Synthesis, crystal structures, anti­proliferative activities and reverse docking studies of eight novel Schiff bases derived from benzil

Tan, X.-J.; Wang, D.; Hei, X.-M.; Yang, F.-C.; Zhu, Y.-L.; Xing, D.-X.; Ma, J.-P.

doi:10.1107/S2053229619015687

Acta Crystallographica Section C
Acta Crystallographica
Section C STRUCTURAL CHEMISTRY

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Figure 1
(a) The molecular structure of BDHFI, showing the atom-labelling scheme, with displacement ellipsoids for non-H atoms drawn at the 30% probability level at 293 K. (b) The Hirshfeld surface for BDHFI, mapped over d_norm (−0.10 to 1.40 Å, same throughout this article). Four red spots correspond to N5—H35⋯N1(−x + 2, y + $[{1\over 2}]$ , −z + $[{1\over 2}]$ ) (marked a) and N6—H36⋯π (marked b) interactions, respectively. (c) The shape-index surface of BDHFI, identifying π–π stacking interactions (marked c). Only red and blue triangles on the surface are shown for clarity. (d) Hydrogen bonds a (green dashed lines) and b (red dashed lines) link molecules into infinite 1D chains parallel to the crystallographic b and a axes, respectively, viewed along the crystallographic [8, $[\overline{1}]$ , 17] direction. Eight molecules are illustrated by the simplified structure (centre of gravity) for clarity and the two colours (red and green) represent two different orientations.

STRUCTURAL
CHEMISTRY

ISSN: 2053-2296

Volume 76| Part 1| January 2020| Pages 44-63

https://doi.org/10.1107/S2053229619015687

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