Formate magnetic susceptibility

The formation and presence of both phases of the Pd-H system in the palladium catalyst samples investigated was confirmed by Brill and Watson by the values of the magnetic susceptibility of the samples investigated under the same conditions as in the kinetic studies. 

The direct proof of hydride formation in situ in a reaction vessel is in principle possible. One can follow changes of resistance (of a film, a wire, etc.) or of magnetic susceptibility of a catalyst. Hydride identification by means of the X-ray diffraction method requires a catalyst sample to be taken out from a reaction vessel, and eventually frozen in order to avoid a rapid decomposition of the hydride under ambient conditions (67). 

Electrobalances suitable for thermogravimetry are readily adapted for measurements of magnetic susceptibility [333—336] by the Faraday method, with or without variable temperature [337] and data processing facilities [338]. This approach has been particularly valuable in determinations of the changes in oxidation states which occur during the decompositions of iron, cobalt and chromium oxides and hydroxides [339] and during the formation of ferrites [340]. The method requires higher concentrations of ions than those needed in Mossbauer spectroscopy, but the apparatus, techniques and interpretation of observations are often simpler. 

In this study, we extend the range of inorganic materials produced from polymeric precursors to include copper composites. Soluble complexes between poly(2-vinylpyridine) (P2VPy) and cupric chloride were prepared in a mixed solvent of 95% methanol 5% water. Pyrolysis of the isolated complexes results in the formation of carbonaceous composites of copper. The decomposition mechanism of the complexes was studied by optical, infrared, x-ray photoelectron and pyrolysis mass spectroscopy as well as thermogravimetric analysis and magnetic susceptibility measurements. 

The electrocrystallization and characterization of a novel molecular metal which displays both electronic and ionic conduction has been reported. The complex Li0.6(15-crown-5-ether)[Ni-(dmit)2] H20 is composed of stacks of [Ni(dmit)2] units which provide pathways for electronic conduction. The stacks are separated by parallel stacks of 15-crown-5-ether moieties in a channellike formation which facilitates ion conduction. The salt has a room temperature conductivity of 240 Scm-1. Temperature-dependent magnetic susceptibility and NMR measurements were used to prove the existence of Li+ movement within the crown ether channels.1030... 

The atomic properties satisfy the necessary physical requirement of paralleling the transferability of their charge distributions - atoms that look the same in two molecules contribute identical amounts to all properties in both molecules, including field-induced properties. Thus the atoms of theory recover the experimentally measurable contributions to the volume, heats of formation, electric polarizability, and magnetic susceptibility in those cases where the group contributions are found to be transferable, as well as additive additive [4], The additivity of the atomic properties coupled with the observation that their transferability parallels the transferability of the atom s physical form are unique to QTAIM and are essential for a theory of atoms in molecules that purports to explain the observations of experimental chemistry. 

The aromaticity of five-membered rings with two or more heteroatoms was discussed in detail in earlier reviews.52 100 111 In a comprehensive survey on the quantitative measurements of aromaticity,112 it has been shown that basicity-based quantification of aromaticity gave more reproducible resonance energies than other methods, such as heats of formation, ring currents, magnetic susceptibilities, and theoretical indices. 

The reaction of an excess of VCp2 with RC=CC=CR (R = SiMc3, PPh2) results in addition of one VCp2 moiety to each C=C moiety and the formation of cw- VCp2 2(M- M-h -RC2C2R) (42). Magnetic susceptibility measurements... 

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