Issue 4, 1999

Configurations of 1,3-bis(aryl)-1,3-diaza-2-thiaallenes in the crystal state

Abstract

The σ,π-mixing responsible for the Z,Z configuration of the title compounds is indifferent to both withdrawing (NO2) and releasing (OMe) π-electron character of ortho-substituents, and the arrangement of aromatic rings in the Z,E configuration orthogonally to the NSN plane is a universal way to overcome steric hindrances due to bulky (But, Br) ortho-substituents.

Article information

Article type
Paper

Mendeleev Commun., 1999,9, 157-158

Configurations of 1,3-bis(aryl)-1,3-diaza-2-thiaallenes in the crystal state

I. Y. Bagryanskaya, Y. V. Gatilov and A. V. Zibarev, Mendeleev Commun., 1999, 9, 157 DOI: 10.1070/MC1999v009n04ABEH001140

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