Abstract
Abstractσ‐Bond metathesis reactions between [(6‐Dipp)CuOtBu] (6‐Dipp=:C({Dipp}NCH2)2CH2, Dipp=2,6‐iPr2−C6H3) and three diboranes gave access to three new copper(I) boryl complexes [(6‐Dipp)CuBcat], [(6‐Dipp)CuBneop], and [(6‐Dipp)CuBhex] (cat=1,2‐O2C6H4; neop=(OCH2)2C(CH3)2; hex=OC(CH3)HCH2C(CH3)2O). Whilst [(6‐Dipp)CuBcat] and [(6‐Dipp)CuBneop] formed rapidly in toluene, access to [(6‐Dipp)CuBhex] required heating to 60 °C for days. The complexes were characterised by single‐crystal X‐ray crystallography which showed in all three cases that the systems were monomers and distorted‐linear at the copper atom. The stability of [(6‐Dipp)CuBneop] was found to be comparable to that of [(IPr*)Cu‐Bneop] (IPr*=1,3‐bis(2,6‐(diphenylmethyl)‐4‐methylphenyl)imidazol‐2‐ylidene); it persisted in solution for days with no sign of decomposition. [(6‐Dipp)CuBhex] is a rare crystallographically characterised example of a complex containing a boryl anion supported by the hexylene glycolato ligand.
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