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Synthesis and comparative study of (NHCF)PdCl2Py and (NHCF)Ni(Cp)Cl complexes: investigation of the electronic properties of NHC ligands and complex characteristics Full article

Journal Dalton Transactions
ISSN: 1477-9234 , E-ISSN: 1477-9226
Output data Year: 2024, Volume: 53, Number: 30, Pages: 12503-12518 Pages count : 16 DOI: 10.1039/d4dt01304b
Authors Pankov Roman O. 1 , Tarabrin Ignatii R. 2,1 , Son Alexandra G. 3 , Minyaev Mikhail E. 1 , Prima Darya O. 1 , Ananikov Valentine P. 1
Affiliations
1 Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospekt 47, Moscow, 119991, Russia
2 Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1-3, Moscow 119991, Russia
3 Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Leninskii pr. 31, Moscow 119991, Russia

Abstract: The electron-donating and electron-accepting properties of N-heterocyclic carbene (NHC) ligands play a pivotal role in governing their interactions with transition metals, thereby influencing the selectivity and reactivity in catalytic processes. Herein, we report the synthesis of Pd/NHCF and Ni/NHCF complexes, wherein the electronic parameters of the NHC ligands were systematically varied. By performing a series of controlled structure modifications, we elucidated the influence of the σ-donor and π-acceptor properties of NHC ligands on interactions with the transition metals Pd and Ni and, consequently, the catalytic behavior of Pd and Ni complexes. The present study deepens our understanding of NHC-metal interactions and provides novel information for the rational design of efficient catalysts for organic synthesis.
Cite: Pankov R.O. , Tarabrin I.R. , Son A.G. , Minyaev M.E. , Prima D.O. , Ananikov V.P.
Synthesis and comparative study of (NHCF)PdCl2Py and (NHCF)Ni(Cp)Cl complexes: investigation of the electronic properties of NHC ligands and complex characteristics
Dalton Transactions. 2024. V.53. N30. P.12503-12518. DOI: 10.1039/d4dt01304b WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:001267914600001
Scopus: 2-s2.0-85198959571
OpenAlex: W4400689198
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OpenAlex 1
Scopus 1
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