2017•Unpublished venueRequires access

Solid‐State NMR Spectroscopy

Stephen R Byrn, George Zografi, Xiaoming (Sean) Chen

Open publisher page 1 citations

Abstract

Solution proton and carbon nuclear magnetic resonance (1H and 13C NMR) are widely used for the study of drugs, being employed for structure elucidation or identification. One advantage of solid-state NMR is that it offers the potential for analysis of mixed crystals or mixtures because signals from crystal-lographically distinct but chemically identical sites are often resolvable. One advantage of solid-state NMR is that it offers the potential for analysis of mixed crystals or mixtures because signals from crystallographically distinct but chemically identical sites are often resolvable. Solid-state NMR spectroscopy was developed by Schaefer and Stejskal who combined high-powered proton decoupling with cross-polarization (CP) and magic-angle spinning (MAS), techniques that provided an enormous increase in the resolution and sensitivity of solid-state spectra. A complete understanding of the CP experiment requires an understanding of the concept of spin temperature and spin diffusion in solids.

About this research paper

What this paper is about

Solution proton and carbon nuclear magnetic resonance (1H and 13C NMR) are widely used for the study of drugs, being employed for structure elucidation or identification. One advantage of solid-state NMR is that it offers the potential for analysis of mixed crystals or mixtures because signals from crystal-lographically distinct but chemically identical sites are often resolvable. One advantage of solid-state NMR is that it offers the potential for analysis of mixed crystals or mixtures because signals from crystallographically distinct but chemically identical sites are often resolvable. Solid-state NMR spectroscopy was developed by Schaefer and Stejskal who combined high-powered proton decoupling with cross-polarization (CP) and magic-angle spinning (MAS), techniques that provided an enormous increase in the resolution and sensitivity of solid-state spectra. A complete understanding of the CP experiment requires an understanding of the concept of spin temperature and spin diffusion in solids.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Solution proton and carbon nuclear magnetic resonance (1H and 13C NMR) are widely used for the study of drugs, being employed for structure elucidation or identification. One advantage of solid-state NMR is that it offers the potential for analysis of mixed crystals or mixtures because signals from crystal-lographically distinct but chemically identical sites are often resolvable. One advantage of solid-state NMR is that it offers the potential for analysis of mixed crystals or mixtures because signals from crystallographically distinct but chemically identical sites are often resolvable. Solid-state NMR spectroscopy was developed by Schaefer and Stejskal who combined high-powered proton decoupling with cross-polarization (CP) and magic-angle spinning (MAS), techniques that provided an enormous increase in the resolution and sensitivity of solid-state spectra. A complete understanding of the CP experiment requires an understanding of the concept of spin temperature and spin diffusion in solids.

Key concepts: Chemistry, Solid-state nuclear magnetic resonance, Spin diffusion, Carbon-13 NMR satellite, Nuclear magnetic resonance spectroscopy, Magic angle spinning, Solid-state, Nuclear magnetic resonance crystallography

Related papers

Back to paper searchBrowse research topicsOriginal source
Solid‐State NMR Spectroscopy — Research Paper | ScholarLens