Sathish Sai, Narayan Govindh, Rao Nageswara, Janardhana Chelli
Department of Chemistry, Sri Sathya Sai Institute of Higher Learning, Prashanthi Nilayam, Anantapur, A.P-515134, India.
J Fluoresc. 2007 Jan;17(1):1-5. doi: 10.1007/s10895-006-0137-1. Epub 2006 Dec 12.
Aluminum chloride addition results in a self-organized TURN-ON fluorescence of 3-hydroxyflavone (3HF) by a complexation reaction in MeOH and subsequent ligand exchange reaction with fluoride or acetate ions causes a fluorescence TURN-OFF of this complex, delivering a quantitative estimation route for fluoride and acetate ions. The ternary complex of 3HF with Al (III), a hard acid provides for a sensitive signalling system for fluoride ion, a hard base in the concentration range from 6 muM to 50 mM by a concerted co-ordination of fluoride ion involving an intermediate mechanistic pathway, while the complex is sensitive to acetate addition between 0-68 muM. The ligand exchange reaction of Al (3HF)(2) complex by fluoride or acetate ion, without interference from other common anions, has been investigated by UV-visible and fluorescence spetroscopies. The structure of the in-situ intermediate isolated at higher Al (3HF)(2) complex and acetate concentrations was inferred from the FT-IR spectrum and ESI-MS of the sample.
在甲醇中,通过络合反应,添加氯化铝会使3-羟基黄酮(3HF)产生自组织开启荧光,随后与氟离子或醋酸根离子发生配体交换反应会导致该络合物荧光关闭,从而为氟离子和醋酸根离子提供了一种定量估算方法。3HF与作为硬酸的铝(III)形成的三元络合物,通过涉及中间机理途径的氟离子协同配位作用,在6 μM至50 mM的浓度范围内为作为硬碱的氟离子提供了一个灵敏的信号系统,而该络合物对0 - 68 μM之间添加的醋酸根敏感。通过紫外可见光谱和荧光光谱研究了Al(3HF)₂络合物与氟离子或醋酸根离子的配体交换反应,不受其他常见阴离子的干扰。从样品的傅里叶变换红外光谱和电喷雾电离质谱推断出在较高Al(3HF)₂络合物和醋酸根浓度下分离出的原位中间体的结构。