The Journal of Physical Chemistry B · 2020 · 25 citations · 31 references
Natural SciencesChemistryMaterials ScienceCrystal StructurePhysical ChemistrySolid-state ChemistryChemical BondingCoordination ChemistryCrystal ChemistryMolecular SymmetryPhotochemistryPhotochromic MaterialsBonding Electron DelocalizationCharge DelocalizationChromophore PhotochemistryElectron DelocalizationSolid-state PhotochromismSolution-phase PhotochromismSpiropyran CompoundsStabilization
Salts containing the merocyanine form of a pyridinium-fused spiropyran ([6′-MC]X; X = I and PF6) were prepared, and their crystal structures were determined. In addition, the photochromic properties of the salts were spectroscopically and kinetically investigated. In the solution state, the salts exhibited negative photochromism. Theoretical calculations revealed that the negative photochromism of the salt originates from the drastic stabilization of the merocyanine structure by electron delocalization of the pyridinium ring. Furthermore, the salts containing the merocyanine and spiropyran forms ([6′-MC]I, [6′-MC]PF6, and [6′-SP]PF6) were obtained by recrystallization. The crystals of [6′-SP]PF6 exhibited positive photochromism in the solid state; however, no photochromism was observed in the [6′-MC]X crystals.
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