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3,6-Dibromo-9-eth­yl-9H-carbazole

✍ Scribed by Huang, Peng-Mian ;Li, Jiang-Sheng ;Duan, Xue-Min ;Zeng, Tao ;Yan, Xi-Long

Publisher
International Union of Crystallography
Year
2005
Tongue
English
Weight
128 KB
Volume
61
Category
Article
ISSN
1600-5368

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✦ Synopsis

The title compound, C 14 H 11 Br 2 N, was synthesized by Nalkylation of bromoethane with 3,6-dibromo-9H-carbazole. The carbazole ring system is essentially planar and makes a dihedral angle of 94.7 (3) with the plane formed by the ethyl C and carbazole N atoms.

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The title compound, C 18 H 12 Br 2 N 2 , was synthesized by Nalkylation of 4-chloromethylpyridine with 3,6-dibromo-9Hcarbazole. The carbazole ring system is essentially planar, with a mean deviation of 0.012 A ˚, and makes a dihedral angle of 83.2 (8) with the plane of the pyridine ring. In the crys

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The carbazole ring system is essentially planar and the n-hexyl chain is in the fully extended conformation.

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The title compound, C 15 H 11 Br 2 N, was synthesized by Nalkylation of 3-bromopropene with 3,6-dibromo-9H-carbazole. The carbazole ring system is essentially planar and perpendicular to the pendant allyl substituent.