Emissive Supramolecular Systems Based on Reversible Bond Formation and Noncovalent Interactions.
luminescence
metal-metal interactions
molecular recognition
supramolecular chemistry
Journal
Chemical record (New York, N.Y.)
ISSN: 1528-0691
Titre abrégé: Chem Rec
Pays: United States
ID NLM: 101085550
Informations de publication
Date de publication:
Mar 2021
Mar 2021
Historique:
received:
07
10
2020
revised:
05
11
2020
pubmed:
26
11
2020
medline:
26
11
2020
entrez:
25
11
2020
Statut:
ppublish
Résumé
Noncovalent interactions and reversible bond formations are widely seen in natural systems for the construction of sophisticated molecular systems that perform various biological processes. Inspired by the natural systems, luminescent supramolecular systems constructed by coordination-driven self-assembly and homometallic metal-metal interations have been studied increasingly. These supramolecular systems show fascinating luminescent behaviors that are not observed from single components. This review summarizes our progress in the development of two types of unique luminescent supramolecular systems. The mononuclear Pt(II) complex units can sandwich coinage metal ions to form heteropolynuclear complexes involving heterometallic metal-metal interactions. A close proximity of the two or three different metal ions by the noncovalent forces lead to orbital overlapping among the coinage metal ions and the Pt(II) complex units, showing emission color change accompanied with structural transformation and reversible metal binding behaviors. Emissive host-guest systems consisting of mononuclear metal complexes and a hydrogen-bonded capsule are also developed, that show a unique encapsulation-induced emission enhancement (EIEE) behavior.
Identifiants
pubmed: 33236813
doi: 10.1002/tcr.202000125
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
469-479Subventions
Organisme : JSPS KAKENHI
ID : JP16H0659
Organisme : JSPS KAKENHI
ID : JP19K15589
Organisme : JSPS KAKENHI
ID : JP19H04587
Organisme : JSPS KAKENHI
ID : JP20K05542
Organisme : JSPS KAKENHI
ID : JP20H05231
Informations de copyright
© 2020 The Chemical Society of Japan & Wiley-VCH GmbH.
Références
J. L. Atwood, J.-M. Lehn, Comprehensive Supramolecular Chemistry, Pergamon, Oxford, 1996.
R. Chakrabarty, P. S. Mukherjee, P. J. Stang, Chem. Rev. 2011, 111, 6810-6918;
A. J. McConnell, C. S. Wood, P. P. Neelakandan, J. N. Nitschke, Chem. Rev. 2015, 115, 7729-7793;
L.-J. Chen, H.-B. Yang, M. Shionoya, Chem. Soc. Rev. 2017, 46, 2555-2576;
W. M. Bloch, G. H. Clever, Chem. Commun. 2017, 53, 8506-8516.
M. Yoshizawa, J. K. Klosterman, M. Fujita, Angew. Chem. Int. Ed. 2009, 48, 3418-3438;
M. J. Wiester, P. A. Ulmann, C. A. Mirkin, Angew. Chem. Int. Ed. 2010, 49, 2-26;
B. Breiner, J. K. Clegg, J. R. Nitschke, Chem. Sci. 2011, 2, 51-56;
S. H. A. M. Leenders, R. Gramage-Doria, B. de Bruin, J. N. H. Reek, Chem. Soc. Rev. 2015, 44, 433-448;
C. J. Brown, F. D. Toste, R. G. Bergman, K. N. Raymond, Chem. Rev. 2015, 115, 3012-3035;
C. Tan, D. Chu, X. Tang, Y. Liu, W. Xuan, Y. Cui, Chem. Eur. J. 2019, 25, 662-672;
Y. Fang, J. A. Powell, E. Li, Q. Wang, Z. Perry, A. Kirchon, X. Yang, Z. Xiao, C. Zhu, L. Zhang, F. Huang, H.-C. Zhou, Chem. Soc. Rev. 2019, 48, 4707-4730;
K. Wang, J. H. Jordan, X.-Y. Hu, L. Wang, Angew. Chem. Int. Ed. 2020, 59, 13712-13721.
A. Kaloudi-Chantzea, N. Karakostas, C. P. Raptopoulou, V. Psycharis, E. Saridakis, J. Griebel, R. Hermann, G. Pistolis, J. Am. Chem. Soc. 2010, 132, 16327-16329;
F. Lin, H.-Y. Peng, J.-X. Chen, D. T. W. Chik, Z. Cai, K. N. C. Wong, V. W. W. Yam, H. N. C. Wong, J. Am. Chem. Soc. 2010, 132, 16383-16392;
Y. Shi, I. Sánchez-Molina, C. Cao, T. R. Cook, P. J. Stang, Proc. Natl. Acad. Sci. USA 2014, 111, 9390-9395;
M. Ebina, A. Kobayashi, T. Ogawa, M. Yoshida, M. Kato, Inorg. Chem. 2015, 54, 8878-8880;
A. K.-W. Chan, W. H. Lam, Y. Tanaka, K. M.-C. Wong, V. W.-W. Yam, Proc. Natl. Acad. Sci. USA 2015, 112, 690-695;
X. Yan, T. R. Cook, P. Wang, F. Huang, P. J. Stang, Nat. Chem. 2015, 7, 342-348;
M. L. Saha, X. Yan, P. J. Stang, Acc. Chem. Res. 2016, 49, 2527-2539;
C. Lescop, Acc. Chem. Res. 2017, 50, 885-894;
M. Zhang, S. Yin, J. Zhang, Z. Zhou, M. L. Saha, C. Lu, P. J. Stang, Proc. Natl. Acad. Sci. USA 2017, 114, 3044-3049;
C.-L. Liu, R.-L. Zhang, C.-S. Lin, L.-P. Zhou, L.-X. Cai, J.-T. Kong, S.-Q. Yang, K.-L. Han, Q.-F. Sun, J. Am. Chem. Soc. 2017, 139, 12474-12479;
S. Datta, M. L. Saha, P. J. Stang, Acc. Chem. Res. 2018, 51, 2047-2063;
Z. Gao, Y. Han, Z. Gao, F. Wang, Acc. Chem. Res. 2018, 51, 2719-2729;
Y.-Q. He, W. Fudickar, J.-H. Tang, H. Wang, X. Li, J. Han, Z. Wang, M. Liu, Y.-W. Zhong, T. Linker, P. J. Stang, J. Am. Chem. Soc. 2020, 142, 2601-2608;
Z. Yang, Y. Wang, X. Liu, R. T. Vanderlinden, R. Ni, X. Li, P. J. Stang, J. Am. Chem. Soc. 2020, 142, 13689-13694;
L. Chen, C. Chen, Y. Sun, S. Lu, H. Huo, T. Tan, A. Li, X. Li, G. Ungar, F. Liu, M. Zhang, Angew. Chem. Int. Ed. 2020, 59, 10143-10150.
D. R. Martir, E. Zysman-Colman, Coord. Chem. Rev. 2018, 364, 86-117;
D. R. Martir, E. Zysman-Colman, Chem. Commun. 2019, 55, 139-158.
K. M.-C. Wong, M. M.-Y. Chan, V. W.-W. Yam, Adv. Mater. 2014, 26, 5558-5568;
K. Li, G. S. M. Tong, Q. Wan, G. Cheng, W.-Y. Tong, W.-H. Ang, W.-L. Kwong, C.-M. Che, Chem. Sci. 2016, 7, 1653;
M. Yoshida, M. Kato, Coord. Chem. Rev. 2018, 355, 101-115;
Z. Gao, Y. Han, Z. Gao, F. Wang, Acc. Chem. Res. 2018, 51, 2719-2729;
A. K.-W. Chan, V. W.-W. Yam, Acc. Chem. Res. 2018, 51, 3041-3051;
Y. Han, Z. Gao, C. Wang, R. Zhong, F. Wang, Coord. Chem. Rev. 2020, 414, 213300.
X. Zhang, B. Li, Z.-H. Chen, Z.-N. Chen, J. Mater. Chem. 2012, 22, 11427-11441;
O. S. Wenger, Chem. Rev. 2013, 113, 3686-3733;
A. Kobayashi, M. Kato, Eur. J. Inorg. Chem. 2014, 4469-4483.
K. Umakoshi, T. Kojima, K. Saito, S. Akatsu, M. Onishi, S. Ishizaka, N. Kitamura, Y. Nakao, S. Sakaki, Y. Ozawa, Inorg. Chem. 2008, 47, 5033-5035.
K. Umakoshi, K. Saito, Y. Arikawa, M. Onishi, S. Ishizaka, N. Kitamura, Y. Nakao, S. Sakaki, Chem. Eur. J. 2009, 15, 4238-4242.
S. Akatsu, Y. Kanematsu, T. Kurihara, S. Sueyoshi, Y. Arikawa, M. Onishi, S. Ishizaka, N. Kitamura, Y. Nakao, S. Sakaki, K. Umakoshi, Inorg. Chem. 2012, 51, 7977-7992.
K. Nishihara, M. Ueda, A. Higashitani, Y. Nakao, Y. Arikawa, S. Horiuchi, E. Sakuda, K. Umakoshi, Dalton Trans. 2016, 45, 4978-4982.
S. Horiuchi, S. Moon, E. Sakuda, A. Ito, Y. Arikawa, K. Umakoshi, Dalton Trans. 2018, 47, 7113-7117.
M. Ueda, S. Horiuchi, E. Sakuda, Y. Nakao, Y. Arikawa, K. Umakoshi, Chem. Commun. 2017, 53, 6405-6408.
S. Horiuchi, H. Tanaka, E. Sakuda, Y. Arikawa, K. Umakoshi, Chem. Eur. J. 2016, 22, 17533-17537.
S. Horiuchi, C. Matsuo, E. Sakuda, Y. Arikawa, G. H. Clever, K. Umakoshi, Dalton Trans. 2020, 49, 8472-8477.
S. Horiuchi, H. Tanaka, E. Sakuda, Y. Arikawa, K. Umakoshi, Dalton Trans. 2019, 48, 5156-5160.
H. Schmidbaur, A. Schier, Chem. Soc. Rev. 2012, 41, 370-412;
H. Schmidbaur, A. Schier, Angew. Chem. Int. Ed. 2015, 54, 746-784;
V. W.-W. Yam, V. K.-M. Au, S. Y.-L. Leung, Chem. Rev. 2015, 115, 7589-7728;
N. V. S. Harisomayajula, S. Makovetskyi, Y.-C. Tsai, Chem. Eur. J. 2019, 25, 8936-8954;
N. Mirzadeh, S. H. Privér, A. J. Blake, H. Schmidbaur, S. K. Bhargava, Chem. Rev. 2020, 120, 7551-7591;
J. Zheng, Z. Lu, K. Wu, G.-H. Ning, D. Li, Chem. Rev. 2020, 120, 9675-9742.
J. R. Berenguer, E. Lalinde, M. T. Moreno, Coord. Chem. Rev. 2010, 254, 832-875;
I. G. Powers, C. Uyeda, ACS Catal. 2017, 7, 936-959;
A. K. Gupta, A. Orthaber, Chem. Eur. J. 2018, 24, 7536-7559;
H. Yu, B. Rao, W. Jiang, S. Yang, M. Zhu, Coord. Chem. Rev. 2019, 378, 595-617.
Z.-N. Chen, N. Zhao, Y. Fan, J. Ni, Coord. Chem. Rev. 2009, 253, 1-20;
Á. Díez, E. Lalinde, M. T. Moreno, Coord. Chem. Rev. 2011, 255, 2426-2447;
J. R. Berenguer, E. Lalinde, M. T. Moreno, Coord. Chem. Rev. 2018, 366, 69-90;
Q.-C. Zhang, H. Xiao, X. Zhang, L.-J. Xu, Z.-N. Chen, Coord. Chem. Rev. 2019, 378, 121-133;
M. Yoshida, M. Kato, Coord. Chem. Rev. 2020, 408, 213194.
A. Bondi, J. Phys. Chem. 1964, 68, 441-451.
R. Visbal, M. C. Gimeno, Chem. Soc. Rev. 2014, 43, 3551-3574;
M. Elie, J.-L. Renaud, S. Gaillard, Polyhedron 2018, 140, 158-168.
L. R. MacGillivray, J. L. Atwood, Nature 1997, 389, 469-472;
A. Shivanyuk, J. Rebek Jr., Proc. Natl. Acad. Sci. USA 2001, 98, 7662-7665;
Q. Zhang, L. Catti, V. R. I. Kaila, K. Tiefenbacher, Chem. Sci. 2017, 8, 1653-1657.
Q. Zhang, L. Catti, K. Tiefenbacher, Acc. Chem. Res. 2018, 51, 2107-2114;
C. Gaeta, C. Talotta, M. D. Rosa, P. L. Manna, A. Soriente, P. Neri, Chem. Eur. J. 2019, 25, 4899-4913.
A. Cavarzan, A. Scarso, P. Sgarbossa, G. Strukul, J. N. H. Reek, J. Am. Chem. Soc. 2011, 133, 2848-2851;
G. Bianchini, A. Scarso, G. L. Sorella, G. Strukul, Chem. Commun. 2012, 48, 12082-12084.
S. Ladouceur, E. Zysman-Colman, Eur. J. Inorg. Chem. 2013, 2985-3007.
S. J. Pike, J. J. Hutchinson, C. A. Hunter, J. Am. Chem. Soc. 2017, 139, 6700-6706.
M. Kvasnica, J. C. Chapin, B. W. Purse, Angew. Chem. Int. Ed. 2011, 50, 2244-2248;
J. C. Chapin, M. Kvasnica, B. W. Purse, J. Am. Chem. Soc. 2012, 134, 15000-15009;
S. N. Journey, K. L. Teppang, C. A. Garcia, S. A. Brim, D. Onofrei, J. B. Addison, G. P. Holland, B. W. Purse, Chem. Sci. 2017, 8, 7737-7745.
J. V. Caspar, T. J. Meyer, J. Am. Chem. Soc. 1983, 105, 5583-5590.