Basic information Safety Supplier Related

3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%

Basic information Safety Supplier Related

3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Basic information

Product Name:
3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%
Synonyms:
  • 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%
  • 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine
  • 3,7-Di([1,1'-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine
  • 10H-Phenoxazine, 3,7-bis([1,1'-biphenyl]-4-yl)-10-(1-naphthalenyl)-
  • Phenox O-PC? A0202
  • 3,7-Di([1,1'-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine
CAS:
1987900-95-7
MF:
C46H31NO
MW:
613.74
Mol File:
1987900-95-7.mol
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3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Chemical Properties

Melting point:
171°C
Density 
1.209±0.06 g/cm3(Predicted)
form 
powder or crystals
pka
-0.29±0.20(Predicted)
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3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Usage And Synthesis

Uses

This phenoxazine-based organic photoredox catalyst (in addition to the dihydrophenazine catalyst 901112) was designed to be a strong excited-state reductant and possesses advanced photophysical and electrochemical properties, enabling it to serve as a sustainable replacement for ruthenium- or iridium-based photoredox catalysts. For example, dihydrophenazine and phenoxazine derivatives were demonstrated to replace ruthenium or iridium complexes in the application of photoredox-catalyzed atom transfer radical polymerization (ATRP) for controlled polymer synthesis and small molecule transformations such as trifluoromethylation, atom transfer radical addition, and dual Nickel/photoredox catalyzed C-N and C-S cross-couplings. Dihydrophenazine- and phenoxazine-based organic photoredox catalysts were introduced in collaboration with the Miyake Research Group.

3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%Supplier

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