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Related Concept Videos

¹H NMR: Long-Range Coupling01:27

¹H NMR: Long-Range Coupling

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The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
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The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
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In the AX proton spin system, proton A can sense the two spin states of a coupled proton X, resulting in a doublet NMR signal with two peaks of equal (1:1) intensity. When proton A is coupled to two equivalent protons (AX2 spin system), the spin states of each X can be aligned with or against the external field, creating three possible scenarios. This results in a 1:2:1  triplet signal, where the central peak corresponds to the chemical shift of A and is twice as large or intense as the...
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NMR Spectrometers: Resolution and Error Correction01:14

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When magnetic nuclei in a sample achieve resonance and undergo relaxation, the signal detected in NMR is an approximately exponential free induction decay. Fourier transform of an exponential decay yields a Lorentzian peak in the frequency domain. Lorentzian peaks in an NMR spectrum are defined by their amplitude, full width at half maximum, and position, where the peak width is governed by the spin-spin relaxation time alone. In real experiments, however, the applied magnetic field is rendered...
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Atomic Nuclei: Types of Nuclear Relaxation01:28

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Nuclear relaxation restores the equilibrium population imbalance and can occur via spin–lattice or spin–spin mechanisms, which are first-order exponential decay processes.
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Single-file nanochannel persistence lengths from NMR.

Muslim Dvoyashkin1, Hrishi Bhase, Navid Mirnazari

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Researchers developed a new NMR method to measure open channel persistence length in nanomaterials. This technique confirmed that dipeptide nanotubes are largely unblocked, but pulverizing them significantly reduces channel persistence.

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Analytical Chemistry

Background:

  • Crystalline solids with sub-nanometer one-dimensional channels are promising for various applications.
  • A critical parameter for these materials is the average open channel persistence length, indicating the distance to the first obstruction.

Purpose of the Study:

  • To introduce and validate a novel Nuclear Magnetic Resonance (NMR)-based methodology for measuring average open channel persistence length.
  • To apply this method to dipeptide nanotubes (l-Ala-l-Val and l-Val-l-Ala) and assess their structural integrity.

Main Methods:

  • Development of an NMR-based protocol to quantify average open channel persistence length.
  • Application of the NMR method to polycrystalline samples of l-Ala-l-Val (AV) and l-Val-l-Ala (VA) nanotubes.
  • Comparison of NMR-derived persistence lengths with crystallite dimensions obtained from Scanning Electron Microscopy (SEM).

Main Results:

  • NMR measurements revealed persistence lengths comparable to crystallite sizes in pristine AV and VA samples, suggesting hollow structures with minimal blockages.
  • Pulverization of an AV sample significantly reduced the average open channel persistence length from 50 μm to 6.6 μm.
  • SEM analysis corroborated the reduction in crystallite size after mechanical stress, consistent with the observed decrease in channel persistence.

Conclusions:

  • The developed NMR methodology effectively measures average open channel persistence length in nanomaterials.
  • Dipeptide nanotubes exhibit excellent open channel structures, but are susceptible to blockage upon mechanical processing.
  • This technique provides valuable insights into the structural integrity and processability of nanomaterials with one-dimensional channels.