Crystal structure, Hirshfeld surface analysis and DFT studies of (E)-1-(4-bromo­phen­yl)-3-(3-fluoro­phen­yl)prop-2-en-1-one

The asymmetric unit of the title halogenated chalcone derivative, C(15)H(10)BrFO, contains two independent mol­ecules, both adopting an s-cis configuration with respect to the C=O and C=C bonds. In the crystal, centrosymmetrically related mol­ecules are linked into dimers via inter­molecular hydrogen bonds, forming rings with R (1) (2)(6), R (2) (2)(10) and R (2) (2)(14) graph-set motifs. The dimers are further connected by C—H⋯O inter­actions into chains parallel to [001]. A Hirshfeld surface analysis suggests that the most significant contribution to the crystal packing is by H⋯H contacts (26.3%). Calculations performed on the optimized structure obtained using density functional theory (DFT) at B3LYP with the 6–311 G++(d,p) basis set reveal that the HOMO–LUMO energy gap is 4.12 eV, indicating the suitability of this crystal for optoelectronic and biological applications. The nucleophilic and electrophilic binding site regions are elucidated using the mol­ecular electrostatic potential (MEP).