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Silicon boron-sulfur bonds

Element-element bonds, addition to G-G multiple bonds arsenic—selenium bonds, 10, 782 boron—boron bonds, 10, 727 boron—sulfur bonds, 10, 778 B-S and B-Ge bonds, 10, 758 chalcogen—chalcogen additions, 10, 752 germanium—germanium bonds, 10, 747 germanium-tin bonds, 10, 780 overview, 10, 725-787 phosphorus—phosphorus bonds, 10, 751 phosphorus—selenium bonds, 10, 782 phosphorus-sulfur bonds, 10, 781 Se-Si and Se-Ge bonds, 10, 779 silicon-germanium bonds, 10, 770 silicon-phosphorus bonds, 10, 780 silicon-silicon bonds, 10, 734 silicon-sulfur bonds, 10, 779 silicon-tin bonds, 10, 770 tin-boron bonds, 10, 767 tin-tin bonds, 10, 748... [Pg.101]

Catenation is defined as the self-linking of an element to form chains and rings. Carbon, then, given the above discussion, is the all-time champion catenator, much better than silicon (or sulfur, boron, phosphorus, germanium, and tin, the other elements that show this ability). Why should this be so A comparison of the relevant carbon and silicon bond energies as shown below is helpful ... [Pg.419]

The methods available for synthesis have advanced dramatically in the past half-century. Improvements have been made in selectivity of conditions, versatility of transformations, stereochemical control, and the efficiency of synthetic processes. The range of available reagents has expanded. Many reactions involve compounds of boron, silicon, sulfur, selenium, phosphorus, and tin. Catalysis, particularly by transition metal complexes, has also become a key part of organic synthesis. The mechanisms of catalytic reactions are characterized by catalytic cycles and require an understanding not only of the ultimate bond-forming and bond-breaking steps, but also of the mechanism for regeneration of the active catalytic species and the effect of products, by-products, and other reaction components in the catalytic cycle. [Pg.1338]

In contrast, use of metalloid elements, such as silicon, tin antimony or boron, which can form weak covalent bonds with oxygen, nitrogen or sulfur substituents during the course of the reaction, results in templated products that may be obtained metal-free by simple hydrolysis. These covalent template reactions (the M—X bond is essentially covalent in these cases) also have the advantage that the... [Pg.637]


See other pages where Silicon boron-sulfur bonds is mentioned: [Pg.118]    [Pg.242]    [Pg.782]    [Pg.123]    [Pg.147]    [Pg.877]    [Pg.1151]    [Pg.16]    [Pg.1034]    [Pg.1]    [Pg.220]    [Pg.17]    [Pg.727]    [Pg.296]    [Pg.65]    [Pg.41]    [Pg.273]    [Pg.208]    [Pg.450]    [Pg.171]    [Pg.21]    [Pg.1051]    [Pg.1660]    [Pg.5995]    [Pg.1014]    [Pg.49]    [Pg.165]    [Pg.1659]    [Pg.5994]    [Pg.63]    [Pg.1033]    [Pg.1]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.4 , Pg.4 , Pg.5 , Pg.5 , Pg.7 , Pg.7 ]




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Boron bonding

Silicon—sulfur bonds

Sulfur bonding

Sulfur bonds

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