1996
DOI: 10.1007/bf01434246
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Synthesis of 1,1-dihydroperfluorooxaalkan-1-ols and their interaction with terephthaloyl chloride

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“…Bp of the products was above 200 °C (0.01 Torr). They were prepared according to the procedure reported in [24] and represent fluoropolyether glycols or fluoropolyether amides containing hydroxymethylated terminal groups ( 1a – b ) or a mixture of fluoropolyether glycols with alcohols of similar structure ( 1c – d ) with ratio 7:1. Molecular weights and compositions of the prepared fluoropolyether diols and alcohols were found from 19 F-NMR and 1 H-NMR data.…”
Section: Methodsmentioning
confidence: 99%
“…Bp of the products was above 200 °C (0.01 Torr). They were prepared according to the procedure reported in [24] and represent fluoropolyether glycols or fluoropolyether amides containing hydroxymethylated terminal groups ( 1a – b ) or a mixture of fluoropolyether glycols with alcohols of similar structure ( 1c – d ) with ratio 7:1. Molecular weights and compositions of the prepared fluoropolyether diols and alcohols were found from 19 F-NMR and 1 H-NMR data.…”
Section: Methodsmentioning
confidence: 99%