Investigation of L(+)-Ascorbic acid with Raman spectroscopy in visible and UV light

References

• Tolbert, B.M., Downing, M.R., Carlson, W., Knight, M.K., and Baker, E.M. (1975) Chemistry and metabolism of ascorbic acid and ascorbate sulfate. Ann. New York Acad. Sci., 258: 48–69.
   PubMedGoogle Scholar
• Neta, P., Huie, R.E., Mosseri, S., Shastri, L.V., Mittal, J.P., Maruthamuthu, P., and Steenken, S. (1989) Rate constants for reduction of substituted methylperoxyl radicals by ascorbate ions and N,N,N,N-tetramethyl-p-phenylenediamine. J. Phys. Chem., 93: 4099–4104.
   Web of Science ®Google Scholar
• Zapata, S. and Dufour, J.-P. (1992) Ascorbic ascorbic, dehydroascorbic and lsoascorbic, acid simultaneous determinations by reverse phase ion interaction HPLC. J. Food Sci., 57 (2): 506–511.
   Web of Science ®Google Scholar
• Allen, R.N., Shukla, M.K., Reed, D., and Leszczynski, J. (2006) Ab inito study of the structural properties of ascorbic acid (vitamin C). Int. J. Quantum Chem., 106 (14): 2934–2943.
   Web of Science ®Google Scholar
• Amorati, R., Pedulli, G.F., and Valgimigli, L. (2011) Kinetic and thermodynamic aspects of the chain-breaking antioxidant activity of ascorbic acid derivatives in non-aqueous media. Org. Biomol. Chem., 9: 3792–3800.
   PubMed Web of Science ®Google Scholar
• Schlueter, A.K. and Johnston, C.S. (2011) Vitamin C: overview and update. J. Evid. Base. Compl. Alternative Med., 16 (1): 49–57.
   Google Scholar
• Padayatti, S.J., Katz, A., Eck, P., Lee, J., Chen, S., Corpe, C., Dutta, S.K., and Levine, M. (2003) Vitamin C as an antioxidant: evaluation of its role in disease prevention. J. Am. Coll. Nutr., 22: 18–35.
   PubMed Web of Science ®Google Scholar
• Peng, Z., Duncan, B., Pocock, K.F., and Sefton, M.A. (1998) The effect of ascorbic acid on oxidative browning of white wines and model wines. Aust. J. Grape Wine Res., 4 (3): 127–135.
   Google Scholar
• Darvin, M.E., Sterry, W., and Lademann, J. (2010) Resonance Raman spectroscopy as an effective tool for the determination of antioxidative stability of cosmetic formulations. J. Biophoton., 3 (1–2): 82–88.
   PubMed Web of Science ®Google Scholar
• Hvoslef, J. (1969) Changes in conformation and bonding of ascorbic acid by ionization. The crystal structure of sodium ascorbate. Acta. Crystallogr., B25: 2214–2223.
   Web of Science ®Google Scholar
• Ogata, Y. and Kosugi, Y. (1970) Ultraviolet spectra of L-ascorbic acid and cupric ascorbate complex. Tetrahedron, 26: 4711–4716.
   PubMed Web of Science ®Google Scholar
• Forsberg, O., Johansson, K., Ulmgren, P., and Wahlberg, O. (1973) Equilibrium studies of l-ascorbate ions. Chem. Scripta, 3: 153–158.
   Google Scholar
• Berger, S. (1984) 13C, 13C spin coupling constants as a probe for mesomeric structures: vitamin C. J. Chem. Soc., Chem. Comm., 1252–1253.
   Google Scholar
• Karayannis, M.I., Samios, D.N., and Gousetis, C.P. (1997) A study of the molar absorptivity of ascorbic acid at different wavelengths and pH values. Anal. Chim. Acta, 93: 275–279.
   Web of Science ®Google Scholar
• Juhasz, J.R., Pisterzi, L.F., Gasparro, D.M., Almeida, D.R.P., and Csizmadia, I.G. (2003), The effect of conformation on the acidity of ascorbic acid: a density functional study. J. Mol. Struct., 666–667: 401–407.
   Web of Science ®Google Scholar
• Sato, H. and Ikeya, M. (2004) Organic molecules and nanoparticles in inorganic crystals: vitamin C in CaCO3 as an ultraviolet absorber. J. Appl. Phys., 95 (6): 3031–3036.
   Web of Science ®Google Scholar
• Köse, D.A. and Zümreoglu-Karan, B. (2009) Complexation of boric acid with vitamin C. New J. Chem., 33 (9): 1874–1881.
   Web of Science ®Google Scholar
• Kanters, J.A., Roelofsen, G., and Alblas, B.P. (1977) Changes in conformation and bonding of D-isoascorbic acid by ionisation. The crystal structure of sodium d-isoascorbate monohydrate. Acta Crystallogr., B33: 1903–1912.
   Google Scholar
• Njus, D. and Kelley, P.M. (1993) The secretory-vesicle ascorbate-regenerating system: a chain of concerted H+/e− transfer reactions. Biochim. Biophys. Acta, 1144 (3): 235–248.
   PubMed Web of Science ®Google Scholar
• Brenner, G.S., Hinkley, D.F., Perkins, L.M., and Weber, S. (1964) Isomerization of the ascorbic acids. J. Org. Chem., 29: 2389–2392.
   Web of Science ®Google Scholar
• Njus, D. and Kelley, P.M. (1991) Vitamins C and E donate single hydrogen atoms in vivo. FEBS Lett., 284 (2): 147–151.
   PubMed Web of Science ®Google Scholar
• Washko, P.W., Welch, R.W., Dhariwal, K.R., Wang, Y., and Levine, M. (1992) Review: ascorbic acid and dehydroascorbic acid analyses in biological samples. Anal. Biochem., 204: 1–14.
   PubMed Web of Science ®Google Scholar
• Costanzo, F., Sulpizi, M., Vandevondele, J., Della Valle, R.G., and Sprik, M. (2007) Ab initio molecular dynamics study of ascorbic acid in aqueous solution. Mol. Phys., 105 (1): 17–23.
   Web of Science ®Google Scholar
• Hvoslef, J. (1968) The crystal structure of L-ascorbic acid, “vitamin C.” I. The X-ray analysis. Acta Crystallogr., B24: 23–35.
   Web of Science ®Google Scholar
• Hvoslef, J. (1968) The crystal structure of L-ascorbic acid, “vitamin C.” II. The neutron diffraction analysis. Acta Crystallogr., B24: 1431–1440.
   Google Scholar
• Milanesio, M., Bianchi, R., Ugliengo, P., Roetti, C., and Viterbo, D. (1997) Vitamin C at 120 K: experimental and theoretical study of the charge density. J. Mol. Struct. (Theochem), 419: 139–154.
   Web of Science ®Google Scholar
• Hearn, R.A. and Bugg, C.E. (1974) Calcium binding to carbohydrates: crystal structure of calcium ascorbate dihydrate. Acta Crystallogr., B30: 2705–2711.
   Web of Science ®Google Scholar
• Hvoslef, J. and Kjellevold, K.E. (1974) The crystal structure of calcium ascorbate dihydrate. Acta Crystallogr., B30: 2711–2716.
   Web of Science ®Google Scholar
• Abrahams, S.C., Bernstein, J.L., Bugg, C.E., and Hvoslef, J. (1978) Comparison of two independent determinations of the structure of calcium L-ascorbate dihydrate. Acta Crystallogr., B34: 2981–2985.
   Web of Science ®Google Scholar
• Ståhl, K., Andersen, J.E.T., and Christgau, S. (2006) Strontium diascorbate dihydrate. Acta Crystallogr., 62: m144–m149.
   Web of Science ®Google Scholar
• Koziol, A.E., Stepniak, K. and Lis, T. (1992) The crystal structure of lithium L-ascorbate dihydrate. Carbohydr. Res., 226: 43–48.
   PubMed Web of Science ®Google Scholar
• Hughes, D.L. (1973) Crystal structure of thallium(I) L-ascorbate. J. Chem. Soc. Dalton Trans., 2209–2215.
   Google Scholar
• McClelland, B.W. (1974) Crystal and molecular structure of barium 2-O-sulfonato-L-ascorbate dihydrate. Acta Crystallogr., B30: 178–186.
   Web of Science ®Google Scholar
• Tajmir-Riahi, H.A. (1990) Coordination chemistry of vitamin C. Part I–III. J. Inorg. Biochem., 40: 181–188.
   PubMed Web of Science ®Google Scholar
• Tajmir-Riahi, H.A. (1991a) Coordination chemistry of vitamin C. Part II. J. Inorg. Biochem., 42: 47–55.
   PubMed Web of Science ®Google Scholar
• Tajmir-Riahi, H.A. (1991b) Coordination chemistry of vitamin C. Part III. J. Inorg. Biochem., 44: 39–45.
   Web of Science ®Google Scholar
• Tajmir-Riahi, H.A. and Boghai, D.M. (1992) Coordination chemistry of vitamin C. Part IV. J. Inorg. Biochem., 45: 73–84.
   Web of Science ®Google Scholar
• Edsall, J.T. and Sagall, E.L. (1943) Raman spectra of L-ascorbic acid, tetronic acid and related compounds. J. Am. Chem. Soc., 65 (7): 1312–1316.
   Google Scholar
• Hvoslef, J. and Klæboe, P. (1971) Vibrational spectroscopic studies of L-ascorbic acid and sodium ascorbate. Acta Chem. Scand., 25: 3043–3053.
   Google Scholar
• Falk, M. and Wojcik, M.J. (1979) Effect of temperature and hydrogen-bond strength on the i.r. absorption of isolated OH oscillators: crystalline L-ascorbic acid. Spectrochim. Acta, 35: 1117–1123.
   Web of Science ®Google Scholar
• Lohmann, W., Pagel, D., and Penka, V. (1984) Structure of ascorbic acid and its biological function. Determination of the conformation of ascorbic acid and isoascorbic acid by infrared and ultraviolet investigations. Eur. J. Biochem., 138 (3): 479–480.
   PubMedGoogle Scholar
• Lohmann, W., Beinhauer, K., and Sapper, H. (1984) Proton- and carbon-13-NMR spectra of ascorbate and isoascorbate. Naturwissenschaften, 71 (9): 477–478.
   Web of Science ®Google Scholar
• Ferrer, E.G. and Baran, E.J. (2001) Reduction of vanadium(V) with ascorbic acid and isolation of the generated oxovanadium(IV) species. Biol. Trace Elem. Res., 83: 111–119.
   PubMed Web of Science ®Google Scholar
• De Gelder, J., De Gussem, K., Vandenabeele, P., and Moens, L. (2007) Reference database of Raman spectra of biological molecules. J. Raman Spectros., 38: 1133–1147.
   Web of Science ®Google Scholar
• Panicker, C.Y., Varghese, H.T., and Philip, D. (2006) FT-IR, FT-Raman and SERS spectra of vitamin C. Spectrochim. Acta, 65: 802–804.
   PubMed Web of Science ®Google Scholar
• Shimada, H., Nibu, Y., and Shimada, R. (2008) Pressure effects on inter- and intramolecular vibrations in hydrogen-bonded L-ascorbic acid crystal. J. Raman Spectros., 39: 32–39.
   Web of Science ®Google Scholar
• Jehlička, J., Vítek, P., and Edwards, H.G.M. (2010) Raman spectra of organic acids obtained using a portable instrument at −5°C in a mountain area at 2000 m above sea level. J. Raman Spectros., 41: 440–444.
   Web of Science ®Google Scholar
• Saraiva, G.D., Lima, J.A., Jr., de Sousa, F.F., Freire, P.T.C., Mendes Filho, J., and Souza Filho, A.G. (2011) Temperature dependent Raman scattering study of L-ascorbic acid. Vib. Spectros., 55: 101–106.
   Web of Science ®Google Scholar
• Adams, D.M. and Berg, R.W. (1976) Low-temperature far-infrared spectra of some tetrachloropalladate(II) and tetrachloroplatinate(II) salts. J. Chem. Soc. Dalton Trans., 1976: 52–58.
   Google Scholar
• Krebs Larsen, F. and Berg, R.W. (1977) A neutron diffraction study of the crystal structure of deuterated ammonium tetrachloropalladate(II) at low and ambient temperature. Acta Chem. Scand., A31: 375–378.
   Google Scholar
• Krebs, B., Greiwing, H., Brendel, C., Taulelle, F., Gaune-Escard, M., and Berg, R.W. (1991) Crystallographic and 27A1-NMR study on premelting phenomena in crystals of sodium tetrachloroaluminate. Inorg. Chem., 30: 981–988.
   Web of Science ®Google Scholar
• Bichara, L.C., Lanus, H.E., Nieto, C.G., and Brandan, S.A. (2010) Density functional theory calculations of the molecular force field of L-ascorbic acid, vitamin C. J. Phys. Chem., A144: 4997–5004.
   Web of Science ®Google Scholar
• Singh, P., Singh N.P., and Yadav, R.A. (2010) Study of the optimized molecular structures and vibrational characteristics of neutral L-ascorbic acid and its anion and cation radical using density functional theory. J. Chem. Pharm. Res., 2 (5): 656–681.
   Google Scholar
• Yadav, R.A., Rani, P., Kumar, M., Singh, R., Singh, P., and Singh, N.P. (2011) Experimental IR and Raman spectra and quantum chemical studies of molecular structures, conformers and vibrational characteristics of L-ascorbic acid and its anion and cation radical. Spectrochim. Acta, A84 (1): 6–21.
   Web of Science ®Google Scholar
• Carlson, G.L., Cable, H., and Pedersen, L.G. (1976) An ab initio study of ascorbic acid. Chem. Phys. Lett., 38 (1): 75–78.
   Web of Science ®Google Scholar
• Al-Laham, M.A., Petersson, G.A., and Haake, P. (1991) Ab initio study of ascorbic acid conformations. J. Comput. Chem., 12(1): 113–118.
   Web of Science ®Google Scholar
• Mora, M.A. and Melendez, F.J. (1998) Conformational ab initio study of ascorbic acid. J. Mol. Struct. (Theochem), 454: 175–185.
   Web of Science ®Google Scholar
• O’Malley, P.J. (2001) Density Functional calculations modelling the spin density distribution, hyperfine couplings, and hydrogen bonding environment of the ascorbate (vitamin C) free radical. J. Phys. Chem., B105: 11290–11293.
   Web of Science ®Google Scholar
• Dimitrova, Y. (2006) Theoretical study of the changes in the vibrational characteristics arising from the hydrogen bonding between vitamin C (L-ascorbic acid) and H2O. Spectrochim. Acta, A63: 427–437.
   Web of Science ®Google Scholar
• Frisch, M.J., Trucks, G.W., Schlegel, H.B., Scuseria, G.E., Robb, M.A., Cheeseman, J.R., Montgomery, J.A., Jr., Vreven, T., Kudin, K.N., Burant, J.C., Millam, J.M., Iyengar, S.S., Tomasi, J., Barone, V., Mennucci, B., Cossi, M., Scalmani, G., Rega, N., Petersson, G.A., Nakatsuji, H., Hada, M., Ehara, M., Toyota, K., Fukuda, R., Hasegawa, J., Ishida, M., Nakajima, T., Honda, Y., Kitao, O., Nakai, H., Klene, M., Li, X., Knox, J.E., Hratchian, H.P., Cross, J.B., Bakken, V., Adamo, C., Jaramillo, J., Gomperts, R., Stratmann, R.E., Yazyev, O., Austin, A.J., Cammi, R., Pomelli, C., Ochterski, J.W., Ayala, P.Y., Morokuma, K., Voth, G.A., Salvador, P., Dannenberg, J.J., Zakrzewski, V.G., Dapprich, S., Daniels, A.D., Strain, M.C., Farkas, O., Malick, D.K., Rabuck, A.D., Raghavachari, K., Foresman, J.B., Ortiz, J.V., Cui, Q., Baboul, A.G., Clifford, S., Cioslowski, J., Stefanov, B.B., Liu, G., Liashenko, A., Piskorz, P., Komaromi, I., Martin, R.L., Fox, D.J., Keith, T., Al-Laham, M.A., Peng, CY., Nanayakkara, A., Challacombe, M., Gill, P.M.W., Johnson, B., Chen, W., Wong, M.W., Gonzalez, C., and Pople, J.A. (2004) Gaussian 03 W, Rev. E.01. Gaussian, Inc.: Wallingford, CT.
   Google Scholar
• Fairchild, S.Z., Bradshaw, C.F., Su, W. and Guharay, S.K. (2009) Predicting Raman spectra using density functional theory. Appl. Spectros., 63 (7): 733–741.
   PubMed Web of Science ®Google Scholar
• Harrand, M. and Lennuier, R. (1946) Exaltation of the intensity of certain bands in the Raman spectra emitted from solids with an absorption band near the excitation wavelength. Compt. Rend. Acad. Sci., 223: 356–357 ( in French).
   Google Scholar
• Liu, C. and Berg, R.W. (2013) Nonlinearity in intensity versus concentration dependence for the deep UV resonance raman spectra of toluene and heptane. Appl. Spectros. Rev., 48: 425–437.
   Web of Science ®Google Scholar
• Shriver, D.F. and Dunn, J.B.R. (1974) The backscattering geometry for Raman spectrometry of colored materials. Appl. Spectros., 28 (4): 319–323.
   Web of Science ®Google Scholar
• Asher, S.A., Ludwig, M., and Johnson, C.R. (1986) UV resonance Raman excitation profiles of the aromatic amino acids. J. Am. Chem. Soc., 108: 3186–3197.
   Web of Science ®Google Scholar
• Asher, S.A. (2002) Ultraviolet Raman spectroscopy. In Handbook of Vibrational Spectroscopy, vol. 50. Chalmers, J.M. and Griffiths, P.R. Eds. J. Wiley & Sons: New York, pp. 557–571.
   Google Scholar
• Wittine, K., Gazivoda, T., Markus, M., Mrvos-Sermek, D., Hergold-Brundic, A., Cetina, M., Ziher, D., Gabelica, V., Mintas, M., and Raic-Malic, S. (2004) Crystal structures, circular dichroism spectra and absolute configurations of some L-ascorbic acid derivatives. J. Mol. Struct., 687 (1–3): 101–106.
   Web of Science ®Google Scholar
• Davey, M.W., Bauw, G., and Van Montagu, M. (1996) Analysis of ascorbate in plant tissues by high-performance capillary zone electrophoresis. Anal. Biochem., 239: 8–19.
   PubMed Web of Science ®Google Scholar
• Kimoto, E., Terada, S., and Yamaguchi, T. (1997) Analysis of ascorbic acid, dehydroascorbic acid, and transformation products by ion-pairing high-performance liquid chromatography with multiwavelength ultraviolet and electrochemical detection. Meth. Enzymol., 279: 3–12.
   PubMed Web of Science ®Google Scholar
• Albrecht, A.C. (1961) On the theory of Raman intensities. J. Chem. Phys., 34: 1476–1484.
   Web of Science ®Google Scholar
• Hassing, S. and Sonnich Mortensen, O. (1980) Kramers-Kronig relations and resonance Raman scattering. J. Chem. Phys., 73 (3): 1078–1083.
   Web of Science ®Google Scholar
• Tuschel, D.D., Mikhonin, A.V., Lemoff, B.E., and Asher, S.A. (2011) Deep ultraviolet resonance Raman excitation enables explosive detection. Appl. Spectros., 64 (4): 425–432.
   Web of Science ®Google Scholar
• Vickers, T.J., Mann, C.K., Zhu, J., and Chong, C.K. (1991) Quantitative resonance Raman spectroscopy. Appl. Spectros. Rev., 26 (4): 341–375.
   Web of Science ®Google Scholar
• McHale, J.L. (2002) Resonance Raman spectroscopy. In Handbook of Vibrational Spectroscopy, vol. 50. Chalmers, J.M. and Griffiths, P.R., Eds. J. Wiley & Sons: New York, pp. 534–556.
   Google Scholar
• Efremov, E.V., Ariese, F. and Gooijer, C. (2008) Achievements in resonance Raman spectroscopy. Review of a technique with a distinct analytical chemistry potential. Anal. Chim. Acta, 606: 119–134.
   PubMed Web of Science ®Google Scholar
• Liu, C. and Berg, R.W. (2012) Determining the spectral resolution of a charge-coupled device (CCD) Raman instrument. Appl. Spectros., 66 (9): 1034–1043.
   Web of Science ®Google Scholar
• Asher, S.A. and Johnson, C.R. (1984) Raman spectroscopy of a coal liquid shows that fluorescence interference is minimized with ultraviolet excitation. Science, New Series, 225 (4659): 311–313.
   PubMed Web of Science ®Google Scholar
• Loppnow, G.R., Shoute, L., Schidt, K.J., Savage, A., Hall, R.H., and Bulmer, J.T. (2004) UV Raman spectroscopy of hydrocarbons. Phil. Trans. R. Soc. Lond., A362: 2461–2476.
   Web of Science ®Google Scholar
• Berg, R.W., Ferré, I.M., and Schäffer, S.J.C. (2006) Raman spectroscopy evidence of 1:1:1 complex formation during dissolution of WO3 in a melt of K2S2O7:K2SO4. Vib. Spectros. 42: 346–352.
   Web of Science ®Google Scholar
• Berg, R.W. and Nørbygaard, T. (2006) Wavenumber calibration of CCD detector Raman spectrometers controlled by a sinus arm drive. Appl. Spectros. Rev., 41: 165–183.
   Web of Science ®Google Scholar
• Liu, C. (2012) Implementation of Deep Ultraviolet Raman Spectroscopy, Ph.D. Thesis, Printed at DTU Chemistry: Lyngby, Denmark.
   Google Scholar
• Berg, R.W., Nørbygaard, T., White, P.C., and Abdali, S. (2011) Ab initio calculations, Raman and SERS spectral analyses of amphetamine species. Appl. Spectros. Rev., 46 (2): 107–131.
   Web of Science ®Google Scholar
• Berg, R.W., Shim, I., White, P.C., and Abdali, S. (2012) ROA and Raman spectra of amphetamine species—quantum chemical model calculations and experiments. Am. J. Anal. Chem., 3: 410–421.
   Google Scholar
• Berg, R.W., Deetlefs, M., Seddon, K.R., Shim, I., and Thompson, J. (2005) Raman and ab initio studies of simple and binary 1-alkyl-3-methylimidazolium ionic liquids. J. Phys. Chem. B, 109 (40): 19018–19025.
   PubMed Web of Science ®Google Scholar
• Berg, R.W. (2007) Raman spectroscopy and ab-initio model calculations on ionic liquids: a review. Monatsh. Chem. Chem. Mon., 138: 1045–1075.
   Web of Science ®Google Scholar
• Turrell, G. (1984) Analysis of polarization measurements in Raman microspectroscopy. J. Raman Spectros., 15 (2): 103–108.
   Web of Science ®Google Scholar
• Porto, S.P.S., Giordmaine, J.A., and Daman T.C. (1966) Depolarization of Raman scattering in calcite. Phys. Rev., 147: 608–611.
   Web of Science ®Google Scholar
• Porto, S.P.S. and Krishnan, R.S. (1961) Raman effect of corundum. J. Chem. Phys., 47: 1009–1012.
   Web of Science ®Google Scholar
• Dawson, P. (1972) Polarisation measurements in Raman spectroscopy. Spectrochim. Acta, 28: 715–723.
   Web of Science ®Google Scholar
• Brooker, M.H., Hancock, G., Rice, B.C., and Shapter, J. (1989) Raman frequency and intensity studies of liquid water (H2O, H218O and D2O). J. Raman Spectros., 20 (10): 683–694.
   Web of Science ®Google Scholar
• Baschenko, S.M. and Marchenko, L.S. (2011) On Raman spectra of water, its structure and dependence on temperature. Semiconductor Physics, Quantum Electronics and Optoelectronics, 11 (1): 77–79.
   Google Scholar