Aromatic excited states

Jonah et al. [178] found that the fluorescence emitted by 9,10-diphenyl-anthracene (or by p-terphenyl) in cyclohexane solution after photostimulation with Cerenkov radiation both grew-in and decayed more rapidly than when the solution was pulse-radiolysed (see Fig. 34). The delay in the formation of the aromatic excited state ( 0.5 ns) was attributed to the slowness of charge capture and of diffusion together of ions to form an excited state (Sect. 3.4). 

Excimers, that is complexes of excited state molecules with corresponding ground state molecules, are ( ) characteristic of aromatic excited states. For our present purposes we wish to consider the lowest Tr->Tr excited state of benzene and substituted derivatives together with the corresponding excimer. ... 

Furrer R, Fujara F, Lange C, Stehlik D, Vieth H and Vollmann W 1980 Transient ESR nutation signals in excited aromatic triplet states Chem. Rhys. Lett. 75 332-9... 

Figure 7, Aromatic and andaromatic systems in the ground state (GS) and the twin excited state (ES). The parameter is the coordinate that transforms A to B.

The bicyclic product is formed by coupling of the two radical sites, while the alkene results from an intramolecular hydrogen-atom transfer. These reactions can be sensitized by aromatic ketones and quenched by typical triplet quenchers and are therefore believed to proceed via triplet excited states. 

Aromatic compounds such as toluene, xylene, and phenol can photosensitize cis-trans interconversion of simple alkenes. This is a case in which the sensitization process must be somewhat endothermic because of the energy relationships between the excited states of the alkene and the sensitizers. The photostationary state obtained under these conditions favors the less strained of the alkene isomers. The explanation for this effect can be summarized with reference to Fig. 13.12. Isomerization takes place through a twisted triplet state. This state is achieved by a combination of energy transfer Irom the sensitizer and thermal activation. Because the Z isomer is somewhat higher in energy, its requirement for activation to the excited state is somewhat less than for the E isomer. If it is also assumed that the excited state forms the Z- and -isomers with equal ease, the rate of... 

These various photoproducts are all valence isomers of the normal benzenoid structure. These alternative bonding patterns are reached from the excited state, but it is difficult to specify a precise mechanism. The presence of the t-butyl groups introduces a steric factor that works in favor of the photochemical valence isomerism. Whereas the t-butyl groups are coplanar with the ring in the aromatic system, the geometry of the bicyclic products results in reduced steric interactions between adjacent t-butyl groups. 

These reactions are believed to proceed through a complex of the alkene with a singlet excited state of the aromatic compound (an exciplex). The alkene and aromatic ring are presumed to be oriented in such a manner that the alkene n system reacts with p orbitals on 1,3-carbons of the aromatic. The structure of the excited-state species has been probed in more detail using CAS-SCF ab initio calculations. ... 

As in the case of benzothiazoles and benzimidazoles, the excited-state proton transfer in 2-(2 -hydroxyphenyl)benzoxazole was studied both experimentally and computationally. The results closely resemble the observations for the other species The cw-enol form is preferred in the Sq ground state and the cw-keto form in the 5i excited state. Moreover, the proton transfer appears to be due to vibrational relaxation rather than thermal activation, suggesting that the aromatic ring has an impact on the transfer reaction of these systems [95JPC12456, 99JST255]. 

The irradiation is usually carried out with light of the near UV region, in order to activate only ihc n n transition of the carbonyl function," thus generating excited carbonyl species. Depending on the substrate, it can be a singlet or triplet excited state. With aromatic carbonyl compounds, the reactive species are usually in a Ti-state, while with aliphatic carbonyl compounds the reactive species are in a Si-state. An excited carbonyl species reacts with a ground state alkene molecule to form an exciplex, from which in turn diradical species can be formed—e.g. 4 and 5 in the following example ... 

Capellos and Suryanarayanan (Ref 28) described a ruby laser nanosecond flash photolysis system to study the chemical reactivity of electrically excited state of aromatic nitrocompds. The system was capable of recording absorption spectra of transient species with half-lives in the range of 20 nanoseconds (20 x lO sec) to 1 millisecond (1 O 3sec). Kinetic data pertaining to the lifetime of electronically excited states could be recorded by following the transient absorption as a function of time. Preliminary data on the spectroscopic and kinetic behavior of 1,4-dinitronaphthalene triplet excited state were obtained with this equipment... 

In electron donor-acceptor (EDA) complexes, there is always a donor molecule and an acceptor. The donor may donate an unshared pair (an n donor) or a pair of electrons in a ti orbital of a double bond or aromatic system (a it donor). One test for the presence of an EDA complex is the electronic spectrum. These complexes generally exhibit a spectrum (called a charge-transfer spectrum) that is not the same as the sum of the spectra of the two individual molecules. Because the first excited state of the complex is relatively close in energy to the ground state, there is usually a... 

The NIR femtosecond laser microscope realized higher order multi photon excitation for aromatic compounds interferometric autocorrelation detection of the fluorescence from the microcrystals of the aromatic molecules confirmed that their excited states were produced not via stepwise multiphoton absorption but by simultaneous absorption of several photons. The microscope enabled us to obtain three-dimensional multiphoton fluorescence images with higher spatial resolution than that limited by the diffraction theory for one-photon excitation. 

The reaction is stereospecific for at least some aliphatic ketones but not for aromatic carbonyls.197 This result suggests that the reactive excited state is a singlet for aliphatics and a triplets for aromatics. With aromatic ketones, the regioselectivity of addition can usually be predicted on the basis of formation of the more stable of the two possible diradical intermediates obtained by bond formation between oxygen and the alkene.198... 

Lukeman, M. Wan, P. Excited state intramolecular proton transfer (ESIPT) in 2-phenylphenol an example of proton transfer to a carbon of an aromatic ring. J. Chem. Soc., Chem. Commun. 2001, 1004-1005. 

Lukeman, M. Wan, P. A new type of excited-state intramolecular proton transfer proton transfer from phenol OH to a carbon atom of an aromatic ring observed for 2-phenyl-phenol. J. Am. Chem. Soc. 2002, 124, 9458-9464. 

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