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相关概念视频

Chirality02:25

Chirality

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...
Molecules with Multiple Chiral Centers02:25

Molecules with Multiple Chiral Centers

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...
Chirality at Nitrogen, Phosphorus, and Sulfur02:30

Chirality at Nitrogen, Phosphorus, and Sulfur

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...
Prochirality02:05

Prochirality

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...
Chirality in Nature02:30

Chirality in Nature

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. The...

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相关实验视频

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Preparation and Photoacoustic Analysis of Cellular Vehicles Containing Gold Nanorods
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一个纳米级的螺旋式超结构,具有设计的性.

Xiang Lan1, Xuxing Lu, Chenqi Shen

  • 1Key Laboratory of Nano-Bio Interface, Division of Nanobiomedicine and i-Lab, CAS Center for Excellence in Brain Science, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences , Suzhou, 215123 China.

Journal of the American Chemical Society
|December 18, 2014
PubMed
概括
此摘要是机器生成的。

研究人员使用DNA原始创建创建了可编程性金纳米基 (AuNR) 螺旋式超结构. 这种方法可以精确控制先进纳米材料的性和组装.

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科学领域:

  • 纳米技术 纳米技术
  • 材料科学 材料科学 材料科学
  • 超分子化学 超分子化学

背景情况:

  • 在纳米技术中,将异性质纳米材料组织成具有特定性质的3D超结构是一个重大挑战.
  • 控制纳米材料组件中的性对于光学和电子学的应用至关重要.

研究的目的:

  • 开发一种可编程的方法,用于构建具有量身定制的性性异型黄金纳米 (AuNR) 螺旋式超结构.
  • 调查DNA原木模板对AuNR螺旋的组装和手术性能的影响.

主要方法:

  • 使用一个二维的DNA原创模板与专门设计的DNA捕获链的"X"模式.
  • 功能化AuNRs与互补的DNA序列,用于精确定位在原木模板上.
  • 在邻近的AuNR之间插入DNA原形模板,形成螺旋式超结构.

主要成果:

  • 通过调整DNA原木"X"图案,成功构建左手 (LH) 和右手 (RH) AuNR螺旋.
  • 实现了对杆间距离 (14 nm) 和杆间角度 (45°) 的精确控制,形成长达220 nm的螺旋,具有9个AuNR.
  • 通过调整 AuNR/原木数比,证明了可调节的 AuNR 组件 (每螺旋体 2 到 9 个 AuNR).
  • 在最长的螺旋中观察到强烈的手术活动,最大的异构系数为~0.02.

结论:

  • 基因原形模板组件提供了一个可编程的路线来制造异构的性超结构.
  • 这一策略使得能够精确控制金纳米石螺旋的性和尺寸.
  • 开发的方法具有创造光学活跃纳米结构的潜力,用于奇拉传感,信号放大和光谱学的应用.