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With silane

Germane is used, along with silane, SiH, to make amorphous or crystalline siUcon solar cells having an extended solar energy absorption range to increase conversion efficiency. [Pg.281]

Clays. Clay, which is generally considered a mild reinforcing filler, is used sparingly in tires. It is most often used in white sidewalls or in low performance tires. Clay toimage in tires worldwide is estimated at 36,000 t annually. Clay can also be coupled to mbber with silanes, and this is the more popular version used in tires. Even with silane coupling, clays are still a weak reinforcing filler compared to both carbon black and siUca. [Pg.250]

Fumed sihca, a highly reinforcing filler, is usually added in amounts ranging from 6 to 20%. Sihca is most often used when a high strength sealant is desired. Several sihcas having different surface areas are available and surface treatment with silanes may be used as well. [Pg.310]

Although the most popular of the processes described above (PAA and CAA) perform very well, there is a continuing need to develop processes that are less hazardous (no chromates, no strong acids or bases) or that are suitable for treatment of repair areas in the field. Two of these treatments are grit blasting coupled with silane coupling agents and sol-gel. [Pg.971]

Silane Flood horizontal panel with silane Using clean acid brushes, brush... [Pg.973]

Attempts have been made to distinguish between these theories on the basis of the AH° and values anticipated for the two theories, but it may be illusory to think of them as independent alternatives. The eavity model has been criticized on the basis that it eannot account for certain observations such as the denaturing effect of urea, but it must be noted that the cavity theory includes not only the cavity term AAy, but also a term (or terms) for the interaction of the solutes and the solvent. A more eogent objeetion might be to the extension of the macroseopic concepts of surface area and tension to the molecular scale. A demonstration of the validity of the cavity concept has been made with silanized glass beads, which aggregate in polar solvents and disperse in nonpolar solvents. [Pg.396]

Silicon cluster reactions are an example of a newly emerging field of research which is very amenable to study with electronic structure methods. This exercise will examine the potential surface for silicon cation reacting with silane (SiH4). Such reactions are central to the growth of large silicon clusters, which occurs by sequential additions of -SiHj ... [Pg.199]

Both PMPPIC and PS contain benzene rings, and their delocalized II electrons provide strong interactions. As a result, that there is an adhesion between PMPPIC and PS (Fig. 8). Comparing both methods, treatment with silanes or treatment with isocyanates, it is obvious that the isocyanatic treatment is more effec-... [Pg.797]

Organofunctional group Chemical structure OSi-Specialties Germany GmbH product Critical surface tension of glass with silane treatment [dyne/cm] Applied polymers (abbreviations according ASTM 1600)... [Pg.798]

In [276] the properties of kaolin-filled polyethylenes were investigated. The filler was pre-treated with silanes of two kinds, vinyl triethoxysilane (VTES) (I) and gamma-methacryloxypropyl trimethoxysilane (II). The results are presented in Table. 9. [Pg.41]

A common deposition reaction, used widely in semiconductor processing, combines ammonia with silane as the silicon source ... [Pg.282]

Nitrous oxide (N2O) is another common oxidizer, which is used with silane in a plasma at 200-350°C, with ratios of N2O to silane of 15/1 to 30/1.0 1 It is also used with dichlorosilane in a deposition temperature range of 850-950°C and at low pressure (<1 Torr) [i4]... [Pg.303]

CVD Reactions. MoSi2 is usually deposited by the reaction of a molybdenum halide with silane. The simplified reactions are as... [Pg.329]

Tantalum disilicide, TaSi2, is very refractory and chemically resistant. It is deposited from the reaction of the chloride, TaCl5, with silane (SiH4), or dichlorosilane (SiH2Cl2), the latter precursor being preferred. The reaction takes place in a plasma as follows ... [Pg.330]

Use of highly dispersible silica together with silanes and high vinyl S-SBR has met all critical magic triangle requirements like good dry and wet traction, reduction in tread wear, and low RR. [Pg.921]

Some reductions with silanes have already been described in previous chapters (in Section 4.8 reaction of 356 to give 359 in Section 5.4 reaction of 121 to give 717, 718 to 719 in Section 12.1 reaction of 1790 to give 1791). Because of the many applications of such reductions with silanes in the chemical literature only a selected number of examples can be given in this chapter. [Pg.267]


See other pages where With silane is mentioned: [Pg.24]    [Pg.41]    [Pg.47]    [Pg.167]    [Pg.461]    [Pg.747]    [Pg.753]    [Pg.163]    [Pg.209]    [Pg.102]    [Pg.404]    [Pg.411]    [Pg.412]    [Pg.427]    [Pg.632]    [Pg.204]    [Pg.797]    [Pg.534]    [Pg.1201]    [Pg.698]    [Pg.718]    [Pg.1053]    [Pg.4]    [Pg.267]    [Pg.269]    [Pg.271]   
See also in sourсe #XX -- [ Pg.195 , Pg.196 , Pg.197 ]




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Acyl radical with tris silane

Adhesion promoters mechanism with silanes

Aldehydes reaction with silane carbanions

Aldehydes reaction with silanes

Aldehydes reactions with allylic silanes

Aldehydes, a-methyl reaction with enol silanes

Aldehydes, p-alkoxy reaction with enol silanes

Aldehydes, reduction with silanes

Alkenes, reduction with silanes

Aminals reaction with enol silanes

Ammonium fluoride, tetrabutylcatalyst enol silane reaction with aldehydes

Annulation with Allylic Silanes

Atomic reaction with silane

Benzenes with silanes

Benzonitrile oxide reaction with silane

Bromine with silanes

Carbonates, a-methoxyreaction with enol silanes

Carbonates, a-methoxyreaction with enol silanes Lewis acid mediated

Carbonyl compounds reaction with enol silanes

Cobalt, octacarbonylbiscatalyst silane reaction with carbonyl compounds

Cross with allyl silane

Cross with vinyl silane

Cumulative Subject reactions with enol silanes

Dienes reaction with silanes

Electrophiles, reaction with allyl silane

Enol silanes reaction with acetals

Enol silanes reaction with aldehydes

Enol silanes reaction with aldehydes, diastereoselectivity

Enol silanes reaction with aldehydes, stereoselectivity

Enol silanes reaction with chiral a-alkoxy aldehydes

Enol silanes reaction with chiral a-methyl aldehydes

Enol silanes reaction with chiral acetals

Enol silanes reaction with chiral azetinones

Enol silanes reaction with dimethyl acetals

Enol silanes reaction with imines

Enol silanes with enones

Enol silanes, nonstereogenic reaction with aldehydes

Enol silanes, nonstereogenic reaction with aldehydes, diastereoselectivity

Enol silanes, stereogenic reaction with aldehydes

Enol silanes, stereogenic reaction with chiral azetinones

Epoxides reaction with allyl silanes

Esters (cont reaction with allylic silanes

Fluoride, tetrabutylammonium reaction with silanes

Fluorides enol silane reaction with aldehydes

Grignard reagents, reactions with silanes

Group reaction with silanes

Hydroxyphenyl)Silanes with Different Types of Bioactivity

Imines (cont reactions with unsaturated silanes

Imines with allyl silanes

Iminium ions reaction with enol silanes

Ketones, reaction with silane carbanions

Ketones, reduction with silanes

Liquid-phase silanization with

Lithium, alkyl-: addn. to 1-alkenyl silanes halogen-metal exchange with

Metal hydrido complexes with silanes

Methane compared with silane

Nickel sulfide silane reaction with carbonyl compounds

Nitrones reaction with enol silanes

Oxonium ions reaction with enol silanes

Phosphine oxides reactions with silanes

Photochemical Reaction with Silanes

Radical photochemical reaction with silane

Radicals reaction with silanes

Reaction with silane carbanions

Reactions of Silanes with CO

Reactions of Silanes with Transition Metals

Reactions of silanes with

Reactions of with Primary and Secondary Silanes

Reactions with Silane (SiH

Reactions with Silanes and Alkali Aluminiumhydrides

Reactions with silanes

Reduction With Silanes (Hydrosilylation)

Reduction conjugate, with silanes

Reduction of CO2 with silanes

Rhodium, chlorotris catalyst silane reaction with carbonyl compounds

Silane Ligands and Exchange with cis Hydrides

Silane carbanions, reaction with aldehydes Silanes

Silane carbanions, reaction with aldehydes ketones

Silane coatings with active ions

Silane coatings with active species

Silane coupling agents reaction with filler surfaces

Silane etherification with

Silane reaction with silyl radical

Silane reaction with thiyl radical

Silane with nitrogen ions

Silane with oxygen reactive ions

Silane with silicon ions

Silane with transition metal ions

Silane, a-phenylthiomethyltrimethylreaction with alkyl halides

Silane, a-phenylthiomethyltrimethylreaction with alkyl halides synthesis of aldehydes

Silane, allenylreaction with acetals

Silane, allenylreaction with acetals Friedel-Crafts reaction

Silane, allenylreaction with acetals Mannich reaction

Silane, allenylreaction with acetals chiral

Silane, allenylreaction with acetals fluoride ion catalysis

Silane, allenylreaction with acetals reactions

Silane, allenylreaction with acetals syn-anti selectivity

Silane, allenylreaction with acetals synthesis

Silane, allyl dimethylreaction with BuLi/TMEDA

Silane, chlorotrimethylreaction with conjugated ketones

Silane, chlorotrimethylreaction with conjugated ketones 1,4-addition

Silane, crotylreaction with iminium salts

Silane, crotylreaction with iminium salts synthesis

Silane, ethynylreaction with acetals

Silane, methyldiphenylchlororeaction with lithium ester enolates

Silane, methyldiphenylchlororeaction with lithium ester enolates regiochemistry of silylation

Silane, propargylacylation reaction with acetals

Silane, propargylacylation reaction with aldehydes

Silane, propargylacylation reaction with ketals

Silane, propargylacylation reaction with ketones

Silane, propargyltrimethylcondensation with acyl cyanide

Silane, triethylionic hydrogenation reaction with unsaturated esters

Silane, triisopropylreaction with acyl chloride

Silane, triisopropylreaction with acyl chloride reductive decarboxylation

Silane, trimethyl protection with

Silane, trimethylreaction with sulfonyl carbanions

Silane, vinylepoxidation reaction with acetals

Silane, vinylepoxidation reaction with aldehydes

Silane, vinylepoxidation reaction with carbonyl compounds

Silane, vinylepoxidation reaction with glycine cation equivalents

Silane, vinylepoxidation reaction with ketals

Silane, vinylepoxidation reaction with ketones

Silane, vinylepoxidation reaction with methoxymethyl chloride

Silanes alkenyl, reactions with electrophiles

Silanes allyl, reactions with electrophilic intermediate

Silanes allylic, reaction with electrophiles

Silanes aryl, ipso substitution with electrophile

Silanes cross-coupling with halides

Silanes performance with

Silanes reaction with alcohols

Silanes reaction with alkenes

Silanes reaction with carbonyl compounds

Silanes reaction with epoxides

Silanes reaction with iminium salts

Silanes reaction with metal halides

Silanes reactions with electrophiles

Silanes vinyl, reaction with electrophiles

Silanes with acyl halides

Silanes with aromatic bridges

Silanes with halogens

Silanes with nitrobenzenes

Silanes, acylreaction with sulfonyl carbanions

Silanes, acylreaction with sulfonyl carbanions synthesis

Silanes, acylreaction with sulfonyl carbanions via Claisen rearrangement

Silanes, allenyl annulations reactions with a,p-unsaturated carbonyl compounds

Silanes, allyl, reaction with

Silanes, comparison with carbon

Silanes, comparison with carbon compounds

Silanes, dimethylfluororeaction with alkenyl iodides

Silanes, dimethylfluororeaction with alkenyl iodides organopalladium catalysis

Silanes, reduction with

Silica compounds silanization reaction with

Silica reaction with silanes

Silicon Reaction of Silanes with Ni, Rh, Pd, Pt

Silicon with silanes

Silyl radical with silanes

Silylene with silanes

Skin contact with silane

Spiroketal reduction with Silane-Lewis acid

Subject reactions with enol silanes

Surface modification with silane coupling agent

Thiyl radical with silane

Transition metal ions, reaction with silane

Treatment with silane coupling reagent

Tris silane with acid chloride

Tris silane with acyl chlorides

Tris silane with aldehyde

Tris silane with alkyl bromide

Tris silane with alkyl chloride

Tris silane with alkyl halide

Tris silane with alkyl iodide

Tris silane with alkyl radical

Tris silane with alkyne

Tris silane with ammonia

Tris silane with aryl iodide

Tris silane with oxygen

Tris silane with phenyl radical

Tris silane with primary amines

Tris silane with sulfone

Tris silane with water

With silane coupling agents

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