Alkylvanadium‐ und Alkylniob‐Reagenzien, III. über zwei unkonventionelle Methoden zur Charakterisierung labiler Organoübergangsmetall‐Komplexe; Anwendungen auf Allylderivate von V III , V V , Cr III und Mn II

Alkylvanadium and Alkylniobium Reagents, III [1] . – Two Unconventional Chemical Methods for the Characterisation of Labile Transition Metal Complexes; Application to Allyl Derivatives of V III , V V , Cr III , and Mn II Two little known chemical methods, the “Competition Constant Method” and the pr...

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Veröffentlicht in:Chemische Berichte 1993-09, Vol.126 (9), p.2093-2100
Hauptverfasser: Kauffmann, Thomas, Bonrath, Werner, Beirich, Christoph, Li, Weichang, Pahde, Claudia, Raedeker, Susanne, Wichmann, Barbara, Wingbermühle, Dorothea
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container_end_page 2100
container_issue 9
container_start_page 2093
container_title Chemische Berichte
container_volume 126
creator Kauffmann, Thomas
Bonrath, Werner
Beirich, Christoph
Li, Weichang
Pahde, Claudia
Raedeker, Susanne
Wichmann, Barbara
Wingbermühle, Dorothea
description Alkylvanadium and Alkylniobium Reagents, III [1] . – Two Unconventional Chemical Methods for the Characterisation of Labile Transition Metal Complexes; Application to Allyl Derivatives of V III , V V , Cr III , and Mn II Two little known chemical methods, the “Competition Constant Method” and the production of “Ligand Concentration/Product Yield Diagrams”, are suitable for the characterisation and identification of allyl and crotyl transition metal species prepared in solution. These methods (Figures 1 – 6) gave the following results: by transmetallation of 1 or 2 equivalents of allylMgBr with 1 equivalent of VCl 3 , CrCl 3 , or MnCl 2 and subsequent reaction with ketones, a diallyl ( 2, 23, 25 ) and not a monoallyl derivative of the transition metal reacts with the ketones, suggesting that the equilibrium: 2 allylMCI (allyl) 2 M + MCl 2 (M = VCl, CrCl, Mn) lies far to the right hand side. This assumption was confirmed by the IR spectrum in the case of vanadation of 1 and 2 equivalents of allylMgBr with VCl 3 and corresponds with the observation that by chromation of allylMgBr with 1 equivalent of CrCl 3 ca. 50% of the CrCl 3 remain unaffected although the allylMgBr is completely consumed. Conversely, according to the results of the “Competition Constant Method” vanadation of 1, 2, or 3 equivalents of allylMgBr with VOCl 3 gives three different allyl complexes which are believed to be allylVOCl 2 ( 5 ), (allyl) 2 VOCl ( 6 ), and (allyl) 3 VO ( 7 ). Vanadation of 1 or 2 equivalents of crotylMgBr with 1 or 2 equivalents of VCl 3 gives analogous results to the corresponding reactions with allylMgBr.
doi_str_mv 10.1002/cber.19931260920
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These methods (Figures 1 – 6) gave the following results: by transmetallation of 1 or 2 equivalents of allylMgBr with 1 equivalent of VCl 3 , CrCl 3 , or MnCl 2 and subsequent reaction with ketones, a diallyl ( 2, 23, 25 ) and not a monoallyl derivative of the transition metal reacts with the ketones, suggesting that the equilibrium: 2 allylMCI (allyl) 2 M + MCl 2 (M = VCl, CrCl, Mn) lies far to the right hand side. This assumption was confirmed by the IR spectrum in the case of vanadation of 1 and 2 equivalents of allylMgBr with VCl 3 and corresponds with the observation that by chromation of allylMgBr with 1 equivalent of CrCl 3 ca. 50% of the CrCl 3 remain unaffected although the allylMgBr is completely consumed. Conversely, according to the results of the “Competition Constant Method” vanadation of 1, 2, or 3 equivalents of allylMgBr with VOCl 3 gives three different allyl complexes which are believed to be allylVOCl 2 ( 5 ), (allyl) 2 VOCl ( 6 ), and (allyl) 3 VO ( 7 ). Vanadation of 1 or 2 equivalents of crotylMgBr with 1 or 2 equivalents of VCl 3 gives analogous results to the corresponding reactions with allylMgBr.</description><identifier>ISSN: 0009-2940</identifier><identifier>DOI: 10.1002/cber.19931260920</identifier><language>eng</language><ispartof>Chemische Berichte, 1993-09, Vol.126 (9), p.2093-2100</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c880-467563fb84b81a9d89e5010081da5945beb2ad5eb0c9fa8a43d77bf51c670b563</citedby><cites>FETCH-LOGICAL-c880-467563fb84b81a9d89e5010081da5945beb2ad5eb0c9fa8a43d77bf51c670b563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kauffmann, Thomas</creatorcontrib><creatorcontrib>Bonrath, Werner</creatorcontrib><creatorcontrib>Beirich, Christoph</creatorcontrib><creatorcontrib>Li, Weichang</creatorcontrib><creatorcontrib>Pahde, Claudia</creatorcontrib><creatorcontrib>Raedeker, Susanne</creatorcontrib><creatorcontrib>Wichmann, Barbara</creatorcontrib><creatorcontrib>Wingbermühle, Dorothea</creatorcontrib><title>Alkylvanadium‐ und Alkylniob‐Reagenzien, III. über zwei unkonventionelle Methoden zur Charakterisierung labiler Organoübergangsmetall‐Komplexe; Anwendungen auf Allylderivate von V III , V V , Cr III und Mn II</title><title>Chemische Berichte</title><description>Alkylvanadium and Alkylniobium Reagents, III [1] . – Two Unconventional Chemical Methods for the Characterisation of Labile Transition Metal Complexes; Application to Allyl Derivatives of V III , V V , Cr III , and Mn II Two little known chemical methods, the “Competition Constant Method” and the production of “Ligand Concentration/Product Yield Diagrams”, are suitable for the characterisation and identification of allyl and crotyl transition metal species prepared in solution. These methods (Figures 1 – 6) gave the following results: by transmetallation of 1 or 2 equivalents of allylMgBr with 1 equivalent of VCl 3 , CrCl 3 , or MnCl 2 and subsequent reaction with ketones, a diallyl ( 2, 23, 25 ) and not a monoallyl derivative of the transition metal reacts with the ketones, suggesting that the equilibrium: 2 allylMCI (allyl) 2 M + MCl 2 (M = VCl, CrCl, Mn) lies far to the right hand side. This assumption was confirmed by the IR spectrum in the case of vanadation of 1 and 2 equivalents of allylMgBr with VCl 3 and corresponds with the observation that by chromation of allylMgBr with 1 equivalent of CrCl 3 ca. 50% of the CrCl 3 remain unaffected although the allylMgBr is completely consumed. Conversely, according to the results of the “Competition Constant Method” vanadation of 1, 2, or 3 equivalents of allylMgBr with VOCl 3 gives three different allyl complexes which are believed to be allylVOCl 2 ( 5 ), (allyl) 2 VOCl ( 6 ), and (allyl) 3 VO ( 7 ). 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These methods (Figures 1 – 6) gave the following results: by transmetallation of 1 or 2 equivalents of allylMgBr with 1 equivalent of VCl 3 , CrCl 3 , or MnCl 2 and subsequent reaction with ketones, a diallyl ( 2, 23, 25 ) and not a monoallyl derivative of the transition metal reacts with the ketones, suggesting that the equilibrium: 2 allylMCI (allyl) 2 M + MCl 2 (M = VCl, CrCl, Mn) lies far to the right hand side. This assumption was confirmed by the IR spectrum in the case of vanadation of 1 and 2 equivalents of allylMgBr with VCl 3 and corresponds with the observation that by chromation of allylMgBr with 1 equivalent of CrCl 3 ca. 50% of the CrCl 3 remain unaffected although the allylMgBr is completely consumed. Conversely, according to the results of the “Competition Constant Method” vanadation of 1, 2, or 3 equivalents of allylMgBr with VOCl 3 gives three different allyl complexes which are believed to be allylVOCl 2 ( 5 ), (allyl) 2 VOCl ( 6 ), and (allyl) 3 VO ( 7 ). Vanadation of 1 or 2 equivalents of crotylMgBr with 1 or 2 equivalents of VCl 3 gives analogous results to the corresponding reactions with allylMgBr.</abstract><doi>10.1002/cber.19931260920</doi><tpages>8</tpages></addata></record>
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title Alkylvanadium‐ und Alkylniob‐Reagenzien, III. über zwei unkonventionelle Methoden zur Charakterisierung labiler Organoübergangsmetall‐Komplexe; Anwendungen auf Allylderivate von V III , V V , Cr III und Mn II
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