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相关概念视频

Metal-Ligand Bonds02:51

Metal-Ligand Bonds

The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Properties of Organometallic Compounds01:23

Properties of Organometallic Compounds

Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H01:13

meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H

All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for the...
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
Heterogeneous Catalysis01:22

Heterogeneous Catalysis

Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...

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Updated: May 11, 2026

Bridging the Bio-Electronic Interface with Biofabrication
16:38

Bridging the Bio-Electronic Interface with Biofabrication

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用动态定位的氨基金属凝进行相变换

Peter J Boul1, Peter D Jarowski2, Carl J Thaemlitz1

  • 1Aramco Research Center , Houston, Texas 77061, United States.

Journal of the American Chemical Society
|October 10, 2017
PubMed
概括
此摘要是机器生成的。

当三价金属结合时,动态聚合物分解成液体,然后在加热时重塑凝. 这种可逆转变为先进材料提供了自我愈合和触发释放功能.

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Multi-Scale Modification of Metallic Implants With Pore Gradients, Polyelectrolytes and Their Indirect Monitoring In vivo
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Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange
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科学领域:

  • 聚合物化学
  • 材料科学
  • 超分子化学

背景情况:

  • 动态共价化学可以创造适应性材料.
  • 半氨基和氨基链接为动态聚合物提供可逆键形成的关键.

研究的目的:

  • 研究三价金属对具有 hemiaminal 和 aminal 功能的动态聚合物的作用.
  • 在聚合物凝中探索平衡和不平衡状态之间的转换.
  • 描述这些动态系统的自我愈合和触发释放特性.

主要方法:

  • 使用 hemiaminal 和 aminal 链接合成动态聚合物.
  • 用于研究凝-溶过渡和材料性能的风湿学分析.
  • 核磁共振 (NMR) 光谱检测反应中间体.
  • 密度函数理论 (DFT) 计算以了解能量景观.

主要成果:

  • 三价金属诱导动态聚合物的可逆碎片化,将凝转化为液体.
  • 加热液相会触发催化转化成闭环六酸产物,形成新的凝.
  • 由系统热力学和动力学决定的受控凝时间得到了实现.
  • 系统展示了可调节的特性,自我修复能力和触发释放潜力.

结论:

  • 基于 hemiaminal/aminal 功能的动态聚合物表现出金属响应,热可切换的行为.
  • 在平衡状态和不平衡状态之间的相互作用允许控制的物质转换.
  • 该系统为开发具有自我愈合和触发释放功能的先进材料提供了一个平台.