TY - JOUR
T1 - Second sphere coordination in oxoanion binding: Synthesis, spectroscopic characterisation and crystal structures of trans-[bis(ethylenediamine)dinitrocobalt(III)] diclofenac and chlorate
AU - Sharmaa, R
AU - Sharmaa, RP
AU - Bala, R
AU - Kariuki, Benson
PY - 2007/1/29
Y1 - 2007/1/29
N2 - 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.
AB - 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.
KW - X-ray crystallography
KW - chlorate
KW - hydrogen bonding
KW - diclofenac
KW - cobalt(III)
KW - second sphere coordination
U2 - 10.1016/j.molstruc.2006.04.045
DO - 10.1016/j.molstruc.2006.04.045
M3 - Article
VL - 826
SP - 177
JO - Journal of Molecular Structure
JF - Journal of Molecular Structure
IS - 2-3
ER -