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Selection of a precursor of a monofunctional polyhedral oligomeric silsesquioxane reacted with aromatic diamines
Author(s) -
Ramírez C.,
Vilariño J. M. L.,
Abad M. J.,
Barral L.,
Bouza R.,
Cano J.,
Díez F. J.,
GarcíaGarabal S.,
López J.
Publication year - 2004
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.20101
Subject(s) - silsesquioxane , polymer chemistry , gel permeation chromatography , epoxy , materials science , diamine , oligomer , chemistry , polymer , organic chemistry
With the aim of selecting a precursor of a polyhedral oligomeric silsesquioxane (POSS) reacted with aromatic diamines for its incorporation into an epoxy network, to generate an organic–inorganic hybrid material containing POSS, a polyhedral oligomeric silsesquioxane (glycidylisobutyl–POSS) was reacted with the diamines 4,4′‐methylenebis(2,6‐diethylaniline) (MDEA), 4,4′‐diaminediphenylmethane (DDM), and 4,4′‐(1,3‐phenylenediisopropylidene)bisaniline (BSA), at 160°C and different times, in a proportion rich in amines. The distribution of species in the reaction was followed by gel permeation chromatography (GPC). From the experimental data obtained the selected precursor was POSS/BSA reacted at 160°C for 20 or 30 min, to ensure that all the POSS was reacted, that there was a maximum of the monosubstituted amines, and that there was no degradation. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1576–1583, 2004