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