1H-13C CPMAS and T2 Relaxation Solid-State NMR Measurements of Melamine-Based Polycondensed Chemical Gels
✍ Scribed by Chrystelle C. Egger; Volker Schädler; Jérôme Hirschinger; Jésus Raya; Burkhard Bechinger
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 298 KB
- Volume
- 208
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Gel networks prepared from aqueous melamine‐formaldehyde resins via a sol–gel route were characterised by ^13^C CPMAS (where MAS stands for magic angle spinning)‐NMR and T~2~ relaxation. We show that within the aqueous networks, the type and amount of functional groups on the melamine ring is strongly influenced by the initial melamine/formaldehyde ratio, the sol concentration and the amount of catalyst. Residual methylol groups can be etherified by postalkoxylation using primary alcohols resulting in chemical gels with different bridging units and residual ether linkages as also confirmed by T~2~ measurements. In addition, in the case of initially alkoxylated gels the alcoholysis process can be followed by varying the amount of catalyst used.
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## Abstract A combination of solid‐state ^13^C CP/MAS NMR methods was used to study the rates of rotation of the phenyl group in 3,5‐dimethyl‐1‐phenylhex‐1‐yn‐3‐ol. The methods used were __T__~1ρ~ measurements, lineshape analysis and 2D exchange spectroscopy over the temperature range 219–284 K. Th