Stimuli Responsive Stable Radical Anion for Conductance Switching
Source abstract
Abstract
Radical anions are important for various uses. However, their generation and stabilization under ambient conditions, which are essential for actual applications, are challenging. A photogenerated NDI-based radical-anion that is stable even in water for more than a month is reported here. The design, synthesis, and the generation of the radical-anion and its stability have been discussed. The photogenerated radical-anion form a stacked supramolecular architecture structure that conducts electricity with a linear I – V curve. This system offers a photoresponsive turn-on behavior of conductance with a response ratio ( I 366nm / I unexposed ) of 22 million of the UV light-exposed samples compared to its neutral precursor.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Perovskite Materials and Applications · Conducting polymers and applications
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) Kolkata, Mohanpur 741246, India
References (49)
Show source-provided references
1. 10.1039/B401630K10.1039/B401630K ↗
2. 10.1039/B615857A10.1039/B615857A ↗
3. 10.1039/C5SC04450B10.1039/C5SC04450B ↗
4. 10.1039/C5CC06140G10.1039/C5CC06140G ↗
5. 10.1021/acsami.6b0001110.1021/acsami.6b00011 ↗
6. 10.1126/science.120596210.1126/science.1205962 ↗
7. 10.1002/adma.20190801510.1002/adma.201908015 ↗
8. 10.1002/anie.20180284210.1002/anie.201802842 ↗
9. 10.1038/nchem.69910.1038/nchem.699 ↗
10. 10.1038/srep2292810.1038/srep22928 ↗
11. 10.1039/C3CP54190H10.1039/C3CP54190H ↗
12. 10.1002/anie.20110765510.1002/anie.201107655 ↗
13. 10.1039/C4CC05429F10.1039/C4CC05429F ↗
14. 10.1002/anie.20140219210.1002/anie.201402192 ↗
15. 10.1039/c0nr00766h10.1039/c0nr00766h ↗
16. 10.1126/science.293.5532.111910.1126/science.293.5532.1119 ↗
17. 10.1021/jacs.6b0586310.1021/jacs.6b05863 ↗
18. 10.1021/acs.chemrev.5b0058610.1021/acs.chemrev.5b00586 ↗
19. 10.1016/j.ccr.2018.01.01810.1016/j.ccr.2018.01.018 ↗
20. Morita Y. · 2010
21. 10.1038/nchem.98510.1038/nchem.985 ↗
22. 10.1021/ja504903j10.1021/ja504903j ↗
23. 10.1021/acs.joc.8b0202310.1021/acs.joc.8b02023 ↗
24. 10.1039/c3sc51174j10.1039/c3sc51174j ↗
25. 10.1021/ja510958k10.1021/ja510958k ↗
26. 10.1126/science.125823210.1126/science.1258232 ↗
27. 10.1039/C5SC00862J10.1039/C5SC00862J ↗
28. 10.1021/ja511952c10.1021/ja511952c ↗
29. 10.1039/B614208G10.1039/B614208G ↗
30. 10.1039/C5SC00862J10.1039/C5SC00862J ↗
31. 10.1021/jo101498b10.1021/jo101498b ↗
32. 10.1002/anie.20060228610.1002/anie.200602286 ↗
33. 10.1002/chem.20110164210.1002/chem.201101642 ↗
34. 10.1021/jp902482r10.1021/jp902482r ↗
35. 10.1039/C4CC06680D10.1039/C4CC06680D ↗
36. 10.1002/anie.20140883110.1002/anie.201408831 ↗
37. 10.1039/C6CC01983H10.1039/C6CC01983H ↗
38. 10.1111/j.1751-1097.2006.tb09808.x10.1111/j.1751-1097.2006.tb09808.x ↗
39. 10.1039/C2CC37497H10.1039/C2CC37497H ↗
40. 10.1039/C4SC03224A10.1039/C4SC03224A ↗
41. 10.1016/j.ymeth.2016.06.00510.1016/j.ymeth.2016.06.005 ↗
42. 10.1016/j.freeradbiomed.2018.12.02210.1016/j.freeradbiomed.2018.12.022 ↗
43. 10.1021/ol403736m10.1021/ol403736m ↗
44. 10.1021/cm034140u10.1021/cm034140u ↗
45. 10.1002/adfm.20110100110.1002/adfm.201101001 ↗
46. 10.1002/chem.20130312310.1002/chem.201303123 ↗
47. 10.1002/adma.20100023210.1002/adma.201000232 ↗
48. 10.1021/acsami.0c1751310.1021/acsami.0c17513 ↗
49. 10.1002/asia.20190095610.1002/asia.201900956 ↗