Borate

For the community in California formerly called Borate, see Boron, California.

Borates are the name for a large number of boron-containing oxyanions. The term "borates" may also refer to tetrahedral boron anions, or more loosely to chemical compounds which contain borate anions of either description. Larger borates are composed of trigonal planar BO3 or tetrahedral BO4 structural units, joined together via shared oxygen atoms[1] and may be cyclic or linear in structure. Boron most often occurs in nature as borates, such as borate minerals and borosilicates.

Structures

Idealized structure of a compound with trigonal planar molecular geometry.

The simplest borate anion, the orthoborate ion, BO33− is known in the solid state, for example in Ca3(BO3)2.[2] In this it adopts a near trigonal planar structure. It is a structural analogue of the carbonate anion CO32−, with which it is isoelectronic. Simple bonding theories point to the trigonal planar structure. In terms of valence bond theory the bonds are formed by using sp2 hybrid orbitals on boron. Some compounds termed orthoborates do not necessarily contain the trigonal planar ion, for example gadolinium orthoborate, GdBO3 contains the polyborate (B3O9)9− ion, whereas the high temperature form contains planar BO33−.[3]

Boric acid

The structure of the tetrahydroxyborate anion

All borates can be considered derivatives of boric acid, B(OH)3. Boric acid is a weak proton donor (pKa ~ 9) in the sense of Brønsted acid, but is a Lewis acid, i.e., it can accept an electron pair. In water, it behaves as a Lewis acid accepting the electron pair of a hydroxyl ion produced by the water autoprotolysis.

So, B(OH)3 is acidic because of its reaction with OH– from water, forming the tetrahydroxyborate complex (B(OH)4–) and releasing the corresponding proton left by the water autoprotolysis:[4]

B(OH)3 + 2H2O   is in equilibrium with   B(OH)−
4 + H3O+                   (pKa = 8.98)[5]

In the presence of cis-diols such as mannitol, glucose, sorbitol and glycerol the pKa is lowered to about 4.[6]

Polymeric ions

Tetraborate (borax) ion structure: pink, boron; red, oxygen; white, hydrogen. This tetrameric boron structure comprises two boron atoms in tetrahedral configuration sharing one common oxygen atom and linked by other oxygens to two other boron atoms present in trigonal configuration. Three cycles are also visible: two with 3 boron atoms and one with 4 boron atoms.

Under acid conditions boric acid undergoes condensation reactions to form polymeric oxyanions:

4 [B(OH)4]− + 2 H+ is in equilibrium with [B4O5(OH)4]2− + 7 H2O

The tetraborate anion (tetramer) includes two tetrahedral and two trigonal boron atoms symmetrically assembled in cyclic structure. The two tetrahedral boron atoms are linked together by a common oxygen atom and each also bears a negative net charge brought by the supplementary OH− groups laterally attached to them. This intricate molecular anion also exhibits three rings: two distorted hexagonal rings and one distorted octagonal ring. Each ring is made of a succession of alternate boron and oxygen atoms.

The tetraborate anion occurs in the mineral borax, as an octahydrate, Na2B4O5(OH)4·8H2O. The borax chemical formula is also commonly written in a more compact but equivalent notation as Na2B4O7·10H2O, simply by converting stoechiometrically 4 OH− as 2 O2− and 2 H2O.

Sodium borate can be obtained in high purity and so can be used to make a standard solution in titrimetric analysis.[7]

A number of metal borates are known. They arise by treating boric acid or boron oxides with metal oxides. Examples hereafter include[1] linear chains of 2, 3 or 4 trigonal BO3 structural units, each sharing only one oxygen atom with adjacent unit(s):

Metaborates, such as LiBO2 contain chains of trigonal BO3 structural units, each sharing two oxygen atoms with adjacent units, whereas NaBO2 and KBO2 contain the cyclic B3O62− ion.[8]

Borosilicates

Borosilicate glass, also known as pyrex, can be viewed as a silicate in which some SiO44− units are replaced by BO45− centers, together with a cation to compensate for the difference in valence states of Si(IV) and B(III). Because of this substitution leads to imperfections, the material is slow to crystallise and forms a glass with low coefficient of thermal expansion and is resistant to cracking when heated, unlike soda glass.

Minerals and uses

borax crystals

Common borate salts include sodium metaborate, NaBO2, and borax. Borax is soluble in water, so mineral deposits only occur in places with very low rainfall. Extensive deposits were found in Death Valley and transported out using the famous twenty-mule teams (1883 to 1889). Later (1925), deposits were found at Boron, California on the edge of the Mojave Desert. The Atacama Desert in Chile also contains mineable borate concentrations.

Lithium metaborate or lithium tetraborate, or a mixture of both, can be used in borate fusion sample preparation of various samples for analysis by XRF, AAS, ICP-OES, ICP-AES and ICP-MS. Borate fusion and energy dispersive X-ray fluorescence spectrometry with polarized excitation have been used in the analysis of contaminated soils.[9]

Disodium octaborate tetrahydrate is used as wood preservatives or fungicide. Zinc borate is used as a flame retardant.

Borate esters

Borate esters are organic compounds of the type B(OR)3 where R is alkyl or aryl. They are conveniently prepared by condensation reaction of boric acid and the alcohol:

B(OH)3 + 3 ROH → B(OR)3 +3 H2O

A dehydrating agent, such as concentrated sulfuric acid is typically added.[10] Borate esters are volatile and can be purified by distillation. This procedure is used for analysis of trace amounts of borate and for analysis of boron in steel.[11] Like all boron compounds, alkyl borates burn with a characteristic green flame. This property is used to determine the presence of boron in qualitative analysis.[12]

Trimethyl borate is a popular borate ester used in organic synthesis.

Borate esters form more spontaneously when treated with diols such as sugars.

Trimethyl borate, B(OCH3)3, is used as a precursor to boronic esters for Suzuki couplings:[13] Unsymmetrical borate esters are prepared from alkylation of trimethyl borate:[14]

ArMgBr + B(OCH3)3 → MgBrOCH3 + ArB(OCH3)2
ArB(OCH3)2 + 2 H2O → ArB(OH)2 + 2 HOCH3

These esters hydrolyze to boronic acids, which are used in Suzuki couplings.

See also

References

  1. 1 2 Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier ISBN 0-12-352651-5
  2. ↑ Vegas, A. (1985). "New description of the Ca3(BO3)2 structure". Acta Crystallographica Section C Crystal Structure Communications 41 (11): 1689–1690. doi:10.1107/S0108270185009052. ISSN 0108-2701.
  3. ↑ Ren, M.; Lin, J. H.; Dong, Y.; Yang, L. Q.; Su, M. Z.; You, L. P. (1999). "Structure and Phase Transition of GdBO3". Chemistry of Materials 11 (6): 1576–1580. doi:10.1021/cm990022o. ISSN 0897-4756.
  4. ↑ Atkins; et al. (2010). Inorganic Chemistry (5th ed.). Oxford University Press. p. 334. ISBN 9780199236176.
  5. ↑ Ingri N. (1962) Acta Chem. Scand., 16, 439.
  6. ↑ Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, p. 357, ISBN 0-582-22628-7
  7. ↑ Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, p. 316, ISBN 0-582-22628-7
  8. ↑ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 205. ISBN 0-08-037941-9.
  9. ↑ Hettipathirana, Terrance D. (2004). "Simultaneous determination of parts-per-million level Cr, As, Cd and Pb, and major elements in low level contaminated soils using borate fusion and energy dispersive X-ray fluorescence spectrometry with polarized excitation". Spectrochimica Acta Part B: Atomic Spectroscopy 59 (2): 223–229. Bibcode:2004AcSpe..59..223H. doi:10.1016/j.sab.2003.12.013.
  10. ↑ Brown, Herbert C.; Mead, Edward J.; Shoaf, Charles J. (1956). "Convenient Procedures for the Preparation of Alkyl Borate Esters". J. Am. Chem. Soc 78 (15): 3613–3614. doi:10.1021/ja01596a015.
  11. ↑ Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, p. 666, ISBN 0-582-22628-7
  12. ↑ Vogel, Arthur I.; Svehla, G. (1979), Vogel's Textbook of Macro and Semimicro Qualitative Inorganic Analysis (5th ed.), London: Longman, ISBN 0-582-44367-9
  13. ↑ Li, W.; Nelson, D. P.; Jensen, M. S.; Hoerrner, R. S.; Cai, D.; Larsen, R. D.; Reider, P. J. (2002). "An Improved Protocol for the Preparation of 3-Pyridyl- and Some Arylboronic Acids". J. Org. Chem. 67. p. 5394. Retrieved 2010-12-16.
  14. ↑ R. L. Kidwell, M. Murphy, and S. D. Darling (1969). "Phenols: 6-Methoxy-2-naphthol". Org. Synth. 49: 90.; Coll. Vol. 10, p. 80

External links

Wikimedia Commons has media related to Borates.
This article is issued from Wikipedia - version of the Tuesday, December 29, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.