## Abstract Paramagnetic nickel(II) complexes which are used as commercial photostabilizers of polyolefins are shown in laser photolysis studies to quench the triplet state of benzophenone in dilute benzene solution. The efficiency of quenching observed is less than that of diamagnetic squareβplana
Quenching of *UF6 (A state) by alkanes
β Scribed by Fred B. Wampler; Walter W. Rice; Richard C. Oldenborg
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 421 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
β¦ Synopsis
The removal of *UF6 (A state) molecules by selected alkanes has been investigated at 25OC. The following rate constants (units of 10" I/mol-sec) were evaluated ~S O -C ~F I ~, 0.0432 f 0.0115; n-C4Flo, 0.0764 f 0.020; CZF6, 0.0192 f 0.0052; CH4, 0.0612 f 0.0061; C&3,3.78 f 0.60; C~HS, 5.08 f 0.60; n-C4Hlo, 5.05 f 0.78; iso-C4H10,4.17 f 1.15; neo-CsHln, 6.59 f 0.93; CF&HJ, 0.0385 f 0.0056; CF2H-CF2H, 0.0729 f 0.0074; and CFzH-CFHz, 0.149 f 0.015. The perfluoro-alkane quenching of *UF6 proceeds via a physical mechanism. The other alkane quenching reactions are consistent with a chemical mechanism also contributing in varying degrees which may involve removal of two hydrogens from the alkane.
π SIMILAR VOLUMES
## Abstract Sensitization of neat __cis__ or __trans__ 1,3βpentadienes by triplet benzophenone leads only to isomerization and dimerization. The quantum yields measured for these processes as well as the photostationary composition are strikingly different from the figures obtained in dilute soluti
Photoinduced hydrogen transfer and electron transfer to excited states of carbonyl compounds are two of the most intensively investigated fundamental processes in photochemistry. [1][2][3] Numerous studies have been performed to elucidate the mechanisms as well as to determine ways to control these
The electronic structure and bonding of UF, and UF; are studied within a relativistic framework using the MOLFDIR program package. A stronger bonding but more ionic molecule is found if one compares the relativistic with the nonrelativistic results. The first peak in the photoelectron spectrum of Ka