ビーチによるグラファイトの減少. 水素によるエッジとインテリアの機能化
Zhiqiang Yang1, Yanqiu Sun, Lawrence B Alemany
1Department of Chemistry, Shared Equipment Authority, Rice University, Houston, Texas 77005, United States.
Journal of the American Chemical Society
|October 18, 2012
まとめ
グラファイトのビーチ還元は,高度に脱皮された,水素化されたグラフェンを生成します. このプロセスは,グラフェン網の端と内部の両方を水素原子で飽和させます.
科学分野:
- マテリアルサイエンス 材料科学
- ケミストリー 化学
背景:
- グラファイトは,ユニークな電子特性を有する層状の材料です.
- 石墨の化学的改変は,さまざまな用途のためにその性質を変更することができます.
研究 の 目的:
- グラファイトのビーチ還元を調査するために.
- 結果として得られる水素化されたグラフェン製品を特徴付けるために.
主な方法:
- 液体アンモニアにリチウムを使用したビーチの減少.
- 固体 (13) C NMRスペクトロスコーピー. 固体 (13) C NMRスペクトロスコーピー.
- エレメンタル分析. エレメンタル分析.
- 原子力顕微鏡 (AFM). 原子力の顕微鏡 (AFM). 原子力の顕微鏡 (AFM). 原子力の顕微鏡 (AFM). 原子力の顕微鏡 (AFM).
- 電子エネルギー損失スペクトロスコーピー (EELS).
主要な成果:
- ビーチ還元は,非常に減少した,脱皮されたグラフェン材料を生成しました.
- NMRとEELSでは,両辺と内側の格子位置の水素化が確認されました.
- 要素解析により, (C) の組成が (C) の組成と (H) の組成と (n) の組成とされた.
- AFMは,減少グラフェンの有意な剥離を示した.
- 4 eVの大きな帯域のギャップが観察され,広範な水素化を示した.
結論:
- ビーチ還元は,グラフィートを水素化する効果的な方法です.
- その結果生成される水素化されたグラフェンは,高度な剥離と水素化を示す.
- この材料は大きな帯域のギャップを有しており,電子アプリケーションの可能性を示唆しています.
関連する概念動画
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Birch reduction uses solvated electrons as reducing agents. The reaction converts benzene to 1,4-cyclohexadiene. The reaction proceeds by the transfer of a single electron to the ring to form a benzene radical anion. This anion is highly basic—it abstracts a proton from the alcohol to form a cyclohexadienyl radical. Another single electron transfer gives the cyclohexadienyl anion. A proton transfer from the alcohol forms 1,4-cyclohexadiene. Since this reduction occurs via radical anion...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
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.
Alcohols from Carbonyl Compounds: Reduction
Reduction is a simple strategy to convert a carbonyl group to a hydroxyl group. The three major pathways to reduce carbonyls to alcohols are catalytic hydrogenation, hydride reduction, and borane reduction.
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
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...
Reduction of Alkenes: Catalytic Hydrogenation
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the surface of...
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the surface of...
Acid Halides to Alcohols: LiAlH4 Reduction
Acid halides are reduced to alcohols in the presence of a strong reducing agent like lithium aluminum hydride.
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...


