Making Nonconjugated Small-Molecule Organic Radicals Conduct
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Updated: Dec 18, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Ilhwan Yu1, Yerin Jo1,2, Jaehyoung Ko1
1Institute of Advanced Composite Materials, Korea Institute of Science and Technology (KIST), 92 Chudong-ro, Bongdong-eup, Wanju-gun, Jeonbuk 55324, Republic of Korea.
Abstract:
Charge neutral, nonconjugated organic radicals have emerged as extremely useful active materials for solid-state electronic applications. This previous achievement confirmed the potential of radical-based macromolecules in organic electronic devices; however, charge transport in radical molecules has not been studied in great detail from a fundamental perspective. Here we demonstrate the charge transport in a nonconjugated organic small radical, 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (h-TEMPO). The chemical component of this radical molecule allows us to form a single crystal via physical vapor deposition (PVD). While the charge transport of this macroscopic open-shell single crystal is rather low, thermal annealing of the well-defined single crystal enables the molecule to have a rapid charge transfer reaction due to the electronic communication of open-shell sites with each other, which results in electrical conductivities greater than 0.05 S m-1. This effort demonstrates a drastically different model than the commonly accepted conjugated polymers or molecules for the creation of next-generation conductors.
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