journal article·2018-05

Elastic Self‐Doping Organic Single Crystals Exhibiting Flexible Optical Waveguide and Amplified Spontaneous Emission

Rui Huang, Chenguang Wang, Yue Wang, Hongyu Zhang

Advanced Materials· Volume 30· Issue 21
Publisher page

Abstract

Abstract Organic crystals are generally brittle and tend to crack under applied stress. Doped organic crystals are even more brittle because of lattice defects. Herein, the first doped organic crystals 1d@2d, which display elastic bending ability under applied stress, are reported. Moreover, the potential applications of elastic‐doped crystals 1d@2d in flexible optoelectronics are impressively demonstrated. The elastic crystals 1d@2d with high quality and large size are crystalized by a simple and unique “self‐doping” process, which is a regular solution evaporation of crude product 1d (2,5‐dihydro‐3,6‐bis(octylamino)terephthalate) containing a minute amount of 2d (3,6‐bis(octylamino)terephthalate) as the oxidized byproduct. The host 1d is easily crystallized to form elastic crystals but is nonfluorescent, while the guest 2d has poor crystallinity and is highly emissive. The doping approach integrates the advantages of both 1d and 2d, and thus endows doped crystals 1d@2d with good elasticity as well as intense orange fluorescence. Taking these advantages, the application potentials of these doped crystals 1d@2d are evaluated by measuring optical waveguide and amplified spontaneous emission in both the straight and bent states.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Supramolecular Self-Assembly in Materials · Crystallography and molecular interactions

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

Affiliations

State Key Laboratory of Supramolecular Structure and Materials College of Chemistry Jilin University Qianjin Street Changchun 130012 P. R. China

Funding

National Natural Science Foundation of China

References (33)

Show source-provided references
1. 10.1021/acs.chemrev.5b0039810.1021/acs.chemrev.5b00398 ↗
2. 10.1002/anie.20120460410.1002/anie.201204604 ↗
3. 10.1002/anie.20141073010.1002/anie.201410730 ↗
4. 10.1002/anie.20150931910.1002/anie.201509319 ↗
5. 10.1038/s41598-017-09848-010.1038/s41598-017-09848-0 ↗
6. 10.1021/acs.cgd.7b0099210.1021/acs.cgd.7b00992 ↗
7. 10.1002/anie.20161119510.1002/anie.201611195 ↗
8. 10.1021/jacs.5b0532410.1021/jacs.5b05324 ↗
9. 10.1039/C6CC03226E10.1039/C6CC03226E ↗
10. 10.1002/chem.20170081310.1002/chem.201700813 ↗
11. 10.1039/C7CC04392A10.1039/C7CC04392A ↗
12. 10.1002/anie.20170197210.1002/anie.201701972 ↗
13. 10.1002/anie.20140256010.1002/anie.201402560 ↗
14. 10.1021/ja410149710.1021/ja4101497 ↗
15. 10.1002/anie.20130120710.1002/anie.201301207 ↗
16. 10.1021/jacs.6b1183510.1021/jacs.6b11835 ↗
17. 10.1021/ja201925p10.1021/ja201925p ↗
18. 10.1021/ja400833r10.1021/ja400833r ↗
19. 10.1002/anie.20160600310.1002/anie.201606003 ↗
20. 10.1021/jacs.6b0740610.1021/jacs.6b07406 ↗
21. 10.1002/anie.20160966710.1002/anie.201609667 ↗
22. 10.1002/anie.20131101410.1002/anie.201311014 ↗
23. 10.1002/anie.20170651710.1002/anie.201706517 ↗
24. 10.1021/cg900712510.1021/cg9007125 ↗
25. 10.1039/C4CE02501F10.1039/C4CE02501F ↗
26. 10.1002/adma.20100073110.1002/adma.201000731 ↗
27. 10.1002/anie.20080257010.1002/anie.200802570 ↗
28. 10.1002/adfm.20120148210.1002/adfm.201201482 ↗
29. 10.1039/c3tc32161d10.1039/c3tc32161d ↗
30. 10.1021/acsami.7b0019510.1021/acsami.7b00195 ↗
31. 10.1016/j.cclet.2017.08.04510.1016/j.cclet.2017.08.045 ↗
32. 10.1021/jacs.5b1035310.1021/jacs.5b10353 ↗
33. 10.1002/anie.20150391410.1002/anie.201503914 ↗