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Comprehensive Basicity Scales for N‐Heterocyclic Carbenes in DMSO: Implications on the Stabilities of N‐Heterocyclic Carbene and CO 2 Adducts
Author(s) -
Wang Zhen,
Xue XiaoSong,
Fu Yanhua,
Ji Pengju
Publication year - 2020
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201901418
Subject(s) - carbene , mesoionic , chemistry , adduct , substituent , medicinal chemistry , alkyl , enantiomer , computational chemistry , stereochemistry , organic chemistry , catalysis
A very broad acidity scale (≈40 p K units) for about 400 N‐heterocyclic carbene precursors (NHCPs) with various backbones and electronic features, including imidazolylidenes, 1,2,4‐triazolylidenes, cyclic diaminocarbenes (CDACs), diamidocarbenes (DACs), thiazolylidenes, cyclic (alkyl)(amino)carbenes (CAACs) and mesoionic carbenes (MICs), was established in DMSO by a well examined computational method. Varying the backbone structure or flanking N‐substituents can have different extent of acidifying effects, depending on both the nature and number of substituent(s). The Gibbs energies (Δ G r s) for the reactions between the corresponding NHCs and CO 2 were also calculated. There is a good linear correlation between the p K a s of most NHCPs and Δ G r s, suggesting that a greater basicity of NHC leads to a more stable NHC‐CO 2 adduct. Interestingly, the nearby asymmetric environment has virtually no differential effect on the acidities of the chiral NHCP enantiomers, but has a pronounced effect on the Δ G r values.