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Total complexity

Lipoproteins. The lipid moiety of lipoproteins is quite variable both qualitatively and quantitatively. The a-lipoprotein of serum contains glyceride, phosphatide and cholesterol to about 30 -40% of the total complex. The -lipoprotein of serum contains some glyceride but the phosphatide and cholesterol account for nearly 75% of the total. [Pg.332]

HF concentration, mol/l Ta concentration, mol/l NH4 +/Ta + Complexes found % TaF72 of total complexes... [Pg.130]

The total (complex) amplitude of the waves at a point r, V(r) is the superposition or sum of the amplitudes due to the waves from each pinhole,... [Pg.12]

The total complexity of the numerical analysis is 0(N n N)). Readers who want more details are referred to Liu [371... [Pg.123]

The rate of reaction (13) can be evaluated from the difference between values at E. = 0.25 V and = 0.6 V, which represents the total amount of complexed potassium arriving at the collector. Dividing this quantity by collection efficiency one gets an estimate for the total complexation rate in the system. To evaluate homogeneous complexation rate the contribution of interfacial complexation (i.e., ig KOBisce) has to be subtracted ... [Pg.396]

Figure 5. Reaction probabilities vs. impact parameter for frei = 0.5 kcal/mol and Trot = 300 K. Part (a) is for nc-cib = 0. The solid lines are for FVib = 0 and the dotted lines are for Fvib = zpe. The squares are for total complex formation and the triangles for long-range complex formation. Part (b) is for nc-clh = 6 and fVib = 0 with ( , —) for total complex formation, (a, —) for long-range complex formation, and (o, ) for attaining the central barrier with one or no ITP (from ref. 38). Figure 5. Reaction probabilities vs. impact parameter for frei = 0.5 kcal/mol and Trot = 300 K. Part (a) is for nc-cib = 0. The solid lines are for FVib = 0 and the dotted lines are for Fvib = zpe. The squares are for total complex formation and the triangles for long-range complex formation. Part (b) is for nc-clh = 6 and fVib = 0 with ( , —) for total complex formation, (a, —) for long-range complex formation, and (o, ) for attaining the central barrier with one or no ITP (from ref. 38).
Species Total concentration mg kg-1 molal Free concentration molal % of total Complexes % of total... [Pg.85]

Fig. 7. The 13C NMR spectra for [WO(X)(13CN)4]m illustrating the variation in chemical shift and MO W- C) coupling constants. For [WO(13CN)5]3 the total complex concentration [W(IV)] = 0.2 m, the total cyanide concentration [13CN] = 0.3 m, pH = 8.8 for [WO(F)(13CN)4]3 the total complex concentration [W(IV)] = 0.2 m, the total cyanide concentration [13CN] = 0.3 m, the total fluoride concentration [KF] = 0.33 m, pH = 5.2 and for [W0(H20)(13CN)4]2 the total complex concentration [W(IV)] = 0.2 m, the total cyanide concentration [13CN] = 0.3 m, pH = 3.1 (8). (Adapted with permission from Abou-Hamdan, A. Roodt, A. Merbach, A. E. Inorg. Chem. 1998, 37, 1278-1288. Copyright 1998 American Chemical Society). Fig. 7. The 13C NMR spectra for [WO(X)(13CN)4]m illustrating the variation in chemical shift and MO W- C) coupling constants. For [WO(13CN)5]3 the total complex concentration [W(IV)] = 0.2 m, the total cyanide concentration [13CN] = 0.3 m, pH = 8.8 for [WO(F)(13CN)4]3 the total complex concentration [W(IV)] = 0.2 m, the total cyanide concentration [13CN] = 0.3 m, the total fluoride concentration [KF] = 0.33 m, pH = 5.2 and for [W0(H20)(13CN)4]2 the total complex concentration [W(IV)] = 0.2 m, the total cyanide concentration [13CN] = 0.3 m, pH = 3.1 (8). (Adapted with permission from Abou-Hamdan, A. Roodt, A. Merbach, A. E. Inorg. Chem. 1998, 37, 1278-1288. Copyright 1998 American Chemical Society).
Fig. 8. Oxygen-17 NMR spectra at pH = 1.3, illustrating the formation of the di-nuclear complex at 25°C after (a) 3 min, (b) 1 h and (c) 6 h of mixing [Re02(CN)4]3 and H2170. The total complex concentration [Re] = 0.2 m, /m = 1.0 m (KN03), NMR chemical shift reference is the nitrate ion (<5(N03) = 413 ppm) (5). (Adapted with permission from Roodt, A. Leipoldt, J. G. Helm, L. Merbach, A. E. Inorg. Chem. 1992, 31, 2864-2868. Copyright 1992 American Chemical Society). Fig. 8. Oxygen-17 NMR spectra at pH = 1.3, illustrating the formation of the di-nuclear complex at 25°C after (a) 3 min, (b) 1 h and (c) 6 h of mixing [Re02(CN)4]3 and H2170. The total complex concentration [Re] = 0.2 m, /m = 1.0 m (KN03), NMR chemical shift reference is the nitrate ion (<5(N03) = 413 ppm) (5). (Adapted with permission from Roodt, A. Leipoldt, J. G. Helm, L. Merbach, A. E. Inorg. Chem. 1992, 31, 2864-2868. Copyright 1992 American Chemical Society).
Fig. 5. Ten types of different structures identified by X-ray diffraction, where the abbreviated N-0 is used to express each bridging amidate ligand and X denotes axial donors such as OH2, N03, N02 (nitro), Cl, and Br. For the compounds involving axial ligands (X), the total complex charge is given assuming that X is a monoanion. Note that, in some cases, amine ligand in cis-Pt(NH3)2 will be replaced with other ligands, such as in Pt(en), cis-Pt(NH3)Cl, cis-PtCl2, and Pt(bpy). Fig. 5. Ten types of different structures identified by X-ray diffraction, where the abbreviated N-0 is used to express each bridging amidate ligand and X denotes axial donors such as OH2, N03, N02 (nitro), Cl, and Br. For the compounds involving axial ligands (X), the total complex charge is given assuming that X is a monoanion. Note that, in some cases, amine ligand in cis-Pt(NH3)2 will be replaced with other ligands, such as in Pt(en), cis-Pt(NH3)Cl, cis-PtCl2, and Pt(bpy).
G. GENERAL TRANSFER FUNCTIONS IN SERIES. The historical reason for the widespread use of Bode plots is that, before the use of computers, they made it possible to handle complex processes fairly easily. A complex transfer function can be broken down into its simple elements leads, lags, gains, deadtimes, etc. Then each of these is plotted on the same Bode plots. Finally the total complex transfer function is obtained by adding the individual log modulus curves and the individual phase curves at each value of frequency. [Pg.434]

On the other hand, the complexity of a molecule increases with the number of heteroatoms, the symmetrical disposition of which is a simplifying factor just as it is for carbon atoms. When all the atoms are the same, C(E) = 0 and the total complexity Cj is equal to C(q) i. e, the complexity due to connectivity. [Pg.33]

The free energy change of the total complexation reaction, AG°, is related principally to step 2 [Eq. (3.18b)], the combination snbreaction ... [Pg.112]

The enthalpy and entropy changes of the total complexation reaction, AH° and AS°, reflect, primarily, step 1 [Eq. (3.18a)], the dehydration snbreaction. [Pg.112]

Using Eqs. (278), (281b), (282), and (301), we can calculate the total complex permittivity s (v) from the above theory. After that we can find the absorption coefficient a(v), its components aor(v) and avib(v) due to the reorientation and vibration processes, and the refraction index n ... [Pg.229]

Taking account of Eq. (343), we express the total complex permittivity in the form of a Lorentz line... [Pg.259]

Now we apply the additivity approximation corresponding to Eq. (387). Namely, we sum up the contributions of three sources of dielectric loss due to (a) reorienting dipoles, (b) oscillating anions, and (c) oscillating cations. Combining Eqs. (387), (388), and (399a), we write the formula for the total complex permittivity ... [Pg.280]

Figure 50. Calculated contributions of the ionic permittivity for the imaginary (a, c) and real (b, d) parts of the total complex permittivity (solid lines) dashed lines refer to the calculation, neglecting the ionic dispersion, (a, b) For NaCl-water solution (c, d) for KCl-water solution. Cm = 0.5 mol/liter, Tion/r = 10. Figure 50. Calculated contributions of the ionic permittivity for the imaginary (a, c) and real (b, d) parts of the total complex permittivity (solid lines) dashed lines refer to the calculation, neglecting the ionic dispersion, (a, b) For NaCl-water solution (c, d) for KCl-water solution. Cm = 0.5 mol/liter, Tion/r = 10.
Polyfunctiomlity refers to the presence of many different coordinating groups on the same molecule. The stronger complexing sites are occupied first by metals. Thus, the overall retention energy of these complexants depends on the total metal to total complexant concentration ratio. [Pg.203]

Pesticide Opportunity Profile. In looking at the total complex of R and D and marketing inputs, there are a number of points which must be understood to anticipate obstacles or roadblocks which can impede or eliminate further development (20). For example (Fig. 6). [Pg.288]

Impedance spectroscopy is an effective technique for probing the features of chemically-modified electrodes and for understanding electrochemical reaction rates (87,88). Impedance is the totally complex resistance encountered... [Pg.58]

A short overview of synthetic strategies that are currently used in combinatorial chemistry is important to get a better understanding of how to characterize a combinatorial library in the most efficient way. Figure 10.3 presents different strategies for synthesis of combinatorial libraries on an example of a library with three points of randomization (X, Y, Z), three building blocks in each randomization (XI, X2, X3, Yl, Y2, etc., correspondingly), and total complexity of 27 compounds. [Pg.249]

For the equivalent circuit in Figure 3.10, the total complex admittance Y and complex impedance Z in Cartesian coordinates can be expressed as... [Pg.118]


See other pages where Total complexity is mentioned: [Pg.415]    [Pg.144]    [Pg.34]    [Pg.66]    [Pg.68]    [Pg.79]    [Pg.446]    [Pg.1054]    [Pg.308]    [Pg.309]    [Pg.279]    [Pg.440]    [Pg.35]    [Pg.36]    [Pg.20]    [Pg.587]    [Pg.454]    [Pg.1031]    [Pg.119]    [Pg.356]    [Pg.216]    [Pg.123]    [Pg.492]   
See also in sourсe #XX -- [ Pg.36 ]




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