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

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

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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.
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Network Covalent Solids02:18

Network Covalent Solids

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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...
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¹H NMR of Conformationally Flexible Molecules: Temporal Resolution00:52

¹H NMR of Conformationally Flexible Molecules: Temporal Resolution

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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...
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Conformations of Cyclohexane02:11

Conformations of Cyclohexane

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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...
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Molecular Models02:00

Molecular Models

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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.
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Adaptability of Cytoskeletal Filaments01:12

Adaptability of Cytoskeletal Filaments

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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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Video Experimental Relacionado

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

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Flexibilidad bajo demanda: marcos orgánicos covalentes multivariados en 3D

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
Resumen

Los investigadores desarrollaron un nuevo método para sintetizar marcos orgánicos covalentes multivariados (MTV). Este avance permite una flexibilidad ajustable y un rendimiento mejorado de separación de gases en COF dinámicos.

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Área de la Ciencia:

  • Ciencias de los materiales
  • Química
  • Nanotecnología

Sus antecedentes:

  • Los marcos orgánicos covalentes dinámicos 3D (dynaCOF) exhiben cambios estructurales con adsorción de invitados.
  • Las estrategias multivariadas (MTV) ofrecen flexibilidad ajustable, pero se enfrentan a desafíos sintéticos debido a las diferencias de reactividad de los enlaces, que a menudo causan separación de fase.

Objetivo del estudio:

  • Desarrollar un protocolo sintético general para las MTV-COF en 3D.
  • Para superar los problemas de separación de fase en la síntesis de MTV-COF con diversas funcionalidades.
  • Para demostrar la aplicación de estos MTV-COF en la separación de gases.

Principales métodos:

  • Sintetizó 15 isostructuras MTV-COF-300 cristalinas y puras de fase utilizando una unidad tetraédrica y ocho soportes ditópicos con grupos funcionales variados.
  • Se utiliza un sistema de disolventes mixtos (aprótico polar y no polar) para equilibrar la reactividad del enlace y mejorar la solubilidad para una cristalización controlada.
  • Investigó el impacto de los grupos de donación y retirada de electrones en la reactividad del enlace y la cristalización del material.

Principales resultados:

  • Sintetizó con éxito MTV-COFs de fase pura equilibrando cuidadosamente la reactividad del enlace y la polaridad del disolvente.
  • Se demostró que las mezclas específicas de disolventes mejoran la solubilidad de los oligómeros y la cinética de reacción moderada, cruciales para la cristalización.
  • Mostró los comportamientos dinámicos de gas sintonizables y la separación eficiente de benceno y ciclohexano utilizando los MTV-COF sintetizados.

Conclusiones:

  • Se estableció un protocolo sintético general para MTV-COFs 3D, superando las limitaciones anteriores.
  • Los MTV-COF sintetizados exhiben flexibilidad bajo demanda, lo que permite una sinergia dinámica para aplicaciones específicas.
  • Estos marcos multivariados superan a las contrapartes monofuncionales en la separación de gases, lo que pone de relieve el potencial de las funcionalidades integradas.