Spirobifluorene and biphenylaminophenyl fluorene with dimesitylboron as multifunctional electroluminescent materials
•2,7-Bis(dimesitylboryl)-9,9-spirobifluorene (5) as an emitter and electron transport.•Multifunctional 2,7-bis(dimesitylboryl)-9,9-bis(4-diphenylaminophenyl)fluorene (6).•5 and 6 exhibited solvatochromism in the different polarities of solvents.•Device A based on 5 emitted a deep blue light at 444nm...
Saved in:
Published in | Optical materials Vol. 50; pp. 154 - 161 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.12.2015
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | •2,7-Bis(dimesitylboryl)-9,9-spirobifluorene (5) as an emitter and electron transport.•Multifunctional 2,7-bis(dimesitylboryl)-9,9-bis(4-diphenylaminophenyl)fluorene (6).•5 and 6 exhibited solvatochromism in the different polarities of solvents.•Device A based on 5 emitted a deep blue light at 444nm with maximum LE of 1.52cd/A.•Device B based on 6 showed a blue emission at 472nm with maximum LE of 1.93cd/A.
By introducing triarylamino and dimesitylboron groups into fluorene derivatives, two symmetric compounds 2,7-bis(dimesitylboryl)-9,9-spirobifluorene (SFMB) and 2,7-bis(dimesitylboryl)-9,9-bis(4-diphenylaminophenyl)fluorene (PAFMB) were prepared. SFMB and PAFMB exhibited solvatochromism in the different polarities of solvents. Devices A1, A2, A3 and A4 based on SFMB displayed emissions at 444, 448, 528, and 444nm with current efficiencies of 1.06, 1.41, 0.84, and 1.52cd/A, respectively. The blue light was close to the National Television Standards Committee standard blue color (x=0.14, y=0.08). Devices B1, B2, B3 and B4 based on PAFMB emitted lights centered at 484, 472, 513 and 472nm, their current efficiencies were 1.80, 0.1, 1.23 and 1.93cd/A, respectively. The results demonstrated that SFMB and PAFMB were multifunctional materials acted as emitters, and hole- and electron-transporting materials. |
---|---|
AbstractList | •2,7-Bis(dimesitylboryl)-9,9-spirobifluorene (5) as an emitter and electron transport.•Multifunctional 2,7-bis(dimesitylboryl)-9,9-bis(4-diphenylaminophenyl)fluorene (6).•5 and 6 exhibited solvatochromism in the different polarities of solvents.•Device A based on 5 emitted a deep blue light at 444nm with maximum LE of 1.52cd/A.•Device B based on 6 showed a blue emission at 472nm with maximum LE of 1.93cd/A.
By introducing triarylamino and dimesitylboron groups into fluorene derivatives, two symmetric compounds 2,7-bis(dimesitylboryl)-9,9-spirobifluorene (SFMB) and 2,7-bis(dimesitylboryl)-9,9-bis(4-diphenylaminophenyl)fluorene (PAFMB) were prepared. SFMB and PAFMB exhibited solvatochromism in the different polarities of solvents. Devices A1, A2, A3 and A4 based on SFMB displayed emissions at 444, 448, 528, and 444nm with current efficiencies of 1.06, 1.41, 0.84, and 1.52cd/A, respectively. The blue light was close to the National Television Standards Committee standard blue color (x=0.14, y=0.08). Devices B1, B2, B3 and B4 based on PAFMB emitted lights centered at 484, 472, 513 and 472nm, their current efficiencies were 1.80, 0.1, 1.23 and 1.93cd/A, respectively. The results demonstrated that SFMB and PAFMB were multifunctional materials acted as emitters, and hole- and electron-transporting materials. |
Author | Zhang, Wenguan He, Zhiqun Zhao, Shengmin Wang, Yongsheng Pang, Hui |
Author_xml | – sequence: 1 givenname: Wenguan surname: Zhang fullname: Zhang, Wenguan email: wenguanzhang@sina.com organization: Lab of Printing & Packaging Material and Technology-Beijing Area Major Laboratory, Beijing Institute of Graphic Communication, Beijing 102600, PR China – sequence: 2 givenname: Zhiqun surname: He fullname: He, Zhiqun organization: Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University, Beijing 100044, PR China – sequence: 3 givenname: Hui surname: Pang fullname: Pang, Hui organization: Lab of Printing & Packaging Material and Technology-Beijing Area Major Laboratory, Beijing Institute of Graphic Communication, Beijing 102600, PR China – sequence: 4 givenname: Yongsheng surname: Wang fullname: Wang, Yongsheng organization: Lab of Printing & Packaging Material and Technology-Beijing Area Major Laboratory, Beijing Institute of Graphic Communication, Beijing 102600, PR China – sequence: 5 givenname: Shengmin surname: Zhao fullname: Zhao, Shengmin organization: Lab of Printing & Packaging Material and Technology-Beijing Area Major Laboratory, Beijing Institute of Graphic Communication, Beijing 102600, PR China |
BookMark | eNp9kM1qwzAQhEVJoUnaN-hBL2BX_44vhRL6B4Ee2p6NLK-Jgi0FSW7J21fBpceevmXZGWZnhRbOO0DolpKSEqruDqU_plGnkhEq86rMuEBLuql4QZlkC7QkNZMFF6q6QqsYD4QQJpVaovR-tMG3th8mH8AB1q7DrT3uwZ0GPVrn5xH_HXzbtMedHSHadBpaH7zDOuJxGpLtJ2eS9U4PGAYwKfhhyh4QDbiEc0IIVg_xGl32GXDzyzX6fHr82L4Uu7fn1-3DrjCcqFQwobQUObkhqqppL6kArru-45JDayiveduJDVeG9DU13LSMCKU4qzpTyVrwNRKzrwk-xgB9cwx21OHUUNKcm2sOzdxcc27uvM3IsvtZBjnbl4XQRGPBGehsyE81nbf_G_wAmTB_aQ |
CitedBy_id | crossref_primary_10_1016_j_tsf_2016_10_073 crossref_primary_10_1016_j_optmat_2022_112870 crossref_primary_10_1016_j_optmat_2020_110425 crossref_primary_10_1016_j_synthmet_2016_02_009 |
Cites_doi | 10.1557/JMR.1996.0403 10.1016/j.dyepig.2013.09.042 10.1016/j.optmat.2014.12.033 10.1039/b105422h 10.1021/cm020948n 10.1039/c2jm15480c 10.1016/j.synthmet.2010.03.006 10.1016/j.orgel.2008.05.013 10.1063/1.98799 10.1016/j.synthmet.2009.11.004 10.1002/(SICI)1521-4095(199903)11:4<283::AID-ADMA283>3.0.CO;2-V 10.1007/s11426-009-0077-0 10.1016/j.dyepig.2009.10.008 10.1002/adfm.200290007 10.1002/chem.200305579 10.1021/ma981443e 10.1021/cm011671e 10.1002/1521-4095(20020605)14:11<809::AID-ADMA809>3.0.CO;2-8 10.1021/cm048617t 10.1016/j.synthmet.2011.08.042 |
ContentType | Journal Article |
Copyright | 2015 Elsevier B.V. |
Copyright_xml | – notice: 2015 Elsevier B.V. |
DBID | AAYXX CITATION |
DOI | 10.1016/j.optmat.2015.10.015 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Physics |
EISSN | 1873-1252 |
EndPage | 161 |
ExternalDocumentID | 10_1016_j_optmat_2015_10_015 S0925346715300756 |
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- AAXKI AAYXX AFJKZ AKRWK CITATION |
ID | FETCH-LOGICAL-c306t-246a54092c06791f514e3adfd353ebc1393bd4836c0f91c3cb20466327dc75943 |
IEDL.DBID | .~1 |
ISSN | 0925-3467 |
IngestDate | Thu Sep 26 16:28:14 EDT 2024 Fri Feb 23 02:31:37 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | Solvatochromism Fluorene Dimesitylboron Electroluminescent device Multifunctional Triphenylamino |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c306t-246a54092c06791f514e3adfd353ebc1393bd4836c0f91c3cb20466327dc75943 |
PageCount | 8 |
ParticipantIDs | crossref_primary_10_1016_j_optmat_2015_10_015 elsevier_sciencedirect_doi_10_1016_j_optmat_2015_10_015 |
PublicationCentury | 2000 |
PublicationDate | December 2015 2015-12-00 |
PublicationDateYYYYMMDD | 2015-12-01 |
PublicationDate_xml | – month: 12 year: 2015 text: December 2015 |
PublicationDecade | 2010 |
PublicationTitle | Optical materials |
PublicationYear | 2015 |
Publisher | Elsevier B.V |
Publisher_xml | – name: Elsevier B.V |
References | Zhang, He, Wang, Zhao (b0095) 2015; 42 Wen, Xiao, Dong, Zheng, Suning, George (b0040) 2005; 17 Zhang, He, Mu, Zou, Wang, Zhao (b0100) 2010; 85 Ego, Grimsdale, Uckert, Yu, Srdanov, Müllen (b0075) 2002; 14 Kinoshita, Kita, Shirota (b0025) 2002; 12 Rothberg, Lovinger (b0005) 1996; 11 Su, Lin, Tao, Ko, Lin, Sun (b0015) 2002; 14 Kim, Jeon, Kim, Lee, Gong (b0070) 2008; 9 Zhang, He, Hui, Mu, Wang, Zhao, Jing (b0080) 2009; 52 Doi, Kinoshita, Okumoto, Shirota (b0030) 2003; 15 Jia, Bai, McCormick, Liu, Motala, Wang, Seward, Tao, Wang (b0035) 2004; 4 Tang, Van Slyke (b0085) 1987; 51 Zhang, Wang, He, Mu, Zou, Liang, Zhao (b0090) 2010; 160 Pang, Tao, Freiberg, Yang, D’lorio, Wang (b0010) 2002; 12 Ranger, Leclerc (b0060) 1999; 32 Xu, Ye, He, Chen, Xiang, Zhou, Lu, Zhao, Qiu (b0045) 2014; 101 Thangthong, Prachumrak, Tarsang, Keawin, Jungsuttiwong, Sudyoadsuk, Promarak (b0050) 2012; 22 Zhang, He, Wang, Zhao (b0055) 2011; 161 Noda, Ogawa, Shirota (b0020) 1999; 11 Jang, Joo, Yook, Kim, Lee, Lee (b0065) 2010; 160 Kinoshita (10.1016/j.optmat.2015.10.015_b0025) 2002; 12 Tang (10.1016/j.optmat.2015.10.015_b0085) 1987; 51 Doi (10.1016/j.optmat.2015.10.015_b0030) 2003; 15 Zhang (10.1016/j.optmat.2015.10.015_b0100) 2010; 85 Zhang (10.1016/j.optmat.2015.10.015_b0090) 2010; 160 Noda (10.1016/j.optmat.2015.10.015_b0020) 1999; 11 Zhang (10.1016/j.optmat.2015.10.015_b0095) 2015; 42 Wen (10.1016/j.optmat.2015.10.015_b0040) 2005; 17 Thangthong (10.1016/j.optmat.2015.10.015_b0050) 2012; 22 Rothberg (10.1016/j.optmat.2015.10.015_b0005) 1996; 11 Jang (10.1016/j.optmat.2015.10.015_b0065) 2010; 160 Jia (10.1016/j.optmat.2015.10.015_b0035) 2004; 4 Ranger (10.1016/j.optmat.2015.10.015_b0060) 1999; 32 Ego (10.1016/j.optmat.2015.10.015_b0075) 2002; 14 Zhang (10.1016/j.optmat.2015.10.015_b0080) 2009; 52 Xu (10.1016/j.optmat.2015.10.015_b0045) 2014; 101 Zhang (10.1016/j.optmat.2015.10.015_b0055) 2011; 161 Kim (10.1016/j.optmat.2015.10.015_b0070) 2008; 9 Pang (10.1016/j.optmat.2015.10.015_b0010) 2002; 12 Su (10.1016/j.optmat.2015.10.015_b0015) 2002; 14 |
References_xml | – volume: 14 start-page: 1884 year: 2002 end-page: 1890 ident: b0015 article-title: Amorphous 2,3-substituted thiophenes: potential electroluminescent materials publication-title: Chem. Mater. contributor: fullname: Sun – volume: 15 start-page: 1080 year: 2003 end-page: 1089 ident: b0030 article-title: A novel class of emitting amorphous molecular materials with bipolar character for electroluminescence publication-title: Chem. Mater. contributor: fullname: Shirota – volume: 4 start-page: 994 year: 2004 end-page: 1006 ident: b0035 article-title: Three-coordinate organoboron compounds BAr publication-title: Chem. Eur. J. contributor: fullname: Wang – volume: 161 start-page: 2323 year: 2011 end-page: 2328 ident: b0055 article-title: Multifunctional electroluminescent material based on dimesitylboron and α-naphthylamino fluorene bridge publication-title: Synth. Met. contributor: fullname: Zhao – volume: 11 start-page: 3174 year: 1996 end-page: 3187 ident: b0005 article-title: Status of and prospects for organic electroluminescence publication-title: J. Mater. Res. contributor: fullname: Lovinger – volume: 42 start-page: 137 year: 2015 end-page: 143 ident: b0095 article-title: Solution-processable phosphorescence based on iridium-cored small molecules with the trifluoromethyl group publication-title: Opti. Mater. contributor: fullname: Zhao – volume: 14 start-page: 809 year: 2002 end-page: 811 ident: b0075 article-title: Triphenyl- amine-substituted polyfluorene — a stable blue-emitter with improved charge injection for light-emitting diodes publication-title: Adv. Mater. contributor: fullname: Müllen – volume: 101 start-page: 136 year: 2014 end-page: 141 ident: b0045 article-title: Dimesitylboryl-functionalized fluorene derivatives: promising luminophors with good electron-transporting ability for deep blue organic light-emitting diodes publication-title: Dyes Pigm. contributor: fullname: Qiu – volume: 12 start-page: 206 year: 2002 end-page: 212 ident: b0010 article-title: Syntheses, structures, and electroluminescence of new blue luminescent star-shaped compounds based on 1,3,5-triazine and 1,3,5-trisubstituted benzene publication-title: J. Mater. Chem. contributor: fullname: Wang – volume: 12 start-page: 780 year: 2002 end-page: 786 ident: b0025 article-title: A novel family of boron-containing hole-blocking amorphous molecular materials for blue- and blue-violet-emitting organic electroluminescent devices publication-title: Adv. Funct. Mater. contributor: fullname: Shirota – volume: 160 start-page: 1184 year: 2010 end-page: 1188 ident: b0065 article-title: Thermally stable fluorescent blue organic light-emitting diodes using spirobifluorene based anthracene host materials with different substitution position publication-title: Synth. Met. contributor: fullname: Lee – volume: 9 start-page: 797 year: 2008 end-page: 804 ident: b0070 article-title: Blue light-emitting OLED using new spiro[fluorene-7,9’-benzofluorene] host and dopant materials publication-title: Org. Electron. contributor: fullname: Gong – volume: 51 start-page: 913 year: 1987 end-page: 915 ident: b0085 article-title: Organic electroluminescent diodes publication-title: Appl. Phys. Lett. contributor: fullname: Van Slyke – volume: 160 start-page: 354 year: 2010 end-page: 360 ident: b0090 article-title: Efficient electrophosphorescence based on 2-(9,9-diethylfluoren-2-yl)-5-trifluoro- methylpyridine iridium complexes publication-title: Synth. Met. contributor: fullname: Zhao – volume: 17 start-page: 164 year: 2005 end-page: 170 ident: b0040 article-title: Mes publication-title: Chem. Mater. contributor: fullname: George – volume: 52 start-page: 952 year: 2009 end-page: 960 ident: b0080 article-title: Synthesis and light-emitting properties of 2-( publication-title: Sci. China Ser. B contributor: fullname: Jing – volume: 11 start-page: 283 year: 1999 end-page: 285 ident: b0020 article-title: A blue-emitting organic electroluminescent device using a novel emitting amorphous molecular material, 5,5’-bis(dimesitylboryl)-2,2’-bithiophene publication-title: Adv. Mater. contributor: fullname: Shirota – volume: 85 start-page: 86 year: 2010 end-page: 92 ident: b0100 article-title: Red non-doped electroluminescent dyes based on arylamino fumaronitrile derivatives publication-title: Dyes Pigm. contributor: fullname: Zhao – volume: 32 start-page: 3306 year: 1999 end-page: 3313 ident: b0060 article-title: New base-doped polyfluorene derivatives publication-title: Macro-molecules contributor: fullname: Leclerc – volume: 22 start-page: 6869 year: 2012 end-page: 6877 ident: b0050 article-title: Blue light-emitting and hole-transporting materials based on 9,9-bis(4-diphenylaminophenyl)fluorenes for efficient electroluminescent devices publication-title: J. Mater. Chem. contributor: fullname: Promarak – volume: 11 start-page: 3174 year: 1996 ident: 10.1016/j.optmat.2015.10.015_b0005 article-title: Status of and prospects for organic electroluminescence publication-title: J. Mater. Res. doi: 10.1557/JMR.1996.0403 contributor: fullname: Rothberg – volume: 101 start-page: 136 year: 2014 ident: 10.1016/j.optmat.2015.10.015_b0045 article-title: Dimesitylboryl-functionalized fluorene derivatives: promising luminophors with good electron-transporting ability for deep blue organic light-emitting diodes publication-title: Dyes Pigm. doi: 10.1016/j.dyepig.2013.09.042 contributor: fullname: Xu – volume: 42 start-page: 137 year: 2015 ident: 10.1016/j.optmat.2015.10.015_b0095 article-title: Solution-processable phosphorescence based on iridium-cored small molecules with the trifluoromethyl group publication-title: Opti. Mater. doi: 10.1016/j.optmat.2014.12.033 contributor: fullname: Zhang – volume: 12 start-page: 206 year: 2002 ident: 10.1016/j.optmat.2015.10.015_b0010 article-title: Syntheses, structures, and electroluminescence of new blue luminescent star-shaped compounds based on 1,3,5-triazine and 1,3,5-trisubstituted benzene publication-title: J. Mater. Chem. doi: 10.1039/b105422h contributor: fullname: Pang – volume: 15 start-page: 1080 year: 2003 ident: 10.1016/j.optmat.2015.10.015_b0030 article-title: A novel class of emitting amorphous molecular materials with bipolar character for electroluminescence publication-title: Chem. Mater. doi: 10.1021/cm020948n contributor: fullname: Doi – volume: 22 start-page: 6869 year: 2012 ident: 10.1016/j.optmat.2015.10.015_b0050 article-title: Blue light-emitting and hole-transporting materials based on 9,9-bis(4-diphenylaminophenyl)fluorenes for efficient electroluminescent devices publication-title: J. Mater. Chem. doi: 10.1039/c2jm15480c contributor: fullname: Thangthong – volume: 160 start-page: 1184 year: 2010 ident: 10.1016/j.optmat.2015.10.015_b0065 article-title: Thermally stable fluorescent blue organic light-emitting diodes using spirobifluorene based anthracene host materials with different substitution position publication-title: Synth. Met. doi: 10.1016/j.synthmet.2010.03.006 contributor: fullname: Jang – volume: 9 start-page: 797 year: 2008 ident: 10.1016/j.optmat.2015.10.015_b0070 article-title: Blue light-emitting OLED using new spiro[fluorene-7,9’-benzofluorene] host and dopant materials publication-title: Org. Electron. doi: 10.1016/j.orgel.2008.05.013 contributor: fullname: Kim – volume: 51 start-page: 913 year: 1987 ident: 10.1016/j.optmat.2015.10.015_b0085 article-title: Organic electroluminescent diodes publication-title: Appl. Phys. Lett. doi: 10.1063/1.98799 contributor: fullname: Tang – volume: 160 start-page: 354 year: 2010 ident: 10.1016/j.optmat.2015.10.015_b0090 article-title: Efficient electrophosphorescence based on 2-(9,9-diethylfluoren-2-yl)-5-trifluoro- methylpyridine iridium complexes publication-title: Synth. Met. doi: 10.1016/j.synthmet.2009.11.004 contributor: fullname: Zhang – volume: 11 start-page: 283 year: 1999 ident: 10.1016/j.optmat.2015.10.015_b0020 article-title: A blue-emitting organic electroluminescent device using a novel emitting amorphous molecular material, 5,5’-bis(dimesitylboryl)-2,2’-bithiophene publication-title: Adv. Mater. doi: 10.1002/(SICI)1521-4095(199903)11:4<283::AID-ADMA283>3.0.CO;2-V contributor: fullname: Noda – volume: 52 start-page: 952 year: 2009 ident: 10.1016/j.optmat.2015.10.015_b0080 article-title: Synthesis and light-emitting properties of 2-(N-phenyl-α-naphthylamino) and 2-dimesitylboron-7-(N-phenyl-α-naphthylamino)-9,9-diethylfluorene publication-title: Sci. China Ser. B doi: 10.1007/s11426-009-0077-0 contributor: fullname: Zhang – volume: 85 start-page: 86 year: 2010 ident: 10.1016/j.optmat.2015.10.015_b0100 article-title: Red non-doped electroluminescent dyes based on arylamino fumaronitrile derivatives publication-title: Dyes Pigm. doi: 10.1016/j.dyepig.2009.10.008 contributor: fullname: Zhang – volume: 12 start-page: 780 year: 2002 ident: 10.1016/j.optmat.2015.10.015_b0025 article-title: A novel family of boron-containing hole-blocking amorphous molecular materials for blue- and blue-violet-emitting organic electroluminescent devices publication-title: Adv. Funct. Mater. doi: 10.1002/adfm.200290007 contributor: fullname: Kinoshita – volume: 4 start-page: 994 year: 2004 ident: 10.1016/j.optmat.2015.10.015_b0035 article-title: Three-coordinate organoboron compounds BAr2R (Ar = Mesityl, R=7-azaindolyl- or 2,2-dipyridylamino-functionalized aryl or thienyl) for electroluminescent devices and supramolecular assembly publication-title: Chem. Eur. J. doi: 10.1002/chem.200305579 contributor: fullname: Jia – volume: 32 start-page: 3306 year: 1999 ident: 10.1016/j.optmat.2015.10.015_b0060 article-title: New base-doped polyfluorene derivatives publication-title: Macro-molecules doi: 10.1021/ma981443e contributor: fullname: Ranger – volume: 14 start-page: 1884 year: 2002 ident: 10.1016/j.optmat.2015.10.015_b0015 article-title: Amorphous 2,3-substituted thiophenes: potential electroluminescent materials publication-title: Chem. Mater. doi: 10.1021/cm011671e contributor: fullname: Su – volume: 14 start-page: 809 year: 2002 ident: 10.1016/j.optmat.2015.10.015_b0075 article-title: Triphenyl- amine-substituted polyfluorene — a stable blue-emitter with improved charge injection for light-emitting diodes publication-title: Adv. Mater. doi: 10.1002/1521-4095(20020605)14:11<809::AID-ADMA809>3.0.CO;2-8 contributor: fullname: Ego – volume: 17 start-page: 164 year: 2005 ident: 10.1016/j.optmat.2015.10.015_b0040 article-title: Mes2B(p-4,4’- biphenyl-NPh(1-naphthyl)): a multifunctional molecule for electroluminescent devices publication-title: Chem. Mater. doi: 10.1021/cm048617t contributor: fullname: Wen – volume: 161 start-page: 2323 year: 2011 ident: 10.1016/j.optmat.2015.10.015_b0055 article-title: Multifunctional electroluminescent material based on dimesitylboron and α-naphthylamino fluorene bridge publication-title: Synth. Met. doi: 10.1016/j.synthmet.2011.08.042 contributor: fullname: Zhang |
SSID | ssj0002566 |
Score | 2.188709 |
Snippet | •2,7-Bis(dimesitylboryl)-9,9-spirobifluorene (5) as an emitter and electron transport.•Multifunctional... |
SourceID | crossref elsevier |
SourceType | Aggregation Database Publisher |
StartPage | 154 |
SubjectTerms | Dimesitylboron Electroluminescent device Fluorene Multifunctional Solvatochromism Triphenylamino |
Title | Spirobifluorene and biphenylaminophenyl fluorene with dimesitylboron as multifunctional electroluminescent materials |
URI | https://dx.doi.org/10.1016/j.optmat.2015.10.015 |
Volume | 50 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV07a8MwEBYhpdCl9EnTR9DQVYlt-TmG0JC2NEsayGYsWQKXYJvGGbr0t_dOsvuA0qGTbSGBuJPuO8nf3RFyCwedMMtih0WwkZgfacFELOHgGig_VpI7uala8rQI5yv_YR2se2TaxcIgrbK1_damG2vdtoxbaY7rohgvncQLOOxz2LMIfJh22wcwgjU9ev-ieQCkm_-V0Jlh7y58znC8qroBvxAJXsEIOV5YHPc3ePoGObMjctj6inRip3NMeqo8IfuGsym3p6RZ1gVmUdKbXYWJKWlW5lQUSNp6Az0XZWVf6WcHvHSlOQZ9gO-9EZi8gGZbakiFCHD2XpC2pXHAbCEnHumbFOZvl-oZWc3unqdz1hZRYCDosGEe6AK8ssSTeGXkanCQFM9yDTrgSkhwALnI_ZiH0tGJK7kUHhyZQ-5FuYyCxOfnpF9WpbogNMiUp13putrFoBKZKK3R4iYAgk6YxwPCOtmltc2VkXYkspfUyjpFWWMrPAYk6gSc_tB5Cub8z5GX_x55RQ7wyxJSrkm_ed2pG3ArGjE062ZI9ib3j_PFB1-qz-M |
link.rule.ids | 315,786,790,4521,24144,27957,27958,45620,45714 |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV07T8MwELZKEYIF8RTl6YHVbRLnOSJEVaDt0lbqFsWOLQVVSUTTgYXfzl2c8JAQA1Mix5asO_vus_PdHSG3cNDxkyS0WAAbibmBFkyEEg6unnJDJbmV1lVLJlN_tHCflt6yQ-7bWBikVTa239j02lo3LYNGmoMyywYzK3I8Dvsc9iw6Pn-LbCOcx_oN_fcvngf49PqHJfRm2L2Nn6tJXkVZATBEhpfXR5IXVsf9zT998znDA7LfgEV6Z-ZzSDoqPyI7NWlTro9JNSszTKOkV5sCM1PSJE-pyJC19QaKzvLCvNLPDnjrSlOM-gDwvRKYvYAma1qzCtHDmYtB2tTGAbuFpHjkb1KYv1mrJ2QxfJjfj1hTRYGBpP2KOaAMgGWRI_HOyNaAkBRPUg1K4EpIQIBcpG7IfWnpyJZcCgfOzD53glQGXuTyU9LNi1ydEeolytG2tG1tY1SJjJTWaHIj8IKWn4Y9wlrZxaVJlhG3LLKX2Mg6RlljKzx6JGgFHP9Qegz2_M-R5_8eeUN2R_PJOB4_Tp8vyB5-MeyUS9KtXjfqCjBGJa7rNfQBVG_RdQ |
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=Spirobifluorene+and+biphenylaminophenyl+fluorene+with+dimesitylboron+as+multifunctional+electroluminescent+materials&rft.jtitle=Optical+materials&rft.au=Zhang%2C+Wenguan&rft.au=He%2C+Zhiqun&rft.au=Pang%2C+Hui&rft.au=Wang%2C+Yongsheng&rft.date=2015-12-01&rft.issn=0925-3467&rft.volume=50&rft.spage=154&rft.epage=161&rft_id=info:doi/10.1016%2Fj.optmat.2015.10.015&rft.externalDBID=n%2Fa&rft.externalDocID=10_1016_j_optmat_2015_10_015 |
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 |