The synthesis of rod-coil diblock copolymers was achieved for the first time by TEMPO-mediated 'living' free radical polymerization of styrene and 2,5-bis [(4-methoxyphenyl)oxycarbonyl] styrene(MPCS). The blo...The synthesis of rod-coil diblock copolymers was achieved for the first time by TEMPO-mediated 'living' free radical polymerization of styrene and 2,5-bis [(4-methoxyphenyl)oxycarbonyl] styrene(MPCS). The block architecture of the two diblock copolymers thus prepared, MPCS-b-St(5400/2400) and MPCS-b-St(10800/8700), was confirmed by GPC, DSC studies and the formation of multimolecular micelles. (Author abstract) 10 Refs.展开更多
Poly{2,5-bis[(p-methoxyphenyl)oxycarbonyl]styrene}was successfully synthesized.This new polymer has a structure characteristic of mesogen-jacketed liquid cyrstalline polymers(MJLCPs)and does form a liquid crystal phas...Poly{2,5-bis[(p-methoxyphenyl)oxycarbonyl]styrene}was successfully synthesized.This new polymer has a structure characteristic of mesogen-jacketed liquid cyrstalline polymers(MJLCPs)and does form a liquid crystal phase above its glass transition.It thus became the starting member of a new series of MJLCPs.The synthesis of the polymer as well as the liquid crystalline properties of the polymer and its monomer was discussed.A brief comparison of the new monomer and polymer with some previously reported counterparts was also included.展开更多
The first TEMPO-mediated 'living' free radical polymerization of liquid crystalline monomer, 2, 5-bis[(4-methoxyphenyl)oxycarbonyl]styrene (MPCS), was carried out at 130 degrees C with BPO as an initiator. The...The first TEMPO-mediated 'living' free radical polymerization of liquid crystalline monomer, 2, 5-bis[(4-methoxyphenyl)oxycarbonyl]styrene (MPCS), was carried out at 130 degrees C with BPO as an initiator. The molecular weight of the polymer can be varied from rather low values to high values while maintaining narrow polydispersity. It was observed that the polymerization of MPCS proceeded much faster than that of styrene. A tentative explanation for this fast polymerization was suggested.展开更多
Monofilament type of polyaromatic amide(PA)and carbon nanotube(CNT)composite fibers is presented.A concept of a lyotropic liquid crystal(LLC)constructed via a spontaneous self-assembly is introduced to mitigate the ex...Monofilament type of polyaromatic amide(PA)and carbon nanotube(CNT)composite fibers is presented.A concept of a lyotropic liquid crystal(LLC)constructed via a spontaneous self-assembly is introduced to mitigate the extremely low com-patibility between PA and CNT.These approaches provide an effective co-processing route of PA and CNT simultaneously to fabricate the uniform,continuous,and reliable composite fibers through a wet-spinning.Interestingly,the addition of a small amount PA into the dope solution of CNT governs the LLC mesophase not only in a spinneret stage but also in a coagulant region.Thus,the developed PA/CNT composite fibers have the high uniaxial orientational order and the close interfacial packing compared to the pure CNT fibers.The PA/CNT composite fibers achieve the outstanding tensile strength,electrical conductivity,and electrochemical response,while maintaining a lightweight.They also exhibit the chemical,mechanical,and thermal robustness.All of these advantages can make flexible,sewable,and washable PA/CNT composite fibers ideal nanocomposite materials for use in next-generation information and energy transporting system by replacing conventional metal electrical conductors.展开更多
A series of poly{2,5-bis[(4-butoxyphenyl)-oxycarbonyl]styrenes}(PBPCS)with low mo-lecular weight distribution was synthesized by atom transfer radical polymerization(ATRP).The me-somorphic properties were investigated...A series of poly{2,5-bis[(4-butoxyphenyl)-oxycarbonyl]styrenes}(PBPCS)with low mo-lecular weight distribution was synthesized by atom transfer radical polymerization(ATRP).The me-somorphic properties were investigated by differential scanning calorimetry(DSC),polarizing optical microscopy(POM)and rheometer.PBPCS showed the phase transition from isotropic into liquid crystal(LC)phase,and the LC phase formed at high temperature and disappeared in the subsequent cooling procedure.Using the WAXD fiber pattern,the phase structure of the PBPCS at higher tem-perature showed hexagonal columnar nematic phase.Experimental results demonstrated that the driving force of the entropy is an important factor during the unusual LC phase formation of PBPCS.展开更多
基金This project was supported by the Foundation of Peking University for Young Scientist and the National Natural Science Foundation of China.
文摘The synthesis of rod-coil diblock copolymers was achieved for the first time by TEMPO-mediated 'living' free radical polymerization of styrene and 2,5-bis [(4-methoxyphenyl)oxycarbonyl] styrene(MPCS). The block architecture of the two diblock copolymers thus prepared, MPCS-b-St(5400/2400) and MPCS-b-St(10800/8700), was confirmed by GPC, DSC studies and the formation of multimolecular micelles. (Author abstract) 10 Refs.
基金This work is supported by the National Natural Science Foundation of China.
文摘Poly{2,5-bis[(p-methoxyphenyl)oxycarbonyl]styrene}was successfully synthesized.This new polymer has a structure characteristic of mesogen-jacketed liquid cyrstalline polymers(MJLCPs)and does form a liquid crystal phase above its glass transition.It thus became the starting member of a new series of MJLCPs.The synthesis of the polymer as well as the liquid crystalline properties of the polymer and its monomer was discussed.A brief comparison of the new monomer and polymer with some previously reported counterparts was also included.
基金This work was supported by the Foundation of Peking University for Young Scientist and the National Natural Science Foundation of China(Grant No.29874003).
文摘The first TEMPO-mediated 'living' free radical polymerization of liquid crystalline monomer, 2, 5-bis[(4-methoxyphenyl)oxycarbonyl]styrene (MPCS), was carried out at 130 degrees C with BPO as an initiator. The molecular weight of the polymer can be varied from rather low values to high values while maintaining narrow polydispersity. It was observed that the polymerization of MPCS proceeded much faster than that of styrene. A tentative explanation for this fast polymerization was suggested.
基金supported by Korea Institute of Science and Technology(KIST)Open Research Program(ORP)and K-Lab Program,and grants from Mid-Career Researcher Program(2021R1A2C2009423)Korea Government MSIT(2021R1R1R1004226)Korea Research Institute for defense Technology planning and advancement(DAPA KRIT-CT-21-014).
文摘Monofilament type of polyaromatic amide(PA)and carbon nanotube(CNT)composite fibers is presented.A concept of a lyotropic liquid crystal(LLC)constructed via a spontaneous self-assembly is introduced to mitigate the extremely low com-patibility between PA and CNT.These approaches provide an effective co-processing route of PA and CNT simultaneously to fabricate the uniform,continuous,and reliable composite fibers through a wet-spinning.Interestingly,the addition of a small amount PA into the dope solution of CNT governs the LLC mesophase not only in a spinneret stage but also in a coagulant region.Thus,the developed PA/CNT composite fibers have the high uniaxial orientational order and the close interfacial packing compared to the pure CNT fibers.The PA/CNT composite fibers achieve the outstanding tensile strength,electrical conductivity,and electrochemical response,while maintaining a lightweight.They also exhibit the chemical,mechanical,and thermal robustness.All of these advantages can make flexible,sewable,and washable PA/CNT composite fibers ideal nanocomposite materials for use in next-generation information and energy transporting system by replacing conventional metal electrical conductors.
基金This work was supported by the National Natural Science Foundation of China(Grant No.20134010)the Ministry of Education of China(Key Project No.104005).
文摘A series of poly{2,5-bis[(4-butoxyphenyl)-oxycarbonyl]styrenes}(PBPCS)with low mo-lecular weight distribution was synthesized by atom transfer radical polymerization(ATRP).The me-somorphic properties were investigated by differential scanning calorimetry(DSC),polarizing optical microscopy(POM)and rheometer.PBPCS showed the phase transition from isotropic into liquid crystal(LC)phase,and the LC phase formed at high temperature and disappeared in the subsequent cooling procedure.Using the WAXD fiber pattern,the phase structure of the PBPCS at higher tem-perature showed hexagonal columnar nematic phase.Experimental results demonstrated that the driving force of the entropy is an important factor during the unusual LC phase formation of PBPCS.
