Double fluorescence of p-dimethylacetophenone (DMAPh) in CHaCN and m-methyl-p-c&nodimethyhudliue (MCDMA) iu CHaCia has been observed and analyzed iu terms of reversible excited state isomerisation of the primary excited form b\* to the strongly poiar rotamer a\*. Using the oxygen quenching technique
Picosecond isomerisation kinetics of excited p-dimethylaminobenzonitriles studied by oxygen quenching of fluorescence
✍ Scribed by Krystyna Rotkiewicz; Zbigniew R. Grabowski; Jan Jasny
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 404 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
Fluorescence quenching v,ith O2 under high pressure ~2s used for the study of reaction kinetics in the 10 picosecond region. Quenching of the dual fluorescence of 2-methyl4dimethylaminohenzonitrile (II) in acetonirrile was analysed. The process B* 4 A* occurs with a n lifetime of 11 ps, rvhile the solvent reorientation correlation time is only 1 ps. lvhich supports the isomeri=tion mechanism which involves twisting the amino group. The lifetime of A* is 4.5 ns.
📜 SIMILAR VOLUMES
## Abstract Two __p__‐phenylenevinylene (PV) trimers, containing 3′‐methylbutyloxyl (in MBOPV3) and 2′‐ethylhexyloxyl (in EHOPV3) side chains, are used as model compounds of PV‐based conjugated polymers (PPV) with the purpose of clarifying the origin of fast (picosecond time) components observed in
The quenching kinetics of N,(B3ng, u),have been determined in a low-prcwre flow system in the abscncc of N atoms. Individual vibration?1 levels of the B staic were populated by laser pumping (firsr-positive bands) of N?(A31G) molecules. The latter were created upstream by energy transfer from Ar met