通过多元组件自组合的Fe-Pt扭曲的异金属循环超分子
Hajar Sepehrpour1, Manik Lal Saha1, Peter J Stang1
1Department of Chemistry, University of Utah , 315 South 1400 East, Room 2020, Salt Lake City, Utah 84112, United States.
Journal of the American Chemical Society
|February 3, 2017
概括
研究人员开发了一种新的多元组件自组装方法,以创建复杂的铁 (Fe-Pt) 双循环结构. 这种方法为新型金属循环合成提供了对分子结构的精确控制.
科学领域:
- 超分子化学
- 协调化学
- 材料科学
背景情况:
- 设计复杂的分子架构需要对组件组装进行精确控制.
- 异金属系统提供独特的特性,但具有定义结构的合成具有挑战性.
研究的目的:
- 引入一种新的多元件自组装策略,用于构建异金属双循环架构.
- 在复杂的金属循环的形成中展示宪法控制.
主要方法:
- 使用了协调方向性,静态度和差异金属离子协调偏好.
- 来自四种独特的前体物种的合成Fe-Pt异金属双循环金属 (6a和6b).
- 使用多核核磁共振,二维核磁共振,质谱 (ESI-TOF) 和紫外线光谱的产品.
主要成果:
- 在约70%的分离产量中成功制备了两个不同的Fe-Pt异金属双循环金属循环.
- 这些结构有九个沟通的组成部分,
- 计算分析显示,一个结构由两个扭曲的[Pt→Fe→II→pyridine]六角组成,由一个[terpyridine→Fe→Fe→II→pyridine]链连接.
结论:
- 开发的多组件自组装方法可以创建前所未有的异金属双循环架构,具有高度的结构控制.
- 这种方法为设计具有可预测结果的复杂超分子结构提供了多功能平台.
- 合成的Fe-Pt金属循环展示了基于受控自组合的新功能材料的潜力.
相关概念视频
Protein Complex Assembly
17.0K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types. Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Many viruses self-assemble into a fully functional unit using the infected host cell to...
17.0K
Olefin Metathesis Polymerization: Overview
2.7K
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 of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
2.7K
Aromatic Hydrocarbon Cations: Structural Overview
4.1K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
Removing one hydrogen from the intervening CH2 group...
4.1K
Thermal and Photochemical Electrocyclic Reactions: Overview
3.1K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
3.1K
Thermal Electrocyclic Reactions: Stereochemistry
2.7K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.7K
Valence Bond Theory
11.5K
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...
11.5K


