The Structure of Cis-2,2′-Azopyridine in the Solid State View Full Text


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Article Info

DATE

2018-10-08

AUTHORS

Iamnica J. Linares Mendez, Jeffrey S. Pleizier, Hong-Bo Wang, James A. Wisner

ABSTRACT

Descriptions of azoheteroaromatic compounds in their cis-isomeric form in the solid state are almost non-existent. Cis-2,2′-azopyridine is a known compound which structure differentiates from the trans-isomer based on spectroscopic evidence (UV–Vis absorption, 1H, and 13C NMR spectroscopy) and with studies regarding its stability, thermal reversion to the trans-isomer, and dipole moment in solution. However, the structure of this compound in the solid state has been unresolved. Herein, we present the crystal structure of cis-2,2′-azopyridine that forms red prismatic crystals in the monoclinic space group C2/c. The unit cell parameters are: a = 23.485 (4), b = 5.9241 (12), c = 21.656 (4) Å, and V = 2717.1 (9) Å3 with 12 molecules per unit cell. Molecules are arranged as two helical conformers (P and M) with C–N=N–C torsion angles and aromatic ring planes’ angles comparable to those reported for cis-azobenzene. The rare structural determination of an azoheteroaromatic cis-isomer of 2-azopyridine that was synthesized, isolated and crystallized is presented. X-ray structure analysis reveals that the molecule forms dimeric complexes containing both M- and P-helical conformers as well as infinite stacked columns in the solid state through a combination of C–H⋯N hydrogen bonds, C–H⋯π interactions and lone pair⋯π contacts. More... »

PAGES

1-6

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10870-018-0737-z

DOI

http://dx.doi.org/10.1007/s10870-018-0737-z

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https://app.dimensions.ai/details/publication/pub.1107484609


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