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An NHC‐Stabilised Phosphinidene for Catalytic Formylation: A DFT‐Guided Approach
Author(s) -
Sreejyothi P.,
Bhattacharyya Kalishankar,
Kumar Shiv,
Kumar Hota Pradip,
Datta Ayan,
Mandal Swadhin K.
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202101202
Subject(s) - phosphinidene , formylation , chemistry , catalysis , lone pair , frustrated lewis pair , photochemistry , phenylsilane , computational chemistry , lewis acids and bases , molecule , organic chemistry
In recent years, the applications of low‐valent main group compounds have gained momentum in the field of catalysis. Owing to the accessibility of two lone pairs of electrons, NHC‐stabilised phosphinidenes have been found to be excellent Lewis bases; however, they cannot yet be used as catalysts. Herein, an NHC‐stabilised phosphinidene, 1,3‐dimethyl‐2‐(phenylphosphanylidene)‐2,3‐dihydro‐1 H imidazole (1), for the activation of CO 2 is reported.A closer inspection of the CO 2 activation process by DFT calculations along with intrinsic bond orbital analysis shows that phosphinidene is associated with phenylsilane through a noncovalent π‐π interaction between two phenyl rings which activates the Si−H bond facilitating hydride transfer to the CO 2 molecule. Detailed DFT studies along with spectroscopic experiments were combined to understand the mechanism of CO 2 activation and its catalytic reductive functionalisation leading to the formylation of a range of chemically inert primary amides under mild reaction conditions.