-penicillamine and L(-)-cystine. Synthesis and spectromagnetic characterization / M. Freni, A. Gervasini, P. Romiti, T. Beringhelli, F. Morazzoni. - In: SPECTROCHIMICA ACTA. PART A, MOLECULAR SPECTROSCOPY. - ISSN 0584-8539. - 39A:1(1983), pp. 85-89. [10.1016/0584-8539(83)80060-9]

Chromium(III) complexes of L(+)-cysteine, DL-penicillamine and L(-)-cystine. Synthesis and spectromagnetic characterization

A. Gervasini
Secondo
;
T. Beringhelli
Penultimo
;
1983

Abstract

Chromium(III) chloro-complexes with L(+)-cysteine, dl-penicillamine and l(-)-cystine were isolated and characterized by their vibrational, electronic and spectromagnetic properties. The coordination of sulphur containing amino acids involves amino and/or carboxylato groups; only in the case of penicillamine the mercapto group shows bonding with metal. The difference in the relative strength of binding sites, in the compounds here reported, is related to the σ -donor and π -acceptor properties of sulphur containing amino acids; specifically coordination of mercapto group becomes possible if amino and carboxylato groups supply to chromium the electronic charge required for the back-donation to dπ sulphur orbitals.
Settore CHIM/02 - Chimica Fisica
1983
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/195110
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 11
  • ???jsp.display-item.citation.isi??? 11
social impact