Triplet state of orotic acid and orotic acid methyl ester in solution

1970 ◽  
Vol 48 (6) ◽  
pp. 987-999 ◽  
Author(s):  
R. W. Yip ◽  
W. D. Riddell ◽  
A. G. Szabo

Flash photolysis of orotic acid and orotic acid methyl ester in aqueous solution was studied. The transients were identified as triplet excited states on the basis of their lifetimes, sensitization, quenching, and self-quenching experiments. The rate constants for self-quenching and for decay of the triplet were measured and discussed in terms of dimerization and competing unimolecular and pseudo-unimolecular processes. A triplet energy of 60 kcal mole−1 was deduced for both orotic acid and orotic acid methyl ester from triplet energy transfer measurements.

1970 ◽  
Vol 48 (20) ◽  
pp. 3265-3268 ◽  
Author(s):  
K. K. Maheshwari ◽  
P. de Mayo ◽  
D. Wiegand

It has been shown that the direct irradiation of cyclic peroxides such as ascaridole, and those derived from cyclohexadiene, 1,3,5,5-tetramethylcyclohexadiene, and levopimaric acid methyl ester rearrange on irradiation. The bisepoxides are obtained, as in the thermal rearrangement, together with, where the structure permits, the ketoepoxide. The reaction can be induced by triplet–triplet energy transfer.


2004 ◽  
Vol 108 (35) ◽  
pp. 7147-7150 ◽  
Author(s):  
Xichen Cai ◽  
Masanori Sakamoto ◽  
Michihiro Hara ◽  
Sachiko Tojo ◽  
Kiyohiko Kawai ◽  
...  

2016 ◽  
Vol 4 (14) ◽  
pp. 2843-2853 ◽  
Author(s):  
Xueyan Wu ◽  
Wenting Wu ◽  
Xiaoneng Cui ◽  
Jianzhang Zhao ◽  
Mingbo Wu

Bodipy–ferrocene dyads were prepared for reversible electrochemical switching of the singlet excited state (fluorescence), as well as the triplet excited states of Bodipy.


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