The polarizationsof three low energy singlet-singlet electronic transitions of several monesubstituted naphthdenes have been measured rctative to the transition moment of fluorescence by the method of photoselection. It is shown that substitution of a hydrosy or a methosy group at the 2 (or &positio
Singlet-singlet electronic absorption and polarization in disubstituted naphthalenes
β Scribed by Asim Kumar Maiti
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 287 KB
- Volume
- 134
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The effects of disubstitution at the 2,6-and 2,7-positions of the naphthalene ring in shifting the energies of the 'L, and 'L+ states and altering the direction of the transition moments have been investigated. It is shown that in the 2,6_disubstituted naphthalenes the first ( 'Ls) and second (IL,) excited electronic states overlap and both the transitions are short-axis polarized, whereas in the 2,7_disubstituted compounds these bands are well separated and IL,, and 'L, bands are polarized mainly along the short and long molecular axis, respectively.
π SIMILAR VOLUMES
Polarized S-S absorption spectra of a-nuphtol single crystals show that the first two electronic absorption systems are respectively lcng-asir and short-axis polarized (A' +A') trnrxitions. The polarized absorp:ion spectra of a-nophtol in a diphcnyl has1 cryml, hon'ever, show that the first electron
By flash photolysis using a pulsed laser, we have examined the following Qttramolecular processes occurring from the lowest excited singlet state of naphthalene in cycloheale at room temperature: fluorescence lifetime, excited singlet-singlet absorption and intersystem crossing kinetics.
The direction of polarization and the oscillator strengths of the S +-Sl absorption spectra df 1,2benzcoronene, 1,12\_benzperylene and 1,2:3.4-dibenzsnthracene in t'he region 15 000 -25 000 cm-l are reported.