Solvent-Regulated Fluorimetric Differentiation of Al3+ and Zn2+ Using an AIE-Active Single Sensor

化学 水溶液中的金属离子 分子内力 光化学 分子轨道 光谱学 离子 激发态 轨道能级差 荧光 密度泛函理论 金属 电子转移 分析化学(期刊) 分子 计算化学 原子物理学 立体化学 有机化学 物理 量子力学
作者
Bhriguram Das,Malay Dolai,Anamika Dhara,Avijit Ghosh,Subhabrata Mabhai,Ajay Misra,Satyajit Dey,Atanu Jana
出处
期刊:Journal of Physical Chemistry A [American Chemical Society]
卷期号:125 (7): 1490-1504 被引量:35
标识
DOI:10.1021/acs.jpca.0c10518
摘要

The absence of d-orbital electrons or presence of full-filled d-orbital electrons in metal ions is a well-known Achilles’ heel problem for the detection of these metal ions by a simple UV-visible study. For this reason, detection of metal ions such as Al3+ with no d-orbital electrons or Zn2+ with filled d-orbital electrons is a challenging task. Herein, we report a 2-naphthol-based fluorescent probe [1-((E)-((E)-(5-bromo-2-hydroxybenzylidene)hydrazono)methyl)naphthalen-2-ol] (H2L) that has been used to sense and discriminate Al3+ and Zn2+ via solvent regulation. The probe exhibits excellent selectivity and swift sensitivity toward Al3+ in MeOH–water (9:1, v/v) and toward Zn2+ in dimethyl sulfoxide (DMSO)–water (9:1, v/v) among various metal ions. The respective detection limit is found to be 9.78 and 3.65 μM. The sensing mechanism is attributed to multiple processes, viz., the inhibition of photo-induced electron transfer (PET) along with the introduction of chelation-enhanced emission (CHEF) and excited-state intramolecular proton transfer (ESIPT) inhibition, which are experimentally well verified by UV–vis absorption spectroscopy, emission spectroscopy, and NMR spectroscopy. The probe shows aggregation-induced emissive (AIE) response in ≥70% aqueous media as well as in the solid state. The experimental results are well corroborated by time-resolved photoluminescence (TRPL) and density functional theory (DFT) calculations. An advanced-level OR-AND-NOT logic gate has been constructed from a different chemical combinational input and emission output. The reversible recognition of both Al3+ in MeOH–water (9:1, v/v) and Zn2+ in DMSO–water (9:1, v/v) is also ascertained in the presence of Na2EDTA, enabling the construction of a molecular memory device. The probe H2L also detects intracellular Al3+/Zn2+ ions in Hela cells. Altogether, our fundamental findings will pave the way for designing and synthesis of unique chemosensors that could be used for cell imaging studies as well as constructing molecular logic gates.
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