2015
DOI: 10.1016/j.jlumin.2014.08.036
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Spectroscopic studies of neutral and chemically oxidized species of β-carotene, lycopene and norbixin in CH2Cl2: Fluorescence from intermediate compounds

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Cited by 16 publications
(8 citation statements)
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“…Finally, the Z ‐isomerized lycopene cation species accept the electron from iron(II) ions to form Z ‐isomers of lycopene in (5) and (6). This proposed mechanism is further supported by a very recent study using fluorescence spectroscopy (Alwis and others ).…”
Section: Resultssupporting
confidence: 73%
“…Finally, the Z ‐isomerized lycopene cation species accept the electron from iron(II) ions to form Z ‐isomers of lycopene in (5) and (6). This proposed mechanism is further supported by a very recent study using fluorescence spectroscopy (Alwis and others ).…”
Section: Resultssupporting
confidence: 73%
“…Rao, Satyanarayana, and Rao (), when assessing the aqueous stability extracts containing different norbixin storage conditions, reported that norbixin is easily degraded by the presence of light, need to be stored in light‐protected media. Alwis, Chandrika, and Jayaweera () reported that norbixin and other carotenoids can be easily oxidized, forming intermediate species of free radicals, dienes, epoxides, and peroxides. Probably, the norbixin present in the films suffered degradation by light absorption of the experiment, forming highly reactive degradation compounds or absorbing and transmitting light energy for singlet oxygen formation.…”
Section: Resultsmentioning
confidence: 99%
“…In the DMF solution, these complexes emit a cyan color with a significant quantum yield. From an application viewpoint, the cyan emission spectra overlap with carotene absorption [ 33 ]. β-carotene is a key compound in grain plants, fruit trees, and other key food resource plants, which absorb solar energy at wavelengths between 500 nm and 550 nm.…”
Section: Introductionmentioning
confidence: 99%