Riedlberger Felix, Todisco Stefano, Mastrorilli Piero, Timoshkin Alexey Y, Seidl Michael, Scheer Manfred
Institut für Anorganische Chemie, Universität Regensburg, 93040, Regensburg, Germany.
Dipartimento di Ingeneria Civile, Ambientale, del Territorito Edile e di Chimica (DICATECh), Politecnico di Bari, Via Orabona 4, 70125, Bari, Italy.
Chemistry. 2020 Dec 9;26(69):16251-16255. doi: 10.1002/chem.202003393. Epub 2020 Oct 29.
The first adducts of NHCs (=N-heterocyclic carbenes) with aromatic polyphosphorus complexes are reported. The reactions of [CpFe(η -P )] (1) (Cp=pentamethyl-cyclopentadienyl) with IMe (=1,3,4,5-tetramethylimidazolin-2-ylidene), IMes (=1,3-bis(2,4,6-trimethylphenyl)-imidazolin-2-ylidene) and IDipp (=1,3-bis(2,6-diisopropylphenyl)-imidazolin-2-ylidene) led to the corresponding neutral adducts which can be isolated in the solid state. However, in solution, they quickly undergo a dissociative equilibrium between the adduct and 1 including the corresponding NHC. The equilibrium is influenced by the bulkiness of the NHC. [Cp''Ta(CO) (η -P )] (Cp''=1,3-di-tert-butylcyclopentadienyl) reacts with IMe under P atom abstraction to give an unprecedented cyclo-P -containing anionic tantalum complex. DFT calculations shed light onto the energetics of the reaction pathways.
报道了氮杂环卡宾(NHCs)与芳香族多磷配合物的首例加合物。[CpFe(η -P )](1)(Cp = 五甲基环戊二烯基)与IMe(= 1,3,4,5 - 四甲基咪唑啉 - 2 - 亚基)、IMes(= 1,3 - 双(2,4,6 - 三甲基苯基)- 咪唑啉 - 2 - 亚基)和IDipp(= 1,3 - 双(2,6 - 二异丙基苯基)- 咪唑啉 - 2 - 亚基)的反应生成了相应的中性加合物,这些加合物可以以固态形式分离出来。然而,在溶液中,它们会迅速在加合物和1(包括相应的氮杂环卡宾)之间经历解离平衡。该平衡受氮杂环卡宾空间位阻的影响。[Cp''Ta(CO) (η -P )](Cp'' = 1,3 - 二叔丁基环戊二烯基)与IMe在磷原子夺取反应下反应,生成一种前所未有的含环 -P 的阴离子钽配合物。密度泛函理论计算揭示了反应途径的能量学。