3129-17-7

Upstream product

• 119-61-9 benzophenone 
• 908093-98-1 diazodiphenylmethane 
• 470-35-9 tetraphenyloxirane 
• 2051-90-3 Dichlorodiphenylmethane 
• 4545-20-4 benzophenone tosylhydrazone 

Downstream Products

• 1016-09-7 benzhydryl methyl ether 
• 2229-07-4 methyl radical 
• 38885-70-0 C₁₄H₁₃S 
• 4471-17-4 diphenylmethyl radical 
• 16812-19-4 tert-butyl mercaptyl radical 
• 38885-72-2 C₁₇H₁₉S 
• 119-61-9 benzophenone 
• 91-01-0 1,1-Diphenylmethanol 
• 632-50-8 1,1,2,2-tetraphenylethane 
• 20799-93-3 (N-diphenylmethyl)butylamine 
• 983-79-9 benzophenone azine 
• 632-51-9 1,1,2,2-tetraphenylethylene 
• 3677-76-7 2-methyl-1,1-diphenyl-propan-2-ol 
• 5670-79-1 isopropyl diphenylmethyl ether 

Relevant academic research and scientific papers

Activation of the B?F Bond by Diphenylcarbene: A Reversible 1,2-Fluorine Migration between Boron and Carbon

Experiments in low-temperature matrices reveal that triplet diphenylcarbene inserts into the very strong B?F bond of BF3in a two-step reaction. The first step is the formation of a strongly bound Lewis acid–base complex between the singlet stat

1-Phenyl-1,2,4,6-cycloheptatetraene: The missing intermediate of the diphenylcarbene to fluorene rearrangement

The photochemistry of diphenylcarbene 5, matrix-isolated in argon at 3-5K was investigated by UV-Vis, IR, and EPR spectros-copy. Although carbene 5 proved to be stable toward broadband UV irradiation, it slowly rearranges to 1-phenyl-1,2,4,6-cycloheptatet

LASER FLASH SPECTROMETRIC INVESTIGATIONS OF BIRADICALS AND CAGED RADICAL PAIRS

The use of laser flash spectroscopic techniques allows the detection, identification and dynamic analysis of biradicals and caged radical pairs in fluid solution at ambient temperatures.The conventional flash spectroscopic device has been advanced with the advent of the Excimer Laser, as an excitation source of the optical multichannel analyzer (OMA) as a detector system and of the transient digitizer (TD) as a data collector and analyzer.The Excimer Laser, in addition to serving as an excitation source, may also induce novel photophysical and/or photochemical events as a result of the unusually high intensities produced by such devices.Examples are given of the use of Excimer Laser-OMA and Excimer Laser-TD systems to study the dynamics of radical pairs that are caged in micelle aggregates and to study novel emissions produced by photoexcitation of benzophenone and substituted benzophenones.