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Macromolecular hydrides

Aluminium and beryllium hydrides react with water in the same way as the salt-like hydrides, to give hydrogen and metal hydroxides. However, the hydroxides are insoluble, so alkaline solutions are not produced for example [Pg.52]


Macromolecular hydrides have extended structures, which differ from those that would be expected of a collection of ions. Thus, BeH2 has a chain structure like that of BeCl2- Each beryllium is surrounded tetrahedrally by four hydrogens, but each hydrogen has just two berylliums on one side (Figure 5.10, overleaf). [Pg.51]

I and Group II except Be), macromolecular (Be and Al) or molecular (boron and Groups IV-VII/14-17.) Salt-like hydrides, which have the characteristics of ionic compounds, and macromolecular hydrides, react with water giving em aqueous or solid hydroxide. [Pg.59]

Usually the Zigler-Natta co-ordination initiator system is used to graft oc-olefins onto other polymers to give stereo block/graft copolymers, which contain isotactic/atactic sequences. In the Zigler-Natta co-ordination catalyst [69] system, the diethyl aluminium hydride reacts with pendant groups to form macromolecular trialkyl aluminium. The residual initiator is freed by extraction methods. [Pg.242]

Chemically modified silica fillers with grafted methyl groups or methyl and silicon hydride groups, influenced the micro- and macrostructures of various copolymers. Changes in cross-linking, orderliness, crystallinity, microtacticity and conformation of macromolecules have been detected in the presence of fillers. Surface functionality of the silica filler determines the disposition of macromolecular chains at the interface. [Pg.110]

Radicals constitute another type of reactive intermediate that have found considerable use in synthesizing seven-membered rings. Pat-tenden provides a rather remarkable example of the way this process can be incorporated into a macrocyclization-transannulation cascade to prepare polycycles. Tributyltin hydride generates a radical intermediate which, upon macromolecular ring closure and two subsequent transannular processes, provides a tricyclic product (Eq. 8)." Aside... [Pg.9]

Because of the small number of truly active centers, the molar masses of the polymers obtained are very high to control the sample molar mass, polymerizations are carried out in the presence of transfer agents and mostly H2 is used upon reaction with a macromolecular alkyltitanium, titanium hydride is produced that is able to reinitiate polymerization ... [Pg.348]

Hydrogen combines with most of the chemical elements. Here we concentrate on binary hydrides of the typical elements, ignoring those of the transition elements, lanthanides and actinides, which often have metallic properties and so resemble alloys. Binary hydrides are compounds of hydrogen and one other element. A useful classification of the highest hydrides of the typical elements is shown in Figure 5.9. It divides them into three classes salt-like, macromolecular and molecular. [Pg.50]


See other pages where Macromolecular hydrides is mentioned: [Pg.51]    [Pg.52]    [Pg.51]    [Pg.52]    [Pg.105]    [Pg.96]    [Pg.1374]    [Pg.453]    [Pg.25]    [Pg.176]    [Pg.141]    [Pg.189]    [Pg.66]    [Pg.5]    [Pg.345]    [Pg.349]    [Pg.737]    [Pg.51]    [Pg.172]   


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