基素和基素结合调制的多组件状自组件
Yiran Xia1, Aiyou Hao1, Pengyao Xing1
1Key Laboratory of Colloid and Interface Chemistry of Ministry of Education and School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, People's Republic of China.
ACS nano
|October 31, 2023
概括
素和素的结合会从无素的前体中产生状螺旋式纳米管. 这种方法控制了新材料中的超分子性和光学特性.
科学领域:
- 材料科学 材料科学 材料科学
- 超分子化学 超分子化学
- 奇拉性是一种精神性.
背景情况:
- 素和素的结合在控制超分子性方面具有有限的用途.
- 开发新的方法来控制材料中的性对于先进的应用至关重要.
研究的目的:
- 为了研究使用石化和化结合来控制超分子性.
- 在多元组件系统中调节奇拉光学特性.
主要方法:
- 与非化氨基酸一起组合的化 - 联合体.
- 实验和计算分析以证明结合相互作用和形态变化的证据.
- 描述手术活动的特征,例如循环二重化和循环极化发光.
主要成果:
- 素和素的结合诱导了从状膜转化为状螺旋纳米管的转化.
- 出现超分子性与倒置的手性和可调整的手术活动.
- 协同结合稳定了电荷转移复杂化,产生了具有增强光学特性的三元性奇拉联合组件.
结论:
- 碳素和核素的结合是有效的操纵超分子和光学.
- 这项研究扩展了含有VA组和VIA组元素的奇拉材料的制造和属性调整.
相关概念视频
Chirality at Nitrogen, Phosphorus, and Sulfur
5.7K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
5.7K
Molecules with Multiple Chiral Centers
11.8K
Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
11.8K
Prochirality
3.8K
The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
3.8K
Complexation Equilibria: The Chelate Effect
525
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...
525
Metal-Ligand Bonds
20.8K
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...
20.8K
Chirality
24.3K
Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
24.3K


