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Rosocyanine

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Rosocyanine
Names
Other names
Rosocyanine
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C42H44BO12.ClH/c1-48-39-21-27(9-17-35(39)44)5-13-31-25-32(14-6-28-10-18-36(45)40(22-28)49-2)53-43(52-31)54-33(15-7-29-11-19-37(46)41(23-29)50-3)26-34(55-43)16-8-30-12-20-38(47)42(24-30)51-4;/h5-24,31-34,44-47H,25-26H2,1-4H3;1H/q+1;/p-1/b13-5+,14-6+,15-7+,16-8+; checkY
    Key: XZWTYNUGOWPDCM-JWMINOHISA-M checkY
  • InChI=1S/C42H44BO12.ClH/c1-48-39-21-27(9-17-35(39)44)5-13-31-25-32(14-6-28-10-18-36(45)40(22-28)49-2)53-43(52-31)54-33(15-7-29-11-19-37(46)41(23-29)50-3)26-34(55-43)16-8-30-12-20-38(47)42(24-30)51-4;/h5-24,31-34,44-47H,25-26H2,1-4H3;1H/q+1;/p-1/b13-5+,14-6+,15-7+,16-8+;
  • Key: XZWTYNUGOWPDCM-JWMINOHISA-M
  • [Cl-].Oc1ccc(cc1OC)/C=C/C5CC(O[B@+]3(OC(CC(/C=C/c2ccc(O)c(OC)c2)O3)/C=C/c4ccc(O)c(OC)c4)O5)/C=C/c6ccc(O)c(OC)c6
Properties
[B(C21H19O6)2]Cl (as chloride)
Molar mass 781.013 g/mol
Appearance dark-green colored solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Rosocyanine and Rubrocurcumin are two red colored materials, which are formed by the reaction between curcumin and borates.

Application

The color reaction between borates and curcumin is used within the spectrophotometrical determination and quantification of boron present in food or materials. Curcumin is a yellow coloring natural pigment found in the root stocks of some Curcuma species, especially Curcuma longa (turmeric), in concentrations up to 3%. In the so called curcumin method for boron quantification it serves as reaction partner for boric acid. The reaction is very sensitive and so the smallest quantities of boron can be detected. The maximum absorbance at 540 nm for rosocyanine is used in this colorimetric method. The formation of rosocyanine depends on the reaction conditions. The reaction is carried out preferentially in acidic solutions containing hydrochloric or sulfuric acid. The color reaction also takes place under different conditions; however, in alkaline solution, gradual decomposition is observed. The reaction might be disturbed at higher pH values, interfering with other compounds.

Space filling model

Rosocyanine is formed as 2:1 complex from curcumin and boric acid in acidic solutions. The boron complexes formed with rosocyanine are dioxaborines (here a 1,3,2-dioxaborine). Curcumin possesses a 1,3-diketone structure and can therefore considered as a chelating agent. Unlike the simpler 1,3-diketone–containing compound acetylacetone (which forms acetylacetonate complexes with metals), the entire skeleton of curcumin is in resonance with the 1,3-dicarbonyl section, making the backbone an extended conjugated system. Investigations of the structure have shown that the positive charge is distributed throughout the molecule. In rosocyanine, the two curcumin moieties are not coplanar but rather perpendicular relative to one another (as seen in the 3D model), as a result of the tetrahedral geometry of tetracoordinate boron. The same applies to rubrocurcumin.

In order to exclude the presence of other materials during the boron quantification using the curcumin method, a variant of the process was developed. In this process, 2,2-dimethyl-1,3-hexanediol or 2-ethyl-1,3-hexanediol are added, in addition to curcumin, to a neutral solution of the boron-containing solution. The complex formed between boron and the 1,3-hexanediol derivative is removed from the aqueous solution by extraction in an organic solvent. Acidification of the organic phase yields rubrocyanine, which can be detected by colorimetric methods. The reaction of curcumin with borates in presence of oxalic acid produces the coloring compound rubrocurcumin.

Characteristics

Rosocyanine is a dark green solid with a glossy, metallic shine that forms red colored solutions. It is almost insoluble in water and some organic solvents, very slightly soluble (up to 0.01%) in ethanol, and somewhat soluble (approximately 1%) in pyridine, sulfuric acid, and acetic acid. An alcoholic solution of rosocyanine temporarily turns deeply blue on treatment with alkali.

In rubrocurcumin one molecule curcumin is replaced with oxalic acid. Rubrocurcumin produces a similar red colored solution. Rosocyanine is an ionic compound, while rubrocurcumin is a neutral complex.

See also

References

  • M. E. Schlumberger: Sur la réaction de l'acide borique sur la curcumine. In: Bulletin de la Société Chimique de Paris N.S. 5, p. 194-202 (1866), ISSN: 0991-6504.
  • L. Clarke and C. L. Jackson: Rosocyanine. In: American Chemical Journal Vol. 39, p. 696-719 (1908); ISSN: 0096-4085, CODEN: ACJOAZ.
  • Spicer, G. S.; Strickland, J. D. H. (1952). "Compounds of Curcumin and Boric acid. Part I. The structure of rosocyanin". Journal of the Chemical Society (London) (article 906): 4644–4650. doi:10.1039/JR9520004644. ISSN 0368-1769. CODEN: JCSOA9.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Bellamy, L. J.; Spicer, G. S.; Strickland, J. D. H. (1952). "Compounds of Curcumin and Boric acid. Part III. Infra-red studies of rosocyanine and allied compounds". Journal of the Chemical Society (London). 1952 (article 908): 4653–4656. doi:10.1039/JR9520004653. ISSN 0368-1769. CODEN: JCSOA9.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Spicer, G. S.; Strickland, J. D. H. (1958). "Determination of microgram and submicrogram amounts of boron. I. Absorptiometric determination with curcumin". Analytica Chimica Acta. 18: 231–239. doi:10.1016/S0003-2670(00)87133-0. ISSN 0003-2670. CODEN: ACACAM.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • H. J. Roth and B. Miller: Zur Kenntnis der Farbreaktion zwischen Borsaeure und Curcumin, I. In: Archiv der Pharmazie, Berichte der Deutschen Pharmazeutischen Gesellschaft Vol. 297, No. 10, p. 617-623 (1964); ISSN: 0376-0367, CODEN: APBDAJ.
  • H. J. Roth and B. Miller: Zur Kenntnis der Farbreaktion zwischen Borsaeure und Curcumin, II. In: Archiv der Pharmazie, Berichte der Deutschen Pharmazeutischen Gesellschaft Vol. 297, No. 11, p. 660-673 (1964); ISSN: 0376-0367, CODEN: APBDAJ.
  • Fritz Umland, Detlef Thierig and Gunther Mueller: Photometrische Bestimmung von Bor im Picogram-Bereich. In: Fresenius Journal of Analytical Chemistry Vol. 215, No. 5, p. 401-406 (1966); ISSN: 0937-0633, CODEN: FJACEP.
  • P. Quint and F. Umland: On the composition of the (1 2)-boron-curcumin-chelate »rosocyanine«. In: Fresenius Journal of Analytical Chemistry Vol. 295, No. 4, p. 269-270 (1979); ISSN: 0937-0633, CODEN: FJACEP.
  • David W. Dyrssen, Yu. P. Novikov and Leif R. Uppstrom: Chemistry of the determination of boron with curcumin. In: Analytica Chimica Acta Vol. 60, No. 1, p. 139-151 (1972); ISSN: 0003-2670, CODEN: ACACAM.
  • C. G. Kowalenko and L. M. Lavkulich: A modified curcumin method for boron analysis of soil extracts. In: Canadian Journal of Soil Science Vol. 56, No. 4, p. 537-539 (1976); ISSN: 0008-4271, CODEN: CJSSAR.
  • Ulrike de la Chevallerie-Haaf, Axel Meyer and Guenter Henze: Photometrische Bestimmung von Bor im Grund- and Oberflächenwasser. In: Fresenius Journal of Analytical Chemistry Vol. 323, No. 3, P. 266-270 (1986); ISSN: 0937-0633, CODEN: FJACEP.
  • Elsie M. Donaldson: Spectrophotometric determination of boron in iron and steel with curcumin after separation by 2-ethyl-1,3-hexanediol-chloroform extraction. In: Talanta Vol. 28, No. 11, p. 825-831 (1981); ISSN: 0039-9140, CODEN: TLNTA2.
  • B. Wikner: Boron determination in natural waters with curcumin using 2,2-dimethyl-1,3-hexanediol to eliminate interferences. In: Communications in Soil Science and Plant Analysis Vol. 12, No. 7, p. 697-709 (1981); ISSN: 0010-3624, CODEN: CSOSA2.
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