4.5 Article

Acetylene Cyclotrimerization with an Iron(II) Bis(imino)pyridine Catalyst

期刊

ORGANOMETALLICS
卷 31, 期 8, 页码 3439-3442

出版社

AMER CHEMICAL SOC
DOI: 10.1021/om300084s

关键词

-

资金

  1. CSIRO
  2. Australian Research Council [FT100100609]
  3. Australian Research Council [FT100100609] Funding Source: Australian Research Council

向作者/读者索取更多资源

Acetylene oligomerization with an activated iron bis(imino)pyridine complex with low steric hindrance leads to benzene as the major product, in contrast to this reaction with a more sterically encumbered analogue, which leads to polyacetylene. The mechanism of benzene formation was studied and likely occurs via metallacycle intermediates; this process can be interrupted by addition of ZnEt2 as a chain transfer agent to generate hexadiene instead.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Engineering, Chemical

The pyrolysis of natural gas: A study of carbon deposition and the suitability of reactor materials

Steven Wang, Woo Jin Lee, Chao'en Li, Benny Kuan, Nick Burke, Jim Patel

AICHE JOURNAL (2019)

Article Engineering, Chemical

Pyrolysis of Natural Gas: Effects of Process Variables and Reactor Materials on the Product Gas Composition

Steven Wang, Woo Jin Lee, Chao'en Li, Benny Kuan, Nick Burke, Jim Patel

CHEMICAL ENGINEERING & TECHNOLOGY (2019)

Article Chemistry, Physical

Heterogeneous iron containing carbon catalyst (Fe-N/C) for epoxidation with molecular oxygen

Daniel Malko, Yanjun Guo, Pip Jones, George Britovsek, Anthony Kucernak

JOURNAL OF CATALYSIS (2019)

Article Chemistry, Physical

From Lignin to Chemicals: Hydrogenation of Lignin Models and Mechanistic Insights into Hydrodeoxygenation via Low-Temperature C-O Bond Cleavage

Charles E. J. J. Vriamont, Tianyi Chen, Charles Romain, Paul Corbett, Phornphit Manageracharath, Janet Peet, Christopher M. Conifer, Jason P. Hallett, George J. P. Britovsek

ACS CATALYSIS (2019)

Article Multidisciplinary Sciences

Fluid-solid phase transition of n-alkane mixtures: Coarse-grained molecular dynamics simulations and diffusion-ordered spectroscopy nuclear magnetic resonance

S. Shahruddin, G. Jimenez-Serratos, G. J. P. Britovsek, O. K. Matar, E. A. Mueller

SCIENTIFIC REPORTS (2019)

Article Chemistry, Applied

The Mathematics of Ethylene Oligomerisation and Polymerisation

Craig T. Young, Richard von Goetze, Atanas K. Tomov, Francesco Zaccaria, George J. P. Britovsek

TOPICS IN CATALYSIS (2020)

Article Chemistry, Physical

gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation

Dillon W. P. Tay, James D. Nobbs, Charles Romain, Andrew J. P. White, Srinivasulu Aitipamula, Martin van Meurs, George J. P. Britovsek

ACS CATALYSIS (2020)

Review Polymer Science

Polyethylene terephthalate degradation under natural and accelerated weathering conditions

Tian Sang, Christopher J. Wallis, Gavin Hill, George J. P. Britovsek

EUROPEAN POLYMER JOURNAL (2020)

Article Chemistry, Inorganic & Nuclear

Directing Selectivity to Aldehydes, Alcohols, or Esters with Diphobane Ligands in Pd-Catalyzed Alkene Carbonylations

Dillon W. P. Tay, James D. Nobbs, Srinivasulu Aitipamula, George J. P. Britovsek, Martin van Meurs

Summary: Phenylene-bridged diphobane ligands with different substituents have been synthesized and studied in palladium-catalyzed carbonylation reactions of various alkenes. The results show different selectivities between hydroformylation and alkoxycarbonylation, with the performance also influenced by the nature and amount of acid cocatalyst.

ORGANOMETALLICS (2021)

Article Chemistry, Inorganic & Nuclear

Photolytic Activation of Late-Transition-Metal-Carbon Bonds and Their Reactivity toward Oxygen

Sarah K. Y. Ho, Francis Y. T. Lam, Adiran de Aguirre, Feliu Maseras, Andrew J. P. White, George J. P. Britovsek

Summary: The study investigates the photolytic activation of palladium(II) and platinum(II) complexes featuring the BPI ligand in various solvents, revealing the reactivity towards oxygen and formation of chloro complexes or peroxide intermediates. The reaction pathways differ for alkyl and aryl complexes based on the strength of the metal-carbon bonds, with UV irradiation affecting the reactivity of other components in the reaction mixture.

ORGANOMETALLICS (2021)

Article Chemistry, Physical

Monitoring Light-Driven Oxygen Insertion Reactions into Metal Carbon Bonds by LED-NMR Spectroscopy

Sarah K. Y. Ho, Chigozie Ezeorah, Suviti Chari, Ali Salehi-Reyhani, George J. P. Britovsek

Summary: The light-driven insertion reaction of oxygen into metal carbon bonds of BPI (1,3-bis(2-pyridylimino)isoindole) complexes [Pt(BPI)Me] and [Pd(BPI)Me] was studied using LED-NMR in CDCl3. The initial reaction formed peroxo complexes [Pt(BPI)OOMe] and [Pd(BPI)OOMe], which further reacted over time. Spectra were recorded at 1-minute intervals, allowing for tracking of the methyl substituent, which eventually produced formaldehyde and methanol in similar proportions. The presence of oxygen and light in the solvent CDCl3 led to side reactions, resulting in the formation of phosgene and DCl, as well as chloro methylformate and dimethyl carbonate.

CHEMPHOTOCHEM (2023)

Article Polymer Science

Towards degradable polyethylene: end-functionalised polyethylene (PE-X) and PE-I/LDPE blends from iron-catalysed chain growth of ZnEt2 with ethylene

Richard von Goetze, Ahmad Aljaber, Koon-Yang Lee, Gavin Hill, Christopher Wallis, George J. P. Britovsek

Summary: A series of end-functionalised polyethylene materials were synthesized via catalysed chain growth reaction. Different functional groups were introduced with varying effects. Blending polyethylene with polymers resulted in potential degradable blends.

POLYMER CHEMISTRY (2022)

Article Chemistry, Physical

Single- and double-bridged PNP ligands in chromium-catalysed ethylene oligomerisation

Quintin Lo, Dominic Pye, Sami Gesslbauer, Ying Sim, Felipe Garcia, Andrew J. P. White, George J. P. Britovsek

Summary: Several PNP-type diphosphine ligands with different N-bridging modes have been synthesized and characterized. These ligands exhibit good activities and selectivities for the tri- and tetramerization of ethylene, comparable to standard ligands. Computational studies also suggest that the binding of ethylene is favorable in these complexes, and the oligomerization mechanism involves both single and double ethylene insertions.

CATALYSIS SCIENCE & TECHNOLOGY (2022)

Article Chemistry, Physical

Using molecular oxygen and Fe-N/C heterogeneous catalysts to achieve Mukaiyama epoxidations via in situ produced organic peroxy acids and acylperoxy radicals

Mengjun Gong, Yanjun Guo, Daniel Malko, Javier Rubio-Garcia, Jack M. S. Dawson, George J. P. Britovsek, Anthony Kucernak

Summary: Under mild conditions, aldehydes are efficiently converted to epoxides using a heterogeneous Fe-N/C catalyst, which forms the corresponding organic peroxy acid and acylperoxy radicals. Real-time monitoring of oxygen consumption and catalyst potential reveals the formation of peroxy acid and subsequent catalytic epoxidation. The involvement of aldehyde and Fe-N/C catalyst is shown to be the rate determining step for the reaction, and the induction time can be increased by adding a radical scavenger.

CATALYSIS SCIENCE & TECHNOLOGY (2022)

Article Chemistry, Inorganic & Nuclear

Biaryl Group 4 Metal Complexes as Non-Metallocene Catalysts for Polyethylene with Long Chain Branching

Maria M. Gragert, Atanas K. Tomov, Serge Bettonville, Gaelle Pannier, Andrew J. P. White, George J. P. Britovsek

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY (2020)

暂无数据