Organometallic Borromean Rings and [2]Catenanes Featuring Di-NHC Ligands.

We report herein a series of organometallic Borromean rings (BRs) and [2]catenanes prepared from benzobiscarbene ligands. The reaction of dinickel complexes of the benzobiscarbenes 1 a-1 c with a thiazolothiazole bridged bipyridyl ligand L2 led by self-assembly to a series of organometallic BRs. Solvophobic effects played a crucial role in the formation and stability of the interlocked species. The stability of BRs is related to the N-alkyl substituents at the precursors 1 a-1 c, where longer alkyl substitutes improve stability and inter-ring interactions. Solvophobic effects are also important for the stability of [2]catenanes prepared from 1 a-1 c and a flexible bipyridyl ligand L3 . In solution, an equilibrium between the [2]catenanes and their macrocyclic building blocks was observed. High proportions of [2]catenanes were obtained in concentrated solutions or polar solvents. The proportion of [2]catenanes in solution could be further enhanced by lengthening of the N-alkyl substitutes.

Chemoselective synthesis of heterobimetallic bis-NHC complexes.

Bis-NHC precursors composed of an azolium and a 2-halogenoazole group connected by different linkers have been site-selectively metallated to give heterobimetallic complexes from a single-frame bis-NHC ligand. The azolium group reacts with a base and oxidized metal centers to give NHC complexes with no participation of the halogenoazole, while the halogenoazole reacts in an oxidative addition with low-valent transition metals to give azolato complexes with no participation of the azolium group.