Reaction pathways for the oxidation of methanol to formaldehyde by an iron-oxo species

Kazunari Yoshizawa, Yoshihisa Kagawa

研究成果: ジャーナルへの寄稿記事

46 引用 (Scopus)

抄録

The reaction mechanism and energetics for the conversion of methanol to formaldehyde by an iron-oxo species, FeO+, is investigated. Three competitive reaction pathways for the catalytic reaction are analyzed from DFT computations at the B3LYP level of theory. In Path 1, the H atom of the OH group of methanol is first abstracted by the oxo group of FeO+ via a four-centered transition state (TS1-1) leading to the intermediate complex HO-Fe+-OCH3, and after that one of the H atoms of the OCH3 group is shifted to the OH ligand via a five-centered transition state (TS1-2) to form the final product complex H2O-Fe+-OCH2. In Path 2, one of the H atoms of the CH3 group of methanol is abstracted by the oxo group via a five-centered transition state (TS2-1) leading to the intermediate complex HO-Fe+-OHCH2, and then the H atom of the OHCH2 group is shifted to the OH ligand via a four-centered transition state (TS2-2) to give the product complex. Unlike Paths 1 and 2, which involve a hydrogen shift, the first step in Path 3 involves a methyl migration that takes place via a four-centered transition state (TS3-1) resulting in the formation of the intermediate complex HO-Fe+-OCH3 and the second half of Path 3 is identical to that of Path 1. From B3LYP computations, Path 1 and Path 2 are competitive in energy and Path 3 is unlikely from the energetic viewpoint. Kinetic isotope effects (kH/kD) for the electronic processes of TS1-1, TS2-1, and TS3-1 are computed and analyzed.

元の言語英語
ページ(範囲)9347-9355
ページ数9
ジャーナルJournal of Physical Chemistry A
104
発行部数41
DOI
出版物ステータス出版済み - 10 19 2000
外部発表Yes

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formaldehyde
Formaldehyde
Methanol
Iron
methyl alcohol
iron
Atoms
Oxidation
oxidation
Ligands
Discrete Fourier transforms
Isotopes
Hydrogen
atoms
Kinetics
ligands
products
isotope effect
shift
kinetics

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry

これを引用

Reaction pathways for the oxidation of methanol to formaldehyde by an iron-oxo species. / Yoshizawa, Kazunari; Kagawa, Yoshihisa.

:: Journal of Physical Chemistry A, 巻 104, 番号 41, 19.10.2000, p. 9347-9355.

研究成果: ジャーナルへの寄稿記事

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title = "Reaction pathways for the oxidation of methanol to formaldehyde by an iron-oxo species",
abstract = "The reaction mechanism and energetics for the conversion of methanol to formaldehyde by an iron-oxo species, FeO+, is investigated. Three competitive reaction pathways for the catalytic reaction are analyzed from DFT computations at the B3LYP level of theory. In Path 1, the H atom of the OH group of methanol is first abstracted by the oxo group of FeO+ via a four-centered transition state (TS1-1) leading to the intermediate complex HO-Fe+-OCH3, and after that one of the H atoms of the OCH3 group is shifted to the OH ligand via a five-centered transition state (TS1-2) to form the final product complex H2O-Fe+-OCH2. In Path 2, one of the H atoms of the CH3 group of methanol is abstracted by the oxo group via a five-centered transition state (TS2-1) leading to the intermediate complex HO-Fe+-OHCH2, and then the H atom of the OHCH2 group is shifted to the OH ligand via a four-centered transition state (TS2-2) to give the product complex. Unlike Paths 1 and 2, which involve a hydrogen shift, the first step in Path 3 involves a methyl migration that takes place via a four-centered transition state (TS3-1) resulting in the formation of the intermediate complex HO-Fe+-OCH3 and the second half of Path 3 is identical to that of Path 1. From B3LYP computations, Path 1 and Path 2 are competitive in energy and Path 3 is unlikely from the energetic viewpoint. Kinetic isotope effects (kH/kD) for the electronic processes of TS1-1, TS2-1, and TS3-1 are computed and analyzed.",
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N2 - The reaction mechanism and energetics for the conversion of methanol to formaldehyde by an iron-oxo species, FeO+, is investigated. Three competitive reaction pathways for the catalytic reaction are analyzed from DFT computations at the B3LYP level of theory. In Path 1, the H atom of the OH group of methanol is first abstracted by the oxo group of FeO+ via a four-centered transition state (TS1-1) leading to the intermediate complex HO-Fe+-OCH3, and after that one of the H atoms of the OCH3 group is shifted to the OH ligand via a five-centered transition state (TS1-2) to form the final product complex H2O-Fe+-OCH2. In Path 2, one of the H atoms of the CH3 group of methanol is abstracted by the oxo group via a five-centered transition state (TS2-1) leading to the intermediate complex HO-Fe+-OHCH2, and then the H atom of the OHCH2 group is shifted to the OH ligand via a four-centered transition state (TS2-2) to give the product complex. Unlike Paths 1 and 2, which involve a hydrogen shift, the first step in Path 3 involves a methyl migration that takes place via a four-centered transition state (TS3-1) resulting in the formation of the intermediate complex HO-Fe+-OCH3 and the second half of Path 3 is identical to that of Path 1. From B3LYP computations, Path 1 and Path 2 are competitive in energy and Path 3 is unlikely from the energetic viewpoint. Kinetic isotope effects (kH/kD) for the electronic processes of TS1-1, TS2-1, and TS3-1 are computed and analyzed.

AB - The reaction mechanism and energetics for the conversion of methanol to formaldehyde by an iron-oxo species, FeO+, is investigated. Three competitive reaction pathways for the catalytic reaction are analyzed from DFT computations at the B3LYP level of theory. In Path 1, the H atom of the OH group of methanol is first abstracted by the oxo group of FeO+ via a four-centered transition state (TS1-1) leading to the intermediate complex HO-Fe+-OCH3, and after that one of the H atoms of the OCH3 group is shifted to the OH ligand via a five-centered transition state (TS1-2) to form the final product complex H2O-Fe+-OCH2. In Path 2, one of the H atoms of the CH3 group of methanol is abstracted by the oxo group via a five-centered transition state (TS2-1) leading to the intermediate complex HO-Fe+-OHCH2, and then the H atom of the OHCH2 group is shifted to the OH ligand via a four-centered transition state (TS2-2) to give the product complex. Unlike Paths 1 and 2, which involve a hydrogen shift, the first step in Path 3 involves a methyl migration that takes place via a four-centered transition state (TS3-1) resulting in the formation of the intermediate complex HO-Fe+-OCH3 and the second half of Path 3 is identical to that of Path 1. From B3LYP computations, Path 1 and Path 2 are competitive in energy and Path 3 is unlikely from the energetic viewpoint. Kinetic isotope effects (kH/kD) for the electronic processes of TS1-1, TS2-1, and TS3-1 are computed and analyzed.

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