{"id":195872,"date":"2021-03-05T20:05:42","date_gmt":"2021-03-05T17:05:42","guid":{"rendered":"https:\/\/en.buradabiliyorum.com\/using-a-radical-to-break-c-f-bonds-one-at-a-time\/"},"modified":"2021-03-05T20:05:42","modified_gmt":"2021-03-05T17:05:42","slug":"using-a-radical-to-break-c-f-bonds-one-at-a-time","status":"publish","type":"post","link":"https:\/\/buradabiliyorum.com\/en\/using-a-radical-to-break-c-f-bonds-one-at-a-time\/","title":{"rendered":"#Using a radical to break C-F bonds one at a time"},"content":{"rendered":"

“#Using a radical to break C-F bonds one at a time<\/strong>”<\/p>\n

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\n Strategies for C\u2013F bond functionalizations of CF3 groups. (A) Defluorination of CF3 groups to difluoro-substituted intermedia<\/a>tes (top) and the challenging goal of controllably generating di- and monofluoroalkyl radicals (bottom). (B) Spin-center shift (SCS) in biochemical conversions and organic synthesis. (C) This work: Two-stage process for sequential C\u2013F bond cleavage via SCS. Credit: Science<\/a><\/i> (2021). DOI: 10.1126\/science.abg0781
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A team of researchers from the University of Science and Technology<\/a> of China and the University of California has found a way to use radicals to break C-F bonds one at a time when working with trifluoroacetamides and acetates. In their paper published in the journal Science<\/i>, the group describes how they found the right radical for such reactions and how their technique might be used in future app<\/a>lications.<\/p>\n


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Chemists have been searching for ways to add fluorine to certain drugs because doing so helps their molecules move through cell membranes. The problem has been finding a way to swap out just one of the fluorine atoms in compounds such as trifluoromethyl to create mono- and\/or difluorinated compounds. With current methods, when a reaction breaks the first C-F bond, the other two grow weaker, resulting in their removal, as well. In this new effort, the researchers have found a way to carry out such reactions without weakening secondary C-F bonds.<\/p>\n

The researchers claim that the solution to the problem lies in finding the right radical\u2014one that can target trifluoroacetate and trifluoroacetamide starting materials. After an extensive search, they found that the amino-boryl radical would target starting compounds as desired. The radical worked, they note, because the CF3<\/sub> carbon molecule was strongly electron deficient. That meant that once the radical broke the first C-F bond, it was much less likely to do the same for the second or third C-F bonds. The end result was a reaction that stopped before all the fluorine bonds had been broken.<\/p>\n

The team tested their radical along with an amino boran by swapping out a C-F bond for either a C-H bond or a C-C bond, while also adding other ingredients such as hydrogen to make a wide variety of mono- and difluorinated acetamides and acetates. They also used their radical to modify existing drug molecules to make them more effective in targeting specific tissue. They suggest their technique should prove useful in the development of new therapies for a host of ailments, ranging from lymphoma to endometriosis.<\/p>\n\n

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Experiments with bifluoride ions show evidence of hybrid bonds\n <\/p><\/div>\n

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\n More information:<\/strong>
\n Sequential C\u2013F bond functionalizations of trifluoroacetamides and acetates via spin-center shifts, Science<\/i> (2021). science.sciencemag.org\/lookup\/ \u2026 1126\/science.abg0781<\/a><\/p><\/div>\n

\n \u00a9 2021 Science X Network<\/p>\n

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Citation<\/strong>:
\n Using a radical to break C-F bonds one at a time (2021, March 5)
\n retrieved 6 March 2021
\n from https:\/\/phys.org\/news<\/a>\/2021-03-radical-c-f-bonds.html<\/p>\n

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