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Polarization type

Olefin polymerization by catalysts based on transition metal halogenides is usually designated as coordinated anionic, after Natta (194). It is believed that the active metal-carbon bond in Ziegler-Natta catalysts is polarized following the type M+ - C. The polarization of the active metal-carbon bond should influence the route of its decomposition by some compounds ( polar-type inhibitors), e.g. by alcohols. When studying polymerization by Ziegler-Natta catalysts tritiated alcohols were used in many works to determine the number of metal-polymer bonds. However, as it was noted above (see Section IV), in two-component systems the polarization of the active bond cannot be judged by the results of the treatment of the system by alcohol, as the radioactivity of the polymer thus obtained results mainly from the decomposition of the aluminum-polymer bonds. [Pg.211]

These dyes, already described in section 2.12, require adequate solubility for the coloration of various organic solvents and must be cheap [79]. The simplest and least polar dyes of this class are used for the coloration of petrol and ball-pen inks, with more polar types being used in lacquers, stains and varnishes. Some products of lower solubility are used in mass coloration. [Pg.211]

Erancl MM, Pietro WJ, Hehre WJ, Binkley JS, Gordon MS, DePrees DJ, Pople JA (1982) Self-consistent molecular-orbital methods. 23. A polarization-type basis set for 2 row elements. J Chem Phys 77 3654-3665... [Pg.99]

Comparing polarity between components is often a good way to predict solubility, regardless of whether those components are liquid, solid, or gas. Why is polarity such a good predictor Because polarity is central to the tournament of forces that underlies solubility. So solids held together by ionic bonds (the most polar type of bond) or polar covalent bonds tend to dissolve well in polar solvents, like water. [Pg.170]

The salient findings from adsorption studies are that reversible H2 of an activated type exists on reduced and sulfided catalysts and that polar-type compounds are strongly adsorbed on these catalysts. [Pg.286]

Polar-type molecules, especially nitrogen compounds, inhibit both hydrogenolysis and hydrogenation, but to differing extents. [Pg.295]

M. M. Francl, W. J. Pietro, W. J. Hehre, J. S. Binkley, M. S. Gordon, D. J. DeFrees, and J. A. Pople, J. Chem. Phys., 77, 3654 (1982). Self-Consistent Molecular Orbital Methods. XXIII. A Polarization-Type Basis Set for Second-Row Elements. [Pg.205]

The reactions with which we are mostly concerned in chemistry take place in solution rather than in the gas phase. The majority of them moreover involve reactants, products, or transition states carrying electric charges. In such cases the entropies of solvation are extremely large, and these entropies cannot be estimated at present. This immediately rules out any possibility of estimating absolute values of equilibrium or rate constants for reactions of this kind. If we are concerned with absolute calculations of rates and equilibria, we must confine ourselves either to gas-phase reactions, or to reactions of non-polar type. Even here we will usually be forced to make estimates of entropies that are of dubious significance chemical theory has not yet progressed to a point where problems of this kind can usefully be discussed. [Pg.66]

All the calculations of F2 are carried out with a simple basis set of double-zeta polarization type, the standard 6-31G(d) basis set, and are performed at a fixed interatomic distance of 1.44 A, which is approximately the optimized distance for a full Cl calculation in this basis set. Only the corresponding orbitals are referred to as the active orbitals , while the orbitals representing the lone pairs, so-called spectator orbitals , remain doubly occupied in all calculations. A common point to the various VB methods we use, except the VBCI method, is that at the dissociation limit, the methods converge to two F fragments at the restricted-open-shell Hartree Fock (ROHF) level. [Pg.271]

A typical separation of platelet phospholipids can be achieved as follows A sample containing 40-50 p,g of phospholipid (by weight) is applied to a p, Porasil (polar-type) column (Waters, Milford, CT) measuring 7 x 30 cm, and a solvent system of acetonitrile-methanol-45% phosphoric acid (130 5 1.5, v/v) is applied, as suggested by Chen and Kou (1982). The flow rate was 1 ml/min, and the elution was monitored by an ultraviolet detector sensitive at 203 nm. The total elution time in this case was 40 min, and the profile is illustrated in Figure 3-4. [Pg.57]

The term "quaternary structure" refers to the interaction of several polypeptide chains in a noncovalent manner to form multisubunit protein particles termed oligomers. Individual subunit polypeptide chains are also referred to as protomers. Oligomers usually have an even number of subunits (two or more). The noncovalent interactions may be of the hydrophobic, hydrogen bond, or the polar type. Examples are hemoglobin and lactate dehydrogenase (four protomers each) and many allosteric enzymes. [Pg.76]

Thus, it is concluded that local isotherm functions of a fairly narrow type such as the Langmuir and Langmuir-plus-lateral interaction types are the rule. Conversely, isotherms of the Frenkel-Halsey and polarization types do not seem applicable in the submonolayer region. [Pg.63]

A polar-type transition state is also supported by the occurrence of Wagner-Meer-wein rearrangements accompanying the elimination of hydrogen chloride, from neo-pentyl - " - - , bornyl > andisobornylchlorides - ° In the case of neopentyl chloride the formation of 2-methylbut-l-ene and 2-methyl-but-2-ene has been explained in terms of a non-classical carbonium ion type transition state. [Pg.168]

T-cells can be subdivided in polarized type I and type II cells, depending on the spectrum of cytokines which they are able to produce. Thl cells are characterized by production by of TNF and IFN-y and activate immunity based on macrophage activation and effector functions. At the other extreme of the spectrum, Th2 cells are characterized by IL-4 and IL-5 production and elicit immune responses based on the effector function of mastocytes and eosinophils. The latter cell types are typically involved in allergic inflammation. [Pg.239]


See other pages where Polarization type is mentioned: [Pg.218]    [Pg.226]    [Pg.236]    [Pg.102]    [Pg.347]    [Pg.98]    [Pg.592]    [Pg.31]    [Pg.437]    [Pg.569]    [Pg.171]    [Pg.21]    [Pg.98]    [Pg.496]    [Pg.13]    [Pg.274]    [Pg.24]    [Pg.37]    [Pg.26]    [Pg.312]    [Pg.93]    [Pg.99]    [Pg.89]    [Pg.183]    [Pg.76]    [Pg.513]    [Pg.168]    [Pg.513]    [Pg.118]    [Pg.120]    [Pg.62]    [Pg.710]    [Pg.568]    [Pg.668]    [Pg.60]   
See also in sourсe #XX -- [ Pg.78 ]

See also in sourсe #XX -- [ Pg.41 ]




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F-type polarization

Polar Solvent-type Fires

Polar reactions, types

Polarization types Atomic

Polarization types Dipolar

Polarization types Electronic

Polarization types Ionic

Polarization types Orientational

Polarizer types

Polarizer types

Rayleigh-type polarization

Solvent types polar aprotic

Surfactants polar headgroups, types

The dissociative type reaction may not depend on solvent polarity

The polarization types and their relaxation times

Three Types of Polarization

Three types of polarization mechanisms

Type I polar stratospheric clouds

Types of Bonds Covalent, Ionic, Polar, Metallic

Types of Polarization

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