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Photoreactions adiabatic

Rettig W, Lapouyade R (1994) Fluorescence probes based on twisted intramolecular charge transfer (TICT) states and other adiabatic photoreactions. Topics in fluorescence spectroscopy 4 109-149... [Pg.301]

Lippert E, Ayuk AA, Rettig W, Wermuth G (1981) Adiabatic photoreactions in dilute solutions of p-substituted N, N -dialkylanilines and related donor-acceptor compounds. J Photochem 17 237-241... [Pg.303]

Rettig W, Vogel M, Lippert E, Otto H (1986) The dynamics of adiabatic photoreactions as studied by means of the time structure of synchrotron radiation. Chem Phys 103 381-390... [Pg.304]

Fluorescence Probes Based on Twisted Intramolecular Charge Transfer (TICT) States and Other Adiabatic Photoreactions... [Pg.109]

In the following, some of the most well-known adiabatic photoreaction mechanisms relevant to fluorescent probes are briefly introduced. [Pg.112]

W. Rettig and W. Majenz, Competing adiabatic photoreaction channels in stilbene derivatives, Chem. Phys. Lett. 143, 335-341 (1989). [Pg.148]

An approximation stating that the motion of nuclei in ordinary molecular vibrations is slow relative to the motions of electrons. Thus, the nuclei can be held in fixed positions when doing calculations of electronic states. Such an assumption is useful in determining potential energy surfaces and is central in studying the quantum mechanical properties of molecules. See also Adiabatic Photoreaction Diabatic Photoreaction... [Pg.96]

BORN-OPPENHEIMER APPROXiMATION ADIABATIC PHOTOREACTION DIABATIC PHOTOREACTION BORNYL PYROPHOSPHATE SYNTHASE BOROHYDRIDE REDUCTION ACYL-PHOSPHATE INTERMEDIATE BOSE-EINSTEIN CONDENSATE Bound water,... [Pg.727]

When the concept of adiabatic photoreactions was first tested on the photolytic cycloreversion of the 9-methylanthracene photodimer 104, the formation of singlet excited 9-methylanthracene A (R=methyl) according to... [Pg.204]

Fluorescence properties of 9-anthrylalkenes, 177 adiabatic photoreaction effect on, 179 Stokes shift, 179... [Pg.382]

There are three processes conneced with each other in the kinetics of the TICT adiabatic photoreaction mechanism in fluid media ... [Pg.11]

Fig. 2.2. Schematic diagrams of the angular dependence of the S, and S2 potentials along 6 from the initial to the final state of adiabatic photoreactions.37... Fig. 2.2. Schematic diagrams of the angular dependence of the S, and S2 potentials along 6 from the initial to the final state of adiabatic photoreactions.37...
For DM ABN in polar solvents, the observed activation energy AB for the backward reaction is larger than BA, that is, the adiabatic photoreaction is exothermic. For example, from the spectra and activation energies shown in Figs. 2.1 and 2.8, the potential energy diagram displayed in Fig. 2.9 can be constructed. Only part of the strong redshift of the A band is... [Pg.21]

As can be seen in Table I, the BA values thus derived correlate with Ev for various series of homologous solvents. This and the fact that BA tj directly lead to the inequality E0< Ev, and we conclude that TICT formation, in the cases considered here, proceeds as a barrierless adiabatic photoreaction. [Pg.36]

In the particular cases of DMABN and DMABEE, specific interactions most probably can occur with certain solvent partners after the adiabatic photoreaction has achieved its final state of orthogonality and... [Pg.47]

Adiabatic photoreaction Within the Born-Oppenheimer approximation , a reaction of an excited state species that occurs on a single potential-energy surface . Compare diabatic photoreaction. [Pg.301]

Non-adiabatic photoreaction Same as diabatic photoreaction. Use of double negative is discouraged. [Pg.326]

Fig. 2. The TICT model involves a twisted product species with charge transfer or charge shift properties (A state) formed through an adiabatic photoreaction from the precursor (B ) state which is often (but not always) of near planar conformation... Fig. 2. The TICT model involves a twisted product species with charge transfer or charge shift properties (A state) formed through an adiabatic photoreaction from the precursor (B ) state which is often (but not always) of near planar conformation...
Experimentally, in all cases studied, intramolecular fluorescence quenching can be observed due to the adiabatic photoreaction towards the photochemical funnel (twisted double bond, close-lying So/Sj, ultrafast nonradiative... [Pg.270]

In adiabatic reactions, the chemical change occurs on the same energy hypersurface (see Sect. 1.2). Most adiabatic photoreactions are proton transfer reactions. All reactions of that sort are reversible insofar as, following deactivation, very fast reverse reactions drive the system back to its original composition so that no permanent change occurs [26b]. [Pg.265]

Examples of alternative photochemical mechanisms. A. An adiabatic photoreaction. B. A hot molecule reaction. [Pg.965]


See other pages where Photoreactions adiabatic is mentioned: [Pg.110]    [Pg.111]    [Pg.111]    [Pg.117]    [Pg.117]    [Pg.125]    [Pg.289]    [Pg.166]    [Pg.179]    [Pg.203]    [Pg.15]    [Pg.18]    [Pg.308]    [Pg.326]    [Pg.255]    [Pg.271]    [Pg.282]    [Pg.303]    [Pg.72]    [Pg.222]    [Pg.997]   
See also in sourсe #XX -- [ Pg.3 , Pg.11 ]




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