NHC-Stabilised Acetylene-How Far Can the Analogy Be Pushed?

Experimental studies suggest that the compound (NHCbz )2 C2 H2 can be considered as a complex of a distorted acetylene fragment which is stabilised by benzoannelated N-heterocyclic carbene ligands (NHCbz )→(C2 H2 )←(NHCbz ). A quantum chemical analysis of the electronic structures shows that the description with dative bonds is more favourable than with electron-sharing double bonds (NHCbz )=(C2 H2 )=(NHCbz ).

A Strong cis-Effect in an Imidazole-Imidazolium-Substituted Alkene.

We report the first example of an alkene with two carbon-bound substituents (imidazole and imidazolium rings) where the Z-isomer has a greater thermodynamic stability than the E-isomer which persists in both the gas phase and in solution. Theoretical calculations, solution fluorescence spectroscopy and gas-phase ion mobility mass spectrometry studies confirm the preference for the Z-isomer, the stability of which is traced to a non-covalent interaction between the imidazole lone pair and the imidazolium ring.

The fate of NHC-stabilized dicarbon.

The attempted synthesis of NHC-stabilized dicarbon (NHC=C=C=NHC) through deprotonation of a doubly protonated precursor ([NHC-CH=CH-NHC](2+) ) is reported. Rather than deprotonation, a clean reduction to NHC=CH-CH=NHC is observed with a variety of bases. The apparent resistance towards deprotonation to the target compound led to a reinvestigation of the electronic structure of NHC→CC←NHC, which showed that the highest occupied molecular orbital/lowest unoccupied molecular orbital (HOMO/LUMO) gap is likely too small to allow for isolation of this species. This is in contrast to the recent isolation of the cyclic alkylaminocarbene analogue (cAAC=C=C=cAAC), which has a large HOMO-LUMO gap. A detailed theoretical study illuminates the differences in electronic structures between these molecules, highlighting another case of the potential advantages of using cAAC rather than NHC as a ligand. The bonding analysis suggests that the dicarbon compounds are well represented in terms of donor-acceptor interactions L→C2 ←L (L=NHC, cAAC).

Reactions of [PhI(pyridine)2]2+ with model Pd and Pt II/IV redox couples.

The results of the reactions of the dicationic iodine(III) family of oxidants [PhI(pyridine)2](2+) with model Pd(II) and Pt(II) complexes are described. Depending on the specific reaction pairs, a variety of outcomes are observed. For palladium, Pd(IV) complexes cannot be observed but are implicated in C-C and C-N bond formation for Pd(II) starting materials based on phenylpyridine and 2,2-bipyridine, respectively. Theoretical comparisons with similar processes for -Cl and -OAc rather than pyridine indicate that these provide greater thermodynamic stability, and our results here show that they also give greater kinetic stability (the failure of MP2 methods for these systems is quite dramatic). In contrast, oxidation and delivery of the pyridine ligands gives dicationic Pt(IV) complexes that may be isolated and structurally characterized.