6,6″-二(2,6-二甲氧基苯)-三联吡啶及其衍生物金属配位自组装的研究进展

doi:10.6023/A23120538

化学学报 ›› 2024, Vol. 82 ›› Issue (3): 336-347.DOI: 10.6023/A23120538 上一篇下一篇

综述

6,6″-二(2,6-二甲氧基苯)-三联吡啶及其衍生物金属配位自组装的研究进展

王敏^a, 陈帮塘^a, 陈桥林^a, 王俊^a, 陈名钊^a, 蒋志龙^a^,^*(), 王平山^a^,^b^,^*()

a 广州大学大湾区环境研究院珠江三角洲水质安全与保护教育部重点实验室广州 510006
b 中南大学化学化工学院长沙 410083

投稿日期:2023-12-19 发布日期:2024-01-18

作者简介:

王敏, 广州大学环境科学与工程学院环境工程专业在读硕士生.

蒋志龙, 广州大学大湾区环境研究院副教授, 主要的研究方向为超分子自组装及功能配合物, 参与国家自然科学基金面上项目3项, 主持贵州省科技厅科技创新项目1项, 广东省教育厅科技创新项目1项, 广州市市校联合基金1项, 目前以第一作者或者通讯作者身份在Nature Communication、J. Am. Chem. Soc.、Angew. Chem. Int. Ed.、iScience、Cell Reports Physical Science、Nano Research、Chem. Commun.、Inorg. Chem.等期刊上发表论文17篇, 授权中国发明专利6项.

王平山, 广州大学大湾区环境研究院教授, 中南大学化学化工学院特聘教授, 入选中组部海外高层次人才计划和湖南省“国家级领军人才”, 主持国家、国际环境署/环保部及美国科研项目20余项, 获省部级科技奖励3项, 目前研究领域主要集中在超分子化学、金属有机高分子能源材料和高分子环保材料, 在Science, Nat. Commun., J. Am. Chem. Soc., Angew. Chem. Int. Ed.等期刊发表学术论文100余篇, 授权国际和中国发明专利30余项, 在超大单分子的构筑策略研究领域有突出贡献, 相关成果在国内外具有重要的影响.

基金资助:
国家自然科学基金(22101060); 国家自然科学基金(21971257); 广州市科技计划项目(202201020201); 广州市科技计划项目(SL2022A03J01050)

Research Progress on Metal-coordination-driven Self-assembly of 6,6"-Bis(2,6-dimethoxy-benzene)-terpyridine and Its Derivatives

Min Wang^a, Bangtang Chen^a, Qiaolin Chen^a, Jun Wang^a, Mingzhao Chen^a, Zhilong Jiang^a(), Pingshan Wang^a^,^b()

a Institute of Environmental Research at Greater Bay Area, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006
b College of Chemistry and Chemical Engineering, Central South University, Changsha 410083

Received:2023-12-19 Published:2024-01-18
Contact: *E-mail: jiangzl@gzhu.edu.cn;chemwps@csu.edu.cn
Supported by:
National Natural Science Foundation of China(22101060); National Natural Science Foundation of China(21971257); Science and Technology Planning Project of Guangzhou(202201020201); Science and Technology Planning Project of Guangzhou(SL2022A03J01050)

文章分享

摘要/Abstract

过去几年里, 6,6"-二(2,6-二甲氧基苯)-三联吡啶及其衍生物在多组分自组装过程中具有自识别能力强, 能够有效抑制副产物的生成等特点, 因此在精确构建多配体参与的金属配位超分子结构及功能研究方面具有独特优势. 这种新型互补型配体的应用不仅丰富了三联吡啶金属配位超分子结构的研究内容, 还展示了在发光材料、主客体化学、药物载体和限域催化等领域的广阔应用前景. 基于此, 本综述对基于6,6"-二(2,6-二甲氧基苯)-三联吡啶的衍生配体配位自组装研究中的最新进展进行了系统总结, 并简要探讨了此领域目前所面临的发展机遇及挑战.

关键词: 三联吡啶, 金属配位自组装, 金属有机配合物, 三联吡啶互补配体对, 功能超分子

In the past few decades, coordination-driven self-assembly of metal ions and organic ligands has been extensively applied in the construction of a variety of functional two-dimensional (2D) and three-dimensional (3D) structures. The majority of these structures are consisted of one type of ligand. Nevertheless, there have been sustained efforts dedicated to constructing heteroleptic assemblies using various strategic methods in order to increase the complexity and sophistication of nano-scale structures. Heteroleptic assemblies involve the use of multiple types of ligands, to assemble metal ions into more intricate structures. This approach allows for the incorporation of different ligand geometries, charge densities, and functional groups, leading to increased structural diversity and potential for new properties. To achieve heteroleptic assemblies, various strategic methods have been employed. One common approach is the use of different ligands with complementary binding properties, allowing for the controlled formation of targeted structures. In recent years, 6,6"-bis(2,6-dimethoxy-phenyl)- terpyridine and its derivatives have received considerable attention in the research of coordination-driven supramolecular self-assembly. These ligands exhibit strong self-recognition ability and effectively suppress the formation of by-products in multicomponent self-assembly processes, giving them unique advantages in the precise construction of metal-coordination supramolecular structures involving multiple ligands. A large number of 2D and 3D supramolecular structures formed by the coordination of 6,6"-bis(2,6-dimethoxy-phenyl)-terpyridine ligands and their derivatives with metal ions have been reported. The successful construction of these 2D and 3D topological structures has not only enriched the research of terpyridine metal-coordination supramolecular structures but also demonstrated significant research value and broad prospects in fields such as luminescent materials, host-guest chemistry, drug delivery systems, and confined catalysis. Based on this, this review systematically summarizes the latest progress in the self-assembly of derivative ligands based on 6,6"-bis(2,6-dimethoxy- phenyl)-terpyridine in terms of ligand synthesis, structure construction and property study, and briefly discusses the current development opportunities and challenges faced in this field.

Key words: terpyridine, metal coordination self-assembly, metal-organic complexes, complementary terpyridine ligand pairing, functional supramolecular

引用此文

王敏, 陈帮塘, 陈桥林, 王俊, 陈名钊, 蒋志龙, 王平山. 6,6″-二(2,6-二甲氧基苯)-三联吡啶及其衍生物金属配位自组装的研究进展[J]. 化学学报, 2024, 82(3): 336-347.

Min Wang, Bangtang Chen, Qiaolin Chen, Jun Wang, Mingzhao Chen, Zhilong Jiang, Pingshan Wang. Research Progress on Metal-coordination-driven Self-assembly of 6,6"-Bis(2,6-dimethoxy-benzene)-terpyridine and Its Derivatives[J]. Acta Chimica Sinica, 2024, 82(3): 336-347.

导出引用 EndNote|Reference Manager|ProCite|BibTeX|RefWorks

分享此文

图/表 22

图1. 配体的自分类和不等边三角形1的合成

Figure 1. Self-sorting of ligands and synthesis of scalene triangle structures

图2. 三联吡啶互补型配体对金属离子配位过程

Figure 2. Complementary terpyridine ligands pairing coordination process versus metal ion

图3. 6,6"-二(2,6-二甲氧基苯)-三联吡啶配体的合成策略

Figure 3. Synthetic strategies of 6,6"-bis(2,6-dimethoxybenzene)- terpyridine ligand

图4. 杂配化合物4的合成

Figure 4. Synthesis of heteroleptic complex 4

图5. 三角形5a和双层三角形5b的自组装

Figure 5. Self-assembly of triangle 5a and ditrigon 5b

图6. 舍宾斯基三角形6a的自组装及其选择性金属转化

Figure 6. Self-assembly of Sierpiński triangle 6a and its site-selective transmetalation

图7. 二维金属超分子大环和三维金属笼的自组装

图8. 四角星7a和六角星7b的自组装

Figure 8. Self-assembly of the four-pointed star 7a and six-pointed star 7b

图9. 三聚六边形8a、星形六角体8b和三角形8c的构建

图10. 星形金属笼9a和9b的构建

图11. 二聚体胶囊10a~10c、舍宾斯基三角棱柱10d和立方星10e的构建

图12. 双层多室截半立方体11的构建

图13. 异金属纳米土星12的自组装

图14. 三叶草形金属环13a和超分子笼13b的自组装

图15. Sierpiński三角形14a、Sierpiński四面体14b和Sierpiński八面体14c的自组装

图16. 二维菱形结构15a和巨型棱锥四面体超分子15b的自组装

化合物	吸收最大值/nm	发射最大值/nm	量子产率^a/%
[Cd₄L¹₂L²₂]	286 (4.5), 355 (1.4)	467	14.4
[Cd₄L¹₂L³₂]	278 (6.7), 330 (1.1)	472	13.3
[Cd₄L¹₂L⁴₂]	283 (19.6), 343 (10.2)	473	6.2
[Cd₆L¹₃L⁵₃]	279 (13.2), 336 (1.9)	473	6.3
[Cd₄L⁵₂L⁷₂]	279 (10.1), 333 (2.5)	393, 463	14.4
[Cd₄L²₂L⁷₂]	280 (9.8), 335 (2.8)	393, 450	21.2
[Cd₉L⁷₃L⁸₃]	281 (10.5), 335 (3.9)	381, 464	8.2
[Cd₃L¹⁰₂]	278 (4.9), 325 (6.3)	407, 492	5.3
[Cd₆L¹₃L¹⁰₂]	280 (10.2), 340 (1.6)	472	2.1
[Cd₆L⁷₃L¹⁰₂]	281 (18.4), 332 (6.0)	395, 495	7.1
[Cd₆L⁹₃L¹⁰₂]	280 (10.8), 335 (1.7)	477	2.1
[Cd₁₂L¹⁰₄L¹¹₄]	286 (3.5), 330 (1.6)	472	3.4

表1. 乙腈中的吸收和发射光谱最大值, 摩尔吸光系数和量子产率

Table 1. Absorption and emission band maxima, molar extinction coefficients, and quantum yields in MeCN

图17. 巨型棱锥四面体15b的催化研究: (a)与2,2,6,6-四甲基-4-哌啶酮混合的15b在氙灯下的电子自旋共振光谱(λ>420 nm, 300 W), (b)氙灯(λ>420 nm, 300 W)下15b催化2-氯乙基硫醚转化的研究, (c) 15b在氙灯(λ>420 nm, 300 W)下不同时间催化2-氯乙基硫醚的1H NMR谱

Figure 17. Catalytic study of Triakis tetrahedron 15b: (a) ESR spectra of the Triakis tetrahedron 15b mixed with 4-oxo-TMP under Xe lamp (λ>420 nm, 300 W), (b) conversion of CEES catalyzed by the Triakis tetrahedron 15b under Xe lamp (λ>420 nm, 300 W), (c) 1H NMR spectra of CEES catalyzed by the Triakis tetrahedron 15b under Xe lamp (λ>420 nm, 300 W) at different time. Reprinted with permission from Ref. [84], copyright 2023, Elsevier

图18. 基于互补配体对组装而成的三种Co2+配合物

Figure 18. Self-assembly of three Co2+ complexes based on complementary terpyridine ligands pairing

图19. (a) 16a、(b) 16b和(c) 16c在连续冷却/加热循环时5000 Oe直流场下磁化率温度依赖性图

Figure 19. Plots of the temperature dependence of χMT under 5000 Oe dc field for (a) 16a, (b) 16b, and (c) 16c for successive cycles. Reprinted with permission from Ref. [88], copyright 2022, CCS Chinese Journal of Inorganic Chemistry

图20. 三种具有不同连接基团的Co2+配合物的合成过程

Figure 20. Synthesis of three Co2+ complexes with different linkers

图21. (a) 17a、(b) 17b和(c) 17c在连续扫描时磁化率温度依赖性图

参考文献 88

[1]	Jiang, Z.; Li, Y.; Wang, M.; Liu, D.; Yuan, J.; Chen, M.; Wang, J.; Newkome, G. R.; Sun, W.; Li, X.; Wang, P. Angew. Chem., Int. Ed. 2017, 56, 11450. doi: 10.1002/anie.v56.38
[2]	Sarkar, R.; Guo, K.; Moorefield, C. N.; Saunders, M. J.; Wesdemiotis, C.; Newkome, G. R. Angew. Chem., Int. Ed. 2014, 53, 12182. doi: 10.1002/anie.v53.45
[3]	Li, Y.; Jiang, Z.; Wang, M.; Yuan, J.; Liu, D.; Yang, X.; Chen, M.; Yan, J.; Li, X.; Wang, P. J. Am. Chem. Soc. 2016, 138, 10041. doi: 10.1021/jacs.6b06021
[4]	Schultz, A.; Li, X.; Barkakaty, B.; Moorefield, C. N.; Wesdemiotis, C.; Newkome, G. R. J. Am. Chem. Soc. 2012, 134, 7672. doi: 10.1021/ja303177v
[5]	Jiang, Z.; Li, Y.; Wang, M.; Song, B.; Wang, K.; Sun, M.; Liu, D.; Li, X.; Yuan, J.; Chen, M.; Guo, Y.; Yang, X.; Zhang, T.; Moorefield, C. N.; Newkome, G. R.; Xu, B.; Li, X.; Wang, P. Nat. Commun. 2017, 8, 15476. doi: 10.1038/ncomms15476
[6]	Zhang, Z.; Wang, H.; Wang, X.; Li, Y.; Song, B.; Bolarinwa, O.; Reese, R. A.; Zhang, T.; Wang, X.-Q.; Cai, J.; Xu, B.; Wang, M.; Liu, C.; Yang, H.-B.; Li, X. J. Am. Chem. Soc. 2017, 139, 8174. doi: 10.1021/jacs.7b01326 pmid: 28558196
[7]	Kaphan, D. M.; Levin, M. D.; Bergman, R. G.; Raymond, K. N.; Toste, F. D. Science 2015, 350, 1235. doi: 10.1126/science.aad3087 pmid: 26785485
[8]	MacGillivray, L. R.; Atwood, J. L. Nature 1997, 389, 469. doi: 10.1038/38985
[9]	Roberts, D. A.; Pilgrim, B. S.; Cooper, J. D.; Ronson, T. K.; Zarra, S.; Nitschke, J. R. J. Am. Chem. Soc. 2015, 137, 10068. doi: 10.1021/jacs.5b05080
[10]	Cao, L.; Wang, P.; Miao, X.; Dong, Y.; Wang, H.; Duan, H.; Yu, Y.; Li, X.; Stang, P. J. J. Am. Chem. Soc. 2018, 140, 7005. doi: 10.1021/jacs.8b03856
[11]	Mahata, K.; Frischmann, P. D.; Wuerthner, F. J. Am. Chem. Soc. 2013, 135, 15656. doi: 10.1021/ja4083039
[12]	Hong, C. M.; Morimoto, M.; Kapustin, E. A.; Alzakhem, N.; Bergman, R. G.; Raymond, K. N.; Toste, F. D. J. Am. Chem. Soc. 2018, 140, 6591. doi: 10.1021/jacs.8b01701
[13]	Suzuki, K.; Tominaga, M.; Kawano, M.; Fujita, M. Chem. Commun. 2009, 1638.
[14]	Meng, W.; Breiner, B.; Rissanen, K.; Thoburn, J. D.; Clegg, J. K.; Nitschke, J. R. Angew. Chem., Int. Ed. 2011, 50, 3479. doi: 10.1002/anie.v50.15
[15]	Tan, C.; Jiao, J.; Li, Z.; Liu, Y.; Han, X.; Cui, Y. Angew. Chem., Int. Ed. 2018, 57, 2085. doi: 10.1002/anie.v57.8
[16]	Xie, T.-Z.; Guo, K.; Guo, Z.; Gao, W.-Y.; Wojtas, L.; Ning, G.-H.; Huang, M.; Lu, X.; Li, J.-Y.; Liao, S.-Y.; Chen, Y.-S.; Moorefield, C. N.; Saunders, M. J.; Cheng, S. Z. D.; Wesdemiotis, C.; Newkome, G. R. Angew. Chem., Int. Ed. 2015, 54, 9224. doi: 10.1002/anie.v54.32
[17]	Clingerman, D. J.; Kennedy, R. D.; Mondloch, J. E.; Sarjeant, A. A.; Hupp, J. T.; Farha, O. K.; Mirkin, C. A. Chem. Commun. 2013, 49, 11485. doi: 10.1039/c3cc44173c
[18]	Ghosh, K.; Hu, J.; White, H. S.; Stang, P. J. J. Am. Chem. Soc. 2009, 131, 6695. doi: 10.1021/ja902045q
[19]	Olenyuk, B.; Levin, M. D.; Whiteford, J. A.; Shield, J. E.; Stang, P. J. J. Am. Chem. Soc. 1999, 121, 10434. doi: 10.1021/ja9931933
[20]	Wang, H.; Ji, X.; Li, Z.; Huang, F. Adv. Mater. 2017, 29, 1606117. doi: 10.1002/adma.v29.14
[21]	Yamashina, M.; Sartin, M. M.; Sei, Y.; Akita, M.; Takeuchi, S.; Tahara, T.; Yoshizawa, M. J. Am. Chem. Soc. 2015, 137, 9266. doi: 10.1021/jacs.5b06195 pmid: 26166243
[22]	Yan, X.; Cook, T. R.; Wang, P.; Huang, F.; Stang, P. J. Nat. Chem. 2015, 7, 342. doi: 10.1038/nchem.2201
[23]	Mugridge, J. S.; Zahl, A.; van Eldik, R.; Bergman, R. G.; Raymond, K. N. J. Am. Chem. Soc. 2013, 135, 4299. doi: 10.1021/ja309949q pmid: 23391095
[24]	Xiao, T.; Elmes, R.; Yao, Y. Front. Chem. 2020, 8, 628200. doi: 10.3389/fchem.2020.628200
[25]	Xiao, T.; Zhou, L.; Sun, X.-Q.; Huang, F.; Lin, C.; Wang, L. Chin. Chem. Lett. 2020, 31, 1. doi: 10.1016/j.cclet.2019.05.011
[26]	Horiuchi, S.; Yamaguchi, T.; Tessarolo, J.; Tanaka, H.; Sakuda, E.; Arikawa, Y.; Meggers, E.; Clever, G. H.; Umakoshi, K. Nat. Commun. 2023, 14, 155. DOI: 10.1038/s41467-023-35850-4
[27]	Jiang, B.; Zhang, J.; Ma, J.-Q.; Zheng, W.; Chen, L.-J.; Sun, B.; Li, C.; Hu, B.-W.; Tan, H.; Li, X.; Yang, H.-B. J. Am. Chem. Soc. 2016, 138, 738. doi: 10.1021/jacs.5b11409 pmid: 26741405
[28]	Bai, L.; Wang, N.; Li, Y. Adv. Mater. 2021, 34, 2102811. doi: 10.1002/adma.v34.22
[29]	Casini, A.; Crowley, J. D. Front. Chem. 2019, 7, 293. doi: 10.3389/fchem.2019.00293
[30]	Lu, Y.-L.; Song, J.-Q.; Qin, Y.-H.; Guo, J.; Huang, Y.-H.; Zhang, X.-D.; Pan, M.; Su, C.-Y. J. Am. Chem. Soc. 2022, 144, 8778. doi: 10.1021/jacs.2c02692
[31]	Tan, C.; Jiao, J.; Li, Z.; Liu, Y.; Han, X.; Cui, Y. Angew. Chem., Int. Ed. 2018, 57, 2085. doi: 10.1002/anie.v57.8
[32]	Clever, G. H.; Punt, P. Acc. Chem. Res. 2017, 50, 2233. doi: 10.1021/acs.accounts.7b00231
[33]	Turunen, L.; Warzok, U.; Schalley, C. A.; Rissanen, K. Chem 2017, 3, 861. doi: 10.1016/j.chempr.2017.08.010
[34]	Winter, A.; Hager, M. D.; Newkome, G. R.; Schubert, U. S. Adv. Mater. 2011, 23, 5728. doi: 10.1002/adma.v23.48
[35]	De, S.; Mahata, K.; Schmittel, M. Chem. Soc. Rev. 2010, 39, 1555. doi: 10.1039/b922293f
[36]	Fujita, D.; Ueda, Y.; Sato, S.; Mizuno, N.; Kumasaka, T.; Fujita, M. Nature 2016, 540, 563. doi: 10.1038/nature20771
[37]	Dietrich-Buchecker, C. O.; Sauvage, J. P.; Kintzinger, J. P. Tetrahedron Lett. 1983, 24, 5095. doi: 10.1016/S0040-4039(00)94050-4
[38]	Sauvage, J. P.; Weiss, J. J. Am. Chem. Soc. 1985, 107, 6108. pmid: 27715037
[39]	Saha, M. L.; Pramanik, S.; Schmittel, M. Chem. Commun. 2012, 48, 9459. doi: 10.1039/c2cc35036j
[40]	Mahata, K.; Saha, M. L.; Schmittel, M. J. Am. Chem. Soc. 2010, 132, 15933. doi: 10.1021/ja108419k
[41]	Saha, M. L.; Bats, J. W.; Schmittel, M. Org. Biomol. Chem. 2013, 11, 5592. doi: 10.1039/c3ob41258j
[42]	Saha, M. L.; Schmittel, M. J. Am. Chem. Soc. 2013, 135, 17743. doi: 10.1021/ja410425k
[43]	Saha, M. L.; Mittal, N.; Bats, J. W.; Schmittel, M. Chem. Commun. 2014, 50, 12189. doi: 10.1039/C4CC05465B
[44]	Wang, S.-Y.; Fu, J.-H.; Liang, Y.-P.; He, Y.-J.; Chen, Y.-S.; Chan, Y.-T. J. Am. Chem. Soc. 2016, 138, 3651. doi: 10.1021/jacs.6b01005
[45]	Mahata, K.; Schmittel, M. J. Am. Chem. Soc. 2009, 131, 16544. doi: 10.1021/ja907185k
[46]	Schmittel, M.; Ganz, A. Chem. Commun. 1997, 999.
[47]	Lal Saha, M.; Schmittel, M. Org. Biomol. Chem. 2012, 10, 4651. doi: 10.1039/c2ob25098e
[48]	Wang, S. Y.; Huang, J. Y.; Liang, Y. P.; He, Y. J.; Chen, Y. S.; Zhan, Y. Y.; Hiraoka, S.; Liu, Y. H.; Peng, S. M.; Chan, Y. T. Chem. - Eur. J. 2018, 24, 9274. doi: 10.1002/chem.v24.37
[49]	Fu, J.-H.; Wang, S.-Y.; Chen, Y.-S.; Prusty, S.; Chan, Y.-T. J. Am. Chem. Soc. 2019, 141, 16217. doi: 10.1021/jacs.9b08731
[50]	Rousseaux, S. A. L.; Gong, J. Q.; Haver, R.; Odell, B.; Claridge, T. D. W.; Herz, L. M.; Anderson, H. L. J. Am. Chem. Soc. 2015, 137, 12713. doi: 10.1021/jacs.5b07956 pmid: 26378660
[51]	Wang, S.-C.; Cheng, K.-Y.; Fu, J.-H.; Cheng, Y.-C.; Chan, Y.-T. J. Am. Chem. Soc. 2020, 142, 16661. doi: 10.1021/jacs.0c06618
[52]	Song, B.; Zhang, Z.; Wang, K.; Hsu, C.-H.; Bolarinwa, O.; Wang, J.; Li, Y.; Yin, G.-Q.; Rivera, E.; Yang, H.-B.; Liu, C.; Xu, B.; Li, X. Angew. Chem., Int. Ed. 2017, 56, 5258. doi: 10.1002/anie.201701417 pmid: 28382756
[53]	Riwar, L.-J.; Trapp, N.; Root, K.; Zenobi, R.; Diederich, F. Angew. Chem., Int. Ed. 2018, 57, 17259. doi: 10.1002/anie.v57.52
[54]	Xie, J.; Peng, H.-J.; Huang, J.-Q.; Xu, W.-T.; Chen, X.; Zhang, Q. Angew. Chem., Int. Ed. 2017, 56, 16415. doi: 10.1002/anie.v56.51
[55]	Yang, Y.; Jing, X.; Shi, Y.; Wu, Y.; Duan, C. J. Am. Chem. Soc. 2023, 145, 10136. doi: 10.1021/jacs.3c00626
[56]	Kohlhaas, M.; Zähres, M.; Mayer, C.; Engeser, M.; Merten, C.; Niemeyer, J. Chem. Commun. 2019, 55, 3298. doi: 10.1039/C8CC10152C
[57]	MacGillivray, L. R.; Atwood, J. L. Nature 1997, 389, 469. doi: 10.1038/38985
[58]	Ugono, O.; Moran, J. P.; Holman, K. T. Chem. Commun. 2008, 1404.
[59]	Kobayashi, K.; Yamada, Y.; Yamanaka, M.; Sei, Y.; Yamaguchi, K. J. Am. Chem. Soc. 2004, 126, 13896. pmid: 15506730
[60]	He, L.; Wang, S.-C.; Lin, L.-T.; Cai, J.-Y.; Li, L.; Tu, T.-H.; Chan, Y.-T. J. Am. Chem. Soc. 2020, 142, 7134. doi: 10.1021/jacs.0c01482
[61]	He, L.; Hsu, H.-K.; Li, L.; Lin, L.-T.; Tu, T.-H.; Ong, T.-G.; Liou, G.-G.; Chan, Y.-T. Chem 2022, 8, 494. doi: 10.1016/j.chempr.2021.11.013
[62]	Toyota, S.; Tsurumaki, E. Chem. Eur. J. 2019, 25, 6878. doi: 10.1002/chem.v25.28
[63]	Yamamoto, Y.; Tsurumaki, E.; Wakamatsu, K.; Toyota, S. Angew. Chem., Int. Ed. 2018, 57, 8199. doi: 10.1002/anie.201804430 pmid: 29846033
[64]	Zhan, S.-Z.; Li, J.-H.; Zhang, G.-H.; Li, M.-D.; Sun, S.; Zheng, J.; Ning, G.-H.; Li, M.; Kuang, D.-B.; Wang, X.-D.; Li, D. Chem. Commun. 2020, 56, 3325. doi: 10.1039/D0CC00532K
[65]	Stasyuk, O. A.; Stasyuk, A. J.; Sola, M.; Voityuk, A. A. Phys. Chem. Chem. Phys. 2021, 23, 2126. doi: 10.1039/d0cp05919f pmid: 33437974
[66]	Zhang, J.; Qiu, Z.; Zhao, C.; Lu, Y.; Li, W.; Liu, L.; Wang, C.; Tan, Y.; Wang, T. Nano Res. 2023, 16, 3372. doi: 10.1007/s12274-022-5158-9
[67]	He, L.; Li, L.; Wang, S.-C.; Chan, Y.-T. Chem. Commun. 2023, 59, 11500. doi: 10.1039/D3CC03414C
[68]	Schultz, A.; Li, X.; McCusker, C. E.; Moorefield, C. N.; Castellano, F. N.; Wesdemiotis, C.; Newkome, G. R. Chem. Eur. J. 2012, 18, 11569. doi: 10.1002/chem.v18.37
[69]	Li, Z.; Luo, S.; Chen, M.; Yu, X.; Li, X. Acta Chim. Sinica 2023, 81, 1447 (in Chinese). doi: 10.6023/A23050201
	(李志凯, 罗思琪, 陈敏, 於秀君, 李霄鹏,, 化学学报, 2023, 81, 1447.) doi: 10.6023/A23050201
[70]	Newkome, G. R.; Cho, T. J.; Moorefield, C. N.; Cush, R.; Russo, P. S.; Godínez, L. A.; Saunders, M. J.; Mohapatra, P. Chem. Eur. J. 2002, 8, 2946.
[71]	Xie, T.-Z.; Li, J.-Y.; Guo, Z.; Ludlow, J. M., III; Lu, X.; Moorefield, C. N.; Wesdemiotis, C.; Newkome, G. R. Eur. J. Inorg. Chem. 2016, 1671.
[72]	Chakraborty, S.; Sarkar, R.; Endres, K.; Xie, T.-Z.; Ghosh, M.; Moorefield, C. N.; Saunders, M. J.; Wesdemiotis, C.; Newkome, G. R. Eur. J. Org. Chem. 2016, 2016, 5091. doi: 10.1002/ejoc.v2016.30
[73]	Liu, D.; Jiang, Z.; Wang, M.; Yang, X.; Liu, H.; Chen, M.; Moorefield, C. N.; Newkome, G. R.; Li, X.; Wang, P. Chem. Commun. 2016, 52, 9773. doi: 10.1039/C6CC04482D
[74]	Zhang, Z.; Ma, L.; Fang, F.; Hou, Y.; Lu, C.; Mu, C.; Zhang, Y.; Liu, H.; Gao, K.; Wang, M.; Zhang, Z.; Li, X.; Zhang, M. JACS Au 2022, 2, 1479. doi: 10.1021/jacsau.2c00245
[75]	Ju, H.; Tsuruoka, Y.; Hayano, M.; Lee, E.; Park, K.-M.; Ikeda, M.; Ishi-i, J.-i.; Kuwahara, S.; Habata, Y. Angew. Chem., Int. Ed. 2021, 60, 650. doi: 10.1002/anie.v60.2
[76]	Jiang, Z.; Zhao, H.; Wang, J.; Chen, B.; Lv, W.; Li, Y.; Dong, Q.; Liu, D.; Liu, W.; Wang, M.; Fu, F.; Hwang, S.-H.; Chen, M.; Wang, P. Chin. Chem. Lett. 2023, 34, 108334. doi: 10.1016/j.cclet.2023.108334
[77]	Elbert, T.; Ray, W. J.; Kowalik, Z. J.; Skinner, J. E.; Graf, K. E.; Birbaumer, N. Physiol. Rev. 1994, 74, 1. doi: 10.1152/physrev.1994.74.1.1 pmid: 8295931
[78]	Jiang, Z.; Liu, D.; Chen, M.; Wang, J.; Zhao, H.; Li, Y.; Zhang, Z.; Xie, T.; Wang, F.; Li, X.; Newkome, G. R.; Wang, P. iScience 2020, 23, 101064. doi: 10.1016/j.isci.2020.101064
[79]	Li, C.; Li, R.; Xu, Z.; Li, J.; Zhang, X.; Li, N.; Zhang, Y.; Shen, Z.; Tang, H.; Wang, Y. J. Am. Chem. Soc. 2021, 143, 14417. doi: 10.1021/jacs.1c05949
[80]	Jiang, Z.; Liu, W.; Wang, J.; Chen, B.; Wu, Z.; Fu, F.; Miao, R.; Ouyang, T.; Lv, W.; Huang, Y.; Liu, D.; Liu, Z.-Q.; Chen, M.; Wang, P. Inorg. Chem. 2023, 62, 8923. doi: 10.1021/acs.inorgchem.3c00587
[81]	Li, C.; Zhang, X.; Li, N.; Wang, Y.; Yang, J.; Gu, G.; Zhang, Y.; Hou, S.; Peng, L.; Wu, K.; Nieckarz, D.; Szabelski, P.; Tang, H.; Wang, Y. J. Am. Chem. Soc. 2017, 139, 13749. doi: 10.1021/jacs.7b05720
[82]	Sarkar, R.; Xie, T.-Z.; Endres, K. J.; Wang, Z.; Moorefield, C. N.; Saunders, M. J.; Ghorai, S.; Patri, A. K.; Wesdemiotis, C.; Dobrynin, A. V.; Newkome, G. R. J. Am. Chem. Soc. 2020, 142, 5526. doi: 10.1021/jacs.0c01168
[83]	Wang, J.; Jiang, Z.; Liu, W.; Wu, Z.; Miao, R.; Fu, F.; Yin, J.-F.; Chen, B.; Dong, Q.; Zhao, H.; Li, K.; Wang, G.; Liu, D.; Yin, P.; Li, Y.; Chen, M.; Wang, P. Angew. Chem., Int. Ed. 2023, 62, e20221423.
[84]	Jiang, Z.; Wang, J.; Zhang, H.; Liu, W.; Wu, Z.; Zhao, H.; Yin, J.-F.; Chen, B.; Li, Y.; Yin, P.; Chan, Y.-T.; Wang, K.; Chen, M.; Wang, P. Cell Rep. Phys. Sci. 2023, 4, 101293.
[85]	Goodall, W.; Williams, J. A. G. Chem. Commun. 2001, 2514.
[86]	Hofmeier, H.; Schubert, U. S. Chem. Soc. Rev. 2004, 33, 373. pmid: 15280970
[87]	Zhang, S.-Y.; Sun, H.-Y.; Wang, R.-G.; Meng, Y.-S.; Liu, T.; Zhu, Y.-Y. Dalton Trans. 2022, 51, 9888. doi: 10.1039/D2DT00436D
[88]	Yang, R.; Zhang, S.-Y.; Wang, R.-G.; Meng, Y.-S.; Liu, T.; Zhu, Y.-Y. Chinese J. Inorg. Chem. 2022, 38, 1477 (in Chinese).
	(杨蕊, 张舒雅, 王润国, 孟银杉, 刘涛, 朱元元, 无机化学学报, 2022, 38, 1477.)

6,6″-二(2,6-二甲氧基苯)-三联吡啶及其衍生物金属配位自组装的研究进展

Research Progress on Metal-coordination-driven Self-assembly of 6,6"-Bis(2,6-dimethoxy-benzene)-terpyridine and Its Derivatives

RichHTML

PDF

可视化

摘要/Abstract

引用此文

分享此文

图/表 22

参考文献 88

相关文章 10

编辑推荐

相关统计

本文评价

[1]	李志凯, 罗思琪, 陈敏, 於秀君, 李霄鹏. 双三联吡啶钌配合物的研究进展^★[J]. 化学学报, 2023, 81(10): 1447-1461.
[2]	杨忠杰, 张小飞, 施亚男, 隆昶, 张彬灏, 闫书豪, 常琳, 唐智勇. 二维疏水铜基纳米片的合成及在硫醚类化合物催化氧化中的应用[J]. 化学学报, 2020, 78(9): 980-988.
[3]	刘明丽, 吴琪, 史慧芳, 安众福, 黄维. 有机/金属有机力致发光材料的研究进展[J]. 化学学报, 2018, 76(4): 246-258.
[4]	钱长涛, 王春红, 陈耀峰. 稀土金属有机配合物化学60年[J]. 化学学报, 2014, 72(8): 883-905.
[5]	王锋, 梁文静, 王文光, 陈彬, 冯科, 张丽萍, 佟振合, 吴骊珠. 三联吡啶锇Os(Ⅱ)配合物为光敏剂的二元铁氢化酶模拟化合物的合成及其光物理过程[J]. 化学学报, 2012, 70(22): 2306-2310.
[6]	潘月秀, 佟斌, 支俊格, 赵玮, 申进波, 石建兵, 董宇平. 基于过渡金属离子与三联吡啶的配位作用构筑全共轭层-层自组装超薄功能膜[J]. 化学学报, 2009, 67(24): 2779-2784.
[7]	丁慧颖, 宋林青, 陈景荣, 王雪松, 张宝文. TiO₂纳米颗粒对钌(II)三联吡啶配合物光损伤小牛胸腺DNA能力的影响[J]. 化学学报, 2006, 64(17): 1799-1804.
[8]	潘敦,吴骊珠,佟振合,张丽萍. 1,3-取代杯[4]芳烃三联吡啶配体的合成及其离子识别性能的研究[J]. 化学学报, 2006, 64(14): 1479-1482.
[9]	丁涪江,何云清,刘柳斜,赵可清. 平面四方金属苯配合物的非线性光学性质的从头算研究[J]. 化学学报, 2005, 63(24): 2199-2204.
[10]	李宏洋, 施锋, 彭孝军, 张蓉, 陈小强, 张丽珠, 孙立成. Mn(Ⅲ,Ⅲ)配合物及含酚配体[N₄O₃]^3--Ru(bPy)₃模型化合物的性能研究[J]. 化学学报, 2004, 62(9): 916-922.