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Alkynes to Carboxylic Acids: Oxidative Cleavage02:01

Alkynes to Carboxylic Acids: Oxidative Cleavage

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Alkynes undergo oxidative cleavage in the presence of oxidizing reagents like potassium permanganate and ozone. The triple bond — one σ bond and two π bonds — is completely cleaved, and the alkyne is oxidized to carboxylic acids. When warm and basic aqueous potassium permanganate is used as an oxidizing agent, alkynes are first converted to carboxylate salts via an unstable α-diketone intermediate. Further, a mild acid treatment protonates the carboxylate anions...
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Oxidative Cleavage of Alkenes: Ozonolysis01:46

Oxidative Cleavage of Alkenes: Ozonolysis

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In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
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Ethers to Alkyl Halides: Acidic Cleavage02:18

Ethers to Alkyl Halides: Acidic Cleavage

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Ethers are generally unreactive and unsuitable for direct nucleophilic substitution reactions since the alkoxy groups are strong bases and, therefore, poor leaving groups. However, ethers readily undergo acidic-cleavage reactions. Ethers can be converted to alkyl halides when heated with strong acids such as HBr and HI in a sequence of two substitution reactions.
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Acid Halides to Carboxylic Acids: Hydrolysis01:01

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Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
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Solubility03:00

Solubility

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Solution, Solubility, and Solubility Equilibrium
A solution is a homogeneous mixture composed of a solvent, the major component, and a solute, the minor component. The physical state of a solution—solid, liquid, or gas—is typically the same as that of the solvent. Solute concentrations are often described with qualitative terms such as dilute (of relatively low concentration) and concentrated (of relatively high concentration).
In a solution, the solute particles (molecules,...
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Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
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可通过酸切割的多氧烯酸表面活性剂.

Joseph A Garcia1, Linglan Zhu1, Ashley Vergara Mendez1

  • 1Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, California 90095, USA.

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概括
此摘要是机器生成的。

新的刺激响应纳米疗法利用可酸分裂的表面活性剂用于向癌症治疗. 这些新型的基于聚氧氨酸的材料增强了药物输送和内体逃逸在酸性瘤环境中.

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科学领域:

  • 生物材料科学 生物材料科学
  • 纳米技术 纳米技术
  • 聚合物化学 聚合物化学

背景情况:

  • 酸性瘤微环境和晚期内体是刺激响应纳米治疗的关键目标.
  • 酸可裂变的表面活性剂,特别是那些具有水链接的表面活性剂,提供稳定性和受控的细胞内有效载荷释放.
  • 有效的内体体逃脱对于有效的癌症纳米医学至关重要.

研究的目的:

  • 为了合成和表征一种新型的与酸结合的基于多 (酸) 的双块共聚合物表面活性剂.
  • 为了评估合成的表面活性剂的pH依赖的裂变行为.
  • 为了证明这种表面活性剂系统对受控有效载荷释放和增强内体逃逸的实用性.

主要方法:

  • 一种基于多 () 的双块共聚合物表面活性剂的合成,具有水链接.
  • pH稳定性研究以确定不同pH值 (pH7.4与pH5.0) 的裂变速率.
  • 纳米乳液制备和有效载荷分离到细胞膜中的评估模仿了分离后的情况.

主要成果:

  • 水结合的聚合物表现出显著的pH依赖性裂变,80%在pH7.4下保持,21小时后只有17%在pH5.0下保持.
  • 分成细胞膜的纳米乳液有效载荷仅在表面活性剂裂变后进行模拟.
  • 通过操纵pH条件,在42小时内有效载荷释放量从26%增加到47%.

结论:

  • 在生物相关条件下证明了一条可行的途径,用于在生物相关条件下制造具有可控释放能力的聚类基纳米材料.
  • 开发的表面活性剂系统在纳米医学中有望改善内体逃生和向癌症.
  • 这项工作为推进癌症治疗的刺激响应纳米疗法提供了基础.