Open Access1,4‐Bis(3,5‐di‐ tert ‐butyl‐2‐hydroxybenzylideneaminomethyl)benzene
Author(s) -
Tooke Duncan M.,
Song Yufei,
Albada Gerard A. van,
Reedijk Jan,
Spek Anthony L.
Publication year - 2004
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536804023633
Subject(s) - intramolecular force , aldehyde , benzene , hydrogen bond , methanol , amine gas treating , schiff base , chemistry , medicinal chemistry , stereochemistry , organic chemistry , molecule , catalysis
The title compound, C 38 H 52 N 2 O 2 , has been obtained by a Schiff base reaction of 3,5‐di‐ tert ‐butylsalicaldehyde and p ‐xylenediamine in methanol. The molecule is located on a crystallographic inversion centre, and the hydrogen bonding is exclusively intramolecular.
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