Molybdenum blue

A sample of one kind of molybdenum blue with the formula Na15[MoVI126MoV28O462H14(H2O)70]1⁄2 [MoVI124MoV28O457H14(H2O)68]1⁄2.[1]

Molybdenum blue is a term applied to:

The "heteropoly-molybdenum blues", are used extensively in analytical chemistry and as catalysts. The formation of "isopoly-molybdenum blues" which are intense blue has been used as a sensitive test for reducing reagents. They have recently been shown to contain very large anionic species based on the so-called "big wheel" containing 154 Mo atoms, with a formula [Mo154O462H14(H2O)70]14−.[2]

The molybdenum blue pigment is historically documented[3] but may not be in use today.

Heteropoly-molybdenum blues

The first heteropoly molybdate and first heteropolymetallate, yellow ammonium phosphomolybdate, (NH4)3PMo12O40 was discovered by Berzelius in 1826.[4] The phosphorus atom in the anion is termed the hetero-atom, other hetero-atoms are silicon and arsenic. The heteropoly-molybdenum blues have structures based on the Keggin structure. The blue colour arises because the near-colourless anion, such as the phosphomolybdate anion, PMo
12O3−
40, can accept more electrons (i.e. be reduced) to form an intensely coloured mixed-valence complex. This can occur in one electron or two electron steps.[4] The reduction process is reversible and the structure of the anion is essentially unchanged.[4]

PMoVI
12O3−
40 + 4 e− ⇌ PMoV
4MoVI
8O7−
40

The structure of the anion, PMoV
4MoVI
8O7−
40, has been determined in the solid state and is a β-isomer (i.e. with one of the four groups of edge-shared octahedra on the α-Keggin ion rotated through 60°).[5] Similar structures have been found with silicon, germanium or arsenic heteroatoms.[4]

The intense blue colour of the reduced anion is the basis for the use of heteropoly-molybdenum blues in quantitative and qualitative analytical techniques. This property is exploited as follows:

Uses in quantitative analysis

Main article: Colorimetric analysis

Colorimetric determination of P, As, Si and Ge

The determination of phosphorus, arsenic, silicon and germanium are examples of the use of heteropoly-molybdenum blue in analytical chemistry. The following example describes the determination of phosphorus. A sample containing the phosphate is mixed with an acid solution of MoVI, for example ammonium molybdate, to produce PMo
12O3−
40, which has an α-Keggin structure. This anion is then reduced by, for example, ascorbic acid or SnCl2, to form the blue coloured β-keggin ion, PMo
12O7−
40.[5] The amount of the blue coloured ion produced is proportional to the amount of phosphate present and the absorption can be measured using a colorimeter to determine the amount of phosphorus. Examples of procedures are:

The comparison of the measured absorption against readings taken for analyses of standard solutions means that a detailed understanding of the structure of the blue complex was unnecessary.

This colorimetric method is not effective when comparable amounts of arsenate are present in solution with phosphate. This is due to the strong chemical likeness of arsenate and phosphate. The resultant molybdenum blue for arsenate, using the same procedure, does produce a slightly different spectral signature, however.[11]

Colorimetric determination of glucose

The Folin–Wu and the Somogyi–Nelson methods are both based on the same principles. In the first step glucose (or a reducing sugar) is oxidised using a solution of Cu(II) ion which in the process is reduced to Cu(I). In the second step the Cu(I) ions are then oxidised back to Cu(II) using a colourless hetero-polymolybdate complex, which is, in the process, reduced to give the characteristic blue colour. Finally the absorption of the hetero-poly molybdenum blue is measured using a colorimeter and compared to standards prepared from reacting sugar solutions of known concentration, to determine the amount of reducing-sugar present.
The Folin–Wu method [12] uses a reagent that contains sodium tungstate. The exact nature of the blue complex in this procedure is not known.
The Somogyi-Nelson method uses an arsenomolybdate complex formed by the reaction of ammonium molybdate, (NH4)6 Mo7O24, with sodium arsenate, Na2HAsO7. [13][14][15]

Colorimetric determination of some drugs containing o-hydroquinone

Some drugs that contain an o-hydroquinone group react with phosphomolbydic acid to give the heteropoly-molybdenum blue colour.[16] Micro quantities of the drugs can be determined.

Uses in qualitative analysis

Examples of simple tests[17] are shown below that rely on the production of the molybdenum blue colour either due to reduction:

or by detection of the heteroatom

Dittmer's spray reagent for phospholipids is used in thin layer chromatography to detect phospholipids. The spray reagent is prepared as follows:

When applied to the TLC plate, compounds containing phosphate ester show up immediately as blue spots.[18]

Isopoly molybdenum blues

The isopoly-molybdenum blues have been known for many years. They are the cause of the "blue waters" found near Idaho Springs, known to Native Americans. They were first documented by Scheele and Berzelius.[2] The compounds responsible for the blue colour were not known until 1995.[19] Before then it was well known that there were polymolybdates of Mo(VI). Molybdenum(VI)oxide, MoO3, when dissolved in aqueous alkali forms the tetrahedral molybdate anion, MoO2−
4. Dissolving molybdate salts in strong acid produces "molybdic acid", MoO3·2H2O. In between these extremes of pH, polymeric ions are produced which are mostly built from MoO6 octahedral units sharing corners and edges. Examples include Mo
7O6−
24, Mo
8O4−
26 and Mo
36O
112(H2O)8−
16, which contain the {(Mo)Mo5}-type unit comprising a central MoO7 pentagonal bipyramid sharing edges with five MoO6 octahedra. The later unit occurs also in the giant mixed-valence molybdenum blue species [HxMo368O1032(H2O)240(SO4)48]48− (x ≈ 16) [20] as well as in the cluster described in the next section. The molybdenum blue species are obtained by reduction of acidified molybdate(VI) solutions.

The big wheel

The first publication of the structure of wheel shaped cluster anion, first determined for the nitrosyl derivative by Achim Müller et al.[19] was announced in New Scientist as "Big Wheel rolls back the molecular frontier".[21] Further work by the same group then refined the initial findings and determined the structure of the wheel produced in molybdate solutions as [Mo154O462H14(H2O)70]14−.[19] The Mo154-type cluster was then shown to be the basic structural type of molybdenum blue compounds obtained under slightly different conditions.[2]

The structure of the big wheel is constructed from units containing 11 Mo atoms ({Mo11}-type units), 14 of which are linked together to form the {Mo154}-type cluster that has an external diameter of 3.4 nm. (12 {Mo11}-type units are also involved in the construction of higher symmetrical spherical systems called Keplerates[2]) These units consist of a central MoO7 bipyramid sharing edges with 5 MoO6 octahedra (an illustration of this is on page 155 of the review [22]). With 5 more linking MoO6 octahedra the repeating {Mo11}-type unit is built up.

The spherical vesicle

Along with other aggregates, a hollow, spherical structure self-assembles from approximately 1,165 Mo154 wheels. This was termed a vesicle by analogy with lipid vesicles. Unlike lipid vesicles that are stabilised by hydrophobic interactions it is believed that the vesicle is stabilised by an interplay of van der Waals attraction, long-range electrostatic repulsion with further stabilization arising from hydrogen bonding involving water molecules encapsulated between the wheel-shaped clusters and in the vesicles' interior. The radius of the vesicle is 45 nm.[23]

Molybdenum blue pigment

A pigment termed molybdenum blue is recorded in 1844 as a mixture of molybdenum with "oxyde of tin or phosphate of lime".[3] An alternative formulation involves "digesting" molybdenum sulfide with nitric acid to form molybdic acid, which is then mixed with tin filings and a little muriatic acid (HCl).[3] This is evaporated and heated with alumina. A 1955 paper states that molybdenum blue is unstable and is not used commercially as a pigment.[24] The chemistry of these pigments has not been investigated.

References

  1. ↑ John R. Shapley (2004). Inorganic Syntheses, Vol 34. John Wiley & Sons, Inc. p. 197. ISBN 978-0-471-64750-8.
  2. 1 2 3 4 From Scheele and Berzelius to MÜller: polyoxometalates (POMs) revisited and the "missing link" between the bottom up and top down approaches P. Gouzerh, M. Che; L’Actualité Chimique, 2006, 298, 9
  3. 1 2 3 A Dictionary of Arts, Manufactures, and Mines: Containing a Clear Exposition of Their Principles, Andrew Ure, Published 1844, D. Appleton & Co.
  4. 1 2 3 4 Greenwood, N. N.; Earnshaw, A. (1997). Chemistry of the Elements, 2nd Edition, Oxford:Butterworth-Heinemann. ISBN 0-7506-3365-4
  5. 1 2 Structure of a heteropoly blue. The four electron reduced beta-12-molybdophosphate anion, JN Barrows, G. B. Jameson, M. T. Pope, J. Am. Chem. Soc., 1985, 107, 1771
  6. ↑ "A single solution method for the determination of soluble phosphate in sea water", Murphy J., Riley J.P., J. Mar. Biol. Assoc. UK, 1958, 37, 9–14
  7. ↑ BS1728-12:1961 "Standard Methods for the analysis of aluminium and aluminium alloys. Determination of silicon (absorptiometric molybdenum blue method)" date of publication 1961-10-14 ISBN 0-580-01569-6
  8. ↑ ISO 7834:1987 "Iron ores – Determination of arsenic content – Molybdenum blue spectrophotometric method"
  9. ↑ ISO 8556:1986 "Title: Aluminium ores – Determination of phosphorus content – Molybdenum blue spectrophotometric method"
  10. ↑ "Determination of Phosphorus, Germanium, Silicon, and Arsenic by the Heteropoly Blue Method" D. F. Boltz, M.G.Mellon, Analytical Chemistry, 19 (1947), 873 doi:10.1021/ac60011a019
  11. ↑ "Determination of phosphate/arsenate by a modified molybdenum blue method and reduction of arsenate by S
    2    O2−
    4    " Susanna Tsang, Frank Phu, Marc M Baum and Gregory A Poskrebyshev; Talanta 71(4): 1560–8 (2007), doi:10.1016/j.talanta.2006.07.043
  12. ↑ "A system of blood analysis" O. Folin, H. Wu, The Journal of Biological Chemistry (1920), 41(3), 367
  13. ↑ Food Analysis S Suzanne Nielson (2003) Springer ISBN 0-306-47495-6
  14. ↑ "A new reagent for the determination of sugars", M. Somogyi, Journal of Biological Chemistry (1945), 160, 61
  15. ↑ "A photometric adaptation of the Somogyi method for the determination of glucose", Nelson N., Journal of Biological Chemistry (1944), 153, 375
  16. ↑ "Spectrophotometric determination of microquantities of Carbidopa, Levodopa and alpha-methyldopa using molybdatophosphoric acid", P. B. Issopoulos, Pharm. Acta Helv. 64, 82 (1989)
  17. ↑ "Spot test analysis", Ervin Jungreis, 'Encyclopedia of Analytical Chemistry, John Wiley and Sons (2000)
  18. ↑ "A simple, specific spray for the detection of phospholipids on thin-layer chromatograms", Dittmer, J. C., R. L. Lester. J. Lipid Res. 5 (1964), 126–127
  19. 1 2 3 "[Mo154(NO)14O420(OH)28(H2O)70](25±5)−: A water-soluble big wheel with more than 700 atoms and a relative molecular mass of about 24000", A. Müller, E. Krickemeyer, J. Meyer, H. Bogge, F. Peters, W. Plass, E. Diemann, S. Dillinger, F. Nonnebruch, M. Randerath, C. Menke, Angew. Chem. Int. Ed. Engl., 1995, 34, 19, 2122. The first formula was published with an error limit for the negative charge, the final formula nowadays accepted is [Mo154(NO)14O448H14(H2O)70]28− (see "Soluble Molybdenum Blue—'des Pudels Kern'", A. Müller, C. Serain, Acc. Chem. Res., 2000, 33, 2).
  20. ↑ "Inorganic Chemistry Goes Protein Size: A Mo368 Nano-Hedgehog Initiating Nanochemistry by Symmetry Breaking", A. Müller, E. Beckmann, H. Bögge, A. Dress, Angew. Chem. Int. Ed., 2002, 41, 1162
  21. ↑ "Big Wheel rolls back the molecular frontier", D. Bradley, New Scientist, 1995, 148, 18
  22. ↑ "En route from the mystery of molybdenum blue via related manipulatable building blocks to aspects of materials science", A. Müller, S. Roy, Coord. Chem. Rev. 2003, 245, 153
  23. ↑ "Self-assembly in aqueous solution of wheel-shaped Mo154 oxide clusters into vesicles", T. Liu, E. Diemann, H. Li, A. W. M. Dress, A. Müller, Nature, 2003, 426, 59
  24. ↑ "Inorganic pigments", W.G. Huckle, E. Lalor, Industrial and Engineering Chemistry (1955), 47, 8, 1501
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