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相关概念视频

Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation01:22

Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation

Baeyer–Villiger oxidation converts aldehydes to carboxylic acids and ketones to esters. The reaction uses peroxy acids or peracids and is often catalyzed by acid. The reaction is named after its pioneers, Adolf von Baeyer and Victor Villiger. The reaction is achieved by a wide range of peracids such as m-chloroperoxybenzoic acid (mCPBA), perbenzoic acid (C6H5COOOH), peracetic acid (CH3COOOH), hydrogen peroxide (H2O2), and tert-butyl hydroperoxide (t-BuOOH).
The carbonyl center is activated by...
β-Dicarbonyl Compounds via Crossed Claisen Condensations01:18

β-Dicarbonyl Compounds via Crossed Claisen Condensations

Crossed Claisen condensations are base-promoted reactions between two different ester molecules producing β-dicarbonyl compounds. The reaction involving esters, with both containing α hydrogen, results in a mixture of four different products that are difficult to isolate. This reduces the synthetic utility of the reaction.
Radical Formation: Elimination00:51

Radical Formation: Elimination

Another method of radical formation is the elimination process. It is the opposite of the addition route and is driven by the instability of the radical. For example, as depicted in Figure 1, dibenzoyl peroxide yields a pair of unstable radicals upon homolysis. Given its instability, this radical spontaneously undergoes elimination via a C–C bond cleavage to form a relatively more stable phenyl radical. The mechanism involves cleavage of the bond between the α and β positions with respect to...
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the polymer...
Phase I Reactions: Reductive Reactions01:27

Phase I Reactions: Reductive Reactions

Phase I biotransformation reductive reactions are chemical processes that modify drugs by introducing or revealing polar functional groups via reduction. Enzymes called reductases catalyze these reactions, playing a pivotal role in drug metabolism by transforming lipophilic drugs into more polar, water-soluble metabolites for easy excretion. An essential type of reductive reaction is the carbonyl group reduction, where aldehydes and ketones are reduced to alcohols. An example is the...

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相关实验视频

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Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation
11:09

Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation

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用于干脱的β-二胺复合物.

Ulrich Fekl1, Werner Kaminsky, Karen I Goldberg

  • 1Department of Chemistry, Box 351700, University of Washington, Seattle, WA 98195-1700, USA.

Journal of the American Chemical Society
|December 11, 2003
PubMed
概括

合成和研究了新的 (IV) 复合物. 一个复合体产生 (II) 种,可以激活基C-H键并执行脱反应.

科学领域:

  • 有机金属化学 有机金属化学
  • 催化剂是一种催化剂.
  • 无机化学 无机化学

背景情况:

  • 由于其独特的反应性,五坐标 (IV) 复合物引起人们的兴趣.
  • 基C-H键激活是有机合成和能源应用中的关键转化.

研究的目的:

  • 合成和表征新的五坐标 (IV) 复合体.
  • 为了研究这些复合物的催化潜力在基功能化.

主要方法:

  • 使用已确定的有机金属方法合成的目标复合物.
  • 使用光谱技术 (NMR,质谱学) 进行复合物的表征.
  • 评估基C-H键激活和脱反应中的催化活性.

主要成果:

  • 成功合成了新的五坐标 ((IV) 复合物,其一般式为[{(o-R2-p-R'-C6H2) NC(R' ') }2CH]PtMe3.3.
  • 发现具有R = Me,R' = tBu,R' ' = Me的特异复合物产生不和 (II) 种.
  • 这种 (二) 种表现出能够激活和脱化静态度基C-H键的能力.

结论:

  • 报告中的 (IV) 复合物代表了一类新的有机金属化合物.

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  • 从的前体中生成活性 (II) 种,为催化应用开辟了道路.
  • 这些发现有助于开发用于C-H键功能化和脱的新催化剂.