\( \require{mhchem} \)
Silicon monoxide is the chemical compound with the formula SiO where silicon is present in the oxidation state +2. In the vapour phase, it is a diatomic molecule.[1] It has been detected in stellar objects[2] and has been described as the most common oxide of silicon in the universe.[3]
Solid form
When SiO gas is cooled rapidly, it condenses to form a brown/black polymeric glassy material, (SiO)n, which is available commercially and used to deposit films of SiO. Glassy (SiO)n is air and moisture sensitive.
Oxidation
Its surface readily oxidizes in air at room temperature, giving an SiO2 surface layer that protects the material from further oxidation. However, (SiO)n irreversibly disproportionates into SiO2 and Si in a few hours between 400 °C and 800 °C and very rapidly between 1,000 °C and 1,440 °C, although the reaction does not go to completion.[4]
Production
The first precise report on the formation of SiO was in 1887[5] by the chemist Charles F. Maybery (1850–1927) at the Case School of Applied Science in Cleveland. Maybery claimed that SiO formed as an amorphous greenish-yellow substance with a vitreous luster when silica was reduced with charcoal in the absence of metals in an electric furnace.[6] The substance was always found at the interface between the charcoal and silica particles.
By investigating some of the chemical properties of the substance, its specific gravity, and a combustion analysis, Maybery deduced that the substance must be SiO. The equation representing the partial chemical reduction of SiO2 with C can be represented as:
- SiO2 + C ⇌ SiO + CO
Complete reduction of SiO2 with twice the amount of carbon yields elemental silicon and twice the amount of carbon monoxide. In 1890, the German chemist Clemens Winkler (the discoverer of germanium) was the first to attempt to synthesize SiO by heating silicon dioxide with silicon in a combustion furnace.[7]
- SiO2 + Si ⇌ 2 SiO
However, Winkler was not able to produce the monoxide since the temperature of the mixture was only around 1000 °C. The experiment was repeated in 1905 by Henry Noel Potter (1869–1942), a Westinghouse engineer. Using an electric furnace, Potter was able to attain a temperature of 1700 °C and observe the generation of SiO.[5] Potter also investigated the properties and applications of the solid form of SiO.[8][9]
Gaseous form
Because of the volatility of SiO, silica can be removed from ores or minerals by heating them with silicon to produce gaseous SiO in this manner.[1] However, due to the difficulties associated with accurately measuring its vapor pressure, and because of the dependency on the specifics of the experimental design, various values have been reported in the literature for the vapor pressure of SiO (g). For the pSiO above molten silicon in a quartz (SiO2) crucible at the melting point of silicon, one study yielded a value of 0.002 atm.[10] For the direct vaporization of pure, amorphous SiO solid, 0.001 atm has been reported.[11] For a coating system, at the phase boundary between SiO2 and a silicide, 0.01 atm was reported.[12]
Silica itself, or refractories containing SiO2, can be reduced with H2 or CO at high temperatures, e.g.:[13]
- SiO2(s) + H2(g) ⇌ SiO(g) + H2O(g)
As the SiO product volatilizes off (is removed), the equilibrium shifts to the right, resulting in the continued consumption of SiO2. Based on the dependence of the rate of silica weight loss on the gas flow rate normal to the interface, the rate of this reduction appears to be controlled by convective diffusion or mass transfer from the reacting surface.[14][15]
Gaseous (molecular) form
Silicon monoxide molecules have been trapped in an argon matrix cooled by helium. In these conditions, the SiO bond length is between 148.9 pm[3] and 151 pm.[16] This bond length is similar to the length of Si=O double bonds (148 pm) in the matrix-isolated linear molecule SiO
2 (O=Si=O), suggestive of the absence of a triple bond as in carbon monoxide.[3] However, the SiO triple bond has a calculated bond length of 150 pm and a bond energy of 794 kJ/mol, which are also very close to those reported for SiO.[16] In the carbon analogues the formal double bonds of carbon dioxide (116 pm) is also close to the triple bond length of carbon monoxide (112.8 pm); in light of this the observed bond length of SiO may be consistent with at least some triple-bond character in the diatomic molecule. The SiO double bond structure is, notably, an exception to Lewis' octet rule for molecules composed of the light main group elements, whereas the SiO triple bond satisfies this rule. That anomaly not withstanding, the observation that monomeric SiO is short-lived and that (SiO)'n' oligomers with 'n' = 2,3,4,5 are known,[17] all having closed ring structures in which the silicon atoms are connected through bridging oxygen atoms (i.e. each oxygen atom is singly bonded to two silicon atoms; no Si-Si bonds), suggests the Si=O double bond structure, with a hypovalent silicon atom, is likely for the monomer.[3]
Condensing molecular SiO in argon matrix together with fluorine, chlorine or carbonyl sulfide (COS), followed by irradiation with light, produces the planar molecules OSiF
2 (with Si-O distance 148 pm) and OSiCl
2 (Si-O 149 pm), and the linear molecule OSiS (Si-O 149 pm, Si-S 190 pm).[3]
Matrix-isolated molecular SiO reacts with oxygen atoms generated by microwave discharge to produce molecular SiO
2 which has a linear structure.
When metal atoms (such as Na, Al, Pd, Ag, and Au) are co-deposited with SiO, triatomic molecules are produced with linear (AlSiO and PdSiO), non-linear (AgSiO and AuSiO), and ring (NaSiO) structures.[3]
Solid (polymeric) form
Potter reported SiO solid as yellowish-brown in color and as being an electrical and thermal insulator. The solid burns in oxygen and decomposes water with the liberation of hydrogen. It dissolves in warm alkali hydroxides and in hydrofluoric acid. Even though Potter reported the heat of combustion of SiO to be 200 to 800 calories higher than that of an equilibrium mixture of Si and SiO2 (which could, arguably, be used as evidence that SiO is a unique chemical compound),[18] some studies characterized commercially available solid silicon monoxide materials as an inhomogeneous mixture of amorphous SiO2 and amorphous Si with some chemical bonding at the interface of the Si and SiO2 phases.[19][20] Recent spectroscopic studies in a correlation with Potter's report suggest that commercially available solid silicon monoxide materials can not be considered as an inhomogeneous mixture of amorphous SiO2 and amorphous Si.[21]
Interstellar occurrence
Interstellar SiO was first reported in 1971 after detection in the giant molecular cloud Sgr B2.[22] SiO is used as a molecular tracer of shocked gas in protostellar outflows.[23]
References
Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.), Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, ISBN 0-12-352651-5
Gibb, A.G.; Davis, C.J.; Moore, T.J.T., A survey of SiO 5 → 4 emission towards outflows from massive young stellar objects. Monthly Notices of the Royal Astronomical Society, 382, 3, 1213-1224. doi:10.1111/j.1365-2966.2007.12455.x, arXiv:0709.3088v1.
Peter Jutzi and Ulrich Schubert (2003) Silicon chemistry: from the atom to extended systems. Wiley-VCH ISBN 3-527-30647-1.
HERTL, W.; PULTZ, W. W. (1967). "Disproportionation and Vaporization of Solid Silicon Monoxide". Journal of the American Ceramic Society. Wiley. 50 (7): 378–381. doi:10.1111/j.1151-2916.1967.tb15135.x. ISSN 0002-7820.
J. W. Mellor "A Comprehensive Treatise on Inorganic and Theoretical Chemistry" Vol VI, Longmans, Green and Co. (1947) p. 235.
C. F. Maybery Amer. Chem. Journ. 9, 11, (1887).
C. Winkler Ber. 23, (1890) p. 2652.
U.S. Patent 182,082, July 26, 1905.
E. F. Roeber H. C. Parmelee (Eds.) Electrochemical and Metallurgical Industry, Vol. 5 (1907) p. 442.
"Handbook of Semiconductor Silicon Technology," W. C. O'Mara, R. B. Herring, L. P. Hunt, Noyes Publications (1990), p. 148
Nuth III, Joseph A.; Ferguson, Frank T. (2006). "Silicates Do Nucleate in Oxygen‐rich Circumstellar Outflows: New Vapor Pressure Data for SiO". The Astrophysical Journal. American Astronomical Society. 649 (2): 1178–1183. Bibcode:2006ApJ...649.1178N. doi:10.1086/506264. ISSN 0004-637X. S2CID 123656840.
"High-Temperature Oxidation-Resistant Coatings ," National Academy of Sciences/National Academy of Engineering (1970), p. 40
Charles A. (2004) Schacht Refractories handbook. CRC Press, ISBN 0-8247-5654-1.
Han, Gilsoo; Sohn, Hong Yong (2005). "Kinetics of the Hydrogen Reduction of Silica Incorporating the Effect of Gas-Volume Change upon Reaction". Journal of the American Ceramic Society. Wiley. 88 (4): 882–888. doi:10.1111/j.1551-2916.2005.00144.x. ISSN 0002-7820.
Gardner, Richard A. (1974). "The kinetics of silica reduction in hydrogen". Journal of Solid State Chemistry. Elsevier BV. 9 (4): 336–344. Bibcode:1974JSSCh...9..336G. doi:10.1016/0022-4596(74)90092-9. ISSN 0022-4596.
Inorganic Chemistry, Holleman-Wiberg, Academic Press (2001) p. 858.
Chrystie, Robin S. M.; Janbazi, Hossein; Dreier, Thomas; Wiggers, Hartmut; Wlokas, Irenäus; Schulz, Christof (2019-01-01). "Comparative study of flame-based SiO2 nanoparticle synthesis from TMS and HMDSO: SiO-LIF concentration measurement and detailed simulation". Proceedings of the Combustion Institute. 37 (1): 1221–1229. doi:10.1016/j.proci.2018.07.024. ISSN 1540-7489. S2CID 139291303.
J. W. Mellor "A Comprehensive Treatise on Inorganic and Theoretical Chemistry" Vol VI, Longmans, Green and Co. (1947) p. 234.
Friede B., Jansen M. (1996) Some comments on so-called silicon monoxide. Journal of Non-Crystalline Solids, 204, 2, 202-203. doi:10.1016/S0022-3093(96)00555-8.
Schulmeister K. and Mader W. (2003) TEM investigation on the structure of amorphous silicon monoxide. Journal of Non-Crystalline Solids, 320, 1-3, 143-150. doi:10.1016/S0022-3093(03)00029-2.
Gunduz, D. C., Tankut, A., Sedani, S., Karaman, M. and Turan, R. (2015) Crystallization and phase separation mechanism of silicon oxide thin films fabricated via e-beam evaporation of silicon monoxide. Phys. Status Solidi C, 12: 1229–1235. doi:10.1002/pssc.201510114.
Wilson, R. W.; Penzias, A. A.; Jefferts, K. B.; Kutner, M.; Thaddeus, P. (1971). "Discovery of Interstellar Silicon Monoxide". The Astrophysical Journal. 167: L97. Bibcode:1971ApJ...167L..97W. doi:10.1086/180769. ISSN 0004-637X.
Martin-Pintado, J.; Bachiller, R.; Fuente, A. (1992-02-01). "SIO Emission as a Tracer of Shocked Gas in Molecular Outflows". Astronomy and Astrophysics. 254: 315. Bibcode:1992A&A...254..315M. ISSN 0004-6361.
vte
Molecules detected in outer space
Molecules
Diatomic
Aluminium monochloride Aluminium monofluoride Aluminium(II) oxide Argonium Carbon cation Carbon monophosphide Carbon monosulfide Carbon monoxide Cyano radical Diatomic carbon Fluoromethylidynium Helium hydride ion Hydrogen chloride Hydrogen fluoride Hydrogen (molecular) Hydroxyl radical Iron(II) oxide Magnesium monohydride Methylidyne radical Nitric oxide Nitrogen (molecular) Imidogen Sulfur mononitride Oxygen (molecular) Phosphorus monoxide Phosphorus mononitride Potassium chloride Silicon carbide Silicon monoxide Silicon monosulfide Sodium chloride Sodium iodide Sulfur monohydride Sulfur monoxide Titanium(II) oxide
Triatomic
Aluminium(I) hydroxide Aluminium isocyanide Amino radical Carbon dioxide Carbonyl sulfide CCP radical Chloronium Diazenylium Dicarbon monoxide Disilicon carbide Ethynyl radical Formyl radical Hydrogen cyanide (HCN) Hydrogen isocyanide (HNC) Hydrogen sulfide Hydroperoxyl Iron cyanide Isoformyl Magnesium cyanide Magnesium isocyanide Methylene radical N2H+ Nitrous oxide Nitroxyl Ozone Phosphaethyne Potassium cyanide Protonated molecular hydrogen Sodium cyanide Sodium hydroxide Silicon carbonitride c-Silicon dicarbide SiNC Sulfur dioxide Thioformyl Thioxoethenylidene Titanium dioxide Tricarbon Water
Four
atoms
Acetylene Ammonia Cyanic acid Cyanoethynyl Formaldehyde Fulminic acid HCCN Hydrogen peroxide Hydromagnesium isocyanide Isocyanic acid Isothiocyanic acid Ketenyl Methylene amidogen Methyl cation Methyl radical Propynylidyne Protonated carbon dioxide Protonated hydrogen cyanide Silicon tricarbide Thioformaldehyde Tricarbon monoxide Tricarbon monosulfide Thiocyanic acid
Five
atoms
Ammonium ion Butadiynyl Carbodiimide Cyanamide Cyanoacetylene Cyanoformaldehyde Cyanomethyl Cyclopropenylidene Formic acid Isocyanoacetylene Ketene Methane Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster
Six
atoms
Acetonitrile Cyanobutadiynyl radical E-Cyanomethanimine Cyclopropenone Diacetylene Ethylene Formamide HC4N Ketenimine Methanethiol Methanol Methyl isocyanide Pentynylidyne Propynal Protonated cyanoacetylene
Seven
atoms
Acetaldehyde Acrylonitrile
Vinyl cyanide Cyanodiacetylene Ethylene oxide Glycolonitrile Hexatriynyl radical Methylacetylene Methylamine Methyl isocyanate Vinyl alcohol
Eight
atoms
Acetic acid Aminoacetonitrile Cyanoallene Ethanimine Glycolaldehyde Hexapentaenylidene Methylcyanoacetylene Methyl formate Propenal
Nine
atoms
Acetamide Cyanohexatriyne Cyanotriacetylene Dimethyl ether Ethanol Methyldiacetylene Octatetraynyl radical Propene Propionitrile
Ten
atoms
or more
Acetone Benzene Benzonitrile Buckminsterfullerene (C60, C60+, fullerene, buckyball) C70 fullerene Cyanodecapentayne Cyanopentaacetylene Cyanotetra-acetylene Ethylene glycol Ethyl formate Methyl acetate Methyl-cyano-diacetylene Methyltriacetylene Propanal n-Propyl cyanide Pyrimidine Heptatrienyl radical
Deuterated
molecules
Ammonia Ammonium ion Formaldehyde Formyl radical Heavy water Hydrogen cyanide Hydrogen deuteride Hydrogen isocyanide Methylacetylene N2D+ Trihydrogen cation
Unconfirmed
Anthracene Dihydroxyacetone Ethyl methyl ether Glycine Graphene Hemolithin (possibly 1st extraterrestrial protein found) H2NCO+ Linear C5 Naphthalene cation Phosphine Pyrene Silylidine
Related
Abiogenesis Astrobiology Astrochemistry Atomic and molecular astrophysics Chemical formula Circumstellar dust Circumstellar envelope Cosmic dust Cosmic ray Cosmochemistry Diffuse interstellar band Earliest known life forms Extraterrestrial life Extraterrestrial liquid water Forbidden mechanism Homochirality Intergalactic dust Interplanetary medium Interstellar medium Photodissociation region Iron–sulfur world theory Kerogen Molecules in stars Nexus for Exoplanet System Science Organic compound Outer space PAH world hypothesis Pseudo-panspermia Polycyclic aromatic hydrocarbon (PAH) RNA world hypothesis Spectroscopy Tholin
Category:Astrochemistry Outer space portal Astronomy portal Chemistry portal
vte
Silicon compounds
Si(II)
SiO SiS
Si(III)
Si2H6 Si2Cl6
Si(IV)
SiBr4 SiC SiCl4 SiF4 SiH4 SiI4 SiAu4 SiO2 SiS2 Si3N4 Si2N2O Si2Cl6O SiF3Cl
vte
Oxides
Mixed oxidation states
Antimony tetroxide (Sb2O4) Boron suboxide (B12O2) Carbon suboxide (C3O2) Chlorine perchlorate (Cl2O4) Chloryl perchlorate (Cl2O6) Cobalt(II,III) oxide (Co3O4) Dichlorine pentoxide (Cl2O5) Iron(II,III) oxide (Fe3O4) Lead(II,IV) oxide (Pb3O4) Manganese(II,III) oxide (Mn3O4) Mellitic anhydride (C12O9) Praseodymium(III,IV) oxide (Pr6O11) Silver(I,III) oxide (Ag2O2) Terbium(III,IV) oxide (Tb4O7) Tribromine octoxide (Br3O8) Triuranium octoxide (U3O8)
+1 oxidation state
Aluminium(I) oxide (Al2O) Copper(I) oxide (Cu2O) Caesium monoxide (Cs2O) Dicarbon monoxide (C2O) Dichlorine monoxide (Cl2O) Gallium(I) oxide (Ga2O) Iodine(I) oxide (I2O) Lithium oxide (Li2O) Nitrous oxide (N2O) Potassium oxide (K2O) Rubidium oxide (Rb2O) Silver oxide (Ag2O) Thallium(I) oxide (Tl2O) Sodium oxide (Na2O) Water (hydrogen oxide) (H2O)
+2 oxidation state
Aluminium(II) oxide (AlO) Barium oxide (BaO) Beryllium oxide (BeO) Bromine monoxide (BrO) Cadmium oxide (CdO) Calcium oxide (CaO) Carbon monoxide (CO) Chlorine monoxide (ClO) Chromium(II) oxide (CrO) Cobalt(II) oxide (CoO) Copper(II) oxide (CuO) Dinitrogen dioxide (N2O2) Europium(II) oxide (EuO) Germanium monoxide (GeO) Iron(II) oxide (FeO) Iodine monoxide (IO) Lead(II) oxide (PbO) Magnesium oxide (MgO) Manganese(II) oxide (MnO) Mercury(II) oxide (HgO) Nickel(II) oxide (NiO) Nitric oxide (NO) Palladium(II) oxide (PdO) Phosphorus monoxide (PO) Protactinium monoxide (PaO) Silicon monoxide (SiO) Strontium oxide (SrO) Sulfur monoxide (SO) Disulfur dioxide (S2O2) Thorium monoxide (ThO) Tin(II) oxide (SnO) Titanium(II) oxide (TiO) Vanadium(II) oxide (VO) Zinc oxide (ZnO)
+3 oxidation state
Actinium(III) oxide (Ac2O3) Aluminium oxide (Al2O3) Americium(III) oxide (Am2O3) Antimony trioxide (Sb2O3) Arsenic trioxide (As2O3) Berkelium(III) oxide (Bk2O3) Bismuth(III) oxide (Bi2O3) Boron trioxide (B2O3) Caesium sesquioxide (Cs2O3) Californium(III) oxide (Cf2O3) Cerium(III) oxide (Ce2O3) Chromium(III) oxide (Cr2O3) Cobalt(III) oxide (Co2O3) Dinitrogen trioxide (N2O3) Dysprosium(III) oxide (Dy2O3) Einsteinium(III) oxide (Es2O3) Erbium(III) oxide (Er2O3) Europium(III) oxide (Eu2O3) Gadolinium(III) oxide (Gd2O3) Gallium(III) oxide (Ga2O3) Holmium(III) oxide (Ho2O3) Indium(III) oxide (In2O3) Iron(III) oxide (Fe2O3) Lanthanum oxide (La2O3) Lutetium(III) oxide (Lu2O3) Manganese(III) oxide (Mn2O3) Neodymium(III) oxide (Nd2O3) Nickel(III) oxide (Ni2O3) Phosphorus trioxide (P4O6) Praseodymium(III) oxide (Pr2O3) Promethium(III) oxide (Pm2O3) Rhodium(III) oxide (Rh2O3) Samarium(III) oxide (Sm2O3) Scandium oxide (Sc2O3) Terbium(III) oxide (Tb2O3) Thallium(III) oxide (Tl2O3) Thulium(III) oxide (Tm2O3) Titanium(III) oxide (Ti2O3) Tungsten(III) oxide (W2O3) Vanadium(III) oxide (V2O3) Ytterbium(III) oxide (Yb2O3) Yttrium(III) oxide (Y2O3)
+4 oxidation state
Americium dioxide (AmO2) Berkelium(IV) oxide (BkO2) Bromine dioxide (BrO2) Californium dioxide (CfO2) Carbon dioxide (CO2) Carbon trioxide (CO3) Cerium(IV) oxide (CeO2) Chlorine dioxide (ClO2) Chromium(IV) oxide (CrO2) Curium(IV) oxide (CmO2) Dinitrogen tetroxide (N2O4) Germanium dioxide (GeO2) Iodine dioxide (IO2) Hafnium(IV) oxide (HfO2) Lead dioxide (PbO2) Manganese dioxide (MnO2) Neptunium(IV) oxide (NpO2) Nitrogen dioxide (NO2) Osmium dioxide (OsO2) Plutonium(IV) oxide (PuO2) Praseodymium(IV) oxide (PrO2) Protactinium(IV) oxide (PaO2) Rhodium(IV) oxide (RhO2) Ruthenium(IV) oxide (RuO2) Selenium dioxide (SeO2) Silicon dioxide (SiO2) Sulfur dioxide (SO2) Technetium(IV) oxide (TcO2) Tellurium dioxide (TeO2) Terbium(IV) oxide (TbO2) Thorium dioxide (ThO2) Tin dioxide (SnO2) Titanium dioxide (TiO2) Tungsten(IV) oxide (WO2) Uranium dioxide (UO2) Vanadium(IV) oxide (VO2) Zirconium dioxide (ZrO2)
+5 oxidation state
Antimony pentoxide (Sb2O5) Arsenic pentoxide (As2O5) Dinitrogen pentoxide (N2O5) Niobium pentoxide (Nb2O5) Phosphorus pentoxide (P2O5) Protactinium(V) oxide (Pa2O5) Tantalum pentoxide (Ta2O5) Vanadium(V) oxide (V2O5)
+6 oxidation state
Chromium trioxide (CrO3) Molybdenum trioxide (MoO3) Rhenium trioxide (ReO3) Selenium trioxide (SeO3) Sulfur trioxide (SO3) Tellurium trioxide (TeO3) Tungsten trioxide (WO3) Uranium trioxide (UO3) Xenon trioxide (XeO3)
+7 oxidation state
Dichlorine heptoxide (Cl2O7) Manganese heptoxide (Mn2O7) Rhenium(VII) oxide (Re2O7) Technetium(VII) oxide (Tc2O7)
+8 oxidation state
Iridium tetroxide (IrO4) Osmium tetroxide (OsO4) Ruthenium tetroxide (RuO4) Xenon tetroxide (XeO4) Hassium tetroxide (HsO4)
Related
Oxocarbon Suboxide Oxyanion Ozonide Peroxide Superoxide Oxypnictide
Hellenica World - Scientific Library
Retrieved from "http://en.wikipedia.org/"
All text is available under the terms of the GNU Free Documentation License
