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Synthesis of new metal‐free 1,2,4,5,9,10,12, 13‐octaaza [16]annulene derivatives using the reaction of vinamidinium salts with thiocarbohydrazide
Author(s) -
Sabet Askar,
Mehranpour Abdolmohammad
Publication year - 2021
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.4218
Subject(s) - chemistry , annulene , salt (chemistry) , metal , ligand (biochemistry) , carbon 13 nmr , organic chemistry , nuclear chemistry , polymer chemistry , combinatorial chemistry , biochemistry , receptor
A new series of marcocyclic ligands, 1,2,4,5,9,10,12,13‐octaaza[16]annulene derivatives were synthesized by using the condensation reaction of the correspondingly [2+2] 2‐heteroaryl‐substituted vinamidinium salts or phenyl vinamidinium salts and derivatives or halo‐substituted vinamidinum salt [1A‐10A] with thiocarbohydrazide in ethanolic medium under mild condition. Metal complexes were formed by reacting of ethanolic solution of Co, Ni, and Zn with macrocyclic ligand in ethanolic medium under mild condition. Purposed complexes have been characterized with the help of elemental analyses, comparative absorption band of ν(C=N), mass, and NMR. Geometry and complex formulation are out of scope of this work. The biological activities of carohydrazide and thiocarbohydrazide base of the ligands and purposed complexes such as antimicrobial, antitumor, and insecticides have attracted significant attention in bioorganic chemistry.
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