Abstract
•Two Schiff's base derivatives synthesized with organic fluorine.•Qualitative study of weak intermolecular interactions.•PIXEL intermolecular interaction energies for dimers.•Topological analysis of intermolecular interactions.•In vitro antimicrobial and antifungal activities.
Crystal structures of two newly synthesized Schiff's bases with organic fluorine {systematic name: (E)-N-(4-Fluorophenyl)-1-(5-nitrothiophen-2-yl)methanimine (1) and (E)-N-(2-trifluorophenyl)-1-(5-nitrothiophen-2-yl)methanimine (2)} are reported. In this contribution, we performed a qualitative analysis of intermolecular interactions using the Hirshfeld surface and 2D-fingerprint plots to understand the effect of -F and –CF3 substituents. Compounds 1 and 2 and their respective isomers, -F in the meta and –CF3 in para position on the phenyl ring, are analyzed and compared. This analysis suggests that three C–H•••O, one C–H•••F and a short S1•••C4 interactions found to be important for stabilization of crystal structure 1 and three C–H•••O, one C–H•••F, one C–F•••π halogen bond and π•••π interactions are found to be vital for stabilization of crystal structure 2. Further, intermolecular interaction energies of molecular dimers in 1 and 2 are obtained using PIXEL energy analysis. The lattice energies for structures 1, 2 and their isomers are calculated. The energetic analysis suggests that structure 2 is more stable than its para isomer and 1. Structure 1 and its meta isomer show 1D structural similarity. The quantitative analysis of intermolecular interactions involved in the molecular dimers of 1, 2 and selected dimers of meta isomer of 1 using Bader's quantum theory of atoms-in-molecules approach. An in vitro evaluation of antimicrobial activities reveals that compounds 1 and 2 exhibit potent and broad spectrum antibacterial activity against selected Gram-positive and Gram-negative bacterial stains.
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