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¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR01:15

¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR

1.1K
The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.
1.1K
Network Covalent Solids02:18

Network Covalent Solids

13.5K
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
13.5K
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution00:52

¹H NMR of Conformationally Flexible Molecules: Temporal Resolution

847
At room temperature, the chair conformer of cyclohexane undergoes rapid ring flipping between two equivalent chair conformers at a rate of approximately 105 times per second. These two chair conformers are in equilibrium. The rapid ring flipping results in the interconversion of the axial proton to an equatorial proton and an equatorial to the axial proton. Such interconversions are too rapid and cannot be detected on the NMR timescale. Hence, the NMR spectrometer cannot distinguish between the...
847
Conformations of Cyclohexane02:11

Conformations of Cyclohexane

12.5K
Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts non-planar chair and boat conformations.
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
12.5K
Molecular Models02:00

Molecular Models

38.4K
Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
38.4K
Adaptability of Cytoskeletal Filaments01:12

Adaptability of Cytoskeletal Filaments

3.7K
The cytoskeleton is a complex dynamic structure performing varied functions based on cellular requirements. The adaptability of the individual filaments in the cytoskeleton determines their ability to perform various functions within the cell. It can undergo rapid reorganization during processes like cell division or remain stable for several hours as in the interphase. The adaptability of these filaments depends on stringent regulatory mechanisms. The microfilament and microtubules of the...
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相关实验视频

Updated: Jul 7, 2025

Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
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Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface

Published on: July 10, 2017

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根据需求的灵活性:多变量3D共价有机框架

Meng Wang1, Tengwu Zeng2, Yi Yu1

  • 1School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, China.

Journal of the American Chemical Society
|December 28, 2023
PubMed
概括

研究人员开发了一种合成多变量 (MTV) 共价有机框架 (COF) 的新方法. 这一突破使得可调节的灵活性和增强的气体分离性能在动态COF.

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Last Updated: Jul 7, 2025

Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
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科学领域:

  • 材料科学
  • 化学学
  • 纳米技术

背景情况:

  • 动态3D共价有机框架 (dynaCOFs) 显示客体吸附的结构变化.
  • 多变量 (MTV) 策略提供可调节的灵活性,但由于链接器反应率差异而面临合成挑战,往往导致相位分离.

研究的目的:

  • 为3DMTV-COF开发一个通用的合成协议.
  • 在合成具有多种功能的MTV-COF时克服相隔问题.
  • 证明这些MTV-COF在气体分离中的应用.

主要方法:

  • 合成了15个晶体和相纯MTV-COF-300异构结构,使用四面体单元和8个具有不同功能组的二面体支架.
  • 采用混合溶剂系统 (极性近极和非极性) 来平衡链接器反应性并提高可溶性以控制结晶.
  • 研究了电子捐赠和电子吸收组对链接器反应和材料结晶的影响.

主要成果:

  • 通过仔细平衡连接器反应性和溶剂极性,成功合成了纯相3DMTV-COF.
  • 证明特定的溶剂混合物增强了寡合物的溶解性和适度的反应动力学,这对于结晶至关重要.
  • 使用合成的MTV-COF展示了可调节的气体动态行为和和环的有效分离.

结论:

  • 建立了3DMTV-COF的一般合成协议,克服了以前的限制.
  • 合成的MTV-COF具有按需的灵活性,可用于特定应用的动态协同作用.
  • 这些多变量框架在气体分离方面表现优于单功能同行,突出显示了集成功能的潜力.