首页> 外文期刊>Journal of the American Chemical Society >Magnetic Bistability in Crystalline Organic Radicals: The Interplay of H-bonding, Pancake Bonding, and Electrostatics in 4-(2'- Benzimidazolyl)-1,2,3,5-dithiadiazolyl
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Magnetic Bistability in Crystalline Organic Radicals: The Interplay of H-bonding, Pancake Bonding, and Electrostatics in 4-(2'- Benzimidazolyl)-1,2,3,5-dithiadiazolyl

机译:结晶有机自由基中的磁性双稳性:4-(2'-苯并咪唑基)-1,2,3,5-二噻二唑基中H键,煎饼键和静电的相互作用

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摘要

The neutral radical 4-(2'-benzimidazolyl)-1,2,3,5-dithiadiazolyl (HbimDTDA) exhibits a first order phase transition around 270 K without symmetry breaking, preserving its orthorhombic Pbca space group between 340 and 100 K. Associated with this reversible single-crystal-to-single-crystal phase transition, thermal hysteresis of the magnetic susceptibility is observed. The low temperature (LT) phase is diamagnetic owing to pancake bonding between the pi-radicals. In the paramagnetic high temperature (HT) phase, the pancake bonds are broken, and new electrostatic contacts are apparent. As a result of the dense 3D network of supramolecular contacts, which includes H-bonds, the HbimDTDA system provides the first example of magnetic bistability for a DTDA radical.
机译:中性自由基4-(2'-苯并咪唑基)-1,2,3,5-二硫二唑基(HbimDTDA)在270 K附近表现出一阶相变而没有对称破坏,保留了其正交的Pbca空间群在340和100 K之间。通过这种可逆的单晶至单晶相变,观察到磁化率的热滞后。由于pi自由基之间的薄饼键合,低温(LT)相是反磁性的。在顺磁性高温(HT)阶段,薄饼键断裂,并且出现了新的静电接触。由于包括H键的超分子接触的密集3D网络,HbimDTDA系统提供了DTDA自由基的磁性双稳态的第一个例子。

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