Systematic color tuning of a family of firefly oxyluciferin analogues suitable for OLED applications. (March 2016)
- Record Type:
- Journal Article
- Title:
- Systematic color tuning of a family of firefly oxyluciferin analogues suitable for OLED applications. (March 2016)
- Main Title:
- Systematic color tuning of a family of firefly oxyluciferin analogues suitable for OLED applications
- Authors:
- Min, Chun-Gang
Leng, Yan
Yang, Xi-Kun
Huang, Shao-Jun
Ren, Ai-Min - Abstract:
- Abstract: The firefly oxyluciferin analogues have great potential application in organic light-emitting devices because of their high fluorescent efficiency. The emission color of these analogues can be tuned by chemical functionalization. To reveal the molecular structures, optoelectronic properties, and structure–property relationships of these analogues, an in-depth theoretical investigation was elaborated via quantum chemical calculation. The calculated ionization potentials, electron affinities, and reorganization energies show that introduction of dimethylamino and double bond can significantly affect the carrier injection and transport characteristics. We also calculated the singlet-to-triplet exciton-formation cross-section ratio ( σ S / σ T ), the exciton formation fractions ( χ s ), the absorption and emission spectra. The calculated σ S / σ T values range from 1.00 to 10.17, and the corresponding χ s are ca. 0.25–0.77. The calculated emission spectra range from 403.93 to 631.09 nm. It can be deduced that these studied firefly oxyluciferin analogues can serve as efficient blue, green, orange and red light-emitting electroluminescent materials. Highlights: The emission color of these analogues can be tuned by chemical functionalization. Double bond can affect the carrier injection and transport characteristics. These analogues can serve as blue, green, orange and red light-emitting materials. The radiative lifetimes of some analogues are close to nature fireflyAbstract: The firefly oxyluciferin analogues have great potential application in organic light-emitting devices because of their high fluorescent efficiency. The emission color of these analogues can be tuned by chemical functionalization. To reveal the molecular structures, optoelectronic properties, and structure–property relationships of these analogues, an in-depth theoretical investigation was elaborated via quantum chemical calculation. The calculated ionization potentials, electron affinities, and reorganization energies show that introduction of dimethylamino and double bond can significantly affect the carrier injection and transport characteristics. We also calculated the singlet-to-triplet exciton-formation cross-section ratio ( σ S / σ T ), the exciton formation fractions ( χ s ), the absorption and emission spectra. The calculated σ S / σ T values range from 1.00 to 10.17, and the corresponding χ s are ca. 0.25–0.77. The calculated emission spectra range from 403.93 to 631.09 nm. It can be deduced that these studied firefly oxyluciferin analogues can serve as efficient blue, green, orange and red light-emitting electroluminescent materials. Highlights: The emission color of these analogues can be tuned by chemical functionalization. Double bond can affect the carrier injection and transport characteristics. These analogues can serve as blue, green, orange and red light-emitting materials. The radiative lifetimes of some analogues are close to nature firefly oxyluciferin. Some derivates were used as highly efficient fluorescent OLED materials. … (more)
- Is Part Of:
- Dyes and pigments. Volume 126(2016)
- Journal:
- Dyes and pigments
- Issue:
- Volume 126(2016)
- Issue Display:
- Volume 126, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 126
- Issue:
- 2016
- Issue Sort Value:
- 2016-0126-2016-0000
- Page Start:
- 202
- Page End:
- 208
- Publication Date:
- 2016-03
- Subjects:
- Ionization potential and electron affinity -- Reorganization energy -- Exciton-formation fractions -- TDDFT -- Firefly oxyluciferin
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2015.12.004 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 282.xml