メタル・オーガニック・フレームワークの二次構造体をエチレンポリメリゼーションのための六核Zr-アルキル触媒に変換する
Pengfei Ji1, Joseph B Solomon1, Zekai Lin1
1Department of Chemistry, The University of Chicago , 929 E 57th Street, Chicago, Illinois 60637, United States.
Journal of the American Chemical Society
|August 12, 2017
まとめ
メタル・オーガニック・フレームワークのノードは,エチレンポリメリゼーションのための固体有機金属触媒に変換されました. これらの新しい触媒は,高分子量ポリエチレンを生成し,均質なシステムに代替案を提供します.
科学分野:
- マテリアルサイエンス 材料科学
- カタリシス カタリシス カタリシス
- ポリマー化学のポリマー化学について
背景:
- メタル・オーガニック・フレームワーク (MOF) は,調節可能な構造を提供します.
- MOF-808のようなZrベースのMOFは,触媒の潜在能力を示しています.
- 効率的で安定したポリメリゼーション触媒の開発は極めて重要です.
研究 の 目的:
- MOFノードが有機金属触媒に段階的に変換される様子を示します.
- エチレンポリメリゼーションのためのこれらの新しい固体触媒の触媒活性を調査する.
- これらの固体触媒の性質を伝統的な均質な触媒と比較する.
主な方法:
- Zr-BTCノードをZrCl2-BTCに,それからZrR2-BTCに段階的に化学変換する.
- ZrCl2-BTCをMMAO-12で活性化してZrMe-BTCを形成する.
- ZrMe-BTCを触媒として使用したエチレンポリメリゼーション.
主要な成果:
- Zr-BTCからZrCl2-BTCとZrR2-BTCノードを合成しました.
- エチレンポリメリゼーションのための効率的な固体触媒であるZrMe-BTCを生成しました.
- 独特の触媒特性を持つ高分子量線形ポリエチレンを生産した.
結論:
- MOFノードは,単一サイト固体有機金属触媒に直接変換することができます.
- これらの固体触媒は,異なる電子およびステリック特性を有する.
- このアプローチは,同質なアナログのない新しいポリメリゼーション触媒への新しい経路を提供します.
関連する概念動画
Ziegler–Natta Chain-Growth Polymerization: Overview
4.1K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
4.1K
Olefin Metathesis Polymerization: Overview
2.6K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
2.6K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
9.1K
Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
9.1K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.9K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.9K
Free-Radical Chain Reaction and Polymerization of Alkenes
10.0K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
10.0K
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
13.1K
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
13.1K


