Swarts fluorination is a process whereby the chlorine atoms in a compound – generally an organic compound, but experiments have been performed using silanes...

hydrolyzing slowly in water. With fluorine, it is oxidized to give antimony pentafluoride. SbF3 + F2 → SbF5 It is used as a fluorination reagent in organic chemistry...

Swarts fluorination, in which chlorocarbon chlorines are substituted for fluorines by hydrogen fluoride under catalysts. Electrochemical fluorination subjects...

potassium permanganate. The trifluorotrichloropropene can be prepared by Swarts fluorination of hexachloropropene. TFA is the precursor to many other fluorinated...

Theodore Swarts (chemist, *1839 Antwerpen; †1911 Kortenberg, Belgium) and a colleague of Leo Baekeland. Kauffman, George B. (1955). "Frederic Swarts: Pioneer...

photodimer, an example of a 1,3-dithietane, is a colourless solid. Swarts fluorination of the dimer and then cracking is the principal route to thiocarbonyl...

on the degree and regiochemistry of fluorination sought and the nature of the precursors. The direct fluorination of hydrocarbons with F2, often diluted...

debromination with a Swarts reagent. From a dihalomethane by an halogen exchange reaction or from a halomethane by catalyzed bromination or fluorination. The method...

compounds by treatment with antimony trifluoride/antimony pentachloride (the Swarts reaction). Another route to trifluoromethyl aromatics is the reaction of...

prepared in 1901 by Frédéric Swarts, the Belgian chemist who was the first to prepare chlorofluorocarbons in 1892. Swarts used the reaction of zinc with...