Bridging linker installation strategy in the engineering of copper(ii) complexes: activation of nitriles, efficient catalysts for the cyanosilylation of aldehydes

A series of bridging linkers such as pyrazine (L1), 4,4′-bipyridine (L2), (E)-1,2-di(pyridin-4-yl)ethene (L3), 1,2-di(pyridin-4-yl)ethane (L4), 1,2-di(pyridin-4-yl)disulfane (L5), 1,2-di(pyridin-4-yl)diazene (L6) and 1,4-di(pyridin-4-yl)benzene (L7) has been used in a Cu(ii)-mediated cyano group activation in sodium 2-(2-(dicyanomethylene)hydrazineyl)benzenesulfonate (NaHL), leading to [{Cu(H2O)(La)}2(μ-L1)]n (1) (La = (Z)-2-(1-cyano-2-imino-2-methoxyethylidene)-1-(2-sulfonatophenyl)hydrazin-1-ide), [{Cu(H2O)(La)}2(μ-L2)]·2H2O (2), [{Cu(X)(La)}2(μ-L3)]·3H2O (3) (X = H2O or CH3OH for the two independent units), [{Cu(CH3OH)(La)}2(μ-L4)]·2H2O (4), [{Cu(La)}2(μ-L5)2]n (5), [{Cu(μ-La)}2(μ-L6)Cu(H2O)(La)]2·4H2O (6) and [{Cu(H2O)(La)}2(μ-L7)] (7), respectively. Depending on the length of the respective linkers, the distance between the two copper(ii) centres in 1-7 can be expanded/adjusted from 6.762 to 15.138 Å. The catalytic activity of the synthesized compounds in the cyanosilylation reaction of aldehydes with trimethylsilyl cyanide in methanol was performed. No linear correlation among the length of the bridging ligands and the yield of 2-phenyl-2-((trimethylsilyl)oxy)acetonitrile was observed in 1-7 catalysed cyanosilylation of benzaldehyde with trimethylsilyl cyanide, but the copper complexes show a higher catalytic activity in comparison to the monomer [Cu(H2O)2(La)]. The higher catalytic activity exhibited by complex 5 was further investigated evaluating the effects of reaction time, catalyst amount, temperature and the activity with different aldehydes. © 2024 The Royal Society of Chemistry.

Authors
Gurbanov A.V. , Mahmoudi G. , Zangrando E. , Zubkov F.I. , Hasanov K.I. , Mahmudov K.T.
Journal
Publisher
Royal Society of Chemistry
Number of issue
47
Language
English
Pages
6692-6700
Status
Published
Volume
26
Year
2024
Organizations
  • 1 Excellence Center, Baku State University, Z. Xalilov Str. 23, Baku, 1148, Azerbaijan
  • 2 Centro de Química Estrutural, Institute of Molecular Sciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Lisboa, 1049-001, Portugal
  • 3 Department of Chemistry, Faculty of Science, University of Maragheh, P.O. Box 55136-83111, Maragheh, Iran
  • 4 Chemistry Department, Faculty of Engineering and Natural Sciences, Istinye University, Sarıyer, Istanbul, 34396, Turkey
  • 5 Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via L. Giorgieri 1, Trieste, 34127, Italy
  • 6 Department of Organic Chemistry, RUDN University, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
  • 7 Azerbaijan Medical University, Scientific Research Centre (SRC), A. Kasumzade Street 14, Baku, AZ 1022, Azerbaijan
  • 8 Western Caspian University, Istiqlaliyyat Street 31, Baku, AZ1001, Azerbaijan
  • 9 Scientific Research Center, Baku Engineering University, Hasan Aliyev str. 120, Absheron, Baku, AZ0101, Azerbaijan
Keywords
Activation analysis; Benzene; Hydrosilylation; Pyridine; Sulfur compounds; Temperature scales; Benzenesulfonates; Bipyridines; Copper complexes; Cyano-groups; Cyanosilylation; Diazenes; Dicyanomethylene; Efficient catalysts; Pyrazines; Trimethylsilyl cyanide; Chemical activation

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