Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes

[Display omitted] •Solution processable organic light emitting diodes (OLEDs).•Bithiophene disubstituted 1,3,4-thiadiazoles as a new class of bluish-green emitters.•Effective guest–host electroluminescent systems for application in OLEDs. Photo- and electroluminescence of five bithiophene disubstitu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Optical materials 2014-11, Vol.37, p.193-199
Hauptverfasser: Grykien, Remigiusz, Luszczynska, Beata, Glowacki, Ireneusz, Kurach, Ewa, Rybakiewicz, Renata, Kotwica, Kamil, Zagorska, Malgorzata, Pron, Adam, Tassini, Paolo, Maglione, Maria Grazia, Mauro, Anna De Girolamo Del, Fasolino, Tommaso, Rega, Romina, Pandolfi, Giuseppe, Minarini, Carla, Aprano, Salvatore
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 199
container_issue
container_start_page 193
container_title Optical materials
container_volume 37
creator Grykien, Remigiusz
Luszczynska, Beata
Glowacki, Ireneusz
Kurach, Ewa
Rybakiewicz, Renata
Kotwica, Kamil
Zagorska, Malgorzata
Pron, Adam
Tassini, Paolo
Maglione, Maria Grazia
Mauro, Anna De Girolamo Del
Fasolino, Tommaso
Rega, Romina
Pandolfi, Giuseppe
Minarini, Carla
Aprano, Salvatore
description [Display omitted] •Solution processable organic light emitting diodes (OLEDs).•Bithiophene disubstituted 1,3,4-thiadiazoles as a new class of bluish-green emitters.•Effective guest–host electroluminescent systems for application in OLEDs. Photo- and electroluminescence of five bithiophene disubstituted 1,3,4-thiadiazoles, constituting a new class of solution processable materials for organic opto-electronics, were studied. It was found that the introduction of alkyl solubilizing substituents bathochromically shifted the photo- and electroluminescence bands. The most pronounced effect was observed for the substitution at the Cα position which changed the emitting light color from bluish to green. All five derivatives were tested in host/guest type organic light emitting diodes (OLEDs) with either poly(N-vinylcarbazole) (PVK) or poly(N-vinylcarbazole)+2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole (PVK+PBD) matrices. The latter matrix turned out especially well suited for these guest molecules yielding devices of varying color coordinates. The best luminance (750cd/m2) was measured for 2,5-bis(5′-octyl-2,2′-bithiophene-5-yl)-1,3,4-thiadiazole with the luminous efficiency exceeding 0.4cd/A.
doi_str_mv 10.1016/j.optmat.2014.05.023
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1651436728</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S092534671400278X</els_id><sourcerecordid>1651436728</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-a1dd58a62ceb1b80f19720f1f46c19fdea59657fe93c58273402ebe683849a0d3</originalsourceid><addsrcrecordid>eNp9kc1u1TAQhSMEEpfCG7DwBolFk_ovTrJBQlWBSpVgAWvLsSc3c5XYwXYqwfPwoPjqVizZzCzmzDma-arqLaMNo0zdnJqw5dXkhlMmG9o2lItn1YH1nagZb_nz6kAH3tZCqu5l9SqlE6WUt0odqj_f5pBDTYx3BBawOYZlX9FDsuAz2WLYIGaERMJERswzhm0GD8Rh2seUMe8ZHGHX4lrWZWocmt9hKfqzY54BIzHbtqA1GYMnpgxsxkcgNqxb8CUkEfQkxKPxaMmCxzkTWDFn9MeSEhyk19WLySwJ3jz1q-rHp7vvt1_qh6-f728_PtRWiiHXhjnX9kZxCyMbezqxoeOlTlJZNkwOTDuotptgELbteSck5TCC6kUvB0OduKreX3zL2T93SFmvWP6wLMZD2JNmqmVSqI73RSovUhtDShEmvUVcTfylGdVnKPqkL1D0GYqmrS5Qytq7pwSTrFmmaLzF9G-X9_0gpDjbf7jooJz7iBB1sgjegsNYIGkX8P9BfwHEO6jY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1651436728</pqid></control><display><type>article</type><title>Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Grykien, Remigiusz ; Luszczynska, Beata ; Glowacki, Ireneusz ; Kurach, Ewa ; Rybakiewicz, Renata ; Kotwica, Kamil ; Zagorska, Malgorzata ; Pron, Adam ; Tassini, Paolo ; Maglione, Maria Grazia ; Mauro, Anna De Girolamo Del ; Fasolino, Tommaso ; Rega, Romina ; Pandolfi, Giuseppe ; Minarini, Carla ; Aprano, Salvatore</creator><creatorcontrib>Grykien, Remigiusz ; Luszczynska, Beata ; Glowacki, Ireneusz ; Kurach, Ewa ; Rybakiewicz, Renata ; Kotwica, Kamil ; Zagorska, Malgorzata ; Pron, Adam ; Tassini, Paolo ; Maglione, Maria Grazia ; Mauro, Anna De Girolamo Del ; Fasolino, Tommaso ; Rega, Romina ; Pandolfi, Giuseppe ; Minarini, Carla ; Aprano, Salvatore</creatorcontrib><description>[Display omitted] •Solution processable organic light emitting diodes (OLEDs).•Bithiophene disubstituted 1,3,4-thiadiazoles as a new class of bluish-green emitters.•Effective guest–host electroluminescent systems for application in OLEDs. Photo- and electroluminescence of five bithiophene disubstituted 1,3,4-thiadiazoles, constituting a new class of solution processable materials for organic opto-electronics, were studied. It was found that the introduction of alkyl solubilizing substituents bathochromically shifted the photo- and electroluminescence bands. The most pronounced effect was observed for the substitution at the Cα position which changed the emitting light color from bluish to green. All five derivatives were tested in host/guest type organic light emitting diodes (OLEDs) with either poly(N-vinylcarbazole) (PVK) or poly(N-vinylcarbazole)+2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole (PVK+PBD) matrices. The latter matrix turned out especially well suited for these guest molecules yielding devices of varying color coordinates. The best luminance (750cd/m2) was measured for 2,5-bis(5′-octyl-2,2′-bithiophene-5-yl)-1,3,4-thiadiazole with the luminous efficiency exceeding 0.4cd/A.</description><identifier>ISSN: 0925-3467</identifier><identifier>EISSN: 1873-1252</identifier><identifier>DOI: 10.1016/j.optmat.2014.05.023</identifier><language>eng</language><publisher>Oxford: Elsevier B.V</publisher><subject>Applied sciences ; Bands ; Bithiophene disubstituted 1,3,4-thiadiazoles ; Color ; Derivatives ; Electroluminescence ; Electronics ; Exact sciences and technology ; Host/guest electroluminescent system ; Luminance ; Optoelectronic devices ; Optoelectronics ; Organic light emitting diodes ; Polyvinyl carbazole ; Semiconductor electronics. Microelectronics. Optoelectronics. Solid state devices</subject><ispartof>Optical materials, 2014-11, Vol.37, p.193-199</ispartof><rights>2014 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-a1dd58a62ceb1b80f19720f1f46c19fdea59657fe93c58273402ebe683849a0d3</citedby><cites>FETCH-LOGICAL-c439t-a1dd58a62ceb1b80f19720f1f46c19fdea59657fe93c58273402ebe683849a0d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.optmat.2014.05.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28893438$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Grykien, Remigiusz</creatorcontrib><creatorcontrib>Luszczynska, Beata</creatorcontrib><creatorcontrib>Glowacki, Ireneusz</creatorcontrib><creatorcontrib>Kurach, Ewa</creatorcontrib><creatorcontrib>Rybakiewicz, Renata</creatorcontrib><creatorcontrib>Kotwica, Kamil</creatorcontrib><creatorcontrib>Zagorska, Malgorzata</creatorcontrib><creatorcontrib>Pron, Adam</creatorcontrib><creatorcontrib>Tassini, Paolo</creatorcontrib><creatorcontrib>Maglione, Maria Grazia</creatorcontrib><creatorcontrib>Mauro, Anna De Girolamo Del</creatorcontrib><creatorcontrib>Fasolino, Tommaso</creatorcontrib><creatorcontrib>Rega, Romina</creatorcontrib><creatorcontrib>Pandolfi, Giuseppe</creatorcontrib><creatorcontrib>Minarini, Carla</creatorcontrib><creatorcontrib>Aprano, Salvatore</creatorcontrib><title>Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes</title><title>Optical materials</title><description>[Display omitted] •Solution processable organic light emitting diodes (OLEDs).•Bithiophene disubstituted 1,3,4-thiadiazoles as a new class of bluish-green emitters.•Effective guest–host electroluminescent systems for application in OLEDs. Photo- and electroluminescence of five bithiophene disubstituted 1,3,4-thiadiazoles, constituting a new class of solution processable materials for organic opto-electronics, were studied. It was found that the introduction of alkyl solubilizing substituents bathochromically shifted the photo- and electroluminescence bands. The most pronounced effect was observed for the substitution at the Cα position which changed the emitting light color from bluish to green. All five derivatives were tested in host/guest type organic light emitting diodes (OLEDs) with either poly(N-vinylcarbazole) (PVK) or poly(N-vinylcarbazole)+2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole (PVK+PBD) matrices. The latter matrix turned out especially well suited for these guest molecules yielding devices of varying color coordinates. The best luminance (750cd/m2) was measured for 2,5-bis(5′-octyl-2,2′-bithiophene-5-yl)-1,3,4-thiadiazole with the luminous efficiency exceeding 0.4cd/A.</description><subject>Applied sciences</subject><subject>Bands</subject><subject>Bithiophene disubstituted 1,3,4-thiadiazoles</subject><subject>Color</subject><subject>Derivatives</subject><subject>Electroluminescence</subject><subject>Electronics</subject><subject>Exact sciences and technology</subject><subject>Host/guest electroluminescent system</subject><subject>Luminance</subject><subject>Optoelectronic devices</subject><subject>Optoelectronics</subject><subject>Organic light emitting diodes</subject><subject>Polyvinyl carbazole</subject><subject>Semiconductor electronics. Microelectronics. Optoelectronics. Solid state devices</subject><issn>0925-3467</issn><issn>1873-1252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1TAQhSMEEpfCG7DwBolFk_ovTrJBQlWBSpVgAWvLsSc3c5XYwXYqwfPwoPjqVizZzCzmzDma-arqLaMNo0zdnJqw5dXkhlMmG9o2lItn1YH1nagZb_nz6kAH3tZCqu5l9SqlE6WUt0odqj_f5pBDTYx3BBawOYZlX9FDsuAz2WLYIGaERMJERswzhm0GD8Rh2seUMe8ZHGHX4lrWZWocmt9hKfqzY54BIzHbtqA1GYMnpgxsxkcgNqxb8CUkEfQkxKPxaMmCxzkTWDFn9MeSEhyk19WLySwJ3jz1q-rHp7vvt1_qh6-f728_PtRWiiHXhjnX9kZxCyMbezqxoeOlTlJZNkwOTDuotptgELbteSck5TCC6kUvB0OduKreX3zL2T93SFmvWP6wLMZD2JNmqmVSqI73RSovUhtDShEmvUVcTfylGdVnKPqkL1D0GYqmrS5Qytq7pwSTrFmmaLzF9G-X9_0gpDjbf7jooJz7iBB1sgjegsNYIGkX8P9BfwHEO6jY</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Grykien, Remigiusz</creator><creator>Luszczynska, Beata</creator><creator>Glowacki, Ireneusz</creator><creator>Kurach, Ewa</creator><creator>Rybakiewicz, Renata</creator><creator>Kotwica, Kamil</creator><creator>Zagorska, Malgorzata</creator><creator>Pron, Adam</creator><creator>Tassini, Paolo</creator><creator>Maglione, Maria Grazia</creator><creator>Mauro, Anna De Girolamo Del</creator><creator>Fasolino, Tommaso</creator><creator>Rega, Romina</creator><creator>Pandolfi, Giuseppe</creator><creator>Minarini, Carla</creator><creator>Aprano, Salvatore</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7U5</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20141101</creationdate><title>Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes</title><author>Grykien, Remigiusz ; Luszczynska, Beata ; Glowacki, Ireneusz ; Kurach, Ewa ; Rybakiewicz, Renata ; Kotwica, Kamil ; Zagorska, Malgorzata ; Pron, Adam ; Tassini, Paolo ; Maglione, Maria Grazia ; Mauro, Anna De Girolamo Del ; Fasolino, Tommaso ; Rega, Romina ; Pandolfi, Giuseppe ; Minarini, Carla ; Aprano, Salvatore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-a1dd58a62ceb1b80f19720f1f46c19fdea59657fe93c58273402ebe683849a0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Applied sciences</topic><topic>Bands</topic><topic>Bithiophene disubstituted 1,3,4-thiadiazoles</topic><topic>Color</topic><topic>Derivatives</topic><topic>Electroluminescence</topic><topic>Electronics</topic><topic>Exact sciences and technology</topic><topic>Host/guest electroluminescent system</topic><topic>Luminance</topic><topic>Optoelectronic devices</topic><topic>Optoelectronics</topic><topic>Organic light emitting diodes</topic><topic>Polyvinyl carbazole</topic><topic>Semiconductor electronics. Microelectronics. Optoelectronics. Solid state devices</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grykien, Remigiusz</creatorcontrib><creatorcontrib>Luszczynska, Beata</creatorcontrib><creatorcontrib>Glowacki, Ireneusz</creatorcontrib><creatorcontrib>Kurach, Ewa</creatorcontrib><creatorcontrib>Rybakiewicz, Renata</creatorcontrib><creatorcontrib>Kotwica, Kamil</creatorcontrib><creatorcontrib>Zagorska, Malgorzata</creatorcontrib><creatorcontrib>Pron, Adam</creatorcontrib><creatorcontrib>Tassini, Paolo</creatorcontrib><creatorcontrib>Maglione, Maria Grazia</creatorcontrib><creatorcontrib>Mauro, Anna De Girolamo Del</creatorcontrib><creatorcontrib>Fasolino, Tommaso</creatorcontrib><creatorcontrib>Rega, Romina</creatorcontrib><creatorcontrib>Pandolfi, Giuseppe</creatorcontrib><creatorcontrib>Minarini, Carla</creatorcontrib><creatorcontrib>Aprano, Salvatore</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Optical materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grykien, Remigiusz</au><au>Luszczynska, Beata</au><au>Glowacki, Ireneusz</au><au>Kurach, Ewa</au><au>Rybakiewicz, Renata</au><au>Kotwica, Kamil</au><au>Zagorska, Malgorzata</au><au>Pron, Adam</au><au>Tassini, Paolo</au><au>Maglione, Maria Grazia</au><au>Mauro, Anna De Girolamo Del</au><au>Fasolino, Tommaso</au><au>Rega, Romina</au><au>Pandolfi, Giuseppe</au><au>Minarini, Carla</au><au>Aprano, Salvatore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes</atitle><jtitle>Optical materials</jtitle><date>2014-11-01</date><risdate>2014</risdate><volume>37</volume><spage>193</spage><epage>199</epage><pages>193-199</pages><issn>0925-3467</issn><eissn>1873-1252</eissn><abstract>[Display omitted] •Solution processable organic light emitting diodes (OLEDs).•Bithiophene disubstituted 1,3,4-thiadiazoles as a new class of bluish-green emitters.•Effective guest–host electroluminescent systems for application in OLEDs. Photo- and electroluminescence of five bithiophene disubstituted 1,3,4-thiadiazoles, constituting a new class of solution processable materials for organic opto-electronics, were studied. It was found that the introduction of alkyl solubilizing substituents bathochromically shifted the photo- and electroluminescence bands. The most pronounced effect was observed for the substitution at the Cα position which changed the emitting light color from bluish to green. All five derivatives were tested in host/guest type organic light emitting diodes (OLEDs) with either poly(N-vinylcarbazole) (PVK) or poly(N-vinylcarbazole)+2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole (PVK+PBD) matrices. The latter matrix turned out especially well suited for these guest molecules yielding devices of varying color coordinates. The best luminance (750cd/m2) was measured for 2,5-bis(5′-octyl-2,2′-bithiophene-5-yl)-1,3,4-thiadiazole with the luminous efficiency exceeding 0.4cd/A.</abstract><cop>Oxford</cop><pub>Elsevier B.V</pub><doi>10.1016/j.optmat.2014.05.023</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0925-3467
ispartof Optical materials, 2014-11, Vol.37, p.193-199
issn 0925-3467
1873-1252
language eng
recordid cdi_proquest_miscellaneous_1651436728
source Elsevier ScienceDirect Journals Complete
subjects Applied sciences
Bands
Bithiophene disubstituted 1,3,4-thiadiazoles
Color
Derivatives
Electroluminescence
Electronics
Exact sciences and technology
Host/guest electroluminescent system
Luminance
Optoelectronic devices
Optoelectronics
Organic light emitting diodes
Polyvinyl carbazole
Semiconductor electronics. Microelectronics. Optoelectronics. Solid state devices
title Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T07%3A29%3A20IST&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=Photo-%20and%20electroluminescent%20properties%20of%20bithiophene%20disubstituted%201,3,4-thiadiazoles%20and%20their%20application%20as%20active%20components%20in%20organic%20light%20emitting%20diodes&rft.jtitle=Optical%20materials&rft.au=Grykien,%20Remigiusz&rft.date=2014-11-01&rft.volume=37&rft.spage=193&rft.epage=199&rft.pages=193-199&rft.issn=0925-3467&rft.eissn=1873-1252&rft_id=info:doi/10.1016/j.optmat.2014.05.023&rft_dat=%3Cproquest_cross%3E1651436728%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=1651436728&rft_id=info:pmid/&rft_els_id=S092534671400278X&rfr_iscdi=true