The energy transfer processes from thioxanthone (TX) and 2,4-diisopentylthioxanthone (DITX) to organic azides, such as ethyl-p-azidobenzoate (EAZB) and vinylbenzyl azide (VBAZ), were studied by measuring the transient absorption spectra and triplet decay rates of TX and DITX using an Nd:YAG laser fl
Triplet—triplet absorption and triplet energy transfer of thioxanthone in solid polymer matrices
✍ Scribed by Hiroshi Morita; Yoshio Sakaguchi; Hisaharu Hayashi
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 508 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1010-6030
No coin nor oath required. For personal study only.
✦ Synopsis
Transient absorption spectra and triplet decay rates k,, of thioxanthone (TX) and 2,4diisopentylthioxanthone (DITX) in solid polymer matrices were measured using an Nd:YAG laser flash photolysis technique. In a polystyrene matrix, the triplet decay rates of TX and DITX are not dependent on their concentration, indicating that the self-quenching of TX and DITX is not effective in a polymer matrix. In a poly(styrene-co-vinylbenzyl azide) (AZMS) matrix, the triplet decay rates of TX and DITX increase as the number of azido groups in the AZMS polymer increases. The energy transfer rate k,, to the azido group in the AZMS polymer matrix is 1.5X lo6 M-' s-' for TX and 1.4~10~ M-' s-l for DITX. The k,/k,, values of TX and DITX in the AZMS polymer matrix are 20-30 times smaller than the values previously obtained from the measurement of the amount of nitrogen evolved under steady state conditions. The disagreement between the two results strongly indicates that the autocatalytic chain decomposition reaction of the azido group takes place in the AZMS polymer matrix.
📜 SIMILAR VOLUMES
Energy transfer has been shown to occur from triplet polyvinylbenzophenone to naphthalene by an exchange mechanism at liquid nitrogen temperature. The radius of the Terenin "critical sphere" is much larger for the polymer containing naphthalene (29.3,) than for mixtures benzophenonenaphthalene in or
The emission spectra of polyaeenaphthylene (PA&T) and polyvinyluaphthalene (PVN) tihus and solutions have heen compared at room temperature and 77°K. In organic glasses at 77'K, normal fluoresceuee and phosphorescence are observed for both polymers. Quenching of PAcN phosphorescence by piperylene in