Chem. J. Chinese Universities ›› 2024, Vol. 45 ›› Issue (7): 20240051.doi: 10.7503/cjcu20240051
• Organic Chemistry • Previous Articles Next Articles
DONG Yiran1, LI Fengjiao1, MIAO Jinling2(), NIE Yong1(
), LI Tianrui1,2, XU Chunyue1, LIU Wei1, LIU Guangning2, JIANG Xuchuan1(
)
Received:
2024-01-29
Online:
2024-07-10
Published:
2024-04-29
Contact:
MIAO Jinling, NIE Yong, JIANG Xuchuan
E-mail:chm_miaojl@ujn.edu.cn;Chm_niey@ujn.edu.cn;ism_jiangxc@ujn.edu.cn
Supported by:
CLC Number:
TrendMD:
DONG Yiran, LI Fengjiao, MIAO Jinling, NIE Yong, LI Tianrui, XU Chunyue, LIU Wei, LIU Guangning, JIANG Xuchuan. Synthesis, Photoluminescence and Stimulus-responsiveness Properties of Bridged Fluorinated Tetraphenylethene Compounds[J]. Chem. J. Chinese Universities, 2024, 45(7): 20240051.
Compd. | λabsa /nm | λemb /nm | λemc /nm | λemd /nm | Φb (%) | τb /ns | 10‒7kre /s‒1 | 10‒8knrf /s‒1 |
---|---|---|---|---|---|---|---|---|
1 | 246, 326 g | 445 i | 497 | 491 | 18 | 0.83 | 21.70 | 9.9 |
2 | 234, 305 g | 444 j | 480 | 447 | 38 | 3.43 | 11.10 | 1.81 |
3 | 238, 308 g | 482 i | — | — | 22 | 4.42 | 4.98 | 1.76 |
4 | 232,304 g | 452 k | — | — | 37 | 3.43 | 10.80 | 1.84 |
5 | 239, 308 h | 462 l | 490 | 486 | 8 | 1.31 | 6.11 | 7.02 |
6 | 237, 305 h | 456 l | 482 | 482 | 32 | 5.16 | 6.20 | 1.32 |
Table 1 Photophysical data of compounds 1—6
Compd. | λabsa /nm | λemb /nm | λemc /nm | λemd /nm | Φb (%) | τb /ns | 10‒7kre /s‒1 | 10‒8knrf /s‒1 |
---|---|---|---|---|---|---|---|---|
1 | 246, 326 g | 445 i | 497 | 491 | 18 | 0.83 | 21.70 | 9.9 |
2 | 234, 305 g | 444 j | 480 | 447 | 38 | 3.43 | 11.10 | 1.81 |
3 | 238, 308 g | 482 i | — | — | 22 | 4.42 | 4.98 | 1.76 |
4 | 232,304 g | 452 k | — | — | 37 | 3.43 | 10.80 | 1.84 |
5 | 239, 308 h | 462 l | 490 | 486 | 8 | 1.31 | 6.11 | 7.02 |
6 | 237, 305 h | 456 l | 482 | 482 | 32 | 5.16 | 6.20 | 1.32 |
1 | Luo J. D., Xie Z. L., Lam J. W. Y., Cheng L., Chen H. Y., Qiu C. F., Kwok H. S., Zhan X. W., Liu Y. Q., Zhu D. B., Tang B. Z., Chem. Commun., 2001, 18, 1740—1741 |
2 | Yao L., Zhang S. T., Wang R., Li W. J., Shen F. Z., Yang B., Ma Y. G., Angew. Chem. Int. Ed., 2014, 53(8), 2119—2123 |
3 | Han P. B., Xu Z., Lin C. W., Ma D. G., Qin A. J., Tang B. Z., J. Mater. Chem. C, 2020, 8(21), 7012—7018 |
4 | Han T., Yan D. Y., Wu Q., Song N., Zhang H. K., Wang D., Chin. J. Chem., 2021, 39(3), 677—689 |
5 | Wu Z. X., Zhu Y. J., Wang H. Z., Wang J. A., He Y., Chem. J. Chinese Universities, 2022, 43(11), 20220371 |
伍泽鑫, 朱渊杰, 王泓中, 王均安, 贺英. 高等学校化学学报, 2022, 43(11), 20220371 | |
6 | Mei J., Hong Y. N., Lam J. W. L., Qin A. J., Tang Y. H., Tang B. Z., Adv. Mater., 2014, 26(31), 5429—5479 |
7 | Huang G. X., Du X. X., Bo H., Li B. S., Mater. Chem. Front., 2024, 8, 104—132 |
8 | Zhao Z. J., Lam J. W. Y., Tang B. Z., J. Mater. Chem., 2012, 22(45), 23726—23740 |
9 | Duan X. L., Han H. M., Zhao M. K., Ren L. X., Chem. J. Chinese Universities, 2023, 44(11), 20230291 |
段小丽, 韩慧敏, 赵明坤, 任丽霞. 高等学校化学学报, 2023 , 44(11), 20230291 | |
10 | Liu W., Yao W., Zhou M. M., You Q., Nie Y., Jiang X. C., Chem. J. Chinese Universities, 2021, 42(8), 2668—2672 |
刘威, 姚伟, 周明明, 游淇, 聂永, 蒋绪川. 高等学校化学学报, 2021, 42(8), 2668—2672 | |
11 | Qin C. Y., Liu W., Nie Y., Gao Y., Miao J. L., Li T. R., Jiang X. C., Chin. J. Org. Chem., 2020, 40(8), 2232—2253 |
秦成远, 刘威, 聂永, 高迎, 苗金玲, 李天瑞, 蒋绪川. 有机化学, 2020, 40(8), 2232—2253 | |
12 | Chopra D., Row T. N. G., CrystEngComm, 2011, 13(7), 2175—2186 |
13 | Milián⁃Medina B., Gierschner J., J. Phys. Chem. Lett., 2017, 8(1), 91—101 |
14 | Deng D., Zhou E. J., Wei Z. X., Acta Phys.⁃Chim. Sin., 2018, 34(11), 1239—1249 |
邓丹, 周二军, 魏志祥. 物理化学学报, 2018, 34(11), 1239—1249 | |
15 | Qin C. Y., Miao J. L., Nie Y., Liu W., Gao Y., Li T. R., Jiang, X. C., Chin. J. Org. Chem., 2021, 41(2), 504—520 |
秦成远, 苗金玲, 聂永, 刘威, 高迎, 李天瑞, 蒋绪川. 有机化学, 2021, 41(2), 504—520 | |
16 | Yang Z. Y., Chi Z. H., Mao Z., Zhang Y., Liu S. W., Zhao J., Aldred M. P., Chi Z. G., Mater. Chem. Front., 2018, 2(5), 861—890 |
17 | Yang J., Huang J., Li Q. Q., Li Z., J. Mater. Chem. C, 2016, 4(14), 2663—2684 |
18 | Zhang J. Y., Kang W. B., Xu X. D., Org. Chem. Front., 2023, 10(24), 6225—6239 |
19 | Zhang M., Guo J. J., Liu T. T., He Z. Y., Irfan M., Zhao Z. J., Zeng Z., J. Mater. Chem. C, 2020, 8(42), 14919—14924 |
20 | Huang J., Sun N., Chen P. Y., Tang R. L., Li Q. Q., Ma D. G., Li Z., Chem. Commun., 2014, 50(17), 2136—2138 |
21 | Huang J., Sun N., Dong Y. Q., Tang R. L., Lu P., Cai P., Li Q. Q., Ma D. G., Qin J. G., Li Z., Adv. Funct. Mater., 2013, 23(18), 2329—2337 |
22 | Huang J., Tang R. L., Zhang T., Li Q. Q., Yu G., Xie S. Y., Liu Y. Q., Ye S. H., Qin J. G., Li Z., Chem. Eur. J., 2014, 20(18), 5317—5326 |
23 | Yang J., Huang J., Sun N., Peng Q., Li Q. Q., Ma D. G., Li Z., Chem. Eur. J., 2015, 21(18), 6862—6868 |
24 | Dang D. F., Qiu Z. J., Han T., Liu Y., Chen M., Kwok R. T. K., Lam J. W. Y., Tang B. Z., Adv. Funct. Mater., 2018, 28(16), 1707210 |
25 | Li C., Gong W. L., Hu Z., Aldred M. P., Zhang G. F., Chen T., Huang Z. L., Zhu M. Q., RSC Adv., 2013, 3(23), 8967—8972 |
26 | Li S. H., Shang Y. L., Wang L. F., Kwok R. T. K., Tang B. Z., J. Mater. Chem. C, 2016, 4(23), 5363—5369 |
27 | Yu C. Y., Hsu C. C., Weng H. C., RSC Advances, 2018, 8(23), 12619—12627 |
28 | Zhao F., Chen Z., Fan C. B., Liu G., Pu S. Z., Dyes Pigments, 2019, 164, 390—397 |
29 | Zhang M., Lu L. P., Yang G. L., Mo X. F., Luo S. Y., Irfan M., Zeng Z., New J. Chem., 2023, 47(12), 5915—5921 |
30 | Li T. R., Miao J. L., Xu C. Y., Nie Y., Liu W., Li Y. X., Liu G. N., Jiang X. C., J. Mater. Chem. C, 2022, 10(22), 8657—8665 |
31 | Zhang H., Nie Y., Miao J. L., Zhang D. Q., Li Y. X., Liu G. N., Sun G. X., Jiang X. C., J. Mater. Chem. C, 2019, 7(11), 3306—3314 |
32 | Xiong J. B., Li X. Y., Yuan C. Q., Semin S., Yao Z. Q., Xu J. L., Rasing T., Bu X.H., Mater. Chem. Front., 2018, 2(12), 2263—2271 |
33 | Chen Z., Zhang J., Song M., Yin J., Yu G.A., Liu S. H., Chem. Commun., 2015, 51(2), 326—329 |
34 | Zeng X., Yu Z., Wang F., Wang X. M., Wang C. X., Lu H. G., Wang Q. S., Dyes Pigments, 2019, 171, 107699 |
35 | Hu M., Ye F. Y., Du C., Wang W. Z., Yu W., Liu M. H., Zheng Y. S., Angew. Chem. Int. Ed., 2021, 61(8), e202115216 |
36 | Li X., Yin Y. H., Yan H., Lu C. S., Chem. Asian J., 2017, 12(17), 2207—2210 |
37 | Siddharth K., Alam P., Hossain M. D., Xie N., Nambafu G. S., Rehman F., Lam J. W. Y., Chen G. H., Cheng J. P., Luo Z. T., Chen G. H., Tang B. Z., Shao M. H., J. Am. Chem. Soc., 2021, 143(5), 2433—2440 |
38 | Wang L. Y., Wu S. M., Tang H., Meier H., Cao D. R., Sensors Actuat. B⁃Chem., 2018, 273, 1085—1090 |
39 | Gan W. J., Zhang Z. H., Zheng X. H., Yu Z. F., Xie C. X., Wen H. Q., Sun L. S., Zhao Y. J., Asian J. Org. Chem., 2022, 12(1), e202200559 |
40 | Cai X. M., Tang Z. G., Chen X. F., Lin Y. T., Zhang X. D., Huang S. L., Dyes Pigments, 2022, 204, 110454 |
41 | Nie Y., Zhang H., Miao J. L., Zhao X. Q., Li Y. X., Sun G. X., J. Organomet. Chem., 2018, 865, 200—205 |
42 | Li D., Liang X. Z., Zhang F., Li J., Zhang Z., Wang S. J., Li Z. J., Xing Y. F., Guo K. P., J. Mater. Chem. C, 2022, 10(30), 11016—11026 |
43 | Chen W. J., Zhang C., Han X., Liu S. H., Tan Y., Yin J., J. Org. Chem., 2019, 84(22),14498—14507 |
44 | Zhu H. C., Zhang S. S., Yang J. J., Wu M. Y., Wu Q. Y., Liu J. Y., Zhang J. N., Kong L., Yang J. X., J. Solid State Chem., 2022, 305, 122706 |
45 | Zhang J. N., Kang H., Li N., Zhou S. M., Sun H. M., Yin S. W., Zhao N., Tang B. Z., Chem. Sci., 2017, 8(1), 577—582 |
[1] | WU Zexin, ZHU Yuanjie, WANG Hongzhong, WANG Junan, HE Ying. Methyl-modified Carbazole/Diphenyl Sulfone-based AIE-TADF Blue Emitter and Its OLEDs [J]. Chem. J. Chinese Universities, 2022, 43(11): 20220371. |
[2] | LIU Wei, YAO Wei, ZHOU Mingming, YOU Qi, NIE Yong, JIANG Xuchuan. Synthesis, Aggregation-induced Emission and Piezofluorochromic Properties of 9,10-Bis(N-phenylindole-3-vinyl)anthracene [J]. Chem. J. Chinese Universities, 2021, 42(8): 2668. |
[3] | DU Xianchao, HAO Hongxia, QIN Anjun, TANG Benzhong. Detection of Cocaine Based on the System of AIEgen, Aptamer and Exonuclease Ⅰ [J]. Chem. J. Chinese Universities, 2020, 41(3): 411. |
[4] | WU Wenbo,LIU Bin. Two-photon Excitable Photosensitizers with Aggregation-induced Emission and Their Biomedical Applications † [J]. Chem. J. Chinese Universities, 2020, 41(2): 191. |
[5] | ZHANG Ronghui, MIN Deng, WANG Lailai, XIE Wenjian. Research Progress of Catalysts for Gas-phase Fluorination to Synthesize Hydorfluoroolefins† [J]. Chem. J. Chinese Universities, 2020, 41(10): 2199. |
[6] | ZHANG Yu, JING Jiangbo, SHAO Yueming, YIN Xin, XU Bin, WEN Xiaoyu. Specific Hepatocellular Carcinoma Imaging Based on Aggregation-Induced Emission Nanoparticles † [J]. Chem. J. Chinese Universities, 2019, 40(11): 2382. |
[7] | LING Yao, LIU Xuejing, HAO Haijing, HAO Xiaohui, BAI Libin, WU Yonggang. Synthesis and Properties of Water-soluble Glycosyl Fluorescent Polymer with Aggregation-induced Emission Effect† [J]. Chem. J. Chinese Universities, 2018, 39(6): 1319. |
[8] | WANG Jun, HUO Hongliang, LI Cuiqin, MA Lili, SHI Weiguang, CHEN Shuai. Synthesis of Novel Dendritic Bridging Nickel Complex for Oligomerization of Olefins† [J]. Chem. J. Chinese Universities, 2015, 36(9): 1813. |
[9] | YANG Hua, QI Qi, WANG Bin-Bin, QIAN Ying. Aggregation-induced Emission Enhance and Electrical Storage Properties of 1,2,4,5-Tetra{4-[N,N-di(4-iodophenyl)amino]styryl}benzene [J]. Chem. J. Chinese Universities, 2013, 34(8): 1880. |
[10] | CHI Zhen-Guo, HE Ke-Qiang, LI Hai-Yin, ZHANG Xi-Qi, XU Bing-Jia, LIU Si-Wei, ZHANG Yi, XU Jia-Rui. Synthesis and Properties of a Dicarbazolyl Tetraphenylethylene Multi-functional Luminophor [J]. Chem. J. Chinese Universities, 2012, 33(04): 725. |
[11] | SHEN Jin-Bo, TONG Bin, SHI Jian-Bing, SUN Shu, FENG Xiao, ZHI Jun-Ge, .... Aggregation-Induced Emission Enhancement Properties of Phosphaphenanthrene-containing Styrene Derivant and Its Application of Detection to Transition Metal Ions [J]. Chem. J. Chinese Universities, 2010, 31(8): 1656. |
[12] | ZHENG Jing-Jing, WANG Lei*, LIU Yang, TAO Xu-Tang*. Aggregation Induced Luminescence in the Λ-Shaped iso-Phoronederivative Nanoparticles [J]. Chem. J. Chinese Universities, 2010, 31(5): 855. |
[13] | ZHOU Quan-Hui, YU Xin-Quan, ZHANG You-Fa*, LI Kang-Ning, CHEN Feng1, GU Zhong-Ze. Fabrication of Superhydrophobic Surface on Aluminum Alloy by Sandblasting-anodizing-fluorination [J]. Chem. J. Chinese Universities, 2010, 31(3): 456. |
[14] | WANG Wei, GONG Shu-Ling, MENG Ling-Zhi, CHEN Yuan-Yin . Preparation and Characterization of Biscalix [4] arene with Alkyne-containing Spacer [J]. Chem. J. Chinese Universities, 2005, 26(8): 1467. |
[15] | HANG Yi-Ping, QIN Yong-Chao, JIANG Zu-Cheng, HU Bin . Direct Analysis of Trace Rare EartHElements Through Nanometer-size Titanium Dioxide Separation/Concentration and Fluorination Assisted ETV-ICP-AES with Slurry Sampling [J]. Chem. J. Chinese Universities, 2003, 24(11): 1980. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||