環膨張メタテシスによる循環的有機ナノ構造への直接的な経路,デンドロン化マクロモノマーのポリメリゼーション
Andrew J Boydston1, Thomas W Holcombe, David A Unruh
1Arnold and Mabel Beckman Laboratory of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Journal of the American Chemical Society
|April 2, 2009
まとめ
研究者らは,環膨張メタテシスポリメリゼーションを用いたサイクル有機ナノ構造を作り出した. この効率的な方法は,直接ナノスケールのリングを生成し,AFMイメージングで toroidal 形状として確認されます.
科学分野:
- ポリマー化学のポリマー化学について
- ナノテクノロジー ナノテクノロジー
- マテリアルサイエンス 材料科学
背景:
- サイクルポリマーにはユニークな特性がありますが,合成することは困難です.
- 環膨張メタテシスポリメリゼーション (ROMP) は,ポリマー合成のための強力なツールです.
研究 の 目的:
- 循環的有機ナノ構造を合成するための直接的かつ効率的な方法を開発する.
- 結果となるナノ構造物の形状を特徴付ける.
主な方法:
- デンドロニズドのノルボネンマクロモノマーのリング膨張メタテシスポリメリゼーション (ROMP).
- 構造分析のための原子力顕微鏡 (AFM).
主要な成果:
- 単一のステップでサイクル有機ナノ構造の成功合成.
- AFM画像は,直径約35~40nmのトロイド状ナノ構造を明らかにした.
結論:
- 開発されたROMP戦略は,循環的有機ナノ構造への効率的な経路です.
- 合成されたナノ構造は,ナノスケールでよく定義されたトロイド形状の形状を持っています.
関連する概念動画
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
Cationic Chain-Growth Polymerization: Mechanism
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Anionic Chain-Growth Polymerization: Mechanism
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
Ziegler–Natta Chain-Growth Polymerization: Overview
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 catalyst, high molecular...
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Radical Chain-Growth Polymerization: Mechanism
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this species into the...


