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Resonance, also

Other frequently used resonators are dielectric cavities and loop-gap resonators (also called split-ring resonators) [12]. A dielectric cavity contains a diamagnetic material that serves as a dielectric to raise the effective filling factor by concentratmg the B field over the volume of the sample. Hollow cylinders machmed from Ilised quartz or sapphire that host the sample along the cylindrical axis are conunonly used. [Pg.1560]

IR-UV double resonance also selective for S and C Reaction of both Isotopes with high selectivity (high fluence)... [Pg.2137]

Stabilizing resonances also occur in other systems. Some well-known ones are the allyl radical and square cyclobutadiene. It has been shown that in these cases, the ground-state wave function is constructed from the out-of-phase combination of the two components [24,30]. In Section HI, it is shown that this is also a necessary result of Pauli s principle and the permutational symmetry of the polyelectronic wave function When the number of electron pairs exchanged in a two-state system is even, the ground state is the out-of-phase combination [28]. Three electrons may be considered as two electron pairs, one of which is half-populated. When both electron pahs are fully populated, an antiaromatic system arises ("Section HI). [Pg.330]

According to the quantum transition state theory [108], and ignoring damping, at a temperature T h(S) /Inks — a/ i )To/2n, the wall motion will typically be classically activated. This temperature lies within the plateau in thermal conductivity [19]. This estimate will be lowered if damping, which becomes considerable also at these temperatures, is included in the treatment. Indeed, as shown later in this section, interaction with phonons results in the usual phenomena of frequency shift and level broadening in an internal resonance. Also, activated motion necessarily implies that the system is multilevel. While a complete characterization of all the states does not seem realistic at present, we can extract at least the spectrum of their important subset, namely, those that correspond to the vibrational excitations of the mosaic, whose spectraFspatial density will turn out to be sufficiently high to account for the existence of the boson peak. [Pg.145]

Multiple resonance was observed at T = 723 K and rs = 0.01 s. The enhancement, exceeds 1 at a cycle period between 0.2 and 0.3 s and also at greater than 1000 s, although quasi steady state is also attained at about that period. Resonance also occurs at two different cycle periods at ts = 0.02 s, T is much smaller. As the space-time increases above 0.25 s, the rate enhancement becomes very small and the multiple resonance phenomenon seems to disappear. [Pg.222]

Clearly high g-factor resonance also benefits the detection of light-absorbing analytes in the fluid region. [Pg.218]

EPR electron paramagnetic resonance (also known as electron spin resonance (ESR))... [Pg.26]

Our study underscores the significance of a quantitative interpretation of STD intensities using the CORCEMA-ST procedure for the characterization of binding epitopes at atomic resolution. In contrast to what was sometimes suggested [84], we show here that the STDs involving methyl resonances also give accurate information about epitopes in quantitative analyses. [Pg.48]

Table 5.2 Summary of selected analytical methods for molecular environmental geochemistry. AAS Atomic absorption spectroscopy AFM Atomic force microscopy (also known as SFM) CT Computerized tomography EDS Energy dispersive spectrometry. EELS Electron energy loss spectroscopy EM Electron microscopy EPR Electron paramagnetic resonance (also known as ESR) ESR Electron spin resonance (also known as EPR) EXAFS Extended X-ray absorption fine structure FUR Fourier transform infrared FIR-TEM Fligh-resolution transmission electron microscopy ICP-AES Inductively-coupled plasma atomic emission spectrometry ICP-MS Inductively-coupled plasma mass spectrometry. Reproduced by permission of American Geophysical Union. O Day PA (1999) Molecular environmental geochemistry. Rev Geophysics 37 249-274. Copyright 1999 American Geophysical Union... Table 5.2 Summary of selected analytical methods for molecular environmental geochemistry. AAS Atomic absorption spectroscopy AFM Atomic force microscopy (also known as SFM) CT Computerized tomography EDS Energy dispersive spectrometry. EELS Electron energy loss spectroscopy EM Electron microscopy EPR Electron paramagnetic resonance (also known as ESR) ESR Electron spin resonance (also known as EPR) EXAFS Extended X-ray absorption fine structure FUR Fourier transform infrared FIR-TEM Fligh-resolution transmission electron microscopy ICP-AES Inductively-coupled plasma atomic emission spectrometry ICP-MS Inductively-coupled plasma mass spectrometry. Reproduced by permission of American Geophysical Union. O Day PA (1999) Molecular environmental geochemistry. Rev Geophysics 37 249-274. Copyright 1999 American Geophysical Union...
In applications where high power density or thermal management is of prime importance, hard- switched converters are not feasible using conventional Si components. In these cases, resonant or quasi-resonant (also termed soft-switching ) topologies can be used. The electrical resonance is obtained through parasitic... [Pg.72]

To test the hypothesis, aliquots of 5.0 mM adenine derivative were mixed with aliquots of 5.0 mM thymine derivative in proportions shown in the table. Each solution also contained 20 mM sodium dodecyl sulfate. The concentration of product measured by nuclear magnetic resonance also is shown in the table. Are the results consistent with formation of a 1 1 complex Explain your answer. [Pg.422]

Fermi resonance also has an effect on the intensities of the two transitions. Overtone or combination transitions generally have less than one tenth the intensity of fundamental transitions. However, the interaction between and which affects the actual energies, also leads to new wave functions which are linear combinations of these two, as explained for secular equations generally in Section 7.1. Thus, the actual excited state whose energy is closest to (v, + v7) will be described by a wave function... [Pg.340]

With stilbene and azobenzene there are two isomers. In these cases a plane structure is realized for the //mf-isomers, in contrast to the cis forms where this is impossible on spatial grounds. The stability of the trans forms is a consequence of the extra resonance (extra R.E. /z -stilbene 7.0 kcal energy content of frmy-azobenzene 10 kcal lower than the cis form). This resonance also appears from the distances, stilbene, trans C—C 1.445 A, C=C 1.33 A azobenzene, trans C—N 1.415 A, cis C—N 1.46 A (sum of atomic distances 1.54 A and 1.47 A, respectively) in this latter compound the planes of the rings make an angle of 50°. [Pg.212]

When on the other hand the resonance is restricted, for example, when two systems of conjugated electron systems are separated by a —CH2— group, then the spectrum is only the superposition of those of the separate parts (isolation effect). For example the spectra of diphenylmethane and of dibenzyl are very much analogous to that of benzene (abs. band around 2600 A). Steric hindrance of the resonance also leads to a displacement towards shorter wave lengths through this isolation effect. [Pg.246]

We have thus far considered coherent processes that take place in RPs (which in some cases been have been modulated by stochastic motion). However, the common spin-lattice and spin-spin relaxation processes familiar from magnetic resonance also come to bear on the dynamics of RPs. Typical values of Ti and T2 for small organic radicals in homogeneous solution are on the microsecond timescale and as such are rather slow relative to coherent mixing and RP diffusion. Thus, for the most part, effects of incoherent spin relaxation are not manifest in such reactions. However, for reactions in which the RP lifetime is substantially extended, for instance, by constraining the RP inside a microreactor such as a micelle (many examples in Ref. 14), relaxation effects become significant. [Pg.167]


See other pages where Resonance, also is mentioned: [Pg.110]    [Pg.110]    [Pg.17]    [Pg.8]    [Pg.524]    [Pg.119]    [Pg.385]    [Pg.45]    [Pg.111]    [Pg.316]    [Pg.514]    [Pg.629]    [Pg.1355]    [Pg.1567]    [Pg.832]    [Pg.467]    [Pg.225]    [Pg.212]    [Pg.15]    [Pg.193]    [Pg.466]    [Pg.212]    [Pg.171]    [Pg.166]    [Pg.390]    [Pg.317]    [Pg.629]    [Pg.331]    [Pg.176]    [Pg.227]   


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