Unusual spectroscopic and photophysical properties of meso-tert-butylBODIPY in comparison to related alkylated BODIPY dyes. Issue 109 (20th October 2015)
- Record Type:
- Journal Article
- Title:
- Unusual spectroscopic and photophysical properties of meso-tert-butylBODIPY in comparison to related alkylated BODIPY dyes. Issue 109 (20th October 2015)
- Main Title:
- Unusual spectroscopic and photophysical properties of meso-tert-butylBODIPY in comparison to related alkylated BODIPY dyes
- Authors:
- Jiao, Lijuan
Yu, Changjiang
Wang, Jun
Briggs, Edward A.
Besley, Nicholas A.
Robinson, David
Ruedas-Rama, María J.
Orte, Angel
Crovetto, Luis
Talavera, Eva M.
Alvarez-Pez, Jose M.
Van der Auweraer, Mark
Boens, Noël - Abstract:
- Abstract : meso-t -Bu-BODIPY produces unusual spectroscopic and photophysical characteristics in comparison to those of related alkylated BODIPY dyes. Abstract : Five alkyl-substituted difluoroboron dipyrrin (BODIPY) dyes have been synthesized: three with a methyl, isopropyl or tert -butyl group at the meso -position of the BODIPY core and two substituted with one or two tert -butyl functions at the 3/5-positions. X-Ray structural analysis, UV-vis absorption spectroscopy and fluorescence (steady-state and time-resolved) techniques have been used to study the structures and the spectroscopic/photophysical properties of these dyes. All but one of these BODIPYs are highly fluorescent in all the solvents tested, the exception being meso-tert -butylBODIPY (2 ). Derivative2 differs from the other alkylated boron dipyrrins as it exhibits a broad and red-shifted fluorescence band with a large Stokes shift. In addition, very low fluorescence quantum yields and short fluorescence lifetimes characterize2 . Quantum chemical calculations indicate that2 has a distorted, nonplanar geometry in the S1 excited state due to the rotation of 8- tert -butyl group. Our results lead us to the conclusion that the torsional rotation about the bond connecting the meso -C and the quarternary C of the tert -butyl group of2 plays a crucial role in the fast radiationless deactivation of this isomer.
- Is Part Of:
- RSC advances. Volume 5:Issue 109(2015)
- Journal:
- RSC advances
- Issue:
- Volume 5:Issue 109(2015)
- Issue Display:
- Volume 5, Issue 109 (2015)
- Year:
- 2015
- Volume:
- 5
- Issue:
- 109
- Issue Sort Value:
- 2015-0005-0109-0000
- Page Start:
- 89375
- Page End:
- 89388
- Publication Date:
- 2015-10-20
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ra17419h ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
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