## Abstract Flash photolysis of 2,4,6‐trinitrotoluene solutions (TNT) indicates a photochemically induced isomerization leading to the aci‐quinoid isomer magnified image with an absorption maximum at 460 nm in nonpolar solvents, or the conjugate base magnified image of the aci‐quinoid isomer with a
The flash photolysis of aqueous solutions of rhodizonic and croconic acids
✍ Scribed by B. Zhao; M. H. Back
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 608 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
The flash photolysis of aqueous solutions of rhodizonic and croconic acids has been studied in the presence and absence of electron acceptors. No transient absorption which could be identified with an excited state was observed with either anion. The rate of recovery of the ground state in the absence of additives was a first-order process with both acids and gave rate constants for deactivation of the excited state, KO, of 2.4 X lo5 s-l for rhodizonate and 2.8 X lo5 s-l for croconate. With croconate dianion in the presence of three acceptors, 4-nitrobenzylbromide, methylviologen, and biacetyl, a transient absorption was detected, with a maximum absorbance at 500 nm, and was tentatively identified with the monoanion radical, formed following electron transfer to the acceptor. From the rate of growth of the transient, rate constants for the rate of electron transfer to the acceptor were measured as follows: 4-nitrobenzylbromide: 2.8 X lo9 M-l s-l; methyl viologen: 3.7 X 1O1O M-l s-l; and biacetyl: 2.0 X lo8 M-l s-l. The significance of the measurements is discussed in relation to the mechanism proposed for the photochemical reactions of these dianions. 0 1994 John Wiley & Sons, Inc.
📜 SIMILAR VOLUMES
## Abstract Flash photolysis of __s__‐trinitrobenzene (TNB) aerated solutions in alcohols generates a transient species with absorption maxima at 430 and 510 nm. The yield of the transient is a function of oxygen concentration, and its rate of formation is viscosity dependent. In deaerated solution
The flash photolysis of HNs was studied by coordinated time-resolved spectroscopic measurements of HN3, NH(u'A), NH(X3z), NH(c'a), NH(A3r), NH2, and N3 following flash photolysis of mixtures of HN3 with argon or helium. The primary photolysis is complex, but when the wavelength distribution of the f
Colloidal solutions of Q-Cd3P2 of different mean particle size were flashed and the changes in optical absorption recorded. An absorption band at long wavelengths in the visible and near-infrared is attributed to surface-trapped holes. A bleaching band close to the onset of absorption is attributed
## Abstract The flash photolysis of the mono and di‐thiocyanate complexes of μ‐oxo __bis__(oxo‐molybdenum(V)) (Mo~2~O~4~(NCS)~__x__~(H~2~O)~6−__x__~^(2−__x__)+^ where __x__ = 1, 2) has been studied in the system composed of perchloric acid solutions of Mo~2~O~4~(H~2~O)~6~^2+^ in the presence of exc
## Abstract Triplet state formation (Φ~isc~) and properties (ε~T‐T~, τ~T~) of phthalocyanine (HPC) and zinc phthalocyanine (ZnPC) have been characterized in homogeneous solutions (1‐chloronaphthalene, 1‐propanol) and in microemulsion by investigating the variation of the transient optical density a