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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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13C CP/MAS NMR study of a phenyl group r
✍ Frank G. Riddell; Murray Bremner; John H. Strange 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 316 KB

## 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