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Green matrix technique

In other words if the Fermi level falls into such a region of states which are still delocalized (the Fermi level is above the mobility edge) Bloch-type (coherent) conduction is possible, while in the opposite case (the Fermi level is below the mobility edge) only hopping-type conduction occurs /44/. For this reason the investigation of localization properties of the states in a disordered system like a protein chain is of utmost importance for which a Green matrix technique has been developed /44,45/. [Pg.351]

However, to do this for every state is practically impossible in the case of really long chains (N> 1000, where N is the number of sites). Therefore, a technique is needed that gives a rough idea as to whether or not the states are localized in a certain eneigy region without explicitly calculating them. Such a method based on the calculation of Green matrix elements of the chain will be examined in the next section. [Pg.162]

A report by Ozin et al. in 1977 describes the formation of Ti(CO)6 via matrix cocondensation techniques (11). This green complex, while not isolated, was characterized by its infrared and ultraviolet-visible spectra. In a pure CO matrix, a color change from green to reddish-brown was observed on warming from 10 K to about 40-50 K. The infrared spectrum of the reddish-brown material showed no evidence for coordinated CO, thus suggesting the extreme thermal instability of Ti(CO)6. [Pg.319]

The HPLC-FTIR technique has recently been used to identify six catechins and two methyl-xanthines present in green tea extracts." " A reversed-phase separation of the compounds was performed on a C-18 column equilibrated at 30°C using an isocratic mobile phase of acetonitrile-0.1% formic acid (15 85), prior to introduction to the deposition interface linked to the FTIR detector. The solvent was evaporated at 130°C and spectra were collected every 6 sec during the run. Two distinct designs for HPLC-FTIR interfaces have been developed flow cells and solvent elimination systems. Flow cell systems acquired spectra of the eluent in the solvent matrix through IR transparent, nonhydroscopic windows. The... [Pg.103]

Although the present section has emphasized the fundamental theory of Weyl as a basis for a reformulation and generalization of conventional scattering theory, our illustrations have focused on the possibility to analytically continue the full differential equation with its spectral function and associated Green s functions and resolvents, the S-matrix etc., into the complex plane. This calls attention to appropriate methods for both rigorous and practical techniques to accomplish this operation. [Pg.51]

One can ask what is the advantage to use the more complex two-time Green functions instead of density matrices There are several reasons. First of all, NGF give, as we shall see below, a clear description of both density of states and distribution of particles over this states. Then, the equations of motion including interactions and the influence of environment can be obtained with the help of a diagrammatic technique, and (very important) all diagrammatic results of equilibrium theory can be easily incorporated. Retardation effects are conveniently taken into account by two-time Green functions. And,. .. finally, one can always go back to the density matrix when necessary. [Pg.259]

An alternative quasiparticle description of the optical response is possible using the nonlinear exciton equations (NEE) (39). The response function is then represented in terms of one-exciton Green functions and exciton-exciton scattering matrix. Four coherent ultrafast 2D techniques have been proposed (16,17), and computer simulations of the 2D response were performed for model aggregates made out of a few two-level chromophores. [Pg.363]


See other pages where Green matrix technique is mentioned: [Pg.374]    [Pg.374]    [Pg.4535]    [Pg.4534]    [Pg.3]    [Pg.187]    [Pg.168]    [Pg.13]    [Pg.1041]    [Pg.180]    [Pg.253]    [Pg.221]    [Pg.116]    [Pg.370]    [Pg.70]    [Pg.237]    [Pg.96]    [Pg.47]    [Pg.104]    [Pg.182]    [Pg.1279]    [Pg.281]    [Pg.215]    [Pg.287]    [Pg.268]    [Pg.150]    [Pg.455]    [Pg.123]    [Pg.128]    [Pg.71]    [Pg.488]    [Pg.601]    [Pg.365]    [Pg.388]    [Pg.216]    [Pg.198]    [Pg.356]    [Pg.858]    [Pg.203]    [Pg.149]    [Pg.566]    [Pg.106]    [Pg.228]   
See also in sourсe #XX -- [ Pg.351 ]




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