B50805
1,4-Bis(5-phenyl-2-oxazolyl)benzene
suitable for scintillation, 98%
Synonym(s):
1,4-Bis(5-phenyl-2-oxazolyl)benzene, 2,2′-p-Phenylene-bis(5-phenyloxazole), Di(phenyl-5-oxazolyl-2)-1,4-benzene, POPOP
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Assay
98%
mp
242-246 °C (lit.)
suitability
suitable for scintillation
SMILES string
c1ccc(cc1)-c2cnc(o2)-c3ccc(cc3)-c4ncc(o4)-c5ccccc5
InChI
1S/C24H16N2O2/c1-3-7-17(8-4-1)21-15-25-23(27-21)19-11-13-20(14-12-19)24-26-16-22(28-24)18-9-5-2-6-10-18/h1-16H
InChI key
MASVCBBIUQRUKL-UHFFFAOYSA-N
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General description
1,4-Bis(5-phenyl-2-oxazolyl)benzene (POPOP) is a scintillation luminophore. It is commonly used as a secondary wavelength shifter. The photochemical and photophysical studies of POPOP in different solvents have been reported.
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Photophysical Parameters, Excitation Energy Transfer, and Photoreactivity of 1,4-Bis (5-phenyl-2-oxazolyl) benzene (POPOP) Laser Dye.
International Journal of Photoenergy, 2012 (2012)
Investigation of the physical and the optical properties of various base solvents for the liquid scintillator in a neutrino detector.
The Journal of the Korean Physical Society, 62(1), 26-33 (2013)
New solution-processable carbazole derivatives as deep blue emitters for organic light-emitting diodes.
Royal Society of Chemistry Advances, 6(11), 9247-9253 (2016)
Luminescence : the journal of biological and chemical luminescence, 16(3), 243-246 (2001-06-16)
The involvement of upper electron-excited states in bacterial bioluminescence process was studied with excitation energy-accepting molecules. The fluorescent aromatic compounds, anthracene and 1.4-bis(5-phenyloxazol-2-yl)benzene, were chosen. Energies of their lowest excited singlet states are higher than the energy of the analogous
Analytical biochemistry, 368(1), 100-110 (2007-06-15)
In this study, micron-sized poly(styrene-co-glycidyl methacrylate) (PSt-GMA) fluorescent microspheres of 5.1microm in diameter were synthesized via dispersion polymerization of styrene and glycidyl methacrylate in the presence of 1,4-bis(5-phenyloxazol-2-yl) benzene (POPOP), which provided surface functional groups for covalent immobilization of enzymes.
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