Temperature- and pressure-dependent kinetics of the competing C–O bond fission reactions of dimethoxymethane

Literature Information

Publication Date 2020-02-27
DOI 10.1039/D0CP00136H
Impact Factor 3.676
Authors

Leonie Golka, Dennis Gratzfeld, Isabelle Weber, Matthias Olzmann


View Original

Abstract

Oxymethylene ethers are often considered as promising fuel additives to reduce the emissions of soot and NOx from diesel engines. Dimethoxymethane (DMM) is the smallest member of this class of compounds and therefore particularly suitable to study the reactivity of the characteristic methylenedioxy group (O–CH2–O). In this context, we investigated the pyrolysis of DMM behind reflected shock waves at temperatures between 1100 and 1600 K and nominal pressures of 0.4 and 4.7 bar by monitoring the formation of H atoms with time-resolved atom resonance absorption spectroscopy. Rate coefficients for the C–O bond fission reactions of DMM were inferred from the recorded [H](t) profiles, and a pronounced temperature and pressure dependence of the rate coefficients was found. To rationalize this finding, we characterized the relevant parts of the potential energy surface of DMM by performing quantum chemical calculations at the CCSD(F12*)(T*)/cc-pVQZ-F12//B2PLYP-D3/def2-TZVPP level of theory. On the basis of the results, a two-channel master equation accounting for the two different C–O bond-fission reactions of DMM was set up and solved. Specific rate coefficients were calculated from the simplified Statistical Adiabatic Channel Model. The branching between the two reaction channels was modeled, and the CH3OCH2O + CH3 product channel was found to be clearly dominating. A Troe parameterization for the pressure dependence of this channel was derived. To enable implementation of both channels into kinetic mechanisms for combustion modeling, ‘log p’ parameterizations of the rate coefficients for both reaction channels are also given and were implemented into a literature mechanism for DMM oxidation. With this slightly modified mechanism, the results of our experiments could be adequately modeled. The role of competing molecular (i.e. nonradical) decomposition channels of DMM was also quantum-chemically checked, but no indications for such channels could be found.

Related Literature

Substituted benzophenone imines for COF synthesis via formal transimination‡

Josefine Sprachmann, Niklas Grabicki, Anna Möckel, Jeremy Maltitz, José Refugio Monroy, Glen J. Smales, Oliver Dumele

2023-10-18 Communication

DOI: 10.1039/D3CC03735E

Organoboron/iodide-catalyzed photoredox N-functionalization of NH-sulfoximines/sulfonimidamides

Jiawei Huang, Xiaoman Li, Yu Wei, Liang Xu

2023-10-24 Communication

DOI: 10.1039/D3CC04351G

A high-performance crystalline Ti2O1.3(PO4)1.6/TiO2 carbon-coated composite as an anode for lithium-ion batteries

Yuefo Yi, Wenbin Zhou, Yichao Wang, Zhengfei Chen

2023-10-26 Communication

DOI: 10.1039/D3CC04633H

Two active species from a single metal halide precursor: a case study of highly productive Mn-catalyzed dehydrogenation of amine-boranes via intermolecular bimetallic cooperation

Elena S. Osipova, Sergey A. Kovalenko, Oleg A. Filippov, Natalia V. Belkova, Laure Vendier, Yves Canac, Elena S. Shubina, Dmitry A. Valyaev

2023-12-07 Edge Article

DOI: 10.1039/D3SC05356C

Copper-catalyzed trichloromethylative carbonylation of ethylene

2023-12-14 Edge Article

DOI: 10.1039/D3SC05530B

Multicolor circularly polarized luminescence inversion of metal–organic supramolecular polymers

Kuo Fu, Guofeng Liu

2023-10-25 Communication

DOI: 10.1039/D3CC04068B

A triad molecular conductor: simultaneous control of charge and molecular arrangements

Naoya Kinoshita, Atsuya Maruyama

2023-10-10 Communication

DOI: 10.1039/D3CC03198E

Chemical remodeling of the mycomembrane with chain-truncated lipids sensitizes mycobacteria to rifampicin

Ishani V. Gaidhane, Helen E. Erickson, Prachi Agarwal, Yashpal S. Chhonker, Donald R. Ronning

2023-10-30 Communication

DOI: 10.1039/D3CC02364H

You might also like

Compound Q&A

What are the main uses of (5-Sulfamoyl-3-pyridinyl)boronic acid (CAS: 951233-61-7)?

(5-Sulfamoyl-3-pyridinyl)boronic acid is primarily used in chemical synthesis, p...

951233-61-7(5-Sulfamoyl-3-pyrid...
Compound Q&A

How is Benzyl 2-methyl-2-(methylsulfonyl)-4-pentenoate (CAS: 1942858-50-5) typically synthesized?

Benzyl 2-methyl-2-(methylsulfonyl)-4-pentenoate is typically synthesized via est...

1942858-50-5Benzyl 2-methyl-2-(m...
Compound Q&A

What precautions should be taken when handling 8-Fluoroquinolin-6-ol (CAS: 209353-22-0)?

When handling 8-Fluoroquinolin-6-ol (CAS: 209353-22-0), it is important to use p...

209353-22-08-Fluoroquinolin-6-o...
Compound Q&A

What are the physical and chemical properties of 1,3-Dibromo-5-(2-methyl-2-propanyl)benzene (CAS: 129316-09-2)?

1,3-Dibromo-5-(2-methyl-2-propanyl)benzene (CAS: 129316-09-2) is a crystalline c...

129316-09-21,3-Dibromo-5-(2-met...
Compound Q&A

What industries use Ethyl 7-chloro-4-oxo-1-(1,3-thiazol-2-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate (CAS: 174726-87-5)?

Ethyl 7-chloro-4-oxo-1-(1,3-thiazol-2-yl)-1,4-dihydro-1,8-naphthyridine-3-carbox...

174726-87-5Ethyl 7-chloro-4-oxo...
Compound Q&A

What precautions should be taken when handling Delta-7-Avenasterol (CAS: 23290-26-8)?

When handling Delta-7-Avenasterol (CAS: 23290-26-8), it is important to wear app...

23290-26-8Delta-7-Avenasterol
872992-20-6N-({(5R)-3-[3-Fluoro...
Compound Q&A

What precautions should be taken when handling 2-Methyl-2-proanyl 4-[(2-aminophenyl)amino]-1-piperidinecarboxylate (CAS: 79099-00-6)?

When handling 2-Methyl-2-proanyl 4-[(2-aminophenyl)amino]-1-piperidinecarboxylat...

79099-00-62-Methyl-2-propanyl ...
Compound Q&A

What is N-Methyl-4-chlorobenzylamine hydrochloride (CAS: 65542-24-7)?

N-Methyl-4-chlorobenzylamine hydrochloride (CAS: 65542-24-7) is a organic compou...

65542-24-7N-Methyl-4-chloroben...
Compound Q&A

Is [2-(Dodecyloxy)ethoxy]acetic acid (CAS: 27306-90-7) safe?

[2-(Dodecyloxy)ethoxy]acetic acid (CAS: 27306-90-7) is generally considered safe...

27306-90-7[2-(Dodecyloxy)ethox...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.