Abstract
A set of three new binary-component charge transfer (CT) complexes (Ia, Ib, and Ic) based on anthracene derivatives 1-acetyl-3-naphthyl-(9-anthryl)-2-pyrazoline (ANNP)/1-acetyl-3-(4-methoxyphenyl)-5-(9-anthryl)-2-pyrazoline (AMAP)/1-acetyl-3-thiophene-5-(9-anthryl)-2-pyrazoline (ATAP) as donors (D) and 1,2,4,5-tetracyanobenzene (TCNB) as acceptor (A) were fabricated via molecular self-assembly and comprehensively characterized. Crystal structural analysis revealed that acceptor molecules become sandwiched in a face-to-face manner between the anthracene units through charge transfer, hydrogen bond, and π···π interactions forming CT organic co-crystals with a unique mixed stacking of D··A··D··A··D (Ib and Ic) and DAD···DAD (Ia) arrangement. All of these crystals displayed significant enhancement and red-shift in fluorescence and color-tunable emission such as blue to orange in the solid state. Remarkably, the solid state luminescence efficiency of these CT co-crystals has been improved in comparison to pris...
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