Kalkuhl Till L, Qin Lei, Zhao Lili, Frenking Gernot, Hadlington Terrance J
Fakultät für Chemie, Technische Universität München Lichtenberg Strasse 4 85747 Garching Germany
Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University Nanjing China
Chem Sci. 2023 Sep 22;14(40):11088-11095. doi: 10.1039/d3sc03772j. eCollection 2023 Oct 18.
σ-complexes of homoatomic E-E bonds are key intermediates in catalytically relevant oxidative addition reactions, but are as yet unknown for the group 13 elements. Here, stable species best described as σ-complexes of a 1,2-dichlorodigallane derivative with Ni and Pd are reported. They are readily accessed through the combination of a 1,2-dichlorodigallane derivative, which features chelating phosphine functionalities, with Ni and Pd synthons. In-depth computational analyses of these complexes importantly reveal considerable Ga-Ga bonding interactions in both Ni and Pd complexes, despite the expected elongation of the Ga-Ga bond upon complexation, suggestive of σ-complex character as opposed to more commonly described bis(gallyl) character. Finally, the well-defined disproportion of the Ni complex is described, leading to a unique Ga-nickel complex, with concomitant expulsion of uncomplexed Ga species.
同原子E-E键的σ-配合物是催化相关氧化加成反应中的关键中间体,但对于13族元素而言,此类中间体迄今仍不为人知。本文报道了一类稳定的物种,它们最好被描述为1,2-二氯二镓烷衍生物与镍和钯形成的σ-配合物。通过具有螯合膦官能团的1,2-二氯二镓烷衍生物与镍和钯合成子的组合,可以很容易地得到它们。对这些配合物的深入计算分析重要地揭示了镍和钯配合物中都存在相当可观的镓-镓键相互作用,尽管在络合时镓-镓键预期会伸长,这表明其具有σ-配合物的特征,而非更常见的双(镓基)特征。最后,描述了镍配合物明确的歧化反应,生成了一种独特的镓-镍配合物,同时排出了未络合的镓物种。