233584-39-9

Upstream product

• 40686-36-0 1-[N-tert-butyl-N-(hydroxylamino)]-3-bromobenzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 917-95-3 t-butylnitrite 
• 108-36-1 1,3-dibromobenzene 

Downstream Products

• 364038-64-2 C₁₀H₁₃N₄O 
• 364038-68-6 3-azido-N-tert-butyl-N-hydroxylaminylbenzene 
• 867198-34-3 1,2-bis[3-(N-tert-butyl-N-oxylamino)phenyl]-1,2-bis[4-{N,N-bis(4-methoxyphenyl)amino}phenyl]ethylene 
• 1352707-76-6 1,2-bis[3-(N-tert-butyl-N-tert-butyldimethylsiloxyamino)phenyl]-1,2-bis[4-{N,N-bis(4-methoxyphenyl)amino}phenyl]ethylene 
• 1352707-75-5 1,2-bis[3-(N-tert-butyl-N-tert-butyldimethylsiloxyamino)phenyl]-1,2-bis[4-{N,N-bis(4-methoxyphenyl)amino}phenyl]ethylene 
• 1352707-77-7 1,2-bis[3-(N-tert-butyl-N-hydroxyamino)phenyl]-1,2-bis[4-{N,N-bis(4-methoxy-phenyl)amino}phenyl]ethylene 
• 1352707-74-4 3-(N-tert-butyl-N-tert-butyldimethylsiloxyamino)-4'-[bis(4-methoxyphenyl)amino]benzophenone 
• 865534-30-1 (N-tert-butyl-N-(tert-butyldimethylsiloxy)amino)phenyl-3-boronic acid 
• 749916-98-1 3-azido-N-tert-butyldimethylsiloxy-N-tert-butylaminobenzene 

Relevant academic research and scientific papers

Redox-switching of intramolecular magnetic interaction through π-conjugation mode change of 1,2-bis(4-dianisylamino)-1,2-bis(3-N-oxylamino)- substituted tetraarylethylene

To develop the redox-switching system of intramolecular magnetic interaction, 1,2-bis[3-(N-tert-butyl-N-oxylamino)phenyl]-1,2-bis[4-{N,N-bis(4- methoxyphenyl)amino}phenyl]ethylene, tetraarylethylene with two nitroxide radical groups at the meta-position,

Photolysis and oxidation of azidophenyl-substituted radicals: Delocalization in heteroatom-based radicals

2-(4-Azidophenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole-3-oxide-1- oxyl (14), 2-(4-azidophenyl)benzimidazole-1-oxide-3-oxyl (16), 2-(4-azidophenyl)-1,2,6-triphenylverdazyl (19), 2-(3-azidophenyl)-4,4,5,5- tetramethyl-4,5-dihydro-1H-imidazole-3-oxid

3,5-Di-tert-butyl-3'-(N-tert-butyl-N-aminoxy)-4-oxybiphenyl: A heterospin diradical with temperature dependent behavior

The title diradical was synthesized and investigated by ESR and UV-vis spectroscopy. It was found to have a lifetime of weeks even in the presence of oxygen, and even survives brief heating in toluene up to about 60°C. In the UV-vis spectrum, the diradica