Synthesis and electrochemical anion recognition by novel redox-responsive ferrocenoyl dipeptide ester derivatives; H-1 NMR anion complexation studies

Authors
Gallagher, JF Kenny, PTM Sheehy, MJ
Citation
Jf. Gallagher et al., Synthesis and electrochemical anion recognition by novel redox-responsive ferrocenoyl dipeptide ester derivatives; H-1 NMR anion complexation studies, INORG CH C, 2(8), 1999, pp. 327-330
Citations number
16
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANIC CHEMISTRY COMMUNICATIONS
ISSN journal
13877003 → ACNP
Volume
2
Issue
8
Year of publication
1999
Pages
327 - 330
Database
ISI
SICI code
1387-7003(199908)2:8<327:SAEARB>2.0.ZU;2-T
Abstract
The synthesis of six N-ferrocenoyl dipeptide eater derivatives FcCOR (Fc=(e ta(5)-C5H5)Fe(eta(5)-C5H4); R=Gly-Gly(OMe) (1), Leu-Leu(OEt) (2), Ala-Phe(O Et) (3), Phe-Phe(OMe) (4), Phe-Leu(OBn) (5) and Phr-Ser(OEt) (6)) is descri bed. The electrochemical anion sensing behaviour (using a platinum microdis k working electrode) and H-1 NMR anion coordination studies of these novel pendant N-ferrocenoyl dipeptide eater derivatives with a range of anions ar e reported. (C) 1999 Elsevier Science S.A. All rights reserved.