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 |
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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 |
format | Article |
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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.</description><identifier>ISSN: 1001-604X</identifier><identifier>EISSN: 1614-7065</identifier><identifier>DOI: 10.1002/cjoc.201200368</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>copper(II) ; diamine ; Ligands ; mixed-chelate ; SMLR method ; solvatochromism ; tetraphenylborate ; X-ray crystal structure</subject><ispartof>Chinese journal of chemistry, 2012-08, Vol.30 (8), p.1873-1880</ispartof><rights>Copyright © 2012 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2012 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3558-3d55494ec42a79a874ce6311fbaa439a5fa60d79a87fea0054da025569c5f6be3</citedby><cites>FETCH-LOGICAL-c3558-3d55494ec42a79a874ce6311fbaa439a5fa60d79a87fea0054da025569c5f6be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcjoc.201200368$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcjoc.201200368$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Golchoubian, Hamid</creatorcontrib><creatorcontrib>Afshar, Zahra Mohseni</creatorcontrib><creatorcontrib>Moayyedi, Golasa</creatorcontrib><creatorcontrib>Bruno, Giuseppe</creatorcontrib><creatorcontrib>Rudbari, Hadi Amiri</creatorcontrib><title>Synthesis, Characterization and Solvatochromism Investigation of Mixed Ligand Chelate Copper(II) Complexes with Acetyleacetonate and Three Diamine Ligands</title><title>Chinese journal of chemistry</title><addtitle>Chin. J. Chem</addtitle><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.</description><subject>copper(II)</subject><subject>diamine</subject><subject>Ligands</subject><subject>mixed-chelate</subject><subject>SMLR method</subject><subject>solvatochromism</subject><subject>tetraphenylborate</subject><subject>X-ray crystal structure</subject><issn>1001-604X</issn><issn>1614-7065</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkMFO3DAQhiPUSlDaa8-WuFCp2dpJ7CRHFMqy1baoWqpyswZnQrwkcbAN7PZR-rR4G4R64zSjme8by38UfWR0xihNvqi1UbOEsoTSVBR70QETLItzKvib0FPKYkGzq_3onXPrwOd5Ig6iv6vt4Ft02n0mVQsWlEer_4DXZiAw1GRlugfwRrXW9Nr1ZDE8oPP6ZiJMQ77rDdZkGSaBrlrswCOpzDiiPV4sPoW2HzvcoCOP2rfkRKHfdgihmGGH7rTL1iKSUw29HvD5lnsfvW2gc_jhuR5Gv86-Xlbn8fJivqhOlrFKOS_itOY8KzNUWQJ5CUWeKRQpY801QJaWwBsQtP63aRAo5VkNNOFclIo34hrTw-houjtac3cfPifX5t4O4UnJciEKWrJCBGo2Ucoa5yw2crS6B7uVjMpd_nKXv3zJPwjlJDzqDrev0LL6dlH978aTq53HzYsL9laKPM25_P1jLs9Oz3_Or1ZLOU-fALzWm8s</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Golchoubian, Hamid</creator><creator>Afshar, Zahra Mohseni</creator><creator>Moayyedi, Golasa</creator><creator>Bruno, Giuseppe</creator><creator>Rudbari, Hadi Amiri</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201208</creationdate><title>Synthesis, Characterization and Solvatochromism Investigation of Mixed Ligand Chelate Copper(II) Complexes with Acetyleacetonate and Three Diamine Ligands</title><author>Golchoubian, Hamid ; Afshar, Zahra Mohseni ; Moayyedi, Golasa ; Bruno, Giuseppe ; Rudbari, Hadi Amiri</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3558-3d55494ec42a79a874ce6311fbaa439a5fa60d79a87fea0054da025569c5f6be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>copper(II)</topic><topic>diamine</topic><topic>Ligands</topic><topic>mixed-chelate</topic><topic>SMLR method</topic><topic>solvatochromism</topic><topic>tetraphenylborate</topic><topic>X-ray crystal structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Golchoubian, Hamid</creatorcontrib><creatorcontrib>Afshar, Zahra Mohseni</creatorcontrib><creatorcontrib>Moayyedi, Golasa</creatorcontrib><creatorcontrib>Bruno, Giuseppe</creatorcontrib><creatorcontrib>Rudbari, Hadi Amiri</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Chinese journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Golchoubian, Hamid</au><au>Afshar, Zahra Mohseni</au><au>Moayyedi, Golasa</au><au>Bruno, Giuseppe</au><au>Rudbari, Hadi Amiri</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, Characterization and Solvatochromism Investigation of Mixed Ligand Chelate Copper(II) Complexes with Acetyleacetonate and Three Diamine Ligands</atitle><jtitle>Chinese journal of chemistry</jtitle><addtitle>Chin. 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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