TY - JOUR
T1 - A new sulfonamide-based chemosensor for potential fluorescent detection of Cu2+ and Zn2+ ions
AU - Amoah, Cephas
AU - Obuah, Collins
AU - Ainooson, Michael Kojo
AU - Hamenu, Louis
AU - Oppong, Anita
AU - Muller, Alfred
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/3/3
Y1 - 2023/3/3
N2 - In recent times, there has been an increased demand in the search for probing materials for numerous substances in the environment such as the detection of metals ions. In this study, a new class of pyrazolyl-sulfonamide derivatives of para-nitroaniline were synthesized following a multistep approach. The ligands and complexes were characterized using NMR spectroscopy, IR spectroscopy, and mass spectrometry. All the compounds C1–C3 were synthesized in very good yields (85%–92%) and their photo-physical properties measured. All the compounds show fluorescence behaviour with emissions within the UV and far visible range with quantum yields between 7.7% and 25.7%. TD-DFT calculations predictions for the electronic transitions present are in good agreement with experimental observations. Fluorescent probing studies conducted on the compounds show that C1–C3 were analytically sensitive and possessed significant selectivity towards Cu2+ (for C3) and Zn2+ (for C1 and C2) ions with detection limits between 0.011 and 0.103 mg/L for Cu2+ ions and 0.002–0.135 mg/L for Zn2+ ions. Overall, C1 was found to be the most sensitive molecule for the metals studied, having good quantum yield and better selectivity for Zn2+ ion compared to Cu2+.
AB - In recent times, there has been an increased demand in the search for probing materials for numerous substances in the environment such as the detection of metals ions. In this study, a new class of pyrazolyl-sulfonamide derivatives of para-nitroaniline were synthesized following a multistep approach. The ligands and complexes were characterized using NMR spectroscopy, IR spectroscopy, and mass spectrometry. All the compounds C1–C3 were synthesized in very good yields (85%–92%) and their photo-physical properties measured. All the compounds show fluorescence behaviour with emissions within the UV and far visible range with quantum yields between 7.7% and 25.7%. TD-DFT calculations predictions for the electronic transitions present are in good agreement with experimental observations. Fluorescent probing studies conducted on the compounds show that C1–C3 were analytically sensitive and possessed significant selectivity towards Cu2+ (for C3) and Zn2+ (for C1 and C2) ions with detection limits between 0.011 and 0.103 mg/L for Cu2+ ions and 0.002–0.135 mg/L for Zn2+ ions. Overall, C1 was found to be the most sensitive molecule for the metals studied, having good quantum yield and better selectivity for Zn2+ ion compared to Cu2+.
KW - Electronic transition
KW - Fluorescent probes
KW - Photophysical properties
KW - Pyrazole derivatives
KW - Quantum yield
UR - http://www.scopus.com/inward/record.url?scp=85147228881&partnerID=8YFLogxK
U2 - 10.1016/j.tet.2023.133276
DO - 10.1016/j.tet.2023.133276
M3 - Article
AN - SCOPUS:85147228881
SN - 0040-4020
VL - 133
JO - Tetrahedron
JF - Tetrahedron
M1 - 133276
ER -