Excited-state dynamics of fluorene/substituted-benzene van der Waals complexes in supersonic jets: dependence of exciplex formation on the relative energies of the lowest excited singlet states of component molecules

1990 ◽  
Vol 94 (6) ◽  
pp. 2631-2637 ◽  
Author(s):  
Hiroyuki. Saigusa ◽  
Edward C. Lim

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.



1985 ◽  
Vol 63 (11) ◽  
pp. 3140-3146 ◽  
Author(s):  
B. Arnold ◽  
L. Donald ◽  
A. Jurgens ◽  
J. A. Pincock

The photochemical cleavage of the 1-naphthylmethyl derivatives, 1–7, has been examined in methanol solvent under both direct and sensitized conditions. The competitition between homolytic and heterolytic cleavage as a function of multiplicity and leaving group has been studied in detail. Only substrates 1, 2, 3, and 7 react on sensitization with xanthone but evidence is presented that the resulting reactivity of 1, 2, and 3 may not be triplet energy transfer but rather exciplex formation. A semi-quantitative scale for photofugacities of the leaving groups from the excited singlet states has been established.





1994 ◽  
Vol 14 (1-3) ◽  
pp. 45-59 ◽  
Author(s):  
Shane M. Ohline ◽  
Joann Romascan ◽  
Peter M. Felker

We report the results of rotational coherence spectroscopy on tolane, tolane–Ar, and tolane–N2. The results on tolane are consistent with a planar geometry for the species. They also provide information about the symmetries of excited vibronic states in the species. The results on the van der Waals complexes provide significant experimental constraints on where the small species bind to tolane. In addition, we report the observation of a rapid excited-state decay process in the complexes and discuss the possible nature of this process.



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.





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