Photoinduced Electron Transfer Reactions of Water Soluble Porphyrins in Zeolite Environment

نویسندگان

چکیده

Excited state interactions of zeolite adsorbed porphyrins have been investigated by steady luminescence quenching technique with certain antioxidants such as reduced glutathione, ascorbic acid and L-cysteine. The supported porphyrins, meso-tetra (N-methyl-4-pyridyl) porphyrin (H2TMPyP4+) zinc tetra(N-methyl-4-pyridyl) (ZnTMPyP4+) were prepared characterized various techniques Diffuse Reflectance Spectra (DRS), Scanning Electron Microscope (SEM), powder X-Ray Diffraction (XRD) BET surface area. interaction zeolites are shown to increase the lifetime singlet excited decays biphasic in nature. splitting emission band occurs 1:1 glycerol: water solution due changes dielectric solvation sphere associated porphyrin. Stern-Volmer plots I0/I vs quencher concentration [Q] linear whole range used. These studies revealed effective for compared free base effect quenchers acidity has also studied rate constant (kq) is found order 109 M−1 s−1. reaction obeys Rehm-Weller Equation be thermodynamically favoured electron transfer from (reductive quenching).

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Dynamics of Bimolecular Photoinduced Electron-Transfer Reactions

From the accumulated results of several research groups over the last 25 years, it is clear that photoinduced electron-transfer reactions have significantly broadened the scope of organic photochemistry.1 The fundamental mechanistic principle is that when quenching of an excited state via electron transfer is sufficiently exothermic, the reaction occurs at or close to the diffusion-controlled l...

متن کامل

ultrafast spectroscopy on bimolecular photoinduced electron transfer reactions

in Figure 1. After excitation of one of the reactants, diffusion is required to bring the reaction partners at distances where charge separation (CS) can occur. The nature of the primary quenching product is still debated.3 For weakly exergonic CS, ∆GCS > ~ -0.4 eV, it is generally accepted that the product is a contact ion pair (CIP), that is, two ions at a distance enabling a substantial over...

متن کامل

Ultrafast photoinduced electron transfer in face-to-face charge-transfer π-complexes of planar porphyrins and hexaazatriphenylene derivatives.

Charge-transfer (CT) π-complexes are formed between planar porphyrins and 1,4,5,8,9,12-hexaazatriphenylene (HAT) derivatives with large formation constants (e.g., 104 M-1), exhibiting broad CT absorption bands. The unusually large formation constants result from close face-to-face contact between two planar π-planes of porphyrins and HAT derivatives. The redox potentials of porphyrins and HAT d...

متن کامل

Photoinduced Electron Transfer in Ionic Media

Title of Document: PHOTOINDUCED ELECTRON TRANSFER IN IONIC MEDIA Rebecca Cristine Vieira, Doctor of Philosophy, 2008 Directed By: Dr. Daniel E. Falvey, Department of Chemistry and Biochemistry The goal of this research was to explore the use of room temperature ionic liquids (RTILs) and ionic liquids crystals (ILCs) as reaction media for photoinduced electron transfer (PET) processes. Photoindu...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Journal of Fluorescence

سال: 2021

ISSN: ['1053-0509', '1573-4994']

DOI: https://doi.org/10.1007/s10895-021-02747-8