协调杂质对聚合的电化学稳定性的影响 (II) 希夫基复合物
Ulyana M Rodionova1, Daniil A Lukyanov1, Peixia Yang2
1Institute of Chemistry, Saint-Petersburg University, 199034 Saint-Petersburg, Russia.
International journal of molecular sciences
|February 27, 2026
概括
基希夫基聚合物薄膜中的固体阻碍通过防止酒精杂质与中心协调,提高了电化学稳定性. 分子设计提高了对降解的抵抗力.
科学领域:
- 电化学 电化学 电化学
- 聚合物科学 聚合物科学
- 材料化学 材料化学
背景情况:
- 希夫基复合物用于聚合物薄膜中.
- 通过协调杂质降解会影响聚合物的性能.
- 了解降解机制对于材料的稳定性至关重要.
研究的目的:
- 为了研究基希夫基聚合物薄膜中的降解机制,这些薄膜是由基溶剂诱导的.
- 为了澄清分子结构在电化学稳定性中的作用.
- 评估固体阻碍对抗协调杂质的影响.
主要方法:
- 聚 (Ni) 和其衍生物的电聚合.
- 循环电压测量 (CV) 和电化学石英晶微平衡 (EQCM) 测量.
- 在现场监测氧化还原活性和重量变化在酸与酒精添加剂.
主要成果:
- 酒精 (甲醇,异醇) 作为Ni中心的轴联体,破坏聚合物的π系统和导电性.
- 不被替代的聚[Ni(Salen) ]显示出快速的容量损失,而受到固体保护的衍生品 (聚[Ni(Salpn-1,2)),聚[Ni(Saltmen) ]显示出更好的稳定性.
- EQCM揭示了不可逆转的质量变化,与轴坐标和溶剂入相一致.
结论:
- 分子设计,特别是在Ni中心周围引入固体障碍,显著提高了聚合物薄膜对协调杂质的抵抗力.
- 基希夫基聚合物薄膜的稳定性严重依赖于它们的分子结构.
- 控制固体阻碍是开发强大的电化学材料的关键策略.
相关概念视频
Formation of Complex Ions
26.4K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
26.4K
Complexation Equilibria: Factors Influencing Stability of Complexes
884
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...
884
EDTA: Auxiliary Complexing Reagents
1.4K
EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...
1.4K
EDTA: Chemistry and Properties
3.6K
Polydentate ligands are most widely used in complexometric titrations because they form more stable complexes with the metal ions than mono- or bidentate ligands due to the chelate effect. Examples of polydentate ligands are ethylenediaminetetraacetic acid (EDTA), crown ethers, and cryptands. The most important feature of optimal polydentate ligands is the ability to form 1:1 complexes in a single-step process. Amino carboxylic acid derivatives are frequently used as complexing agents. EDTA is...
3.6K
Extraction: Advanced Methods
1.2K
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
1.2K
Metal-Ligand Bonds
24.8K
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...
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...
24.8K


