Aluminium(II) oxide

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Aluminium(II) oxide
Aluminium(II)-oxide-3D-vdW.png
Names
IUPAC name
Aluminium(II) oxide
Systematic IUPAC name
Oxoalumanyl radical
Other names
Aluminium monoxide
Oxidoaluminium
Oxoaluminum
Aluminious oxide
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
349
PubChem CID
  • InChI=1S/Al.O Yes check.svgY
    Key: AIRCTMFFNKZQPN-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/Al.O/rAlO/c1-2
    Key: AIRCTMFFNKZQPN-IPBSAJSUAY
  • O=[Al]
Properties
AlO
Molar mass 42.98 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Aluminium(II) oxide or aluminium monoxide is a compound of aluminium and oxygen with the chemical formula AlO. It has been detected in the gas phase after explosion of aluminized grenades in the upper atmosphere [1] [2] [3] and in stellar absorption spectra. [4]

Aluminium(II) oxide is one of the aluminium oxides (the most common is Aluminium oxide Al2O3), as it was the rare example of aluminium(II) compound since aluminium usually exists in its +3 oxidation state.

See also

Related Research Articles

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<span class="mw-page-title-main">Thorium dioxide</span> Chemical compound

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<span class="mw-page-title-main">Copper(II) oxide</span> Chemical compound – an oxide of copper with formula CuO

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<span class="mw-page-title-main">Sulfur monoxide</span> Chemical compound

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<span class="mw-page-title-main">Dichlorine monoxide</span> Chemical compound

Dichlorine monoxide is an inorganic compound with the molecular formula Cl2O. It was first synthesised in 1834 by Antoine Jérôme Balard, who along with Gay-Lussac also determined its composition. In older literature it is often referred to as chlorine monoxide, which can be a source of confusion as that name now refers to the ClO radical.

<span class="mw-page-title-main">Metal carbonyl</span> Coordination complexes of transition metals with carbon monoxide ligands

Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands. Metal carbonyls are useful in organic synthesis and as catalysts or catalyst precursors in homogeneous catalysis, such as hydroformylation and Reppe chemistry. In the Mond process, nickel tetracarbonyl is used to produce pure nickel. In organometallic chemistry, metal carbonyls serve as precursors for the preparation of other organometallic complexes.

<span class="mw-page-title-main">Niobium pentoxide</span> Chemical compound

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<span class="mw-page-title-main">Iodine oxide</span> Class of chemical compounds

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<span class="mw-page-title-main">Cyclopentanepentone</span> Chemical compound

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<span class="mw-page-title-main">Cyclobutanetetrone</span> Chemical compound

Cyclobutanetetrone, also called tetraoxocyclobutane, is an organic compound with formula C4O4 or (CO)4, the fourfold ketone of cyclobutane. It would be an oxide of carbon, indeed a tetramer of carbon monoxide.

<span class="mw-page-title-main">Disulfur monoxide</span> Chemical compound

Disulfur monoxide or sulfur suboxide is an inorganic compound with the formula S2O, one of the lower sulfur oxides. It is a colourless gas and condenses to give a roughly dark red coloured solid that is unstable at room temperature.

<span class="mw-page-title-main">Disulfur dioxide</span> Chemical compound

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Scandium compounds are compounds containing the element scandium. The chemistry of scandium is almost completely dominated by the trivalent ion, Sc3+, due to its electron configuration, [Ar] 3d14s2. The radii of M3+ ions in the table below indicate that the chemical properties of scandium ions have more in common with yttrium ions than with aluminium ions. In part because of this similarity, scandium is often classified as a lanthanide-like element.

<span class="mw-page-title-main">1,2-Dimethyldiborane</span> Chemical compound

1,2-Dimethyldiborane is an organoboron compound with the formula [(CH3)BH2]2. Structurally, it is related to diborane, but with methyl groups replacing terminal hydrides on each boron. It is the dimer of methylborane, CH3BH2, the simplest alkylborane. 1,2-Dimethyldiborane can exist in a cis- and a trans arrangement. 1,2-Dimethyldiborane is an easily condensed, colorless gas that ignites spontaneously in air.

<span class="mw-page-title-main">Tetramethyldiborane</span> Chemical compound

Dimethylborane, (CH3)2BH is the simplest dialkylborane, consisting of a methyl group substituted for a hydrogen in borane. As for other boranes it normally exists in the form of a dimer called tetramethyldiborane or tetramethylbisborane or TMDB ((CH3)2BH)2. Other combinations of methylation occur on diborane, including monomethyldiborane, trimethyldiborane, 1,2-dimethylborane, 1,1-dimethylborane and trimethylborane. At room temperature the substance is at equilibrium between these forms. The methylboranes were first prepared by H. I. Schlesinger and A. O. Walker in the 1930s.

<span class="mw-page-title-main">Aluminium compounds</span>

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<span class="mw-page-title-main">Phosphorus monoxide</span> Chemical compound

Phosphorus monoxide is an unstable radical inorganic compound with molecular formula PO.

References

  1. D. C. Tyte (1964). "Red (B2Π–A2σ) Band System of Aluminium Monoxide". Nature. 202 (4930): 383. Bibcode:1964Natur.202..383T. doi:10.1038/202383a0. S2CID   4163250.
  2. D. C. Tyte (1967). "The dissociation energy of aluminium monoxide". Proc. Phys. Soc. 92 (4): 1134–1137. Bibcode:1967PPS....92.1134T. doi:10.1088/0370-1328/92/4/339.
  3. Johnson E. R.; Low C. H. (1967). "Further spectral observations of grenade glow clouds in the lower thermosphere". Australian Journal of Physics. 20 (5): 577. Bibcode:1967AuJPh..20..577J. doi: 10.1071/ph670577 .
  4. Merrill, P. W.; Deutsch, A. J. & Keenan, P. C. (1962). "Absorption Spectra of M-Type Mira Variables". Astrophysical Journal. 136: 21. Bibcode:1962ApJ...136...21M. doi:10.1086/147348.