2-(9-Anthrylmethyl-ideneamino)-4-methyl-phenol.
Andrés Villalpando, Frank R Fronczek, Ralph Isovitsch
Index: Acta Crystallogr. Sect. E Struct. Rep. Online 66(Pt 6) , o1353, (2010)
Full Text: HTML
Abstract
The title compound, C(22)H(17)NO, is a novel Schiff base synthesized via a condensation reaction between 9-anthracenecarboxaldehyde and 2-amino-p-cresol. The asymmetric unit contains two independent mol-ecules that are joined by an O-H⋯OH hydrogen bond. An intra-molecular O-H⋯N hydrogen bond occurs in each mol-ecule. π-stacking about inversion centers was observed between adjacent phenol rings [centroid-centroid distance = 3.850 (2) Å] and adjacent anthracene rings [centroid-centroid distance = 3.834 (2) Å]. The C-N=C-C torsion angles between the phenol and anthracene rings are close to 180° with values of 174.06 (15) and 179.85 (14)°.
Related Compounds
Related Articles:
2014-08-21
[Dalton Trans. 43(31) , 11988-99, (2014)]
2011-08-15
[Chem. Res. Toxicol. 24(8) , 1223-30, (2011)]
2012-12-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 98 , 14-17, (2012)]
2015-01-01
[Anal. Chim. Acta 853 , 596-601, (2014)]
1991-10-01
[Anal. Biochem. 198(1) , 134-7, (1991)]