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中性、配位饱和的三羰基锰(I)-PNP钳型配合物催化二氧化碳加氢生成甲酸盐

Carbon Dioxide Hydrogenation to Formate Catalyzed by a Neutral, Coordinatively Saturated Tris-Carbonyl Mn(I)-PNP Pincer-Type Complex.

作者信息

Kostera Sylwia, Manca Gabriele, Gonsalvi Luca

机构信息

Istituto di Chimica dei Composti Organometallici (ICCOM), Consiglio Nazionale delle Ricerche (CNR), Via Madonna del Piano 10, 50019, Sesto, Fiorentino (Florence), Italy.

出版信息

Chemistry. 2023 Dec 14;29(70):e202302642. doi: 10.1002/chem.202302642. Epub 2023 Oct 27.

Abstract

CO catalytic hydrogenation to formate was achieved (TON =ca. 3800) in the presence of the neutral, halide-free, coordinatively saturated tris(carbonyl) manganese pincer-type complex [Mn(PNP)(CO) ], bearing a diarylamido pincer-type PNP ligand, using DBU as base and LiOTf as Lewis acid additive, under mild reaction conditions (60 bar, 80 °C). DFT calculations suggest that the precatalyst activation key step occurs by intermolecular, base assisted dihydrogen heterolytic splitting rather than by the expected ligand-assisted intramolecular MLC-type mechanism.

摘要

在温和的反应条件(60巴,80°C)下,使用DBU作为碱和LiOTf作为路易斯酸添加剂,在带有二芳基酰胺钳型PNP配体的中性、无卤化物、配位饱和的三(羰基)锰钳型配合物[Mn(PNP)(CO)]存在下,实现了CO催化加氢生成甲酸盐(TON约为3800)。密度泛函理论计算表明,预催化剂活化的关键步骤是通过分子间碱辅助的二氢异裂分裂发生的,而不是通过预期的配体辅助分子内MLC型机制。

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