This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility: In a new publication in the journal Nature Chemistry, chemists in professor Holger Braunschweig's team at the University of Würzburg, supported by computational work from the team of professor Ashwini K. Phukan at Tezpur University in India, detail their discovery of a method for preparing and isolating a range of surprisingly stable oxoboranes—a challenge that has stood for over 60 years.
The element boron does not like to form triple bonds—this challenge has motivated Würzburg chemist Braunschweig to make molecules with boron-containing triple bonds for over 15 years. In 2012, his team reported the first molecule with a boron-boron triple bond, and in 2025 they reported the first neutral molecule with a boron-carbon triple bond. In the first row of the periodic table's p-block, just one challenge remained: organic oxoboranes, compounds with boron-oxygen triple bonds.
Since at least the early 1960s, oxoboranes have been the target of decades of synthetic attempts from a wide range of inorganic and organic chemists around the world. They have been trapped and detected under extreme conditions, their existence has been inferred from chemical reactions and a number of derivatives have been made—but isolation of stable examples remained elusive. When Würzburg chemistry doctoral students Lukas Lubczyk and Christian Markl combined a molecule called a diboracumulene with different ketones—standard reagents in organic chemistry—they independently noted that the reactions had led to unusual orange or yellow solids.
"The discovery was a pleasant surprise. I never thought the diboracumulene would react the way it did, let alone with multiple different, simple substrates. And when Christian came to me with his compound, I knew we were on to something," says Lubczyk.
It was a great surprise that, out of many other seemingly more likely outcomes, and despite decades of attempts to prepare these compounds, the elusive oxoboranes would be the main products of these reactions. "Nearly everybody in the field had given up on oxoboranes, as they were thought to be just too unstable to be isolated. So we were stunned to see them spontaneously form in these reactions and stick around long enough that we could study them," says Braunschweig.
Three oxoboranes were prepared, showing that the method could lead to many new oxoboranes in the future. The team is now trying to see just how far the method can be pushed to prepare other elusive molecules across the periodic table. Lukas Lubczyk et al., Synthesis and isolation of stable oxoboranes, Nature Chemistry (2026).
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