Department of Chemistry, Gauhati University, Guwahati, 781014, Assam, India.
J Fluoresc. 2013 Jul;23(4):823-8. doi: 10.1007/s10895-013-1192-z. Epub 2013 Mar 24.
The first fluorescent sensor for HF2(-) anion, N(1), N(3)-di(naphthalene-1-yl)isophthalamide (L) has been derived from α-Napthylamine and isopthaloyl chloride. In 1:1 (v/v) DMSO:H2O, L exhibits high selectivity towards HF2(-) anion with a 4-fold enhancement in fluorescent intensity. Very little enhancement in fluorescence intensity is observed for F(-), Cl(-), Br(-), I(-), SCN(-), PO4(3-), SO4(2-), and CH3COO(-) anions. The stoichiometry interaction between L and HF2 (-) is found to be 1:1 from fluorescence and UV/Visible spectral data. DFT calculation shows that binding between HF2(-) and L is 1:1 and increases the relative planarity between the two naphthyl rings causing fluorescence enhancement. A shift of 0.080 V in oxidation potential of L is observed on interaction with HF2(-) by cyclic voltammetry and square wave voltammetry.
第一个 HF2(-)阴离子的荧光传感器,N(1),N(3)-二(萘-1-基)间苯二甲酰胺(L)是由α-萘胺和异苯二甲酰氯衍生而来。在 1:1(v/v)DMSO:H2O 中,L 对 HF2(-)阴离子表现出高选择性,荧光强度增强了 4 倍。对于 F(-)、Cl(-)、Br(-)、I(-)、SCN(-)、PO4(3-)、SO4(2-)和 CH3COO(-)阴离子,荧光强度几乎没有增强。从荧光和紫外/可见光谱数据可以发现,L 与 HF2 (-)之间的化学计量相互作用为 1:1。DFT 计算表明,HF2(-)与 L 的结合为 1:1,并增加了两个萘环之间的相对平面性,导致荧光增强。通过循环伏安法和方波伏安法观察到 L 与 HF2(-)相互作用时氧化电位向正方向移动了 0.080 V。