Silicon-containing poly(esters) with halogenated bulky side groups. Synthesis, characterization and thermal studies
Poly(esters) ( PEs ) derived from diacids containing bulky side groups, which have an halogenated (Cl, Br) imide ring, an aminoacidic residue (glycine, l -alanine, l -valine) and an amide group were obtained with a silicon-containing diphenol. Also PEs without the aminoacidic residue were obtained....
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Published in | RSC advances Vol. 5; no. 61; pp. 49132 - 49142 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2015
|
Subjects | |
Online Access | Get full text |
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Summary: | Poly(esters) (
PEs
) derived from diacids containing bulky side groups, which have an halogenated (Cl, Br) imide ring, an aminoacidic residue (glycine,
l
-alanine,
l
-valine) and an amide group were obtained with a silicon-containing diphenol. Also
PEs
without the aminoacidic residue were obtained.
PEs
were characterized by IR and NMR spectroscopy, and the results were in agreement with the proposed structures.
PEs
were obtained with good yields and moderate or high
η
inh
values.
PEs
were soluble in aprotic polar solvents and were swollen in other solvents like
m
-cresol and THF. The
T
g
values were determined and it was possible to see a tendency in the sense that when the size of the atom (Cl, Br) bonded to the imidic ring is increased, the
T
g
values decreased, also for those
PEs
obtained without the aminoacidic residue. The thermal decomposition temperatures showed that only two
PEs
can be considered as thermostable, considering TDT values above 400 °C at 10% of weight lost. The other
PEs
showed good thermal stability, showing in general a decrease of the TDT values when the volume of the side group, is increased.
PEs
showed UV-vis transparency at 400 nm lower than 20%, but between 500 and 600 nm, showed 80% transparency.
PEs
containing halogen atoms showed flame retardancy in a simple essay, with respect to
PEs
without halogen atoms in which the combustion was complete.
Synthesis of poly(esters)
X-PE-(a-c)
and poly(esters)
X-PE
. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c5ra06896g |