用立方体,混合Pd(II) 和Pt(II) M6L12的聚合物网络:合成和压力放松行为
Julia Zhao1, Eduard O Bobylev1, David J Lundberg2
1Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Journal of the American Chemical Society
|September 29, 2023
概括
这项研究引入了使用 (II) 和 (II) 离子的聚合物金属有机 (polyMOC) 凝. 这些新型聚MOC通过控制金属 - 连接物交换动态来显示可调节的能量消散特性.
科学领域:
- 材料科学
- 聚合物化学
- 超分子化学
背景情况:
- 金属有机/多面体 (MOC) 是高级聚合物网络的关键构件.
- 之前的研究还没有从稳定的Pt (II) 基MOC或混合Pd (II) /Pt (II) 系统中探索多MOC.
- 金属-连接物交换动态对多MOC能耗的影响在很大程度上尚未研究.
研究的目的:
- 引入一种新的聚合物金属有机 (polyMOC) 架构.
- 使用 (II) 和 (II) 离子的混合物来证明多MOC的合成.
- 调查金属-联体交换动态和多MOC能耗之间的关系.
主要方法:
- 由M6L12立方体 (M=Pd(II),Pt(II) 或混合物交联的聚乙烯糖醇 (PEG) 纤维合成的聚MOC凝.
- 在多MOC网络结构中变化了Pd (II) 含量.
- 分析了M6L12连接层的应力放松率和金属连接物交换动态.
主要成果:
- 开发了一种具有可调节网络结构的新型聚MOC凝.
- 通过变化的Pd (II) 和Pt (II) 含量实现了跨越3个数量级的调节式应力放松率.
- 在混合金属多MOC中观察到独特的放松行为,这表明了连接内部的合作相互作用.
结论:
- 介绍了用于多MOC设计和合成的新型MOC架构.
- 从Pd (II) /Pt (II) 金属离子的混合物中成功制备的多MOC.
- 证明了由于多价结,多MOCs表现出独特的放松行为,使其能够独立控制材料属性.
相关概念视频
Valence Bond Theory
8.6K
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...
8.6K
Stability of Substituted Cyclohexanes
12.7K
This lesson discusses the stability of substituted cyclohexanes with a focus on energies of various conformers and the effect of 1,3-diaxial interactions.
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
12.7K
Metallic Solids
18.5K
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
18.5K
Ziegler–Natta Chain-Growth Polymerization: Overview
3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K
Crystal Field Theory - Tetrahedral and Square Planar Complexes
42.8K
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
42.8K
Crystal Field Theory - Octahedral Complexes
26.7K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
26.7K


