155504-10-2Relevant articles and documents
Ferromagnetic spin alignment in head-to-tail coupled oligo(1,4-phenyleneethynylene)s and oligo(1,4-phenylenevinylene)s bearing pendant p-phenylenediamine radical cations
Van Meurs, Pauline J.,Janssen, Rene A. J.
, p. 5712 - 5719 (2007/10/03)
The intramolecular and long-range ferromagnetic coupling between p-phenylenediamine radical cations in head-to-tail coupled oligo(1,4-phenyleneethynylene)s and oligo(1,4-phenylenvinylene)s between neighbors and next-nearest neighbors is described. UV/vis/near-IR experiments show that the radical cations are localized in the pendant p-phenylenediamine units of the conjugated oligomers. The ESR spectra of these oligo(1,4-phenyleneethynylene) and oligo(1,4-phenylenvinylene) di(radical cation)s are consistent with those of a triplet state. A linear behavior is observed for the doubly integrated ESR intensity of the ΔM(s) = ±1 and ΔM(s) = ±2 signals with the inverse temperature (I ~ 1/T), consistent with Curie's law. This behavior indicates a triplet ground-state diradical with a large triplet-singlet energy gap or possibly a degeneracy of singlet and triplet states.
MAGNETIC COUPLING BETWEEN TWO PHENOXYL RADICALS ATTACHED TO THE PHENYL RINGS OF CIS- AND TRANS-STILBENES
Mitsumori, Teruyuki,Koga, Noboru,Iwamura, Hiizu
, p. 43 - 49 (2007/10/02)
Magnetic coupling between two sterically protected phenoxyl radicals through the cis- and trans-stilbene chromophores was studied by means of their EPR fine structures.While the zero-field splitting parameters D, which are governed by the magnitude of dip
