𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Spectroscopy and dynamics of DCM encapsulated in MCM-41 and Y zeolite mesoporous materials

✍ Scribed by Haiquan Guo; Xiaoming Zhang; Metin Aydin; Wei Xu; Han-Ru Zhu; Daniel L. Akins


Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
149 KB
Volume
689
Category
Article
ISSN
0022-2860

No coin nor oath required. For personal study only.

✦ Synopsis


The laser dye 4-(dicyanomethylene)-2-methyl-6-( p-dimethylaminostyryl)-4H-pyran (referred to as DCM) was encapsulated in mesoporous MCM-41 and Y-zeolite. The resultant composites were studied by X-ray diffraction, UV-Vis absorption and emission spectroscopies, and fluorescence lifetime spectrophometry at room temperature. The interactions between occluded DCM and the internal surfaces of the porous materials are found to modify the optical spectra and dynamics of the confined DCM molecules. In particular, two fluorescence bands are observed for DCM occluded within MCM-41, while one fluorescence band is observed for DCM occluded within Y-zeolite or dissolved in DMSO. The dual bands are attributed to emissions from the lowest excited (LE) state and a state created as a result of intramolecular charge transfer, specifically, the twisted intramolecular charge transfer (TICT) state. The decay lifetimes for the LE and TICT states are found to be 0.6 ^0.1 and 1.9 ^0.1 ns, respectively, with 480 nm excitation; the decay lifetimes for 514 excitation are essentially the same. The single emissions from the DCM/Y-zeolite composite and the homogeneous DMSO solution show single exponential decays with lifetimes of 1.3 ^0.1 and 2.0 ^0.1 ns, respectively, both assigned to the TICT state.


πŸ“œ SIMILAR VOLUMES


Acidity and catalytic activity of mesopo
✍ K. Suzuki; Y. Aoyagi; N. Katada; M. Choi; R. Ryoo; M. Niwa πŸ“‚ Article πŸ“… 2008 πŸ› Elsevier Science 🌐 English βš– 821 KB

Acidity of mesoporous HZSM-5 prepared using amphiphilic organosilane template molecules was measured. BrΓΈnsted acid sites were observed in the prepared sample, and the number and the strength of BrΓΈnsted acid sites were determined quantitatively by a method of infrared-mass spectroscopy/temperature-