Highly fluorescent single crystals of a 4-ethoxy-1, 3-thiazole. (February 2018)
- Record Type:
- Journal Article
- Title:
- Highly fluorescent single crystals of a 4-ethoxy-1, 3-thiazole. (February 2018)
- Main Title:
- Highly fluorescent single crystals of a 4-ethoxy-1, 3-thiazole
- Authors:
- Habenicht, Stefanie H.
Kupfer, Stephan
Nowotny, Jürgen
Schramm, Stefan
Weiß, Dieter
Beckert, Rainer
Görls, Helmar - Abstract:
- Abstract: 4-Ethoxy-2-(pyridin-2-yl)-5-(3, 4, 5-trimethoxyphenyl)thiazole (EPTT ) was prepared in a four-step synthetic protocol. Column shaped single crystals of EPTT were obtained from a saturated EtOH solution. Both single crystals and a THF solution of EPTT were investigated in terms of their photophysical properties and electronic structure. The crystals showed very intense fluorescence upon photoexcitation as well as a red shifted emission maximum compared to a THF solution of EPTT (single crystals: λem = 523 nm, ΦFL = 0.82, THF solution λem = 477 nm, ΦFL = 0.67). Quantum chemical methods were then employed to unravel the underlying fundamental transitions and explain the experimental results. Calculations for a small dye cluster modeled after the x-ray crystal structure predicted three dark intermolecular CT states, S1 -S3, below the intramolecular CT state (S4 ) for EPTT in the crystalline state. Photoexcitation and subsequent relaxation along the excited states relaxation pathways may populate the low-lying dark intermolecular CT states, which in consequence leads to an exciton moving along the stacked dyes in the crystal. This finding explains the significantly enhanced red-shift of the solid-state fluorescence of EPTT compared to the dissolved dye. Graphical abstract: Highlights: A new 4-alkoxythiazole fluorophore EPTT was synthesized. EPTT exhibits sky-blue fluorescence (477 nm) with 67% quantum yield in THF. EPTT shows enhanced and red-shifted fluorescenceAbstract: 4-Ethoxy-2-(pyridin-2-yl)-5-(3, 4, 5-trimethoxyphenyl)thiazole (EPTT ) was prepared in a four-step synthetic protocol. Column shaped single crystals of EPTT were obtained from a saturated EtOH solution. Both single crystals and a THF solution of EPTT were investigated in terms of their photophysical properties and electronic structure. The crystals showed very intense fluorescence upon photoexcitation as well as a red shifted emission maximum compared to a THF solution of EPTT (single crystals: λem = 523 nm, ΦFL = 0.82, THF solution λem = 477 nm, ΦFL = 0.67). Quantum chemical methods were then employed to unravel the underlying fundamental transitions and explain the experimental results. Calculations for a small dye cluster modeled after the x-ray crystal structure predicted three dark intermolecular CT states, S1 -S3, below the intramolecular CT state (S4 ) for EPTT in the crystalline state. Photoexcitation and subsequent relaxation along the excited states relaxation pathways may populate the low-lying dark intermolecular CT states, which in consequence leads to an exciton moving along the stacked dyes in the crystal. This finding explains the significantly enhanced red-shift of the solid-state fluorescence of EPTT compared to the dissolved dye. Graphical abstract: Highlights: A new 4-alkoxythiazole fluorophore EPTT was synthesized. EPTT exhibits sky-blue fluorescence (477 nm) with 67% quantum yield in THF. EPTT shows enhanced and red-shifted fluorescence (523 nm, 82% quantum yield). Calculations revealed three dark intramolecular CT states in the crystalline state. Population of the dark CT states explains the red-shifted solid state emission. … (more)
- Is Part Of:
- Dyes and pigments. Volume 149(2018)
- Journal:
- Dyes and pigments
- Issue:
- Volume 149(2018)
- Issue Display:
- Volume 149, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 149
- Issue:
- 2018
- Issue Sort Value:
- 2018-0149-2018-0000
- Page Start:
- 644
- Page End:
- 651
- Publication Date:
- 2018-02
- Subjects:
- 4-Hydroxy-1, 3-Thiazoles -- DFT-calculations -- Single crystals -- Solid state fluorescence
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.2017.11.016 ↗
- 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:
- 14511.xml