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1,3-Benzothia-zole-2(3H)-selone.


ABSTRACT: The title compound, C(7)H(5)NSSe, is the product of the reaction of 2-chloro-benzothia-zole with sodium hydro-selenide. The mol-ecule is almost planar (r.m.s. deviation = 0.018?Å) owing to the presence of the long chain of conjugated bonds (Se=C-N-C=C-C=C-C=C). The geometrical parameters correspond well to those of the analog N-methyl-benzothia-zole-2(3H)-selone, demonstrating that the S atom does not take a significant role in the electron delocalization within the mol-ecule. In the crystal, mol-ecules form centrosymmetric dimers by means of inter-molecular N-H?Se hydrogen bonds. The dimers have a nonplanar ladder-like structure. Furthermore, the dimers are linked into ribbons propagating in [010] by weak attractive Se?S [3.7593?(4)?Å] inter-actions.

SUBMITTER: Mammadova GZ 

PROVIDER: S-EPMC3247443 | biostudies-literature | 2011 Nov

REPOSITORIES: biostudies-literature

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1,3-Benzothia-zole-2(3H)-selone.

Mammadova Gunay Z GZ   Matsulevich Zhanna V ZV   Osmanov Vladimir K VK   Borisov Alexander V AV   Khrustalev Victor N VN  

Acta crystallographica. Section E, Structure reports online 20111029 Pt 11


The title compound, C(7)H(5)NSSe, is the product of the reaction of 2-chloro-benzothia-zole with sodium hydro-selenide. The mol-ecule is almost planar (r.m.s. deviation = 0.018 Å) owing to the presence of the long chain of conjugated bonds (Se=C-N-C=C-C=C-C=C). The geometrical parameters correspond well to those of the analog N-methyl-benzothia-zole-2(3H)-selone, demonstrating that the S atom does not take a significant role in the electron delocalization within the mol-ecule. In the crystal, mo  ...[more]

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