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 7
(a) The molecular structure of BMHMFI, 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 BMHMFI, mapped over d_norm. The intermolecular hydrogen bonds a calculated using PLATON, but another kind of hydrogen bond [C11—H11⋯N1(x, −y − $[{1\over 2}]$ , z − $[{1\over 2}]$ ), which can be found as red spots] was not suggested by PLATON. (c) The shape-index surface of BMHMFI, identifying π–π stacking interactions b and c. (d) 1D chains formed by C—H⋯π interactions a (shown with red dashed lines) can be woven into a 2D layer structure by π–π interactions b and c (shown with green and blue dashed lines, respectively), viewed along the a axis.

STRUCTURAL
CHEMISTRY

ISSN: 2053-2296

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

https://doi.org/10.1107/S2053229619015687

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