Time-resolved excited state dynamics of a cyanine dye

نویسندگان

  • Tieqiao Zhang
  • Ciping Chen
  • Qihuang Gong
  • Wenpeng Yan
  • Shufeng Wang
  • Hong Yang
  • Huahua Jian
  • Guangzi Xu
چکیده

X Ž . The photophysics and isomerization dynamics in the excited state of a cyanine dye, 3,3 -di 3-sulfopropyl -thiacyanine triethylaminium salt was investigated. Using the femotosecond time-resolved fluorescence up-conversion technique, wavelength-dependent fluorescence dynamics was observed and the theoretical prediction of the dual fluorescence behavior was vindicated. The results were explained using a barrierless isomerization reaction model. The origins of two decay components were assigned to the relaxation within the excited state and the S TMS transition, respectively, and the time 1 0 constants were obtained. q 1998 Elsevier Science B.V. All rights reserved.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ultrafast excited-state dynamics associated with the photoisomerization of a cyanine dye.

The ultrafast excited-state dynamics of a cyanine dye, 3,3'-bis(3-sulfopropyl)-5,5'-dimethoxy-thiacyanine triethylaminium salt, was investigated by using conventional time-resolved fluorescence up-conversion technique. The fluorescence decay can be well described as tri-exponential kinetics, which indicates the excited-state population decays through the bond-twist, vibrational and radiative re...

متن کامل

Watching ultrafast barrierless excited-state isomerization of pseudocyanine in real time.

The photoinduced excited-state processes in 1,1'-diethyl-2,2'-cyanine iodine are investigated using femtosecond time-resolved pump-probe spectroscopy. Using a broad range of probe wavelengths, the relaxation of the initially prepared excited-state wavepacket can be followed down to the sink region. The data directly visualize the directed downhill motion along the torsional reaction coordinate ...

متن کامل

Ultrafast charge transfer in solid-state films of pristine cyanine borate and blends with fullerene

Photoinduced electron transfer in light-absorbing materials is the first step towards charge separation and extraction in small molecule-based organic solar cells. The excited state dynamics of the cyanine dye cation Cy3 paired with a tetraphenylborate counter-anion (Cy3-B) was studied in pristine solid-state films of the dye and in blends with the electron acceptor material PCBM. Here we show ...

متن کامل

Femtosecond pump-probe study of molecular vibronic structures and dynamics of a cyanine dye in solution

Time-resolved pump–probe spectra of 1,18,3,3,38,38-hexamethyl-4,48,5,58-dibenzo-2,28indotricarbocyanine ~HDITC!, a cyanine dye, in ethylene glycol are obtained using 11 fs and 90 fs duration pulses and analyzed in order to study its potential energy surfaces and vibrational dynamics. Ten oscillatory frequencies ranging from 30 cm to 1400 cm are observed in the 11 fs duration wavelength-resolved...

متن کامل

Photoinduced dynamics of a cyanine dye: parallel pathways of non-radiative deactivation involving multiple excited-state twisted transients

Cyanine dyes are broadly used for fluorescence imaging and other photonic applications. 3,3'-Diethylthiacyanine (THIA) is a cyanine dye composed of two identical aromatic heterocyclic moieties linked with a single methine, -CH 0000000000000000000000000000000000 0000000000000000000000000000000000 0000000000000000000000000000000000 0000000000000000000000000000000000 000000000000000000000000000000...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 1998