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Structural Isomerism02:34

Structural Isomerism

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Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
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Covalent Bonds

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Covalent Bonds01:08

Covalent Bonds

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When two atoms share electrons to complete their valence shells, they create a covalent bond. An atom's electronegativity—the force with which shared electrons are pulled towards an atom—determines how the electrons are shared. Molecules formed with covalent bonds can be either polar or nonpolar. Atoms with similar electronegativities form nonpolar covalent bonds; the electrons are shared equally. Atoms with different electronegativities share electrons unequally,...
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Isomerism02:43

Isomerism

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Isomers are molecules with the same molecular formula but different structural arrangements. Isomers can be further classified into constitutional isomers and stereoisomers. Constitutional isomers differ in the connectivity of their constituent atoms. For example, 2-butanol and diethyl ether are constitutional isomers, as they have the same chemical formula, C4H10O, but differ in the connectivity of the carbon and oxygen atoms. Constitutional isomers have different physical and chemical...
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Network Covalent Solids02:18

Network Covalent Solids

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Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
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Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
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  2. オレフィンのe-zイソメリゼーションのためのトリアジン機能化された多孔共性有機フレームワーク
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  2. オレフィンのe-zイソメリゼーションのためのトリアジン機能化された多孔共性有機フレームワーク

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オレフィンのE-Zイソメリゼーションのためのトリアジン機能化された多孔共性有機フレームワーク

Mohitosh Bhadra1,2, Sharath Kandambeth2, Manoj K Sahoo1,2

  • 1Academy of Scientific and Innovative Research (AcSIR) , CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road , Pune - 411008 , India.

Journal of the American Chemical Society
|April 5, 2019

PubMed で要約を見る

まとめ
この要約は機械生成です。

非金属の共性有機フレームワークは,可視光光触媒の貴金属触媒に持続可能な代替手段を提供します. 新しいトリアジン・ケト・フレームワーク (TpTt) は,青い光を使ってトランス・スティルベンをシス・スティルベンに効率的に変換します.

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科学分野:

  • 有機化学
  • 材料科学
  • 光触媒

背景:

  • 可視光光触媒は熱有機反応の 持続可能な代替手段です
  • 貴金属や有機染料を基にした均質な光触媒は有毒で,再利用できず,工業的な応用が制限されています.
  • 効率的で再利用可能で無毒な異質光触媒の開発は極めて重要です.

研究 の 目的:

  • 異質光触媒のための新しい非金属基の共性有機フレームワーク (TpTt) を合成する.
  • 可視光照射下でTpTtの光触媒的活動を調査する.
  • トランス・スティルベンのシス・スティルベンの上昇変換におけるTpTtの応用を証明する.

主な方法:

  • トリアジンとケトの機能化された非金属基の共性有機構造体 (TpTt) の合成
  • TpTtの光学および構造特性の特徴
  • 青い発光ダイオードを使った光触媒反応装置
  • トランス・スティルベンのシス・スティルベンの変換の分析

主要な成果:

  • 合成されたTpTtは可視光スペクトルにおいて有意な吸収を示した.
  • TpTtは,トランス・スティルベンのシス・スティルベンの光触媒的変換において高い効率性を示した.
  • 反応は,広範囲の基板を持つエネルギー転送メカニズムによって進行した.
  • 結論:

    • 非金属基の共性有機フレームワーク (TpTt) は,可視光駆動の有機変換のための効果的な異質な光触媒である.
    • TpTtは従来の同質光触媒の持続可能で再利用可能な代替品です.
    • この研究は,グリーン化学における大規模な応用のためのTpTtの可能性を強調しています.