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OHS Reference

The general formula for a family of simple organic compounds is R + functional group. The letter R stands for any alkyl group. (If more than one alkyl group is present, R and R" are also used.) For example, the general formula R—OH refers to any of the following compounds ... [Pg.21]

FIGURE 11.15 Measurement of OH using DOAS as a function of time (UT) after subtraction of the contributions of other known absorbers. The solid lines through the data are OH reference spectra (adapted from Dorn et al., 1996). [Pg.560]

FIGURE 11.42 (a) Energy levels and some allowed transitions for the OH(X2n - A21 + ) absorption, (b) a typical broadband laser emission line profile, and an OH reference spectrum with absorption lines in this region. (Adapted from Mount, 1992 and Dorn et al., 1995a.)... [Pg.599]

Figure 11.44 is a schematic diagram of one LIF instrument (Stevens et al., 1994 Brune et al., 1998). An air-cooled copper-vapor laser pumps a dye laser whose output at 616 nm is doubled to generate the 308-nm exciting radiation. An OH reference cell in which OH is generated from the thermal dissociation of water... [Pg.600]

CO H- refers to the amino terminus while -OH refers to the carboxyl terminus of ... [Pg.161]

For the 2 2g and 5T2g-terms of the Oh-reference the Griffith theory could be appropriate. In the case of the Cl-interacting terms 3Tig or 4 Tig, the Figgis isotropic Hamiltonian can be applied. These theories offer the magnetic susceptibility formulae in closed forms. However, these approaches... [Pg.199]

For the s g- or 2 g-terms of the Oh-reference no simple treatment is appropriate and one needs to solve the secular equation numerically. [Pg.200]

Taft, R. W., Gurka, D., Joris, L., Schleyer, P. V., Rakshys, J. W., Studies of hydrogen-bonded complex formation with P-fluorophenol. V. linear free energy relationships with OH reference acids. J. Am. Chem. Soc. 1969, 91, 4801-4808. [Pg.566]

MDDR (MDL Drag Data Report), DiscoveryGate, OHS Reference, xPharm, etc. Prous/MDL 175 http //www. mdli. com... [Pg.275]

Taft RW, Gurka D,Joris L, Schleyer P, von R, and RakshysJW. Studies of Hydrogen-bonded complex formation with p-fluorophenol. V. Linear Free Energy Relationships with OH Reference Acids./Am Chem Soc 1969 91 4801-4808. [Pg.27]

Hydroxyls vibrating in small cages are disturbed by the electrostatic field created by the nearest oxygen (14). This decreases their wavenumber as compared to the unperturbed OH referred to above. [Pg.196]

Relative retention times for the columns labeled OH refer to methyl deoxycholate = 1.00 for the columns labeled TMS (trimethylsilyl ethers) refer to the bis (TMS) ether of methyl deoxycholate = 1.00. Absolute times of elution of methyl deoxycholate were 3% QF-1, 29.0 min 3% OV-1, 38.4 min 3% OV-17, 44.0 min methyl deoxycholate was injected simultaneously with each ester. Absolute times of elution of the bis (TMS) ether of methyl deoxycholate were 3% QF-1, 10.0 m in 3% OV-1, 27.3 min 3% OV-17, 14.2 min this derivative was injected simultaneously with each ether (60). [Pg.61]

One of metabolites of tannic add formed on in vitro incnbation with rat liver miaosomes. HO OH - Refer to Chem. Abstr., 108,1953y (1988). ... [Pg.40]

Ligand L R Anion R L Space group Complex spedes (with symmetry) CN Mean R-X distances (A) R-ligand R-anion and/or R-OH References ... [Pg.342]


See other pages where OHS Reference is mentioned: [Pg.318]    [Pg.231]    [Pg.200]    [Pg.162]    [Pg.35]    [Pg.91]    [Pg.605]    [Pg.698]    [Pg.699]    [Pg.175]    [Pg.318]    [Pg.427]    [Pg.562]    [Pg.572]    [Pg.574]    [Pg.122]    [Pg.263]    [Pg.284]    [Pg.156]    [Pg.3285]    [Pg.110]    [Pg.36]    [Pg.276]    [Pg.423]    [Pg.454]    [Pg.469]    [Pg.474]    [Pg.1369]    [Pg.1599]    [Pg.1976]    [Pg.50]    [Pg.284]   
See also in sourсe #XX -- [ Pg.175 ]




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References for OH-Radical Probes

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