Unknown

Dataset Information

0

1-(3-Bromo-prop-yl)-4-(2-pyrid-yl)-1H-1,2,3-triazole.


ABSTRACT: In the structure of the title compound, C(10)H(11)BrN(4), the plane of the substituted 1,2,3-triazole ring is tilted by 14.84?(10)° with respect to the mean plane of the pyridine ring. The pyridine and closest triazole N atoms adopt an anti arrangement which removes any lone pair-lone pair repulsions between the N atoms. This conformation is further stabilized by weak intermolecular C-H?N inter-actions. There are two mol-ecules in the unit cell, which form a centrosymmetric head-to-tail dimer. The dimers are stabilized through ?-? inter-actions [centroid-centroid distance = 3.733?(4)?Å and mean inter-planar distance = 3.806?(12)?Å] between the substituted 1,2,3-triazole ring and the pyridine rings in adjacent mol-ecules. Each dimer inter-acts with two neighbouring dimers above and below, forming a slipped stack of dimers through the crystal. The 3-bromo-propyl chain sits over the pyridine ring of a neighbouring mol-ecule and the triazole rings of nearby mol-ecules are adjacent.

SUBMITTER: Crowley JD 

PROVIDER: S-EPMC2977690 | biostudies-literature | 2009 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

1-(3-Bromo-prop-yl)-4-(2-pyrid-yl)-1H-1,2,3-triazole.

Crowley James D JD   Bandeen Pauline H PH   Hanton Lyall R LR  

Acta crystallographica. Section E, Structure reports online 20090408 Pt 5


In the structure of the title compound, C(10)H(11)BrN(4), the plane of the substituted 1,2,3-triazole ring is tilted by 14.84 (10)° with respect to the mean plane of the pyridine ring. The pyridine and closest triazole N atoms adopt an anti arrangement which removes any lone pair-lone pair repulsions between the N atoms. This conformation is further stabilized by weak intermolecular C-H⋯N inter-actions. There are two mol-ecules in the unit cell, which form a centrosymmetric head-to-tail dimer. T  ...[more]

Similar Datasets

| S-EPMC2969765 | biostudies-literature
| S-EPMC3344657 | biostudies-literature
| S-EPMC3151948 | biostudies-literature
| S-EPMC3200735 | biostudies-literature
| S-EPMC4120528 | biostudies-literature
| S-EPMC4120607 | biostudies-literature
| S-EPMC3008971 | biostudies-literature
| S-EPMC3515254 | biostudies-literature
| S-EPMC3379506 | biostudies-literature
| S-EPMC3050293 | biostudies-literature