Simone V. Hirmer, Shicheng Dong, Sebastian Stigler, Arseni Kostenko, John A. Kelly, Zihan Zhang, Karsten Meyer, Jun Zhu, Shigeyoshi Inoue
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引用次数: 0
摘要
我们报道了利用乙烯桥接双[(二烷基氨基)环丙烯胺](bisCPI)配体LCPI来获得新的主基团E(II)卤化物配合物(E = Ge, Sn, Pb;随后用科尔曼试剂(Na2Fe(CO)4•二氧六环)还原,可以分离出一系列单原子零价四炔-四羰基铁配合物(LCPI)E(Fe(CO)4 (E = Ge (4), Sn (5), Pb(6))。化合物4 ~ 6与五羰基铁进一步反应,得到双四羰基铁配合物(LCPI)E[(Fe(CO)4]2 (E = Ge (7), Sn (8), Pb(9))。通过57Fe Mössbauer光谱和密度泛函理论计算研究了这些配合物的电子结构。
Utilization of a Chelating Bis[(dialkylamino)cyclopropenimine] to Isolate a Series of Heavier Zero-Valent Group 14 Tetracarbonyl Iron Complexes
We report on the utilization of the ethylene-bridged bis[(dialkylamino)cyclopropenimine] (bisCPI) ligand, LCPI, to give access to new main-group E(II) halide complexes (E = Ge, Sn, Pb; 1, 2, 3). Subsequent reduction with Collman's reagent (Na2Fe(CO)4 • dioxane) enables the isolation of a series of zero-valent tetrylone-tetracarbonyl iron complexes, (LCPI)E(Fe(CO)4 (E = Ge (4), Sn (5), Pb (6)). Compounds 4 – 6 were reacted further with iron pentacarbonyl to yield the bis-tetracarbonyl iron complexes (LCPI)E[(Fe(CO)4]2 (E = Ge (7), Sn (8), Pb (9)). The electronic structure of these complexes was studied by 57Fe Mössbauer spectroscopy and computationally by density functional theory calculations.
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