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Influence of n-alkyl substituents on the thermal behaviour of Polyhedral Oligomeric Silsesquioxanes (POSSs) with different cage's periphery

•POSS thermal stability increases with aromatic substituents instead of cycloaliphatic.•Residues at 700°C were a further confirmation of higher phenyl POSS thermal stability.•Thermal stability linearly increases as a function of (CH2) groups in alkyl chain. Polyhedral Oligomeric Silsesquioxanes (POS...

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Bibliographic Details
Published in:Thermochimica acta 2016-01, Vol.623, p.50-57
Main Authors: Blanco, I., Bottino, F.A., Abate, L.
Format: Article
Language:English
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Summary:•POSS thermal stability increases with aromatic substituents instead of cycloaliphatic.•Residues at 700°C were a further confirmation of higher phenyl POSS thermal stability.•Thermal stability linearly increases as a function of (CH2) groups in alkyl chain. Polyhedral Oligomeric Silsesquioxanes (POSSs) of general formula R7R′(SiO1.5)8, where R=isobutyl, cyclopentyl or phenyl and R′=(CH2)5CH3, (CH2)7 CH3 or (CH2)9CH3, were prepared by corner capping reaction of trisilanols with suitable alkyltriethoxysilane. The compounds obtained were characterized by elemental analysis and 1H NMR spectroscopy, and the results were in very good agreement with those of expected products. The prepared POSSs were degraded in dynamic heating conditions from r.t. to 700°C, in both inert and oxidative atmospheres, and the temperatures at 5% weight loss (T5%) were determined and compared with each other, in order to investigate how the various groups affect the resistance to thermal degradation. The results did not evidence any substantial difference between the two investigated atmospheres, but indicated clearly an increasing resistance to the thermal degradation according to the following order: isobutyl POSSs
ISSN:0040-6031
1872-762X
DOI:10.1016/j.tca.2015.11.013