scholarly journals Erratum: On the quantitation of light emission from cytochrome c in the low quantum yield limit [J. Chem. Phys. 73, 5947 (1980)]

1981 ◽  
Vol 74 (9) ◽  
pp. 5334-5334
Author(s):  
P. M. Champion ◽  
R. Lange
2018 ◽  
Vol 124 (11) ◽  
Author(s):  
Puja Bhattacharyya ◽  
Swarupananda Bhattacharjee ◽  
Manoranjan Bar ◽  
Uttam Kumar Ghorai ◽  
Mrinal Pal ◽  
...  

2015 ◽  
Vol 51 (15) ◽  
pp. 3094-3097 ◽  
Author(s):  
Ze-Ping Wang ◽  
Jin-Yun Wang ◽  
Jian-Rong Li ◽  
Mei-Ling Feng ◽  
Guo-Dong Zou ◽  
...  

Presented is an antimony-based photoluminescent material, namely [Bmim]2SbCl5, exhibiting bright yellow and white light photoluminescence with quantum yield as high as 86.3%.


2017 ◽  
Vol 19 (47) ◽  
pp. 32143-32143
Author(s):  
Hendrik Mohrmann ◽  
Jovan Dragelj ◽  
Federico Baserga ◽  
Ernst-Walter Knapp ◽  
Sven T. Stripp ◽  
...  

Retraction of ‘The reductive phase of Rhodobacter sphaeroides cytochrome c oxidase disentangled by CO ligation’ by Hendrik Mohrmann et al., Phys. Chem. Chem. Phys., 2017, DOI: 10.1039/c7cp06480b.


1980 ◽  
Vol 187 (1) ◽  
pp. 131-140 ◽  
Author(s):  
Enrique Cadenas ◽  
Alberto Boveris ◽  
Britton Chance

Ferricytochrome c showed low-level chemiluminescence, with a light-emission measured of about 1×103–3×103 counts/s, when supplemented with organic hydroperoxides. Tertiary hydroperoxides (cumene hydroperoxide and t-butyl hydroperoxide) showed a saturation behaviour at about 5mm-hydroperoxide, whereas primary hydroperoxides showed a quadratic dependence on the hydroperoxide concentration. Chemiluminescence depended linearly on cytochrome c concentration, and optimal light-emission was observed at [t-butyl hydroperoxide]/[ferricytochrome c] ratios of 160–500. Hydroperoxide-supplemented ferricytochrome c consumed O2 at a rate of 1.0μmol/min per μmol of cytochrome c; the rate of O2 uptake was linearly related to the concentration of cytochrome c. The Soret absorption band of ferricytochrome c decreased about 64% after incubation with t-butyl hydroperoxide, whereas the 530nm band was almost totally abolished. Light-emission was (a) inhibited competitively by cyanide. (b) inhibited by singlet-oxygen quenchers (e.g. β-carotene), scavengers (e.g. dimethylfuran) and traps (e.g. histidine and tryptophan) and (c) increased by singlet-oxygen-chemiluminescence enhancer 1,4-diazabicyclo[2.2.2]-octane. Superoxide dismutase had no effect on the present system. The participation of free radicals is suggested by the effect of the radical trap 2,5-di-t-butylquinol. Singlet-oxygen dimol emission seems to be mainly responsible for the observed light-emission; a mechanism that can account for the major part of the present experimental observations is proposed.


2017 ◽  
Vol 53 (2) ◽  
pp. 392-395 ◽  
Author(s):  
Wen-Chao Geng ◽  
Yan-Cen Liu ◽  
Yu-Ying Wang ◽  
Zhe Xu ◽  
Zhe Zheng ◽  
...  

White light emission was successfully achieved with high quantum yield in a novel FRET platform based on a macrocyclic amphiphile.


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