Excited-state reactivities. II. Basicities of some polymethylbenzenes in their excited singlet states

1967 ◽  
Vol 71 (3) ◽  
pp. 589-592 ◽  
Author(s):  
Robert L. Flurry ◽  
R. Keith Wilson

2019 ◽  
Vol 21 (27) ◽  
pp. 14766-14774 ◽  
Author(s):  
Marie-Luise Hebestreit ◽  
Michael Schneider ◽  
Hilda Lartian ◽  
Vivienne Betz ◽  
Michael Heinrich ◽  
...  

The rotationally resolved electronic Stark spectrum of 4-cyanoindole and some N-D and C-D deuterated isotopologues has been measured and analyzed.



2003 ◽  
Vol 81 (10) ◽  
pp. 1083-1095 ◽  
Author(s):  
J A Pincock ◽  
I S Young

The photochemistry of the indenyl acetates 1 and pivalates 2, substituted with X = H, 5-CH3O, and 6-CH3O, have been examined in both methanol and cyclohexane. The precursor alcohols 3 were also found to be photoreactive. Although only radical-derived products were obtained in cyclohexane, both ion- and radical-derived products were formed in methanol. The absence of significant fluorescence emission from any of the substrates 1, 2, and 3 indicates that the excited singlet states are highly reactive. A mechanism is proposed for the ion-derived products that proceeds through direct heterolytic cleavage to give an indenyl cation – carboxylate anion pair. The indenyl cations generated are anti-aromatic in the ground state and their efficient generation by this photochemical solvolysis is in sharp contrast to the very low reactivity of related ground-state substrates. For the pivalate esters 2, an excited-state migratory decarboxylation is proposed for the formation of tert-butyl derived products.Key words: ester photochemistry, indenyl cations, indenyl radicals.



1959 ◽  
Vol 37 (8) ◽  
pp. 1367-1372 ◽  
Author(s):  
Robin M. Hochstrasser

The relative fluorescence yields of a variety of double molecules have been measured as a function of the wavelength of exciting light. In some cases the yield from the second excited state is lower than from the first. This effect is attributed to either photodecomposition or to the enhancement of intramolecular energy transfer processes which can compete with the internal conversion between the excited singlet states. The experiments on bianthrone have suggested a method of elucidating the mechanism of the photochromic isomerization of this compound.



2011 ◽  
Vol 13 (28) ◽  
pp. 12912 ◽  
Author(s):  
Martin Rosenberg ◽  
Henrik Ottosson ◽  
Kristine Kilså


1987 ◽  
Vol 109 ◽  
Author(s):  
Paul Tavan ◽  
Klaus Schulten

ABSTRACTWe apply the Pariser-Parr-Pople Hamiltonian to study many-electron excitations in polyenes and polyacetylene. The excited singlet states of polyenes, calculated by a multireference double excitation expansion, are classified as quasi-particle excitations, namely as triplet-triplet magnons and particle-hole excitons. From finite polyene spectra we derive approximate dispersion relations for these quasi-particles in the infinite polyene, i.e. polyacetylene.



Sign in / Sign up

Export Citation Format

Share Document