TY - JOUR
T1 - Synthesis and characterization of telechelic phosphine oxide polyesters and cobalt(II) chloride complexes
AU - Lin, Qin
AU - Unal, Serkan
AU - Fornof, Ann R.
AU - Armentrout, R. Scott
AU - Long, Timothy Edward
PY - 2006/5/17
Y1 - 2006/5/17
N2 - A monofunctional phosphine oxide containing endcapping reagent, 4-carboxyphenyl biphenyl phosphine oxide, was synthesized for the preparation of telechelic polyester oligomers. The chemical structure of the endcapping reagent was verified using NMR spectroscopy, mass spectroscopy, and elemental analysis. Phosphine oxide telechelic polyesters were prepared for the first time via copolymerization of a low molar mass polyester oligomer precursor and the phosphine oxide endcapping reagent in the melt state. The quantitative incorporation of telechelic phosphine oxide functionality was confirmed using 1H NMR spectroscopy and elemental analysis. The corresponding complexes of phosphine oxide terminated polyesters and cobalt(II) chloride were prepared via charging the cobalt salt at the onset of melt polymerization. 31P {1H} NMR spectroscopy, FT-IR spectroscopy, and UV-vis spectroscopy indicated that the cobalt(II) ion preferentially coordinated with the phosphine oxide end groups. The complexes exhibited higher melt viscosity than their salt-free analogues due to the formation of coordinated polymers. The presence of the telechelic phosphine oxide end groups also aided in the homogeneous dispersion of the cobalt salt in a poly(ethylene terephthalate) (PET) matrix.
AB - A monofunctional phosphine oxide containing endcapping reagent, 4-carboxyphenyl biphenyl phosphine oxide, was synthesized for the preparation of telechelic polyester oligomers. The chemical structure of the endcapping reagent was verified using NMR spectroscopy, mass spectroscopy, and elemental analysis. Phosphine oxide telechelic polyesters were prepared for the first time via copolymerization of a low molar mass polyester oligomer precursor and the phosphine oxide endcapping reagent in the melt state. The quantitative incorporation of telechelic phosphine oxide functionality was confirmed using 1H NMR spectroscopy and elemental analysis. The corresponding complexes of phosphine oxide terminated polyesters and cobalt(II) chloride were prepared via charging the cobalt salt at the onset of melt polymerization. 31P {1H} NMR spectroscopy, FT-IR spectroscopy, and UV-vis spectroscopy indicated that the cobalt(II) ion preferentially coordinated with the phosphine oxide end groups. The complexes exhibited higher melt viscosity than their salt-free analogues due to the formation of coordinated polymers. The presence of the telechelic phosphine oxide end groups also aided in the homogeneous dispersion of the cobalt salt in a poly(ethylene terephthalate) (PET) matrix.
KW - Macroligands
KW - Phosphine oxide
KW - Polyesters
UR - http://www.scopus.com/inward/record.url?scp=33646781967&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33646781967&partnerID=8YFLogxK
U2 - 10.1016/j.polymer.2006.02.028
DO - 10.1016/j.polymer.2006.02.028
M3 - Article
AN - SCOPUS:33646781967
SN - 0032-3861
VL - 47
SP - 4085
EP - 4093
JO - Polymer (United Kingdom)
JF - Polymer (United Kingdom)
IS - 11
ER -