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Glucose transformation to 5‐hydroxymethylfurfural in acidic ionic liquid: A quantum mechanical study
Author(s) -
Puripat Maneeporn,
Yokogawa Daisuke,
Parasuk Vudhichai,
Irle Stephan
Publication year - 2016
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.24214
Subject(s) - ionic liquid , 5 hydroxymethylfurfural , quantum , transformation (genetics) , chemistry , quantum chemical , computational chemistry , ionic bonding , quantum chemistry , chemical engineering , chemical physics , organic chemistry , ion , biochemistry , catalysis , physics , quantum mechanics , molecule , engineering , gene
Isomerization and transformation of glucose and fructose to 5‐hydroxymethylfurfural (HMF) in both ionic liquids (ILs) and water has been studied by the reference interaction site model self‐consistent field spatial electron density distribution (RISM‐SCF‐SEDD) method coupled with ab initi o electronic structure theory, namely coupled cluster single, double, and perturbative triple excitation (CCSD(T)). Glucose isomerization to fructose has been investigated via cyclic and open chain mechanisms. In water, the calculations support the cyclic mechanism of glucose isomerization; with the predicted activation free energy is 23.8 kcal mol −1 at experimental condition. Conversely, open ring mechanism is more favorable in ILs with the energy barrier is 32.4 kcal mol −1 . Moreover, the transformation of fructose into HMF via cyclic mechanism is reasonable; the calculated activation barriers are 16.0 and 21.5 kcal mol −1 in aqueous and ILs solutions, respectively. The solvent effects of ILs could be explained by the decomposition of free energies and radial distribution functions of solute‐solvent that are produced by RISM‐SCF‐SEDD. © 2015 Wiley Periodicals, Inc.