CN112940015A - 一种有机金属配合物和含有该化合物的有机光电元件 - Google Patents
一种有机金属配合物和含有该化合物的有机光电元件 Download PDFInfo
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- CN112940015A CN112940015A CN202110122677.2A CN202110122677A CN112940015A CN 112940015 A CN112940015 A CN 112940015A CN 202110122677 A CN202110122677 A CN 202110122677A CN 112940015 A CN112940015 A CN 112940015A
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Classifications
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
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- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/08—Copper compounds
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
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Abstract
Description
实施例 | 化合物 | 启亮电压(伏) | EQE | 发光峰(纳米) | LT90(小时) |
对比器件 | GD-1 | 2.7 | 22.5% | 527 | 183 |
对比器件2 | RD-1 | 2.5 | 18.7% | 625 | 240 |
器件例1 | 化合物1 | 2.7 | 20.1% | 523 | 179 |
器件例2 | 化合物2 | 2.6 | 23.3% | 525 | 232 |
器件例3 | 化合物3 | 2.8 | 17.3% | 522 | 155 |
器件例4 | 化合物4 | 2.6 | 22.6% | 530 | 180 |
器件例5 | 化合物5 | 2.6 | 22.8% | 532 | 204 |
器件例6 | 化合物6 | 2.6 | 21.2% | 536 | 170 |
器件例7 | 化合物7 | 2.8 | 19.3% | 540 | 160 |
器件例8 | 化合物8 | 2.8 | 17.4 | 536 | 152 |
器件例9 | 化合物9 | 2.7 | 18.1% | 522 | 148 |
器件例10 | 化合物10 | 2.6 | 22.7% | 528 | 240 |
器件例11 | 化合物11 | 2.6 | 21.5% | 530 | 195 |
器件例12 | 化合物12 | 2.8 | 19.3% | 533 | 190 |
器件例13 | 化合物13 | 2.4 | 20.7% | 622 | 260 |
器件例14 | 化合物14 | 2.8 | 18.5% | 540 | 89 |
器件例15 | 化合物15 | 2.8 | 17.6% | 533 | 163 |
Claims (14)
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120220922A1 (en) * | 2009-06-26 | 2012-08-30 | Universidad De Buenos Aires | Photolabile compounds |
US20130252273A1 (en) * | 2012-03-26 | 2013-09-26 | The Florida International University Board Of Trustees | Organometallic fluorescent sensors for nitric oxide detection and imaging |
CN107573383A (zh) * | 2016-07-05 | 2018-01-12 | 三星电子株式会社 | 有机金属化合物、包括其的有机发光器件、和包括该有机金属化合物的诊断组合物 |
-
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120220922A1 (en) * | 2009-06-26 | 2012-08-30 | Universidad De Buenos Aires | Photolabile compounds |
US20130252273A1 (en) * | 2012-03-26 | 2013-09-26 | The Florida International University Board Of Trustees | Organometallic fluorescent sensors for nitric oxide detection and imaging |
CN107573383A (zh) * | 2016-07-05 | 2018-01-12 | 三星电子株式会社 | 有机金属化合物、包括其的有机发光器件、和包括该有机金属化合物的诊断组合物 |
Non-Patent Citations (2)
Title |
---|
KARUPPIAH NAGARAJ: "Synthesis, Micellization Behaviour, DNA/RNA Binding and Biological Studies of a Surfactant Cobalt(III) Complex With Dipyrido[3, 2-a:2′, 4′-c](6, 7, 8, 9-tetrahydro)phenazine", 《J FLUORESC》, no. 24, pages 1701 * |
NAHO IIZUKA: "Mixed-ligand ruthenium(II) complexes capable of hydrogen-bonding interactions with DNA: DNA binding, nuclease activity, cytotoxicity, and topoisomerase inhibition", 《POLYHEDRON》, no. 137, pages 34 * |
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