Kathiravan A, Renganathan R
School of Chemistry, Bharathidasan University, Tiruchirappalli-620 024, Tamil Nadu, India.
J Colloid Interface Sci. 2009 Mar 15;331(2):401-7. doi: 10.1016/j.jcis.2008.12.001. Epub 2008 Dec 3.
The interaction of porphyrins (TCPP, TSPP, TMeOPP and TPP) with colloidal TiO(2) nanoparticles was studied by infra-red, UV-visible absorption, steady state and time resolved fluorescence spectroscopy. The porphyrins (TCPP, TSPP and TMeOPP) adsorbed on the surface of colloidal TiO(2) nanoparticles through electrostatic interaction. According to absorption and fluorescence changes the apparent association constants (K(app)) were calculated. However, TPP did not interact with surface of colloidal TiO(2) nanoparticles due to the absence of anchoring group. The fluorescence quenching is attributable mainly to electron transfer from the excited state porphyrins to the conduction band of colloidal TiO(2). The rate of electron transfer process (k(et)) was calculated using lifetime measurement. The electron transfer mechanism has been proved by the calculation of free energy change (DeltaG(et)) by applying Rehm-Weller equation. Using all the spectroscopic measurements we confirmed that the presence of anchoring group plays major role in the adsorption as well as the electron transfer processes.
通过红外、紫外可见吸收、稳态和时间分辨荧光光谱研究了卟啉(四羧基苯基卟啉、四磺酸苯基卟啉、四甲基苯基卟啉和四苯基卟啉)与胶体二氧化钛纳米颗粒的相互作用。卟啉(四羧基苯基卟啉、四磺酸苯基卟啉和四甲基苯基卟啉)通过静电相互作用吸附在胶体二氧化钛纳米颗粒表面。根据吸收和荧光变化计算了表观缔合常数(K(app))。然而,由于没有锚定基团,四苯基卟啉不与胶体二氧化钛纳米颗粒表面相互作用。荧光猝灭主要归因于从激发态卟啉到胶体二氧化钛导带的电子转移。使用寿命测量计算了电子转移过程的速率(k(et))。通过应用雷姆-韦勒方程计算自由能变化(DeltaG(et)),证明了电子转移机制。通过所有光谱测量,我们证实了锚定基团的存在在吸附以及电子转移过程中起主要作用。