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...

Full description

Saved in:

Bibliographic Details
Published in:	Optical materials Vol. 37; pp. 193 - 199
Main Authors:	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:	Journal Article
Language:	English
Published:	Oxford Elsevier B.V 01-11-2014 Elsevier
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 Organic light emitting diodes Bithiophene disubstituted 1,3,4-thiadiazoles Host/guest electroluminescent system Biphenyl Oxadiazole derivatives Benzenic compound Electroluminescence Organic light-emitting devices Organic compounds
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

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.
AbstractList	[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. 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 C sub( alpha ) 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 (750 cd/m super(2)) was measured for 2,5-bis(5'-octyl-2,2'-bithiophene-5-yl)-1,3,4-thiadia zole with the luminous efficiency exceeding 0.4 cd/A.
Author	Kurach, Ewa Mauro, Anna De Girolamo Del Luszczynska, Beata Maglione, Maria Grazia Aprano, Salvatore Glowacki, Ireneusz Tassini, Paolo Pandolfi, Giuseppe Minarini, Carla Grykien, Remigiusz Rybakiewicz, Renata Pron, Adam Zagorska, Malgorzata Kotwica, Kamil Fasolino, Tommaso Rega, Romina
Author_xml	– sequence: 1 givenname: Remigiusz surname: Grykien fullname: Grykien, Remigiusz organization: Department of Molecular Physics, Technical University of Lodz, Zeromskiego 116, 90924 Lodz, Poland – sequence: 2 givenname: Beata surname: Luszczynska fullname: Luszczynska, Beata email: beata.luszczynska@p.lodz.pl organization: Department of Molecular Physics, Technical University of Lodz, Zeromskiego 116, 90924 Lodz, Poland – sequence: 3 givenname: Ireneusz surname: Glowacki fullname: Glowacki, Ireneusz organization: Department of Molecular Physics, Technical University of Lodz, Zeromskiego 116, 90924 Lodz, Poland – sequence: 4 givenname: Ewa surname: Kurach fullname: Kurach, Ewa organization: Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00664 Warsaw, Poland – sequence: 5 givenname: Renata surname: Rybakiewicz fullname: Rybakiewicz, Renata organization: Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00664 Warsaw, Poland – sequence: 6 givenname: Kamil surname: Kotwica fullname: Kotwica, Kamil organization: Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00664 Warsaw, Poland – sequence: 7 givenname: Malgorzata surname: Zagorska fullname: Zagorska, Malgorzata organization: Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00664 Warsaw, Poland – sequence: 8 givenname: Adam surname: Pron fullname: Pron, Adam organization: Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00664 Warsaw, Poland – sequence: 9 givenname: Paolo surname: Tassini fullname: Tassini, Paolo organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 10 givenname: Maria Grazia surname: Maglione fullname: Maglione, Maria Grazia organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 11 givenname: Anna De Girolamo Del surname: Mauro fullname: Mauro, Anna De Girolamo Del organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 12 givenname: Tommaso surname: Fasolino fullname: Fasolino, Tommaso organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 13 givenname: Romina surname: Rega fullname: Rega, Romina organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 14 givenname: Giuseppe surname: Pandolfi fullname: Pandolfi, Giuseppe organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 15 givenname: Carla surname: Minarini fullname: Minarini, Carla organization: ENEA C.R. Portici, P.le E. Fermi no. 1, Località Granatello, 80055 Portici, NA, Italy – sequence: 16 givenname: Salvatore surname: Aprano fullname: Aprano, Salvatore organization: SESMAT S.r.l., S.S.7 Appia no.36, 82018 San Giorgio del Sannio, BN, Italy
BackLink	http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28893438$$DView record in Pascal Francis
BookMark	eNp9kUuLFTEQhYOM4J3Rf-AiG8HFdJtHpx8bQYbxAQO60HVIJ9W369KdtEl6QH-PP9Rc7uDSTbKoU-dw6rsmVz54IOQ1ZzVnvH13qsOWV5NrwXhTM1UzIZ-RA-87WXGhxBU5sEGoSjZt94Jcp3RijAnVtgfy59sccqio8Y7CAjbHsOwrekgWfKZbDBvEjJBomOiIecawzeCBOkz7mDLmPYOj_FbeNlWZGofmd1iK_uyYZ8BIzbYtaE3G4KkpA5vxEagN61Zq-Jwoehri0Xi0dMHjnCmsmDP6Y0kJDtJL8nwyS4JXT_8N-fHx_vvd5-rh66cvdx8eKtvIIVeGO6d60woLIx97NvGhE-WdmtbyYXJg1NCqboJBWtWLTjZMwAhtL_tmMMzJG_L24ltq_9whZb1iucOyGA9hT5q3ijey7URfpM1FamNIKcKkt4irib80Z_oMRZ_0BYo-Q9FM6QKlrL15SjDJmmWKxltM_3ZF3w-ykWf79xcdlLqPCFEni-AtOIwFknYB_x_0F3liqpY
CitedBy_id	crossref_primary_10_1016_j_saa_2016_01_034 crossref_primary_10_1246_bcsj_20220107 crossref_primary_10_3762_bjoc_13_34 crossref_primary_10_1002_macp_201600222 crossref_primary_10_1002_ajoc_202100745 crossref_primary_10_1002_jhet_2743 crossref_primary_10_1021_acs_jpcc_5b01557 crossref_primary_10_3762_bjoc_10_165 crossref_primary_10_21597_jist_426556 crossref_primary_10_3390_ma14112714 crossref_primary_10_1021_acs_joc_3c00589 crossref_primary_10_1016_j_dyepig_2021_109248 crossref_primary_10_3390_cryst12030434 crossref_primary_10_1016_j_optmat_2017_11_019 crossref_primary_10_1007_s10853_015_9529_4 crossref_primary_10_1016_j_optmat_2015_07_011 crossref_primary_10_1016_j_tet_2017_06_006
Cites_doi	10.1002/anie.200701920 10.1007/s13391-011-0601-1 10.1007/978-3-540-38235-5_24 10.1063/1.368981 10.1016/S0925-3467(97)00145-6 10.1039/c0cs00204f 10.1016/j.orgel.2005.01.002 10.1039/c3cs35440g 10.1016/j.displa.2004.09.016 10.1021/cm101937p 10.1002/1521-4095(20020916)14:18<1317::AID-ADMA1317>3.0.CO;2-S 10.1246/cl.2001.420 10.1021/jp4033832 10.1021/cr0501386 10.1002/adma.200400670 10.1039/b907999h 10.1002/adma.200305621 10.1016/j.tet.2007.02.051 10.1039/b415587d 10.1063/1.124258 10.1063/1.1404995 10.1063/1.98799 10.1002/polb.10648 10.1002/ejoc.200900964 10.1088/0022-3727/43/29/295101 10.1002/adma.201002636 10.1016/j.orgel.2009.02.006 10.1039/a902800e 10.1016/0032-3861(96)81597-7 10.1063/1.126173 10.1016/j.synthmet.2013.06.023 10.1039/C0CP01553A 10.1016/S1369-7021(10)70083-3 10.1002/pi.2915 10.1007/s13391-013-3061-y 10.1021/cr8004229 10.1039/b922714h 10.1021/cr900357e 10.1063/1.1469692 10.1063/1.368299
ContentType	Journal Article
Copyright	2014 Elsevier B.V. 2015 INIST-CNRS
Copyright_xml	– notice: 2014 Elsevier B.V. – notice: 2015 INIST-CNRS
DBID	IQODW AAYXX CITATION 7SP 7U5 8FD H8D L7M
DOI	10.1016/j.optmat.2014.05.023
DatabaseName	Pascal-Francis CrossRef Electronics & Communications Abstracts Solid State and Superconductivity Abstracts Technology Research Database Aerospace Database Advanced Technologies Database with Aerospace
DatabaseTitle	CrossRef Aerospace Database Solid State and Superconductivity Abstracts Technology Research Database Advanced Technologies Database with Aerospace Electronics & Communications Abstracts
DatabaseTitleList	Aerospace Database
DeliveryMethod	fulltext_linktorsrc
Discipline	Physics Applied Sciences
EISSN	1873-1252
EndPage	199
ExternalDocumentID	10_1016_j_optmat_2014_05_023 28893438 S092534671400278X
GroupedDBID	--K --M .DC .~1 0R~ 123 1B1 1RT 1~. 1~5 29N 4.4 457 4G. 53G 5VS 7-5 71M 8P~ 9JN AABXZ AACTN AAEDT AAEDW AAEPC AAIAV AAIKJ AAKOC AALRI AAOAW AAQFI AAXUO ABFNM ABJNI ABMAC ABNEU ABTAH ABXDB ABXRA ABYKQ ACDAQ ACFVG ACGFS ACNNM ACRLP ADBBV ADEZE AEBSH AEKER AENEX AEZYN AFFNX AFKWA AFRZQ AFTJW AGHFR AGUBO AGYEJ AHHHB AIEXJ AIKHN AITUG AIVDX AJBFU AJOXV ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ ASPBG AVWKF AXJTR AZFZN BBWZM BKOJK BLXMC CS3 DU5 EBS EFJIC EFLBG EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU FYGXN G-2 G-Q GBLVA HMV HVGLF HZ~ IHE J1W KOM M24 M38 M41 MAGPM MO0 N9A NDZJH O-L O9- OAUVE OGIMB OZT P-8 P-9 P2P PC. Q38 R2- RIG RNS ROL RPZ SDF SDG SES SEW SMS SPC SPCBC SPD SPG SSM SSQ SSZ T5K UHS WUQ XPP ZMT ZY4 ~G- AALMO ABPIF ABPTK ADALY IPNFZ IQODW AAXKI AAYXX AFJKZ AKRWK CITATION 7SP 7U5 8FD H8D L7M
ID	FETCH-LOGICAL-c439t-a1dd58a62ceb1b80f19720f1f46c19fdea59657fe93c58273402ebe683849a0d3
ISSN	0925-3467
IngestDate	Fri Oct 25 07:35:49 EDT 2024 Thu Sep 26 16:28:10 EDT 2024 Fri Nov 25 01:09:11 EST 2022 Fri Feb 23 02:31:36 EST 2024
IsPeerReviewed	true
IsScholarly	true
Keywords	Organic light emitting diodes Bithiophene disubstituted 1,3,4-thiadiazoles Host/guest electroluminescent system Biphenyl Oxadiazole derivatives Benzenic compound Electroluminescence Organic light-emitting devices Organic compounds
Language	English
License	CC BY 4.0
LinkModel	OpenURL
MergedId	FETCHMERGED-LOGICAL-c439t-a1dd58a62ceb1b80f19720f1f46c19fdea59657fe93c58273402ebe683849a0d3
Notes	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
PQID	1651436728
PQPubID	23500
PageCount	7
ParticipantIDs	proquest_miscellaneous_1651436728 crossref_primary_10_1016_j_optmat_2014_05_023 pascalfrancis_primary_28893438 elsevier_sciencedirect_doi_10_1016_j_optmat_2014_05_023
PublicationCentury	2000
PublicationDate	2014-11-01
PublicationDateYYYYMMDD	2014-11-01
PublicationDate_xml	– month: 11 year: 2014 text: 2014-11-01 day: 01
PublicationDecade	2010
PublicationPlace	Oxford
PublicationPlace_xml	– name: Oxford
PublicationTitle	Optical materials
PublicationYear	2014
Publisher	Elsevier B.V Elsevier
Publisher_xml	– name: Elsevier B.V – name: Elsevier
References	Pron, Gawrys, Zagorska, Djurado, Demadrille (b0110) 2010; 39 Clavier, Audebert (b0140) 2010; 110 Fariola, Ragni (b0055) 2011; 40 Murphy, Frechet (b0095) 2007; 107 Chang, He, Chen, Guo, Yang (b0170) 2001; 79 Glowacki, Szamel (b0195) 2010; 43 Botiz, Darling (b0020) 2010; 13 Weiss, Krause, Paetzold, Weiss, Krause, Paetzold (b0030) 2007; 46 Cuendias, Hiorns, Cloutet, Vignau, Cramail (b0065) 2010; 59 Noda, Ogawa, Noma, Shirota (b0115) 1999; 9 Tang, Van Slyke (b0005) 1987; 51 Gong, Miomandre, Meallet-Renault, Badre, Galmiche, Tang, Audebert, Clavier (b0130) 2009; 35 Allard, Forster, Souharce, Thiem, Scherf (b0100) 2008; 47 Chen, Chang, He, Pyo, Yang, Kurotaki, Kido (b0165) 2003; 41 Saracoglu (b0135) 2007; 63 Sainova, Miteva, Nothofer, Scherf, Głowacki, Ulanski, Fukijawa, Neher (b0205) 2000; 76 Zhang, Wang, Dai, Liu, Wang, Ma (b0045) 2009; 10 Zhu, Yang (b0010) 2013; 42 Wang, Teng, Ma, Xu, Hou, Yang, Wang, Xu (b0040) 2004; 25 Yang, Neher, Hertel, Daubler (b0190) 2004; 16 Sakai, Itaya, Masuhara, Sasaki, Kawata (b0175) 1996; 37 Kurach, Djurado, Rimarcik, Kornet, Wlostowski, Lukes, Pécaut, Zagorska, Pron (b0145) 2011; 13 Fisyuk, Demadrille, Querner, Zagorska, Bleuse, Pron (b0150) 2005; 29 Borsenberger, Weiss (b0180) 1993 Jiang, Register, Killeen, Thompson, Pschenitzka, Hebner, Strum (b0200) 2002; 91 Gather, Köhnen, Meerholz (b0015) 2011; 23 Baldo, Lamansky, Burrows, Thompson, Forrest (b0070) 1999; 75 Hong, Lee (b0025) 2011; 7 P. Tassini, M. G. Maglione, E. Romanelli, P. Vacca, C. Minarini, Patent US 2009/0066244 A1, March 12, 2009. Shaheen, Jabbour, Morrell, Kawabe, Kippelen, Peyghambarian, Nabor, Schlaf, Mash, Armstrong (b0035) 1998; 84 Campbell, Bradley, Lidzey (b0210) 1998; 9 Mazzeo, Vitale, Della Sala, Anni, Barbarella, Favaretto, Sotgiu, Cingolani, Gigli (b0120) 2005; 17 D’Andrade, Datta, Forrest, Djurovich, Polikarpov, Thompson (b0160) 2005; 6 Kurach, Kotwica, Zapala, Knor, Nowakowski, Djurado, Toman, Pfleger, Zagorska, Pron (b0080) 2013; 117 Aso, Okai, Kawaguchi, Otsubo (b0125) 2001; 30 Mishra, Ma, Baeuerle (b0105) 2009; 109 McCairn, Kreouzis, Turner (b0155) 2010; 20 Xu, Kim, Un Kim, Mi, Cho, Lee, Yoon, Hwang (b0075) 2013; 178 Zhong, Duan, Huang, Wu, Cao (b0060) 2011; 23 Li, Fung, Xie, Lee, Hung, Shi (b0050) 2002; 14 Kim, Granström, Friend, Johansson, Salaneck, Daik, Feast, Cacialli (b0085) 1998; 84 Lee, Lee, Lee, Park (b0185) 2013; 9 Xu (10.1016/j.optmat.2014.05.023_b0075) 2013; 178 Sakai (10.1016/j.optmat.2014.05.023_b0175) 1996; 37 Allard (10.1016/j.optmat.2014.05.023_b0100) 2008; 47 Mazzeo (10.1016/j.optmat.2014.05.023_b0120) 2005; 17 Hong (10.1016/j.optmat.2014.05.023_b0025) 2011; 7 Shaheen (10.1016/j.optmat.2014.05.023_b0035) 1998; 84 Botiz (10.1016/j.optmat.2014.05.023_b0020) 2010; 13 10.1016/j.optmat.2014.05.023_b0090 Sainova (10.1016/j.optmat.2014.05.023_b0205) 2000; 76 Weiss (10.1016/j.optmat.2014.05.023_b0030) 2007; 46 Kurach (10.1016/j.optmat.2014.05.023_b0080) 2013; 117 Baldo (10.1016/j.optmat.2014.05.023_b0070) 1999; 75 Clavier (10.1016/j.optmat.2014.05.023_b0140) 2010; 110 Chen (10.1016/j.optmat.2014.05.023_b0165) 2003; 41 Mishra (10.1016/j.optmat.2014.05.023_b0105) 2009; 109 Campbell (10.1016/j.optmat.2014.05.023_b0210) 1998; 9 Fisyuk (10.1016/j.optmat.2014.05.023_b0150) 2005; 29 Jiang (10.1016/j.optmat.2014.05.023_b0200) 2002; 91 Gather (10.1016/j.optmat.2014.05.023_b0015) 2011; 23 Zhu (10.1016/j.optmat.2014.05.023_b0010) 2013; 42 Murphy (10.1016/j.optmat.2014.05.023_b0095) 2007; 107 Zhong (10.1016/j.optmat.2014.05.023_b0060) 2011; 23 Fariola (10.1016/j.optmat.2014.05.023_b0055) 2011; 40 Gong (10.1016/j.optmat.2014.05.023_b0130) 2009; 35 Chang (10.1016/j.optmat.2014.05.023_b0170) 2001; 79 Tang (10.1016/j.optmat.2014.05.023_b0005) 1987; 51 Li (10.1016/j.optmat.2014.05.023_b0050) 2002; 14 Pron (10.1016/j.optmat.2014.05.023_b0110) 2010; 39 Yang (10.1016/j.optmat.2014.05.023_b0190) 2004; 16 Noda (10.1016/j.optmat.2014.05.023_b0115) 1999; 9 Borsenberger (10.1016/j.optmat.2014.05.023_b0180) 1993 Kim (10.1016/j.optmat.2014.05.023_b0085) 1998; 84 Wang (10.1016/j.optmat.2014.05.023_b0040) 2004; 25 Cuendias (10.1016/j.optmat.2014.05.023_b0065) 2010; 59 Aso (10.1016/j.optmat.2014.05.023_b0125) 2001; 30 Glowacki (10.1016/j.optmat.2014.05.023_b0195) 2010; 43 Kurach (10.1016/j.optmat.2014.05.023_b0145) 2011; 13 McCairn (10.1016/j.optmat.2014.05.023_b0155) 2010; 20 Zhang (10.1016/j.optmat.2014.05.023_b0045) 2009; 10 Saracoglu (10.1016/j.optmat.2014.05.023_b0135) 2007; 63 D’Andrade (10.1016/j.optmat.2014.05.023_b0160) 2005; 6 Lee (10.1016/j.optmat.2014.05.023_b0185) 2013; 9
References_xml	– volume: 23 start-page: 233 year: 2011 end-page: 248 ident: b0015 publication-title: Adv. Mater. contributor: fullname: Meerholz – volume: 84 start-page: 6859 year: 1998 end-page: 6869 ident: b0085 publication-title: J. Appl. Phys. contributor: fullname: Cacialli – volume: 47 start-page: 4070−4098 year: 2008 ident: b0100 publication-title: Angew. Chem. Int. Edit. contributor: fullname: Scherf – volume: 76 start-page: 1810 year: 2000 end-page: 1812 ident: b0205 publication-title: Appl. Phys. Lett. contributor: fullname: Neher – volume: 75 start-page: 4 year: 1999 end-page: 6 ident: b0070 publication-title: Appl. Phys. Lett. contributor: fullname: Forrest – volume: 13 start-page: 2690 year: 2011 end-page: 2700 ident: b0145 publication-title: Phys. Chem. Chem. Phys. contributor: fullname: Pron – volume: 41 start-page: 2681 year: 2003 end-page: 2690 ident: b0165 publication-title: J. Polym. Sci., Part B: Polym. Phys. contributor: fullname: Kido – volume: 84 start-page: 2324 year: 1998 end-page: 2327 ident: b0035 publication-title: J. Appl. Phys. contributor: fullname: Armstrong – volume: 91 start-page: 6717 year: 2002 end-page: 6724 ident: b0200 publication-title: J. Appl. Phys. contributor: fullname: Strum – volume: 30 start-page: 420 year: 2001 end-page: 421 ident: b0125 publication-title: Chem. Lett. contributor: fullname: Otsubo – volume: 14 start-page: 1317 year: 2002 end-page: 1321 ident: b0050 publication-title: Adv. Mater. contributor: fullname: Shi – volume: 59 start-page: 1452 year: 2010 end-page: 1476 ident: b0065 publication-title: Polym. Int. contributor: fullname: Cramail – volume: 107 start-page: 1066 year: 2007 end-page: 1096 ident: b0095 publication-title: Chem. Rev. contributor: fullname: Frechet – volume: 117 start-page: 15316 year: 2013 end-page: 15326 ident: b0080 publication-title: J. Phys. Chem. C contributor: fullname: Pron – volume: 63 start-page: 4199 year: 2007 end-page: 4236 ident: b0135 publication-title: Tetrahedron contributor: fullname: Saracoglu – volume: 7 start-page: 77 year: 2011 end-page: 91 ident: b0025 publication-title: Electron. Mater. Lett. contributor: fullname: Lee – year: 1993 ident: b0180 article-title: Organic Photoreceptors for Imaging Systems contributor: fullname: Weiss – volume: 6 start-page: 11 year: 2005 end-page: 20 ident: b0160 publication-title: Org. Electron. contributor: fullname: Thompson – volume: 23 start-page: 326 year: 2011 end-page: 340 ident: b0060 publication-title: Chem. Mater. contributor: fullname: Cao – volume: 9 start-page: 2177 year: 1999 end-page: 2181 ident: b0115 publication-title: J. Mater. Chem. contributor: fullname: Shirota – volume: 25 start-page: 237 year: 2004 end-page: 239 ident: b0040 publication-title: Displays contributor: fullname: Xu – volume: 9 start-page: 663 year: 2013 end-page: 668 ident: b0185 publication-title: Electron. Mater. Lett. contributor: fullname: Park – volume: 13 start-page: 42 year: 2010 end-page: 51 ident: b0020 publication-title: Mater. Today contributor: fullname: Darling – volume: 42 start-page: 4963 year: 2013 end-page: 4976 ident: b0010 publication-title: Chem. Soc. Rev. contributor: fullname: Yang – volume: 110 start-page: 3299 year: 2010 end-page: 3314 ident: b0140 publication-title: Chem. Rev. contributor: fullname: Audebert – volume: 40 start-page: 3467 year: 2011 end-page: 3482 ident: b0055 publication-title: Chem. Soc. Rev. contributor: fullname: Ragni – volume: 37 start-page: 31 year: 1996 end-page: 43 ident: b0175 publication-title: Polymer contributor: fullname: Kawata – volume: 109 start-page: 1141 year: 2009 end-page: 1176 ident: b0105 publication-title: Chem. Rev. contributor: fullname: Baeuerle – volume: 39 start-page: 2577 year: 2010 end-page: 2632 ident: b0110 publication-title: Chem. Soc. Rev. contributor: fullname: Demadrille – volume: 9 start-page: 114 year: 1998 end-page: 119 ident: b0210 publication-title: Opt. Mater. contributor: fullname: Lidzey – volume: 46 start-page: 321 year: 2007 end-page: 332 ident: b0030 publication-title: Adv. Solid State Phys. contributor: fullname: Paetzold – volume: 29 start-page: 707 year: 2005 end-page: 713 ident: b0150 publication-title: New J. Chem. contributor: fullname: Pron – volume: 20 start-page: 1999 year: 2010 end-page: 2006 ident: b0155 publication-title: J. Mater. Chem. contributor: fullname: Turner – volume: 51 start-page: 913 year: 1987 end-page: 915 ident: b0005 publication-title: Appl. Phys. Lett. contributor: fullname: Van Slyke – volume: 43 start-page: 295101 year: 2010 ident: b0195 publication-title: J. Phys. D Appl. Phys. contributor: fullname: Szamel – volume: 79 start-page: 2088 year: 2001 end-page: 2090 ident: b0170 publication-title: Appl. Phys. Lett. contributor: fullname: Yang – volume: 10 start-page: 491 year: 2009 end-page: 495 ident: b0045 publication-title: Org. Electron. contributor: fullname: Ma – volume: 35 start-page: 6121 year: 2009 end-page: 6128 ident: b0130 publication-title: Eur. J. Org. Chem. contributor: fullname: Clavier – volume: 16 start-page: 161 year: 2004 end-page: 166 ident: b0190 publication-title: Adv. Mater. contributor: fullname: Daubler – volume: 17 start-page: 34−39 year: 2005 ident: b0120 publication-title: Adv. Mater. contributor: fullname: Gigli – volume: 178 start-page: 10 year: 2013 end-page: 17 ident: b0075 publication-title: Synth. Met. contributor: fullname: Hwang – volume: 47 start-page: 4070−4098 year: 2008 ident: 10.1016/j.optmat.2014.05.023_b0100 publication-title: Angew. Chem. Int. Edit. doi: 10.1002/anie.200701920 contributor: fullname: Allard – volume: 7 start-page: 77 year: 2011 ident: 10.1016/j.optmat.2014.05.023_b0025 publication-title: Electron. Mater. Lett. doi: 10.1007/s13391-011-0601-1 contributor: fullname: Hong – volume: 46 start-page: 321 year: 2007 ident: 10.1016/j.optmat.2014.05.023_b0030 publication-title: Adv. Solid State Phys. doi: 10.1007/978-3-540-38235-5_24 contributor: fullname: Weiss – volume: 84 start-page: 6859 year: 1998 ident: 10.1016/j.optmat.2014.05.023_b0085 publication-title: J. Appl. Phys. doi: 10.1063/1.368981 contributor: fullname: Kim – volume: 9 start-page: 114 year: 1998 ident: 10.1016/j.optmat.2014.05.023_b0210 publication-title: Opt. Mater. doi: 10.1016/S0925-3467(97)00145-6 contributor: fullname: Campbell – volume: 40 start-page: 3467 year: 2011 ident: 10.1016/j.optmat.2014.05.023_b0055 publication-title: Chem. Soc. Rev. doi: 10.1039/c0cs00204f contributor: fullname: Fariola – volume: 6 start-page: 11 year: 2005 ident: 10.1016/j.optmat.2014.05.023_b0160 publication-title: Org. Electron. doi: 10.1016/j.orgel.2005.01.002 contributor: fullname: D’Andrade – volume: 42 start-page: 4963 year: 2013 ident: 10.1016/j.optmat.2014.05.023_b0010 publication-title: Chem. Soc. Rev. doi: 10.1039/c3cs35440g contributor: fullname: Zhu – volume: 25 start-page: 237 year: 2004 ident: 10.1016/j.optmat.2014.05.023_b0040 publication-title: Displays doi: 10.1016/j.displa.2004.09.016 contributor: fullname: Wang – volume: 23 start-page: 326 year: 2011 ident: 10.1016/j.optmat.2014.05.023_b0060 publication-title: Chem. Mater. doi: 10.1021/cm101937p contributor: fullname: Zhong – volume: 14 start-page: 1317 year: 2002 ident: 10.1016/j.optmat.2014.05.023_b0050 publication-title: Adv. Mater. doi: 10.1002/1521-4095(20020916)14:18<1317::AID-ADMA1317>3.0.CO;2-S contributor: fullname: Li – volume: 30 start-page: 420 year: 2001 ident: 10.1016/j.optmat.2014.05.023_b0125 publication-title: Chem. Lett. doi: 10.1246/cl.2001.420 contributor: fullname: Aso – volume: 117 start-page: 15316 year: 2013 ident: 10.1016/j.optmat.2014.05.023_b0080 publication-title: J. Phys. Chem. C doi: 10.1021/jp4033832 contributor: fullname: Kurach – volume: 107 start-page: 1066 year: 2007 ident: 10.1016/j.optmat.2014.05.023_b0095 publication-title: Chem. Rev. doi: 10.1021/cr0501386 contributor: fullname: Murphy – volume: 17 start-page: 34−39 year: 2005 ident: 10.1016/j.optmat.2014.05.023_b0120 publication-title: Adv. Mater. doi: 10.1002/adma.200400670 contributor: fullname: Mazzeo – volume: 39 start-page: 2577 year: 2010 ident: 10.1016/j.optmat.2014.05.023_b0110 publication-title: Chem. Soc. Rev. doi: 10.1039/b907999h contributor: fullname: Pron – volume: 16 start-page: 161 year: 2004 ident: 10.1016/j.optmat.2014.05.023_b0190 publication-title: Adv. Mater. doi: 10.1002/adma.200305621 contributor: fullname: Yang – volume: 63 start-page: 4199 year: 2007 ident: 10.1016/j.optmat.2014.05.023_b0135 publication-title: Tetrahedron doi: 10.1016/j.tet.2007.02.051 contributor: fullname: Saracoglu – volume: 29 start-page: 707 year: 2005 ident: 10.1016/j.optmat.2014.05.023_b0150 publication-title: New J. Chem. doi: 10.1039/b415587d contributor: fullname: Fisyuk – volume: 75 start-page: 4 year: 1999 ident: 10.1016/j.optmat.2014.05.023_b0070 publication-title: Appl. Phys. Lett. doi: 10.1063/1.124258 contributor: fullname: Baldo – volume: 79 start-page: 2088 year: 2001 ident: 10.1016/j.optmat.2014.05.023_b0170 publication-title: Appl. Phys. Lett. doi: 10.1063/1.1404995 contributor: fullname: Chang – volume: 51 start-page: 913 year: 1987 ident: 10.1016/j.optmat.2014.05.023_b0005 publication-title: Appl. Phys. Lett. doi: 10.1063/1.98799 contributor: fullname: Tang – ident: 10.1016/j.optmat.2014.05.023_b0090 – volume: 41 start-page: 2681 year: 2003 ident: 10.1016/j.optmat.2014.05.023_b0165 publication-title: J. Polym. Sci., Part B: Polym. Phys. doi: 10.1002/polb.10648 contributor: fullname: Chen – year: 1993 ident: 10.1016/j.optmat.2014.05.023_b0180 contributor: fullname: Borsenberger – volume: 35 start-page: 6121 year: 2009 ident: 10.1016/j.optmat.2014.05.023_b0130 publication-title: Eur. J. Org. Chem. doi: 10.1002/ejoc.200900964 contributor: fullname: Gong – volume: 43 start-page: 295101 year: 2010 ident: 10.1016/j.optmat.2014.05.023_b0195 publication-title: J. Phys. D Appl. Phys. doi: 10.1088/0022-3727/43/29/295101 contributor: fullname: Glowacki – volume: 23 start-page: 233 year: 2011 ident: 10.1016/j.optmat.2014.05.023_b0015 publication-title: Adv. Mater. doi: 10.1002/adma.201002636 contributor: fullname: Gather – volume: 10 start-page: 491 year: 2009 ident: 10.1016/j.optmat.2014.05.023_b0045 publication-title: Org. Electron. doi: 10.1016/j.orgel.2009.02.006 contributor: fullname: Zhang – volume: 9 start-page: 2177 year: 1999 ident: 10.1016/j.optmat.2014.05.023_b0115 publication-title: J. Mater. Chem. doi: 10.1039/a902800e contributor: fullname: Noda – volume: 37 start-page: 31 year: 1996 ident: 10.1016/j.optmat.2014.05.023_b0175 publication-title: Polymer doi: 10.1016/0032-3861(96)81597-7 contributor: fullname: Sakai – volume: 76 start-page: 1810 year: 2000 ident: 10.1016/j.optmat.2014.05.023_b0205 publication-title: Appl. Phys. Lett. doi: 10.1063/1.126173 contributor: fullname: Sainova – volume: 178 start-page: 10 year: 2013 ident: 10.1016/j.optmat.2014.05.023_b0075 publication-title: Synth. Met. doi: 10.1016/j.synthmet.2013.06.023 contributor: fullname: Xu – volume: 13 start-page: 2690 year: 2011 ident: 10.1016/j.optmat.2014.05.023_b0145 publication-title: Phys. Chem. Chem. Phys. doi: 10.1039/C0CP01553A contributor: fullname: Kurach – volume: 13 start-page: 42 year: 2010 ident: 10.1016/j.optmat.2014.05.023_b0020 publication-title: Mater. Today doi: 10.1016/S1369-7021(10)70083-3 contributor: fullname: Botiz – volume: 59 start-page: 1452 year: 2010 ident: 10.1016/j.optmat.2014.05.023_b0065 publication-title: Polym. Int. doi: 10.1002/pi.2915 contributor: fullname: Cuendias – volume: 9 start-page: 663 year: 2013 ident: 10.1016/j.optmat.2014.05.023_b0185 publication-title: Electron. Mater. Lett. doi: 10.1007/s13391-013-3061-y contributor: fullname: Lee – volume: 109 start-page: 1141 year: 2009 ident: 10.1016/j.optmat.2014.05.023_b0105 publication-title: Chem. Rev. doi: 10.1021/cr8004229 contributor: fullname: Mishra – volume: 20 start-page: 1999 year: 2010 ident: 10.1016/j.optmat.2014.05.023_b0155 publication-title: J. Mater. Chem. doi: 10.1039/b922714h contributor: fullname: McCairn – volume: 110 start-page: 3299 year: 2010 ident: 10.1016/j.optmat.2014.05.023_b0140 publication-title: Chem. Rev. doi: 10.1021/cr900357e contributor: fullname: Clavier – volume: 91 start-page: 6717 year: 2002 ident: 10.1016/j.optmat.2014.05.023_b0200 publication-title: J. Appl. Phys. doi: 10.1063/1.1469692 contributor: fullname: Jiang – volume: 84 start-page: 2324 year: 1998 ident: 10.1016/j.optmat.2014.05.023_b0035 publication-title: J. Appl. Phys. doi: 10.1063/1.368299 contributor: fullname: Shaheen
SSID	ssj0002566
Score	2.2257497
Snippet	[Display omitted] •Solution processable organic light emitting diodes (OLEDs).•Bithiophene disubstituted 1,3,4-thiadiazoles as a new class of bluish-green... Photo- and electroluminescence of five bithiophene disubstituted 1,3,4-thiadiazoles, constituting a new class of solution processable materials for organic...
SourceID	proquest crossref pascalfrancis elsevier
SourceType	Aggregation Database Index Database Publisher
StartPage	193
SubjectTerms	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
URI	https://dx.doi.org/10.1016/j.optmat.2014.05.023 https://search.proquest.com/docview/1651436728
Volume	37
hasFullText	1
inHoldings	1
isFullTextHit
isPrint
link	http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1da9swFBVpymAwxj5Z2q1osLfUxR-yLT-WLqPdYBtrB3kzimS3bjfbxAml-T37obvSle2EMPYBe4gJTmyLnJOrI-noXkLesFDMRKLJK2IYoHDJHAG61BEhk9DBBbkwyapPz-OPU_52wiaDQZvZoz_3X5GGc4C13jn7F2h3N4UT8B4whyOgDsc_wv3zVbWoHLMmYEvcQPjR3nZtw9R2rFo7qTHV7KxYXBU6sQAoTVU0EEPQOKDGEN9OAngxB76h0xesdOKn1m5ZzMdrC9-6VI0wYdMY1KvSbJorSlsxSo6_6QmAcfa9QI-1KiplnYtWFX-qcUYd1DP-RL0r6O6mwMD4Ba6_LJbNqrMQwXu5uiubG6weneEuu9aZeiskVuQ-M0k7--s-LOcC619NbsX6pIfH7O6_biZuazcOTmn6oRMwLO9xlGFA53HggIjbiPiYZsaGbA8rNNre38NyTVsdC85xXB9V9QJ-C20JZCbjqx_0HWlnbzzXLdENgdGrXtmd7pBdHwIhG5Ld47PJ9H2nFUBwmtX0tuXt5k7jQNx-1q_E04NaNABTjrVYtmSF0UoXj8hDO8ihx8jOx2SQlU_IPWM2ls1T8gM5SoFNdJujtOcorXK6xlG6wVHqHQaHm_w0dzT8pGv8pAI-MPykPT9pUVLLT2r4SVt-UuTnM_L13eTi5NSx1UIcCaJ64QhPqZCLyJcgP2bczXVBPTjmLJJekqtMhEkUxnmWBDLkOquT60MEi3jAWSJcFTwnwxKa8IJQN58lLhd-5Hkg2JWEUcgsihOZMMaUF4Uj4rQwpDUmhUlbt-R1irClGrbUDVOAbUTiFqvUClsUrCnQ6zdXHmxA2z3O5zDQYAEfkdct1il0DHq1T5RZtWxSaCeMhaLY53v__Ph9cr__970kw8V8mb0iO41aHlgm_wThj-d7
link.rule.ids	315,782,786,27934,27935
linkProvider	Elsevier
openUrl	ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Photo-+and+electroluminescent+properties+of+bithiophene+disubstituted+1%2C3%2C4-thiadiazoles+and+their+application+as+active+components+in+organic+light+emitting+diodes&rft.jtitle=Optical+materials&rft.au=Grykien%2C+Remigiusz&rft.au=Luszczynska%2C+Beata&rft.au=Glowacki%2C+Ireneusz&rft.au=Kurach%2C+Ewa&rft.date=2014-11-01&rft.pub=Elsevier+B.V&rft.issn=0925-3467&rft.eissn=1873-1252&rft.volume=37&rft.spage=193&rft.epage=199&rft_id=info:doi/10.1016%2Fj.optmat.2014.05.023&rft.externalDocID=S092534671400278X
thumbnail_l	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0925-3467&client=summon
thumbnail_m	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0925-3467&client=summon
thumbnail_s	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0925-3467&client=summon