Resonance ionic

Reactions that are fast at room temperature and do not show a translational energy dependence up to KE n, of a few eV In these cases, large Franck-Condon factors (FCF), i.e., FCF > 10 , usually exist between the ground state of the neutral reactant and its resonant ionic state (resonant with respect to resonant charge transfer). 

V.V. Sinitsyn, A.I. Privalov, O. Lips, A.f. Baranov, D. Kruk, F. Fujara, Transport properties of CSHSO4 investigated by impedance spectroscopy and nuclear magnetic resonance. Ionics 14 (2008) 223—226. 

Most of the qualitative relationships between color and structure of methine dyes based on the resonance theory were established independently during the 1940 s by Brooker and coworkers (16, 72-74) and by Kiprianov (75-78), and specific application to thiazolo dyes appeared later with the studies of Knott (79) and Rout (80-84). In this approach, the absorptions of dyes belonging to amidinium ionic system are conveyed by a group of contributing structures resulting from the different ways of localization of the 2n rr electrons on the 2n l atoms of the chromophoric cationic chain, rather than by a single formula ... 

A great number of monoaza or polyaza. either symmetrica] or unsym-metrical, mono trimethine thiazolocyainines have been synthesized in order to verify or to obtain semiempirical rules, more or less based on the resonance theory, concerning the relation between the color of a thiazolo dye and the number and place of nitrogen atoms in the chromophoric chain. For example. Forster s rule applies to ionic dyes and stipulates that the will increase with the decreasing tendency of chromophoric atoms lying between the two auxochromes to take up the characteristic charges (90). 

For most vinyl polymers, head-to-tail addition is the dominant mode of addition. Variations from this generalization become more common for polymerizations which are carried out at higher temperatures. Head-to-head addition is also somewhat more abundant in the case of halogenated monomers such as vinyl chloride. The preponderance of head-to-tail additions is understood to arise from a combination of resonance and steric effects. In many cases the ionic or free-radical reaction center occurs at the substituted carbon due to the possibility of resonance stabilization or electron delocalization through the substituent group. Head-to-tail attachment is also sterically favored, since the substituent groups on successive repeat units are separated by a methylene... 

Other imaging techniques such as magnetic resonance and ultrasound have opened up avenues of tremendous potential for contrast medium enhancement (123). Ultrasound contrast media developments have centered around encapsulated air micro-bubbles. Magnetic resonance contrast agents iavolve metal—ligand complexes and have evolved from ionic to nonionic species, much as radiopaques have. 

Lieber et have come to the same conclusion by an investigation of the ultraviolet spectra and dipole moments of 5-amino-, 5-methyl-amino-, and 5-dimethylamino-l, 2,3,4-thiatriazole. The dimethylamino derivative, in which no tautomerism is possible, shows the same characteristic absorption near 250 m/A as the unsubstituted compound and the monomethyl derivative. The dipole moments of the three compounds differ very little. These moments are quite large (5.8 Debye), showing that ionic resonance forms of type 9 contribute considerably to the structure of these compounds. 

The surface behavior of Na is similar to that of Cs, except that inner sphere complexes are not observed. Although Na has the same charge as Cs, it has a smaller ionic radius and thus a larger hydration energy. Conseguently, Na retains its shell of hydration waters. For illite (Figure 6), outer sphere complexes resonate between -7.7 and -1.1 ppm and NaCl... 

We have limited our investigations to the action of gamma-rays and fast neutrons on aromatic, alicyclic, aliphatic, and ionic compounds. The absorption coefficients for these types of radiation have an order of magnitude of lO /cm which is particularly adequate. Shallow penetrating radiations would only alter the superficial layers and would obviously not be able to affect the intensity of the quadrupole line substantially. This is for instance the case for ultraviolet light which has been shown to be unable to produce any effect on the resonance line of iodoform (CHI3 3Sg)... 

Nakamura, T., Ohno, K., Kotani, M., and Hijikata, K., Progr. Theoret. Phys. Kyoto) 8, 387, Interaction of -electrons in the acetylene molecule/ Calculations using both MO-CI and HL with ionic-homopolar resonance. 

Fig. 4.1.17 Graphic illustration of Forster-type resonance energy transfer from aequorin to Aequorea GFP. In the vessel at left, a solution contains the molecules of aequorin and GFP randomly distributed in a low ionic strength buffer. The vessel at right contains a solution identical with the left, except that it contains some particles of DEAE cellulose. In the solution at right, the molecules of aequorin and GFP are coadsorbed on the surface of DEAE particles. Upon an addition of Ca2+, the solution at left emits blue light from aequorin (Xmax 465 nm), and the solution at right emits green light from GFP (Xmax 509 nm).

Yoshida, H. and Hayashi, K. Initiation Process of Radiation-induced Ionic Polymerization as Studied by Electron Spin Resonance. Vol. 6, pp. 401—420. 

NQR spectra of the two isomers give resonances at different frequencies and also show that the Pt—Cl bond is more ionic in the ds-isomer, while there are significant differences in both the absorption and MCD spectra [79]. 

Magnetic resonance techniques, EPR (ESR) and NMR, can be used [341,342] to obtain information about atomic, ionic, molecular and crystallographic states before, during and after solid state reactions. Only a very restricted use has been made of the NMR of solids [342—345]. 

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