イオン性液中のカルコゲニド化学:ダブルキューバンの化合物[Sb7S8Br2](AlCl4) 3の非線形光波混合特性
Qichun Zhang1, In Chung, Joon I Jang
1Department of Chemistry, Northwestern University, Evanston, Illinois 60208, USA.
Journal of the American Chemical Society
|July 8, 2009
まとめ
新しいアンチモニウム-硫黄-ブロミンカチオン, [Sb(7) S(8) Br(2) ](3+) が合成されました. この非中心対称性化合物は,重要な非線形光学特性を示し,光学アプリケーションに有望である.
科学分野:
- 無機化学 無機化学とは
- 材料科学 材料科学とは
- 固体化学 固体化学
背景:
- イオン性液体は,新しい化合物を合成するためのユニークな反応環境を提供します.
- アンチモニー・カルコゲニド材料は,その光電子特性により興味を惹きます.
研究 の 目的:
- 新しいアンチモニー-硫黄-ブロミンカチオンを合成し,特徴づけること.
- 合成された化合物の非線形光学 (NLO) 性質を調査する.
主な方法:
- 165°CのEMIMBr-AlCl(3) イオン液から[AlCl(4) ](-) 塩として[Sb(7) S(8) Br(2) ](3+) カチオンの合成.
- 非中心対称構造を決定する結晶分析 (空間群P2(1))
- 2次和音と差異周波数生成を評価するための光学スペクトルスコピー.
主要な成果:
- 二重立方体の構造を持つ新しいカチオンの形成: [Sb(7) S(8) Br(2) ](3+).
- 化合物は,非中心対称な空間群 P2(1)2(1)2(1) で結晶化する.
- ブロードバンド非線形光学応答は,可視領域と近赤外線領域で観察されました.
結論:
- 非線形光学における潜在的な応用を持つ新しいアンチモニー-硫黄-ブロミンクラスタの成功合成.
- 独特の二重立方体の構造は,観察されたNLO特性に寄与しています.
- この研究は,イオン性液体から派生した機能的無機材料のライブラリを拡張します.
関連する概念動画
Ionic Crystal Structures
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Preparation and Reactions of Sulfides
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
Alkyl Halides
Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Halogenation of Alkenes
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Molecular Orbital Theory II
Molecular Orbital Energy Diagrams
Electrophilic Addition to Alkynes: Halogenation
Introduction
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.


