journal article·2022-01

Phthalocyanine‐Triggered Helical Dipeptide Nanotubes with Intense Circularly Polarized Luminescence

Xiqian Wang, Luyang Zhao, Chiming Wang, Xuenan Feng, Qing Ma, Gengxiang Yang, Tianyu Wang, Xuehai Yan, Jianzhuang Jiang

Small· Volume 18· Issue 4
Publisher page

Abstract

Abstract Nanotubes with circularly polarized luminescence (CPL) are attracting much attention due to many potential applications, such as chiroptical materials, displays, and sensing. However, it remains a challenge to change the assemblies of ordinarily molecular building blocks into CPL supramolecular nanotubes. Herein, the regulation of quite common dipeptide (Fmoc‐FF) assemblies into unprecedented helical nanotubes exhibiting intense CPL is reported by simply doping a few phthalocyanine (octakis(carboxyl)phthalocyaninato zinc complex (Pc)) molecules. Interestingly, altering the Fmoc‐FF/Pc molar ratios over a wide range cannot change the nanotubes structures according to transmission electron microscopy (TEM) and atomic force microscope (AFM) measurements. Although molecular dynamics simulations suggest that the noncovalent interactions between Fmoc‐FF and Pc are quite weak, few Pc molecules can still change the secondary structures of a large number of Fmoc‐FF assemblies, which hierarchically form helical supramolecular nanotubes with long‐range ordered molecular packing, leading to intense CPL signals with large luminescence dissymmetry factor (glum = 0.04). Consequently, the chiral reorganization of Fmoc‐FF assemblies is dependent on the coassembly between Pc molecule and Fmoc‐FF supramolecular architectures. These results open the possibility for the fine‐tuning of helix and supramolecular nanotubes with CPL properties by using a small number of cofactors.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Synthesis and Properties of Aromatic Compounds · Polydiacetylene-based materials and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Beijing Advanced Innovation Center for Materials Genome Engineering Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials Department of Chemistry and Chemical Engineering School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing 100083 China

State Key Laboratory of Biochemical Engineering Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 China

Funding

National Natural Science Foundation of China · Major Science and Technology Program for Water Pollution Control and Treatment · Beijing Municipal Commission of Education · University of Science and Technology Beijing

References (60)

Show source-provided references
1. 10.1126/science.115363410.1126/science.1153634 ↗
2. 10.1038/nature0160010.1038/nature01600 ↗
3. 10.1016/j.cell.2017.05.02810.1016/j.cell.2017.05.028 ↗
4. 10.1016/j.ejmech.2017.11.06210.1016/j.ejmech.2017.11.062 ↗
5. 10.2174/156802661766617010414564010.2174/1568026617666170104145640 ↗
6. 10.1021/nl035159z10.1021/nl035159z ↗
7. 10.1038/nnano.2006.13910.1038/nnano.2006.139 ↗
8. 10.1038/s41467-017-01447-x10.1038/s41467-017-01447-x ↗
9. 10.1002/anie.20170467810.1002/anie.201704678 ↗
10. 10.1002/anie.20180634710.1002/anie.201806347 ↗
11. 10.1002/anie.20200557510.1002/anie.202005575 ↗
12. 10.1002/anie.20150981010.1002/anie.201509810 ↗
13. 10.1039/C6CS00176A10.1039/C6CS00176A ↗
14. 10.1002/adma.20050152210.1002/adma.200501522 ↗
15. 10.1002/anie.20131115810.1002/anie.201311158 ↗
16. 10.1021/acsami.0c1329510.1021/acsami.0c13295 ↗
17. 10.1021/acsnano.6b0158710.1021/acsnano.6b01587 ↗
18. 10.1021/acs.accounts.0c0001210.1021/acs.accounts.0c00012 ↗
19. 10.1002/anie.20191178210.1002/anie.201911782 ↗
20. 10.1021/la804271d10.1021/la804271d ↗
21. 10.1016/j.mattod.2019.04.00210.1016/j.mattod.2019.04.002 ↗
22. 10.1002/admt.20190082910.1002/admt.201900829 ↗
23. 10.1021/acs.jpcc.9b0441410.1021/acs.jpcc.9b04414 ↗
24. 10.1002/advs.20190021810.1002/advs.201900218 ↗
25. 10.1039/C9TB01043B10.1039/C9TB01043B ↗
26. 10.1038/s42004-019-0170-z10.1038/s42004-019-0170-z ↗
27. 10.1039/C8SC04361B10.1039/C8SC04361B ↗
28. 10.1021/acs.jpclett.5b0145210.1021/acs.jpclett.5b01452 ↗
29. 10.1021/acs.accounts.0c0011210.1021/acs.accounts.0c00112 ↗
30. 10.1016/j.ccr.2020.21332910.1016/j.ccr.2020.213329 ↗
31. 10.3390/sym1211178610.3390/sym12111786 ↗
32. 10.1002/adma.20190011010.1002/adma.201900110 ↗
33. 10.1002/chem.20190095510.1002/chem.201900955 ↗
34. 10.1038/nphoton.2010.15610.1038/nphoton.2010.156 ↗
35. 10.1021/acsnano.1c0113410.1021/acsnano.1c01134 ↗
36. 10.1002/anie.20181264210.1002/anie.201812642 ↗
37. 10.1039/C9NR08032E10.1039/C9NR08032E ↗
38. 10.1002/anie.20210559310.1002/anie.202105593 ↗
39. 10.1002/anie.20210484310.1002/anie.202104843 ↗
40. 10.1021/cr030072j10.1021/cr030072j ↗
41. 10.1021/acs.chemrev.9b0050910.1021/acs.chemrev.9b00509 ↗
42. 10.1038/ncomms1572710.1038/ncomms15727 ↗
43. 10.1021/jacs.7b0461110.1021/jacs.7b04611 ↗
44. 10.1002/anie.20171064210.1002/anie.201710642 ↗
45. 10.1021/acsnano.5b0769010.1021/acsnano.5b07690 ↗
46. 10.1021/la900653q10.1021/la900653q ↗
47. 10.1002/chem.20210068110.1002/chem.202100681 ↗
48. 10.1021/ja047176b10.1021/ja047176b ↗
49. 10.1021/ja903467w10.1021/ja903467w ↗
50. 10.1021/jacs.7b0591610.1021/jacs.7b05916 ↗
51. 10.1039/c0sm01200a10.1039/c0sm01200a ↗
52. 10.1002/adma.20070122110.1002/adma.200701221 ↗
53. 10.1021/la202113j10.1021/la202113j ↗
54. 10.1021/cr900181u10.1021/cr900181u ↗
55. 10.1039/C8SC04687E10.1039/C8SC04687E ↗
56. 10.1039/b515476f10.1039/b515476f ↗
57. 10.1021/ja072536r10.1021/ja072536r ↗
58. 10.1021/ja803962910.1021/ja8039629 ↗
59. 10.1039/C8CC09401B10.1039/C8CC09401B ↗
60. 10.34133/2020/645212310.34133/2020/6452123 ↗