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Magnetic Bistability in a Discrete Organic Radical
Abstract
Molecular assembly with magnetic bistability has been of considerable interest for application as electronic devices. In contrast to transition-metal complexes, magnetic bistability so far observed in organic radical crystals is mainly caused by intermolecular electron-exchange interaction. We now report that the magnetic bistability in an organic radical can also be caused by intramolecular electron-exchange interaction. The diradical salt of 1,4-di(bisphenylamino)-2,3,5,6,-tetramethylbenzene undergoes a phase transition with a thermal hysteresis loop over the temperature range from 118 to 131 K. The phases above and below the loop correspond to two different singlet states of the diradical dication. The results provide a novel organic radical material as an unprecedented instance of an intramolecular magnetic bistability revalent to the design of functional materials- Text
- Journal contribution
- Biochemistry
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- singlet states
- diradical dication
- bistability revalent
- Discrete Organic Radical Molecular assembly
- intramolecular
- hysteresis loop
- phase transition
- diradical salt
- material
- Magnetic Bistability
- interaction
- 131 K
- temperature range