
A new cross-linkable monomer containing 1,3-diphenylethenylcarbazolyl-based hole-transporting moieties and four reactive epoxy groups, was prepared by a multistep synthesis route from 1,3-bis(2,2-diphenylethenyl)-9H-carbazol-2-ol and its application for the in situ formation of cross-linked hole transporting layers was investigated. A high concentration of flexible aliphatic epoxy chains ensures good solubility and makes this compound an attractive cross-linking agent. The synthesized compounds were characterized by various techniques, including differential scanning calorimetry, xerographic time of flight, and electron photoemission in air methods.
Models, Molecular, Macromolecular Substances, Carbazole, Carbazoles, hole drift mobility, Organic chemistry, Electrons, Article, QD241-441, carbazole, Ionization potential, Epoxide, Molecular glass, Cross-Linking Reagents, Solubility, molecular glass, epoxide, ionization potential, Hole drift mobility, Cross-linking, cross-linking
Models, Molecular, Macromolecular Substances, Carbazole, Carbazoles, hole drift mobility, Organic chemistry, Electrons, Article, QD241-441, carbazole, Ionization potential, Epoxide, Molecular glass, Cross-Linking Reagents, Solubility, molecular glass, epoxide, ionization potential, Hole drift mobility, Cross-linking, cross-linking
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