通过动态二硫化物键交叉连接的自组合的多伪多素作为性金属纳米粒子的模块化功能
Xiang Xu1,2, Bing Zan2,3, Yuanyang Xie4
1Institute of Pharmaceutical Science, King's College London, Franklin Wilkins Building, Stamford Street, London, SE1 9NH, UK.
Angewandte Chemie (International ed. in English)
|September 8, 2025
概括
我们开发了一种富含硫醇的多伪多 (SPPR) 平台,用于功能化纳米粒子. 这种适应性强的材料可以创建响应性强的水凝,并增强纳米粒子癌症细胞毒性.
科学领域:
- 超分子化学 超分子化学
- 材料科学是一种材料科学.
- 聚合物化学 聚合物化学
背景情况:
- 多重伪多素 (PPR) 为功能性材料提供模块化和可编程性.
- 富含醇的超分子组合对于动态功能化是可取的.
研究的目的:
- 报告一种自我组装的富含硫醇的多伪多达 (SPPR) 的单制剂.
- 为了证明SPPR的实用性作为一个平台,用于功能化性金属纳米粒子 (NP).
主要方法:
- 在聚合物上 thiolated-α-cyclodextrins 的自组装.
- 通过热触发的醇氧化进行交叉连接,形成二硫化键.
- 使用小角度中子散射和风学进行表征.
主要成果:
- 通过一式方法合成了SPPR.
- SPPR形成了包含NP的热响应性水凝,增强了机械性能,光响应性凝和厚度.
- SPPR聚合物包裹了NP,通过醇介导途径增强了它们的癌症细胞毒性.
结论:
- SPPR作为一个多功能平台,用于功能化金属纳米粒子.
- 这种方法可以开发定制的超分子材料,用于响应性水凝和药物输送.
相关概念视频
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...
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...
Structural Isomerism
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Valence Bond Theory
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
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.
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 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...


