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Intramolecular energy transfer dynamics in differently linked zinc porphyrin-dithiaporphyrin dyads

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Title Intramolecular energy transfer dynamics in differently linked zinc porphyrin-dithiaporphyrin dyads
 
Creator GHOSH, R
YEDUKONDALU, M
RAVIKANTH, M
PALIT, DK
 
Subject LIGHT-HARVESTING ARRAYS
ELECTRONIC COMMUNICATION
MULTIPORPHYRIN ARRAYS
THIOPHEN RINGS
FREE-BASE
DIMERS
ZN
SUBUNITS
DENSITY
BRIDGE
 
Description Intramolecular energy transfer dynamics in two molecular dyads, in which zinc porphyrin (ZnN4) and dithiaporphyrin (N2S2) units were linked covalently by different bridges, namely phenylene (ph) and diphenylethyne (dpe), were studied employing ultrafast time-resolved transient absorption and fluorescence spectroscopic techniques. The rates of energy transfer in both these dyads are slower than in the corresponding ZnN4-N-4 dyads, in spite of the better gradient for energy flow in the case of the ZnN4-N2S2 dyads. Quantum chemical calculations reveal that the frontier orbital characteristics of the porphyrins are not significantly altered by sulphur substitution at the acceptor porphyrin core, and thus this does not modify the electronic factor in the energy transfer mechanism. However, a significant decrease in overlap between the absorption spectrum of the donor and the emission spectrum of the acceptor results in lower efficiency of the intramolecular energy transfer. The energy transfer process in dpe-linked dyads follows a through-bond super-exchange mechanism, whereas, in ph-linked dyads, the through-space multipole resonance interaction plays an important role.
 
Publisher ROYAL SOC CHEMISTRY
 
Date 2016-01-15T07:24:45Z
2016-01-15T07:24:45Z
2015
 
Type Article
 
Identifier RSC ADVANCES, 5(104)85296-85304
2046-2069
http://dx.doi.org/10.1039/c5ra12600b
http://dspace.library.iitb.ac.in/jspui/handle/100/18043
 
Language en