Insight in the activity and diastereoselectivity of various Lewis acid catalysts for the citronellal cyclization

Both experiment and theory predict ATPH as most active and selective Lewis acid catalyst in the citronellal cyclization. [Display omitted] •Combined experimental and theoretical study on citronellal cyclization toward isopulegol stereoisomers.•Lewis acid homogeneous catalysts (ZnBr2 and ATPH) versus...

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Published in:Journal of catalysis Vol. 305; pp. 118 - 129
Main Authors: Vandichel, Matthias, Vermoortele, Frederik, Cottenie, Stijn, De Vos, Dirk E., Waroquier, Michel, Van Speybroeck, Veronique
Format: Journal Article
Language:English
Published: Amsterdam Elsevier Inc 01.09.2013
Elsevier
Elsevier BV
Subjects:
Acids
Activity
aluminum
ATPH
Catalysis
Catalysts
Chemical kinetics
Chemistry
citronellal
Citronellal cyclization
Cu-BTC
Diastereoselective catalysis
energy
Exact sciences and technology
General and physical chemistry
Heterogeneous catalysis
hydrogen
Hydrogenation
Lewis acids
ligands
nitrogen dioxide
Selectivity
stereoisomers
temperature
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
ZnBr2
Heterogeneous catalysis
Citronellal cyclization
ATPH
Chemical kinetics
Lewis acids
Diastereoselective catalysis
Activity
ZnBr2
Selectivity
Cu-BTC
Lewis acid
Citronellal
Catalytic reaction
Diastereoselectivity
ZnBr
Cyclization
Kinetics
Catalyst
ISSN:0021-9517, 1090-2694
Online Access:Get full text
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Summary:Both experiment and theory predict ATPH as most active and selective Lewis acid catalyst in the citronellal cyclization. [Display omitted] •Combined experimental and theoretical study on citronellal cyclization toward isopulegol stereoisomers.•Lewis acid homogeneous catalysts (ZnBr2 and ATPH) versus Cu3BTC2 as hetereogeneous MOF catalyst.•Search for catalyst with the highest activity and highest selectivity toward (−)-isopulegol diastereomer.•ATPH is the most active catalyst with selectivity of about 94% at 298K.•Catalytic conversion in Cu3BTC2 strongly dependent on size of catalyst particles due to diffusional restrictions. Industrial (−)-menthol production generally relies on the hydrogenation of (−)-isopulegol, which is in turn produced with high selectivity by cyclization of (+)-citronellal. This paper uses a combined theoretical and experimental approach to study the activity and selectivity of three Lewis acid catalysts for this reaction, namely ZnBr2, aluminum tris(2,6-diphenylphenoxide) (ATPH), and the heterogeneous metal–organic framework Cu3BTC2 (BTC=benzene-1,3,5-tricarboxylate). ATPH is a strong Lewis acid homogeneous catalyst with bulky ligands which provides very high selectivities for the desired stereoisomer (>99%). The performance of the catalysts was evaluated as a function of temperature, which revealed that a higher catalyst activity allows working at lower temperatures and improves the selectivity for isopulegol. The selectivity distribution is kinetically driven for ZnBr2 and ATPH. The theoretical selectivity distributions rely on the determination of an extensive set of diastereomeric transition states, for which the differences in free energy have been calculated using a complementary set of ab initio techniques. Given the sensitivity of the selectivity to small Gibbs free-energy differences, the agreement between experimental and theoretical selectivities is satisfactory. On basis of the obtained insights, rational design of new catalysts may be obtained. As proof of concept, the hypothetical Cu3(BTC-(NO2)3)2 Lewis catalyst – in which each phenyl hydrogen of the BTC ligand is replaced by a nitro group – is predicted to be very selective.
Bibliography:http://dx.doi.org/10.1016/j.jcat.2013.04.017
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ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2013.04.017