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The band at 1737.808 cm−1 was for C=O stretching, usually present in the esters.
In the same way, the most influential hemicellulose signal in the loading plot was the 1,732 cm-1, this signal was a minimum in both cases and relates the modifications in the esters found in the hemicellulose.
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The carbonyl group in the ester linkage of lipids is capable of absorbing infrared energy.
The dielectric transitions related to the local mobility in the ester aromatic fragment were observed.
The molecular structure deviates slightly from the fully extended conformation in the ester part.
Indium stearate, which was used as indium precursor in the ester elimination reactions, was prepared as follows [15].
The ion selectivity is very sensitive to the structure of polyoxyethylene spacer and the R in the ester moiety.
Growth in the ester alkoxy chain length from one to four carbon atoms had minimal effect on the ignition delay.
An increase in the ester units in the network results in materials that are less thermally stable and whose controlled degradability is greater.
The sharp and symmetric characteristic absorption peak at 1,735 cm−1 is due to the stretching vibration of C=O in the ester carbonyl group[48].
The important incentive, impetus to intensify the research on the termination of the course of bimolecular condensation of primary alcohols in the ester phase is the potential increase in the ethyl acetate demand.
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