Abstract

Organic light-emitting molecular glasses (OEMGs) are synthesized through the introduction of nonplanar donor and branched aliphatic chain into electroluminescent emitters. The target OEMGs are characterized by 1H NMR, 13C NMR, IR, UV–vis and fluorescent spectra as well as elemental analysis, TG and DSC. The results indicated that the optical, electrochemical and electroluminescent properties of OEMGs are adjusted successfully by the replacement of electron-donating group. The non-doped OLED device with a standard red electroluminescent emission is achieved by spin-coating the THF solution of OEMG with a triphenylamine moiety. This non-doped red OLED device takes on an electrically stable electroluminescent performance, including the stable maximum electroluminescent wavelength of 640nm, the stable luminous efficiency of 2.4cd/A and the stable CIE1931 coordinate of (x, y)=(0.64, 0.35), which is basically in accord with the CIE1931 coordinate (x, y)=(0.64, 0.33) of standard red light in PAL system.

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