Two Roads Converged in a Yellow Dye: Unusual Spectral Broadening in the Emission of Auramine-O Possibly Caused by Low-Friction Intramolecular Rotation

Yuval Erez, Ron Simkovitch, Katherine Akulov, Rinat Gepshtein, Tal Schwartz, Dan Huppert

نتاج البحث: نشر في مجلةمقالةمراجعة النظراء

ملخص

Steady-state and time-resolved optical techniques were employed to study the rather complex relaxation of excited states of Auramine-O (AuO) in several liquids at room temperature. We found three relaxation times in the decay of the pumpprobe signals of the excited states of AuO. We focused our study on the short time decay, with a duration of within about 150-300 fs. We found that the temporal changes of the emission band of AuO could be divided into three behaviors, depending on the solvent characteristics. In dimethyl sulfoxide (DMSO), a hydrogen-bond-accepting solvent, AuO, shows, at short times, a relatively broad emission band with small changes in its peak position and width as a function of time. In acetonitrile and in acetic acid, both hydrogen-bond-donating solvents, we found large changes in the band peak and width as a function of time. Dichloromethane is a solvent lacking strong solvent interactions, it is apolar and is neither a strong hydrogen-bond-donator nor a strong hydrogen-bond-acceptor. For AuO in dichloromethane we found an oscillation with a time constant of 200 fs in the time-resolved emission signal. We attribute the rather large changes of the emission band with time in the short time window to the twist of the dimethylamino groups of the aniline groups of AuO.
اللغة الأصليةالإنجليزيّة
الصفحات (من إلى)27063-27073
عدد الصفحات11
دوريةJournal of Physical chemistry c
مستوى الصوت118
رقم الإصدار46
المعرِّفات الرقمية للأشياء
حالة النشرنُشِر - 20 نوفمبر 2014

All Science Journal Classification (ASJC) codes

  • !!Electronic, Optical and Magnetic Materials
  • !!General Energy
  • !!Surfaces, Coatings and Films
  • !!Physical and Theoretical Chemistry

بصمة

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