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相关概念视频

Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.2K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.2K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

1.9K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
1.9K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.2K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.2K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.5K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
3.5K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

2.6K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
2.6K
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

320
Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
320

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相关实验视频

Updated: Jul 14, 2025

Rapid, Scalable Assembly and Loading of Bioactive Proteins and Immunostimulants into Diverse Synthetic Nanocarriers Via Flash Nanoprecipitation
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动态元稳定聚合体使得连续流量制造成为可能.

Chin Ken Wong1, Rebecca Y Lai2, Martina H Stenzel3

  • 1School of Chemistry, University of New South Wales (UNSW), Sydney, NSW, 2052, Australia. c.kenwong@unsw.edu.au.

Nature communications
|October 6, 2023
PubMed
概括
此摘要是机器生成的。

一种新的连续流法使得可扩展的聚合体体 (聚合物囊泡) 的生产成为可能. 这些转移稳定的聚合体允许在流中操纵大小和形状,为临床应用铺平了道路.

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Microfluidic Fabrication of Polymeric and Biohybrid Fibers with Predesigned Size and Shape
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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Rapid, Scalable Assembly and Loading of Bioactive Proteins and Immunostimulants into Diverse Synthetic Nanocarriers Via Flash Nanoprecipitation
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Rapid, Scalable Assembly and Loading of Bioactive Proteins and Immunostimulants into Diverse Synthetic Nanocarriers Via Flash Nanoprecipitation

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Microfluidic Fabrication of Polymeric and Biohybrid Fibers with Predesigned Size and Shape
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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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科学领域:

  • 材料科学 材料科学 材料科学
  • 生物技术是生物技术.
  • 化学工程是化学工程的重要组成部分.

背景情况:

  • 聚合体,脂质体的聚合类相似物,具有独特的特性,但在临床转化方面面临挑战.
  • 目前的生产方法缺乏可扩展性和对聚合物特性的控制.

研究的目的:

  • 开发用于可扩展的聚合物体生产的连续流程方法.
  • 在相同的连续过程中,使得聚合体属性的下游操纵成为可能.

主要方法:

  • 一个连续流系统被设计用于聚合体合成.
  • 该方法利用产生的聚合体的固有转移稳定性.
  • 用于大小和形状操纵的下游处理被集成到流系统中.

主要成果:

  • 实现了≥3g/h的近单分散聚合体的可扩展生产.
  • 聚合体表现出~7天的转移稳定性,允许有控制的生长.
  • 证明了聚合体体大小和形状的内流操纵.

结论:

  • 开发的连续流方法克服了聚合物体生产的可扩展性限制.
  • 聚合体的转移性质被利用为多功能下游加工.
  • 这种方法有助于将聚合体转化为工业和临床应用.