A monoclinic modification of 2-[(1,3-benzothia­zol-2-yl)imino­meth­yl]phenol

In the title Schiff base, C(14)H(10)N(2)OS, the azomethine double bond is in an E configuration; the benzothiazolyl ring (r.m.s. deviation = 0.007 Å) is coplanar with the phenyl­ene ring (r.m.s. deviation = 0.007 Å), the two rings being slightly bent at 2.6 (1)°. The hy­droxy H atom forms an intra­m...

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Detalles Bibliográficos
Autores principales: Asiri, Abdullah M., Khan, Salman A., Tan, Kong Wai, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006974/
https://www.ncbi.nlm.nih.gov/pubmed/21588032
http://dx.doi.org/10.1107/S1600536810023755
Descripción
Sumario:In the title Schiff base, C(14)H(10)N(2)OS, the azomethine double bond is in an E configuration; the benzothiazolyl ring (r.m.s. deviation = 0.007 Å) is coplanar with the phenyl­ene ring (r.m.s. deviation = 0.007 Å), the two rings being slightly bent at 2.6 (1)°. The hy­droxy H atom forms an intra­molecular hydrogen bond to the imino group. The bond dimensions of the monoclinic modification are similar to those of the ortho­rhom­bic modification [Liu et al. (2009 ▶). Acta Cryst. E65, o738].

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