在水中的多化环法-二烯二胺复合物中,高效的宿主-客体能量转移
Seán T J Ryan1, Jesús Del Barrio, Indrajit Ghosh
1Melville Laboratory for Polymer Synthesis, Department of Chemistry, University of Cambridge , Lensfield Road, Cambridge CB2 1EW, United Kingdom.
Journal of the American Chemical Society
|June 4, 2014
概括
高电荷的超分子复合体在水中自组装. 这些复合物形成一个具有增强光物理性质的3-多假多,并作为氨酸的选择性传感器.
科学领域:
- 超分子化学 超分子化学
- 材料科学 材料科学 材料科学
- 化学传感器 化学传感器
背景情况:
- 循环宿主-客化学对于开发先进材料至关重要.
- 二胺 (PDI) 是具有可调节光物理性质的多功能染色体.
- 在水性介质中自组装提供了环保的合成途径.
研究的目的:
- 研究高度充电的超分子复合体的自我组装.
- 探索宿主和客分子之间的能量转移 (ET) 动态.
- 开发具有增强功能和传感能力的新型超分子架构.
主要方法:
- 合成和表征ExBox和二元化的PDI衍生品.
- 在水溶液中进行自组装研究.
- 光谱技术 (UV-Vis,光) 用于监测复杂的形成和ET.
- 复杂化研究与黄素[7]uril (CB[7]) 形成多伪多多素.
- 对黑激素的化学传感能力的评估.
主要成果:
- 在ExBox和PDIs之间形成稳定的六化超分子复合体.
- 在ExBox和PDIs之间观察有效的能量传输.
- 使用ExBox,PDIs和CB[7],成功地自组装了一种3-多重伪多多.
- 显著增强PDI光物理性质在多伪多多结构内.
- 使用二进制复合体对黑激素进行选择性化学传感的演示.
结论:
- 高电荷的超分子组件可以很容易地在水中形成.
- 3-多伪多结构导致了优越的光物理性能.
- 这些超分子系统显示出选择性神经递质检测的前景.
相关概念视频
Stability of Substituted Cyclohexanes
13.3K
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...
13.3K
Aromatic Hydrocarbon Cations: Structural Overview
3.4K
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...
3.4K
Intermolecular Forces
62.4K
Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are ion–dipole, dipole–dipole, hydrogen bonds, and dispersion; among these, dipole–dipole, hydrogen...
62.4K
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
8.0K
The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.
8.0K
Stability of Conjugated Dienes
3.3K
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
3.3K
Thermal Electrocyclic Reactions: Stereochemistry
1.6K
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.
1.6K


