Mechanism for the formaldehyde to formic acid and the formic acid to carbon dioxide conversions mediated by an iron-oxo species

Takashi Yumura, Tatsuhiko Amenomori, Yoshihisa Kagawa, Kazunari Yoshizawa

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

The mechanism and energetics for the formaldehyde to formic acid and the formic acid to carbon dioxide conversions are investigated using the FeO+ complex as an oxidant from theoretical calculations at the B3LYP DFT level. In the oxidation processes, there are a lot of reaction branches which are comparable in energy. The elementary processes can be viewed as C-H and O-H cleavage reactions by oxo and hydroxo ligands as well as OH group migrations. In formaldehyde oxidation, the initially formed complex OFe+-OCH2 is converted by a C-H bond cleavage to intermediate HO-Fe+-OCH, which is next transformed to the formic acid complex Fe+-OCHOH by an OH ligand migration and to the carbon monoxide complex H20-Fe+CO by a C-H bond cleavage. There are two possible reaction pathways for the formic acid to carbon dioxide conversion, both reaction pathways being downhill and highly exothermic. In an energetically favorable reaction pathway, complex OFe+-OCHOH is first converted to intermediate HO-Fe+-OCHO by an O-H bond cleavage, and after that, HO-Fe+-OCHO is transformed to the product complex H20-Fe+-O2C by a C-H bond cleavage. Formaldehyde and formic acid are easily oxidized by an excess of oxidants to carbon dioxide and carbon monoxide. The overall reaction from methane to carbon dioxide is exothermic by 117.9 kcal/mol, and there is no high barrier after methanol formation, which can cause the well-known overoxidation problem in methane and alkane oxidation. Our calculations are in good agreement with previous experiments on methane oxidation over Fe-ZSM-5 zeolite with respect to the product branching ratio, suggesting that a surface ironoxo species should have relevance to the interesting catalytic functions of Fe-ZSM-5 zeolite.

Original languageEnglish
Pages (from-to)621-630
Number of pages10
JournalJournal of Physical Chemistry A
Volume106
Issue number4
DOIs
Publication statusPublished - Jan 31 2002

Fingerprint

formic acid
formaldehyde
Carbon Dioxide
Formaldehyde
carbon dioxide
Iron
cleavage
Methane
iron
Carbon Monoxide
Oxidation
oxidation
methane
Oxidants
carbon monoxide
Ligands
Alkanes
ligands
Discrete Fourier transforms
Methanol

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry

Cite this

Mechanism for the formaldehyde to formic acid and the formic acid to carbon dioxide conversions mediated by an iron-oxo species. / Yumura, Takashi; Amenomori, Tatsuhiko; Kagawa, Yoshihisa; Yoshizawa, Kazunari.

In: Journal of Physical Chemistry A, Vol. 106, No. 4, 31.01.2002, p. 621-630.

Research output: Contribution to journalArticle

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N2 - The mechanism and energetics for the formaldehyde to formic acid and the formic acid to carbon dioxide conversions are investigated using the FeO+ complex as an oxidant from theoretical calculations at the B3LYP DFT level. In the oxidation processes, there are a lot of reaction branches which are comparable in energy. The elementary processes can be viewed as C-H and O-H cleavage reactions by oxo and hydroxo ligands as well as OH group migrations. In formaldehyde oxidation, the initially formed complex OFe+-OCH2 is converted by a C-H bond cleavage to intermediate HO-Fe+-OCH, which is next transformed to the formic acid complex Fe+-OCHOH by an OH ligand migration and to the carbon monoxide complex H20-Fe+CO by a C-H bond cleavage. There are two possible reaction pathways for the formic acid to carbon dioxide conversion, both reaction pathways being downhill and highly exothermic. In an energetically favorable reaction pathway, complex OFe+-OCHOH is first converted to intermediate HO-Fe+-OCHO by an O-H bond cleavage, and after that, HO-Fe+-OCHO is transformed to the product complex H20-Fe+-O2C by a C-H bond cleavage. Formaldehyde and formic acid are easily oxidized by an excess of oxidants to carbon dioxide and carbon monoxide. The overall reaction from methane to carbon dioxide is exothermic by 117.9 kcal/mol, and there is no high barrier after methanol formation, which can cause the well-known overoxidation problem in methane and alkane oxidation. Our calculations are in good agreement with previous experiments on methane oxidation over Fe-ZSM-5 zeolite with respect to the product branching ratio, suggesting that a surface ironoxo species should have relevance to the interesting catalytic functions of Fe-ZSM-5 zeolite.

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