Tuning Emission Properties via Aromatic Guest Inclusion in Organic Salts Composed of 4,4′-Dinitro-2,2′,6,6′-tetracarboxybiphenyl and Acridine
Source abstract
Abstract
An organic salt composed of 4,4′-dinitro-2,2′,6,6′-tetracarboxybiphenyl and acridine has been shown to act as host to accommodate large polyaromatic guest molecules. Carboxylate–pyridinium hydrogen bonds, π–π and cation···π interactions are found to play a pivotal role in these host–guest complexes. All the complexes are found to exhibit distinct colors and photoluminescence which correlate with the charge-transfer interactions between acridinium ion and guest molecules, and ionization potential or donor ability of the guest molecules.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Crystallography and molecular interactions · Molecular Sensors and Ion Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Kolkata 700106, India
Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur 721302, India
Funding
Science and Engineering Research Board · Indian Institute of Technology Kharagpur
References (59)
Show source-provided references
1. Desiraju G. R. · 1989
2. 10.1039/b007127g10.1039/b007127g ↗
3. 10.1039/C5CC08216A10.1039/C5CC08216A ↗
4. 10.1021/cg200492w10.1021/cg200492w ↗
5. 10.1007/s41745-017-0026-410.1007/s41745-017-0026-4 ↗
6. 10.1021/ja105166d10.1021/ja105166d ↗
7. 10.1039/b510081j10.1039/b510081j ↗
8. 10.1039/b813721h10.1039/b813721h ↗
9. 10.1039/c0ce00612b10.1039/c0ce00612b ↗
10. 10.1021/cg200681s10.1021/cg200681s ↗
11. 10.1021/am401961s10.1021/am401961s ↗
12. 10.1021/ja210284s10.1021/ja210284s ↗
13. 10.1021/ja312197b10.1021/ja312197b ↗
14. 10.1039/C3TC32245A10.1039/C3TC32245A ↗
15. 10.1038/nchem.125610.1038/nchem.1256 ↗
16. Kwon M. S. · Nat. Commun. · 2014 · 5 · 446010.1038/ncomms5460 ↗
17. 10.1002/adom.20160031010.1002/adom.201600310 ↗
18. 10.1002/anie.19952311110.1002/anie.199523111 ↗
19. 10.1107/S205225251401208110.1107/S2052252514012081 ↗
20. 10.1021/cg049595q10.1021/cg049595q ↗
21. 10.1021/cg101300n10.1021/cg101300n ↗
22. 10.1021/cg301015a10.1021/cg301015a ↗
23. 10.1021/cg400805c10.1021/cg400805c ↗
24. 10.1021/cg500790q10.1021/cg500790q ↗
25. 10.1021/cg800565a10.1021/cg800565a ↗
26. 10.1021/cg801132r10.1021/cg801132r ↗
27. 10.1039/B908492D10.1039/B908492D ↗
28. 10.1039/C5CE00102A10.1039/C5CE00102A ↗
29. 10.1021/cg500502j10.1021/cg500502j ↗
30. 10.1021/cg900199410.1021/cg9001994 ↗
31. 10.1039/b509162d10.1039/b509162d ↗
32. 10.1021/acs.cgd.7b0029910.1021/acs.cgd.7b00299 ↗
33. 10.1039/b102150h10.1039/b102150h ↗
34. 10.1039/b922085b10.1039/b922085b ↗
35. 10.1039/C6CE00518G10.1039/C6CE00518G ↗
36. 10.1021/cg401596s10.1021/cg401596s ↗
37. 10.1021/cg900759e10.1021/cg900759e ↗
38. 10.1002/chem.20160413310.1002/chem.201604133 ↗
39. 10.1021/cg901132g10.1021/cg901132g ↗
40. 10.1021/cg501380m10.1021/cg501380m ↗
41. 10.1002/anie.20160771210.1002/anie.201607712 ↗
42. 10.1039/c3ce27102a10.1039/c3ce27102a ↗
43. 10.1039/c3cp53929f10.1039/c3cp53929f ↗
44. 10.1039/C5CE02019K10.1039/C5CE02019K ↗
45. 10.1039/C5TC01518A10.1039/C5TC01518A ↗
46. 10.1021/cg300485510.1021/cg3004855 ↗
47. 10.1021/cg301492710.1021/cg3014927 ↗
48. 10.1002/smll.20160151610.1002/smll.201601516 ↗
49. 10.1002/adfm.20130207210.1002/adfm.201302072 ↗
50. 10.1039/C7CE00950J10.1039/C7CE00950J ↗
51. 10.1021/cg301055j10.1021/cg301055j ↗
52. 10.1021/cm502724910.1021/cm5027249 ↗
53. 10.1002/anie.20170208410.1002/anie.201702084 ↗
54. 10.1002/anie.20110639110.1002/anie.201106391 ↗
55. 10.1021/ol060862q10.1021/ol060862q ↗
56. 10.1021/jacs.5b0417810.1021/jacs.5b04178 ↗
57. 10.1021/cg400661d10.1021/cg400661d ↗
58. 10.1021/cg200690c10.1021/cg200690c ↗
59. 10.1002/ange.20120582210.1002/ange.201205822 ↗