SUBSTITUENT EFFECTS ON THE PROTOLYTIC DISSOCIATION OF ELECTRONICALLY EXCITED PHENOLS
โ Scribed by William Bartok; Richard B. Hartman; Peter J. Lucchesi
- Book ID
- 114890962
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- English
- Weight
- 350 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0031-8655
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Electronically excited CH was produced by multiphoton dissociation of acetone at 248 nm. Measurements of the electronic relaxation of specific rotational levels of CH( A 'A) by acetone show that the quenching efficiency decreases as N' is increased, in accordance with room temperature results on OH\
Carbonylation of 4-iodotoluene in the presence of a series of 3-or 4-substituted phenols as nucleophiles using a catalytic amount of PdCl,(PPh,), and tributylamine as base to give aryl 4-methylbenzoates has been carried out. It was found that both electron-withdrawing and donating substituents on ph