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Structurally characterised intermediate of the oxidative addition of a heteroleptic germylene to gallanediyle
Chemical Communications ( IF 4.3 ) Pub Date : 2022-08-08 , DOI: 10.1039/d2cc03561h
Anna Bücker 1 , Christoph Wölper 1 , Gebhard Haberhauer 2 , Stephan Schulz 1, 3
Affiliation  

Bond activation reactions using main group metal complexes are gaining increasing interest. We report on reactions of LGa (L = HC[C(Me)N(Ar)]2, Ar = Dipp = 2,6-i-Pr2C6H3,) with heteroleptic tetrylenes L′ECl (E = Ge, Sn; L′ = N(SiMe3)Ar), yielding the donor–acceptor complex LGa–Sn(Cl)L′ (1) or the oxidative addition product L(Cl)GaGeL′ (3). The reaction with DMPGeCl (DMP = 2,6-Mes2C6H3, Mes = 2,4,6-Me3C6H2) yielded LGa(μ–Cl)GeDMP (2), which represents an intermediate of the oxidative addition reaction. 1–3 were characterized by NMR and IR spectroscopy as well as by single crystal X-ray diffraction (sc-XRD), while their electronic nature was analyzed by quantum chemical calculations.

中文翻译:

杂配子锗烯与没食子二烯的氧化加成的结构特征中间体

使用主族金属配合物的键活化反应越来越受到关注。我们报告了 LGa (L = HC[C(Me)N(Ar)] 2 , Ar = Dipp = 2,6- i -Pr 2 C 6 H 3 ,) 与杂配四萘嵌苯 L'ECl (E = Ge , Sn; L' = N(SiMe 3 )Ar),得到供体-受体复合物 LGa-Sn(Cl)L' ( 1 ) 或氧化加成产物 L(Cl)GaGeL' ( 3 )。与 DMPGeCl (DMP = 2,6-Mes 2 C 6 H 3 , Mes = 2,4,6-Me 3 C 6 H 2 ) 反应生成 LGa(μ–Cl)GeDMP ( 2),它代表氧化加成反应的中间体。通过核磁共振和红外光谱以及单晶 X 射线衍射 (sc-XRD) 对1-3进行了表征,而通过量子化学计算分析了它们的电子性质。
更新日期:2022-08-12
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