Bonding reactivity and

The application of the foregoing routes has led to the preparation and characterization of fluorides of virtually every element in the periodic table except the three lightest noble gases, Fie, Ne and Ar. The structures, bonding, reactivity, and industrial applications of these compounds will be found in the treatment of the individual elements and it is an instructive exercise to gather this information together in the form of comparative tables. [Pg.821]

H. Sakurai (ed.), Organosilicon and Bioorganosilicon Chemistry—Structure, Bonding, Reactivity, and Synthetic Application. Ellis Horwood. Chichester, 1985. [Pg.97]

The similarity between the bonding models for transition metal carbene and carbyne complexes was noted in Section II. That the reactivity of the metal-carbon double and triple bonds in isoelectronic carbene and carbyne complexes should be comparable, then, is not surprising. In this section, the familiar relationship between metal-carbon bond reactivity and metal electron density is examined for Ru and Os carbyne complexes. [Pg.190]

Cline DJ, et al. New water-soluble phosphines as reductants of peptide and protein disulfide bonds reactivity and membrane permeability. Biochemistry 2004 43 15195. [Pg.125]

Reviews Tamao, K. In Organosilicon and Bioorganosilicon Chemistry Structure, Bonding, Reactivity and Synthetic Application Sakurai, H., Ed. Halsted Press New York, 1985 pp. 231-242 Tamao, K. J. Synth. Org. Chem. Japan 1988, 41, 861. [Pg.105]

Sogah DY, Farnham WB (1985) In Sakurai (ed) Organosilicon and biooganosilicon chemistry stucture, bonding, reactivity and synthetic application. Ellis Horwood, Chichester, chap 20, p 219... [Pg.33]

R. Bloch, Additions of Organometallic Reagents to C N Bonds Reactivity and Selectivity, Chem. Rev. 1998, 98, 1407-1438. [Pg.455]

The goal of this chapter is to illustrate supported catalytic nanomaterials, with an emphasis on those that are simple and well-defined structurally (and thus relatively well understood), and to summarize generally important conclusions about their structure, bonding, reactivity, and catalytic properties. This summary is not exhaustive, and references to related reviews are cited. [Pg.50]

In the following paragraphs, methods of preparation and characterization of structurally simple supported metal complexes are summarized, and examples are presented that illustrate characterization data and support general conclusions about structure, bonding, reactivity, and catalysis. [Pg.51]

Transition-metal complexes of indium and indium adducts are available.Structures, bonding, reactivity, and their materials-related applications are of current interest in the early 2000s. [Pg.416]

Sogah, D. Y Farnham, W. B. In Organosilicon andBioorganosilicon Chemistry Structure, Bonding, Reactivity and Synthetic Applications Sakurai, H., ed., John Wiley Sons New York 1985, Chapter 20. [Pg.34]

In 1972, Mock considered double-bond reactivity and its relationship to torsional strain, by which he understood the strain imposed on a double bond in medium-ring fra 5-cycloalkenes or by steric compression of large cis substituents [28]. He argued that the loss of 7t overlap due to a torsion about the double bond can be partially compensated by rehybridization in these two situations, leading, respectively, to syn and anti pyramidalization of the double bond consequently, such bonds will favor different modes of addition (cis and trans). The proposition was supported by examples of X-ray structures of strained olefins, STO-3G energy calculations for the twisted and pyramidalized ethylene geometries, and by analysis of the out-of-plane vibrational frequencies of ethylene. Mock concluded that small ground-state distortions may produce sizable effects in the transition states. [Pg.289]

R. Tacke, Recent Results in Bioorganosilicon Chemistry Novel Sila-Drugs and Microbial Transformations of Organosilicon Compounds , in Organosilicon and Bioorganosilicon Chemistry Structure, Bonding, Reactivity and Synthetic Application (Ed. H. Sakurai), Ellis Horwood, Chichester, 1985, pp. 251-262. [Pg.32]

We draw upon each of these notions as necessary to explain various aspects of bonding, reactivity, and structure. We will add solvation effects later in the book. For particular reactions or structures, we may have to refine and/or combine these notions to get the optimal model for the molecule. In some cases we may even need to completely re-think and modify these foundations. However, there is often a tendency in physical organic chemistry to become quite focused on the "exceptions to the rule". We should keep in mind that the vast majority of organic structures are well described by this simple model. [Pg.26]

When these results are viewed in terms of the hormonal activity of the substituted insulins, an interesting parallelism is noted between the effects of the substitutions on disulphide bonds reactivity and on the biological activity the disulphide bonds reactivity appears to be affected only by those substitutions which are known to abolish the biological activity of the hormone, when carried beyond a certain level. It was therefore planned to study the changes of biological activity and of -S-S- bonds reactivity as a function of the degree of substitution. This aspect was studied in detail on iodinated and methylated insulins. [Pg.342]

S-S- Bonds Reactivity and Biological Activity of Insulins Iodinated or Methylated at Different Extents... [Pg.342]

Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...