Abstract
| Original language | English |
|---|---|
| Pages (from-to) | 941-965 |
| Number of pages | 24 |
| Journal | Journal of Macromolecular Science B: Physics |
| Volume | 44 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Jan 2005 |
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Keywords
- rheology
- hydrogen bonding
- acrylic copolymers
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Synthesis and physical property evaluation of a series of poly(N-2-pyridylmethyl methacrylamide-co-methyl methacrylate)s and related polymers. / Stolbova, M.; Hudson, N.E.; Pethrick, R.A.; Sherrington, D.C.; Slark, A.
In: Journal of Macromolecular Science B: Physics, Vol. 44, No. 6, 01.2005, p. 941-965.Research output: Contribution to journal › Article
TY - JOUR
T1 - Synthesis and physical property evaluation of a series of poly(N-2-pyridylmethyl methacrylamide-co-methyl methacrylate)s and related polymers
AU - Stolbova, M.
AU - Hudson, N.E.
AU - Pethrick, R.A.
AU - Sherrington, D.C.
AU - Slark, A.
PY - 2005/1
Y1 - 2005/1
N2 - The synthesis and physical properties of a series of poly(N-2-pyridylmethyl methacrylamide-co-methyl methacrylate)s and related copolymers is presented. High yields of the copolymers were obtained starting from copolymers of methacryloyl chloride with methyl methacrylate, which reacted almost quantitatively with 2-pyridylmethylamine or a related amine, to give copolymers that are capable of interpolymer chain hydrogen bonding. Copolymers of (N-2-pyridylmethylmethacrylamide) (PyMeMA) were obtained in high yield and investigated in detail. The variation in the molar mass data obtained using different methods was interpreted as being a consequence of solvent-induced aggregation effects. Examination of the solution properties indicated that the polymers are indeed able to form transient aggregates through hydrogen bonding interactions that, when subject to shear, separate into smaller aggregates or individual polymer chains. These hydrogen bond interactions are also evident in the solid state physical properties as observed in variation of the glass transition temperature, but to a lesser extent than they are in the dynamic mechanical analysis. Adhesion measurements once more indicate the potential of these materials to exhibit enhanced properties as a consequence of hydrogen bonding interactions.
AB - The synthesis and physical properties of a series of poly(N-2-pyridylmethyl methacrylamide-co-methyl methacrylate)s and related copolymers is presented. High yields of the copolymers were obtained starting from copolymers of methacryloyl chloride with methyl methacrylate, which reacted almost quantitatively with 2-pyridylmethylamine or a related amine, to give copolymers that are capable of interpolymer chain hydrogen bonding. Copolymers of (N-2-pyridylmethylmethacrylamide) (PyMeMA) were obtained in high yield and investigated in detail. The variation in the molar mass data obtained using different methods was interpreted as being a consequence of solvent-induced aggregation effects. Examination of the solution properties indicated that the polymers are indeed able to form transient aggregates through hydrogen bonding interactions that, when subject to shear, separate into smaller aggregates or individual polymer chains. These hydrogen bond interactions are also evident in the solid state physical properties as observed in variation of the glass transition temperature, but to a lesser extent than they are in the dynamic mechanical analysis. Adhesion measurements once more indicate the potential of these materials to exhibit enhanced properties as a consequence of hydrogen bonding interactions.
KW - rheology
KW - hydrogen bonding
KW - acrylic copolymers
UR - http://dx.doi.org/10.1080/00222340500323680
U2 - 10.1080/00222340500323680
DO - 10.1080/00222340500323680
M3 - Article
VL - 44
SP - 941
EP - 965
JO - Journal of Macromolecular Science B: Physics
JF - Journal of Macromolecular Science B: Physics
SN - 0022-2348
IS - 6
ER -