Synthesis, characterization, biological determination and catalytic evaluation of ruthenium() complexes bearing benzimidazole-based NHC ligands in transfer hydrogenation catalysis
A new series of ruthenium( ii ) N-heterocyclic carbene complexes has been synthesized via transmetalation. These complexes are easily handled in very good yields via synthesis of silver-NHC complexes and subsequent reaction with [RuCl 2 ( p -cymene)] 2 in dichloromethane (DCM) under argon atmosphere...
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Veröffentlicht in: | New journal of chemistry 2020-04, Vol.44 (14), p.539-5323 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A new series of ruthenium(
ii
) N-heterocyclic carbene complexes has been synthesized
via
transmetalation. These complexes are easily handled in very good yields
via
synthesis of silver-NHC complexes and subsequent reaction with [RuCl
2
(
p
-cymene)]
2
in dichloromethane (DCM) under argon atmosphere. The new ruthenium(
ii
)-NHC complexes were applied to transfer hydrogenation of ketone derivatives using 2-propanol as a hydrogen source and KOH as a co-catalyst. The results show that the corresponding alcohols could be obtained in good yield with high catalyst activity (up to 76%) under mild conditions. All new compounds were characterized by spectroscopic and analytical methods. The antibacterial activities of the corresponding ruthenium(
ii
)-NHC complexes
4a-i
were tested against positive and negative bacteria using the agar dilution procedure and their IC
50
values have been determined. A cytotoxicity study of the ruthenium(
ii
)-NHC complexes
4
was performed against the two human cancer cell lines MDA-MB-231 and MCF-7. In addition, the scavenging activity of the synthesized complexes for the DPPH radical was also determined.
A new series of ruthenium (
ii
) N-heterocyclic carbene complexes has been synthesized
via
transmetalation. The obtained complexes were applied to transfer hydrogenation of ketone derivatives. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/d0nj00311e |