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Bond frequency

When propylene chemisorbs to form this symmetric allylic species, the double-bond frequency occurs at 1545 cm-1, a value 107 cm-1 lower than that found for gaseous propylene hence, by the usual criteria, the propylene is 7r-bonded to the surface. For such a surface ir-allyl there should be gross similarities to known ir-allyl complexes of transition metals. Data for allyl complexes of manganese carbonyls (SI) show that for the cr-allyl species the double-bond frequency occurs at about 1620 cm-1 formation of the x-allyl species causes a much larger double-bond frequency shift to 1505 cm-1. The shift observed for adsorbed propylene is far too large to involve a simple o--complex, but is somewhat less than that observed for transition metal r-allyls. Since simple -complexes show a correlation of bond strength to double-bond frequency shift, it seems reasonable to suppose that the smaller shift observed for surface x-allyls implies a weaker bonding than that found for transition metal complexes. [Pg.34]

Fig. 27. A plot of the v00 bond frequency for dioxygen species in the solid state as a function of the bond order. The value for 02 refers to the gas phase value for oxygen in the triplet state (21). Fig. 27. A plot of the v00 bond frequency for dioxygen species in the solid state as a function of the bond order. The value for 02 refers to the gas phase value for oxygen in the triplet state (21).
Related research has been reported by Elder and Worley (39), in which MNDO was used to examine the structure of coniferyl alcohol, and its corresponding phenolate anion and free radical. This method represents an improvement over the PPP method, in that MNDO is an all-electron technique, and performs geometry optimizations. It was found that the calculated spin densities and charge values for the reactive sites did not correlate quantitatively with observed bond frequency, but it was observed that positions with partial negative charge and positive spin densities are the positions through which the polymerization has been found to occur. [Pg.273]

Fig. 5. Data for frequency shift, Av monomer frequency minus H-bonded frequency), band width at half maximum iq, and integrated molar absorption coefficient per bonded OH minus integrated molar absorption coefficient for monomer, AB. Curves are those... Fig. 5. Data for frequency shift, Av monomer frequency minus H-bonded frequency), band width at half maximum iq, and integrated molar absorption coefficient per bonded OH minus integrated molar absorption coefficient for monomer, AB. Curves are those...
In the paper of Brato2, Had i and Sheppard [9] some papers are mentioned dealing with the infrared absorption spectra in which such satellites have been observed. The frequency differences of the latter and the fundamental 0—H band are about 200-100 cm"1 which corresponds to the frequencies of the intermolecular vibrations. It should be pointed out that on the basis of thermodynamics. Harford [10] has obtained for the hydrogen bond frequency a value of the order of approximately 200 cm-1. [Pg.210]

The Sn—C bond frequencies are rather less sensitive to electronic effects in methyltin halides and depend weakly on either the number or the nature of the halogens. The increases associated with complex formation are also insignificant. Vibrational spectroscopy is a good tool not only for studying the spatial arrangement and ionicities of Sn—X bonds but also for measur-... [Pg.64]

Figure 7.4 Bond frequency for hydrolysis of maltodextrins [G3 to G8] by porcine pancreatic a-amylase. (From Robyt and French19)... Figure 7.4 Bond frequency for hydrolysis of maltodextrins [G3 to G8] by porcine pancreatic a-amylase. (From Robyt and French19)...
Gravimetric and elemental analysis lead to the following bruto-formula for the products of fullerene chlorination C6oCln (n=2 8). The broad bands in IR spectra (Fig. 2) close to characteristic vibrations for C-Cl bonds (frequencies 885, 850 and 808 cm"1) evidenced the presence of the mixture different isomers in the sample... [Pg.157]

The first reported gas phase electronic spectra of DNA base pairs described hydrogen bond frequencies of GC clusters, measured by REMPI [26], On the one hand these frequencies agreed quite well with theoretical predictions. On the other hand, the six hydrogen bonding modes between two molecules of a given mass are only very weakly dependent on cluster structure and can therefore neither serve as a structural tool nor as a good benchmark for theory. Moreover, REMPI only measures excited state vibrations, while the best calculations apply to the ground state. [Pg.326]

Incorporation of electron-releasing substituents is related to the increase of metal-oxygen bond frequency v(M—O) and the decrease of v(C—O) and v(C—C) in the following order hexafluoroacetylacetonates < trifluoroacetylacetonates < acetylacetonates... [Pg.87]

Table XLVII. Ethylenic Bond Frequency where Resonance Cannot Occur... Table XLVII. Ethylenic Bond Frequency where Resonance Cannot Occur...
Many Vqh vs. bond length correlation curves are found in the literature . However, strong distinction has not been made in all cases for the various acceptor groups, the geometry of the H-bonds, frequency shifts due to intermolecular coupling (use of frequencies of coupled modes instead of uncoupled ones) etc. The best fits available have been given by Mikenda (see Figs. 6 and 7). [Pg.111]

It provides a kind of bond-frequency pattern. It is also independent of conformational flexibility. In this case, the smoothing parameter B has the unit 1 (one). [Pg.134]

H bonding and potential dependence of ion concentrations in the double layer ) of the transition state in the interphase rather than, e.g., from changes in anharmonicity or OH-bond frequency with potential, which could lead only to small changes of AS. ... [Pg.182]


See other pages where Bond frequency is mentioned: [Pg.15]    [Pg.394]    [Pg.32]    [Pg.35]    [Pg.37]    [Pg.159]    [Pg.169]    [Pg.175]    [Pg.105]    [Pg.28]    [Pg.361]    [Pg.372]    [Pg.264]    [Pg.718]    [Pg.12]    [Pg.144]    [Pg.688]    [Pg.168]    [Pg.178]    [Pg.231]    [Pg.639]    [Pg.158]    [Pg.347]    [Pg.284]    [Pg.1301]    [Pg.228]    [Pg.37]    [Pg.21]    [Pg.60]    [Pg.278]    [Pg.179]    [Pg.312]   
See also in sourсe #XX -- [ Pg.114 ]




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Absorption Frequencies of Single Bonds to Hydrogen

Absorption Frequencies of Triple Bonds

Bond frequency pattern

Bond rotation frequencies

Bond vibration frequency

Bond-bending frequencies

Bond-stretching frequencies

Bond-switching-mode frequency

Bonding frequencies

Bonds infrared stretching frequency

Carbon-hydrogen bonds stretching frequencies

Carbon-oxygen bonds, infrared absorption frequencies

Characteristic bond frequencies

Cumulated double bonds Raman frequencies

Debye frequency, hydrogen bonds

Double bonds Raman frequencies

Double bonds infrared frequencies

Double bonds vibrational frequency

Fast mode frequency, hydrogen bonds

Frequency, hydrogen bonding

Frequency-bond length relationships

H Bond Length versus Vibrational Frequency

Hydrogen bonding frequency shifts related

Hydrogen-carbon bonds Raman frequencies

Hydrogen-carbon bonds infrared absorption frequencies

IR Frequency Depends on Type of Bond

Infrared active bond frequencies

Inter-nodal bond separation frequencies

Low-frequency Motions in Condensed Phase Hydrogen Bonding and Transfer

Polysaccharides 1 -» 3 bond, frequency

Raman Frequencies of Other Double Bonds

Raman Frequencies of Single Bonds to Hydrogen and Carbon

Raman frequencies of cumulated double bonds

Raman frequencies of triple bonds

Resonance, among bond structures frequency

Single bonds infrared stretching frequencies

Slow mode frequency, hydrogen bonds

Temperature Dependence of NQR Frequencies and Bond Parameters

Triple bond molecule frequencies

Triple bonds Raman frequencies

Triple bonds infrared absorption frequencies

Triple bonds infrared frequencies

Vibrational frequency hydrogen bonding cooperativity

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