Highly Stereoselective Photochemical Oxidative Addition Reactions. Preliminary Communication
Cyclometallated complexes of the type cis‐bis(2‐phenylpyridine)platinum(II) (C22H16N2Pt) and cis‐bis(2‐(2′‐thienyl)pyridine)platinum(II) (C18H12N2S2Pt) undergo thermal or photochemical oxidative addition (TOA or POA) reactions with a number of substrates. TOA (with CH3I, CH3CH2I etc.) yield mixtures...
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Veröffentlicht in: | Helvetica chimica acta 1986-12, Vol.69 (8), p.1855-1857 |
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description | Cyclometallated complexes of the type cis‐bis(2‐phenylpyridine)platinum(II) (C22H16N2Pt) and cis‐bis(2‐(2′‐thienyl)pyridine)platinum(II) (C18H12N2S2Pt) undergo thermal or photochemical oxidative addition (TOA or POA) reactions with a number of substrates. TOA (with CH3I, CH3CH2I etc.) yield mixtures of several isomers which rearrange slowly (within ca. one week at room temperature) to one of the possible cis‐isomers. CH2Cl2, CHCl3, or (E)ClCHCHCl, e.g., do not react thermally. POA yield directly complexes of Pt(IV) with the halide and a σ‐bonded C‐atom in cis‐position. The configuration, as assigned by extensive use of 1H‐NMR data, can be characterized for the two chelating ligands C …︁ N and C′ …︁ N′ by C,C′‐cis; N,N′‐cis and C(chelate), Cl‐trans. |
doi_str_mv | 10.1002/hlca.19860690812 |
format | Article |
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The configuration, as assigned by extensive use of 1H‐NMR data, can be characterized for the two chelating ligands C …︁ N and C′ …︁ N′ by C,C′‐cis; N,N′‐cis and C(chelate), Cl‐trans.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.19860690812</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag GmbH</publisher><ispartof>Helvetica chimica acta, 1986-12, Vol.69 (8), p.1855-1857</ispartof><rights>Copyright © 1986 Verlag GmbH & Co. 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The configuration, as assigned by extensive use of 1H‐NMR data, can be characterized for the two chelating ligands C …︁ N and C′ …︁ N′ by C,C′‐cis; N,N′‐cis and C(chelate), Cl‐trans.</description><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PwzAMhiMEEmNw59g_0OEka9ocOEwFNqSJjfEphBSliUsD7YraAtu_p2UIwYmTrdd-LOsh5JDCgAKwoyw3ekBlJEBIiCjbIj0aMOYzEQbbpAdAIx-ovN8le3X9DABSQtgjjxP3lOVr76rBCssaczSNe0dvnpVNaTIsnNG5N1s5q7_ykbWuceXSW6A2XVMPvHmFuSvcUldrLy6L4m3ZQt1sn-ykOq_x4Lv2yc3Z6XU88aez8Xk8mvqGDSPmc-Qhh0joBAUzaZtxG0rkAhM2TIRlzAZgTQAGGZUJWC61Nmg1TxM0acT7BDZ3TVXWdYWpeq1c0b6jKKjOjursqF92WuR4g3y4HNf_7qvJNB795f0N7-oGVz-8rl6UCHkYqLuLsTq5jORCPNyqIf8ExZ58mw</recordid><startdate>19861210</startdate><enddate>19861210</enddate><creator>Chassot, Laurent</creator><creator>von Zelewsky, Alex</creator><general>WILEY-VCH Verlag GmbH</general><general>WILEY‐VCH Verlag GmbH</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19861210</creationdate><title>Highly Stereoselective Photochemical Oxidative Addition Reactions. Preliminary Communication</title><author>Chassot, Laurent ; von Zelewsky, Alex</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2482-3e373086abe62cf2483d79e36eb24b6d22d50dc50ce219b0d39aaceda3fbecf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chassot, Laurent</creatorcontrib><creatorcontrib>von Zelewsky, Alex</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chassot, Laurent</au><au>von Zelewsky, Alex</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly Stereoselective Photochemical Oxidative Addition Reactions. Preliminary Communication</atitle><jtitle>Helvetica chimica acta</jtitle><addtitle>HCA</addtitle><date>1986-12-10</date><risdate>1986</risdate><volume>69</volume><issue>8</issue><spage>1855</spage><epage>1857</epage><pages>1855-1857</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>Cyclometallated complexes of the type cis‐bis(2‐phenylpyridine)platinum(II) (C22H16N2Pt) and cis‐bis(2‐(2′‐thienyl)pyridine)platinum(II) (C18H12N2S2Pt) undergo thermal or photochemical oxidative addition (TOA or POA) reactions with a number of substrates. TOA (with CH3I, CH3CH2I etc.) yield mixtures of several isomers which rearrange slowly (within ca. one week at room temperature) to one of the possible cis‐isomers. CH2Cl2, CHCl3, or (E)ClCHCHCl, e.g., do not react thermally. POA yield directly complexes of Pt(IV) with the halide and a σ‐bonded C‐atom in cis‐position. The configuration, as assigned by extensive use of 1H‐NMR data, can be characterized for the two chelating ligands C …︁ N and C′ …︁ N′ by C,C′‐cis; N,N′‐cis and C(chelate), Cl‐trans.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag GmbH</pub><doi>10.1002/hlca.19860690812</doi><tpages>3</tpages></addata></record> |
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title | Highly Stereoselective Photochemical Oxidative Addition Reactions. Preliminary Communication |
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