journal article·2025-02-03

Engineering Host–Guest Interactions to Drive Enhanced and Tunable Chiral Emission in Achiral Porphyrin Nanostructures

Ashok Badrinarayan Jadhav, Arunima Cheran, Camelia Dutta, M. Praveen Kumar, Ravi Kumar Pujala, Jatish Kumar

ACS Materials Letters· Volume 7· Issue 2
Publisher page

Abstract

Circularly polarized luminescence (CPL), an emergent technique to study excited state optical activity, is recently finding vast applications in diverse fields. The research focus has been to develop facile strategies to overcome the low luminescence dissymmetry exhibited by molecules and materials. We herein demonstrate a host–guest approach to achieve intense chiral luminescence in a series of achiral porphyrin nanostructures through their self-assembly with a chiral gelator. Efforts focused toward formulating a structure–property correlation revealed that modulating the host–guest interactions is critical to the generation as well as tuning of the CPL activity. Luminescence dissymmetry as high as 0.015 could be achieved through a judicious design strategy. The applicability of the as synthesized nanohybrid as a potential chiral light emitting device is demonstrated by coating the nanocomposite onto an LED surface.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Luminescence and Fluorescent Materials · Synthesis and Properties of Aromatic Compounds

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

Affiliations

Department of Chemistry

Indian Institute of Science Education and Research (IISER) Tirupati

Soft and Active Matter Group, Department of Physics

Funding

Science and Engineering Research Board · Ministry of Education, India · Indian Institute of Science Education and Research Tirupati · Science and Engineering Research Board, Core Research Grant

References (61)

Show source-provided references
1. 10.1126/science.aaz794910.1126/science.aaz7949 ↗
2. 10.1038/s41557-019-0320-z10.1038/s41557-019-0320-z ↗
3. 10.1126/sciadv.adi994410.1126/sciadv.adi9944 ↗
4. 10.1002/adom.20180053810.1002/adom.201800538 ↗
5. 10.1002/adma.20120496110.1002/adma.201204961 ↗
6. 10.1002/adma.20231239610.1002/adma.202312396 ↗
7. 10.1021/acsami.3c0743110.1021/acsami.3c07431 ↗
8. 10.1021/acs.jpclett.5b0145210.1021/acs.jpclett.5b01452 ↗
9. 10.1039/D2TC02193E10.1039/D2TC02193E ↗
10. 10.1039/D2SC05794H10.1039/D2SC05794H ↗
11. 10.1039/D3SC00686G10.1039/D3SC00686G ↗
12. 10.1002/adma.20190011010.1002/adma.201900110 ↗
13. 10.1039/C7SC04312K10.1039/C7SC04312K ↗
14. 10.1039/D0CS01583K10.1039/D0CS01583K ↗
15. 10.1021/acs.jpclett.3c0312710.1021/acs.jpclett.3c03127 ↗
16. 10.3389/fchem.2020.55765010.3389/fchem.2020.557650 ↗
17. 10.1002/chem.20160132810.1002/chem.201601328 ↗
18. 10.1016/j.tet.2019.04.02510.1016/j.tet.2019.04.025 ↗
19. 10.1002/chem.20210187710.1002/chem.202101877 ↗
20. 10.1021/jacs.9b0258210.1021/jacs.9b02582 ↗
21. 10.1021/acsnano.1c0818210.1021/acsnano.1c08182 ↗
22. 10.1002/anie.20230828110.1002/anie.202308281 ↗
23. 10.1021/acs.jpclett.1c0086510.1021/acs.jpclett.1c00865 ↗
24. 10.1016/j.tetlet.2019.15123210.1016/j.tetlet.2019.151232 ↗
25. 10.1039/C7CC01351E10.1039/C7CC01351E ↗
26. 10.1039/C9QM00652D10.1039/C9QM00652D ↗
27. 10.1002/chem.20240225710.1002/chem.202402257 ↗
28. 10.1039/D4NR02110J10.1039/D4NR02110J ↗
29. 10.1021/ja412294s10.1021/ja412294s ↗
30. 10.1002/ange.20200118610.1002/ange.202001186 ↗
31. 10.1002/chem.20160268410.1002/chem.201602684 ↗
32. 10.1016/j.dyepig.2020.10859310.1016/j.dyepig.2020.108593 ↗
33. 10.1039/C3CS60443H10.1039/C3CS60443H ↗
34. 10.1007/BFb003682710.1007/BFb0036827 ↗
35. 10.1071/CH0814510.1071/CH08145 ↗
36. 10.1021/acsomega.9b0138010.1021/acsomega.9b01380 ↗
37. 10.1002/adma.20190612910.1002/adma.201906129 ↗
38. 10.1002/adma.20180662610.1002/adma.201806626 ↗
39. 10.1021/acs.jpcc.3c0354310.1021/acs.jpcc.3c03543 ↗
40. 10.1002/agt2.19810.1002/agt2.198 ↗
41. 10.1021/ja000052o10.1021/ja000052o ↗
42. 10.1002/chir.117610.1002/chir.1176 ↗
43. 10.1021/acs.jpclett.4c0187310.1021/acs.jpclett.4c01873 ↗
44. 10.1039/C8CC09114E10.1039/C8CC09114E ↗
45. 10.1002/slct.20180021310.1002/slct.201800213 ↗
46. 10.1016/j.molliq.2024.12554410.1016/j.molliq.2024.125544 ↗
47. 10.1021/jacs.0c0770710.1021/jacs.0c07707 ↗
48. 10.1039/C5CC08488A10.1039/C5CC08488A ↗
49. 10.1039/D1CC03314J10.1039/D1CC03314J ↗
50. 10.1016/j.dyepig.2021.10933210.1016/j.dyepig.2021.109332 ↗
51. 10.1039/D1NR08506A10.1039/D1NR08506A ↗
52. 10.1039/C4CC04228J10.1039/C4CC04228J ↗
53. 10.1002/chem.20150219310.1002/chem.201502193 ↗
54. 10.1016/j.molstruc.2024.13809810.1016/j.molstruc.2024.138098 ↗
55. 10.1142/S108842462330001X10.1142/S108842462330001X ↗
56. 10.1002/anie.20200058910.1002/anie.202000589 ↗
57. 10.1021/acsami.0c0208010.1021/acsami.0c02080 ↗
58. 10.1021/acs.jpclett.3c0132810.1021/acs.jpclett.3c01328 ↗
59. 10.1021/jacs.9b1318410.1021/jacs.9b13184 ↗
60. 10.1021/acsnano.9b0325510.1021/acsnano.9b03255 ↗
61. 10.1002/ange.20231513610.1002/ange.202315136 ↗