Photophysical properties and excited state dynamics of 4,7-dithien-2-yl-2,1,3-benzothiadiazole
The relationships between the photophysics and structural properties of 4,7-dithien-2-yl-2,1,3-benzothiadiazole as a function of solvent polarity are investigated both experimentally and by computational methods. Stationary fluorescence measurements are consistent with a model envisaging the presenc...
Gespeichert in:
Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2017, Vol.19 (21), p.13604-13613 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 13613 |
---|---|
container_issue | 21 |
container_start_page | 13604 |
container_title | Physical chemistry chemical physics : PCCP |
container_volume | 19 |
creator | Iagatti, Alessandro Patrizi, Barbara Basagni, Andrea Marcelli, Agnese Alessi, Andrea Zanardi, Stefano Fusco, Roberto Salvalaggio, Mario Bussotti, Laura Foggi, Paolo |
description | The relationships between the photophysics and structural properties of 4,7-dithien-2-yl-2,1,3-benzothiadiazole as a function of solvent polarity are investigated both experimentally and by computational methods. Stationary fluorescence measurements are consistent with a model envisaging the presence of three types of conformers in equilibrium in the ground state. They are characterized by different relative orientations of the thiophene rings. Due to a low rotational barrier, the sample in solution is characterized by a distribution of relative internal orientations. By applying the Kawski method, we evaluate the average dipole moment of ground and excited states of the three types of conformers. The ground state dipole moments are small and similar for the three types of conformers. On the contrary, dipole moments differ substantially in the excited state. X-ray diffraction of a single crystal confirms the presence of an orientational disorder of thiophene rings. Transient absorption UV-visible spectroscopy experiments allows the identification of the main mechanisms responsible for the large Stokes shift observed in this push-pull molecule. Time dependent spectra provide a picture of the relaxation processes occurring after excitation: the primary step is an internal charge transfer assisted by thiophene ring planarization which occurs on a time scale ranging from 0.88 to 1.3 picoseconds depending on solvent polarity. Moreover, time-resolved fluorescence measurements are consistent with a mechanism involving planarization accompanied by a stabilization of the charge transfer state as observed in polar solvents. In the latter, longer fluorescence lifetimes are observed along with a quantum yield decrease due to the activation of specific non-radiative relaxation channels. The photophysical behavior of 4,7-dithien-2-yl-2,1,3-benzothiadiazole in a solid matrix of polymethyl methacrylate is similar to that observed in solution, but the overall non-radiative process rate is slow with respect to that in the liquid phase. As a consequence, the radiative processes are enhanced giving rise to a fluorescence quantum yield of 90%. Such behavior is consistent with the proposed relaxation model. |
doi_str_mv | 10.1039/c6cp08721c |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1915323726</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1915323726</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-2e0ed78888759d0c33edeca1060d37eeba8ed86a3f65ca94f2af337735c66cb23</originalsourceid><addsrcrecordid>eNqNkE1LxDAQhoMo7rp68QdIjyIbzUebpEcpfsGCe9CrJU2mbKTb1CYLdn-91dU9O5cZXh5emAehc0quKeH5jRGmI0oyag7QlKaC45yo9HB_SzFBJyG8E0JoRvkxmjCVUUVzNUVvy5WPvlsNwRndJF3vO-ijg5Do1ibwaVwEm4SoIyR2aPXamZD4OknnElsXVw5azPDQYDanc44raLd-TLV1eusbOEVHtW4CnP3uGXq9v3spHvHi-eGpuF1gw5WImAEBK9U4MsstMZyDBaMpEcRyCVBpBVYJzWuRGZ2nNdM151LyzAhhKsZn6HLXOz7wsYEQy7ULBppGt-A3oaQ5zTjjkol_oKMmplhORvRqh5reh9BDXXa9W-t-KCkpv9WXhSiWP-qLEb747d1Ua7B79M81_wLi2X4M</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1900128290</pqid></control><display><type>article</type><title>Photophysical properties and excited state dynamics of 4,7-dithien-2-yl-2,1,3-benzothiadiazole</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Iagatti, Alessandro ; Patrizi, Barbara ; Basagni, Andrea ; Marcelli, Agnese ; Alessi, Andrea ; Zanardi, Stefano ; Fusco, Roberto ; Salvalaggio, Mario ; Bussotti, Laura ; Foggi, Paolo</creator><creatorcontrib>Iagatti, Alessandro ; Patrizi, Barbara ; Basagni, Andrea ; Marcelli, Agnese ; Alessi, Andrea ; Zanardi, Stefano ; Fusco, Roberto ; Salvalaggio, Mario ; Bussotti, Laura ; Foggi, Paolo</creatorcontrib><description>The relationships between the photophysics and structural properties of 4,7-dithien-2-yl-2,1,3-benzothiadiazole as a function of solvent polarity are investigated both experimentally and by computational methods. Stationary fluorescence measurements are consistent with a model envisaging the presence of three types of conformers in equilibrium in the ground state. They are characterized by different relative orientations of the thiophene rings. Due to a low rotational barrier, the sample in solution is characterized by a distribution of relative internal orientations. By applying the Kawski method, we evaluate the average dipole moment of ground and excited states of the three types of conformers. The ground state dipole moments are small and similar for the three types of conformers. On the contrary, dipole moments differ substantially in the excited state. X-ray diffraction of a single crystal confirms the presence of an orientational disorder of thiophene rings. Transient absorption UV-visible spectroscopy experiments allows the identification of the main mechanisms responsible for the large Stokes shift observed in this push-pull molecule. Time dependent spectra provide a picture of the relaxation processes occurring after excitation: the primary step is an internal charge transfer assisted by thiophene ring planarization which occurs on a time scale ranging from 0.88 to 1.3 picoseconds depending on solvent polarity. Moreover, time-resolved fluorescence measurements are consistent with a mechanism involving planarization accompanied by a stabilization of the charge transfer state as observed in polar solvents. In the latter, longer fluorescence lifetimes are observed along with a quantum yield decrease due to the activation of specific non-radiative relaxation channels. The photophysical behavior of 4,7-dithien-2-yl-2,1,3-benzothiadiazole in a solid matrix of polymethyl methacrylate is similar to that observed in solution, but the overall non-radiative process rate is slow with respect to that in the liquid phase. As a consequence, the radiative processes are enhanced giving rise to a fluorescence quantum yield of 90%. Such behavior is consistent with the proposed relaxation model.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c6cp08721c</identifier><identifier>PMID: 28518198</identifier><language>eng</language><publisher>England</publisher><subject>Charge transfer ; Dipole moments ; Excitation ; Fluorescence ; Ground state ; Mathematical models ; Solvents ; Thiophenes</subject><ispartof>Physical chemistry chemical physics : PCCP, 2017, Vol.19 (21), p.13604-13613</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-2e0ed78888759d0c33edeca1060d37eeba8ed86a3f65ca94f2af337735c66cb23</citedby><cites>FETCH-LOGICAL-c386t-2e0ed78888759d0c33edeca1060d37eeba8ed86a3f65ca94f2af337735c66cb23</cites><orcidid>0000-0003-2696-1611</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28518198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iagatti, Alessandro</creatorcontrib><creatorcontrib>Patrizi, Barbara</creatorcontrib><creatorcontrib>Basagni, Andrea</creatorcontrib><creatorcontrib>Marcelli, Agnese</creatorcontrib><creatorcontrib>Alessi, Andrea</creatorcontrib><creatorcontrib>Zanardi, Stefano</creatorcontrib><creatorcontrib>Fusco, Roberto</creatorcontrib><creatorcontrib>Salvalaggio, Mario</creatorcontrib><creatorcontrib>Bussotti, Laura</creatorcontrib><creatorcontrib>Foggi, Paolo</creatorcontrib><title>Photophysical properties and excited state dynamics of 4,7-dithien-2-yl-2,1,3-benzothiadiazole</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>The relationships between the photophysics and structural properties of 4,7-dithien-2-yl-2,1,3-benzothiadiazole as a function of solvent polarity are investigated both experimentally and by computational methods. Stationary fluorescence measurements are consistent with a model envisaging the presence of three types of conformers in equilibrium in the ground state. They are characterized by different relative orientations of the thiophene rings. Due to a low rotational barrier, the sample in solution is characterized by a distribution of relative internal orientations. By applying the Kawski method, we evaluate the average dipole moment of ground and excited states of the three types of conformers. The ground state dipole moments are small and similar for the three types of conformers. On the contrary, dipole moments differ substantially in the excited state. X-ray diffraction of a single crystal confirms the presence of an orientational disorder of thiophene rings. Transient absorption UV-visible spectroscopy experiments allows the identification of the main mechanisms responsible for the large Stokes shift observed in this push-pull molecule. Time dependent spectra provide a picture of the relaxation processes occurring after excitation: the primary step is an internal charge transfer assisted by thiophene ring planarization which occurs on a time scale ranging from 0.88 to 1.3 picoseconds depending on solvent polarity. Moreover, time-resolved fluorescence measurements are consistent with a mechanism involving planarization accompanied by a stabilization of the charge transfer state as observed in polar solvents. In the latter, longer fluorescence lifetimes are observed along with a quantum yield decrease due to the activation of specific non-radiative relaxation channels. The photophysical behavior of 4,7-dithien-2-yl-2,1,3-benzothiadiazole in a solid matrix of polymethyl methacrylate is similar to that observed in solution, but the overall non-radiative process rate is slow with respect to that in the liquid phase. As a consequence, the radiative processes are enhanced giving rise to a fluorescence quantum yield of 90%. Such behavior is consistent with the proposed relaxation model.</description><subject>Charge transfer</subject><subject>Dipole moments</subject><subject>Excitation</subject><subject>Fluorescence</subject><subject>Ground state</subject><subject>Mathematical models</subject><subject>Solvents</subject><subject>Thiophenes</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkE1LxDAQhoMo7rp68QdIjyIbzUebpEcpfsGCe9CrJU2mbKTb1CYLdn-91dU9O5cZXh5emAehc0quKeH5jRGmI0oyag7QlKaC45yo9HB_SzFBJyG8E0JoRvkxmjCVUUVzNUVvy5WPvlsNwRndJF3vO-ijg5Do1ibwaVwEm4SoIyR2aPXamZD4OknnElsXVw5azPDQYDanc44raLd-TLV1eusbOEVHtW4CnP3uGXq9v3spHvHi-eGpuF1gw5WImAEBK9U4MsstMZyDBaMpEcRyCVBpBVYJzWuRGZ2nNdM151LyzAhhKsZn6HLXOz7wsYEQy7ULBppGt-A3oaQ5zTjjkol_oKMmplhORvRqh5reh9BDXXa9W-t-KCkpv9WXhSiWP-qLEb747d1Ua7B79M81_wLi2X4M</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Iagatti, Alessandro</creator><creator>Patrizi, Barbara</creator><creator>Basagni, Andrea</creator><creator>Marcelli, Agnese</creator><creator>Alessi, Andrea</creator><creator>Zanardi, Stefano</creator><creator>Fusco, Roberto</creator><creator>Salvalaggio, Mario</creator><creator>Bussotti, Laura</creator><creator>Foggi, Paolo</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-2696-1611</orcidid></search><sort><creationdate>2017</creationdate><title>Photophysical properties and excited state dynamics of 4,7-dithien-2-yl-2,1,3-benzothiadiazole</title><author>Iagatti, Alessandro ; Patrizi, Barbara ; Basagni, Andrea ; Marcelli, Agnese ; Alessi, Andrea ; Zanardi, Stefano ; Fusco, Roberto ; Salvalaggio, Mario ; Bussotti, Laura ; Foggi, Paolo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-2e0ed78888759d0c33edeca1060d37eeba8ed86a3f65ca94f2af337735c66cb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Charge transfer</topic><topic>Dipole moments</topic><topic>Excitation</topic><topic>Fluorescence</topic><topic>Ground state</topic><topic>Mathematical models</topic><topic>Solvents</topic><topic>Thiophenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iagatti, Alessandro</creatorcontrib><creatorcontrib>Patrizi, Barbara</creatorcontrib><creatorcontrib>Basagni, Andrea</creatorcontrib><creatorcontrib>Marcelli, Agnese</creatorcontrib><creatorcontrib>Alessi, Andrea</creatorcontrib><creatorcontrib>Zanardi, Stefano</creatorcontrib><creatorcontrib>Fusco, Roberto</creatorcontrib><creatorcontrib>Salvalaggio, Mario</creatorcontrib><creatorcontrib>Bussotti, Laura</creatorcontrib><creatorcontrib>Foggi, Paolo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iagatti, Alessandro</au><au>Patrizi, Barbara</au><au>Basagni, Andrea</au><au>Marcelli, Agnese</au><au>Alessi, Andrea</au><au>Zanardi, Stefano</au><au>Fusco, Roberto</au><au>Salvalaggio, Mario</au><au>Bussotti, Laura</au><au>Foggi, Paolo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photophysical properties and excited state dynamics of 4,7-dithien-2-yl-2,1,3-benzothiadiazole</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2017</date><risdate>2017</risdate><volume>19</volume><issue>21</issue><spage>13604</spage><epage>13613</epage><pages>13604-13613</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>The relationships between the photophysics and structural properties of 4,7-dithien-2-yl-2,1,3-benzothiadiazole as a function of solvent polarity are investigated both experimentally and by computational methods. Stationary fluorescence measurements are consistent with a model envisaging the presence of three types of conformers in equilibrium in the ground state. They are characterized by different relative orientations of the thiophene rings. Due to a low rotational barrier, the sample in solution is characterized by a distribution of relative internal orientations. By applying the Kawski method, we evaluate the average dipole moment of ground and excited states of the three types of conformers. The ground state dipole moments are small and similar for the three types of conformers. On the contrary, dipole moments differ substantially in the excited state. X-ray diffraction of a single crystal confirms the presence of an orientational disorder of thiophene rings. Transient absorption UV-visible spectroscopy experiments allows the identification of the main mechanisms responsible for the large Stokes shift observed in this push-pull molecule. Time dependent spectra provide a picture of the relaxation processes occurring after excitation: the primary step is an internal charge transfer assisted by thiophene ring planarization which occurs on a time scale ranging from 0.88 to 1.3 picoseconds depending on solvent polarity. Moreover, time-resolved fluorescence measurements are consistent with a mechanism involving planarization accompanied by a stabilization of the charge transfer state as observed in polar solvents. In the latter, longer fluorescence lifetimes are observed along with a quantum yield decrease due to the activation of specific non-radiative relaxation channels. The photophysical behavior of 4,7-dithien-2-yl-2,1,3-benzothiadiazole in a solid matrix of polymethyl methacrylate is similar to that observed in solution, but the overall non-radiative process rate is slow with respect to that in the liquid phase. As a consequence, the radiative processes are enhanced giving rise to a fluorescence quantum yield of 90%. Such behavior is consistent with the proposed relaxation model.</abstract><cop>England</cop><pmid>28518198</pmid><doi>10.1039/c6cp08721c</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2696-1611</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1463-9076 |
ispartof | Physical chemistry chemical physics : PCCP, 2017, Vol.19 (21), p.13604-13613 |
issn | 1463-9076 1463-9084 |
language | eng |
recordid | cdi_proquest_miscellaneous_1915323726 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Charge transfer Dipole moments Excitation Fluorescence Ground state Mathematical models Solvents Thiophenes |
title | Photophysical properties and excited state dynamics of 4,7-dithien-2-yl-2,1,3-benzothiadiazole |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T17%3A26%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photophysical%20properties%20and%20excited%20state%20dynamics%20of%204,7-dithien-2-yl-2,1,3-benzothiadiazole&rft.jtitle=Physical%20chemistry%20chemical%20physics%20:%20PCCP&rft.au=Iagatti,%20Alessandro&rft.date=2017&rft.volume=19&rft.issue=21&rft.spage=13604&rft.epage=13613&rft.pages=13604-13613&rft.issn=1463-9076&rft.eissn=1463-9084&rft_id=info:doi/10.1039/c6cp08721c&rft_dat=%3Cproquest_cross%3E1915323726%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1900128290&rft_id=info:pmid/28518198&rfr_iscdi=true |