Exciplex Formation Dynamics of Photoexcited Copper(II) Tetrakis(4-N-methylpyridyl)porphyrin with Synthetic Polynucleotides Probed by Transient Absorption and Raman Spectroscopic Techniques

To elucidate the interaction mechanism of water-soluble copper(II) tetrakis(4-N-methylpyridyl)porphyrin (CuII(TMpy-P4)) with synthetic polynucleotides such as poly(dA-dT)2 and poly(dG-dC)2, the exciplex formation dynamics of photoexcited CuII(TMpy-P4) with added polynucleotides have been investigate...

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Veröffentlicht in:The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 1997-07, Vol.101 (30), p.5412-5417
Hauptverfasser: Jeoung, Sae Chae, Eom, Hyo Soon, Kim, Dongho, Cho, Dae Won, Yoon, Minjoong
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container_issue 30
container_start_page 5412
container_title The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory
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creator Jeoung, Sae Chae
Eom, Hyo Soon
Kim, Dongho
Cho, Dae Won
Yoon, Minjoong
description To elucidate the interaction mechanism of water-soluble copper(II) tetrakis(4-N-methylpyridyl)porphyrin (CuII(TMpy-P4)) with synthetic polynucleotides such as poly(dA-dT)2 and poly(dG-dC)2, the exciplex formation dynamics of photoexcited CuII(TMpy-P4) with added polynucleotides have been investigated by using femtosecond transient absorption as well as transient Raman spectroscopic methods. The nanosecond transient Raman spectra of CuII(TMpy-P4) mixed with poly(dA-dT)2 clearly demonstrate the exciplex formation between photoexcited CuII(TMpy-P4) and poly(dA-dT)2. On the other hand, the exciplex formation of photoexcited CuII(TMpy-P4) with poly(dG-dC)2 is not so manifest as compared with that mixed with poly(dA-dT)2. The transient absorption of CuII(TMpy-P4) mixed with poly(dG-dC)2 exhibits a rise component of 1.3 ps in addition to the very slow decay component (τ ∼ 22 ns). This observation is quite different from that of CuII(TMpy-P4) in aqueous solution or CuII(TMpy-P4) mixed with poly(dA-dT)2, because the exciplex formed in poly(dG-dC)2, if any, is so short-lived that it returns quickly back to four-coordinate CuII(TMpy-P4) intercalated at poly(dG-dC)2, which blocks the axial coordination by water molecules and consequently gives rise to a long lifetime (τ ∼ 22 ns).
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The nanosecond transient Raman spectra of CuII(TMpy-P4) mixed with poly(dA-dT)2 clearly demonstrate the exciplex formation between photoexcited CuII(TMpy-P4) and poly(dA-dT)2. On the other hand, the exciplex formation of photoexcited CuII(TMpy-P4) with poly(dG-dC)2 is not so manifest as compared with that mixed with poly(dA-dT)2. The transient absorption of CuII(TMpy-P4) mixed with poly(dG-dC)2 exhibits a rise component of 1.3 ps in addition to the very slow decay component (τ ∼ 22 ns). This observation is quite different from that of CuII(TMpy-P4) in aqueous solution or CuII(TMpy-P4) mixed with poly(dA-dT)2, because the exciplex formed in poly(dG-dC)2, if any, is so short-lived that it returns quickly back to four-coordinate CuII(TMpy-P4) intercalated at poly(dG-dC)2, which blocks the axial coordination by water molecules and consequently gives rise to a long lifetime (τ ∼ 22 ns).</description><identifier>ISSN: 1089-5639</identifier><identifier>EISSN: 1520-5215</identifier><identifier>DOI: 10.1021/jp970983v</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>The journal of physical chemistry. 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A, Molecules, spectroscopy, kinetics, environment, &amp; general theory</title><addtitle>J. Phys. Chem. A</addtitle><description>To elucidate the interaction mechanism of water-soluble copper(II) tetrakis(4-N-methylpyridyl)porphyrin (CuII(TMpy-P4)) with synthetic polynucleotides such as poly(dA-dT)2 and poly(dG-dC)2, the exciplex formation dynamics of photoexcited CuII(TMpy-P4) with added polynucleotides have been investigated by using femtosecond transient absorption as well as transient Raman spectroscopic methods. The nanosecond transient Raman spectra of CuII(TMpy-P4) mixed with poly(dA-dT)2 clearly demonstrate the exciplex formation between photoexcited CuII(TMpy-P4) and poly(dA-dT)2. On the other hand, the exciplex formation of photoexcited CuII(TMpy-P4) with poly(dG-dC)2 is not so manifest as compared with that mixed with poly(dA-dT)2. 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A, Molecules, spectroscopy, kinetics, environment, &amp; general theory</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeoung, Sae Chae</au><au>Eom, Hyo Soon</au><au>Kim, Dongho</au><au>Cho, Dae Won</au><au>Yoon, Minjoong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exciplex Formation Dynamics of Photoexcited Copper(II) Tetrakis(4-N-methylpyridyl)porphyrin with Synthetic Polynucleotides Probed by Transient Absorption and Raman Spectroscopic Techniques</atitle><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, &amp; general theory</jtitle><addtitle>J. Phys. Chem. A</addtitle><date>1997-07-24</date><risdate>1997</risdate><volume>101</volume><issue>30</issue><spage>5412</spage><epage>5417</epage><pages>5412-5417</pages><issn>1089-5639</issn><eissn>1520-5215</eissn><abstract>To elucidate the interaction mechanism of water-soluble copper(II) tetrakis(4-N-methylpyridyl)porphyrin (CuII(TMpy-P4)) with synthetic polynucleotides such as poly(dA-dT)2 and poly(dG-dC)2, the exciplex formation dynamics of photoexcited CuII(TMpy-P4) with added polynucleotides have been investigated by using femtosecond transient absorption as well as transient Raman spectroscopic methods. The nanosecond transient Raman spectra of CuII(TMpy-P4) mixed with poly(dA-dT)2 clearly demonstrate the exciplex formation between photoexcited CuII(TMpy-P4) and poly(dA-dT)2. On the other hand, the exciplex formation of photoexcited CuII(TMpy-P4) with poly(dG-dC)2 is not so manifest as compared with that mixed with poly(dA-dT)2. The transient absorption of CuII(TMpy-P4) mixed with poly(dG-dC)2 exhibits a rise component of 1.3 ps in addition to the very slow decay component (τ ∼ 22 ns). This observation is quite different from that of CuII(TMpy-P4) in aqueous solution or CuII(TMpy-P4) mixed with poly(dA-dT)2, because the exciplex formed in poly(dG-dC)2, if any, is so short-lived that it returns quickly back to four-coordinate CuII(TMpy-P4) intercalated at poly(dG-dC)2, which blocks the axial coordination by water molecules and consequently gives rise to a long lifetime (τ ∼ 22 ns).</abstract><pub>American Chemical Society</pub><doi>10.1021/jp970983v</doi><tpages>6</tpages></addata></record>
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title Exciplex Formation Dynamics of Photoexcited Copper(II) Tetrakis(4-N-methylpyridyl)porphyrin with Synthetic Polynucleotides Probed by Transient Absorption and Raman Spectroscopic Techniques
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