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231225s2019 xx |||||o 00| ||eng c |
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|a 10.1002/jcc.25812
|2 doi
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|a pubmed25n0982.xml
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|a (NLM)30847957
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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| 100 |
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|a Wang, Qing
|e verfasserin
|4 aut
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|a Aluminum alkoxy-catalyzed biomass conversion of glucose to 5-hydroxymethylfurfural
|b Mechanistic study of the cooperative bifunctional catalysis
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|c 2019
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 11.08.2020
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|a Date Revised 11.08.2020
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2019 Wiley Periodicals, Inc.
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|a Density functional theory calculations were performed to understand the detailed reaction mechanism of aluminum alkoxy-catalyzed conversion of glucose to 5-hydroxymethylfurfural (HMF) using Al(OMe)3 as catalyst. Potential energy surfaces were studied for aggregates formed between the organic compounds and Al(OMe)3 and effects of the medium were considered via continuum solvent models. The reaction takes place via two stages: isomerization from glucose to fructose (stage I) and transformation of fructose to HMF (stage II). Stage II includes three successive dehydrations, which begins with a 1,2-elimination to form an enolate (i.e., B), continues with the formation of the acrolein moiety (i.e., D), and ends with the formation of the furan ring (i.e., HMF). All of these steps are facilitated by aluminum alkoxy catalysis. The highest barriers for stage I and stage II are 23.9 and 31.2 kcal/mol, respectively, and the overall catalytic reaction is highly exothermic. The energetic and geometric results indicate that the catalyzed reaction path has feasible kinetics and thermodynamics and is consistent with the experimental process under high temperature (i.e., 120 °C). Remarkably, the released water molecules in stage II act as the product, reactant, proton shuttle, as well as stabilizer in the conversion of fructose to HMF. The metal-ligand functionality of the Al(OMe)3 catalyst, which combines cooperative Lewis acid and Lewis base properties and thereby enables proton shuttling, plays a crucial role in the overall catalysis and is responsible for the high reactivity. © 2019 Wiley Periodicals, Inc
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a DFT calculations
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|a HMF
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|a aluminum alkoxy catalyst
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|a glucose
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|a reaction mechanism
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|a Alcohols
|2 NLM
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|a Organometallic Compounds
|2 NLM
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|a alkoxyl radical
|2 NLM
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|a 5-hydroxymethylfurfural
|2 NLM
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|a 70ETD81LF0
|2 NLM
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|a Aluminum
|2 NLM
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|a CPD4NFA903
|2 NLM
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|a Furaldehyde
|2 NLM
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|a DJ1HGI319P
|2 NLM
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|a Glucose
|2 NLM
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|a IY9XDZ35W2
|2 NLM
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1 |
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|a Fu, Mingxing
|e verfasserin
|4 aut
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|a Li, Xiaojun
|e verfasserin
|4 aut
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|a Huang, Runfeng
|e verfasserin
|4 aut
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|a Glaser, Rainer E
|e verfasserin
|4 aut
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|a Zhao, Lili
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Journal of computational chemistry
|d 1984
|g 40(2019), 16 vom: 15. Juni, Seite 1599-1608
|w (DE-627)NLM098138448
|x 1096-987X
|7 nnas
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| 773 |
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|g volume:40
|g year:2019
|g number:16
|g day:15
|g month:06
|g pages:1599-1608
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|u http://dx.doi.org/10.1002/jcc.25812
|3 Volltext
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