Abstract
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.
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Lu, Y., Dutschke, P. D., Kinas, J., Hepp, A., Jin, G. X., & Hahn, F. E. (2023). Organometallic Borromean Rings and [2]Catenanes Featuring Di- NHC Ligands. Angewandte Chemie - International Edition, 62(11). https://doi.org/10.1002/anie.202217681
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