Science & Technology - Posted by Robert Perkins-USC on Monday, December 10, 2012 12:11 - 2 Comments
Teflon leftover can fuel drug discovery
USC (US) — Chemists have found a way to turn ozone-destroying greenhouse gas leftover from Teflon manufacture into reagents for producing pharmaceuticals.
Because of the popularity of Teflon—used on everything from cooking pans to armor-piercing bullets—there’s no shortage of its waste byproduct, fluoroform.
Straight from the Source
Major chemical companies, such as DuPont, Arkema Inc., and others, have huge tanks of it and are unable to simply release it because of the potential damage to the environment. Fluoroform has an estimated global warming potential 11,700 times higher than carbon dioxide.
But one man’s trash is another man’s treasure, and G.K. Surya Prakash—who has spent decades working with fluorine reagents—saw the tanks of fluoroform as an untapped opportunity.
Prakash, professor of chemistry at the University of Southern California and director of the USC Loker Hydrocarbon Research Institute, describes fluorine as “the kingpin of drug discovery.”
About 20 to 25 percent of drugs on the market today contain at least one fluorine atom; fluorine can be found in all kinds of drugs, from 5-Fluorouracil (a widely used cancer treatment discovered by Charles Heidelberger at USC in the ’70s) to Prozac to Celebrex.
“It’s a small atom with a big ego,” Prakash says, referring to the fact that while fluorine is about the same size as a tiny hydrogen atom—so similar that living cells cannot tell the two elements apart—it is also extremely electronegative (that is, it has a strong attraction for electrons) making carbon-fluorine chemical bond quite strong, which improves the bioavailability of drugs made with fluorine.
Prakash led a team that included longtime colleague George Olah, professor of chemistry, and research associates Parag Jog and Patrice Batamack.
The discovery was the product of many years of trial-and-error tests, which the postdocs performed under Prakash’s direction. Eventually, the team pinned down the precise conditions needed to coax the harmful fluoroform (CF3H) into useful reagents, including the silicon-based Ruppert-Prakash Reagent for efficient CF3 transfer.
Fluoroform with elemental sulfur was also converted to trifluoromethanesulfonic acid, a widely used superacid 100 times stronger than sulfuric acid.
“In real estate, everything is ‘location, location, location,’ Prakash says. “In chemistry, it is ‘conditions, conditions, conditions.’”
The Loker Hydrocarbon Research Institute funded the research, which the researchers report in the December 7 issue of Science. The method is also being patented.