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Chemical compound
Silicon disulfide is the inorganic compound with the formula SiS2. Like silicon dioxide, this material is polymeric, but it adopts a 1-dimensional structure
Silicon_disulfide
Chemical compound
polymer, in contrast to silicon disulfide, which is a one-dimensional polymer. The Ge-S distance is 2.19 Å. Germanium disulfide was first found in samples
Germanium_disulfide
Functional group with the chemical structure R–S–S–R′
In chemistry, a disulfide (or disulphide in British English) is a compound containing a R−S−S−R′ functional group or the S2−2 anion. In inorganic chemistry
Disulfide
Chemical compound
Molybdenum disulfide (or moly) is an inorganic compound composed of molybdenum and sulfur. Its chemical formula is MoS2. The compound is classified as
Molybdenum_disulfide
Oxide of silicon
Silicon dioxide, also known as silica, is an oxide of silicon with the chemical formula SiO2, and is commonly found in nature as quartz. In many parts
Silicon_dioxide
Chemical compounds with at least one silicon atom
Silicon compounds are compounds containing the element silicon (Si). As a carbon group element, silicon often forms compounds in the +4 oxidation state
Silicon_compounds
Poisonous and flammable gas
nonmetal sulfides, e.g. aluminium sulfide, phosphorus pentasulfide, silicon disulfide liberate hydrogen sulfide upon exposure to water: 6 H2O + Al2S3 →
Hydrogen_sulfide
Central atom with four substituents located at the corners of a tetrahedron
motif, the two tetrahedra share a common edge. The inorganic polymer silicon disulfide features an infinite chain of edge-shared tetrahedra. Inversion of
Tetrahedral molecular geometry
Tetrahedral_molecular_geometry
Chemical compound
radical chain reactions. It was first prepared by alcoholysis of silicon disulfide and purified by distillation: 3 (CH3)3COH + SiS2 → [(CH3)3CO]3SiSH
Tris(tert-butoxy)silanethiol
Chemical element with atomic number 32 (Ge)
appearance to silicon. It is a metalloid (sometimes considered a nonmetal) in the carbon group that is chemically similar to silicon. Like silicon, germanium
Germanium
System of detailed crystal structure classification
P6222 C41 → C14 C42 SiS2 Ibam Silicon disulfide structure C43 ZrO2 P21/c Baddeleyite structure C44 GeS2 Fdd2 Germanium disulfide structure C46 AuTe2 Pma2 Krennerite
Strukturbericht_designation
Chemical compound
crystallography. The material is a polymer with the same connectivity as silicon disulfide, featuring tetrahedral magnesium centres, each surrounded by bridging
Dimethylmagnesium
Index of articles associated with the same name
non-rechargeable battery with lithium as an anode Lithium–air battery Lithium–iron disulfide battery Lithium–sulfur battery Nickel–lithium battery Rechargeable lithium
Lithium_battery
Particle with size less than 100 nm
Platinum nanoparticle Quantum dot Self-assembly of nanoparticles Silicon quantum dot Silicon Silver Nano Sol–gel process Synthesis of nanoparticles by fungi
Nanoparticle
Inorganic silicon compound
[Si2OS6]6−. Silicon is tetrahedral in all thiosilicates and sulfur is bridging or terminal. Formally such materials are derived from silicon disulfide in analogy
Thiosilicate
Class of organosilicon compounds
Driess, Matthias (2015-07-06). "From Silylone to an Isolable Monomeric Silicon Disulfide Complex". Angewandte Chemie International Edition. 54 (35): 10254–10257
Silylone
Chemical compound
ethanol and carbon disulfide. Cyclohexasilane is an important precursor for the deposition of silicon layers from liquid silicon inks in the semiconductor
Cyclohexasilane
Chemical compound
Silicon monosulfide is a chemical compound of silicon and sulfur. The chemical formula is SiS. Molecular SiS has been detected at high temperature in
Silicon_monosulfide
Any organic compound having a sulfanyl group (–SH)
an oxidation reaction can generate a cystine unit with a disulfide bond (−S−S−). Disulfide bonds can contribute to a protein's tertiary structure if
Thiol
Organic compounds of the form >C=O
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Ketone
Chemical group (–OH)
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Hydroxy_group
Chemical group (–CH3) derived from methane
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Methyl_group
Periodic table group
carbon dioxide. Carbon forms a disulfide an a diselenide. Silicon forms several hydrides; two of them are SiH4 and Si2H6. Silicon forms tetrahalides with fluorine
Carbon_group
Chemical element with atomic number 16 (S)
at 100 °C (212 °F). Sulfur is insoluble in water but soluble in carbon disulfide and, to a lesser extent, in other nonpolar organic solvents, such as benzene
Sulfur
semiconductor materials differ in their properties. Thus, in comparison with silicon, compound semiconductors have both advantages and disadvantages. For example
List of semiconductor materials
List_of_semiconductor_materials
Class of minerals containing sulfide or disulfide as the major anion
sulfide minerals are a class of minerals containing sulfide (S2−) or disulfide (S2−2) as the major anion. Some sulfide minerals are economically important
Sulfide_mineral
Chemical compound
and can be stored under water. P4 is soluble in benzene, oils, carbon disulfide, and disulfur dichloride. White phosphorus exists as molecules of four
White_phosphorus
Chemical compounds with the structure R–O–O–R'
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Peroxide
Functional group (C=O)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Carbonyl_group
Topics referred to by the same term
software suite Carbon disulfide, CS2, an inorganic compound Dicaesium, Cs2, an allotrope of elemental caesium CS2, a siliconized, micro-pulverized form
CS2
Cyclic chemical group (–C6H5)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Phenyl_group
Organic compound with the structure >C(O–)2
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Acetal
Process
Silanization of silicon and mica is the coating of these materials with a thin layer of self assembling units. Nanoscale analysis of proteins using atomic
Silanization of silicon and mica
Silanization_of_silicon_and_mica
Organic compound or functional group containing a C=N bond
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Imine
Cage-like allotrope of carbon
molecules. Fullerenes are sparingly soluble in aromatic solvents and carbon disulfide, but insoluble in water. Solutions of pure C 60 have a deep purple color
Buckminsterfullerene
Measure of the electric polarizability of a dielectric, compared with that of a vacuum
Polystyrene 2.4–2.7 Carbon disulfide 2.6 BoPET 3.1 Paper, printing 1.4 (200 kHz) Electroactive polymers 2–12 Mica 3–6 Silicon dioxide 3.9 Sapphire 8.9–11
Relative_permittivity
Chemical group (R–S–Cl)
obtained by chlorination of carbon disulfide. Sulfenyl chlorides are typically prepared by chlorination of disulfides: R2S2 + Cl2 → 2 R−SCl This reaction
Sulfenyl_chloride
Organic compounds of the form >C=N–OH
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Oxime
Group of chemical compounds derived from alkanes containing one or more halogens
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Haloalkane
Chemical group (–C(=O)C6H5
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Benzoyl_group
Chemical group (–CH2–CH3)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Ethyl_group
Chemical compound
can be considered to be intermediate between carbon dioxide and carbon disulfide, both of which are valence isoelectronic with it. Carbonyl sulfide is
Carbonyl_sulfide
Chemical element with atomic number 34 (Se)
Applications in electronics, once important, have been mostly replaced with silicon semiconductor devices. Selenium is still used in a few types of DC power
Selenium
Used in semiconductor integrated circuits
metal as well as the introduction of barrier metal layers to isolate the silicon from potentially damaging copper atoms. Although the methods of superconformal
Copper_interconnects
Early radio receiver component
are used with the wire cat whisker contact; silicon is used with a heavier point contact, while silicon carbide (carborundum) can tolerate the heaviest
Crystal_detector
Chemical compounds and groups containing nitrogen with a lone pair (:N)
Primary amines only Hofmann's mustard oil test Isothiocyanate Carbon disulfide CS2 and mercury(II) chloride HgCl2 are used. Thiocyanate smells like mustard
Amine
Organic molecule with two different functional groups
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Bifunctionality
Chemical group (–CH=CH2)
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Vinyl_group
Chemical group (R–O)
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Alkoxy_group
Organic compounds with a carbon-carbon-oxygen ring
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Epoxide
Salt that is a metal-thioate/O-esters of dithiocarbonate
metals are produced by the treatment of an alcohol, alkali, and carbon disulfide. The process is called xanthation. In chemical terminology, the alkali
Xanthate
Class of chemical compounds
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Imide
Thin semiconductors
molybdenum disulfide by laser to produce single or multi-layer molybdenum disulfide nanosheets. This allows for synthesis of molybdenum disulfide nanosheets
Transition metal dichalcogenide monolayers
Transition_metal_dichalcogenide_monolayers
Short chains of 2–50 amino acids
phosphorylation, hydroxylation, sulfonation, palmitoylation, glycosylation, and disulfide formation. In general, peptides are linear, although lariat structures
Peptide
Chemical compound
indicative of particularly strong hydrogen bonding. Diphosphane and hydrogen disulfide exhibit only weak hydrogen bonding and have little chemical similarity
Hydrogen_peroxide
Chemical compound
Grunwell (1970). "Reaction of Grignard reagents with tetramethylthiuram disulfide [yielding dithiocarbamates]". J. Org. Chem. 35 (5): 1500–1501. doi:10
Methylenebis(dibutyldithiocarbamate)
Methylenebis(dibutyldithiocarbamate)
Class of organic compounds
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Hydrazone
Chemical group (–C4H9) derived from butane
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Butyl_group
Organic compounds with the tautomeric structures RC(S)OH or RC(O)SH
decay over the course of several hours to the free halogen and the diacyl disulfide. Dithiocarboxylic acid Thiocarbamate Thiocarbonate Thiocarbonic acid Thioformic
Thiocarboxylic_acid
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Ether
Third row of the periodic table
The third period contains eight elements: sodium, magnesium, aluminium, silicon, phosphorus, sulfur, chlorine and argon. The first two, sodium and magnesium
Period_3_element
Chemical group made of an –S(=O)2 group bound to a halogen
Reduction with tetrathiotungstate ions (WS2−4) induces dimerization to the disulfide. Chlorosulfonated polyethylene (CSPE) is produced industrially by chlorosulfonation
Sulfonyl_halide
31 (4): 931–970. Bibcode:2002JPCRD..31..931S. doi:10.1063/1.1497384. "Silicon Carbide (SiC) - Optical properties". Ioffe Institute. Retrieved 6 June
List_of_refractive_indices
Organosulfur compound of the form R–SOH
cysteine residue to a sulfenic acid. The sulfenic acid then converts to a disulfide by reaction with another residue of cysteine. Sulfenic acids are produced
Sulfenic_acid
Class of chemical compounds
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Hydroperoxide
Chemical group (–C3H7) derived from propane
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Propyl_group
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Amide_(functional_group)
Hydrocarbon compound (H2C=CH2)
Phosphorus monoxide Phosphorus mononitride Potassium chloride Silicon carbide Silicon monoxide Silicon monosulfide Sodium chloride Sodium iodide Sulfanyl Sulfur
Ethylene
Organic compound containing an –NO2 group
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Nitro_compound
Functional group
are the first of the series of functional groups containing an oxidized disulfide bond. Other members of this family include thiosulfonates (R−SO2−S−R)
Thiosulfinate
Chemical group (–CH2–C6H5)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Benzyl_group
Organic compounds of the form R–O–O–R′
thiol groups to disulfide bonds. Then, when flour is mixed with water, the glutenin and gliadin combine to form gluten. More disulfide bonds increases
Organic_peroxides
Organic compounds that contain sulfur
Methionine, an amino acid containing a sulfide Diphenyl disulfide, a representative disulfide Dibenzothiophene, a component of crude oil Perfluorooctanesulfonic
Organosulfur_chemistry
Thickened and hardened area of skin
proteins and hydrophobic keratin intermediate filaments containing many disulfide bonds. It is the natural reaction of the palmar or plantar skin. Too much
Callus
Organic compounds with the structure R–S(=O)2–OH
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Sulfonic_acid
Any chemical compound having at least one germanium atom in its structure
monoxide, (GeO). The dioxide, GeO2 can be obtained by roasting germanium disulfide (GeS 2) or by allowing elemental germanium to slowly oxidize in air, and
Germanium_compounds
Chemical compound
Earth's atmosphere by the reaction of HO•, the hydroxyl radical, on carbon disulfide, carbon oxysulfide and hydrogen sulfide with side products of carbon dioxide
Sulfanyl
Organosulfur compounds containing –S(=O)2–N< functional group
deprotonated by amines. They are often prepared by one-pot oxidation of disulfides or thiols linked to amines. An alternative synthesis of sultams involves
Sulfonamide
Organic compound containing a sulfinyl group (>SO)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Sulfoxide
Organic molecule containing a neutral carbon with two unbound valence electrons
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Carbene
Chemical group, –C(=O)CH3
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Acetyl_group
Chemical reaction
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Hydrodealkylation
Any chemical compound having two acyl groups bonded to the same oxygen atom
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Organic_acid_anhydride
Chemical compound with the group –N+≡C–
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Isocyanide
Simplest secondary alcohol
esterified to give isopropyl acetate, another solvent. It reacts with carbon disulfide and sodium hydroxide to give sodium isopropylxanthate, which has use as
Isopropyl_alcohol
Organic compound (H–CHO); simplest aldehyde
Phosphorus monoxide Phosphorus mononitride Potassium chloride Silicon carbide Silicon monoxide Silicon monosulfide Sodium chloride Sodium iodide Sulfanyl Sulfur
Formaldehyde
Organic compound containing C–PO(OR)2 groups
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Phosphonate
Chemical group (–OCH3)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Methoxy_group
Chemical compound of sulfur and oxygen
Phosphorus monoxide Phosphorus mononitride Potassium chloride Silicon carbide Silicon monoxide Silicon monosulfide Sodium chloride Sodium iodide Sulfanyl Sulfur
Sulfur_dioxide
Chemical group (–CH2–CH=CH2)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Allyl_group
Organic ammonia derivative
simple reagents include: with phosgene to methyl isocyanate, with carbon disulfide and sodium hydroxide to the sodium methyldithiocarbamate, with chloroform
Methylamine
Battery with solid electrodes and a solid electrolyte
domination of lithium batteries: some learnings from β-alumina and titanium disulfide". MRS Bulletin. 46 (2): 168–173. Bibcode:2021MRSBu..46..168W. doi:10
Solid-state_battery
Chemical group (–OC(O)CH3)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Acetoxy_group
Chemical group (R–C=O)
doi:10.1039/B407654K. Hermannsdorfer, André; Driess, Matthias (2021). "Silicon Tetrakis(trifluoromethanesulfonate): A Simple Neutral Silane Acting as
Acyl_group
Chemical group (–CH=S)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Thial
Nitrogen-based molecule
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Nitrene
Chemical group (>S(=O)2)
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Sulfonyl_group
Functional group
Cyanate Isocyanate Nitrate Nitrite Nitro Nitroso NONOate Triazole Tetrazole Silicon Silane Hydrosilane Chlorosilane Silene Silanol Siloxide Siloxane Silanone
Methylenedioxy
Free radical
acid Arsole Sulfur Thiol Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone
Propenyl_group
Carbon compound
carbon disulfide through a porcelain tube. Prior to the 1950s, carbon tetrachloride was manufactured by the chlorination of carbon disulfide at 105 to
Carbon_tetrachloride
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