N-bonding vs. S-bonding in thiocyanato-copper(II) complexes

► Mononuclear thiocyanato-Cu(II) complexes. ► Structure determination of the complexes by single crystal X-ray crystallography. ► UV–vis and IR spectroscopic characterization of the complexes. Three mononuclear thiocyanato-Cu(II) complexes have been synthesized: the mono-thiocyanato [Cu(cyclen-tpam)...

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Veröffentlicht in:Journal of molecular structure 2011-12, Vol.1006 (1), p.570-575
Hauptverfasser: Mautner, Franz A., Albering, Jörg H., Harrelson, Emily V., Gallo, August A., Massoud, Salah S.
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Sprache:eng
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Zusammenfassung:► Mononuclear thiocyanato-Cu(II) complexes. ► Structure determination of the complexes by single crystal X-ray crystallography. ► UV–vis and IR spectroscopic characterization of the complexes. Three mononuclear thiocyanato-Cu(II) complexes have been synthesized: the mono-thiocyanato [Cu(cyclen-tpam)(NCS)]ClO 4·3H 2O ( 1) and [Cu(DPA)(NCS)ClO 4] ( 2), and the dithiocyanato complex Cu(bdmpzpy)(NCS) 2 ( 3), where cyclen-tpam = 1,4,7,10-tetrakis(propionamide)-1,4,7,10-tetraazacyclododecane, DPA = bis(2-pyridylmethyl)amine, and bdmpzpy = 2,6-bis[(2,5-dimethyl-1-pyrazolyl)methyl]pyridine. The single crystal X-ray crystallography of the complexes confirmed the perfect square pyramidal geometry (SP) in 1 and distorted SP geometry in 2 and 3 with N-bonding coordination mode for the thiocyanato ligands. The IR spectra of the complexes which were consistent with the N-bonding coordination mode of the thiocyanate group(s) and the visible spectra which revealed the square pyramidal geometry around the central Cu 2+ ion were in complete agreement with the X-ray structural determination.
ISSN:0022-2860
1872-8014
DOI:10.1016/j.molstruc.2011.10.005