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Copper Imidazolin-imine Coordination Compounds as Precursors for a Cu/Al Complex
The reactions of [(CF3SO3Cu)2(C6H6)] with the sterically hindered imidazolin-2-imine ligands DippImTMS (1,3-Bis(2,6-diisopropylphenyl)-2-(trimethylsilylimino)imidazoline) or DippImH (1,3-bis(2,6-diisopropylphenyl) imidazolin-2-imine) lead to the formation of the linear copper(I) complexes [Cu(D...
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Published in: | Inorganic chemistry 2024-09, Vol.63 (38), p.17331-17339 |
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creator | Antsiburov, Ivan Stephan, Johannes Weininger, Richard J.J. Gemel, Christian Fischer, Roland A. |
description | The reactions of [(CF3SO3Cu)2(C6H6)] with the sterically hindered imidazolin-2-imine ligands DippImTMS (1,3-Bis(2,6-diisopropylphenyl)-2-(trimethylsilylimino)imidazoline) or DippImH (1,3-bis(2,6-diisopropylphenyl) imidazolin-2-imine) lead to the formation of the linear copper(I) complexes [Cu(DippImTMS)(OTf)] (1) and [Cu(DippImH)2][OTf] (2), respectively. The triflate counteranion in 2 can be easily exchanged to the weakly coordinating [BArF] giving [Cu(DippImH)2][BArF] (3) (BArF = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate). Substitution of the N-heterocyclic imine (NHI) ligand in 3 by AlCp* (Cp* = pentamethylcyclopentadienyl) gives the tetrahedral [Cu(AlCp*)4][BArF] (5). The reaction between lithiated imidazolin-2-iminate DippImLi and CuCl results in the triangular cluster [Cu3(DippIm)2Cl] (4). All products have been fully characterized by 1H- and 13C NMR, mass spectrometry, as well as SC-XRD. |
doi_str_mv | 10.1021/acs.inorgchem.4c02530 |
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The triflate counteranion in 2 can be easily exchanged to the weakly coordinating [BArF] giving [Cu(DippImH)2][BArF] (3) (BArF = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate). Substitution of the N-heterocyclic imine (NHI) ligand in 3 by AlCp* (Cp* = pentamethylcyclopentadienyl) gives the tetrahedral [Cu(AlCp*)4][BArF] (5). The reaction between lithiated imidazolin-2-iminate DippImLi and CuCl results in the triangular cluster [Cu3(DippIm)2Cl] (4). All products have been fully characterized by 1H- and 13C NMR, mass spectrometry, as well as SC-XRD.</description><identifier>ISSN: 0020-1669</identifier><identifier>ISSN: 1520-510X</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/acs.inorgchem.4c02530</identifier><identifier>PMID: 39258868</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2024-09, Vol.63 (38), p.17331-17339</ispartof><rights>2024 The Authors. 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Chem</addtitle><description>The reactions of [(CF3SO3Cu)2(C6H6)] with the sterically hindered imidazolin-2-imine ligands DippImTMS (1,3-Bis(2,6-diisopropylphenyl)-2-(trimethylsilylimino)imidazoline) or DippImH (1,3-bis(2,6-diisopropylphenyl) imidazolin-2-imine) lead to the formation of the linear copper(I) complexes [Cu(DippImTMS)(OTf)] (1) and [Cu(DippImH)2][OTf] (2), respectively. The triflate counteranion in 2 can be easily exchanged to the weakly coordinating [BArF] giving [Cu(DippImH)2][BArF] (3) (BArF = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate). Substitution of the N-heterocyclic imine (NHI) ligand in 3 by AlCp* (Cp* = pentamethylcyclopentadienyl) gives the tetrahedral [Cu(AlCp*)4][BArF] (5). The reaction between lithiated imidazolin-2-iminate DippImLi and CuCl results in the triangular cluster [Cu3(DippIm)2Cl] (4). 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Chem</addtitle><date>2024-09-23</date><risdate>2024</risdate><volume>63</volume><issue>38</issue><spage>17331</spage><epage>17339</epage><pages>17331-17339</pages><issn>0020-1669</issn><issn>1520-510X</issn><eissn>1520-510X</eissn><abstract>The reactions of [(CF3SO3Cu)2(C6H6)] with the sterically hindered imidazolin-2-imine ligands DippImTMS (1,3-Bis(2,6-diisopropylphenyl)-2-(trimethylsilylimino)imidazoline) or DippImH (1,3-bis(2,6-diisopropylphenyl) imidazolin-2-imine) lead to the formation of the linear copper(I) complexes [Cu(DippImTMS)(OTf)] (1) and [Cu(DippImH)2][OTf] (2), respectively. The triflate counteranion in 2 can be easily exchanged to the weakly coordinating [BArF] giving [Cu(DippImH)2][BArF] (3) (BArF = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate). Substitution of the N-heterocyclic imine (NHI) ligand in 3 by AlCp* (Cp* = pentamethylcyclopentadienyl) gives the tetrahedral [Cu(AlCp*)4][BArF] (5). The reaction between lithiated imidazolin-2-iminate DippImLi and CuCl results in the triangular cluster [Cu3(DippIm)2Cl] (4). All products have been fully characterized by 1H- and 13C NMR, mass spectrometry, as well as SC-XRD.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39258868</pmid><doi>10.1021/acs.inorgchem.4c02530</doi><tpages>9</tpages><orcidid>https://orcid.org/0009-0007-9209-8592</orcidid><orcidid>https://orcid.org/0000-0002-0594-9093</orcidid><orcidid>https://orcid.org/0000-0003-4087-0070</orcidid><orcidid>https://orcid.org/0000-0002-7532-5286</orcidid><oa>free_for_read</oa></addata></record> |
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title | Copper Imidazolin-imine Coordination Compounds as Precursors for a Cu/Al Complex |
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