Unknown

Dataset Information

0

2-[N-(4-{4-[(E)-(2-Hydroxybenzyl-idene)amino]phenoxy}phenyl)carbox-imidoyl]phenol.


ABSTRACT: The mol-ecular structure of the title Schiff base compound, C(26)H(20)N(2)O(3), shows that respective methyl-idene residues are almost coplanar with the adjacent terminal benzene ring owing to the presence of intra-molecular O-H?N hydrogen bonds [the N-C-C-C torsion angles are -6.6?(7) and -6.7?(7)°]. However, twists are exhibited about each methyl-idene and respective benzene ring connected to the central O atom; the dihedral angles formed between the two inner and two outer benzene rings are 54.6?(2) and 45.6?(3)°, respectively. The conformation about each of the C=N bonds [1.285?(5) and 1.295?(5)?Å] is E. In the crystal, extensive C-H?? contacts involving all benzene rings results in the formation of layers in the ac plane.

SUBMITTER: Shahverdizadeh GH 

PROVIDER: S-EPMC3100046 | biostudies-literature | 2011 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

2-[N-(4-{4-[(E)-(2-Hydroxybenzyl-idene)amino]phenoxy}phenyl)carbox-imidoyl]phenol.

Shahverdizadeh Gholam Hossein GH   Tiekink Edward R T ER  

Acta crystallographica. Section E, Structure reports online 20110305 Pt 4


The mol-ecular structure of the title Schiff base compound, C(26)H(20)N(2)O(3), shows that respective methyl-idene residues are almost coplanar with the adjacent terminal benzene ring owing to the presence of intra-molecular O-H⋯N hydrogen bonds [the N-C-C-C torsion angles are -6.6 (7) and -6.7 (7)°]. However, twists are exhibited about each methyl-idene and respective benzene ring connected to the central O atom; the dihedral angles formed between the two inner and two outer benzene rings are 5  ...[more]

Similar Datasets

| S-EPMC3415026 | biostudies-literature
| S-EPMC3470348 | biostudies-literature
| S-EPMC3152012 | biostudies-literature
| S-EPMC3344564 | biostudies-literature
| S-EPMC2979767 | biostudies-literature
| S-EPMC3200954 | biostudies-literature
| S-EPMC3238898 | biostudies-literature
| S-EPMC3685059 | biostudies-literature
| S-EPMC4011306 | biostudies-literature
| S-EPMC4011262 | biostudies-literature