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

IUCr IT WDC

home archive editors for authors for readers submit subscribe open access

view article

Figure 5
(a) The molecular structure of BMHFI, 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 BMHFI, mapped over d_norm. Three red spots correspond to N3—H24⋯O1(x + $[{1\over 2}]$ , −y + $[{1\over 2}]$ , −z) (marked a) and C3—H3⋯O1(x + 1, y, z) (marked b) interactions. (c) 1D chains formed by NCIs a and b (shown with green and red dashed lines, respectively), viewed perpendicular to the extending direction, i.e. the a axis. The upper two lines are illustrated by the simplified structure (centre of gravity). (d) 1D chains formed by the aforementioned NCIs a and b, viewed along the extending direction, i.e. the a axis, aiming to show the packing mode of four different orientations (simplified structure with four different colours).

STRUCTURAL
CHEMISTRY

ISSN: 2053-2296

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

https://doi.org/10.1107/S2053229619015687

Follow Acta Cryst. C

Search IUCr Journals		doi		Advanced search
Author		volume	page