Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
3723903
Reference Type
Journal Article
Title
Photophysical and photochemical properties of manganese complexes with cationic porphyrin ligands: Effects of alkyl substituents and micellar environment
Author(s)
Fodor, MA; Horvath, O; Fodor, L; Vazdar, K; Grampp, G; Wankmueller, A
Year
2016
Is Peer Reviewed?
Yes
Journal
Journal of Photochemistry and Photobiology A: Chemistry
ISSN:
1010-6030
EISSN:
1873-2666
Volume
328
Page Numbers
233-239
DOI
10.1016/j.jphotochem.2016.06.011
Web of Science Id
WOS:000381165200028
Abstract
Although Mn(III) porphyrins were considered earlier to be very weakly emissive, the fluorescence displayed by Mn(III) complexes with the cationic TMPyP2+ ligand (H2TMPyP4+ = 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin) as well as with its other alkyl (such as hexyl and dodecyl) derivatives proved to be strong enough for a comparative study. Elongation of the alkyl substituent increased both the quantum yield and the lifetime of the emission for the Mn(III) porphyrins, while resulted in an opposite effect for the corresponding free bases in homogeneous solutions. The presence of cationic micelles, however, reversed this tendency regarding the emission lifetime of the complexes. These cationic metalloporphyrins were applied in a photocatalytic system involving triethanolamine (TEOA) as a sacrificial electron donor and methylviologen (MV2+) as an acceptor. In the first step of the catalytic process outer-sphere photoinduced reduction of the metal center took place via quenching of the triplet excited state of these metalloporphyrins by TEOA. The corresponding manganese(II) porphyrins formed in this way were also photoactive; they forwarded an electron to MV2+ upon irradiation, regenerating the starting complex. Elongation of the alkyl substituents increased the quantum yield of the formation of methylviologen radical (MV(sic)+) in this system, but considerably decreased the durability of the photocatalyst. Anionic micelles totally hindered the photoinduced generation of Mn(II) porphyrins, while cationic micellar environment appreciably increased the efficiency of the accumulation of MV(sic)+. (C) 2016 Elsevier B.V. All rights reserved.
Keywords
Cationic manganese(III) porphyrins; Amphiphilic; Micellar; Fluorescence; Photocatalysis; Triplet state
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity