Crystalline anions based on classical N‐heterocyclic carbenes

Abstract

Herein, the first stable anions K[SIPrBp] (4 a‐K) and K[IPrBp] (4 b‐K) (SIPrBp=BpC{N(Dipp)CH2}2, IPrBp=BpC{N(Dipp)CH}2; Bp=4‐PhC6H4; Dipp=2,6‐iPr2C6H3) derived from classical N‐heterocyclic carbenes (NHCs) (i.e. SIPr and IPr) have been isolated as violet crystalline solids. 4 a‐K and 4 b‐K are prepared by KC8 reduction of the neutral radicals [SIPrBp] (3 a) and [IPrBp] (3 b), respectively. The radicals 3 a and 3 b as well as [Me‐IPrBp] 3 c (Me‐IPrBp=BpC{N(Dipp)CMe}2) are accessible as crystalline solids on treatment of the respective 1,3‐imidazoli(ni)um bromides (SIPrBp)Br (2 a), (IPrBp)Br (2 b), and (Me-IPrBp)Br (2 c) with KC8. The cyclic voltammograms of 2 a-2 c exhibit two one‐electron reversible redox processes in -0.5 to -2.5 V region that correspond to the radicals 3 a-3 c and the anions (4 a-4 c)-. Computational calculations suggest a closed‐shell singlet ground state for (4 a-4 c)- with the singlet‐triplet energy gap of 17-24 kcal mol-1.