Comparison between J-aggregates in a self-assembled multilayer and polymer-bound J-aggregates in solution: a steady-state and time-resolved spectroscopic study

2002 ◽  
Vol 1 (6) ◽  
pp. 395-406 ◽  
Author(s):  
Els Rousseau ◽  
Marc M. Koetse ◽  
Mark Van der Auweraer ◽  
Frans C. De Schryver
2013 ◽  
Vol 134 ◽  
pp. 401-407 ◽  
Author(s):  
Bipattaran Paramanik ◽  
Santanu Bhattacharyya ◽  
Amitava Patra

2011 ◽  
Vol 10 (04n05) ◽  
pp. 867-871
Author(s):  
TAPASI SEN ◽  
AMITAVA PATRA

The photophysical properties of the confined dye inside the γ-CD in presence of Au nanoparticles have been studied by steady state and time resolved spectroscopy. It is found that the photoluminescence quenching of C480 dye increases from 26% to 49% due to confinement of dye inside γ-CD. The designing of such new optical based materials having coumarin 480 dye inside the γ-CD in presence of Au nanoparticles may have potential applications for light harvesting system.


2001 ◽  
Vol 3 (3) ◽  
pp. 147-151 ◽  
Author(s):  
Pavel Kubát ◽  
Kamil Lang ◽  
Vladimír Král ◽  
Franz P. Schmidtchen

Photophysical properties of two novel guanidiniocarbonyl (I) and monocyclic guanidine (II) tetraphenylporphyrins and their interaction with DNA were investigated by steady-state and time-resolved absorption and emission spectroscopies.Istays predominantly monomeric in aqueous solutions. It produces singlet oxygen with high quantum yield(ΦΔ=0.67)that is typical for monomeric porphyrins. The electronic absorption spectra ofIare not influenced by interaction with DNA. This is in contrast with monomeric tetratolylporphyrins bearing phosphonium,ammonium and pyridinium groups where the formation of stable complexes with DNA is accompanied by a characteristic red shift of the Soret band.IIextensively forms Hand J-aggregates,which do not produce singlet oxygen(ΦΔ<0.01). In the presence of DNA only a small fraction ofIIremains in monomeric form that is bound to DNA exterior.


2016 ◽  
Vol 26 (4) ◽  
pp. 1249-1259 ◽  
Author(s):  
M. G. Kotresh ◽  
K. S. Adarsh ◽  
M. A. Shivkumar ◽  
Sanjeev R. Inamdar

1991 ◽  
Vol 11 (1) ◽  
pp. 1-12 ◽  
Author(s):  
K.-H. Feller ◽  
R. Gadonas ◽  
V. Krasauskas ◽  
V. Fidler ◽  
S. Vajda

The deactivation process of J-aggregates of DDEOCI (3,3'-diethyl-5,5'-diphenyl-9-ethyl-oxacarbocyanine iodide) was investigated by means of steady-state and time-resolved absorption and fluorescence spectroscopy. The decay kinetics as well as the transient absorption spectra have been analyzed including different aggregate structures and exciton-exciton annihilation.


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