Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, D-35032 Marburg, Germany.
Chem Soc Rev. 2014 Jul 21;43(14):5106-39. doi: 10.1039/c4cs00073k. Epub 2014 Jun 11.
Recent theoretical studies are reviewed which show that the naked group 14 atoms E = C-Pb in the singlet (1)D state behave as bidentate Lewis acids that strongly bind two σ donor ligands L in the donor-acceptor complexes L→E←L. Tetrylones EL2 are divalent E(0) compounds which possess two lone pairs at E. The unique electronic structure of tetrylones (carbones, silylones, germylones, stannylones, plumbylones) clearly distinguishes them from tetrylenes ER2 (carbenes, silylenes, germylenes, stannylenes, plumbylenes) which have electron-sharing bonds R-E-R and only one lone pair at atom E. The different electronic structures of tetrylones and tetrylenes are revealed by charge- and energy decomposition analyses and they become obvious experimentally by a distinctively different chemical reactivity. The unusual structures and chemical behaviour of tetrylones EL2 can be understood in terms of the donor-acceptor interactions L→E←L. Tetrylones are potential donor ligands in main group compounds and transition metal complexes which are experimentally not yet known. The review also introduces theoretical studies of transition metal complexes [TM]-E which carry naked tetrele atoms E = C-Sn as ligands. The bonding analyses suggest that the group-14 atoms bind in the (3)P reference state to the transition metal in a combination of σ and π∥ electron-sharing bonds TM-E and π⊥ backdonation TM→E. The unique bonding situation of the tetrele complexes [TM]-E makes them suitable ligands in adducts with Lewis acids. Theoretical studies of [TM]-E→W(CO)5 predict that such species may becomes synthesized.
最近的理论研究表明,处于 singlet (1)D 态的裸露 Group 14 原子 E = C-Pb 作为双齿路易斯酸,在供体-受体络合物 L→E←L 中强烈结合两个 σ 供体配体 L。三唑酮 EL2 是二价 E(0)化合物,在 E 原子上具有两个孤对电子。三唑酮(碳烯、硅烯、锗烯、锡烯、铅烯)的独特电子结构清楚地将它们与具有电子共享键 R-E-R 和在 E 原子上只有一个孤对电子的三唑啉 ER2(卡宾、硅烯、锗烯、锡烯、铅烯)区分开来。电荷和能量分解分析揭示了三唑酮和三唑啉的不同电子结构,实验上通过明显不同的化学活性变得明显。三唑酮 EL2 的不寻常结构和化学行为可以根据供体-受体相互作用 L→E←L 来理解。三唑酮是主族化合物和过渡金属配合物中潜在的供体配体,目前在实验中尚未被发现。该综述还介绍了对携带裸露四氮烯原子 E = C-Sn 的过渡金属配合物 [TM]-E 的理论研究。键合分析表明,Group 14 原子在 (3)P 参考态下以 σ 和 π∥ 电子共享键 TM-E 和 π⊥ 反馈 TM→E 的组合与过渡金属结合。四氮烯配合物 [TM]-E 的独特键合情况使其成为路易斯酸加合物中的合适配体。对 [TM]-E→W(CO)5 的理论研究预测,这些物种可能会被合成。