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Excited state behaviour of substituted dipyridophenazine Cr(III) complexes in the presence of nucleic acids
Date Issued
2010
Date Available
2013-05-16T09:12:35Z
Abstract
The photophysics and photochemistry of [Cr(phen)2(dppz)]3+ and its 11,12-substituted derivatives [Cr(phen)2(X2dppz)]3+
{X = Me or F} have been studied in the presence of purine nucleotides
or DNA using steady state and time-resolved absorption and luminescence
spectroscopy. 5'-Adenosine monophosphate (5'-AMP) shows only a weak
interaction with the excited states of each complex. By contrast they
are efficiently quenched by 5'-guanosine monophosphate (5'-GMP),
consistent with photo-induced electron transfer. Laser flash photolysis
spectroscopy in the presence of 5'--GMP suggests that both forward and
back electron-transfers are rapid. All complexes also display a strong
affinity for DNA and evidence for both static and dynamic quenching
mechanisms is provided.
{X = Me or F} have been studied in the presence of purine nucleotides
or DNA using steady state and time-resolved absorption and luminescence
spectroscopy. 5'-Adenosine monophosphate (5'-AMP) shows only a weak
interaction with the excited states of each complex. By contrast they
are efficiently quenched by 5'-guanosine monophosphate (5'-GMP),
consistent with photo-induced electron transfer. Laser flash photolysis
spectroscopy in the presence of 5'--GMP suggests that both forward and
back electron-transfers are rapid. All complexes also display a strong
affinity for DNA and evidence for both static and dynamic quenching
mechanisms is provided.
Type of Material
Journal Article
Publisher
RSC Publishing
Journal
Photochemical and photobiological sciences
Volume
9
Issue
9
Start Page
1196
End Page
1202
Copyright (Published Version)
2010, Royal Society of Chemistry
Language
English
Status of Item
Peer reviewed
This item is made available under a Creative Commons License
File(s)
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2010_PCCP__Cr_Complexes.pdf
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629.26 KB
Format
Adobe PDF
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