Cyclic olefin polymers（COPs） with high glass transition temperature, high transparency（higher than 80%） in the visible light range, excellent thermal stability and outstanding mechanical properties have been synth...Cyclic olefin polymers（COPs） with high glass transition temperature, high transparency（higher than 80%） in the visible light range, excellent thermal stability and outstanding mechanical properties have been synthesized by effective ring opening metathesis polymerization（ROMP） of exo-1,4,4 a,9,9 a,10-hexahydro-9,10（1′,2′）-benzeno-l,4-methanoanthracene（HBM） and dicyclopentadiene（DCPD） or norbornene（NBE） using WCl6/i-Bu3Al/ethanol/1-hexene catalyst system, followed by hydrogenation of double bonds. 1-Hexene acted as a molecular weight controller in the polymerization reaction, tuning the number-average molecular weight（Mn） of P-HBM from 5.8 × 10^4 to 41.1 × 10^4. The monomer composition and thermal properties of the copolymers were characterized by nuclear magnetic resonance（NMR）, differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA）. The saturated polymers exhibited high decomposition temperatures（Td） around 340 ℃ and glass transition temperatures（Tg） in the range from 117.5 ℃ to 219.7 ℃. What is more, tensile tests indicated that the mechanical properties of the COPs could be effectively tuned in a wide range by introducing varying amount of small cyclic olefin such as DCPD or NBE.展开更多
(Imido)vanadium(V)-alkylidene complexes of type V(CHSiMe3)(NR)(OR?)(PMe3)2 [R = Ad, C6H5, 2,6-Me2C6H3, 2,6-Cl2C6H3;R?= 2,6-Me2C6H3, 2,6-i Pr2C6H3, 2,6-F2C6H3, C6F5, C6Cl5] exhibited from moderate to remarkable catalyt...(Imido)vanadium(V)-alkylidene complexes of type V(CHSiMe3)(NR)(OR?)(PMe3)2 [R = Ad, C6H5, 2,6-Me2C6H3, 2,6-Cl2C6H3;R?= 2,6-Me2C6H3, 2,6-i Pr2C6H3, 2,6-F2C6H3, C6F5, C6Cl5] exhibited from moderate to remarkable catalytic activities for ringopening metathesis polymerization(ROMP) of norbornene(NBE). The catalytic activities were affected by the ligand substituents, and V(CHSiMe3)(N-2,6-Cl2C6H3)(OC6X5)(PMe3)2(X = F, Cl) demonstrated the exceptionally high catalytic activities for ROMP of NBE.The complexes polymerized cycloheptene(CHPE) and cis-cyclooctene(COE), and ROMP of COE by the OC6 Cl5 analogue proceeded in a living manner even at 80℃, and the activity increased with increasing the temperature up to 120 ℃. Highly active catalysts for ROMP of cyclic olefins(NBE, cyclopentene, and CHPE) can be generated in situ by premixing isolated V(CHSiMe3)(NC6F5)(O-2,6-iPr2C6H3)(PMe3)2 with 1.0 equiv. of C6F5OH or C6Cl5OH via immediate phenoxy exchange;the activity was affected by the kind of phenol added [TOF in the ROMPs of NBE: 4.62 × 10^4 min^–1(upon addition of C6F5OH) versus 37.3 min^–1(none)].展开更多
基金financial support by the National Natural Science Foundation of China(Nos.21234006 and U1510124)
文摘Cyclic olefin polymers（COPs） with high glass transition temperature, high transparency（higher than 80%） in the visible light range, excellent thermal stability and outstanding mechanical properties have been synthesized by effective ring opening metathesis polymerization（ROMP） of exo-1,4,4 a,9,9 a,10-hexahydro-9,10（1′,2′）-benzeno-l,4-methanoanthracene（HBM） and dicyclopentadiene（DCPD） or norbornene（NBE） using WCl6/i-Bu3Al/ethanol/1-hexene catalyst system, followed by hydrogenation of double bonds. 1-Hexene acted as a molecular weight controller in the polymerization reaction, tuning the number-average molecular weight（Mn） of P-HBM from 5.8 × 10^4 to 41.1 × 10^4. The monomer composition and thermal properties of the copolymers were characterized by nuclear magnetic resonance（NMR）, differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA）. The saturated polymers exhibited high decomposition temperatures（Td） around 340 ℃ and glass transition temperatures（Tg） in the range from 117.5 ℃ to 219.7 ℃. What is more, tensile tests indicated that the mechanical properties of the COPs could be effectively tuned in a wide range by introducing varying amount of small cyclic olefin such as DCPD or NBE.
基金partly supported by Grant-in-Aid for Scientific Research on Innovative Areas ("3D Active-Site Science", No. 26105003) from The Ministry of Education, Culture, Sports, Science and Technology (MEXT), JapanGrant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (JSPS, Nos. 15H03812, 18H01982)the Tokyo Metropolitan government (Tokyo Human Resources Fund for City Diplomacy) for pre-doctoral fellowship
文摘(Imido)vanadium(V)-alkylidene complexes of type V(CHSiMe3)(NR)(OR?)(PMe3)2 [R = Ad, C6H5, 2,6-Me2C6H3, 2,6-Cl2C6H3;R?= 2,6-Me2C6H3, 2,6-i Pr2C6H3, 2,6-F2C6H3, C6F5, C6Cl5] exhibited from moderate to remarkable catalytic activities for ringopening metathesis polymerization(ROMP) of norbornene(NBE). The catalytic activities were affected by the ligand substituents, and V(CHSiMe3)(N-2,6-Cl2C6H3)(OC6X5)(PMe3)2(X = F, Cl) demonstrated the exceptionally high catalytic activities for ROMP of NBE.The complexes polymerized cycloheptene(CHPE) and cis-cyclooctene(COE), and ROMP of COE by the OC6 Cl5 analogue proceeded in a living manner even at 80℃, and the activity increased with increasing the temperature up to 120 ℃. Highly active catalysts for ROMP of cyclic olefins(NBE, cyclopentene, and CHPE) can be generated in situ by premixing isolated V(CHSiMe3)(NC6F5)(O-2,6-iPr2C6H3)(PMe3)2 with 1.0 equiv. of C6F5OH or C6Cl5OH via immediate phenoxy exchange;the activity was affected by the kind of phenol added [TOF in the ROMPs of NBE: 4.62 × 10^4 min^–1(upon addition of C6F5OH) versus 37.3 min^–1(none)].
