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相关概念视频

Chirality02:25

Chirality

29.7K
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...
29.7K
Chirality in Nature02:30

Chirality in Nature

17.3K
Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
17.3K
Chirality at Nitrogen, Phosphorus, and Sulfur02:30

Chirality at Nitrogen, Phosphorus, and Sulfur

7.0K
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...
7.0K
Molecules with Multiple Chiral Centers02:25

Molecules with Multiple Chiral Centers

15.1K
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...
15.1K
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

30.9K
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...
30.9K
Structures of Solids02:22

Structures of Solids

18.0K
Solids in which the atoms, ions, or molecules are arranged in a definite repeating pattern are known as crystalline solids. Metals and ionic compounds typically form ordered, crystalline solids. A crystalline solid has a precise melting temperature because each atom or molecule of the same type is held in place with the same forces or energy. Amorphous solids or non-crystalline solids (or, sometimes, glasses) which lack an ordered internal structure and are randomly arranged. Substances that...
18.0K

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Assembly of Gold Nanorods into Chiral Plasmonic Metamolecules Using DNA Origami Templates
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化等离子场探测器生物界面的结构顺序

Christopher Kelly1, Ryan Tullius1, Adrian J Lapthorn1

  • 1School of Chemistry , Joseph Black Building, University of Glasgow , Glasgow G12 8QQ , United Kingdom.

Journal of the American Chemical Society
|June 19, 2018
PubMed
概括

现在可以监测复杂蛋白质层的结构顺序. 这一突破使得研究真正的生物界面无需已知的成分.

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Probing the Structure and Dynamics of Interfacial Water with Scanning Tunneling Microscopy and Spectroscopy
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科学领域:

  • 生物物理
  • 表面科学
  • 光谱学

背景情况:

  • 生物聚合物在接口上的结构顺序对于生物相互作用至关重要.
  • 现有的光谱方法仅限于简单的单元系统,通常需要标签.
  • 复杂多元生物层具有具有挑战性的光谱特征.

研究的目的:

  • 证明超性等离子场对蛋白质层的全球定向顺序的敏感性.
  • 使用数值模拟和模型系统验证方法.
  • 建立一个分析复杂生物界面的工具.

主要方法:

  • 使用超性等离子场探测蛋白质层.
  • 监测免疫球蛋白G层的方向顺序演变.
  • 分析血清蛋白层的结构顺序变化,而没有先前的成分知识.

主要成果:

  • 超性检测异构电偶极-磁偶极反应,表示结构秩序.
  • 该方法成功监测了模型和复杂蛋白质层的方向顺序.
  • 血清蛋白质层组成的定性变化与结构秩序的变化相关.

结论:

  • 超性对蛋白质层的全球定向顺序很敏感.
  • 这种技术克服了复杂生物界面的传统方法的局限性.
  • 超性为研究真实生物系统的结构动态提供了一个强大的新工具.