Photophysics and electrochemistry of a platinum-acetylide disubstituted perylenediimide
The synthesis and photophysical study of a perylene diimide (PDI) functionalised with platinum acetylide units of the type, trans {-C&z.tbd;C-Pt(PBu 3 ) 2 -C&z.tbd;C-Ph} and comparison with a phenylacetylide substituted model compound are reported. The model compound demonstrates typical per...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2014-01, Vol.43 (1), p.85-94 |
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container_title | Dalton transactions : an international journal of inorganic chemistry |
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creator | Llewellyn, Ben A Slater, Anna G Goretzki, Gudrun Easun, Timothy L Sun, Xue-Zhong Davies, E. Stephen Argent, Stephen P Lewis, William Beeby, Andrew George, Michael W Champness, Neil R |
description | The synthesis and photophysical study of a perylene diimide (PDI) functionalised with platinum acetylide units of the type,
trans
{-C&z.tbd;C-Pt(PBu
3
)
2
-C&z.tbd;C-Ph} and comparison with a phenylacetylide substituted model compound are reported. The model compound demonstrates typical perylene absorption and photoluminescence spectra characteristic of singlet excited state formation and decay. The Pt-substitution, however, appears to induce spin-orbit coupling into the chromophore and giving rise to a triplet excited state which was confirmed by transient absorption measurements. This excited state is quenched by oxygen, leading to the formation of singlet oxygen in dichloromethane, recorded by time-resolved near-infrared luminescence measurements.
Photophysical studies of a perylene diimide (PDI) functionalised with platinum acetylide units reveal the formation of a triplet state upon excitation. |
doi_str_mv | 10.1039/c3dt50874a |
format | Article |
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trans
{-C&z.tbd;C-Pt(PBu
3
)
2
-C&z.tbd;C-Ph} and comparison with a phenylacetylide substituted model compound are reported. The model compound demonstrates typical perylene absorption and photoluminescence spectra characteristic of singlet excited state formation and decay. The Pt-substitution, however, appears to induce spin-orbit coupling into the chromophore and giving rise to a triplet excited state which was confirmed by transient absorption measurements. This excited state is quenched by oxygen, leading to the formation of singlet oxygen in dichloromethane, recorded by time-resolved near-infrared luminescence measurements.
Photophysical studies of a perylene diimide (PDI) functionalised with platinum acetylide units reveal the formation of a triplet state upon excitation.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c3dt50874a</identifier><identifier>PMID: 24077462</identifier><language>eng</language><publisher>England</publisher><subject>Decay ; Diimide ; Excitation ; Excitation spectra ; Luminescence ; Platinum ; Quenching (cooling) ; Spectra</subject><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2014-01, Vol.43 (1), p.85-94</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-794830ff1567e26ef6116ffdc18de50de1e3aeddc63c8a755af9750e7ce65f7d3</citedby><cites>FETCH-LOGICAL-c477t-794830ff1567e26ef6116ffdc18de50de1e3aeddc63c8a755af9750e7ce65f7d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24077462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Llewellyn, Ben A</creatorcontrib><creatorcontrib>Slater, Anna G</creatorcontrib><creatorcontrib>Goretzki, Gudrun</creatorcontrib><creatorcontrib>Easun, Timothy L</creatorcontrib><creatorcontrib>Sun, Xue-Zhong</creatorcontrib><creatorcontrib>Davies, E. Stephen</creatorcontrib><creatorcontrib>Argent, Stephen P</creatorcontrib><creatorcontrib>Lewis, William</creatorcontrib><creatorcontrib>Beeby, Andrew</creatorcontrib><creatorcontrib>George, Michael W</creatorcontrib><creatorcontrib>Champness, Neil R</creatorcontrib><title>Photophysics and electrochemistry of a platinum-acetylide disubstituted perylenediimide</title><title>Dalton transactions : an international journal of inorganic chemistry</title><addtitle>Dalton Trans</addtitle><description>The synthesis and photophysical study of a perylene diimide (PDI) functionalised with platinum acetylide units of the type,
trans
{-C&z.tbd;C-Pt(PBu
3
)
2
-C&z.tbd;C-Ph} and comparison with a phenylacetylide substituted model compound are reported. The model compound demonstrates typical perylene absorption and photoluminescence spectra characteristic of singlet excited state formation and decay. The Pt-substitution, however, appears to induce spin-orbit coupling into the chromophore and giving rise to a triplet excited state which was confirmed by transient absorption measurements. This excited state is quenched by oxygen, leading to the formation of singlet oxygen in dichloromethane, recorded by time-resolved near-infrared luminescence measurements.
Photophysical studies of a perylene diimide (PDI) functionalised with platinum acetylide units reveal the formation of a triplet state upon excitation.</description><subject>Decay</subject><subject>Diimide</subject><subject>Excitation</subject><subject>Excitation spectra</subject><subject>Luminescence</subject><subject>Platinum</subject><subject>Quenching (cooling)</subject><subject>Spectra</subject><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkUtLAzEUhYMotj427pVZijCax0wyWZb6hIIuKi6HNLmhkXmZZBbz7x1trUtd3Qvn43DgQ-iM4GuCmbzRzMQcFyJTe2hKMiFSSVm2v_spn6CjEN4xphTn9BBNaIaFyDidoreXdRvbbj0Ep0OiGpNABTr6Vq-hdiH6IWltopKuUtE1fZ0qDXGonIHEuNCvQnSxj2CSDvxQQQPGuXpMT9CBVVWA0-09Rq_3d8v5Y7p4fniazxapHrfFVMisYNhaknMBlIPlhHBrjSaFgRwbIMAUGKM504USea6sFDkGoYHnVhh2jC43vZ1vP3oIsRxXa6gq1UDbh5IIhrGUBWZ_o5nMGKGMk3-gnDKBpZAjerVBtW9D8GDLzrta-aEkuPzSU87Z7fJbz2yEL7a9_aoGs0N_fIzA-QbwQe_SX7_sE_uKlf8</recordid><startdate>20140107</startdate><enddate>20140107</enddate><creator>Llewellyn, Ben A</creator><creator>Slater, Anna G</creator><creator>Goretzki, Gudrun</creator><creator>Easun, Timothy L</creator><creator>Sun, Xue-Zhong</creator><creator>Davies, E. Stephen</creator><creator>Argent, Stephen P</creator><creator>Lewis, William</creator><creator>Beeby, Andrew</creator><creator>George, Michael W</creator><creator>Champness, Neil R</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7SR</scope><scope>8BQ</scope><scope>JG9</scope></search><sort><creationdate>20140107</creationdate><title>Photophysics and electrochemistry of a platinum-acetylide disubstituted perylenediimide</title><author>Llewellyn, Ben A ; Slater, Anna G ; Goretzki, Gudrun ; Easun, Timothy L ; Sun, Xue-Zhong ; Davies, E. Stephen ; Argent, Stephen P ; Lewis, William ; Beeby, Andrew ; George, Michael W ; Champness, Neil R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-794830ff1567e26ef6116ffdc18de50de1e3aeddc63c8a755af9750e7ce65f7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Decay</topic><topic>Diimide</topic><topic>Excitation</topic><topic>Excitation spectra</topic><topic>Luminescence</topic><topic>Platinum</topic><topic>Quenching (cooling)</topic><topic>Spectra</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Llewellyn, Ben A</creatorcontrib><creatorcontrib>Slater, Anna G</creatorcontrib><creatorcontrib>Goretzki, Gudrun</creatorcontrib><creatorcontrib>Easun, Timothy L</creatorcontrib><creatorcontrib>Sun, Xue-Zhong</creatorcontrib><creatorcontrib>Davies, E. Stephen</creatorcontrib><creatorcontrib>Argent, Stephen P</creatorcontrib><creatorcontrib>Lewis, William</creatorcontrib><creatorcontrib>Beeby, Andrew</creatorcontrib><creatorcontrib>George, Michael W</creatorcontrib><creatorcontrib>Champness, Neil R</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Materials Research Database</collection><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Llewellyn, Ben A</au><au>Slater, Anna G</au><au>Goretzki, Gudrun</au><au>Easun, Timothy L</au><au>Sun, Xue-Zhong</au><au>Davies, E. Stephen</au><au>Argent, Stephen P</au><au>Lewis, William</au><au>Beeby, Andrew</au><au>George, Michael W</au><au>Champness, Neil R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photophysics and electrochemistry of a platinum-acetylide disubstituted perylenediimide</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><addtitle>Dalton Trans</addtitle><date>2014-01-07</date><risdate>2014</risdate><volume>43</volume><issue>1</issue><spage>85</spage><epage>94</epage><pages>85-94</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>The synthesis and photophysical study of a perylene diimide (PDI) functionalised with platinum acetylide units of the type,
trans
{-C&z.tbd;C-Pt(PBu
3
)
2
-C&z.tbd;C-Ph} and comparison with a phenylacetylide substituted model compound are reported. The model compound demonstrates typical perylene absorption and photoluminescence spectra characteristic of singlet excited state formation and decay. The Pt-substitution, however, appears to induce spin-orbit coupling into the chromophore and giving rise to a triplet excited state which was confirmed by transient absorption measurements. This excited state is quenched by oxygen, leading to the formation of singlet oxygen in dichloromethane, recorded by time-resolved near-infrared luminescence measurements.
Photophysical studies of a perylene diimide (PDI) functionalised with platinum acetylide units reveal the formation of a triplet state upon excitation.</abstract><cop>England</cop><pmid>24077462</pmid><doi>10.1039/c3dt50874a</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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issn | 1477-9226 1477-9234 |
language | eng |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Decay Diimide Excitation Excitation spectra Luminescence Platinum Quenching (cooling) Spectra |
title | Photophysics and electrochemistry of a platinum-acetylide disubstituted perylenediimide |
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