Rigid-rod conjugated compounds based on N-7-azaindole and 2,2%-dipyridylamine functional groups have been synthesized as potential compounds for molecular electronic devices via Pd-mediated Sonogashira couplings. Their photoluminescent properties have been investigated.
N heteroatomic effect on the photophysics of a polyphenyl system: 2,2′-dipyridylamine
✍ Scribed by P. Jana; T. Ganguly; S.K. Sarkar; A. Mitra; P.K. Mallick
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 560 KB
- Volume
- 94
- Category
- Article
- ISSN
- 1010-6030
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✦ Synopsis
A detailed investigation of the absorption and emission characteristics of 2,2'-dipyridylamine (DPyA) and diphenylamine (DPA) has been carried out in different polar and non-polar solvents at room temperature (300 K) and at 77 K. A dramatic change in both the characteristics has been observed in DPyA in comparison with DPA. Measured fluorescence and phosphorescence lifetimes and critical study of the absorption and emission spectral data suggest that DPyA is more planar than DPA and its lowest-energy singlet state is of IL a type containing a little charge transfer character. Evidence of the presence of a ~n'tr* state has been found in DPyA on protonation in the binary mixture of water and sulphuric acid at room temperature.
📜 SIMILAR VOLUMES
The thermal decomposition rate constant of AIBN ( k d ) in N,N-dimethylformamide (DMF)/ acrylonitrile (AN) mixtures of various compositions at 60°C is studied. The k d value is (6.45 +. 0.3) X min-' for pure acrylonitrile. The k d values of DMF/AN mixtures were found to be dependent on the mixture