Spectroscopic identification

Butane, 2-Butene, 2-Butyne R. M. Silverstein, G. C. Bassler and T. C. Morril, Spectroscopic Identification of Organic Compounds, 5th ed. (Wiley, New York, 1991), 236-239. [Pg.37]

Currently there are four major lines of approach towards gas-phase epoxidation of propylene (1) mechanistic studies of Au/Ti02 catalysts through kinetics, spectroscopic identification of adsorbed species and... [Pg.191]

For the IR spectroscopic identification of additives in polymeric products, in many cases it is necessary to first isolate the additive either by solvent extraction, chromatographic separation or removal of interfering constituents by ashing, etc. [Pg.568]

These studies have allowed the spectroscopic identification of a number of electronically excited states of the metal oxides, but there appear to have been no analytical applications of the reactions to date. The emitting states, as summarized by Toby [14], are CaO(A n), SrO(ATl), PbO(a32+, b32+), ScO(C2II), YO(C2n), FcO(C ), A10(A2ni B2X+), and BaO(A i)1, D 2+). Nickel carbonyl reacts with ozone to produce chemiluminescence from an excited electronic state of NiO, which is probably produced in the Ni + 03 reaction [42, 43],... [Pg.359]

We will discuss in some detail examples where various methods of separation, including chemical derivatization, were complemented by spectroscopic identification. However, even the use of the most advanced analytical methods frequently yields only partial... [Pg.485]

As has already been discussed (Section m.B.3) we were able to demonstrate that the three C3H2 isomers cyclopropenylidene (2), propargylene (36), and vinylidenecarbene (37), interconvert photochemically in low-temperature matrices. Unlike 36 vinylidenecarbene (37) was predicted to be a singlet.108-110 To aid the spectroscopic identification of S-37 we calculated (MP2/6-31G ) IR frequencies and intensities of this species.26 Comparison with the experimental IR spectrum (most intense band at 1952 cm-1) confirmed the allenic structure S-37. For T-37 a completely different IR spectrum was expected. An additional structural proof for S-37 was its reversible transformation into the other two C3H2 isomers S-2 and T-36. [Pg.134]

The spectroscopic identifications in Eq. (2.69) enable us to take the harmonic limit where the anharmonicity vanishes, xe — 0, and the well is deep (To —> oo) such that the harmonic frequency (oe, coe =4xeVQ, remains finite. In our notation, this is the N — oo, A - 0, AN finite, limit. In the earlier days of the algebraic approach the harmonic limit (Levine, 1982) served as a useful guide to the connection with the geometrical picture. Since the harmonic limit is so well understood, taking it still provides a good intuitive link. [Pg.38]

The spectroscopic identification of the y3-keto ester and the reduction mechanism leading to it have been previously described by Aurbach and co-workers when studying the surface chemistry of yBL-based electrolytes on various electrodes polarized to low potentials. 123,208,209... [Pg.142]

Li, C Domen, K Maruya K Onishi, T. Spectroscopic identification of adsorbed species derived from adsorption and decomposition of formic acid, methanol, and formaldehyde on cerium oxide, J. Catal, 1990, Volume 125, Issue 2, 445-455. [Pg.78]

Matrix isolation is a powerful tool for studying highly reactive species. The matrix provides an inert environment, which increases the lifetime of the reactive species to the extent that it may be thought of as a stable species. This allows for its spectroscopical identification and/or characterization using normal-type spectrometers. It is also possible to learn something about the intrinsic reactivity of the species, because, under such conditions, intermolecular reactions can be excluded. [Pg.179]

Jalal MAF, van der Helm D (1991) Isolation and Spectroscopic Identification of Fungal Siderophores. In Winkelmann G (ed) Handbook of Microbial Iron Chelates. CRC, Boca... [Pg.63]

Elemental composition C 18.19%, F 57.57%, O 24.24%. Carbonyl fluoride may be analyzed by FTIR, GC or GC/MS. For the GC analysis, it may be transported with the carrier gas helium from the reaction vessel into a cryo-genically cooled injector port, then thermally desorbed and analysed by FID. The system should be free of moisture. The characteristic ions for mass spectroscopic identification are 66, 26, and 40. [Pg.196]

Krypton may be analysed most conveniently by GC/MS. The characteristic masses for its mass spectroscopic identification are 84, 86, and 83, the most abundant natural isotopes of the element. It also may be analyzed by gas-sohd chromatography by its retention times. [Pg.442]

Cheon J, Kang HK, et al (2000) Spectroscopic identification of gas phase photofragments from coordination compound chemical vapor deposition precimsors. Coordination Chemistry Reviews 200, 1009-1032... [Pg.225]

Pitts, J. N., Jr., H. W. Biermann, A. M. Winer, and E. C. Tuazon, Spectroscopic Identification and Measurement of Gaseous Nitrous Acid in Direct Auto Exhaust, Atmos. Emiron., 18, 847-854 (1984b). [Pg.291]

Studies of stoichiometric hydroformylation, spectroscopic identification, isolation, and transformation of intermediates provided valuable information of the understanding of the catalytic reaction. Despite the complexity of the process, important conclusions were also drawn from kinetic studies. [Pg.372]

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