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Article type: Research Article
Authors: Salunke, Shrikrishna T.a; b | Shelar, Divyesh S.a | Salunkhe, Snehal S.a | Singh, Pinky R.c | Vaidya, Shashikant P.c | Manjare, Sudesh T.a; *
Affiliations: [a] Department of Chemistry, University of Mumbai, Mumbai, India | [b] Department of Chemistry, T.C. College, Baramati, India | [c] Department of Clinical Pathology, Haffkine Institute, Mumbai, India
Correspondence: [*] Corresponding author: Sudesh T. Manjare, Department of Chemistry, University of Mumbai, Mumbai, 400098, India. E-mail: [email protected]
Abstract: Herein, we have reported the highly effective use of the Knoevenagel condensation reaction to synthesize organoselenium containing quinoline-based probe. The probe was characterized by Nuclear Magnetic Resonance and Infra-Red spectroscopy and mass spectrometry. The probe selectively detects KO2 with high sensitivity over other reactive oxygen species and biothiols. Photo-induced electron transfer process is responsible for fluorescence “turn-on” event through transformation of selenide to selenoxide. The probe reacted with KO2 in less than a second with lower detection limit (0.14μM). The probe have better anticancer potency as compared to standard drug Cisplatin.
Keywords: Quinoline, BODIPY, sensor, turn-on response, selenium
DOI: 10.3233/MGC-230106
Journal: Main Group Chemistry, vol. Pre-press, no. Pre-press, pp. 1-12, 2024
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