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Theoretical Interpretation of the Ionic Liquid Phase Role in the (R)-Ru-BINAP Catalyzed Hydrogenation of Methylacetoacetate
- 1.0427591 - ÚCHP 2015 RIV NL eng J - Článek v odborném periodiku
Dytrych, Pavel - Klusoň, Petr - Slater, M. - Šolcová, Olga
Theoretical Interpretation of the Ionic Liquid Phase Role in the (R)-Ru-BINAP Catalyzed Hydrogenation of Methylacetoacetate.
Reaction Kinetics Mechanism and Catalysis. Roč. 111, č. 2 (2014), s. 475-487. ISSN 1878-5190. E-ISSN 1878-5204
Grant CEP: GA MPO FR-TI3/057
Institucionální podpora: RVO:67985858
Klíčová slova: Ionic liquids * chiral catalysis * Ru-BINAP complex
Kód oboru RIV: CC - Organická chemie
Impakt faktor: 1.170, rok: 2014
ecently, the work focusing on the role of alkyl chain length in the N[R,222][Tf2N] ionic liquids and its reflection in the kinetic parameters of stereoselective hydrogenation of methylacetoacetate over (R)-[RuCl(binap)(p-cymene)]Cl complex was reported. Irregular trends in the principle parameter of enantioselectivity were observed. Here, a possible theoretical explanation of such irregular trends elucidated with the help of molecular simulations methods is presented. A stepwise approach is proposed for evaluating the energetically most stable conformers of a series of individual N[R,222][Tf2N] for the interpretation of selectivity-structure effects observed experimentally. Initially, Monte Carlo molecular mechanics was used followed by a semi-empirical PM3 method to elucidate also the characteristic thermodynamic functions of state and theoretical molecular spectra. The density functional theory was finally applied. The specific absolute entropy data revealed that due to the partition of the cation and anion twisted closer approach the ionic liquids N[8,222][Tf2N] and N[12,222][Tf2N] may stabilize the structures of the (R)-[RuCl(binap)(p-cymene)]Cl complex.
Trvalý link: http://hdl.handle.net/11104/0233124
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