Naturally occurring molecules as well as man-made pharmaceuticals and plastics are strung together by strong amide bonds.
Although amide bonds can give great strength to plastics, when it comes to their recycling at a later point, the difficultly of breaking these bonds usually prevents recovery of useful products.
Researchers from Nagoya University in Japan developed a series of organometallic ruthenium catalysts to break down even the toughest amide bonds effectively under mild conditions.
"Our previous catalysts could hydrogenate most amide bonds, but the reactions needed a long time at high temperature and high pressure. This new ruthenium catalyst can hydrogenate difficult substrates under much milder conditions," said Takashi Miura of Nagoya University.
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Hydrogenation is the key step leading to the breakdown of amide bonds. The catalyst features a ruthenium atom supported in an organic framework.
This ruthenium atom can adsorb hydrogen and deliver it to the amide bond to initiate the breakdown, researchers said.
The team probed the position of hydrogen on the catalyst in the reaction pathway and modified the shape of the supporting framework.
"The changes we made to the catalyst allowed some tricky amide bonds to be selectively cleaved for the first time," said Susumu Saito from Nagoya University.
"This catalyst has great potential for making designer peptides for pharmaceutics and could also be used to recover materials from waste plastics to help realise an anthropogenic chemical carbon cycle," Saito said.
The study was published in the journal Scientific Reports.