journal article·2022-04-08

Luminescent Conjugated Microporous Polymers for Selective Sensing and Ultrafast Detection of Picric Acid

Yogendra Nailwal, Manisha Devi, Santanu Kumar Pal

ACS Applied Polymer Materials· Volume 4· Issue 4
Publisher page

Abstract

Luminescent conjugated microporous polymers (CMPs) are one of the important class of porous organic materials that possess a fully π-conjugated skeleton and high surface area and have been utilized as light-emitting materials. In this work, we have designed and developed three luminescent CMPs based on truxene core (Tx-CMPs) via Suzuki–Miyaura cross-coupling reaction in one step. The flexible aryl linker in Tx-CMPs prevents the possibility of aggregation-caused quenching (ACQ) due to π–π stacking of layers and thus offers a high luminescence in the synthesized Tx-CMPs. All Tx-CMPs possess a high BET surface area (SBET = 788–915 m2 g–1) and excellent thermal stability. Utilizing the fluorescent nature and electron-rich property of the Tx-CMPs, we exploited them as a sensor for the selective and sensitive detection of picric acid (PA) among various nitroaromatic explosives. The Stern–Volmer constant (KSV) for PA was estimated as 3.97 × 104, 7.35 × 104, and 2.39 × 104 M–1 for Tx-CMP-1, Tx-CMP-2, and Tx-CMP-3, respectively, indicating that PA can quench the fluorescence intensity of Tx-CMP-2 most efficiently. The detection limits of Tx-CMPs toward PA were found in the nanomolar range.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Luminescence and Fluorescent Materials

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

Affiliations

Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, Knowledge City, Manauli 140306, India

Funding

Science and Engineering Research Board · Indian Institute of Science Education and Research Mohali

References (61)

Show source-provided references
1. Akhavan J. · 200410.1039/9781847552020 ↗
2. 10.1007/s00244-004-0112-210.1007/s00244-004-0112-2 ↗
3. 10.1039/C4CS00010B10.1039/C4CS00010B ↗
4. 10.1039/D0CE01087A10.1039/D0CE01087A ↗
5. 10.1021/acs.chemrev.6b0043910.1021/acs.chemrev.6b00439 ↗
6. 10.1021/acs.chemrev.9b0039910.1021/acs.chemrev.9b00399 ↗
7. 10.1039/C7CS00071E10.1039/C7CS00071E ↗
8. 10.1039/C3CS60160A10.1039/C3CS60160A ↗
9. 10.1126/science.aaa807510.1126/science.aaa8075 ↗
10. 10.1039/C9CS00315K10.1039/C9CS00315K ↗
11. 10.1021/ja801017610.1021/ja8010176 ↗
12. 10.1021/ma901801s10.1021/ma901801s ↗
13. 10.1021/acscatal.8b0403210.1021/acscatal.8b04032 ↗
14. 10.1002/anie.20171177310.1002/anie.201711773 ↗
15. 10.1021/acscatal.8b0147810.1021/acscatal.8b01478 ↗
16. 10.1039/C8CC08918C10.1039/C8CC08918C ↗
17. 10.1039/D0TA10232F10.1039/D0TA10232F ↗
18. 10.1039/c9cc05051e10.1039/c9cc05051e ↗
19. 10.1002/anie.20180111210.1002/anie.201801112 ↗
20. 10.1039/d0qm00384k10.1039/d0qm00384k ↗
21. 10.1021/ja303448r10.1021/ja303448r ↗
22. 10.1021/mz400024910.1021/mz4000249 ↗
23. 10.1039/c6ta04623a10.1039/c6ta04623a ↗
24. 10.1002/chem.20150224110.1002/chem.201502241 ↗
25. 10.1038/s41598-018-32383-510.1038/s41598-018-32383-5 ↗
26. 10.1002/adfm.20170543210.1002/adfm.201705432 ↗
27. 10.1039/D0CS00021C10.1039/D0CS00021C ↗
28. 10.1016/j.nanoen.2021.10595810.1016/j.nanoen.2021.105958 ↗
29. 10.1039/D0TC03139A10.1039/D0TC03139A ↗
30. 10.1039/C4RA11559G10.1039/C4RA11559G ↗
31. 10.1039/C7TA05043G10.1039/C7TA05043G ↗
32. 10.1021/acsami.9b2341610.1021/acsami.9b23416 ↗
33. 10.1021/acscatal.8b0062310.1021/acscatal.8b00623 ↗
34. 10.1039/C8PY01082J10.1039/C8PY01082J ↗
35. 10.1021/acsami.6b1241910.1021/acsami.6b12419 ↗
36. 10.1039/C6SC05532J10.1039/C6SC05532J ↗
37. 10.1021/acs.macromol.1c0057410.1021/acs.macromol.1c00574 ↗
38. 10.1021/acs.chemmater.9b0143210.1021/acs.chemmater.9b01432 ↗
39. 10.1039/C8RA06463F10.1039/C8RA06463F ↗
40. 10.1039/C8NJ01306C10.1039/C8NJ01306C ↗
41. 10.1021/acsami.9b1676710.1021/acsami.9b16767 ↗
42. 10.1016/j.snb.2017.01.00510.1016/j.snb.2017.01.005 ↗
43. 10.1039/D0QM00769B10.1039/D0QM00769B ↗
44. 10.1039/C9RA06583K10.1039/C9RA06583K ↗
45. 10.1007/s12039-017-1403-210.1007/s12039-017-1403-2 ↗
46. 10.1039/C6RA01717G10.1039/C6RA01717G ↗
47. 10.1039/C8CC00203G10.1039/C8CC00203G ↗
48. 10.1039/C8TA05070H10.1039/C8TA05070H ↗
49. 10.1021/acs.chemrev.9b0055010.1021/acs.chemrev.9b00550 ↗
50. 10.1039/C5CC00987A10.1039/C5CC00987A ↗
51. 10.1021/acsami.8b0633910.1021/acsami.8b06339 ↗
52. 10.1021/acs.inorgchem.9b0261110.1021/acs.inorgchem.9b02611 ↗
53. 10.1039/C6DT00753H10.1039/C6DT00753H ↗
54. 10.1016/j.dyepig.2017.12.03210.1016/j.dyepig.2017.12.032 ↗
55. 10.1039/C6CE00421K10.1039/C6CE00421K ↗
56. 10.1039/C6CE00244G10.1039/C6CE00244G ↗
57. 10.1021/acs.cgd.8b0020410.1021/acs.cgd.8b00204 ↗
58. 10.1039/b809631g10.1039/b809631g ↗
59. 10.1002/anie.20120888510.1002/anie.201208885 ↗
60. 10.1039/C5CS00496A10.1039/C5CS00496A ↗
61. Lakowicz J. R. · 200610.1007/978-0-387-46312-4 ↗