Chirality of Perylene Diimides: Design Strategies and Applications.

Chiral Substituents Chirality Perylene Diimides Supramolecules Twisted Plane

Journal

Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543

Informations de publication

Date de publication:
04 07 2022
Historique:
received: 16 02 2022
pubmed: 1 4 2022
medline: 30 6 2022
entrez: 31 3 2022
Statut: ppublish

Résumé

Chirality is a particularly important concept in nature and exists at all length scales, ranging from the molecular level to the supramolecular level. Over the last two decades, various design strategies have been developed to construct chiral materials based on perylene diimides (PDIs) and to mimic the chiral assembly process in biological systems, but applications of these chiral aggregates are still at an early stage. This Minireview summarizes recent progress in the synthesis and properties of chiral PDIs. The chirality in PDI-based materials can be generated by three different approaches: from the twisted planes of PDIs, the chiral substituents of PDIs, and the co-assembly of achiral PDIs and chiral guests. A comprehensive understanding of the applications of chiral PDIs as well as potential future developments is also provided.

Identifiants

pubmed: 35357065
doi: 10.1002/anie.202202532
doi:

Substances chimiques

Imides 0
Perylene 5QD5427UN7

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202202532

Informations de copyright

© 2022 Wiley-VCH GmbH.

Références

G. Albano, G. Pescitelli, L. Di Bari, Chem. Rev. 2020, 120, 10145-10243.
 
S. Huang, H. Yu, Q. Li, Adv. Sci. 2021, 8, 2002132;
M. Rodin, J. Li, D. Kuckling, Chem. Soc. Rev. 2021, 50, 8147-8177;
K. Ariga, T. Mori, T. Kitao, T. Uemura, Adv. Mater. 2020, 32, 1905657.
 
C. Schaack, A. M. Evans, F. Ng, M. L. Steigerwald, C. Nuckolls, J. Am. Chem. Soc. 2022, 144, 42-51;
X. Yan, Q. Wang, X. Chen, Y. B. Jiang, Adv. Mater. 2020, 32, 1905667.
E. Krieg, A. Niazov-Elkan, E. Cohen, Y. Tsarfati, B. Rybtchinski, Acc. Chem. Res. 2019, 52, 2634-2646.
 
F. Würthner, C. R. Saha-Möller, B. Fimmel, S. Ogi, P. Leowanawat, D. Schmidt, Chem. Rev. 2016, 116, 962-1052;
J. Yang, B. Xiao, A. Tang, J. Li, X. Wang, E. Zhou, Adv. Mater. 2019, 31, 1804699;
K. Liu, Z. Xu, M. Yin, Prog. Polym. Sci. 2015, 46, 25-54.
 
S. Chen, P. Slattum, C. Wang, L. Zang, Chem. Rev. 2015, 115, 11967-11998;
M. Hecht, F. Würthner, Acc. Chem. Res. 2021, 54, 642-653.
 
M. Sun, K. Müllen, M. Yin, Chem. Soc. Rev. 2016, 45, 1513-1528;
D. Bialas, E. Kirchner, M. I. S. Röhr, F. Würthner, J. Am. Chem. Soc. 2021, 143, 4500-4518;
R. S. Wilson-Kovacs, X. Fang, M. J. L. Hagemann, H. E. Symons, C. F. J. Faul, Chem. Eur. J. 2022, 28, e202103443;
Z. Yang, X. Chen, Acc. Chem. Res. 2019, 52, 1245-1254;
A. Nowak-Król, F. Würthner, Org. Chem. Front. 2019, 6, 1272-1318.
 
M. Weh, J. Rühe, B. Herbert, A. M. Krause, F. Würthner, Angew. Chem. Int. Ed. 2021, 60, 15323-15327;
Angew. Chem. 2021, 133, 15451-15455;
A. Nowak-Król, M. I. S. Röhr, D. Schmidt, F. Würthner, Angew. Chem. Int. Ed. 2017, 56, 11774-11778;
Angew. Chem. 2017, 129, 11936-11940.
M. Hecht, P. Leowanawat, T. Gerlach, V. Stepanenko, M. Stolte, M. Lehmann, F. Würthner, Angew. Chem. Int. Ed. 2020, 59, 17084-17090;
Angew. Chem. 2020, 132, 17232-17238.
P. Osswald, F. Würthner, J. Am. Chem. Soc. 2007, 129, 14319-14326.
Z. Xie, F. Würthner, Org. Lett. 2010, 12, 3204-3207.
Z. Xie, V. Stepanenko, K. Radacki, F. Würthner, Chem. Eur. J. 2012, 18, 7060-7070.
B. Teichmann, A. Krause, M.-J. Lin, F. Würthner, Angew. Chem. Int. Ed. 2022, 61, e202117625;
Angew. Chem. 2022, 134, e202117625.
R. K. Dubey, M. M. Franco, A. M. Alonso, J. Am. Chem. Soc. 2022, 144, 2765-2774.
 
P. Osswald, M. Reichert, G. Bringmann, F. Würthner, J. Org. Chem. 2007, 72, 3403-3411;
M. M. Safont-Sempere, P. Osswald, K. Radacki, F. Würthner, Chem. Eur. J. 2010, 16, 7380-7384.
W. Qiu, S. Chen, X. Sun, Y. Liu, D. Zhu, Org. Lett. 2006, 8, 867-870.
 
R. Renner, B. Mahlmeister, O. Anhalt, M. Stolte, F. Würthner, Chem. Eur. J. 2021, 27, 11997-12006;
B. Mahlmeister, R. Renner, O. Anhalt, M. Stolteab, F. Würthner, J. Mater. Chem. C 2022, 10, 2581-2591.
T. Mori, Chem. Rev. 2021, 121, 2373-2412.
W. Yue, W. Jiang, M. Böckmann, N. L. Doltsinis, Z. Wang, Chem. Eur. J. 2014, 20, 5209-5213.
L. Zhang, I. Song, J. Ahn, M. Han, M. Linares, M. Surin, H. J. Zhang, J. H. Oh, J. Lin, Nat. Commun. 2021, 12, 142.
B. Liu, M. Bockmann, W. Jiang, N. L. Doltsinis, Z. Wang, J. Am. Chem. Soc. 2020, 142, 7092-7099.
Z. Ma, T. Winands, N. Liang, D. Meng, W. Jiang, N. L. Doltsinis, Z. Wang, Sci. China Chem. 2020, 63, 208-214.
G. Liu, T. Koch, Y. Li, N. L. Doltsinis, Z. Wang, Angew. Chem. Int. Ed. 2019, 58, 178-183;
Angew. Chem. 2019, 131, 184-189.
D. Meng, G. Liu, C. Xiao, Y. Shi, L. Zhang, L. Jiang, K. K. Baldridge, Y. Li, J. S. Siegel, Z. Wang, J. Am. Chem. Soc. 2019, 141, 5402-5408.
 
N. J. Schuster, R. H. Sánchez, D. Bukharina, N. A. Kotov, N. Berova, F. Ng, M. L. Steigerwald, C. Nuckolls, J. Am. Chem. Soc. 2018, 140, 6235-6239;
M. Milton, N. J. Schuster, D. W. Paley, R. H. Sánchez, F. Ng, M. L. Steigerwald, C. Nuckolls, Chem. Sci. 2019, 10, 1029-1034.
X. Xiao, S. K. Pedersen, D. Aranda, J. Yang, R. A. Wiscons, M. Pittelkow, M. L. Steigerwald, F. Santoro, N. J. Schuster, C. Nuckolls, J. Am. Chem. Soc. 2021, 143, 983-991.
D. Aranda, N. J. Schuster, X. Xiao, F. J. Ávila Ferrer, F. Santoro, C. Nuckolls, J. Phys. Chem. C 2021, 125, 2554-2564.
M. Sapotta, P. Spenst, C. R. Saha-Möller, F. Würthner, Org. Chem. Front. 2019, 6, 892-899.
R. F. Fink, J. Seibt, V. Engel, M. Renz, M. Kaupp, S. Lochbrunner, H. Zhao, J. Pfister, F. Würthner, B. Engels, J. Am. Chem. Soc. 2008, 130, 12858-12859.
J. C. Hu, W. F. Kuang, K. Deng, W. J. Zou, Y. W. Huang, Z. X. Wei, C. F. J. Faul, Adv. Funct. Mater. 2012, 22, 4149-4158.
M. Wehner, M. I. S. Röhr, V. Stepanenko, F. Würthner, Nat. Commun. 2020, 11, 5460.
 
F. Würthner, C. Bauer, V. Stepanenko, S. Yagai, Adv. Mater. 2008, 20, 1695-1698;
T. E. Kaiser, V. Stepanenko, F. Würthner, J. Am. Chem. Soc. 2009, 131, 6719-6732.
J. van Herrikhuyzen, A. Syamakumari, A. P. H. J. Schenning, E. W. Meijer, J. Am. Chem. Soc. 2004, 126, 10021-10027.
 
C. Roche, H. J. Sun, P. Leowanawat, F. Araoka, B. E. Partridge, M. Peterca, D. A. Wilson, M. E. Prendergast, P. A. Heiney, R. Graf, H. W. Spiess, X. Zeng, G. Ungar, V. Percec, Nat. Chem. 2016, 8, 80-89;
L. Wang, B. E. Partridge, N. Huang, J. T. Olsen, D. Sahoo, X. Zeng, G. Ungar, R. Graf, H. W. Spiess, V. Percec, J. Am. Chem. Soc. 2020, 142, 9525-9536.
S. Amiralaei, D. Uzun, H. Icil, Photochem. Photobiol. Sci. 2008, 7, 936-947.
S. Asir, A. S. Demir, H. Icil, Dyes Pigm. 2010, 84, 1-13.
A. Pucci, F. Donati, S. Nazzi, G. U. Barretta, G. Pescitelli, L. D. Bari, G. Ruggeri, React. Funct. Polym. 2010, 70, 951-960.
X. Shang, I. Song, H. Ohtsu, Y. H. Lee, T. Zhao, T. Kojima, J. H. Jung, M. Kawano, J. H. Oh, Adv. Mater. 2017, 29, 1605828.
 
C. D. Schmidt, C. Böttcher, A. Hirsch, Eur. J. Org. Chem. 2009, 5337-5349;
D. Wei, Y. Yu, L. Ge, Z. Wang, C. Chen, R. Guo, Langmuir 2021, 37, 9232-9243.
P. K. Sukul, S. Malik, Chem. Lett. 2018, 47, 576-579.
S. Bai, S. Debnath, N. Javid, P. W. Frederix, S. Fleming, C. Pappas, R. V. Ulijn, Langmuir 2014, 30, 7576-7584.
 
X. T. Liu, Z. J. Huang, Y. W. Huang, L. Y. Zhu, J. Y. Fu, J. Phys. Chem. C 2017, 121, 7558-7563;
Y. Huang, J. Hu, W. Kuang, Z. Wei, C. F. Faul, Chem. Commun. 2011, 47, 5554-5556.
 
K. R. Wang, H. W. An, L. Wu, J. C. Zhang, X. L. Li, Chem. Commun. 2012, 48, 5644-5646;
K. R. Wang, H. W. An, Y. Q. Wang, J. C. Zhang, X. L. Li, Org. Biomol. Chem. 2013, 11, 1007-1012;
K. R. Wang, D. Han, G. J. Cao, X. L. Li, Chem. Asian J. 2015, 10, 1204-1214.
A. P. H. J. Schenning, J. van Herrikhuyzen, P. Jonkheijm, Z. J. Chen, F. Würthner, E. W. Meijer, J. Am. Chem. Soc. 2002, 124, 10252-10253.
F. Würthner, Z. J. Chen, F. J. M. Hoeben, P. Osswald, C. C. You, J. van Herrikhuyzen, A. P. H. J. Schenning, P. P. A. M. Schoot, E. W. Meijer, E. H. A. Beckers, S. C. J. Meskers, R. A. J. Janssen, J. Am. Chem. Soc. 2004, 126, 10611-10618.
C. Thalacker, F. Würthner, Adv. Funct. Mater. 2002, 12, 209-218.
F. Silly, A. Q. Shaw, M. R. Castell, G. A. Briggs, Chem. Commun. 2008, 1907-1909.
D. Franke, M. Vos, M. Antonietti, N. A. J. M. Sommerdijk, C. F. J. Faul, Chem. Mater. 2006, 18, 1839-1847.
Y. Huang, Y. Yan, B. M. Smarsly, Z. Wei, C. F. J. Faul, J. Mater. Chem. 2009, 19, 2356-2362.
J. M. Abendroth, N. Nakatsuka, M. Ye, D. Kim, E. E. Fullerton, A. M. Andrews, P. S. Weiss, ACS Nano 2017, 11, 7516-7526.
B. Roy, T. Noguchi, Y. Tsuchiya, D. Yoshihara, T. Yamamoto, S. Shinkai, J. Mater. Chem. C 2015, 3, 2310-2318.
Y. Liu, X. Gao, F. Lu, M. Hu, L. Shi, L. Zheng, Soft Matter 2017, 13, 3072-3075.
H. Zhao, S. Hussain, X. Y. Liu, S. L. Li, F. T. Lv, L. B. Liu, S. Wang, Chem. Eur. J. 2019, 25, 9834-9839.
M. Kumar, S. J. George, Chem. Sci. 2014, 5, 3025-3030.
M. Kumar, M. D. Reddy, A. Mishra, S. J. George, Org. Biomol. Chem. 2015, 13, 9938-9942.
Y. Tidhar, H. Weissman, S. G. Wolf, A. Gulino, B. Rybtchinski, Chem. Eur. J. 2011, 17, 6068-6075.
J. Kumar, T. Nakashima, H. Tsumatori, T. Kawai, J. Phys. Chem. Lett. 2014, 5, 316-321.
J. Kumar, H. Tsumatori, J. Yuasa, T. Kawai, T. Nakashima, Angew. Chem. Int. Ed. 2015, 54, 5943-5947;
Angew. Chem. 2015, 127, 6041-6045.
F. Li, Y. Li, G. Wei, Y. Wang, S. Li, Y. Cheng, Chem. Eur. J. 2016, 22, 12910-12915.
D. Han, J. Han, S. Huo, Z. Qu, T. Jiao, M. Liu, P. Duan, Chem. Commun. 2018, 54, 5630-5633.
X. Shang, I. Song, J. H. Lee, W. Choi, J. Ahn, H. Ohtsu, J. C. Kim, J. Y. Koo, S. K. Kwak, J. H. Oh, ACS Nano 2020, 14, 14146-14156.
 
D. G. Blackmond, Cold Spring Harbor Perspect. Biol. 2019, 11, a032540;
X. Zhao, S. Q. Zang, X. Chen, Chem. Soc. Rev. 2020, 49, 2481-2503;
C. Hao, L. Xu, H. Kuang, C. Xu, Adv. Mater. 2020, 32, 1802075;
J. Yeom, P. P. G. Guimaraes, H. M. Ahn, B. Jung, Q. Hu, K. McHugh, M. J. Mitchell, C. Yun, R. Langer, A. Jaklene, Adv. Mater. 2020, 32, 1903878.
Y. Cai, D. Ni, W. Cheng, C. Ji, Y. Wang, K. Müllen, Z. Su, Y. Liu, C. Chen, M. Yin, Angew. Chem. Int. Ed. 2020, 59, 14014-14018;
Angew. Chem. 2020, 132, 14118-14122.
P. Sun, P. Yuan, G. Wang, W. Deng, S. Tian, C. Wang, X. Lu, W. Huang, Q. Fan, Biomacromolecules 2017, 18, 3375-3386.
 
C. Liu, S. Zhang, J. Li, J. Wei, K. Müllen, M. Yin, Angew. Chem. Int. Ed. 2019, 58, 1638-1642;
Angew. Chem. 2019, 131, 1652-1656;
S. Zhang, W. Guo, J. Wei, C. Li, X. J. Liang, M. Yin, ACS Nano 2017, 11, 3797-3805;
W. Cheng, H. Chen, C. Liu, C. Ji, G. Ma, M. Yin, View 2020, 1, 20200055;
C. Ji, W. Cheng, Q. Yuan, K. Müllen, M. Yin, Acc. Chem. Res. 2019, 52, 2266-2277.
W. Cheng, H. Cheng, S. Wan, X. Zhang, M. Yin, Chem. Mater. 2017, 29, 4218-4226.
B. He, Y. Chu, M. Yin, K. Müllen, C. An, J. Shen, Adv. Mater. 2013, 25, 4580-4584.
Y. Zheng, S. You, C. Ji, M. Yin, W. Yang, J. Shen, Adv. Mater. 2016, 28, 1375-1380.

Auteurs

Jie Li (J)

State Key Laboratory of Chemical Resource Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Pengyu Li (P)

State Key Laboratory of Chemical Resource Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Mingyu Fan (M)

State Key Laboratory of Chemical Resource Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Xian Zheng (X)

State Key Laboratory of Chemical Resource Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Jun Guan (J)

Key Lab of Organic Optoelectronics & Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, P. R. China.

Meizhen Yin (M)

State Key Laboratory of Chemical Resource Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Articles similaires

Perylene Dopamine Electrochemical Techniques Imides Luminescent Measurements
Hypericum Anthracenes Perylene Plant Breeding Flowers
1.00
Reactive Oxygen Species Perylene Energy Metabolism Mitochondria Quinones
1.00
Silver Perylene Metal Nanoparticles Anthracenes Fluorescent Dyes

Classifications MeSH