Color‐Tuned, Highly Emissive Dicyanodistyrylbenzene Single Crystals: Manipulating Intermolecular Stacking Interactions for Spontaneous and Stimulated Emission Characteristics
Source abstract
Abstract
Solid-state, luminescent, aggregation-induced enhanced emission (AIEE)-active dicyanodistyrylbenzene-based organic π-conjugated materials, i.e. α-MODCS, α-MODBDCS, β-MODCS, and β-MODBDCS, are designed. In virtue of the systematically substituted modular molecular systems combined with thorough structural analyses, photophysical studies, and electronic structure calculations, the spontaneous and stimulated emission properties are quantified and rationalized from a perspective of well-established structure–property correlations. 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 Light-Emitting Diodes Research · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Suprameolcular Optoelectronic Materials and WCU Hybrid Materials Program Department of Materials Science and Engineering Seoul National University 1 Gwanak‐ro, Gwanak‐gu Seoul 151–744 Korea
Madrid Institute for Advanced Studies IMDEA Nanoscience C/Faraday 9, Ciudad Universitaria de Cantoblanco 28049 Madrid Spain
References (26)
Show source-provided references
1. 10.1021/ar100043u10.1021/ar100043u ↗
2. 10.1038/nature0249810.1038/nature02498 ↗
3. 10.1038/419353a10.1038/419353a ↗
4. 10.1021/ar200195210.1021/ar2001952 ↗
5. 10.1021/jz200099p10.1021/jz200099p ↗
6. 10.1021/ja026908210.1021/ja0269082 ↗
7. 10.1021/ja046215g10.1021/ja046215g ↗
8. 10.1002/1521-4095(20021118)14:22<1625::AID-ADMA1625>3.0.CO;2-Q10.1002/1521-4095(20021118)14:22<1625::AID-ADMA1625>3.0.CO;2-Q ↗
9. 10.1021/cm034447t10.1021/cm034447t ↗
10. 10.1021/jp973225d10.1021/jp973225d ↗
11. 10.1021/ja104466510.1021/ja1044665 ↗
12. 10.1039/c0jm03711g10.1039/c0jm03711g ↗
13. 10.1039/c1jm14558d10.1039/c1jm14558d ↗
14. 10.1002/adfm.20110181810.1002/adfm.201101818 ↗
15. 10.1021/jp103453610.1021/jp1034536 ↗
16. 10.1002/adfm.20110078310.1002/adfm.201100783 ↗
17. 10.1021/cm801427s10.1021/cm801427s ↗
18. 10.1063/1.206202810.1063/1.2062028 ↗
19. 10.1021/jp036952j10.1021/jp036952j ↗
20. 10.1002/adma.20080358810.1002/adma.200803588 ↗
21. 10.1351/pac19651103037110.1351/pac196511030371 ↗
22. 10.1002/adma.20120252510.1002/adma.201202525 ↗
23. 10.1146/annurev.physchem.57.032905.10455710.1146/annurev.physchem.57.032905.104557 ↗
24. 10.1063/1.43706210.1063/1.437062 ↗
25. 10.1016/0022-2313(92)90054-D10.1016/0022-2313(92)90054-D ↗
26. 10.1016/S0925-3467(97)00068-210.1016/S0925-3467(97)00068-2 ↗