Department of Chemistry, Center of Excellence in Corrosion and Surface Engineering, National Institute of Technology, Tiruchirappalli 620015, Tamilnadu, India.
Mater Sci Eng C Mater Biol Appl. 2013 Aug 1;33(6):3346-52. doi: 10.1016/j.msec.2013.04.018. Epub 2013 Apr 11.
An efficient colorimetric receptor was developed by a simple convenient method which exhibited naked-eye sensitivity for fluoride and acetate in a biologically competing solvent like DMSO. The receptor developed, portrayed a substantial change in the UV-visible absorption characteristics upon addition of fluoride and acetate anions over other anions. The binding constants showed that the binding ability of receptor towards F(-) anion was slightly higher than that of the AcO(-) anion. Job's plots indicated the formation of a (1:1) complex (receptor:anion) of receptor with fluoride and acetate anions respectively. A "turn on" fluorescence response with a red shift was observed upon fluorescence titration. (1)H NMR titration experiments revealed the mechanism to be driven by the hydrogen bonding interaction of amide NH and phenol OH of the receptor molecule which was followed by deprotonation in the receptor by the F(-) and AcO(-) anions.
一种高效的比色受体通过一种简单方便的方法开发出来,该受体在 DMSO 等生物竞争溶剂中对氟化物和乙酸根离子具有肉眼灵敏度。所开发的受体在加入氟化物和乙酸根阴离子时,其紫外可见吸收特性发生了显著变化,而对其他阴离子则没有明显变化。结合常数表明,受体与 F(-)阴离子的结合能力略高于 AcO(-)阴离子。Job 图表明,受体与氟化物和乙酸根阴离子分别形成了(1:1)络合物(受体:阴离子)。荧光滴定实验观察到荧光滴定实验观察到,在荧光滴定过程中,观察到了一个“开启”的荧光响应,伴随着红移。(1)H NMR 滴定实验表明,该机制是由受体分子中的酰胺 NH 和酚 OH 的氢键相互作用驱动的,随后 F(-)和 AcO(-)阴离子使受体分子脱质子化。