Interaction between methyl glyoxal and ascorbic acid: experimental and theoretical aspects
The absorption spectral change of methyl glyoxal (MG) due to the interaction with ascorbic acid (AA or Vitamin C) has been investigated using steady-state spectroscopic technique. A plausible explanation for the spectral change has been discussed on the basis of hydrogen bonding interaction between...
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Veröffentlicht in: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2004-06, Vol.60 (7), p.1523-1526 |
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container_title | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy |
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creator | Banerjee, D. Koll, A. Filarowski, A. Bhattacharyya, S.P. Mukherjee, S. |
description | The absorption spectral change of methyl glyoxal (MG) due to the interaction with ascorbic acid (AA or Vitamin C) has been investigated using steady-state spectroscopic technique. A plausible explanation for the spectral change has been discussed on the basis of hydrogen bonding interaction between the two interacting species. The equilibrium constant for the complex formation due to hydrogen bonding interaction between MG and AA has been obtained from absorption spectral changes. Ab inito calculations with DFT B3LYP/6/31G (d,p) basis sets have been used to find out the molecular structure of the hydrogen bonded complex. The O⋯H distance found in the OH⋯O hydrogen bond turns out to be quite short (1.974
Å) which is in conformity with the large value of the equilibrium constant determined experimentally. |
doi_str_mv | 10.1016/j.saa.2003.08.022 |
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Å) which is in conformity with the large value of the equilibrium constant determined experimentally.</description><subject>Ascorbic acid</subject><subject>Ascorbic Acid - chemistry</subject><subject>Hydrogen Bonding</subject><subject>Interaction</subject><subject>Macromolecular Substances</subject><subject>Methyl glyoxal</subject><subject>Models, Molecular</subject><subject>Pyruvaldehyde - chemistry</subject><subject>Spectrophotometry, Ultraviolet</subject><issn>1386-1425</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLtOwzAUhj2AaCk8AAvKxNZwbCepAxOquFSqxAILi2U7J9RVLsV2oX17XDUSG9PR0X-R_o-QKwopBVrcrlOvVMoAeAoiBcZOyJhyUUxpxvIROfd-DQBUMDgjI5rTbFaUfEw-Fl1Ap0ywfZdoDD-IXdJiWO2b5LPZ9zvVJKqrEuVN77Q1iTK2uktwt0FnW-zCoIcV9g6DNYffb9AEf0FOa9V4vBzuhLw_Pb7NX6bL1-fF_GE5NTwrwzSnWmhesbIWHHReU6Y1rSgvMiUyATPKNUJuKi6yGpjJQUBd1IWIKhRMFXxCbo69G9d_bdEH2VpvsGlUh_3WyxktWclEHo30aDSu995hLTdxg3J7SUEeIMq1jBDlAaIEISPEmLkeyre6xeovMRCMhvujAePEb4tOemOxM1hZFynIqrf_1P8CiiiEkA</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Banerjee, D.</creator><creator>Koll, A.</creator><creator>Filarowski, A.</creator><creator>Bhattacharyya, S.P.</creator><creator>Mukherjee, S.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040601</creationdate><title>Interaction between methyl glyoxal and ascorbic acid: experimental and theoretical aspects</title><author>Banerjee, D. ; Koll, A. ; Filarowski, A. ; Bhattacharyya, S.P. ; Mukherjee, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-51b8b3d29f830b5f12bb1d1364a8480713be05cd384f02c5080f6f68a84062a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Ascorbic acid</topic><topic>Ascorbic Acid - chemistry</topic><topic>Hydrogen Bonding</topic><topic>Interaction</topic><topic>Macromolecular Substances</topic><topic>Methyl glyoxal</topic><topic>Models, Molecular</topic><topic>Pyruvaldehyde - chemistry</topic><topic>Spectrophotometry, Ultraviolet</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banerjee, D.</creatorcontrib><creatorcontrib>Koll, A.</creatorcontrib><creatorcontrib>Filarowski, A.</creatorcontrib><creatorcontrib>Bhattacharyya, S.P.</creatorcontrib><creatorcontrib>Mukherjee, S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Banerjee, D.</au><au>Koll, A.</au><au>Filarowski, A.</au><au>Bhattacharyya, S.P.</au><au>Mukherjee, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction between methyl glyoxal and ascorbic acid: experimental and theoretical aspects</atitle><jtitle>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</jtitle><addtitle>Spectrochim Acta A Mol Biomol Spectrosc</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>60</volume><issue>7</issue><spage>1523</spage><epage>1526</epage><pages>1523-1526</pages><issn>1386-1425</issn><abstract>The absorption spectral change of methyl glyoxal (MG) due to the interaction with ascorbic acid (AA or Vitamin C) has been investigated using steady-state spectroscopic technique. A plausible explanation for the spectral change has been discussed on the basis of hydrogen bonding interaction between the two interacting species. The equilibrium constant for the complex formation due to hydrogen bonding interaction between MG and AA has been obtained from absorption spectral changes. Ab inito calculations with DFT B3LYP/6/31G (d,p) basis sets have been used to find out the molecular structure of the hydrogen bonded complex. The O⋯H distance found in the OH⋯O hydrogen bond turns out to be quite short (1.974
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subjects | Ascorbic acid Ascorbic Acid - chemistry Hydrogen Bonding Interaction Macromolecular Substances Methyl glyoxal Models, Molecular Pyruvaldehyde - chemistry Spectrophotometry, Ultraviolet |
title | Interaction between methyl glyoxal and ascorbic acid: experimental and theoretical aspects |
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