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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/206388
Towards the tailored design of benzotriazinyl-based organic radicals displaying a spin transition
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The mechanism of the phase transition of 1-phenyl-3-trifluoromethyl- 1,4-dihydrobenzo[e][1,2,4]triazin-4-yl (1), the first reported triazinyl radical to present such a feature, is unveiled. In so doing, we identify the key ingredients that are crucial to enable the phase transition in this family of radicals, and how those can be exploited by a rational design of the spin-carrying units.
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FUMANAL QUINTANA, María, et al. Towards the tailored design of benzotriazinyl-based organic radicals displaying a spin transition. Chemical Communications. 2015. Vol. 51, num. 15776-15779. ISSN 1359-7345. [consulted: 13 of June of 2026]. Available at: https://hdl.handle.net/2445/206388