Cobalt(II) complexes with aromatic carboxylates and N-functionalized cyclam bearing 2-pyridylmethyl pendant arms
Author(s) -
Gordana Vučković,
Vojislav Stanić,
Sofija P. Sovilj,
Mirjana Antonijević Nikolić,
J. Mrozynski
Publication year - 2005
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc0509121v
Subject(s) - cyclam , chemistry , cobalt , phthalate , chelation , cyclic voltammetry , medicinal chemistry , carboxylate , aromaticity , polymer chemistry , stereochemistry , electrochemistry , inorganic chemistry , molecule , organic chemistry , metal , electrode
Novel binuclear Co(II) complexes with N-functionalized cyclam, N,N',N",N''' -te- trakis(2-pyridylmethyl)tetraazacyclotetradecane (tpmc) and one of the aromatic mono- or dicarboxylato ligands (benzoate, phthalate or isophthalate ions) were prepared. They were analyzed and studied by elemental analyses (C, H, N), electrical conductivities, VIS and IR spectroscopy and magnetic as well as cyclic voltammetric measurements. In Co2(C6H5COO)2tpmc(ClO4)2.3H2O, the benzoate ligands are most probably coordi- nated as chelates in the trans-position to each Co(II) and the macrocycle adopts a chair conformation. In the complexes Co2(Y)tpmc(ClO4)2.zH2O, (Y = phthalate or i-phtha- late dianizon, z = 2; 4), it is proposed that the isomeric dicarboxylates are bonded com- bined as bridges and chelates. The composition and the assumed geometries of the com- plexes are compared with the, earlier reported, corresponding Cu(II) complexes. Cyclic voltammetry measurements showed that the compounds are electrochemically stable.
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