4.5 Article

Synthesis and coordination chemistry of new tetradentate N2S2 donor Schiff-base ligand ca2-dapte: Mononuclear and dinuclear copper(I) complexes [Cu(ca2dapte)]ClO4 and [{Cu(PPh3)(X)}2(ca2dapte)] (X = I and Br)

Journal

POLYHEDRON
Volume 28, Issue 1, Pages 167-171

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.poly.2008.10.018

Keywords

N/S donor; Copper(I) complexes; Mononuclear; Dinuclear; Single-crystal X-ray diffraction

Funding

  1. Isfahan University of Technology Research Council
  2. Gorgan University of Agricultural Sciences and Natural Resources

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A mononuclear copper(I) complex, [Cu(ca(2)dapte)]ClO4 (1), and two dinuclear copper(I) complexes, [{Cu(PPh3)(X)}(2)(ca(2)dapte)] (X = 1 (2) and Br (3)), of a new tetradentate N2S2 donor Schiff-base ligand ca2dapte have been prepared (ca(2)dapte = N,N'-bis(trans-cinnamaidehyde)-1,2-di(o-iminophenylthio)ethane). These compounds have been characterized by elemental analyses (CHN), FT-IR, UV-Vis and H-1 NMR spectroscopy. The crystal structures of these copper(l) complexes have been determined by single-crystal X-ray diffraction. The coordination geometry around Cu(I) centers in these complexes is a distorted tetrahedron. The Ca(2)dapte is coordinated to Cu(I) as a tetradentate ligand in 1, while it acts as a bis-bidentate bridging ligand in 2 and 3. (C) 2008 Elsevier Ltd. All rights reserved.

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