Ground and excited-state interactions of coumarin and nucleotide base
Steady-state and time-resolved fluorescence measurements for a series of bichromophoric compounds containing 7-methoxy-coumarin and nucleotide base residues have been performed in water and in organic solvents. The data from these studies have been used to calculate the relative proportion of folded...
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Veröffentlicht in: | Canadian journal of chemistry 1988-03, Vol.66 (3), p.513-516 |
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description | Steady-state and time-resolved fluorescence measurements for a series of bichromophoric compounds containing 7-methoxy-coumarin and nucleotide base residues have been performed in water and in organic solvents. The data from these studies have been used to calculate the relative proportion of folded and extended conformations of bichromophores. Ground-state stacking interactions of coumarin and nucleotide base have been found to be limited to aqueous solution. The contribution of the dynamic quenching mechanism to the total fluorescence quenching in water has been estimated. The absence of dynamic quenching in organic solvents is.explained on the basis of the very short lifetime of the fluorophore in methanol. |
doi_str_mv | 10.1139/v88-087 |
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The data from these studies have been used to calculate the relative proportion of folded and extended conformations of bichromophores. Ground-state stacking interactions of coumarin and nucleotide base have been found to be limited to aqueous solution. The contribution of the dynamic quenching mechanism to the total fluorescence quenching in water has been estimated. 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The data from these studies have been used to calculate the relative proportion of folded and extended conformations of bichromophores. Ground-state stacking interactions of coumarin and nucleotide base have been found to be limited to aqueous solution. The contribution of the dynamic quenching mechanism to the total fluorescence quenching in water has been estimated. The absence of dynamic quenching in organic solvents is.explained on the basis of the very short lifetime of the fluorophore in methanol.</description><subject>Atomic and molecular physics</subject><subject>Exact sciences and technology</subject><subject>Fluorescence and phosphorescence; radiationless transitions, quenching (intersystem crossing, internal conversion)</subject><subject>Molecular properties and interactions with photons</subject><subject>Physics</subject><issn>0008-4042</issn><issn>1480-3291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNp9z8FKAzEQBuAgCtYqvsIeREGIJrvZTXKUUqtQ8NL7kp1MMFKzJUlF397YFm96GIaBj5_5Cbnk7I7zRt9_KEWZkkdkwoVitKk1PyYTxpiigon6lJyl9FZOyep2QuaLOG6DrUwZ_ASf0dKUTcbKh4zRQPZjSNXoKhi37yb6sKNhC2scs7dYDSbhOTlxZp3w4rCnZPU4X82e6PJl8Tx7WFIQXGY6GMa4cbUWQrYtdGiswlZp0yJI1LW2gg9CIh86kK1Ep6RuYOgs1Ngia6bkZh8LcUwpous30ZenvnrO-p_yfSnfl_JFXu3lxiQwaxdNAJ9-uWRSy04XdrtnIULEhCbC6z-Z13_jA-o31jXfX1d1dg</recordid><startdate>19880301</startdate><enddate>19880301</enddate><creator>Wenska, Grażyna</creator><creator>Paszyc, Stefan</creator><general>NRC Research Press</general><general>National Research Council of Canada</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19880301</creationdate><title>Ground and excited-state interactions of coumarin and nucleotide base</title><author>Wenska, Grażyna ; Paszyc, Stefan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-ba001af2944755c6ead8e589a5ec7e929d41b47e1b6c757ef8793cb6dc2e5e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Atomic and molecular physics</topic><topic>Exact sciences and technology</topic><topic>Fluorescence and phosphorescence; radiationless transitions, quenching (intersystem crossing, internal conversion)</topic><topic>Molecular properties and interactions with photons</topic><topic>Physics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wenska, Grażyna</creatorcontrib><creatorcontrib>Paszyc, Stefan</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Canadian journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wenska, Grażyna</au><au>Paszyc, Stefan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ground and excited-state interactions of coumarin and nucleotide base</atitle><jtitle>Canadian journal of chemistry</jtitle><addtitle>Revue canadienne de chimie</addtitle><date>1988-03-01</date><risdate>1988</risdate><volume>66</volume><issue>3</issue><spage>513</spage><epage>516</epage><pages>513-516</pages><issn>0008-4042</issn><eissn>1480-3291</eissn><coden>CJCHAG</coden><abstract>Steady-state and time-resolved fluorescence measurements for a series of bichromophoric compounds containing 7-methoxy-coumarin and nucleotide base residues have been performed in water and in organic solvents. The data from these studies have been used to calculate the relative proportion of folded and extended conformations of bichromophores. Ground-state stacking interactions of coumarin and nucleotide base have been found to be limited to aqueous solution. The contribution of the dynamic quenching mechanism to the total fluorescence quenching in water has been estimated. The absence of dynamic quenching in organic solvents is.explained on the basis of the very short lifetime of the fluorophore in methanol.</abstract><cop>Ottawa, Canada</cop><pub>NRC Research Press</pub><doi>10.1139/v88-087</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Atomic and molecular physics Exact sciences and technology Fluorescence and phosphorescence radiationless transitions, quenching (intersystem crossing, internal conversion) Molecular properties and interactions with photons Physics |
title | Ground and excited-state interactions of coumarin and nucleotide base |
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