Solid-state nuclear magnetic resonance (NMR) spectroscopy has become an integral technique in the field of pharmaceutical sciences. This review focuses on the use of solid-state NMR techniques for the characterization of pharmaceutical solids (drug substance and dosage form). These techniques includ
Silicon-29 solid-state nuclear magnetic resonance spectroscopy of composite interfaces
✍ Scribed by Ka-Pi Hoh; Hatsuo Ishida; Jack L. Koenig
- Book ID
- 104511311
- Publisher
- Society for Plastic Engineers
- Year
- 1990
- Tongue
- English
- Weight
- 436 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0272-8397
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The types of structures and bonds that are formed with silicons in the composite interface were studied using ^29^Si cross‐polarization/magic angle sample spinning (CP/MAS) nuclear magnetic resonance spectroscopy (NMR). The change in mobility of silane coupling agent bonded to silica, as compared with bulk hydrolyzed silane coupling agent, can be monitored by the change in line width and the shift of resonances to higher fields, as well as by the change in the silicon‐proton cross‐polarization time T~SiH~. In the silane coupling agent‐matrix resin interface, the T~SiH~ values reflect the change in mobility as a function of the concentration and degree of hydrolysis of the silane coupling agent. It has been demonstrated that quantitative measurements of T~SiH~ can be used to investigate relative mobilities.
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