Efficient Spontaneous and Stimulated Emission from 1,4‐Bis(2,2‐diphenylvinyl)benzene Single Crystals with Cross‐Dipole Stacking
Source abstract
Abstract
Organic single crystals with cross-dipole stacking based on 1,4-bis(2,2-diphenylvinyl)benzene are prepared. X-ray diffraction shows that adjacent molecules in the single crystal adopt a rotational angle of ≈62°. Such a stacking mode is highly beneficial for spontaneous and stimulated emission, resulting in high solid-state fluorescence efficiency and excellent amplified spontaneous emission characteristics. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Supramolecular Structure and Materials Jilin University Qianjin Street No. 2699 Changchun 130012 China
References (38)
Show source-provided references
1. 10.1038/3869310.1038/38693 ↗
2. 10.1038/419353a10.1038/419353a ↗
3. 10.1021/ar100043u10.1021/ar100043u ↗
4. 10.1021/cr100380z10.1021/cr100380z ↗
5. 10.1021/ar200195210.1021/ar2001952 ↗
6. 10.1063/1.213836110.1063/1.2138361 ↗
7. 10.1002/adfm.20110078310.1002/adfm.201100783 ↗
8. 10.1002/ange.20130289410.1002/ange.201302894 ↗
9. 10.1002/anie.20130289410.1002/anie.201302894 ↗
10. 10.1002/adma.20140111410.1002/adma.201401114 ↗
11. 10.1002/adom.20120006410.1002/adom.201200064 ↗
12. 10.1021/ja400881n10.1021/ja400881n ↗
13. 10.1002/adfm.20090002810.1002/adfm.200900028 ↗
14. 10.1063/1.170487410.1063/1.1704874 ↗
15. 10.1351/pac19651103037110.1351/pac196511030371 ↗
16. 10.1021/ja973761j10.1021/ja973761j ↗
17. 10.1021/cm991194o10.1021/cm991194o ↗
18. 10.1021/ja054661d10.1021/ja054661d ↗
19. 10.1002/adma.20050123910.1002/adma.200501239 ↗
20. 10.1002/adma.20130363910.1002/adma.201303639 ↗
21. 10.1021/ja00170a01610.1021/ja00170a016 ↗
22. 10.1002/1521-4095(200107)13:14<1053::AID-ADMA1053>3.0.CO;2-710.1002/1521-4095(200107)13:14<1053::AID-ADMA1053>3.0.CO;2-7 ↗
23. Bernard V. · 2002
24. 10.1021/ja104466510.1021/ja1044665 ↗
25. 10.1002/adma.20120252510.1002/adma.201202525 ↗
26. 10.1021/cr050152i10.1021/cr050152i ↗
27. Siegman A. E. · 1986 · Ch. 13
28. 10.1021/cm801427s10.1021/cm801427s ↗
29. 10.1002/adma.20110418210.1002/adma.201104182 ↗
30. 10.1002/adma.20039004810.1002/adma.200390048 ↗
31. 10.1002/adma.20120157910.1002/adma.201201579 ↗
32. 10.1063/1.149447310.1063/1.1494473 ↗
33. 10.1103/PhysRevB.58.703510.1103/PhysRevB.58.7035 ↗
34. 10.1002/adma.20100379710.1002/adma.201003797 ↗
35. 10.1021/ja050872710.1021/ja0508727 ↗
36. 10.1002/1521-4095(200011)12:22<1655::AID-ADMA1655>3.0.CO;2-210.1002/1521-4095(200011)12:22<1655::AID-ADMA1655>3.0.CO;2-2 ↗
37. 10.1063/1.276183310.1063/1.2761833 ↗
38. 10.1364/OL.35.00044110.1364/OL.35.000441 ↗