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What is the structure of pyrophosphorous acid?

I asked this question here because the answer which I found on web and other resources are inconsistent which each other. For example, following data is given regarding the structure of pyrophosphorus acid in my textbook, which is not consistent with the number of oxygen atoms.

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On checking here,and here there are no double bonds of phosphorus with oxygen, however here there are. And here both the structures are given on the same website.

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    $\begingroup$ The website in your last statement "And here both the structures are given on the same website," is not a secure website. Please ensure it has https: instead of http: $\endgroup$ – Mathew Mahindaratne Feb 18 at 16:38
  • $\begingroup$ And the first structure on the last website you mentioned should be that of diphosphinic acid according to this by considering the CAS no. mentioned corresponding to it. $\endgroup$ – Eagle Feb 18 at 16:50
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Oxyphosphorus compounds, all of which contain phosphorus-oxygen linkages, are the most dominated subset in Phosphorus Chemistry. You may find good review of oxyphosphorus compounds in Ref.1. In particular, most of these commonly known as phosphates are described in Chapter 3 of Ref. 1 (Pages 169-305) which states that:

Oxyphosphorus compounds may be defined as compounds which contain phosphorus-oxygen linkages. They may contain up to six oxygen atoms linked to a central phosphorus atom. Pyramidal derivatives are represented by phosphite esters (la), tetrahedral compounds by orthophosphate salts (lb) and esters (lc), trigonal bipyramidal compounds by pentaoxyphosphoranes (Id), and octahedral compounds by a few hexaoxyphosphorides (hexaphosphates) of type (le). In addition, there are the comparatively rare 2-connected angular phosphenites (If) and 3-connected planar phosphenates (lg).

OxyPhosporousCpds

The term normal phosphates is used to described the compounds, in which only $\ce{P—O}$ linkages are present (e.g., structures 1a-g). Compounds such as 1b containing discrete $\ce{PO4^{3-}}$ anions are known as orthophosphates. If the neutralizing cation is $\ce{H+}$, then it is called phosphoric acid or orthophosphoric acid.

On the other hand, if some of the oxygen linkages are replaced by other atoms or groups (e.g., $\ce{H, NR2, CR3}$, etc.), the compounds can be termed substituted phosphates. For example, if one $\ce{P—O}$ linkage is replaced by a $\ce{P-H}$ linkage, the compound series are called phosphites (2a) while when the two $\ce{P—O}$ linkages are replaced by two $\ce{P-H}$ linkages, that series is known as hypophosphites (2b). Similar to phosphates, if the neutralizing cation is $\ce{H+}$ in 2a and 2b, then they are traditionally called phosphorus acid (Wikipedia1) or hypophosphorus acid (Wikipedia2), respectively. The IUPAC names of these acids are phosphonic acid and phosphinic acid, respectively. Meanwhile, substituted phosphates containing a single $\ce{P=O}$ linkage (e.g., 2c) are usually referred to as phosphoryl compounds.

When $\ce{PO4^{3-}}$ anions are linked together with sharing oxygen atom in common, they are called condensed phosphates (e.g., pyrophosphate, 3a). If the neutralizing cation is, again, $\ce{H+}$, then it is called pyrophosphoric acid or diphosphoric acid (IUPAC name). On the other hand, one can expect when the two anions linked together with sharing oxygen atom in common are phosphites, they would be called pyrophosphites, 4a (Wikipedia3). However, recent research showed that there are some controversies on the structures, not only on pyrophosphites, but also on phosphite itself.

Phosphorous acid, $\ce{H3PO3}$ (systematic IUPAC name is phosphonic acid), exists in two tautomeric forms: An one with tricoordinate about phosphorous $(\ce{P(OH)3})$; and another with tetracoordinate about phosphorous $(\ce{HP(O)(OH)2})$ (See Scheme below), which is the favored tautomer between two (Ref.2).

Tautomerism

The $\ce{P(OH)3}$ form of two tautomer is rarely isolated or directly obtained, yet its presence in the equilibrium has been repeatedly postulated from kinetics studies (Ref.3,4) and thermodynamic studies (Ref.5,6).

According to most literature, the $\ce{P(OH)3}$ form of tautomers is possible only in triesters such as 1a $(\ce{P(OR)3})$. Even in such cases, there is a strong tendency to rearrange to the tetracoordinate species, $\ce{RP(O)(OR)2}$ (Ref.5). Hence, it is safe to say that pyrophosphites has high tendency to have a structure resembling of 4a (See first scheme).

References:

  1. D. E. C. Corbridge, In Studies in Inorganic Chemistry, Volume 20: Phosphorus – An Outline of its Chemistry, Biochemistry and Uses; Elsevier B.V.: New York, NY, 1995, Pages 1-1208 (https://www.sciencedirect.com/bookseries/studies-in-inorganic-chemistry/vol/20).
  2. F.A. Cotton, G. Wilkinson, C.A. Murillo, M. Bochmann, Advanced Inorganic Chemistry, 6th Edn.; Wiley-Interscience: New York, NY, 1999, “Chapter 10: The Group 15 Elements: $\ce{P, As, Sb, Bi}$,” pp. 380-443.
  3. G.A. Haight Jr., M. Rose, J. Preer, “Reactions of chromium(VI) with phosphorus(III) and phosphorus(I). I. Dihydrogen phosphite, phosphorous acid, and hypophosphorous acid,” J. Am. Chem. Soc. 1968, 90(18), 4809-4814 (DOI: 10.1021/ja01020a011).
  4. R.O. Griffith, A. Mckeown, “Kinetics of the reaction of iodine with phosphorous acid and with phosphites,” Trans. Faraday Soc. 1940, 36, 766-779 (DOI: 10.1039/TF9403600766).
  5. J. P. Guthrie, “Tautomerization equilibria for phosphorous acid and its ethyl esters, free energies of formation of phosphorous and phosphonic acids and their ethyl esters, and $\mathrm{p}K_a$ values for ionization of the $\ce{P—H}$ bond in phosphonic acid and phosphonic esters,” Canadian Journal of Chemistry 1979, 57(2), 236-239 (https://doi.org/10.1139/v79-039).
  6. J. P. Guthrie, “Carbonyl Addition Reactions: Factors Affecting the Hydrate–Hemiacetal and Hemiacetal–Acetal Equilibrium Constants,” Canadian Journal of Chemistry 1975, 53(68), 898-906 (https://doi.org/10.1139/v75-125).
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Most of the online data banks such as PubChem don't bother with showing proper bond multiplicity since they are focused on searching for the compounds based on connectivity graphs. It doesn't mean that those are bad or unreliable, it's just not their primary focus.

The source of confusion here, I think, is terminology. Pyrophosphorous acid is an obsolete name for first member of the group of two isomeric diphosphonic acids (di- and tribasic) with $\ce{H4P2O5}$ formula featuring $\ce{P-O-P}$ and $\ce{P-P}$ bridges [1, p. 125; 2, p. 810]:

Diphosphonic(III,III) acid

Diphosphonic(III,III) acid

Salts of diphosphonic(III,III) acid are obtained by heating of phosphonates $\ce{H2PO3-}$ to $\pu{150 °C}$ in vacuum:

$$\ce{2 H3PO4- → H2P2O5^2- + H2O}$$

The acid itself can be obtained from the barium salt by via treatment with sulfuric acid. A reaction between phosphonic acid and phosphorous trichloride also yields in diphosphonic acid provided that the hydrogen chloride formed is bound in order to shift the equilibrium:

Scheme 1

Diphosphonic(II,IV) acid

Diphosphonic(II,IV) acid

Synthesized similarly to diphosphonic(III,III) acid from phosphonic acid by treating it with phoshorous tribromide or triiodite instead of trichloride. Another way is oxidation of diphosphoric(II,II) acid $\ce{H4P2O4}$ (aka hypodiphosphonic acid):

Scheme 2

Notes

Illustrations for Lewis structures are adapted from Abb. 13.6 Sauerstoffsäuren des Phosphors [1, p. 125]. Syntheses and reaction schemes within are from Holleman's Lehrbuch der anorganischen Chemie [2, p. 810]; German text was translated and adapted by me (I tried to get it as close as possible, but no warranty).

References

  1. Kuhn, N.; Klapötke, T. M.; Walker, I. Allgemeine und anorganische Chemie: eine Einführung; Springer Spektrum: Berlin, 2014. ISBN 978-3-642-36866-0.
  2. Holleman, A. F.; Wiberg, E.; Wiberg, N. Lehrbuch der anorganischen Chemie, 102nd ed.; Fischer, G., Ed.; Walter de Gruyter: Berlin; New York, 2007. ISBN 978-3-11-017770-1.
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Pyrophosphorous acid is the acid anhydride of phophorous acid:

$$\ce{H3PO3 + H3PO3 -> H4P2O5 + H2O}$$

Phosphorous acid in water occurs in two forms, $\ce{H3PO3}$ and $\ce{H2PHO3}$, with no direct bonds between phosphorous and hydrogen in the first case, and one direct bond between phosphorous and hydrogen in the second case, see Why is phosphorous acid diprotic and not triprotic?

In the anhydride, you have the same possibility for tautomerism. I'm not sure which form is the most populated one under which conditions.

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As you can see that the textbook has not considered the P-O-P and thus has one less oxygen. Just remember that in any oxo acid if the number of oxygen is one more than twice the number of phosphorous/sulphur (like in the case above where the number of O=(2*P or S)+1), then it has a bridge bond and if two more than twice the number of phosphorous/sulphur (O=(2*P or S)+2) then it has a peroxide bond like in peroxodisulphuric acid (H2S2O8).

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    $\begingroup$ "Just remember that in any oxo acid if the number of oxygen is one more than twice the number of phosphorous/sulphur (like in the case above where the number of O=(2*P or S)+1), then it has a bridge bond" but this is not the case with pyrosulphurous acid (H2S2O5) $\endgroup$ – Eagle Feb 18 at 19:23
  • $\begingroup$ @Natasha it is a general rule but there are always exceptions $\endgroup$ – Jeel Pandya Feb 19 at 13:29

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