CN1260214C - 具有强双光子吸收特性的杂芴多枝衍生物 - Google Patents
具有强双光子吸收特性的杂芴多枝衍生物 Download PDFInfo
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- CN1260214C CN1260214C CN 200410041260 CN200410041260A CN1260214C CN 1260214 C CN1260214 C CN 1260214C CN 200410041260 CN200410041260 CN 200410041260 CN 200410041260 A CN200410041260 A CN 200410041260A CN 1260214 C CN1260214 C CN 1260214C
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- 150000002220 fluorenes Chemical class 0.000 claims description 32
- 230000021615 conjugation Effects 0.000 claims description 5
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- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 229910052731 fluorine Chemical group 0.000 claims description 2
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- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
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- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- XCEUHXVTRJQJSR-UHFFFAOYSA-N bromo(phenyl)phosphane Chemical compound BrPC1=CC=CC=C1 XCEUHXVTRJQJSR-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
实施例 | 单光子性质 | 双光子性质 | |||||||
溶剂 | λOPA/λOPF(nm) | Φf | τ(ns) | λTPE(nm) | λTPF(nm) | TPF(integral) | δTPA(GM) | δTPF | |
1 | 甲苯 | 368/436 | 0.84 | 1.34 | 760 | 444 | 46446 | 165.8 | 7.7 |
CH2Cl2 | 366/456 | 0.84 | 1.74 | 760 | 460 | 14782 | 55.5 | 2.6 | |
DMF | 368/460 | 0.67 | 2.24 | 840 | 470 | 75800 | 355.0 | 13.3 | |
3 | CH2Cl2 | 361/441 | 0.62 | 1.35 | / | / | / | / | / |
DMF | 361/444 | 0.94 | 1.56 | 720 | 418 | 18378 | 62 | 3.2 |
实施例 | X |
实施例4 | NC4H9 |
实施例5 | NC8H17 |
实施例6 | NC12H23 |
实施例7 | NC22H45 |
环己烷 | 甲苯 | THF | 二氯乙烷 | 丙酮 | DMF | 乙醇 | |
λab max,nm吸光度λem max,nmI(×107)量子产率(Φf) | 3990.1134443.0050.763 | 4040.1734533.390.563 | 4010.1434802.940.59 | 4010.1654932.560.445 | 4000.1934932.400.357 | 4010.19765031.620.235 | 4010.06284880.3090.141 |
实施例 | X |
实施例9 | O |
实施例10 | NC2H5 |
实施例11 | NC4H9 |
实施例12 | NC8H17 |
实施例13 | NC12H23 |
实施例14 | NC22H45 |
实施例 | R | X |
实施例16 | OC2H5 | S |
实施例17 | C(CH3)3 | S |
实施例18 | F | S |
实施例19 | OC2H5 | O |
实施例20 | OC4H9 | O |
实施例21 | C(CH3)3 | O |
实施例22 | F | O |
实施例23 | OC2H5 | NC2H5 |
实施例24 | OC2H5 | NC4H9 |
实施例25 | OC2H5 | NC8H17 |
实施例26 | OC2H5 | NC12H25 |
实施例27 | OC2H5 | NC22H45 |
实施例28 | OC4H9 | NC2H5 |
实施例29 | OC4H9 | NC4H9 |
实施例30 | OC4H9 | NC8H17 |
实施例31 | OC4H9 | NC12H25 |
实施例32 | OC4H9 | NC22H45 |
实施例33 | C(CH3)3 | NC2H5 |
实施例34 | C(CH3)3 | NC4H9 |
实施例35 | C(CH3)3 | NC8H17 |
实施例36 | C(CH3)3 | NC12H25 |
实施例37 | C(CH3)3 | NC22H45 |
实施例38 | F | NC2H5 |
实施例39 | F | NC4H9 |
实施例40 | F | NC8H17 |
实施例41 | F | NC12H25 |
实施例42 | F | NC22H45 |
实施例 | 单光子性质 | 双光子性质 | |||||||
溶剂 | λOPA/λOPF(nm) | Φf | τ(ns) | λTPE(nm) | λTPF(nm) | TPF(integral) | δTPA(GM) | δTPF | |
15 | 甲苯 | 388/471 | 0.46 | 1.0 | 760 | 480 | 56580 | 368.9 | 9.4 |
CH2Cl2 | 389/490 | 0.26 | 1.03 | 760 | 509 | 16125 | 195.5 | 2.8 | |
DMF | 391/500 | 0.31 | 1.01 | 840 | 517 | 93824 | 950.2 | 16.4 | |
28 | CH2Cl2 | 370/486 | 0.14 | 0.95 | 720 | 513 | 1584 | 36 | 0.03 |
DMF | 371/488 | 0.17 | 1.58 | 720 | 498 | 8714 | 161 | 1.5 |
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN 200410041260 CN1260214C (zh) | 2004-06-10 | 2004-06-10 | 具有强双光子吸收特性的杂芴多枝衍生物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CN 200410041260 CN1260214C (zh) | 2004-06-10 | 2004-06-10 | 具有强双光子吸收特性的杂芴多枝衍生物 |
Publications (2)
Publication Number | Publication Date |
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CN1583722A CN1583722A (zh) | 2005-02-23 |
CN1260214C true CN1260214C (zh) | 2006-06-21 |
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Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
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JP5229521B2 (ja) * | 2006-09-15 | 2013-07-03 | 株式会社リコー | π共役系化合物とその用途、およびそれらを用いた素子、装置 |
TWI431003B (zh) * | 2010-10-21 | 2014-03-21 | Ind Tech Res Inst | 有機化合物及包含其之有機電激發光裝置 |
CN104710344A (zh) * | 2015-04-03 | 2015-06-17 | 齐鲁工业大学 | 一种以咔唑为中心的希夫碱类荧光探针化合物及其制备 |
CN105203517A (zh) * | 2015-09-29 | 2015-12-30 | 中国科学院上海光学精密机械研究所 | 2,8-二(4-乙烯基吡啶)-二苯并噻吩阳离子衍生物及其制备方法和应用 |
US11034709B2 (en) * | 2019-05-29 | 2021-06-15 | The Hong Kong University Of Science And Technology | Organic long persistence luminescence compositions |
CN110204694A (zh) * | 2019-06-12 | 2019-09-06 | 南昌航空大学 | 一种含季铵盐末端离子基团的超支化共轭聚合物电解质阴极界面层的制备方法 |
CN111909076B (zh) * | 2020-07-07 | 2023-04-07 | 中山大学 | 一种单/双咔唑空穴传输材料及其制备方法和应用 |
CN114644836B (zh) * | 2021-03-09 | 2023-05-12 | 浙江大学 | 一种以芴环为母体的羧酸盐双光子染料、合成方法及应用 |
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2004
- 2004-06-10 CN CN 200410041260 patent/CN1260214C/zh not_active Expired - Lifetime
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