Carbon Nanotube-Supported Iron Complex Catalyzes 1-Hexene Dimerization

IF 2.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Molly Davis, Caroline E. Arnall, Caroline M. Vanderloo, Charlotte J. Angermeier and Emmanuelle Despagnet-Ayoub*, 
{"title":"Carbon Nanotube-Supported Iron Complex Catalyzes 1-Hexene Dimerization","authors":"Molly Davis,&nbsp;Caroline E. Arnall,&nbsp;Caroline M. Vanderloo,&nbsp;Charlotte J. Angermeier and Emmanuelle Despagnet-Ayoub*,&nbsp;","doi":"10.1021/acs.organomet.5c0010910.1021/acs.organomet.5c00109","DOIUrl":null,"url":null,"abstract":"<p >Supported catalysts for ethylene polymerization and oligomerization have gathered significant interest due to the benefits of catalyst recyclability and ease of removal from reaction media. However, reports on the oligomerization of heavy olefins remain scarce. This heterogenization process typically involves immobilizing an efficient homogeneous catalyst onto a selected support such as zeolites, silica, or metal–organic/covalent-organic frameworks. Carbon nanotubes (CNTs) present a promising support platform due to their high mechanical strength and low solubility in organic solvents. In this study, we report the heterogenization of a pyridine bis-imine iron complex on CNTs and its activity in the dimerization of 1-hexene. The CNT/iron complex was synthesized using imido linkage and characterized by TEM/EDS and inductively coupled plasma–optical emission spectroscopy to determine the distribution and loading of the catalyst. An optimal iron/CNT ratio of 1:1 by weight was identified. The system exhibited high reactivity in the dimerization of 1-hexene, achieving 94% olefin consumption and 64% C12 formation. Characterization of the resulting oligomers indicated that the CNT-supported catalyst operates via a mechanism similar to that of the homogeneous catalyst.</p>","PeriodicalId":56,"journal":{"name":"Organometallics","volume":"44 8","pages":"959–963 959–963"},"PeriodicalIF":2.5000,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organometallics","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.organomet.5c00109","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

Supported catalysts for ethylene polymerization and oligomerization have gathered significant interest due to the benefits of catalyst recyclability and ease of removal from reaction media. However, reports on the oligomerization of heavy olefins remain scarce. This heterogenization process typically involves immobilizing an efficient homogeneous catalyst onto a selected support such as zeolites, silica, or metal–organic/covalent-organic frameworks. Carbon nanotubes (CNTs) present a promising support platform due to their high mechanical strength and low solubility in organic solvents. In this study, we report the heterogenization of a pyridine bis-imine iron complex on CNTs and its activity in the dimerization of 1-hexene. The CNT/iron complex was synthesized using imido linkage and characterized by TEM/EDS and inductively coupled plasma–optical emission spectroscopy to determine the distribution and loading of the catalyst. An optimal iron/CNT ratio of 1:1 by weight was identified. The system exhibited high reactivity in the dimerization of 1-hexene, achieving 94% olefin consumption and 64% C12 formation. Characterization of the resulting oligomers indicated that the CNT-supported catalyst operates via a mechanism similar to that of the homogeneous catalyst.

Abstract Image

碳纳米管负载铁配合物催化1-己烯二聚化
由于催化剂的可回收性和易于从反应介质中去除的优点,乙烯聚合和低聚负载催化剂引起了人们的极大兴趣。然而,关于重烯烃低聚反应的报道仍然很少。这种多相化过程通常包括将高效的均相催化剂固定在选定的载体上,如沸石、二氧化硅或金属有机/共价有机框架。碳纳米管因其高机械强度和在有机溶剂中的低溶解度而成为一种很有前途的支撑平台。在这项研究中,我们报道了吡啶-二亚胺铁配合物在碳纳米管上的异质化及其在1-己烯二聚化中的活性。利用亚胺键合成了碳纳米管/铁配合物,并用TEM/EDS和电感耦合等离子体发射光谱对其进行了表征,以确定催化剂的分布和负载。确定了铁/碳纳米管重量比为1:1的最佳比例。该体系在1-己烯二聚化反应中表现出较高的反应活性,烯烃消耗94%,C12生成64%。对所得低聚物的表征表明,碳纳米管负载的催化剂通过类似于均相催化剂的机制起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Organometallics
Organometallics 化学-无机化学与核化学
CiteScore
5.60
自引率
7.10%
发文量
382
审稿时长
1.7 months
期刊介绍: Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信