Search results
Results from the WOW.Com Content Network
The carbon–fluorine bond is organic chemistry's strongest, [156] and gives stability to organofluorines. [157] It is almost non-existent in nature, but is used in artificial compounds. Research in this area is usually driven by commercial applications; [158] the compounds involved are diverse and reflect the complexity inherent in organic ...
Fluorine's chemistry is dominated by its strong tendency to gain an electron. It is the most electronegative element and elemental fluorine is a strong oxidant. The removal of an electron from a fluorine atom requires so much energy that no known reagents are known to oxidize fluorine to any positive oxidation state. [20]
Introducing the carbon–fluorine bond to organic compounds is the major challenge for medicinal chemists using organofluorine chemistry, as the carbon–fluorine bond increases the probability of having a successful drug by about a factor of ten. [30] Over half of agricultural chemicals contain C-F bonds. A common example is trifluralin. [31]
Fluorine, in the form of fluoride, is considered to be a micronutrient for human health, necessary to prevent dental cavities, and to promote healthy bone growth. [28] The tea plant (Camellia sinensis L.) is a known accumulator of fluorine compounds, released upon forming infusions such as the common beverage. The fluorine compounds decompose ...
Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...
And science and industry have figured out how to put that to use. An isotope of the element fluorine, known as Fluorine-18, is frequently used in medical PET scans.
Moissan's fluorine cell, from his 1887 publication. Fluorine is a relatively new element in human applications. In ancient times, only minor uses of fluorine-containing minerals existed. The industrial use of fluorite, fluorine's source mineral, was first described by early scientist Georgius Agricola in the 16th century, in the context of ...
While different PFAS have different chemical structures, all PFAS have at least one common trait: the presence of carbon-fluorine bonds, which are among the strongest bonds in chemistry.