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Nucleus structure

For example, in the case of relatively light nuclei, structures composed of several helium nuclei, such as " Mg, Si, and so on, are more stable than their neighbonrs. Moreover, nnclei with even mass numbers (an even total nnmber of nentrons and protons) are more robnst than those with odd mass nnmbers. [Pg.68]

The minimum molecular weights of these primary oxidations of aniline are in accordance with an eight-nuclei structure. [Pg.506]

See also Nitrogen NMR NMR Principles NQR Applications NQR, Theory Parameters in NMR Spectroscopy, Theory of Solid State NMR, Methods Solid State NMR Using Quadrupolar Nuclei Structural Chemistry Using NMR Spectroscopy, Inorganic Molecules. [Pg.690]

Tropane alkaloids have a tropane (C4N skeleton -f) nucleus. Structurally, these alkaloids synthesize as postcursors of pyrrolines (Figure 57). a, /3,

tropane alkaloids (e.g., atropine, hyoscyamine, cocaine, tropinone, tropine, littorine and cuscohy-grine) have a strong biological activity, especially as neurotransmitters. [Pg.103]

A second chemical class of synthetic progestins contains the pregnane nucleus structure of progesterone along with some additional substitutions. Alkyl chain additions to the C17 position increase the biological... [Pg.707]

The physical and chemical properties of the elements are directly related to their electron configurations. For example, chemical properties such as gaining, giving and sharing of electrons are dependent on the valence electrons and nucleus structure. As a result, chemical behaviors of the elements are closely related to the nucleus structure and electron configuration of the element. Elements in the same period contain different numbers of electrons in the valence shells. [Pg.31]

Reactions of these ligands have not been studied in aqueous solution. However, their complexes are readily synthesized and are stable but reactive towards heteroligands [41,42], The reported structures all show the vanadium coordinated in monomeric units after the fashion depicted in Scheme 4.9. The multidentate thiolato complexes with tri- or tetradentate functionality are sufficient to satisfy the coordination requirements of the vanadium nucleus. Structurally, the compounds are not much different from analogous complexes formed with oxygen ligands (Section 4.4.2). [Pg.53]

Ibogaine was isolated in 1901 from Tabemanthe iboga roots by Dybowski and Landrin and by Haller and Heckel. The most abundant alkaloid in the shrub s root bark, ibogaine exhibts the indole nucleus structure common to most psychedelics. Its stereochemistry (the dotted lines are at angles to the rest of the molecule) was established in the late 1960s ... [Pg.455]

Compound Nucleus Structure Type (87) Resonance Freq. (MHz) Ref. [Pg.107]

The methyl derivative thus produced forms a multi-nucleus structure by the dehydration condensation. Generally, the numbers of benzene nuclei contained in resol for making phenolic foam are less than 10. The addition and condensation reactions used in synthesizing resol, and the reaction during foaming and curing are summarized as follows ... [Pg.186]

Voigt H.E and Davis K.A. (1996). Computer simulations of neural correlations in the dorsal cochlear nucleus. In Cochlear Nucleus structure and function in relation to modeling. Ainsworth W.A. (Ed.), London JAl Press, pp. 351-375. [Pg.90]

Yau, S. T. and Vekilov, P. G. 2000. Quasi-planar nucleus structure in apoferritin crystallization. [Pg.370]

The concern at this point is limited to the temperature dependence. Therefore, the specifics of the nucleus structure, which are embodied in the parameters k2, ks, g2 and go, do not have to be specified at this time. The second term of the exponential argument should dominate in the present temperature range of interest. [Pg.102]

A key problem is to theoretically establish the appropriate primary and secondary nucleation processes that are operative. This includes defining the geometry of the rate controlling nucleus, i.e. whether it is two-dimensional or three-dimensional. It should be recalled that the experimental results can fit either model. Of crucial importance is the chain conformation within the nucleus. Conventional type data are not discriminatory. They can be fitted by either a bundle type nucleus, or one in which the chains are regularly folded with adjacent re-entry. At present, either type of nucleus is consistent with the experimental results. It is important that it be recognized that it is not necessary for there to be a one-to-one relation between the nucleus structure and the mature crystallite that evolves. It is not necessary to assume a regularly folded chain nucleus in order for a mature lamellar crystallite to evolve. It is important that the crucial role of nucleation in polymer crystallization be taken from the realm of assumption and placed on a first principled theoretical base. Similar concerns can be expressed with respect to the transport term. [Pg.203]

The wave function T i oo ( = 11 / = 0, w = 0) corresponds to a spherical electronic distribution around the nucleus and is an example of an s orbital. Solutions of other wave functions may be described in terms of p and d orbitals, atomic radii Half the closest distance of approach of atoms in the structure of the elements. This is easily defined for regular structures, e.g. close-packed metals, but is less easy to define in elements with irregular structures, e.g. As. The values may differ between allo-tropes (e.g. C-C 1 -54 A in diamond and 1 -42 A in planes of graphite). Atomic radii are very different from ionic and covalent radii. [Pg.45]

In addition to this electron spin fine structure there are often still finer lines present. These are known as the hyperfine structure, which arises from the dilTerent weights of the isotopes of an element or from the spin of the nucleus. [Pg.267]

To provide further insight why the SCF mean-field model in electronic structure theory is of limited accuracy, it can be noted that the average value of the kinetic energy plus the attraction to the Be nucleus plus the SCF interaction potential for one of the 2s orbitals of Be with the three remaining electrons in the s 2s configuration is ... [Pg.232]

The most notable studies are those of Ingold, on the orienting and activating properties of substituents in the benzene nucleus, and of Dewar on the reactivities of an extensive series of polynuclear aromatic and related compounds ( 5.3.2). The former work was seminal in the foundation of the qualitative electronic theory of the relationship between structure and reactivity, and the latter is the most celebrated example of the more quantitative approaches to the same relationship ( 7.2.3). Both of the series of investigations employed the competitive method, and were not concerned with the kinetics of reaction. [Pg.76]

The name found its origin in the fact that the first dyes known were all derived from quinoline as, for example, 2,2 -cyanine (Scheme 1). In the case of an asymmetrical or symmetrical dye involving one or two nuclei that are different from the quinoline ring, the name of the nucleus becomes the prefix in the name of the dye. So 3.3 -dimethyl-4-phenyl thiazolo cyanine is the dye of structure 1 and 3.1 -dimethyl 4-phenyl thiazolo 2 -cyanine is represented by the formula structure 2 (Scheme 2). [Pg.25]


See other pages where Nucleus structure is mentioned: [Pg.799]    [Pg.800]    [Pg.1068]    [Pg.1069]    [Pg.746]    [Pg.100]    [Pg.838]    [Pg.138]    [Pg.442]    [Pg.366]    [Pg.79]    [Pg.244]    [Pg.441]    [Pg.112]    [Pg.1682]    [Pg.196]    [Pg.201]    [Pg.349]    [Pg.470]    [Pg.366]    [Pg.361]    [Pg.1098]    [Pg.283]    [Pg.283]    [Pg.65]    [Pg.24]    [Pg.1469]    [Pg.567]    [Pg.250]    [Pg.726]    [Pg.1115]    [Pg.3]   
See also in sourсe #XX -- [ Pg.93 ]

See also in sourсe #XX -- [ Pg.533 ]




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