Second sphere coordination in oxoanion binding: Synthesis, spectroscopic characterisation and crystal structures of trans-[bis(ethylenediamine)dinitrocobalt(III)] diclofenac and chlorate

R Sharmaa, RP Sharmaa, R Bala, Benson Kariuki

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

In the exploration of cationic cobaltammine [trans-Co(en)(2)(NO2)(2)](+) as an anion receptor, binding with oxoanions diclofenac and chlorate ions has been investigated. Yellow crystals of [trans-Co(en)(2)(NO2)(2)]C14H10Cl2NO2. 2H(2)O 1, and [trans-Co(en)(2)(NO2)(2)]ClO3 II, have been obtained from a mixture of trans-[bis(ethylened iamine)dinitrocobalt(III)] nitrate solution with sodium diclofenac and sodium chlorate. respectively, in aqueous medium. The products were characterised by elemental analyses, IR, UV/vis, H-1 and C-13 NMR spectroscopy. Single crystal X-ray structure determinations revealed that electrostatic forces of attraction besides second sphere hydrogen bonding interactions stabilize the crystal lattice. Oxygen atoms of the halate and carboxylate group in diclofenac ions act as hydrogen bond acceptors thereby forming N-(HenO)-O-... bonds. The results show that [trans-Co(en)(2)(NO2)(2)](+) is a promising anion receptor for the weakly coordinating halate and diclofenac ions in aqueous medium. Solubility measurements indicate that the affinity of cationic cobaltammine [trans-Co(en)(2)(NO2)(2)](+) is greater for diclofenac than for the chlorate ion. (c) 2006 Elsevier B.V. All rights reserved.
Original languageEnglish
Pages (from-to)177
Number of pages1
JournalJournal of Molecular Structure
Volume826
Issue number2-3
DOIs
Publication statusPublished - 29 Jan 2007

Keywords

  • X-ray crystallography
  • chlorate
  • hydrogen bonding
  • diclofenac
  • cobalt(III)
  • second sphere coordination

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