Abstract
A synthetic route is reported towards ruthenium-based structural mimics of the [Fe]-hydrogenase metal cofactor in which the acyl moiety is replaced by an N-heterocyclic carbene. It is observed that the pyridyl-NHC ligand has a rather different trans influence from that of a simple NHC in their ruthenium derivatives. The basis for this difference is explored crystallographically and computationally, and it accounts for their different behaviour towards thiolation.
Original language | English |
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Pages (from-to) | 10775-10780 |
Number of pages | 6 |
Journal | ChemistrySelect |
Volume | 5 |
Issue number | 34 |
DOIs | |
Publication status | Published - Sept 14 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 Wiley-VCH GmbH
ASJC Scopus Subject Areas
- General Chemistry
Keywords
- N-heterocyclic carbene
- Ruthenium
- trans effect
- [Fe]-hydrogenase