The singlet-oxygen-sensitized delayed fluorescence in mammalian cells: a time-resolved microscopy approach

2015 ◽  
Vol 14 (4) ◽  
pp. 700-713 ◽  
Author(s):  
Marek Scholz ◽  
Anna-Louisa Biehl ◽  
Roman Dědic ◽  
Jan Hála

Microsecond kinetics of singlet-oxygen-sensitized delayed fluorescence (SOSDF) have been detected from individual living fibroblast cells as a proof-of-concept. These provide valuable information about excited state lifetimes and their changes during PDT-like treatment.

2015 ◽  
Vol 17 (43) ◽  
pp. 29090-29096 ◽  
Author(s):  
Dawn M. Marin ◽  
Sonia Payerpaj ◽  
Graham S. Collier ◽  
Angy L. Ortiz ◽  
Gaurav Singh ◽  
...  

Singly halogenated carbomethoxyphenylporphyrins show decreased singlet fluorescence lifetimes and increased rates of triplet excited state formation.


1999 ◽  
Vol 19 (1-4) ◽  
pp. 245-251 ◽  
Author(s):  
J. J. Turner ◽  
M. W. George ◽  
I. P. Clark ◽  
I. G. Virrels

For coordination compounds containing CO or CN groups, fast time-resolved infrared spectroscopy (TRIR) provides a convenient method of probing excited states and intermediates. TRIR has proved particularly powerful for probing the structure and kinetics of organometallic intermediates. The interpretation is particularly straightforward when combined with IR data from matrix isolation experiments, although there can be some subtle differences. In excited state studies, shifts in ν(CO) and ν(CN) frequencies, from ground to excited state, are sensitive to the changes in electron distribution on excitation, thus allowing the distinction between charge-transfer and non-charge-transfer transitions. Subtle effects on excited state ν(CO) band positions occur with change from fluid to rigid solvent-“infrared rigidochromism”. There is often a change in ν(CO) band width on excitation; this can be interpreted in terms of specific interactions between the excited species and the solvent. This paper presents some of our recent work in this area.


2015 ◽  
Vol 17 (20) ◽  
pp. 13245-13256 ◽  
Author(s):  
Dariusz M. Niedzwiedzki ◽  
Laura Cranston

Photophysical properties of two typical aryl carotenoids, okenone and chlorobactene, were studied with application of femtosecond and microsecond time-resolved absorption spectroscopies.


2013 ◽  
Vol 117 (17) ◽  
pp. 5180-5187 ◽  
Author(s):  
Yoichi Murakami ◽  
Hitomi Kikuchi ◽  
Akio Kawai

1988 ◽  
Vol 42 (1) ◽  
pp. 27-31
Author(s):  
A. N. Dharamsi ◽  
Shawpin Jong

Time-resolved excited-state triplet-triplet absorption spectra were measured for solutions of 2,5 diphenyloxazole (PPO) in various solvents, with the use of a pump and probe technique. The rate constants for intersystem crossing, triplet deactivation by oxygen, and triplet-triplet self-quenching are obtained. The latter two rate constants are substantially larger than the corresponding rate constants for 2-(1 naphthyl)-5-phenyloxazole-αNPO.


2021 ◽  
Author(s):  
Yuushi Shimoda ◽  
Masaki Saigo ◽  
Tomohiro Ryu ◽  
Takumi Ehara ◽  
Kiyoshi Miyata ◽  
...  

We have investigated the correlation between the photophysical properties and the excited-state detailed characteristics in a multiple-resonance-type thermally activated delayed fluorescence (TADF) molecule, DABNA-1, using time-resolved infrared vibrational spectroscopy. In comparison of the distinctive vibrational spectra in the fingerprint region, 1000 - 1700 cm<sup>-1</sup>, to the simulated spectra by density functional theory calculations, we found the best calculation condition. On the basis of the calculations, we determined the excited-state geometries and molecular orbitals of the lowest excited singlet (S<sub>1</sub>) and triplet (T<sub>1</sub>) states as well as the ground state (S<sub>0</sub>). We revealed that the similarity of the potential surfaces between T<sub>1</sub> and S<sub>0</sub> suppresses the nonradiative decay and causes the high fluorescence quantum yield via TADF process.


2017 ◽  
Vol 16 (11) ◽  
pp. 1643-1653 ◽  
Author(s):  
Marek Scholz ◽  
Roman Dědic ◽  
Jan Hála

Singlet Oxygen Feedback Delayed Fluorescence (SOFDF) is a novel semi-direct modality for microscopic imaging of singlet oxygen in cells. SOFDF enables time-resolved experiments and it can be much stronger than the singlet oxygen phosphorescence.


2020 ◽  
Vol 56 (79) ◽  
pp. 11831-11834
Author(s):  
Dorottya Sárosiné Szemes ◽  
Tamás Keszthelyi ◽  
Mariann Papp ◽  
László Varga ◽  
György Vankó

DFT predicts the ability to tune the energy barrier between the quintet and singlet states of an iron complex, and thus the quintet lifetime, with selected substituents on the ligand; this prediction is confirmed by time-resolved spectroscopy.


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