TY - JOUR
T1 - Ionene segmented block copolymers containing imidazolium cations
T2 - Structure-property relationships as a function of hard segment content
AU - Williams, Sharlene R.
AU - Salas-de la Cruz, David
AU - Winey, Karen I.
AU - Long, Timothy E.
N1 - Funding Information:
This material is based upon work supported in part by the Macromolecular Interfaces with Life Sciences (MILES) Integrative Graduate Education and Research Traineeship (IGERT) of the National Science Foundation under agreement no. DGE-0333378. This material is based upon work supported in part by the U.S. Army Research Office under grant number W911NF-07-1-0452 Ionic Liquids in Electro-Active Devices (ILEAD) MURI. This material is based upon work supported in part by the Kimberly Clark Corporation.
PY - 2010/3/11
Y1 - 2010/3/11
N2 - Imidazolium ionene segmented block copolymers were synthesized from 1,1′-(1,4-butanediyl)bis(imidazole) and 1,12-dibromododecane hard segments and 2000 g/mol PTMO dibromide soft segments. The polymeric structures were confirmed using 1H NMR spectroscopy, and resonances associated with methylene spacers from 1,12-dibromododecane became more apparent as the hard segment content increased. TGA revealed thermal stabilities ≥250 °C for all imidazolium ionene segmented block copolymers. These ionene segmented block copolymers containing imidazolium cations showed evidence of microphase separation when the hard segment was 6-38 wt%. The thermal transitions found by DSC and DMA analysis found that the Tg and Tm of the PTMO segments were comparable to PTMO polymers, namely approximately -80 °C and 22 °C, respectively. In the absence of PTMO soft segments the Tg increased to 27 °C The crystallinity of the PTMO segments was further evidence of microphase separation and was particularly evident at 6, 9 and 20 wt% hard segment, as indicated in X-ray scattering. The periodicity of the microphase separation was well-defined at 20 and 38 wt% hard segment and found to be approximately 10.5 and 13.0 nm, respectively, for these ionenes wherein the PTMO soft segment is 2000 g/mol. Finally, the 38 and 100 wt% hard segment ionenes exhibited scattering from correlations within the hard segment on a length scale of approximately 2-2.3 nm. These new materials present structure on a variety of length scales and thereby provide various routes to controlling mechanical and transport properties.
AB - Imidazolium ionene segmented block copolymers were synthesized from 1,1′-(1,4-butanediyl)bis(imidazole) and 1,12-dibromododecane hard segments and 2000 g/mol PTMO dibromide soft segments. The polymeric structures were confirmed using 1H NMR spectroscopy, and resonances associated with methylene spacers from 1,12-dibromododecane became more apparent as the hard segment content increased. TGA revealed thermal stabilities ≥250 °C for all imidazolium ionene segmented block copolymers. These ionene segmented block copolymers containing imidazolium cations showed evidence of microphase separation when the hard segment was 6-38 wt%. The thermal transitions found by DSC and DMA analysis found that the Tg and Tm of the PTMO segments were comparable to PTMO polymers, namely approximately -80 °C and 22 °C, respectively. In the absence of PTMO soft segments the Tg increased to 27 °C The crystallinity of the PTMO segments was further evidence of microphase separation and was particularly evident at 6, 9 and 20 wt% hard segment, as indicated in X-ray scattering. The periodicity of the microphase separation was well-defined at 20 and 38 wt% hard segment and found to be approximately 10.5 and 13.0 nm, respectively, for these ionenes wherein the PTMO soft segment is 2000 g/mol. Finally, the 38 and 100 wt% hard segment ionenes exhibited scattering from correlations within the hard segment on a length scale of approximately 2-2.3 nm. These new materials present structure on a variety of length scales and thereby provide various routes to controlling mechanical and transport properties.
KW - Imidazolium
KW - Ionenes
KW - X-ray scattering
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U2 - 10.1016/j.polymer.2009.06.051
DO - 10.1016/j.polymer.2009.06.051
M3 - Article
AN - SCOPUS:77649235557
SN - 0032-3861
VL - 51
SP - 1252
EP - 1257
JO - Polymer (United Kingdom)
JF - Polymer (United Kingdom)
IS - 6
ER -