Sculpting the tunable mesoscopic helical chirality into poly(m-phenylenediamine) via Mn2+ coordination
Bibliographic record
Abstract
No abstract is available for this record. The assistant can identify its topic from the title, but cannot infer the study’s results.
Source: Not provided · Quality: missing
Research context
OpenAlex topics: Synthesis and Properties of Aromatic Compounds · Supramolecular Self-Assembly in Materials · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (37)
Show source-provided references
1. Xu L, Wang X, Wang W, et al. Enantiomer-dependent immunological response to chiral nanoparticles. Nature, 2022, 601: 366–37310.1038/s41586-021-04243-2 ↗
2. Dou X, Mehwish N, Zhao C, et al. Supramolecular hydrogels with tunable chirality for promising biomedical applications. Acc Chem Res, 2020, 53: 852–86210.1021/acs.accounts.0c00012 ↗
3. Liu M, Zhang L, Wang T. Supramolecular chirality in self-assembled systems. Chem Rev, 2015, 115: 7304–739710.1021/cr500671p ↗
4. Liu G, Humphrey MG, Zhang C, et al. Self-assembled stereomutation with supramolecular chirality inversion. Chem Soc Rev, 2023, 52: 4443–448710.1039/D2CS00476C ↗
5. Xu C, Yin C, Wu W, et al. Tunable room-temperature phosphorescence and circularly polarized luminescence encoding helical supramolecular polymer. Sci China Chem, 2022, 65: 75–8110.1007/s11426-021-1104-9 ↗
6. Fu K, Liu G. Full-color circularly polarized luminescence of supramolecular polymers with handedness inversion regulated by anion and temperature. ACS Nano, 2024, 18: 2279–228910.1021/acsnano.3c10151 ↗
7. Wen X, Du S, Zhang L, et al. Chiral deep eutectic solvents enable full-color and white circularly polarized luminescence from achiral luminophores. Angew Chem Int Ed, 2023, 62: e20231181610.1002/anie.202311816 ↗
8. Huang Z, He Z, Ding B, et al. Photoprogrammable circularly polarized phosphorescence switching of chiral helical polyacetylene thin films. Nat Commun, 2022, 13: 784110.1038/s41467-022-35625-3 ↗
9. Hu Y, Huang Z, Willner I, et al. Multicolor circularly polarized luminescence of a single-component system revealing multiple information encryption. CCS Chem, 2023, 6: 518–52710.31635/ccschem.023.202302904 ↗
10. Sun S, Li X, Xu C, et al. Scale effect of circularly polarized luminescent signal of matter. Natl Sci Rev, 2023, 10: nwad07210.1093/nsr/nwad072 ↗
11. Zhao J, Zhang P, Qiao H, et al. Supramolecular chirality suppresses molecular chirality: selective chiral recognition in hierarchically coassembled pyridine-benzimidazole conjugates with precise ee% detection. J Phys Chem Lett, 2021, 12: 2912–292110.1021/acs.jpclett.1c00548 ↗
12. Shen Z, Sang Y, Wang T, et al. Asymmetric catalysis mediated by a mirror symmetry-broken helical nanoribbon. Nat Commun, 2019, 10: 397610.1038/s41467-019-11840-3 ↗
13. Yang F, Yue B, Zhu L. Light-triggered modulation of supramolecular chirality. Chem Eur J, 2023, 29: e20220379410.1002/chem.202203794 ↗
14. Xiong T, Yuan X, Wang H, et al. Integrating the (311) facet of MnO2 and the fuctional groups of poly(m-phenylenediamine) in core-shell MnO2@poly(m-phenylenediamine) adsorbent to remove Pb ions from water. J Hazard Mater, 2020, 389: 12215410.1016/j.jhazmat.2020.122154 ↗
15. Wang M, Huang Z, Feng Z, et al. Recyclable poly-m-phenylenediamine selectively recovers gold from acidic solutions. New J Chem, 2023, 47: 14217–1422410.1039/D3NJ01885G ↗
16. Li C, Peng H, Cai J, et al. Emulsion-guided controllable construction of anisotropic particles: droplet size determines particle structure. Adv Mater, 2021, 33: 210293010.1002/adma.202102930 ↗
17. Qin Y, Miao L, Mansuer M, et al. Spatial confinement strategy for micelle-size-mediated modulation of mesopores in hierarchical porous carbon nanosheets with an efficient capacitive response. ACS Appl Mater Interfaces, 2022, 14: 33328–3333910.1021/acsami.2c08342 ↗
18. Zhou C, Ren Y, Han J, et al. Controllable supramolecular chiral twisted nanoribbons from achiral conjugated oligoaniline derivatives. J Am Chem Soc, 2018, 140: 9417–942510.1021/jacs.7b12178 ↗
19. Zhang Y, Deng J. Chiral helical polymer materials derived from achiral monomers and their chiral applications. Polym Chem, 2020, 11: 5407–542310.1039/D0PY00934B ↗
20. Yao H, Zhang H, Zheng H. The construction of helical carbon-based skeletons for enhanced electrocatalytic performance. ChemCatChem, 2024, e20240017710.1002/cctc.202400177 ↗
21. Wang Y, Yang T, Fan X, et al. Anchoring Fe species on the highly curved surface of S and N Co-doped carbonaceous nanosprings for oxygen electrocatalysis and a flexible zinc-air battery. Angew Chem Int Ed, 2024, 63: e20231303410.1002/anie.202313034 ↗
22. Han F, Shi F, Li H, et al. High-efficiency circularly polarized luminescence from twisted tetraarylethylene-bridged polybissilsesquioxane nanotubes. ACS Appl Polym Mater, 2022, 4: 6742–674810.1021/acsapm.2c01112 ↗
23. Zha X, Chen Y, Fan H, et al. Handedness inversion of chiral 3-aminophenol formaldehyde resin nanotubes mediated by metal coordination. Angew Chem Int Ed, 2021, 60: 7759–776910.1002/anie.202013790 ↗
24. Zha X, Xu G, Khan NA, et al. Sculpting mesoscopic helical chirality into covalent organic framework nanotubes from entirely achiral building blocks. Angew Chem Int Ed, 2024, 63: e20231638510.1002/anie.202316385 ↗
25. Zha X, Zuo M, Xu G, et al. Chiral transfer amidst one-dimensional linear polymers and two-dimensional network covalent organic frameworks: striking a fine balance between helicity and crystallinity. Nano Res, 2024, 17: 5726–573410.1007/s12274-024-6523-7 ↗
26. Zha X, Xu G, Xiong Y, et al. Modulating the macroscopic helicity of poly(m-phenylenediamine) by achiral monomer copolymerization. Adv Funct Mater, 2023, 33: 221195610.1002/adfm.202211956 ↗
27. Wang X, Li Y, Dai T, et al. Preparation of pectin/poly(m-phenylenediamine) microsphere and its application for Pb2+ removal. Carbohydrate Polyms, 2021, 260: 11781110.1016/j.carbpol.2021.117811 ↗
28. Bai T, Ai J, Liao L, et al. Chiral mesostructured NiO films with spin polarisation. Angew Chem Int Ed, 2021, 60: 9421–942610.1002/anie.202101069 ↗
29. Liang Z, Fan X, Lei H, et al. Cobalt-nitrogen-doped helical carbonaceous nanotubes as a class of efficient electrocatalysts for the oxygen reduction reaction. Angew Chem Int Ed, 2018, 57: 13187–1319110.1002/anie.201807854 ↗
30. Liu S, Duan Y, Feng X, et al. Synthesis of enantiopure carbonaceous nanotubes with optical activity. Angew Chem Int Ed, 2013, 52: 6858–686210.1002/anie.201301199 ↗
31. Liu G, Sheng J, Wu H, et al. Controlling supramolecular chirality of two-component hydrogels by J- and H-aggregation of building blocks. J Am Chem Soc, 2018, 140: 6467–647310.1021/jacs.8b03309 ↗
32. Wang Z, Hao A, Xing P. Chiroptical helices of N-terminal aryl amino acids through orthogonal noncovalent interactions. Angew Chem Int Ed, 2020, 59: 11556–1156510.1002/anie.202003351 ↗
33. Wang F, Feng C. Metal-ion-mediated supramolecular chirality of L-phenylalanine based hydrogels. Angew Chem Int Ed, 2018, 57: 5655–565910.1002/anie.201800251 ↗
34. Zhao J, Liu Y, Hao A, et al. High-throughput synthesis of chiroptical nanostructures from synergistic hydrogen-bonded coassemblies. ACS Nano, 2020, 14: 2522–253210.1021/acsnano.0c00352 ↗
35. Gao C, Li S, Zhao C, et al. Self-assembled metal-coordination nanohelices as efficient and robust chiral supramolecular catalysts for enantioselective reactions. Small, 2023, 20: 231023410.1002/smll.202310234 ↗
36. Wang F, Feng C. Stoichiometry-controlled inversion of supramolecular chirality in nanostructures Co-assembled with bipyridines. Chem Eur J, 2018, 24: 1509–151310.1002/chem.201704431 ↗
37. Zou H, Wang R, Shi Z, et al. One-dimensional periodic mesoporous organosilica helical nanotubes with amphiphilic properties for the removal of contaminants from water. J Mater Chem A, 2016, 4: 4145–415410.1039/C6TA00708B ↗