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,)
Polarization of singlet-singlet electronic transitions in substituted naphtahlenes
✍ Scribed by Suzanne M. Lyle; E.C. Lim
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- English
- Weight
- 262 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
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 &position of naphthalene leads to mixing between the 'Lb 2nd 'La states, resulting in the short-axis polarization of the electronic transition to the former state. 1 (or a> substituted compounds exhibit no such mixin g. and the transition to the rLb state is polarized Iargely along the long .-is of the molecuie. Substitution of a cyono group at the 2-position also leads to short-axis polarization of the Lb band. These results are consistent with the predictions based on molecular orbital calculations.
📜 SIMILAR VOLUMES
## Abstract Density functional theory and CASSCF calculations have been used to determine equilibrium geometries and vibrational frequencies of metal‐capped one‐dimensional π‐conjugated complexes (H~3~P)Au(CC)~n~(Ph) (__n__ = 1–6), (H~3~P)Au(CCC~6~H~4~)(CCPh), and H~3~PAu(CCC~6~H~4~)CCAuPH~3
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