TY - JOUR
T1 - Synthesis, characterization and self-assembly of well-defined linear heptablock quaterpolymers
AU - Ntaras, Christos
AU - Polymeropoulos, George
AU - Zapsas, Georgios
AU - Ntetsikas, Konstantinos
AU - Liontos, George
AU - Karanastasis, Apostolos
AU - Moschovas, Dimitrios
AU - Rangou, Sofia
AU - Stewart-Sloan, Charlotte
AU - Hadjichristidis, Nikos
AU - Thomas, Edwin L.
AU - Avgeropoulos, Apostolos
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2016/5/17
Y1 - 2016/5/17
N2 - Two well-defined heptablock quaterpolymers of the ABCDCBA type [Α: polystyrene (PS), B: poly(butadiene) with ∼90% 1,4-microstructure (PB1,4), C: poly(isoprene) with ∼55% 3,4-microstructure (PI3,4) and D: poly(dimethylsiloxane) (PDMS)] were synthesized by combining anionic polymerization high vacuum techniques and hydrosilylation/chlorosilane chemistry. All intermediates and final products were characterized by size exclusion chromatography, membrane osmometry, and proton nuclear magnetic resonance spectroscopy. Fourier transform infrared spectroscopy was used to further verify the chemical modification reaction of the difunctional PDMS. The self-assembly in bulk of these novel heptablock quarterpolymers, studied by transmission electron microscopy and small angle X-ray scattering, revealed 3-phase 4-layer alternating lamellae morphology of PS, PB1,4, and mixed PI3,4/PDMS domains. Differential scanning calorimetry was used to further confirm the miscibility of PI3,4 and PDMS blocks. It is the first time that PDMS is the central segment in such multiblock polymers (≥3 chemically different blocks). © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 1443–1449. © 2016 Wiley Periodicals, Inc.
AB - Two well-defined heptablock quaterpolymers of the ABCDCBA type [Α: polystyrene (PS), B: poly(butadiene) with ∼90% 1,4-microstructure (PB1,4), C: poly(isoprene) with ∼55% 3,4-microstructure (PI3,4) and D: poly(dimethylsiloxane) (PDMS)] were synthesized by combining anionic polymerization high vacuum techniques and hydrosilylation/chlorosilane chemistry. All intermediates and final products were characterized by size exclusion chromatography, membrane osmometry, and proton nuclear magnetic resonance spectroscopy. Fourier transform infrared spectroscopy was used to further verify the chemical modification reaction of the difunctional PDMS. The self-assembly in bulk of these novel heptablock quarterpolymers, studied by transmission electron microscopy and small angle X-ray scattering, revealed 3-phase 4-layer alternating lamellae morphology of PS, PB1,4, and mixed PI3,4/PDMS domains. Differential scanning calorimetry was used to further confirm the miscibility of PI3,4 and PDMS blocks. It is the first time that PDMS is the central segment in such multiblock polymers (≥3 chemically different blocks). © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 1443–1449. © 2016 Wiley Periodicals, Inc.
UR - http://hdl.handle.net/10754/621713
UR - https://onlinelibrary.wiley.com/doi/abs/10.1002/polb.24058
UR - http://www.scopus.com/inward/record.url?scp=84969964503&partnerID=8YFLogxK
U2 - 10.1002/polb.24058
DO - 10.1002/polb.24058
M3 - Article
SN - 0887-6266
VL - 54
SP - 1443
EP - 1449
JO - Journal of Polymer Science Part B: Polymer Physics
JF - Journal of Polymer Science Part B: Polymer Physics
IS - 15
ER -