標題: Comparative Investigation of Ultrafast Photoinduced Processes in Salicylidene-Aminopyridine in Solution and Solid State
作者: Sliwa, Michel
Mouton, Nicolas
Ruckebusch, Cyril
Aloise, Stephane
Poizat, Olivier
Buntinx, Guy
Metivier, Remi
Nakatani, Keitaro
Masuhara, Hiroshi
Asahi, Tsuyoshi
應用化學系
應用化學系分子科學碩博班
Department of Applied Chemistry
Institute of Molecular science
公開日期: 9-Jul-2009
摘要: Photodynamics and excited-state intramolecular proton transfer (ESIPT) of N-(3,5-ditert-butylsalicylidene)-4-aminopyridine (4P) and N-(3,5-ditert-butylsalicylidene)-2-aminopyridine (2P) are studied by steady-state and transient optical spectroscopy in solution and solid state (microcrystalline powder). These two compounds are representative of anils Classes A and B, respectively. The results confirm that in solution both compounds have a similar dynamic behavior: upon excitation at 390 nm, ESIPT leads to different cis-keto* fluorescent species which relax to the photochromic trans-keto photoproduct within a few tens of picoseconds. Furthermore, for the first time, picosecond data are recorded for the two classes of anils in the solid state: in 2P, two cis-keto* fluorescent excited state species (23 and 250 ps lifetime) are relaxing exclusively to the cis-keto ground state, whereas in 4P, a single cis-keto* fluorescent species is observed which leads to the trans-keto photoproduct in 250 ps via an intermediate metastable species.
URI: http://dx.doi.org/10.1021/jp901849a
http://hdl.handle.net/11536/6976
ISSN: 1932-7447
DOI: 10.1021/jp901849a
期刊: JOURNAL OF PHYSICAL CHEMISTRY C
Volume: 113
Issue: 27
起始頁: 11959
結束頁: 11968
Appears in Collections:Articles


Files in This Item:

  1. 000267694900071.pdf

If it is a zip file, please download the file and unzip it, then open index.html in a browser to view the full text content.