## Abstract Copper(I) bromide complexes (2a and 2b) of NHC–phenolimine ligand precursors {3‐[(1__R__,2__R__)‐2‐{[1‐(3,5‐di‐__tert__‐butyl‐2‐hydroxyphenyl)meth‐(__E__)‐ylidene]amino}cyclohexyl]‐1‐isopropyl‐4‐phenyl‐3__H__‐imidazol‐1‐ium bromide (1a) and 3‐[(1__R__,2__R__)‐2‐{[1‐(2‐hydroxyphenyl)meth
Synthesis, Structural Diversity, and Ligand-Transfer Potential of (Carbene)copper(I) Complexes
✍ Scribed by Galmari Venkatachalam; Marion Heckenroth; Antonia Neels; Martin Albrecht
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- German
- Weight
- 457 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
Copper(I) complexes comprising different N‐heterocyclic carbene ligands were prepared via in situ deprotonation and metallation. Depending on the wingtip groups on the carbene ligand (alkyl vs. aryl, chelating or monodentate), a variety of different structural motifs were identified, such as a trigonal planar geometry (alkyl wingtips) and an unprecedented see‐saw‐type structure (pyridinyl wingtip groups). While aryl wingtip groups increase the stability of the complexes, alkyl substituents induce rapid demetallation in the presence of moisture. The reactivity of these complexes was used to establish a carbene‐transfer protocol, which is illustrated by the formation of new cyclic thiourea compounds (transfer to sulfur) and new (carbene)ruthenium(II) complexes (transfer to ruthenium). This suggests that (carbene)copper(I) complexes could become valuable alternatives to (carbene)silver(I) complexes for synthesizing (carbene)metal systems via transmetallation.
📜 SIMILAR VOLUMES
## Abstract Di‐ and trinuclear complexes of copper(I) bearing bis‐ or tris‐N‐heterocyclic carbene ligands have been prepared and evaluated as catalysts in nitrene transfer reactions from PhI=NTs to unsaturated and saturated substrates (olefin aziridination and C–H bond amidation) and carbene transf
The tris-carotenoid macrobicycles 1 and 2 were obtained in good yields in a one-step macrobicyclisation condensation between the tripode N(CH,CH2NH2), and the polyolefinic dialdehydes 5 and 6. They form dinuclear cryptates by complexation of two Cu' ions. The crystal structure of the tris-carotenoid