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Extended molecular systems, component

Cizek J 1966 On the correlation problem in atomic and molecular systems. Calculation of wave function components in Ursell-type expansion using quantum-field theoretical methods J. Chem. Phys. 45 4256-66 Paldus J, Cizek J and Shavitt I 1972 Correlation problems in atomic and molecular systems IV. Extended coupled-pair many-electron theory and its applioation to the BHg molecule Phys. Rev A 5 50-67... [Pg.2198]

Yeast cell-surface engineering has been established to display enzymes, functional proteins, antibodies, and combinatorial protein libraries (Kondo and Ueda, 2004). The cell surface is a functional interface between the inside and outside of the cell allowing some surface proteins to extend across the plasma membrane, while others are bound by non-covalent or covalent interactions to the cell surface components. For anchoring surface-specific proteins, yeast cells have molecular systems to confine... [Pg.205]

Quite recently, fused TTF analogs having one or two [5]radialene unit(s) 40—42 have also been prepared (Figure 8.18), because the extended TTF moieties are of interest as multi-redox systems, components for molecular conductors, positive electrode materials for rechargeable batteries, and so on [48]. [Pg.321]

Many simple systems that could be expected to form ideal Hquid mixtures are reasonably predicted by extending pure-species adsorption equiUbrium data to a multicomponent equation. The potential theory has been extended to binary mixtures of several hydrocarbons on activated carbon by assuming an ideal mixture (99) and to hydrocarbons on activated carbon and carbon molecular sieves, and to O2 and N2 on 5A and lOX zeoHtes (100). Mixture isotherms predicted by lAST agree with experimental data for methane + ethane and for ethylene + CO2 on activated carbon, and for CO + O2 and for propane + propylene on siUca gel (36). A statistical thermodynamic model has been successfully appHed to equiUbrium isotherms of several nonpolar species on 5A zeoHte, to predict multicomponent sorption equiUbria from the Henry constants for the pure components (26). A set of equations that incorporate surface heterogeneity into the lAST model provides a means for predicting multicomponent equiUbria, but the agreement is only good up to 50% surface saturation (9). [Pg.285]

Several colloidal systems, that are of practical importance, contain spherically symmetric particles the size of which changes continuously. Polydisperse fluid mixtures can be described by a continuous probability density of one or more particle attributes, such as particle size. Thus, they may be viewed as containing an infinite number of components. It has been several decades since the introduction of polydispersity as a model for molecular mixtures [73], but only recently has it received widespread attention [74-82]. Initially, work was concentrated on nearly monodisperse mixtures and the polydispersity was accounted for by the construction of perturbation expansions with a pure, monodispersive, component as the reference fluid [77,80]. Subsequently, Kofke and Glandt [79] have obtained the equation of state using a theory based on the distinction of particular species in a polydispersive mixture, not by their intermolecular potentials but by a specific form of the distribution of their chemical potentials. Quite recently, Lado [81,82] has generalized the usual OZ equation to the case of a polydispersive mixture. Recently, the latter theory has been also extended to the case of polydisperse quenched-annealed mixtures [83,84]. As this approach has not been reviewed previously, we shall consider it in some detail. [Pg.154]


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Extended molecular systems, component relations

Molecular components

System component

System extended

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