Department of Chemistry, Jadavpur University, Kolkata-700032, India.
J Phys Chem A. 2011 Aug 25;115(33):9169-79. doi: 10.1021/jp204165j. Epub 2011 Aug 3.
This paper investigates how solution conditions, especially solvent polarity and hydrogen bonding, influence the fluorescence of an anticancer drug, doxorubicin hydrochloride (DOX). When excited at 480 nm, this molecule shows single fluorescence. However, when excited at 346 nm, it shows dual fluorescence. The ground and excited state intramolecular double proton transfer in DOX has been observed and investigated to shed light on their corresponding spectroscopy and dynamics in different protic and aprotic solvents. An increase in pH results in enhancement of emission from the ionic conformer with parallel dwindling of emission of the neutral species. Based on the experimental and theoretical studies on DOX, a ground and excited state intramolecular double proton transfer mechanism is proposed to explain the unusual excitation-dependent dual fluorescence of DOX.
本文研究了溶液条件,特别是溶剂极性和氢键,如何影响抗癌药物盐酸多柔比星(DOX)的荧光。当用 480nm 的光激发时,该分子显示单荧光。然而,当用 346nm 的光激发时,它显示出双荧光。已经观察到 DOX 中的基态和激发态分子内双质子转移,并对其在不同质子性和非质子性溶剂中的相应光谱和动力学进行了研究。pH 值的增加导致具有平行结构的离子型构象的发射增强,而中性物种的发射则相应减弱。基于对 DOX 的实验和理论研究,提出了一个基态和激发态分子内双质子转移机制,以解释 DOX 异常的激发依赖性双荧光。