Highly luminescent crystals of a novel linear π‐conjugated thiophene–phenylene co‐oligomer with a benzothiadiazole fragment

The synthesis, growth from solutions and structure of crystals of a new linear thiophene–phenylene co‐oligomer with a central benzothiadiazole fragment with a conjugated core, (TMS‐2T‐Ph)2‐BTD, are presented. Single‐crystal samples in the form of needles with a length of up to 7 mm were grown and th...

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Veröffentlicht in:Acta crystallographica Section B, Structural science, crystal engineering and materials Structural science, crystal engineering and materials, 2019-12, Vol.75 (6), p.1076-1085
Hauptverfasser: Postnikov, Valery A., Sorokina, Nataliya I., Kulishov, Artem A., Lyasnikova, Maria S., Grebenev, Vadim V., Voloshin, Alexey E., Borshchev, Oleg V., Skorotetcky, Maxim S., Surin, Nikolay M., Svidchenko, Evgeniya A., Ponomarenko, Sergei A.
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Sprache:eng
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Zusammenfassung:The synthesis, growth from solutions and structure of crystals of a new linear thiophene–phenylene co‐oligomer with a central benzothiadiazole fragment with a conjugated core, (TMS‐2T‐Ph)2‐BTD, are presented. Single‐crystal samples in the form of needles with a length of up to 7 mm were grown and their crystal structure was determined at 85 K and 293 K using single‐crystal X‐ray diffraction. The conformational differences between the crystal structures are insignificant. The parameters of melting and liquid crystalline phase transitions of (TMS‐2T‐Ph)2‐BTD were established using differential scanning calorimetry and the thermal stability of the crystals was investigated using thermogravimetric analysis. The optical absorption and photoluminescence spectra of the solutions and crystals of (TMS‐2T‐Ph)2‐BTD were obtained, and the kinetics of their photodegradation under the action of UV radiation were studied. The synthesis, growth from solutions, structure and photoluminescence of crystals of a new linear thiophene‐phenylene co‐oligomer (TMS‐2T‐Ph)2‐BTD with a central benzothiadiazole fragment within the conjugated core are presented.
ISSN:2052-5206
2052-5192
2052-5206
DOI:10.1107/S2052520619012484