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Synlett 2025; 36(05): 464-467
DOI: 10.1055/s-0043-1775039
DOI: 10.1055/s-0043-1775039
letter
Thieme Chemistry Journals Awardees 2024
1,2-Diaroyl Benzofurans: Synthesis and Photochromic Properties
Financial support from the National Natural Science Foundation of China (No. 22071051), the Natural Science Foundation of Hunan Province (No. 2024JJ5255), and Hunan Normal University are greatly appreciated.

Abstract
A cascade reaction involving a base-promoted nucleophilic substitution reaction between diketones and α-bromoacetophenone derivatives and the subsequent selective condensation–cyclization was developed for the synthesis of 1,2-diaroyl benzofurans. 1,2-Diaroyl benzofurans with different functional groups and structures exhibit reversible photochromic behaviors in solution, solid state, and thin films with diverse colors, demonstrating a potential application in the field of optical functional materials.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2204-8461.
- Supporting Information
Publikationsverlauf
Eingereicht: 14. Juni 2024
Angenommen nach Revision: 23. Juli 2024
Artikel online veröffentlicht:
15. August 2024
© 2024. Thieme. All rights reserved
Georg Thieme Verlag KG
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References and Notes
- 1a Stevens M, Merilaita S. Philos. Trans. R. Soc., B 2009; 364: 423
- 1b Stress Response in Microbiology . Requena JM. Calster Academic Press; Norfolk: 2012
- 2a Costil R, Holzheimer M, Crespi S, Simeth NA, Feringa BL. Chem. Rev. 2021; 121: 13213
- 2b Pooler DR. S, Lubbe AS, Crespi S, Feringa BL. Chem. Sci. 2021; 12: 14964
- 2c Feng Y, Ovalle M, Seale JS. W, Lee CK, Kim DJ, Astumian RD, Stoddart JF. J. Am. Chem. Soc. 2021; 143: 5569
- 3a Erbas-Cakmak S, Leigh DA, McTernan CT, Nussbaumer AL. Chem. Rev. 2015; 115: 10081
- 3b Krause S, Feringa BL. Nat. Chem. Rev. 2020; 4: 550
- 4a Weißenfels M, Gemen J, Klajn R. Chem 2021; 7: 23
- 4b Lee H, Tessarolo J, Langbehn D, Baksi A, Herges R, Clever GH. J. Am. Chem. Soc. 2022; 144: 3099
- 5a Lerch MM, Hansen MJ, van Dam GM, Szymanski W, Feringa BL. Angew. Chem. Int. Ed. 2016; 55: 10978
- 5b Hüll K, Morstein J, Trauner D. Chem. Rev. 2018; 118: 10710
- 5c Morstein J, Trauner D. Curr. Opin. Chem. Biol. 2019; 50: 145
- 5d Fuchter MJ. J. Med. Chem. 2020; 63: 11436
- 6a Göstl R, Senf A, Hecht S. Chem. Soc. Rev. 2014; 43: 1982
- 6b Dorel R, Feringa BL. Chem. Commun. 2019; 55: 6477
- 7a Sun C.-L, Wang C, Boulatov R. ChemPhotoChem 2019; 3: 268
- 7b Goulet-Hanssens A, Eisenreich F, Hecht S. Adv. Mater. 2020; 32: e1905966
- 7c Wang H, Ji X, Page ZA, Sessler JL. Mater. Chem. Front. 2020; 4: 1024
- 7d Danowski W, van Leeuwen T, Browne WR, Feringa BL. Nanoscale Adv. 2021; 3: 24
- 7e Wang Z, Hölzel H, Moth-Poulsen K. Chem. Soc. Rev. 2022; 51: 7313
- 7f Thaggard GC, Haimerl J, Park KC, Lim J, Fischer RA, Maldeni Kankanamalage BK. P, Yarbrough BJ, Wilson GR, Shustova NB. J. Am. Chem. Soc. 2022; 144: 23249
- 8a Irie M. Chem. Rev. 2000; 100: 1685
- 8b Tian H, Yang S. Chem. Soc. Rev. 2004; 33: 85
- 9a Berkovic G, Krongauz V, Weiss V. Chem. Rev. 2000; 100: 1741
- 9b Minkin VI. Chem. Rev. 2004; 104: 2751
- 9c Molecular Switches, Parts 1 and 2, 2nd ed. Feringa BL, Browne WR. Wiley-VCH; Weinheim: 2011
- 9d Klajn R. Chem. Soc. Rev. 2014; 43: 148
- 9e Pianowski Z. Molecular Photoswitches. Chemistry, Properties, and Applications. Wiley-VCH; Weinheim: 2022
- 9f Zhang Z, Wang W, O’Hagan M, Dai J, Zhang J, Tian H. Angew. Chem. Int. Ed. 2022; 61: e202205758
- 10a Bandara HM. D, Burdette SC. Chem. Soc. Rev. 2012; 41: 1809
- 10b Beharry AA, Woolley GA. Chem. Soc. Rev. 2011; 40: 4422
- 10c Crespi S, Simeth NA, König B. Nat. Rev. Chem. 2019; 3: 133
- 10d Mukherjee A, Seyfried MD, Ravoo BJ. Angew. Chem. Int. Ed. 2023; 62: e202304437
- 11a Zhang S, Sun C, Zhang J, Qin S, Liu J, Ren Y, Zhang L, Hu W, Yang H, Yang D. Adv. Funct. Mater. 2023; 33: 2305364
- 11b Demchenko AP. Methods Appl. Fluoresc. 2020; 8: 022001
- 13 Si X, Jia Y, Luan X, Yang L, Pei Y, Zhou W. Angew. Chem. Int. Ed. 2019; 58: 2660
- 14 Zhang T, Lou X.-Y, Li X, Tu X, Han J, Zhao B, Yang Y.-W. Adv. Mater. 2023; 35: 2210551
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