Publication Type Journal Article
Title Thermochemistry of 2,2,5,7,8-pentamethylchroman-6-ol (PMC) and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox)
Authors Carlos E. S. Bernardes R. A. G. Simões H. P. Diogo M. E. M. Piedade
Groups MET BioMol
Journal JOURNAL OF CHEMICAL THERMODYNAMICS
Year 2014
Month June
Volume 73
Number 0
Pages 140-147
Abstract 2,2,5,7,8-Pentamethylchroman-6-ol (PMC, CAS number 950-99-2) and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox, CAS number 53188-07-1) are perhaps the two most widely used model compounds for alpha-tocoferol, the main active antioxidant form of vitamin E. Because the antioxidant activity of alpha-tocoferol, and of phenol derivatives (ArOH) in general (such as PMC and trolox), is intimately related to the breaking of the ArO-H bond, considerable efforts have been made to investigate how the energetics of that bond is linked to the structure and energetics of both the ArO radical and the ArOH parent compound, which are reflected by the corresponding enthalpies of formation. In this work the standard molar enthalpies of formation of crystalline PMC (triclinic, space group P (1) over bar phase) and trolox (monoclinic, space group P2(1)/c phase), at T = 298.15 K, were obtained as Delta H-f(m)o = -(513.7 +/- 3.4) kJ.mol (1) and Delta H-f(m)o (trolox, cr l) = -(892.5 +/- 4.1) kJ . mol (1) by combustion calorimetry. The results of drop-sublimation Calvet microcalorimetry experiments and vapor pressure vs. temperature measurements by the Knudsen effusion method, combined with C-p,m(o)(cr) and C-p,m(o)(g) data obtained by differential scanning calorimetry and calculated at the B3LYP/6-31+G(d,p) level of theory, respectively, led to Delta H-sub(m)o(PMC) = (107.4 +/- 0.8) kJ.mol (1) and Delta H-sub(m)o = (136.9 +/- 2.5) kJ.mol (1) at T = 298.15 K. From the obtained Delta H-sub(m)o(cr) and Delta H-sub(m)o values it was possible to derive Delta H-sub(m)o(PMC,g) = -(406.3 +/- 3.5) kJ.mol (1) and Delta H-sub(m)o = (755.6 +/- 4.8) kJ.mol (1) at T = 298.15 K. These results led to the conclusion that, in terms of the homodesmotic stabilization enthalpy criteria the replacement of a CH3 group in PMC by a COOH group in trolox approximately conforms to group additivity with no significant contribution from the possible presence of a weak intramolecular hydrogen bond in trolox. (C) 2013 Elsevier Ltd. All rights reserved.
DOI http://dx.doi.org/10.1016/j.jct.2013.11.032
ISBN
Publisher ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
Book Title
ISSN 0021-9614
EISSN 1096-3626
Conference Name
Bibtex ID ISI:000335846900021
Observations
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