Photoluminescence organic wide-band gap semiconductors investigated for optoelectronic applications and cellular imaging
Bibliographic record
Abstract
No abstract is available for this record. The assistant can identify its topic from the title, but cannot infer the study’s results.
Source: Not provided · Quality: missing
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (24)
Show source-provided references
1. Recent advances in organic semiconductor crystalline microwire field-effect transistors
2. Recent advances in small-molecule organic fluorescent semiconductors
3. Charge carrier trapping in organic semiconductors: origins, impact and strategies for mitigation
4. Supramolecular engineering of charge transfer in wide bandgap organic semiconductors with enhanced visible-to-NIR photoresponse
5. A multifluorination strategy toward wide bandgap polymers for highly efficient organic solar cells
6. π-Conjugated polymers and molecules enabling small photon energy loss simultaneously with high efficiency in organic photovoltaics10.1039/D0TA05108J ↗
7. Molecular understanding of diphenylether-, 9,9-biphenylfluorene- and tetraphenylsilane-centered wide bandgap host materials for highly efficient blue phosphorescent OLEDs10.1016/j.dyepig.2018.09.019 ↗
8. Wide bandgap polymer donors containing dihalovinyl thiophene building blocks for organic solar cells10.1021/acs.macromol.4c00195 ↗
9. Doped crystalline thin-film deep-blue organic light-emitting diodes
10. Large-area OLED lightings and their applications10.1088/0268-1242/26/3/034002 ↗
11. An overview of Joule heating in energy storage materials and applications
12. 2,2 – dicyanovinyl derivatives - thermal, photophysical, electrochemical and electroluminescenceinvestigations10.1016/j.matchemphys.2018.02.001 ↗
13. „Photoelectrochemical and thermal characterizationofaromatichydrocarbonssubstitutedwith a dicyanovinylunit
14. „thermal, spectroscopic, electrochemical, and electroluminescent characterization of malononitrile derivatives with triphenylamine structure10.1016/j.saa.2018.11.025 ↗
15. „Malononitrile derivatives as push-pull molecules: structure – propertiesrelationshipscharacterization10.1016/j.jlumin.2018.06.071 ↗
16. „Novel 1,8-napthalimides substituted at 3-C position: synthesis and evaluation of thermal, electrochemical and luminescentproperties10.1016/j.dyepig.2018.05.017 ↗
17. Six new unsymmetrical Imino-1,8-naphthalimide derivatives substituted at 3-C position—photophysical investigations
18. Luminescence and electrochemical activity of new unsymmetrical 3-Imino-1,8-naphthalimide derivatives
19. Live cell imaging by 3-imino-(2-phenol)-1,8-naphthalimides: the effect of ex vivo hydrolysis10.1016/j.saa.2020.118442 ↗
20. 1,8-Naphthalimides 3-substituted with imine or β-ketoenamine unit evaluated as compounds for organic electronics and cell imaging10.1016/j.dyepig.2021.109508 ↗
21. Spectroscopic and biological properties of the 3-Imino-1,8-naphthalimide derivatives as fluorophores for cellular imaging10.3390/molecules28176255 ↗
22. New acceptor–donor–acceptor systems based on Bis-(Imino-1,8-Naphthalimide)10.3390/ma14112714 ↗
23. Symmetrical and asymmetrical imino-naphthalimides in perovskite solar cells
24. Strategy for the synthesis of new 3- or 4-substituted-1,8-naphthalimides with –N=C– and –C–C– bonds as well as differences in the optical properties between tchem10.1039/D5TC03651H ↗