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Chemical compound (SiH4)
somewhat similar to that of acetic acid. Silane is of practical interest as a precursor to elemental silicon. Silanes with alkyl groups are effective water
Silane
Class of organosilicon compounds with the formula SiR4
Most silanes contain Si-C bonds, and are discussed under organosilicon compounds. Some contain Si-H bonds and are discussed under hydrosilanes. Silane SiH
Silanes
Class of antimicrobials developed by Dow Corning in the 1970s
produce concentrated Silane-Quats that range from 42% to 72% active ingredient by weight, with the remainder of the formulation being silanes, alkylamines and
Silane_quats
Chemical compounds with at least one silicon atom
The names silanes and boranes are his, based on analogy with the alkanes. The Moissan and Smiles method of preparation of silanes and silane derivatives
Silicon_compounds
Chemical compounds used in adhesives and sealants
Silyl-modified polymers (SMP; also silane-modified polymers, modified-silane polymers, MS polymers, silane-terminated polymers, etc.) are polymers terminating
Silyl_modified_polymers
Alloy of silicon and iron
Ferrosilicon is an alloy of iron and silicon. It has a typical silicon content of 15–90% by weight and a high proportion of iron silicides. Ferrosilicon
Ferrosilicon
Spanish energy company
Naturgy Energy Group S.A., formerly Gas Natural Fenosa (Spanish pronunciation: [ˈɡas natuˈɾal feˈnosa]), is a Spanish multinational natural gas and electrical
Naturgy
reactions involving thiols and tertiary silanes or disilanes. As well as being coupled to each other, tertiary silanes can be coupled with carboxylic acids
Dehydrogenative coupling of silanes
Dehydrogenative_coupling_of_silanes
Chemical compound
More commonly used than the parent vinylsilane are vinyl-substituted silanes with other substituents on silicon. In the area of organic synthesis, vinylsilanes
Vinylsilane
Chemical compound
Trichloro(dichlorophenyl)silane is a family of chemical compounds, all with formula Si(C6H3Cl2)Cl3. It is used as an intermediate in the manufacture of
Trichloro(dichlorophenyl)silane
Trichloro(dichlorophenyl)silane
Void between celestial bodies
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Outer_space
Neologism questioning importance of carbon for life
Water as a solvent would also react with silanes, but again, this only matters if for some reason silanes are used or mass-produced by such organisms
Carbon_chauvinism
Chemical compound
is a colorless liquid. It is the simplest tetraorganosilane. Like all silanes, the TMS framework is tetrahedral. TMS is a building block in organometallic
Tetramethylsilane
Organometallic chemical
Octadecyltrichlorosilane Names Preferred IUPAC name Trichloro(octadecyl)silane Other names Trichlorooctadecylsilane Stearyltrichlorosilane Identifiers
Octadecyltrichlorosilane
Chemical compound
trans-isomers of 2-, 3-, 4-chlorodimethyl(methylcyclohexyl)silanes and chlorodimethyl(cyclohexylmethyl)silane. The poor selectivity is due to the migration of the
1-Methylcyclohexene
Chemical compound
Amino-functional silanes such as (3-aminopropyl)triethoxysilane and epoxy-functional silanes are used for the same purpose. The silane group attaches to
Vinyltriethoxysilane
unsaturated silane controls the site of reaction and stereoselectivity. Formation of the new carbon-carbon bond is at the γ position of allyl silanes and the
Electrophilic substitution of unsaturated silanes
Electrophilic_substitution_of_unsaturated_silanes
Special type of hyperconjugation
mechanisms of hydrolysis of such compounds. They prepared a series of α-silanes and γ-silanes and tested their reactivity in different pH (acidic and basic regime)
Negative hyperconjugation in silicon
Negative_hyperconjugation_in_silicon
Chemical compound
Methyltrimethoxysilane Names Preferred IUPAC name Trimethoxy(methyl)silane Other names MTM, Trimethoxymethylsilane Identifiers CAS Number 1185-55-3 Y 3D
Methyltrimethoxysilane
Natural or synthetic substance that is significantly longer than it is wide
of the carbon atoms are replaced by silicon atoms, so-called poly-carbo-silanes. The pyrolysis yields an amorphous silicon carbide, including mostly other
Fiber
American economist
Robert W. Vishny, Rafael La Porta, Simeon Djankov and Florencio Lopez de Silanes, Shleifer has also made significant contributions to the study of corporate
Andrei_Shleifer
Organic compound
An ylide (/ˈɪlaɪd/) or ylid (/ˈɪlɪd/) is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached
Ylide
Mexican footballer (born 1970)
Carlos López de Silanes (born April 18, 1970) is a Mexican former footballer who played as a defender. He was a member of the Mexico national football
Carlos López (footballer, born 1970)
Carlos_López_(footballer,_born_1970)
Chemical compound
Tetrakis(trimethylsilyl)silane is the organosilicon compound with the formula (Me3Si)4Si (where Me = CH3). It is a colorless sublimable solid with a high
Tetrakis(trimethylsilyl)silane
Tetrakis(trimethylsilyl)silane
react extensively with metal silanes, producing either M–C–O–Si or Si–C–O–M, depending on the reagents. Transition metal silane complexes are coordination
Transition metal silyl complexes
Transition_metal_silyl_complexes
Chemical compound
Tetrakis(trimethylsilyloxy)silane (TTMS) is an organosilicon compound with the formula Si[OSi(CH3)3]4. This colourless liquid is used as a reagent in organic
Tetrakis(trimethylsilyloxy)silane
Tetrakis(trimethylsilyloxy)silane
Chilean actress, author, and screenwriter
Patricia Paola Fernández Silanes (born 23 June 1971), better known as Nona Fernández, is a Chilean actress, author, and screenwriter. She is a recipient
Nona_Fernández
Chemical compound
one of the most useful compounds of germanium. Like the related compounds silane and methane, germane is tetrahedral. It burns in air to produce GeO2 and
Germane
against salt attack, such as efflorescence and spalling. Uses silanes or modified silanes. These are a type of penetrating sealer, which penetrate deeply
Stone_sealer
Chemical compound of hydrogen and oxygen
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Water
American chemical company
The company produces silicones, resins, specialty chemicals, siloxanes, silanes, additives, ceramics and quartz. The company traces its origins back to
Momentive
American economist
Andrei Shleifer, and many also with Rafael La Porta, Florencio Lopez-de-Silanes, and Shleifer, known as LLSV) have been extremely influential, especially
Robert_W._Vishny
Chemical compound with hydrogen and carbon group atoms
hydrocarbons, such as silanes SinH2n+2 are known for n = 1–8, in which thermal stability decreasing as n increases (e.g. silane SiH4 and disilane Si2H6)
Group_14_hydride
Unmanned US experimental hypersonic aircraft, 1991-2000
Simone, Domenico; Bruno, Claudio (July 2008). "Review of the potential of silanes as rocket/scramjet fuels". Acta Astronautica. 63 (1): 379–388. doi:10.1016/j
NASA_X-43
Chemical compound
Tris(trimethylsilyl)silane is the organosilicon compound with the formula (Me3Si)3SiH (where Me = CH3). It is a colorless liquid that is classified as
Tris(trimethylsilyl)silane
Sequence of organic compounds with similar chemical properties
series (e.g. VnO2n − 1 for 2 < n < 10), called Magnéli phases, as do the silanes, SinH2n + 2 (with n up to 8) that are analogous to the alkanes, CnH2n +
Homologous_series
silicides. This method produces a mixture of silanes, which required separation on a high vacuum line. The silanes (SinH2n+2) are less thermally stable than
Binary silicon-hydrogen compounds
Binary_silicon-hydrogen_compounds
Chemical compound
fungicide. Its chemical formula is C26H58NO3SiCl. It is also used as a silane coupling agent. Dimethyldioctadecylammonium chloride 3-(Trimethoxysilyl)propyl
Dimethyloctadecyl(3-trimethoxysilylpropyl)ammonium chloride
Dimethyloctadecyl(3-trimethoxysilylpropyl)ammonium_chloride
Addition of Si-H bonds across unsaturated bonds
unsaturated organic compounds. Alkenes and alkynes give alkyl and vinyl silanes; aldehydes and ketones give silyl ethers, while esters provide alkyl silyl
Hydrosilylation
Media under editorial control of a government
doi:10.1177/1464884917724621. S2CID 149138184. Djankov, La Porta, Lopez-de-Silanes & Sheleifer, 2002, 28-29 Djankov, McLeish, Nenova & Shleifer, 2003, p.
State_media
Vehicle not powered by petrol or diesel
and requires special safety measures due to its high rotational speed. Silanes higher than heptasilane can be stored like gasoline and may also work as
Alternative_fuel_vehicle
Class of chemical compounds
hexamethyldisilane: RCOCl + tms−tms → RC(O)tms + tmsCl Some acyl silanes are prepared by oxidation of a suitable silanes. Acylsilanes are starting compounds in the Brook
Acylsilane
Chemical naming suffix
non-metals end with the suffix -ane: the hydrides of silicon are called silanes (SiH4); the hydrides of boron are boranes (B2H6). The final "-e" is dropped
-ane
especially tires. SI363 is the trade name of a silane bonding agent in the trialkoxymercaptoalkyl-silane class and of formula SH(CH2)H3Si(OCHH2CHH3)(O
Si_363
Chemical compound
Trichloro(chloromethyl)silane is a compound with formula Si(CH2Cl)Cl3. Organosilicon#Silyl_halides v t e
Trichloro(chloromethyl)silane
Chemical compound
deprotection of a peptide as it can act as a hydride donor in acidic conditions. Silanes may be preferred as scavengers in place of sulfur-based scavengers. Pearson
Triisopropylsilane
Lowest temperature at which a substance spontaneously combusts
780±5[C] Paper 218–246 °C (424–475 °F) Phosphorus (white) 34 °C (93 °F) [A][B] Silane 21 °C (70 °F) or below Strontium 1,075 °C (1,967 °F) 1075±120[C] Tin 940 °C
Autoignition_temperature
Si–OH functional group in silicon chemistry
dioxiranes, and potassium permanganate (for hindered silanes). In the presence of metal catalysts, silanes undergo hydrolysis: R3Si–H + H2O → R3Si–OH + H2
Silanol
Family of chemical substances
are used to compatibilize a polymeric system and a filler (inorganic). Silane coupling agents are denoted by the general monomeric structure X-R-Si-(OR)3
Adhesion_promoter
Class of organosilicon compounds of the form R3Si–O–CR=CR2
functional group R3Si−O−CR=CR2, composed of an enolate (R3C−O−R) bonded to a silane (SiR4) through its oxygen end and an ethene group (R2C=CR2) as its carbon
Silyl_enol_ether
Chemical compound
The decomposition is usually facilitated by mixing WF6 with hydrogen, silane, germane, diborane, phosphine, and related hydrogen-containing gases. WF6
Tungsten_hexafluoride
Attachment of an organosilyl group to some chemical species
ISBN 978-0-471-23896-6. Arkles, Barry (1977). "Tailoring Surfaces with Silanes". Chemtech. 7: 766–777 – via ResearchGate. Žuvela, Petar; Skoczylas, Magdalena;
Silanization
Chemical compound
composed of Na+ and H− ions, in contrast to molecular hydrides such as borane, silane, germane, ammonia, and methane. It is an ionic material that is insoluble
Sodium_hydride
Matter with biological processes
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Life
Chemical compound
ISBN 978-1138561632. "Disilane CAS#:1590-87-0". Barry Arkles "Silicon Compounds, Silanes" in Kirk-Othmer Encyclopedia of Chemical Technology John Wiley & Sons,
Disilane
Chemical compound
sodium aluminium hydride (NaAlH4) (or other alkali metal hydride) to produce silane (SiH4). In 2001 it was listed by New Jersey authorities as a hazardous substance
Silicon_tetrafluoride
generally an organic compound, but experiments have been performed using silanes – are replaced with fluorine, by treatment with antimony trifluoride in
Swarts_fluorination
4-dichlorobutene Triamiphos Triazofos Trichloro(chloromethyl)silane Trichloro(dichlorophenyl)silane Trichloroacetyl chloride Trichloroethylsilane Trichloronate
EPA list of extremely hazardous substances
EPA_list_of_extremely_hazardous_substances
Chemical compounds containing at least one silicon-chlorine bond
a group of reactive, chlorine-containing chemical compounds, related to silane (SiH4) and used in many chemical processes. Each such chemical has at least
Chlorosilane
Thionyl chloride 7719-09-7 250 Trichloro(chloromethyl)silane 1558-25-4 100 Trichloro(dichlorophenyl)silane 27137-85-5 2500 Trichlorosilane 10025-78-2 5000
Highly_hazardous_chemical
Organic compounds of the form RC(=O)NR′R″
Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone Silether
Amide
Class of chemical compounds
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
Boranes
Species of scorpion
antivenom, Anascorp [Antivenin Centruroides (scorpion) F(ab′)2, Laboratorios Silanes, Instituto Bioclon SA de CV], received FDA approval on August 3, 2011,
Arizona_bark_scorpion
Organic compound (H3C–CH3)
'dicarbane', 'tricarbane', and 'tetracarbane' as recommended for analogues of silane, 'disilane'; phosphane, 'triphosphane'; and sulfane, 'tetrasulfane'." "Ethane
Ethane
Chemical compound
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
1-Butyne
Chemical compounds
1002/047084289X.rp101. ISBN 0-471-93623-5. Colvin, Ernest W. (1981). "Silanes as Reducing Agents". Silicon in Organic Synthesis. pp. 325–336. doi:10
Hydrosilanes
Organometallic compound containing carbon–silicon bonds
toward oxygen and water, at least under ambient conditions. Unsaturated silanes are susceptible to electrophilic substitution. Some strong acids will protodesilate
Organosilicon_chemistry
Chemical compound with formula NaCl
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Sodium_chloride
German chemist (1800–1882)
form. He was the first to prepare several inorganic compounds, including silane and silicon nitride. Wöhler is also known for seminal contributions in organic
Friedrich_Wöhler
Hydrocarbon compound with the formula C8H18
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
Octane
chemicals and an appropriately receptive surface. Often bi-functional silanes are used in which one termination of the molecule is reactive. For example
Molecular_vapor_deposition
Chemical compound
when the contaminated brine is electrolyzed. Like other chlorosilanes or silanes, silicon tetrachloride reacts readily with water: SiCl4 + 2 H2O → SiO2
Silicon_tetrachloride
Possible alternative biochemicals used by life forms
varied coordination number. Silanes, silicon analogues to the alkanes, react rapidly with water, and long-chain silanes spontaneously decompose. Consequently
Hypothetical types of biochemistry
Hypothetical_types_of_biochemistry
Organosilicon compound
convenient to operate. Trimethoxysilane is an important substance for producing silane coupling agents. It contains both hydrolyzable siloxane bonds as well as
Trimethoxysilane
Chemical compounds in which hydroxyl group is attached directly to an aromatic ring
diazonium salts, the salts are converted to phenol by the oxidation of aryl silanes—an aromatic variation of the Fleming-Tamao oxidation catalytic synthesis
Phenols
Chemical compound
abbreviated DMCS, is a chemical compound with the formula (CH3)2SiHCl. It is a silane, with a silicon atom bonded to two methyl groups, a chlorine atom, and a
Chlorodimethylsilane
Any organic compound having a sulfanyl group (–SH)
Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone Silether
Thiol
Inert carbon-oxygen gas
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Carbon_dioxide
Type of plastic
the temperature may vary from 160 °C to 220 °C. Silane crosslinking (PE-Xb): In the presence of silanes (e.g. trimethoxyvinylsilane) polyethylene can initially
Cross-linked_polyethylene
Flammable organic fuel (C4H10)
'dicarbane', 'tricarbane', and 'tetracarbane' as recommended for analogues of silane, 'disilane'; phosphane, 'triphosphane'; and sulfane, 'tetrasulfane'. W.
Butane
Organic compound
Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone Silether
Urea
High purity form of silicon
Polysilicon layers can be deposited using 100% silane at a pressure of 25–130 Pa (0.19–0.98 Torr) or with 20–30% silane (diluted in nitrogen) at the same total
Polycrystalline_silicon
Capital of Lower Saxony, Germany
Blume (born 1969), engineering technology professor, works on silica and silane chemistry. Herbert Bötticher (1928-2008), actor Walter Bruch (1908–1990)
Hanover
Law created by judicial precedent
of Law Assistance Impact Assessment: Armenia Porta, Rafael La; Lopez‐de‐Silanes, Florencio; Shleifer, Andrei; Vishny, Robert W. (1998). "Law and Finance"
Common_law
SiC silicon carbide 409–21–2 SiCl4 silicon(IV) chloride 10026–04–7 SiH4 silane 7803–62–5 SiI4 silicon(IV) iodide 13465–84–4 SiO2 silicon(IV) dioxide silica
Glossary_of_chemical_formulae
Method of depositing thin films onto a substrate
using a combination of silicon precursor gasses like dichlorosilane or silane and oxygen precursors, such as oxygen and nitrous oxide, typically at pressures
Plasma-enhanced chemical vapor deposition
Plasma-enhanced_chemical_vapor_deposition
Chemical compound (C6H14)
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
Hexane
Chemical group (>N–C(=O)–O–)
Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone Silether
Carbamate
Chemical compound
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
Ammonia
Chemical compound
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
Semiheavy_water
Inorganic compound with the formula FeO
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Iron(II)_oxide
Molecule containing main group elements with more than eight valence electrons
nucleophilic attack of the tetracoordinated silane by the nucleophile (or water) in which a hypervalent pentacoordinated silane is formed. This is followed by a
Hypervalent_molecule
Process
types of silanes, including aminosilanes, octadecyltrimethoxysilane and fluoalkyl silanes. However, the nature of the attachment of the silane molecules
Silanization of silicon and mica
Silanization_of_silicon_and_mica
Chemical group (–N=C=O)
Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone Silether
Isocyanate
Chemical acid found in vinegar
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Acetic_acid
American economist
Lopez-de-Silanes; Andrei Shleifer (2007). The Economic Consequences of Legal Origins. National Bureau of Economic Research. La Porta, Rafael; Lopez-De-Silanes
Rafael_La_Porta
Method used to apply surface coatings
usually performed in LPCVD systems, with either pure silane feedstock, or a solution of silane with 70–80% nitrogen. Temperatures between 600 and 650 °C
Chemical_vapor_deposition
Chemical compound
alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18 Si9H20 Si10H22 more
Pentaoxidane
Laboratory technique
Nuclear Resonance Shielding Values by "Internal Referencing" with Tetramethyl-silane". The Journal of Physical Chemistry. 62 (9): 1151–1152. Bibcode:1958JPhCh
Nuclear magnetic resonance spectroscopy
Nuclear_magnetic_resonance_spectroscopy
Hexagonal lattice made of carbon atoms
Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical Cyclopropenone
Graphene
SILANES
SILANES
SILANES
SILANES
Girl/Female
Hebrew
Fiery-winged. The name Seraphina comes from 'seraphim', who were the most powerful angels.
Girl/Female
Tamil
Daughter
Boy/Male
Danish, Finnish, German, Swedish
Active; Sprightly
Boy/Male
Tamil
Shanyuth | ஷாநà¯à®¯à¯à®¤
Benevolent
Boy/Male
Muslim
Determined
Girl/Female
Indian
Excellent, Highest social standing, Tall, Towering (Celebrity Name: Pooja Bedi)
Girl/Female
British, English
Twig Head
Girl/Female
British, English
Wealthy Defender
Girl/Female
Indian, Telugu
Silent
Boy/Male
Hebrew
Shall be redeemed.
SILANES
SILANES
SILANES
SILANES
SILANES