Issue 31, 2021

Novel cationic 1,2,4-selenadiazoles: synthesis via addition of 2-pyridylselenyl halides to unactivated nitriles, structures and four-center Se⋯N contacts

Abstract

2-Pyridylselenyl halides undergo facile coupling with a triple CN bond of unactivated nitriles. Unprecedented heterocyclization allowed the preparation of a novel class of cationic 1,2,4-selenadiazoles in remarkably high yields. Cationic 1,2,4-selenadiazoles form supramolecular dimers in the crystal via Se⋯N chalcogen bonding, which was studied theoretically.

Graphical abstract: Novel cationic 1,2,4-selenadiazoles: synthesis via addition of 2-pyridylselenyl halides to unactivated nitriles, structures and four-center Se⋯N contacts

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Article information

Article type
Communication
Submitted
21 Apr 2021
Accepted
09 Jun 2021
First published
09 Jun 2021

Dalton Trans., 2021,50, 10689-10691

Novel cationic 1,2,4-selenadiazoles: synthesis via addition of 2-pyridylselenyl halides to unactivated nitriles, structures and four-center Se⋯N contacts

V. N. Khrustalev, M. M. Grishina, Z. V. Matsulevich, J. M. Lukiyanova, G. N. Borisova, V. K. Osmanov, A. S. Novikov, A. A. Kirichuk, A. V. Borisov, E. Solari and A. G. Tskhovrebov, Dalton Trans., 2021, 50, 10689 DOI: 10.1039/D1DT01322J

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