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Configurational charges

In effect, the lanthanide contraction has shrunk these elements. Since electronic configuration, charge, and ionic size generally determine chemical behavior, we should expect that Zr+4 and Hf+4 have extremely similar behaviors and that the same should be true for Nb+5 and Ta+5. Such similarities are indeed observed and prove exceedingly troublesome in the course of chemical separations. [Pg.120]

In other studies, the above research group synthesised a number of related one-and two-station, photoactive [2]-rotaxanes incorporating either ferrocene or anthracene stoppers or a combination of each type. In these systems, the terminal stoppers associate with the exterior of the bis(4-4 -bipyridinium)cyclophane tetracation via 7U-stacking. Such proximity has obvious implications for the required rapid electron-transfer to a terminal (ferrocenyl) group in order to be competitive with the simple charge recombination process discussed previously. The relationship between the photoactivity, electron-transfer behaviour and concomitant configurational charges in the above systems has now been described in some detail. " ... [Pg.73]

An agonist, by virtue of the molecular information it contains (e.g., size, 3D configuration, charge distribution, hydrogen- or ionic-bonding residues, chirality), selectively binds to a complementary 3D surface or binding site domain formed by amino acid residues of a receptor protein and initiates a... [Pg.3113]

Fig. 1.79. Relaxed atomic configurations of H2O and O2 coadsorbed on free Ans and Au3o clusters (top) and on Aug/MgO(lOO) (bottom). For the free and snpported Ang cases, the difference-charge-density between the compiete adsorption system and the separated Au8/MgO(100) and O2-H2O complex are displayed, superimposed on the atomic configuration. Charge depletion is shown in dark grey and charge accumulation in gray-white. Light grey, dark, and white spheres correspond to An, O, and H atoms, respectively... Fig. 1.79. Relaxed atomic configurations of H2O and O2 coadsorbed on free Ans and Au3o clusters (top) and on Aug/MgO(lOO) (bottom). For the free and snpported Ang cases, the difference-charge-density between the compiete adsorption system and the separated Au8/MgO(100) and O2-H2O complex are displayed, superimposed on the atomic configuration. Charge depletion is shown in dark grey and charge accumulation in gray-white. Light grey, dark, and white spheres correspond to An, O, and H atoms, respectively...
The rate of the substitution of a given solvent molecule in the inner coordination sphere depends mainly on the nature (electron configuration, charge and size) of the metal ion rather than that of the incoming ligand. [Pg.7]

Additional hieh-integritv requirements l C comms will be to other hIgh-Integrity systems and to control systems only, and unidirectional Security for configuration charges... [Pg.54]

Point defects and complexes exliibit metastability when more than one configuration can be realized in a given charge state. For example, neutral interstitial hydrogen is metastable in many semiconductors one configuration has H at a relaxed bond-centred site, bound to the crystal, and the other has H atomic-like at the tetrahedral interstitial site. [Pg.2885]

The unequal distribution of charge produced when elements of different electronegativities combine causes a polarity of the covalent bond joining them and, unless this polarity is balanced by an equal and opposite polarity, the molecule will be a dipole and have a dipole moment (for example, a hydrogen halide). Carbon tetrachloride is one of a relatively few examples in which a strong polarity does not result in a molecular dipole. It has a tetrahedral configuration... [Pg.51]


See other pages where Configurational charges is mentioned: [Pg.147]    [Pg.567]    [Pg.60]    [Pg.329]    [Pg.111]    [Pg.334]    [Pg.47]    [Pg.114]    [Pg.338]    [Pg.23]    [Pg.567]    [Pg.147]    [Pg.567]    [Pg.60]    [Pg.329]    [Pg.111]    [Pg.334]    [Pg.47]    [Pg.114]    [Pg.338]    [Pg.23]    [Pg.567]    [Pg.155]    [Pg.424]    [Pg.403]    [Pg.438]    [Pg.1926]    [Pg.2225]    [Pg.2873]    [Pg.2885]    [Pg.2886]    [Pg.153]    [Pg.219]    [Pg.238]    [Pg.601]    [Pg.608]    [Pg.4]    [Pg.79]    [Pg.361]    [Pg.254]    [Pg.342]    [Pg.1278]    [Pg.34]    [Pg.49]    [Pg.218]    [Pg.67]    [Pg.224]    [Pg.195]    [Pg.216]    [Pg.217]    [Pg.404]    [Pg.428]   


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