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  2. Metal aquo complex - Wikipedia

    en.wikipedia.org/wiki/Metal_aquo_complex

    Structure of an octahedral metal aquo complex. Chromium(II) ion in aqueous solution. Most aquo complexes are mono-nuclear, with the general formula [M(H 2 O) 6] n+, with n = 2 or 3; they have an octahedral structure. The water molecules function as Lewis bases, donating a pair of electrons to the metal ion and forming a dative covalent bond ...

  3. Metal ions in aqueous solution - Wikipedia

    en.wikipedia.org/wiki/Metal_ions_in_aqueous_solution

    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.

  4. Stability constants of complexes - Wikipedia

    en.wikipedia.org/wiki/Stability_constants_of...

    The formation of a complex between a metal ion, M, and a ligand, L, is in fact usually a substitution reaction. For example, in aqueous solutions, metal ions will be present as aqua ions, so the reaction for the formation of the first complex could be written as

  5. List of aqueous ions by element - Wikipedia

    en.wikipedia.org/wiki/List_of_aqueous_ions_by...

    The model is defined in terms of a list of those complex species which are present in solutions in significant amounts. In the present context the complex species have the general formula [M p O q (OH) r] n±. where p, q and r define the stoichiometry of the species and n± gives the electrical charge of the ion. The experimental data are ...

  6. Ion association - Wikipedia

    en.wikipedia.org/wiki/Ion_association

    The nature of this solvation shell is generally not known with any certainty. In aqueous solution and in other donor solvents, metal cations are surrounded by between 4 and 9 solvent molecules in the primary solvation shell, [6] An alternative name for a solvent-shared ion pair is an outer-sphere complex.

  7. Ferric EDTA - Wikipedia

    en.wikipedia.org/wiki/Ferric_edta

    In the absence of EDTA or similar chelating agents, ferric ions form insoluble solids and are thus not bioavailable. [1] Together with pentetic acid (DTPA), EDTA is widely used for sequestering metal ions. Otherwise these metal ions catalyze the decomposition of hydrogen peroxide, which is used to bleach pulp in papermaking. Several million ...

  8. Metal ammine complex - Wikipedia

    en.wikipedia.org/wiki/Metal_ammine_complex

    An ammine ligand bound to a metal ion is markedly more acidic than a free ammonia molecule, although deprotonation in aqueous solution is still rare. One example is the reaction of mercury(II) chloride with ammonia (Calomel reaction) where the resulting mercuric amidochloride is highly insoluble. HgCl 2 + 2 NH 3 → HgCl(NH 2) + [NH 4]Cl

  9. Vanadate - Wikipedia

    en.wikipedia.org/wiki/Vanadate

    Conventionally this ion is represented with a single double bond, however this is a resonance form as the ion is a regular tetrahedron with four equivalent oxygen atoms. Additionally a range of polyoxovanadate ions exist which include discrete ions and "infinite" polymeric ions. [ 2 ]