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Attempts to prepare some carboxylate complexes, especially for electrophilic metals, often gives oxo derivatives. Examples include the oxo-acetates of Fe(III), Mn(III), and Cr(III). Pyrolysis of metal carboxylates affords acid anhydrides and the metal oxide. This reaction explains the formation of basic zinc acetate from anhydrous zinc diacetate.
It is an oxocarbon anion that consists solely of carbon and oxygen. It is the anion of peroxycarbonic acid [1] [2] also called hydroperoxyformic acid, [3] HO−O−CO−OH. The peroxycarbonate anion is formed, together with peroxydicarbonate C 2 O 2− 6, at the negative electrode during electrolysis of molten lithium carbonate. [4]
The latter is consistent with the pK a ’s of carbonic acid: pK 1 = 6.77 and pK 2 = 9.93. To a single metal ion, carbonate is observed to bind in both unidentate (κ 1-) and bidentate (κ 2-) fashions. [5] In the covalent bond classification method, κ 1-carbonate is anX ligand and κ 2-carbonate is an X 2 ligand.
A polycarbonate is an oxocarbon dianion consisting of a chain of carbonate units, where successive carbonyl groups are directly linked to each other by shared additional oxygen atoms. That is, they are the conjugate bases of polycarbonic acids, the conceptual anhydrides of carbonic acid, or polymers of carbon dioxide.
A carbon–oxygen bond is a polar covalent bond between atoms of carbon and oxygen. [1] [2] [3]: 16–22 Carbon–oxygen bonds are found in many inorganic compounds such as carbon oxides and oxohalides, carbonates and metal carbonyls, [4] and in organic compounds such as alcohols, ethers, and carbonyl compounds.
Carbonation is the chemical reaction of carbon dioxide to give carbonates, bicarbonates, and carbonic acid. [1] In chemistry, the term is sometimes used in place of carboxylation, which refers to the formation of carboxylic acids. In inorganic chemistry and geology, carbonation is common.
Transition metal carbon dioxide complexes undergo a variety of reactions. Metallacarboxylic acids protonate at oxygen and eventually convert to metal carbonyl complexes: [L n MCO 2] − + 2 H + → [L n MCO] + + H 2 O. This reaction is relevant to the potential catalytic conversion of CO 2 to fuels. [5]
Metal aqua ions are often involved in the formation of complexes. The reaction may be written as pM x+ (aq) + qL y− → [M p L q] (px-qy)+ In reality this is a substitution reaction in which one or more water molecules from the first hydration shell of the metal ion are replaced by ligands, L. The complex is described as an inner-sphere complex.