Author/Authors :
Miura، نويسنده , , Yousuke and Momotake، نويسنده , , Atsuya and Shinohara، نويسنده , , Yoshihiro and Wahadoszamen، نويسنده , , Md. and Nishimura، نويسنده , , Yoshinobu and Arai، نويسنده , , Tatsuo، نويسنده ,
Abstract :
We report that both singlet and triplet energy transfers in stilbene-cored benzophenone dendrimers (trans-BPST) took place quite efficiently. On excitation (290 nm) of stilbene group, the intramolecular singlet energy transfer from the excited core stilbene to the benzophenone part (99.7%) was confirmed by quenching of the fluorescence from the core stilbene. The benzophenone in the excited singlet state is known to undergo intersystem crossing to give its excited triplet state quantitatively. However, the very weak phosphorescence from benzophenone part in trans-BPST was observed even at 77 K. The phosphorescence intensity of trans-BPST is only 1% of that of model compound (4-methylbenzophenone) at 77 K. During the irradiation, the absorption spectra also changed due to the trans–cis isomerization. This is probably due to the ultrafast triplet energy transfer from the benzophenone to produce the triplet state stilbene.