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Cyclopropanation reactions of styrene derivatives with donor–acceptor carbenes formed in situ are significantly more enantioselective when catalyzed by the heterobimetallic bismuth–rhodium complex 5 a endowed with N‐phthalimido tert‐leucine paddlewheel ligands rather than by its homobimetallic dirhodium analogue 1 a. This virtue is likely the result of two synergizing factors: the conical shape of 5 a translates into a narrower calyx‐like chiral binding site about the catalytically active Rh center; the Bi atom, although fully solvent exposed, does not decompose aryl diazoacetates and is hence incapable of promoting a racemic background reaction. Moreover, ligand variation proved that successful catalyst design mandates that the anisotropy of the conical heterobimetallic core be matched by proper directionality of the ligand sphere. [ABSTRACT FROM AUTHOR]

The synthesis of the Cu-borate complexes [(6Mes)Cu(HBR3)] featuring the unusual [HBEt3]− ( 5) and [HB(C6F5)3]− ( 6) ligands is described. Experimental and computational studies show both compounds feature a direct Cu-H interaction, but that while 5 is two-coordinate, 6 displays an additional, stabilizing Cu-Cipso(C6F5) interaction. [ABSTRACT FROM AUTHOR]

The synthesis of the Cu-borate complexes [(6Mes)Cu(HBR3)] featuring the unusual [HBEt3]− ( 5) and [HB(C6F5)3]− ( 6) ligands is described. Experimental and computational studies show both compounds feature a direct Cu-H interaction, but that while 5 is two-coordinate, 6 displays an additional, stabilizing Cu-Cipso(C6F5) interaction. [ABSTRACT FROM AUTHOR]

The synthesis of the Cu-borate complexes [(6Mes)Cu(HBR3)] featuring the unusual [HBEt3]− ( 5) and [HB(C6F5)3]− ( 6) ligands is described. Experimental and computational studies show both compounds feature a direct Cu-H interaction, but that while 5 is two-coordinate, 6 displays an additional, stabilizing Cu-Cipso(C6F5) interaction. [ABSTRACT FROM AUTHOR]

The synthesis of the Cu-borate complexes [(6Mes)Cu(HBR3)] featuring the unusual [HBEt3]− ( 5) and [HB(C6F5)3]− ( 6) ligands is described. Experimental and computational studies show both compounds feature a direct Cu-H interaction, but that while 5 is two-coordinate, 6 displays an additional, stabilizing Cu-Cipso(C6F5) interaction. [ABSTRACT FROM AUTHOR]

Thetwo-coordinate ring-expanded N-heterocyclic carbene copper(I)complexes [Cu(RE-NHC)2]+(RE-NHC = 6-Mes, 7-o-Tol, 7-Mes) have been prepared and shown to be effectivecatalysts under neat conditions for the 1,3-dipolar cycloadditionof alkynes and azides. In contrast, the cationic diamidocarbene analogue[Cu(6-MesDAC)2]+and the neutral species [(6-MesDAC)CuCl]2and [(6-MesDAC)2(CuCl)3] show goodactivity when the catalysis is performed on water. [ABSTRACT FROM AUTHOR]