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Reversible Bergman cyclization, AFM image

Reversible Bergman cyclization, AFM image

C032/5432

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Credit

IBM RESEARCH / SCIENCE PHOTO LIBRARY IBM RESEARCH / SCIENCE PHOTO LIBRARY

Caption

Reversible Bergman cyclization. Atomic force microscopy (AFM) image of the starting point (a brominated aromatic compound) for a reversible Bergman cyclization. Researchers used non-contact AFM to observe this molecular rearrangement, a key step in several organic synthesis and pharmacology reactions. It was first described in 1972 by American chemist Robert George Bergman. An aromatic diradical was prepared and rearranged into a highly strained ten-membered diyne using atomic manipulation. It was found that the diradical and the diyne exhibit different properties associated with the bond changes. The results were published in 2016 in the journal 'Nature Chemistry', in a collaboration between IBM researchers in Zurich, Switzerland, and CiQUS researchers at the University of Santiago de Compostela, Spain. For the full set of structures observed, see image C032/5431.

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