Unknown

Dataset Information

0

2-(4-Chloro-phen-yl)naphtho-[1,8-de][1,3,2]diaza-borinane.


ABSTRACT: The title compound, C(16)H(12)BClN(2), is one in a series of diaza-borinanes, derived from 1,8-diaminona-phthalene, featuring substitution at the 1, 2 and 3 positions in the nitro-gen-boron heterocycle. The structure deviates from planarity, the torsion angle subtended by the p-chloro-phenyl ring relative to the nitro-gen-boron heterocycle being -44-.3(3)°. The mol-ecules form infinite chains with strong inter-actions between the vacant pz orbital of the B atom and the ?-system of an adjacent mol-ecule. The distance between the B atom and the 10-atom centroid of an adjacent naphthalene ring is 3.381?(4)?Å. One N-H H atom is weakly hydrogen bonded to the Cl atom of an adjacent mol-ecule. This combination of inter-molecular inter-actions leads to the formation of an infinite two-dimensional network perpendic-ular to the c axis.

SUBMITTER: Akerman MP 

PROVIDER: S-EPMC3212269 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

2-(4-Chloro-phen-yl)naphtho-[1,8-de][1,3,2]diaza-borinane.

Akerman Matthew P MP   Robinson Ross S RS   Slabber Cathryn A CA  

Acta crystallographica. Section E, Structure reports online 20110702 Pt 8


The title compound, C(16)H(12)BClN(2), is one in a series of diaza-borinanes, derived from 1,8-diaminona-phthalene, featuring substitution at the 1, 2 and 3 positions in the nitro-gen-boron heterocycle. The structure deviates from planarity, the torsion angle subtended by the p-chloro-phenyl ring relative to the nitro-gen-boron heterocycle being -44-.3(3)°. The mol-ecules form infinite chains with strong inter-actions between the vacant pz orbital of the B atom and the π-system of an adjacent mo  ...[more]

Similar Datasets

| S-EPMC3213450 | biostudies-literature
| S-EPMC3120534 | biostudies-other
| S-EPMC3051938 | biostudies-literature
| S-EPMC3099943 | biostudies-literature
| S-EPMC2960627 | biostudies-literature
| S-EPMC2960192 | biostudies-literature
| S-EPMC3790409 | biostudies-literature
| S-EPMC3393280 | biostudies-literature
| S-EPMC3151928 | biostudies-literature
| S-EPMC2961724 | biostudies-literature