## In Ths reaillts of an e~~eu~i study of the V-N trausition of ethylene in solid and IZqs.&I LXWZ goes demonstrate the. fntravaXence character of this excitation.
A comment on the rotational isomerization of ethylene
โ Scribed by L. Giroux; M.H. Back; R.A. Back
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 244 KB
- Volume
- 154
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
Recent spectroscopic measurements have established a torsional barrier m ethylene of 95.5 kcal/mol, a 30 kcal/mol higher than the activation energy for thermal cis-trans isomerization.
It is shown that this difference can be explained in terms of a modest (11%1) increase in the C-C bond length as the molecule is twisted through 90", and its effect on the potential-energy surface for the isomerization.
๐ SIMILAR VOLUMES
The rate constants of isomerization, k and k', were determined at 68 "C to be 3.7 x s-', respectively. The activation energy is 30 kcal. mol -'. The re-
Reflectance absorbance infrared spectroscopy (RAIRS) and thermal desorption data for ethyl formate on Ni(ll 1) display a surface coverage dependence consistent with rotational isomerization within the chemisorbed layer. The (Z)-gauche adsorbate conformation is selectively populated at low surface co