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A Cu(ii) based sensor (1) prepared by the complexation between (quinolin-8-ylamino)-acetic acid hydrazide (L2) and Cu2+ ions has been developed for a highly sensitive and selective recognition of HNO and S2− over other biologically abundant anions with prominent enhancement in absorption and emission intensities. The sensor (1) shows weak fluorescence due to ET (electron transfer) but upon addition of HNO and S2− a large enhancement in the fluorescence intensity (F.I.) was observed over other possible competitive anions on the basis of reduction of Cu(ii) to Cu(i) and formation of CuS, respectively. The 1 : 1 complexation was characterized by mass spectrometry (MS), elemental analysis and Job's plot. The corresponding Kf value was evaluated to be (4.934 ± 0.05) × 104 M−1 for Cu2+ from UV-Vis absorption titration. Quantum yields of L2 and [Cu-L2 + S2−] and [Cu-L2 + HNO] complexes in acetonitrile (CH3CN) are found to be 0.107, 0.09 and 0.07, respectively, using quinine sulphate as the standard. [ABSTRACT FROM AUTHOR]

We report, herein, the development of an easily synthesizable novel dansyl-based turn-on NO sensor L2. The UV-Vis titration data of L2 with Cu2+ display a gradual increase in absorbance at 418 nm with [Cu2+], which were analyzed by using a non-linear least-squares computer-fit program yielding K = (1.16 ± 0.36) × 10-1 M6 and n = (1.28 ± 0.03) indicating a 1 : 1 complexation. The ground state geometries of L2 as well as its complex [Cu(L2)Cl]+ (1) were optimized by DFT calculations which showed that in complex 1 the central metal ion is in distorted tetrahedral geometry with bond distances very close to those found in analogous Cu2+ complexes. The fluorescence of L2 was dramatically quenched (∼60-fold) through complexation with paramagnetic Cu2+ to form [Cu(L2)Cl]+ in MeCN-H2O (9 : 1, v/v) at pH 7.2 in HEPES buffer, which on further treatment with Angeli's salt (Na2N2O3) restores its fluorescence property by ∼15-fold due to the reduction of Cu2+ to Cu+ by NO generated in solution from Na2N2O3. The lifetime measurements displayed a substantial decrease in the lifetime of free ligand L2 (τ0 = 12 ns) on complexation with Cu2+ (τ0 = 2.1 ns). The detection limit of NO calculated by the 3σ method gives a value of 1.6 nM. The NO induced fluorescence enhancement of [CuII(L2)Cl]+ was due to the reduction of [CuII(L2)Cl]+ (1) to [CuI(L2)]+ (2) and is supported by the disappearance of the d-d transition band at 850 nm as well as the X-band EPR signal of 1. The selective "turn on" fluorogenic behavior of L2 was examined on HeLa cells of human cervical cancer origin by fluorescence microscopy which showed very intense intracellular fluorescence that was strongly suppressed by the addition of Cu2+ but it regains its fluorescence property on further incubation with Angeli's salt (Na2N2O3). The existence of [CuII(L2)Cl]+ and [CuI(L2)]+ in solution was confirmed by ESI-MS+ (m/z) analysis. The effect of different biologically relevant cations and anions on the fluorescence property of L2 indicates that it was only the [CuII(L2)Cl]+ which displayed high selectivity for NO, indicating its suitability for intracellular application without much worry about its cytotoxicity in a specified dose. [ABSTRACT FROM AUTHOR]