Detailed Picosecond Kerr-Gated Time-Resolved Resonance Raman Spectroscopy and Time-Resolved Emission Studies of Merocyanine 540 in Various Solvents
By using the unique fluorescence rejection method of Kerr-gating, detailed picosecond time-resolved resonance Raman experiments have been performed on the highly fluorescent photodynamic therapy dye, Merocyanine 540 (MC540). This has enabled collection of the first-singlet trans excited resonance Ra...
Gespeichert in:
Veröffentlicht in: | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2003-06, Vol.107 (22), p.4347-4353 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4353 |
---|---|
container_issue | 22 |
container_start_page | 4347 |
container_title | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory |
container_volume | 107 |
creator | Benniston, Andrew C Matousek, Pavel McCulloch, Iain E Parker, Anthony W Towrie, Michael |
description | By using the unique fluorescence rejection method of Kerr-gating, detailed picosecond time-resolved resonance Raman experiments have been performed on the highly fluorescent photodynamic therapy dye, Merocyanine 540 (MC540). This has enabled collection of the first-singlet trans excited resonance Raman spectra of this dye in a range of protic and aprotic solvents of varying viscosity and polarity, as well as an organized reverse micelle. The detailed vibrational spectra support the idea that protic solvents form a H-bonded cluster around the oxygen groups of the thiobarbiturate group, which lock the group in position and hinder its rotation. In the reverse micelle containing hexane/AOT and a water pool (ωo = 32) the dye is orientated to permit the thiobarbiturate group to interact with water pool molecules. Using the Kerr-gate setup, time-resolved emission spectra of MC540 were also recorded in various solvents. The dye undergoes fast vibrational cooling (2−10 ps), which can be related to the solvent's thermal diffusivity. A second slower process (20−100 ps) also occurs, which is viscosity dependent and is associated with structural relaxation of the polymethine unit within the dye. |
doi_str_mv | 10.1021/jp027343z |
format | Article |
fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_jp027343z</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_TPS_MFJRMH6P_K</sourcerecordid><originalsourceid>FETCH-LOGICAL-a295t-743bd017d90c735f1eca0b490d0494f600382169714840cc1c75cd609358c35c3</originalsourceid><addsrcrecordid>eNptkM1OAjEUhSdGExFd-AbduHBRvZ2287M0yI8CkQC6bUqnkxSZdtIORnwNX9ghGBbG1T335rsnOSeKrgncEYjJ_bqGOKWMfp1EHcJjwDwm_LTVkOWYJzQ_jy5CWAMAoTHrRN-PupFmows0M8oFrZwt0Fh7j4eyaa9LU2k818FtPtptL6y0SqO5rKRFi1qrxrugXL1D0v7F-5UJwbiWa7aF0QG5Ek21d2onrbEacQbIWPQmvXHbgBb7L9uEy-islJugr35nN3od9Je9EZ68DJ96DxMs45w3OGV0VQBJixxUSnlJtJKwYjkUwHJWJgA0i0mSp4RlDJQiKuWqSCCnPFOUK9qNbg--qo0QvC5F7U0l_U4QEPs2xbHNlsUH1oRGfx5B6d9FktKUi-VsIaaD5_l0lMzEuOVvDrxUQazd1ts2yT--P9XBhAo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Detailed Picosecond Kerr-Gated Time-Resolved Resonance Raman Spectroscopy and Time-Resolved Emission Studies of Merocyanine 540 in Various Solvents</title><source>American Chemical Society Journals</source><creator>Benniston, Andrew C ; Matousek, Pavel ; McCulloch, Iain E ; Parker, Anthony W ; Towrie, Michael</creator><creatorcontrib>Benniston, Andrew C ; Matousek, Pavel ; McCulloch, Iain E ; Parker, Anthony W ; Towrie, Michael</creatorcontrib><description>By using the unique fluorescence rejection method of Kerr-gating, detailed picosecond time-resolved resonance Raman experiments have been performed on the highly fluorescent photodynamic therapy dye, Merocyanine 540 (MC540). This has enabled collection of the first-singlet trans excited resonance Raman spectra of this dye in a range of protic and aprotic solvents of varying viscosity and polarity, as well as an organized reverse micelle. The detailed vibrational spectra support the idea that protic solvents form a H-bonded cluster around the oxygen groups of the thiobarbiturate group, which lock the group in position and hinder its rotation. In the reverse micelle containing hexane/AOT and a water pool (ωo = 32) the dye is orientated to permit the thiobarbiturate group to interact with water pool molecules. Using the Kerr-gate setup, time-resolved emission spectra of MC540 were also recorded in various solvents. The dye undergoes fast vibrational cooling (2−10 ps), which can be related to the solvent's thermal diffusivity. A second slower process (20−100 ps) also occurs, which is viscosity dependent and is associated with structural relaxation of the polymethine unit within the dye.</description><identifier>ISSN: 1089-5639</identifier><identifier>EISSN: 1520-5215</identifier><identifier>DOI: 10.1021/jp027343z</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2003-06, Vol.107 (22), p.4347-4353</ispartof><rights>Copyright © 2003 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a295t-743bd017d90c735f1eca0b490d0494f600382169714840cc1c75cd609358c35c3</citedby><cites>FETCH-LOGICAL-a295t-743bd017d90c735f1eca0b490d0494f600382169714840cc1c75cd609358c35c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jp027343z$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jp027343z$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>Benniston, Andrew C</creatorcontrib><creatorcontrib>Matousek, Pavel</creatorcontrib><creatorcontrib>McCulloch, Iain E</creatorcontrib><creatorcontrib>Parker, Anthony W</creatorcontrib><creatorcontrib>Towrie, Michael</creatorcontrib><title>Detailed Picosecond Kerr-Gated Time-Resolved Resonance Raman Spectroscopy and Time-Resolved Emission Studies of Merocyanine 540 in Various Solvents</title><title>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</title><addtitle>J. Phys. Chem. A</addtitle><description>By using the unique fluorescence rejection method of Kerr-gating, detailed picosecond time-resolved resonance Raman experiments have been performed on the highly fluorescent photodynamic therapy dye, Merocyanine 540 (MC540). This has enabled collection of the first-singlet trans excited resonance Raman spectra of this dye in a range of protic and aprotic solvents of varying viscosity and polarity, as well as an organized reverse micelle. The detailed vibrational spectra support the idea that protic solvents form a H-bonded cluster around the oxygen groups of the thiobarbiturate group, which lock the group in position and hinder its rotation. In the reverse micelle containing hexane/AOT and a water pool (ωo = 32) the dye is orientated to permit the thiobarbiturate group to interact with water pool molecules. Using the Kerr-gate setup, time-resolved emission spectra of MC540 were also recorded in various solvents. The dye undergoes fast vibrational cooling (2−10 ps), which can be related to the solvent's thermal diffusivity. A second slower process (20−100 ps) also occurs, which is viscosity dependent and is associated with structural relaxation of the polymethine unit within the dye.</description><issn>1089-5639</issn><issn>1520-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNptkM1OAjEUhSdGExFd-AbduHBRvZ2287M0yI8CkQC6bUqnkxSZdtIORnwNX9ghGBbG1T335rsnOSeKrgncEYjJ_bqGOKWMfp1EHcJjwDwm_LTVkOWYJzQ_jy5CWAMAoTHrRN-PupFmows0M8oFrZwt0Fh7j4eyaa9LU2k818FtPtptL6y0SqO5rKRFi1qrxrugXL1D0v7F-5UJwbiWa7aF0QG5Ek21d2onrbEacQbIWPQmvXHbgBb7L9uEy-islJugr35nN3od9Je9EZ68DJ96DxMs45w3OGV0VQBJixxUSnlJtJKwYjkUwHJWJgA0i0mSp4RlDJQiKuWqSCCnPFOUK9qNbg--qo0QvC5F7U0l_U4QEPs2xbHNlsUH1oRGfx5B6d9FktKUi-VsIaaD5_l0lMzEuOVvDrxUQazd1ts2yT--P9XBhAo</recordid><startdate>20030605</startdate><enddate>20030605</enddate><creator>Benniston, Andrew C</creator><creator>Matousek, Pavel</creator><creator>McCulloch, Iain E</creator><creator>Parker, Anthony W</creator><creator>Towrie, Michael</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20030605</creationdate><title>Detailed Picosecond Kerr-Gated Time-Resolved Resonance Raman Spectroscopy and Time-Resolved Emission Studies of Merocyanine 540 in Various Solvents</title><author>Benniston, Andrew C ; Matousek, Pavel ; McCulloch, Iain E ; Parker, Anthony W ; Towrie, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a295t-743bd017d90c735f1eca0b490d0494f600382169714840cc1c75cd609358c35c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Benniston, Andrew C</creatorcontrib><creatorcontrib>Matousek, Pavel</creatorcontrib><creatorcontrib>McCulloch, Iain E</creatorcontrib><creatorcontrib>Parker, Anthony W</creatorcontrib><creatorcontrib>Towrie, Michael</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Benniston, Andrew C</au><au>Matousek, Pavel</au><au>McCulloch, Iain E</au><au>Parker, Anthony W</au><au>Towrie, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detailed Picosecond Kerr-Gated Time-Resolved Resonance Raman Spectroscopy and Time-Resolved Emission Studies of Merocyanine 540 in Various Solvents</atitle><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</jtitle><addtitle>J. Phys. Chem. A</addtitle><date>2003-06-05</date><risdate>2003</risdate><volume>107</volume><issue>22</issue><spage>4347</spage><epage>4353</epage><pages>4347-4353</pages><issn>1089-5639</issn><eissn>1520-5215</eissn><abstract>By using the unique fluorescence rejection method of Kerr-gating, detailed picosecond time-resolved resonance Raman experiments have been performed on the highly fluorescent photodynamic therapy dye, Merocyanine 540 (MC540). This has enabled collection of the first-singlet trans excited resonance Raman spectra of this dye in a range of protic and aprotic solvents of varying viscosity and polarity, as well as an organized reverse micelle. The detailed vibrational spectra support the idea that protic solvents form a H-bonded cluster around the oxygen groups of the thiobarbiturate group, which lock the group in position and hinder its rotation. In the reverse micelle containing hexane/AOT and a water pool (ωo = 32) the dye is orientated to permit the thiobarbiturate group to interact with water pool molecules. Using the Kerr-gate setup, time-resolved emission spectra of MC540 were also recorded in various solvents. The dye undergoes fast vibrational cooling (2−10 ps), which can be related to the solvent's thermal diffusivity. A second slower process (20−100 ps) also occurs, which is viscosity dependent and is associated with structural relaxation of the polymethine unit within the dye.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp027343z</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1089-5639 |
ispartof | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2003-06, Vol.107 (22), p.4347-4353 |
issn | 1089-5639 1520-5215 |
language | eng |
recordid | cdi_crossref_primary_10_1021_jp027343z |
source | American Chemical Society Journals |
title | Detailed Picosecond Kerr-Gated Time-Resolved Resonance Raman Spectroscopy and Time-Resolved Emission Studies of Merocyanine 540 in Various Solvents |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T19%3A44%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Detailed%20Picosecond%20Kerr-Gated%20Time-Resolved%20Resonance%20Raman%20Spectroscopy%20and%20Time-Resolved%20Emission%20Studies%20of%20Merocyanine%20540%20in%20Various%20Solvents&rft.jtitle=The%20journal%20of%20physical%20chemistry.%20A,%20Molecules,%20spectroscopy,%20kinetics,%20environment,%20&%20general%20theory&rft.au=Benniston,%20Andrew%20C&rft.date=2003-06-05&rft.volume=107&rft.issue=22&rft.spage=4347&rft.epage=4353&rft.pages=4347-4353&rft.issn=1089-5639&rft.eissn=1520-5215&rft_id=info:doi/10.1021/jp027343z&rft_dat=%3Cistex_cross%3Eark_67375_TPS_MFJRMH6P_K%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |