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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.

Michelle B MillsTobie WohlhauserBenjamin SteinWillem R VerduynEllen SongPierre DechambenoitMathieu RouzièresRodolphe CléracKathryn E Preuss
Published in: Journal of the American Chemical Society (2018)
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 π-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.
Keyphrases
  • molecularly imprinted
  • high temperature
  • computed tomography
  • molecular dynamics simulations
  • quantum dots
  • simultaneous determination
  • tandem mass spectrometry