Photorefractivity in Nematic Liquid Crystals Using a Donor−Acceptor Dyad with a Low-Lying Excited Singlet State for Charge Generation

2001 ◽  
Vol 105 (30) ◽  
pp. 7216-7219 ◽  
Author(s):  
Michael J. Fuller ◽  
Michael R. Wasielewski
2010 ◽  
Vol 81 (20) ◽  
Author(s):  
Annamaria Petrozza ◽  
Frédéric Laquai ◽  
Ian A. Howard ◽  
Ji-Seon Kim ◽  
Richard H. Friend

1980 ◽  
Vol 35 (7) ◽  
pp. 777-778
Author(s):  
I. Gryczyński ◽  
D. Gloyna ◽  
A. Kawski

The electric dipole moments of some substituted stilbenes in the ground (μg) and the first excited singlet state (μe) have been determined and discussed in regard of the donor-acceptor- interactions. A linear correlation between the Hammett σp-constants and the values of μg, μe and Δμ = μe - μg for different substituted stilbenes was found.


1971 ◽  
Vol 44 (12) ◽  
pp. 3310-3316 ◽  
Author(s):  
Hiroshi Masuhara ◽  
Motoo Shimada ◽  
Nobuyuki Tsujino ◽  
Noboru Mataga

1980 ◽  
Vol 35 (12) ◽  
pp. 1411-1414 ◽  
Author(s):  
D. Gloyna ◽  
A. Kawski ◽  
I. Gryczyński

AbstractThe effect of substituents on the fluorescence quantum yield φf of trans-stilbenes (1) in dimethylformamide, acetonitrile, and n-propanol, as well as in n-heptane, is mainly due to radiationless deactivation. Contrary to n-heptane, the rate kd of radiationless deactivation in the above mentioned polar solvents for compounds 1 of similar structure is not a monotoneous function of the polarity of the first excited singlet state. The maximum of kd corresponds to compounds with medium polarity (1h, 1i). The effect of substituents on the fluorescence rate kfn in polar and nonpolar solvents is small compared to that on kd. In all solvents kfn drops with increasing polarity of the first excited singlet state.


2002 ◽  
Vol 76 (1) ◽  
pp. 47 ◽  
Author(s):  
Joakim Andréasson ◽  
Gerdenis Kodis ◽  
Su Lin ◽  
Ana L. Moore ◽  
Thomas A. Moore ◽  
...  

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