Rajendiran N, Balasubramanian T
CAS in Marine Biology, Annamalai University, Parangipettai 608502, Tamil Nadu, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Nov;68(3):867-76. doi: 10.1016/j.saa.2006.12.072. Epub 2007 Jan 12.
Spectral characteristics of N-phenylanthranilic acid (NPAA) have been studied in different solvents, pH and beta-cyclodextrin (beta-CD) and compared with anthranilic acid (2-aminobenzoic acid, 2ABA). In all solvents a dual fluorescence is observed in NPAA, whereas 2ABA gives single emission. Combining the results observed in the absorption, fluorescence emission and fluorescence excitation spectra, it is found that strong intramolecular hydrogen bonding (IHB) interactions present in NPAA molecule. The inclusion complex of NPAA with beta-CD is analysed by UV-vis, fluorimetry, FT-IR, (1)H NMR, scanning electron microscope and AM 1 method. The above spectral studies show that NPAA forms a 1:1 inclusion complex with beta-CD and COOH group present in the beta-CD cavity. A mechanism is proposed to explain the inclusion process.
已在不同溶剂、pH值和β-环糊精(β-CD)条件下研究了N-苯基邻氨基苯甲酸(NPAA)的光谱特性,并与邻氨基苯甲酸(2-氨基苯甲酸,2ABA)进行了比较。在所有溶剂中,NPAA均观察到双重荧光,而2ABA则产生单一发射。综合吸收光谱、荧光发射光谱和荧光激发光谱的观察结果,发现NPAA分子中存在强烈的分子内氢键(IHB)相互作用。采用紫外可见光谱、荧光光谱、傅里叶变换红外光谱、核磁共振氢谱、扫描电子显微镜和AM1方法对NPAA与β-CD的包合物进行了分析。上述光谱研究表明,NPAA与β-CD形成了1:1的包合物,且β-CD空腔中存在COOH基团。提出了一种机制来解释包合过程。