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作为多磷配合物中性供体的氮杂环卡宾

NHCs as Neutral Donors towards Polyphosphorus Complexes.

作者信息

Riedlberger Felix, Todisco Stefano, Mastrorilli Piero, Timoshkin Alexey Y, Seidl Michael, Scheer Manfred

机构信息

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.

出版信息

Chemistry. 2020 Dec 9;26(69):16251-16255. doi: 10.1002/chem.202003393. Epub 2020 Oct 29.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4088/7756228/4aead6d43e89/CHEM-26-16251-g001.jpg

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