Header menu link for other important links
X
A facile access to sterically less crowded to more crowded organo triselones
, A. Sathyanarayana, K. Srinivas, P. Suresh, I. Nath
Published in Wiley-Blackwell
2018
Volume: 3
   
Issue: 4
Pages: 1294 - 1299
Abstract
The reaction of 2,4,6-N’-imidazolium(N-alkyl or N-aryl)-mesitylene bromides (alkyl=Me, isopropyl, vinyl, allyl; aryl=2,6- dimethyl-phenyl and 2,6-diiospropyl-phenyl) with six equivalents of selenium powder and potassium carbonate gave corresponding 2,4,6-N’-imidazole(N-alkyl or N-aryl)-selone-mesitylenes in very good yield. These new compounds were characterized by multinuclear (1D and 2D) NMR, FT-IR, UV-vis and single-crystal X-ray diffraction techniques. These trisimidazole selones are the first structurally characterized triselones supported by aryl platform. An interesting geometrical orientation of imidazole selones was observed from the solid-state structures of trisimidazole selones. The orientation of imidazole selones in isopropyl and vinyl trisimidazole selone derivatives are in propeller shape, while methyl, allyl, 2,6-dimethyl-phenyl and 2,6-diiospropyl-phenyl derivatives of trisimidazole selone derivatives are in twisted propeller shape. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
About the journal
JournalChemistrySelect
PublisherWiley-Blackwell
ISSN23656549