Synthesis, Characterization and Solvatochromism Investigation of Mixed Ligand Chelate Copper(II) Complexes with Acetyleacetonate and Three Diamine Ligands

The syntheses of three mixed ligand chelate copper(II) complexes of the type [Cu(L)(acac)(H2O)]BPh4 where acac=acetyleacetonate; L=N,N‐dimethyl,N′‐benzylethane‐1,2‐diamine (L1), N,N‐dimethyl, N′‐2‐methylbenzylethane‐1,2‐diamine (L2) or N,N‐dimethyl,N′‐2‐chlorobenzylethane‐1,2‐diamine (L3) are report...

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Veröffentlicht in:Chinese journal of chemistry 2012-08, Vol.30 (8), p.1873-1880
Hauptverfasser: Golchoubian, Hamid, Afshar, Zahra Mohseni, Moayyedi, Golasa, Bruno, Giuseppe, Rudbari, Hadi Amiri
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container_end_page 1880
container_issue 8
container_start_page 1873
container_title Chinese journal of chemistry
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creator Golchoubian, Hamid
Afshar, Zahra Mohseni
Moayyedi, Golasa
Bruno, Giuseppe
Rudbari, Hadi Amiri
description The syntheses of three mixed ligand chelate copper(II) complexes of the type [Cu(L)(acac)(H2O)]BPh4 where acac=acetyleacetonate; L=N,N‐dimethyl,N′‐benzylethane‐1,2‐diamine (L1), N,N‐dimethyl, N′‐2‐methylbenzylethane‐1,2‐diamine (L2) or N,N‐dimethyl,N′‐2‐chlorobenzylethane‐1,2‐diamine (L3) are reported and characterized by elemental analyses, spectroscopic and molar conductance measurements. The X‐ray structure of complex 1 shows that the central copper atom is placed in a distorted square pyramidal geometry made by acac and diamine chelate in the base and a H2O molecule on the apex. The prepared complexes are fairly soluble in a large number of organic solvents and show positive solvatochromism. Calculations of SMLR (stepwise multiple linear regression) method was utilized to find the best model explaining the observed solvatochromic behavior and showed that among different solvent parameters, donor number (DN) is a dominant factor responsible for the shift in the d‐d absorption band of the complexes to the lower wavenumber with increasing its values. The importance of substituent effect in diamine ligand on the spectral and SMLR measurements is also discussed.
doi_str_mv 10.1002/cjoc.201200368
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J. Chem</addtitle><date>2012-08</date><risdate>2012</risdate><volume>30</volume><issue>8</issue><spage>1873</spage><epage>1880</epage><pages>1873-1880</pages><issn>1001-604X</issn><eissn>1614-7065</eissn><abstract>The syntheses of three mixed ligand chelate copper(II) complexes of the type [Cu(L)(acac)(H2O)]BPh4 where acac=acetyleacetonate; L=N,N‐dimethyl,N′‐benzylethane‐1,2‐diamine (L1), N,N‐dimethyl, N′‐2‐methylbenzylethane‐1,2‐diamine (L2) or N,N‐dimethyl,N′‐2‐chlorobenzylethane‐1,2‐diamine (L3) are reported and characterized by elemental analyses, spectroscopic and molar conductance measurements. The X‐ray structure of complex 1 shows that the central copper atom is placed in a distorted square pyramidal geometry made by acac and diamine chelate in the base and a H2O molecule on the apex. The prepared complexes are fairly soluble in a large number of organic solvents and show positive solvatochromism. Calculations of SMLR (stepwise multiple linear regression) method was utilized to find the best model explaining the observed solvatochromic behavior and showed that among different solvent parameters, donor number (DN) is a dominant factor responsible for the shift in the d‐d absorption band of the complexes to the lower wavenumber with increasing its values. The importance of substituent effect in diamine ligand on the spectral and SMLR measurements is also discussed.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/cjoc.201200368</doi><tpages>8</tpages></addata></record>
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subjects copper(II)
diamine
Ligands
mixed-chelate
SMLR method
solvatochromism
tetraphenylborate
X-ray crystal structure
title Synthesis, Characterization and Solvatochromism Investigation of Mixed Ligand Chelate Copper(II) Complexes with Acetyleacetonate and Three Diamine Ligands
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