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Complex reflection factor

Coaxial line reflectometry has to be employed at frequencies from 1 MHz to -1 GHz. In contrast to the low-frequency techniques already described, here the sample capacitor is used as the termination of a low-loss precision coaxial line. The complex reflection factor is measured with a microwave reflectometer at the analyzer end of the fine, depending on the sample impedance. For this purpose, the incoming and reflected waves are separated with two directional couplers and their amplitudes are measured. The BDS concept 70 is a commercially available system (Novocontrol Instruments) that uses the coaxial line reflectometry method. This system covers the frequency range between IMHz and 3 GHz with loss factor tan 5 resolution of less than 3 x 10 . The... [Pg.524]

Coaxial line reflectometry (6.3.3) 1 MHz-1 GHz The sample capacitor is placed at the end of a low-loss precision coaxial impedance is determined from complex reflection factor, measured with a microwave reflectometer at analyzer end of coaxial line Special sample cells are available for sample thicknesses ranging from 1 pm (thin films) to 20 mm (liquids or solid samples) The turnkey BDS concept 70 system, available from Novocontrol, combines the Agilent HP E4991A RF impedance analyzer with the BDS 2200 RF sample cell the complex permeability of polymers can also be measured by using a magnetic sample cell... [Pg.594]

The constant s, characteristic of the substrate complex, reflects its sensitivity to variation in nucleophilicity as assessed by the Ptpy2Cl2 reaction. It is called the nucleophilic discrimination factor (ndf). The intercept log k turns out to be related to the value of the k term in the rate law for the solvent in question. Some representative ligands involved in attack on Pt(II) complexes may be listed in order of decreasing as follows ... [Pg.22]

Krishnaswamy. They emphasize the importance of a phase factor in the complex reflection coefficient of electrons from the surface, and propose that field ion energy distributions may be used to measure the phase of electron reflection at the crystal surface. However, neither is the potential barrier known accurately enough nor are the available experimental data good enough, and to this date no such information has been obtained. [Pg.28]

Summarizing as follows, we could say that we learned the following from the thermodynamic studies (1) The different stability of the copper(H) ternary complexes with functionalized P-cyclodextrins is enthalpy driven, in accordance with what was previously found for the ternary system without the CD cavity (2) The cis-disposition of the amine groups of the two ligands seems to be the discriminating factor, in some cases allowing the interaction of the aromatic residues of one the two isomers with the cavity (3) The difference in AH° values between the two copper(II) diastereoisomeric complexes reflects the different interactions of the aromatic moieties of the two amino acid enantiomers. [Pg.359]

Visible spectra of (a) [Co(OH2)6] and (b) [CoCLj] - Note that the intensity scales differ by a factor of 50, the tetrahedral complex giving a much more intense band. The energy of the transition is smaller for the tetrahedral complex, reflecting the smaller crystal-field splitting in this case. Redrawn with permission from [12]. Copyright 1999 John Wiley Sons. [Pg.291]

Borrowed from heat-transport science the convective flux equation enjoys the simple, linear, and theoretically correct concentration functionality. However, the MTC has one adjustable parameter that must reflect all the complex interacting factors... [Pg.22]

The modes of thermal decomposition of the halates and their complex oxidation-reduction chemistry reflect the interplay of both thermodynamic and kinetic factors. On the one hand, thermodynamically feasible reactions may be sluggish, whilst, on the other, traces of catalyst may radically alter the course of the reaction. In general, for a given cation, thermal stability decreases in the sequence iodate > chlorate > bromate, but the mode and ease of decomposition can be substantially modified. For example, alkali metal chlorates decompose by disproportionation when fused ... [Pg.863]

The same reasoning applies to the synthesis of pure enantiomers as to organic synthesis in general processes should be atom efficient and have low E factors, i.e. involve catalytic methodologies. This is reflected in the increasing attention being focused on enantioselective catalysis, using either enzymes or chiral metal complexes. [Pg.53]


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