Abstract
An investigation of the monoligand complex of 1,4,7-tris(β-diphenylphosphinylethyl)-1,4,7-triazacyclononane with divalent copper has been carried out in various solvents using electronic, IR, and ESR spectroscopy. It was found that the five-coordination polyhedron formed in the complex involves only donor atoms of the ligand and has the structure of a tetragonally elongated square pyramid with two nitrogen atoms and two oxygen atoms at the base and a nitrogen atom at the apex. Compared with the copper(II) complex with the corresponding acid, 1,4,7-tris(β-dihydroxyphosphinylethyl)-1,4,7-triazacyclononane, the coordination compound studied has a higher order of symmetry. The absence of observable distortions in the case of the acid is probably connected with steric interaction of the bulky phenyl substituents in the test ligand.
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A. N. Nesmeyanov Institute of Heteroorganic Compounds, Russian Academy of Sciences, Moscow 117813. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 3, pp. 594–601, March, 1992.
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Tolkachev, D.V., Pasechnik, M.P., Goryunova, I.B. et al. Complex formation of 1,4,7-tris(β-diphenylphosphinylethyl)-1,4,7-triazacyclononane with divalent copper salts. Russ Chem Bull 41, 468–473 (1992). https://doi.org/10.1007/BF00863065
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DOI: https://doi.org/10.1007/BF00863065