Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives
Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were inves...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Zhao, Yuling [verfasserIn] |
|---|
| Format: |
Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2011 |
|---|
| Schlagwörter: |
|---|
| Anmerkung: |
© Springer Science+Business Media, LLC 2011 |
|---|
| Übergeordnetes Werk: |
Enthalten in: Journal of fluorescence - Springer US, 1991, 22(2011), 2 vom: 19. Okt., Seite 631-638 |
|---|---|
| Übergeordnetes Werk: |
volume:22 ; year:2011 ; number:2 ; day:19 ; month:10 ; pages:631-638 |
| Links: |
|---|
| DOI / URN: |
10.1007/s10895-011-0999-8 |
|---|
| Katalog-ID: |
OLC2070051277 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | OLC2070051277 | ||
| 003 | DE-627 | ||
| 005 | 20230508175627.0 | ||
| 007 | tu | ||
| 008 | 200819s2011 xx ||||| 00| ||eng c | ||
| 024 | 7 | |a 10.1007/s10895-011-0999-8 |2 doi | |
| 035 | |a (DE-627)OLC2070051277 | ||
| 035 | |a (DE-He213)s10895-011-0999-8-p | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | 4 | |a 620 |q VZ |
| 100 | 1 | |a Zhao, Yuling |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives |
| 264 | 1 | |c 2011 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
| 338 | |a Band |b nc |2 rdacarrier | ||
| 500 | |a © Springer Science+Business Media, LLC 2011 | ||
| 520 | |a Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. | ||
| 650 | 4 | |a Synthesis | |
| 650 | 4 | |a UV-vis Absorption | |
| 650 | 4 | |a Photoluminescence | |
| 650 | 4 | |a Electroluminescence | |
| 650 | 4 | |a Coumarin derivative | |
| 650 | 4 | |a Benzoxazolyl derivative | |
| 700 | 1 | |a Yu, Tianzhi |4 aut | |
| 700 | 1 | |a Wu, Youzhi |4 aut | |
| 700 | 1 | |a Zhang, Hui |4 aut | |
| 700 | 1 | |a Fan, Duowang |4 aut | |
| 700 | 1 | |a Gan, Zunwei |4 aut | |
| 700 | 1 | |a Yang, Liangliang |4 aut | |
| 700 | 1 | |a Han, Xiaoqian |4 aut | |
| 700 | 1 | |a Zhang, Yumei |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of fluorescence |d Springer US, 1991 |g 22(2011), 2 vom: 19. Okt., Seite 631-638 |w (DE-627)130988731 |w (DE-600)1079500-5 |w (DE-576)030293898 |x 1053-0509 |7 nnns |
| 773 | 1 | 8 | |g volume:22 |g year:2011 |g number:2 |g day:19 |g month:10 |g pages:631-638 |
| 856 | 4 | 1 | |u https://doi.org/10.1007/s10895-011-0999-8 |z lizenzpflichtig |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a SYSFLAG_A | ||
| 912 | |a GBV_OLC | ||
| 912 | |a SSG-OLC-TEC | ||
| 912 | |a SSG-OLC-CHE | ||
| 912 | |a SSG-OLC-PHA | ||
| 912 | |a SSG-OLC-DE-84 | ||
| 912 | |a GBV_ILN_70 | ||
| 912 | |a GBV_ILN_2004 | ||
| 912 | |a GBV_ILN_4125 | ||
| 951 | |a AR | ||
| 952 | |d 22 |j 2011 |e 2 |b 19 |c 10 |h 631-638 | ||
| author_variant |
y z yz t y ty y w yw h z hz d f df z g zg l y ly x h xh y z yz |
|---|---|
| matchkey_str |
article:10530509:2011----::yteipooneetouiecnefbnoao2 |
| hierarchy_sort_str |
2011 |
| publishDate |
2011 |
| allfields |
10.1007/s10895-011-0999-8 doi (DE-627)OLC2070051277 (DE-He213)s10895-011-0999-8-p DE-627 ger DE-627 rakwb eng 620 VZ Zhao, Yuling verfasserin aut Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative Yu, Tianzhi aut Wu, Youzhi aut Zhang, Hui aut Fan, Duowang aut Gan, Zunwei aut Yang, Liangliang aut Han, Xiaoqian aut Zhang, Yumei aut Enthalten in Journal of fluorescence Springer US, 1991 22(2011), 2 vom: 19. Okt., Seite 631-638 (DE-627)130988731 (DE-600)1079500-5 (DE-576)030293898 1053-0509 nnns volume:22 year:2011 number:2 day:19 month:10 pages:631-638 https://doi.org/10.1007/s10895-011-0999-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_4125 AR 22 2011 2 19 10 631-638 |
| spelling |
10.1007/s10895-011-0999-8 doi (DE-627)OLC2070051277 (DE-He213)s10895-011-0999-8-p DE-627 ger DE-627 rakwb eng 620 VZ Zhao, Yuling verfasserin aut Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative Yu, Tianzhi aut Wu, Youzhi aut Zhang, Hui aut Fan, Duowang aut Gan, Zunwei aut Yang, Liangliang aut Han, Xiaoqian aut Zhang, Yumei aut Enthalten in Journal of fluorescence Springer US, 1991 22(2011), 2 vom: 19. Okt., Seite 631-638 (DE-627)130988731 (DE-600)1079500-5 (DE-576)030293898 1053-0509 nnns volume:22 year:2011 number:2 day:19 month:10 pages:631-638 https://doi.org/10.1007/s10895-011-0999-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_4125 AR 22 2011 2 19 10 631-638 |
| allfields_unstemmed |
10.1007/s10895-011-0999-8 doi (DE-627)OLC2070051277 (DE-He213)s10895-011-0999-8-p DE-627 ger DE-627 rakwb eng 620 VZ Zhao, Yuling verfasserin aut Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative Yu, Tianzhi aut Wu, Youzhi aut Zhang, Hui aut Fan, Duowang aut Gan, Zunwei aut Yang, Liangliang aut Han, Xiaoqian aut Zhang, Yumei aut Enthalten in Journal of fluorescence Springer US, 1991 22(2011), 2 vom: 19. Okt., Seite 631-638 (DE-627)130988731 (DE-600)1079500-5 (DE-576)030293898 1053-0509 nnns volume:22 year:2011 number:2 day:19 month:10 pages:631-638 https://doi.org/10.1007/s10895-011-0999-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_4125 AR 22 2011 2 19 10 631-638 |
| allfieldsGer |
10.1007/s10895-011-0999-8 doi (DE-627)OLC2070051277 (DE-He213)s10895-011-0999-8-p DE-627 ger DE-627 rakwb eng 620 VZ Zhao, Yuling verfasserin aut Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative Yu, Tianzhi aut Wu, Youzhi aut Zhang, Hui aut Fan, Duowang aut Gan, Zunwei aut Yang, Liangliang aut Han, Xiaoqian aut Zhang, Yumei aut Enthalten in Journal of fluorescence Springer US, 1991 22(2011), 2 vom: 19. Okt., Seite 631-638 (DE-627)130988731 (DE-600)1079500-5 (DE-576)030293898 1053-0509 nnns volume:22 year:2011 number:2 day:19 month:10 pages:631-638 https://doi.org/10.1007/s10895-011-0999-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_4125 AR 22 2011 2 19 10 631-638 |
| allfieldsSound |
10.1007/s10895-011-0999-8 doi (DE-627)OLC2070051277 (DE-He213)s10895-011-0999-8-p DE-627 ger DE-627 rakwb eng 620 VZ Zhao, Yuling verfasserin aut Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative Yu, Tianzhi aut Wu, Youzhi aut Zhang, Hui aut Fan, Duowang aut Gan, Zunwei aut Yang, Liangliang aut Han, Xiaoqian aut Zhang, Yumei aut Enthalten in Journal of fluorescence Springer US, 1991 22(2011), 2 vom: 19. Okt., Seite 631-638 (DE-627)130988731 (DE-600)1079500-5 (DE-576)030293898 1053-0509 nnns volume:22 year:2011 number:2 day:19 month:10 pages:631-638 https://doi.org/10.1007/s10895-011-0999-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_4125 AR 22 2011 2 19 10 631-638 |
| language |
English |
| source |
Enthalten in Journal of fluorescence 22(2011), 2 vom: 19. Okt., Seite 631-638 volume:22 year:2011 number:2 day:19 month:10 pages:631-638 |
| sourceStr |
Enthalten in Journal of fluorescence 22(2011), 2 vom: 19. Okt., Seite 631-638 volume:22 year:2011 number:2 day:19 month:10 pages:631-638 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| topic_facet |
Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative |
| dewey-raw |
620 |
| isfreeaccess_bool |
false |
| container_title |
Journal of fluorescence |
| authorswithroles_txt_mv |
Zhao, Yuling @@aut@@ Yu, Tianzhi @@aut@@ Wu, Youzhi @@aut@@ Zhang, Hui @@aut@@ Fan, Duowang @@aut@@ Gan, Zunwei @@aut@@ Yang, Liangliang @@aut@@ Han, Xiaoqian @@aut@@ Zhang, Yumei @@aut@@ |
| publishDateDaySort_date |
2011-10-19T00:00:00Z |
| hierarchy_top_id |
130988731 |
| dewey-sort |
3620 |
| id |
OLC2070051277 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">OLC2070051277</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230508175627.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200819s2011 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10895-011-0999-8</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2070051277</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)s10895-011-0999-8-p</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">620</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Zhao, Yuling</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2011</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer Science+Business Media, LLC 2011</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Synthesis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">UV-vis Absorption</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Photoluminescence</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Electroluminescence</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Coumarin derivative</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Benzoxazolyl derivative</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yu, Tianzhi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wu, Youzhi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Hui</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Fan, Duowang</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gan, Zunwei</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yang, Liangliang</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Han, Xiaoqian</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Yumei</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of fluorescence</subfield><subfield code="d">Springer US, 1991</subfield><subfield code="g">22(2011), 2 vom: 19. Okt., Seite 631-638</subfield><subfield code="w">(DE-627)130988731</subfield><subfield code="w">(DE-600)1079500-5</subfield><subfield code="w">(DE-576)030293898</subfield><subfield code="x">1053-0509</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:22</subfield><subfield code="g">year:2011</subfield><subfield code="g">number:2</subfield><subfield code="g">day:19</subfield><subfield code="g">month:10</subfield><subfield code="g">pages:631-638</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10895-011-0999-8</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-DE-84</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2004</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">22</subfield><subfield code="j">2011</subfield><subfield code="e">2</subfield><subfield code="b">19</subfield><subfield code="c">10</subfield><subfield code="h">631-638</subfield></datafield></record></collection>
|
| author |
Zhao, Yuling |
| spellingShingle |
Zhao, Yuling ddc 620 misc Synthesis misc UV-vis Absorption misc Photoluminescence misc Electroluminescence misc Coumarin derivative misc Benzoxazolyl derivative Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives |
| authorStr |
Zhao, Yuling |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)130988731 |
| format |
Article |
| dewey-ones |
620 - Engineering & allied operations |
| delete_txt_mv |
keep |
| author_role |
aut aut aut aut aut aut aut aut aut |
| collection |
OLC |
| remote_str |
false |
| illustrated |
Not Illustrated |
| issn |
1053-0509 |
| topic_title |
620 VZ Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives Synthesis UV-vis Absorption Photoluminescence Electroluminescence Coumarin derivative Benzoxazolyl derivative |
| topic |
ddc 620 misc Synthesis misc UV-vis Absorption misc Photoluminescence misc Electroluminescence misc Coumarin derivative misc Benzoxazolyl derivative |
| topic_unstemmed |
ddc 620 misc Synthesis misc UV-vis Absorption misc Photoluminescence misc Electroluminescence misc Coumarin derivative misc Benzoxazolyl derivative |
| topic_browse |
ddc 620 misc Synthesis misc UV-vis Absorption misc Photoluminescence misc Electroluminescence misc Coumarin derivative misc Benzoxazolyl derivative |
| format_facet |
Aufsätze Gedruckte Aufsätze |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
nc |
| hierarchy_parent_title |
Journal of fluorescence |
| hierarchy_parent_id |
130988731 |
| dewey-tens |
620 - Engineering |
| hierarchy_top_title |
Journal of fluorescence |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)130988731 (DE-600)1079500-5 (DE-576)030293898 |
| title |
Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives |
| ctrlnum |
(DE-627)OLC2070051277 (DE-He213)s10895-011-0999-8-p |
| title_full |
Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives |
| author_sort |
Zhao, Yuling |
| journal |
Journal of fluorescence |
| journalStr |
Journal of fluorescence |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
600 - Technology |
| recordtype |
marc |
| publishDateSort |
2011 |
| contenttype_str_mv |
txt |
| container_start_page |
631 |
| author_browse |
Zhao, Yuling Yu, Tianzhi Wu, Youzhi Zhang, Hui Fan, Duowang Gan, Zunwei Yang, Liangliang Han, Xiaoqian Zhang, Yumei |
| container_volume |
22 |
| class |
620 VZ |
| format_se |
Aufsätze |
| author-letter |
Zhao, Yuling |
| doi_str_mv |
10.1007/s10895-011-0999-8 |
| dewey-full |
620 |
| title_sort |
synthesis, photo- and electro-luminescence of 3-benzoxazol-2-yl-coumarin derivatives |
| title_auth |
Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives |
| abstract |
Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. © Springer Science+Business Media, LLC 2011 |
| abstractGer |
Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. © Springer Science+Business Media, LLC 2011 |
| abstract_unstemmed |
Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $. © Springer Science+Business Media, LLC 2011 |
| collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_4125 |
| container_issue |
2 |
| title_short |
Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives |
| url |
https://doi.org/10.1007/s10895-011-0999-8 |
| remote_bool |
false |
| author2 |
Yu, Tianzhi Wu, Youzhi Zhang, Hui Fan, Duowang Gan, Zunwei Yang, Liangliang Han, Xiaoqian Zhang, Yumei |
| author2Str |
Yu, Tianzhi Wu, Youzhi Zhang, Hui Fan, Duowang Gan, Zunwei Yang, Liangliang Han, Xiaoqian Zhang, Yumei |
| ppnlink |
130988731 |
| mediatype_str_mv |
n |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| doi_str |
10.1007/s10895-011-0999-8 |
| up_date |
2024-07-04T00:06:21.100Z |
| _version_ |
1803604806708756480 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">OLC2070051277</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230508175627.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200819s2011 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10895-011-0999-8</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2070051277</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)s10895-011-0999-8-p</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">620</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Zhao, Yuling</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis, Photo- and Electro-Luminescence of 3-Benzoxazol-2-yl-Coumarin Derivatives</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2011</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer Science+Business Media, LLC 2011</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Two coumarin derivatives containing electron-transporting benzoxazolyl moiety, 7-(diethylamino)-3-(benzoxazol-2-yl)coumarin (DABOC) and 3-(benzoxazol-2-yl)benzo[5,6]coumarin (BOBC), were synthesized and characterized. The photoluminescence and electroluminescence of the compounds were investigated detailedly. The compounds exhibited strong blue-green emissions in both solution and solid states, but the devices with DABOC as the emitting layer exhibited orange emission and maximum luminous efficiency of 2.8 cd/A and maximum luminance of 8,800 cd/$ m^{2} $, and the devices with BOBC displayed orange-white emission and maximum luminous efficiency of 0.13 cd/A and maximum luminance of 540 cd/$ m^{2} $.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Synthesis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">UV-vis Absorption</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Photoluminescence</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Electroluminescence</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Coumarin derivative</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Benzoxazolyl derivative</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yu, Tianzhi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wu, Youzhi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Hui</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Fan, Duowang</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gan, Zunwei</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yang, Liangliang</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Han, Xiaoqian</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Yumei</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of fluorescence</subfield><subfield code="d">Springer US, 1991</subfield><subfield code="g">22(2011), 2 vom: 19. Okt., Seite 631-638</subfield><subfield code="w">(DE-627)130988731</subfield><subfield code="w">(DE-600)1079500-5</subfield><subfield code="w">(DE-576)030293898</subfield><subfield code="x">1053-0509</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:22</subfield><subfield code="g">year:2011</subfield><subfield code="g">number:2</subfield><subfield code="g">day:19</subfield><subfield code="g">month:10</subfield><subfield code="g">pages:631-638</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10895-011-0999-8</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-DE-84</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2004</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">22</subfield><subfield code="j">2011</subfield><subfield code="e">2</subfield><subfield code="b">19</subfield><subfield code="c">10</subfield><subfield code="h">631-638</subfield></datafield></record></collection>
|
| score |
7.399102 |