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 4
(a) The molecular structure of BDHFN, showing the atom-labelling scheme, with displacement ellipsoids for non-H atoms drawn at the 30% probability level at 293 K [symmetry code: (A) −x, y, −z + $[{1\over 2}]$ ]. (b) The contribution of C⋯C contacts in the 2D fingerprints of BDHFN, indicating π–π interaction a. (c) The shape-index surface of BDHFN, identifying π–π stacking interaction a (not marked as there is only one type of interaction). (d) 1D chains formed by π–π stacking interaction a (shown with red dashed lines), viewed along the [501] direction. The upper one is illustrated by the simplified structure (centre of gravity).

STRUCTURAL
CHEMISTRY

ISSN: 2053-2296

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

https://doi.org/10.1107/S2053229619015687

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