A new quinazoline functionalized benzimidazole-based compound as a selective and sensitive fluorogenic chemosensor for Cu²⁺and sequential recognition of S²⁻, also being used as live cell imaging.

A series of new benzimidazole containing compounds 2-((1-R-1-H-benzimidazol-2-yl)phenyl-imino)naphthol HL^1–3 (R = methyl, ethyl or propyl, respectively) have been synthesized by Schiff base condensation of 2-(1-R-1-H-benzo[d]imidazol-2-yl)aniline and 2-hydroxy-1-naphthaldehyde. The reactions of HL^1–3 with Cu(NO₃)₂·2.5H₂O led to the corresponding copper(II) complexes [Cu(L)(NO₃)] 1–3. All the compounds were characterized by conventional analytical techniques and, for 1 and 3, also by single-crystal X-ray analysis. The interactions of complexes 1–3 with calf thymus DNA were studied by absorption and fluorescence spectroscopic techniques and the calculated binding constants (K_b) are in the range of 3.5 × 10⁵ M⁻¹–3.2 × 10⁵ M⁻¹. Complexes 1–3 effectively bind DNA through an intercalative mode, as proved by molecular docking studies. The binding affinity of the complexes decreases with the size increase of the N-alkyl substituent, in the order of 1 > 2 > 3, which is also in accord with the calculated LUMO_complex energies. They show substantial in vitro cytotoxic effect against human lung (A-549), breast (MDA-MB-231) and cervical (HeLa) cancer cell lines. Complex 1 exhibits a significant inhibitory effect on the proliferation of the A-549 cancer cells. The antiproliferative efficacy of 1 has also been analysed by a DNA fragmentation assay, fluorescence activated cell sorting (FACS) and nuclear morphology using a fluorescence microscope. The possible mode for the apoptosis pathway of 1 has also been evaluated by a reactive oxygen species (ROS) generation study.