Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF
Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in si...
Ausführliche Beschreibung
Autor*in: |
Guo, An-ru [verfasserIn] Yang, Fan [verfasserIn] Yu, Rui [verfasserIn] Wu, Yi-xian [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2014 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Chinese Journal of Polymer Science - Chinese Chemical Society and Institute of Chemistry, CAS, 2009, 33(2014), 1 vom: 25. Nov., Seite 23-35 |
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Übergeordnetes Werk: |
volume:33 ; year:2014 ; number:1 ; day:25 ; month:11 ; pages:23-35 |
Links: |
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DOI / URN: |
10.1007/s10118-015-1571-9 |
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Katalog-ID: |
SPR009227458 |
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245 | 1 | 0 | |a Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF |
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520 | |a Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. | ||
650 | 4 | |a Cationic ring-opening polymerization |7 (dpeaa)DE-He213 | |
650 | 4 | |a Living polymerization |7 (dpeaa)DE-He213 | |
650 | 4 | |a Tetrahydrofuran |7 (dpeaa)DE-He213 | |
650 | 4 | |a Equilibrium |7 (dpeaa)DE-He213 | |
650 | 4 | |a Kinetics |7 (dpeaa)DE-He213 | |
700 | 1 | |a Yang, Fan |e verfasserin |4 aut | |
700 | 1 | |a Yu, Rui |e verfasserin |4 aut | |
700 | 1 | |a Wu, Yi-xian |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Chinese Journal of Polymer Science |d Chinese Chemical Society and Institute of Chemistry, CAS, 2009 |g 33(2014), 1 vom: 25. Nov., Seite 23-35 |w (DE-627)356885143 |w (DE-600)2093161-X |x 1439-6203 |7 nnns |
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2014 |
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2014 |
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10.1007/s10118-015-1571-9 doi (DE-627)SPR009227458 (SPR)s10118-015-1571-9-e DE-627 ger DE-627 rakwb eng Guo, An-ru verfasserin aut Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. Cationic ring-opening polymerization (dpeaa)DE-He213 Living polymerization (dpeaa)DE-He213 Tetrahydrofuran (dpeaa)DE-He213 Equilibrium (dpeaa)DE-He213 Kinetics (dpeaa)DE-He213 Yang, Fan verfasserin aut Yu, Rui verfasserin aut Wu, Yi-xian verfasserin aut Enthalten in Chinese Journal of Polymer Science Chinese Chemical Society and Institute of Chemistry, CAS, 2009 33(2014), 1 vom: 25. Nov., Seite 23-35 (DE-627)356885143 (DE-600)2093161-X 1439-6203 nnns volume:33 year:2014 number:1 day:25 month:11 pages:23-35 https://dx.doi.org/10.1007/s10118-015-1571-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 33 2014 1 25 11 23-35 |
spelling |
10.1007/s10118-015-1571-9 doi (DE-627)SPR009227458 (SPR)s10118-015-1571-9-e DE-627 ger DE-627 rakwb eng Guo, An-ru verfasserin aut Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. Cationic ring-opening polymerization (dpeaa)DE-He213 Living polymerization (dpeaa)DE-He213 Tetrahydrofuran (dpeaa)DE-He213 Equilibrium (dpeaa)DE-He213 Kinetics (dpeaa)DE-He213 Yang, Fan verfasserin aut Yu, Rui verfasserin aut Wu, Yi-xian verfasserin aut Enthalten in Chinese Journal of Polymer Science Chinese Chemical Society and Institute of Chemistry, CAS, 2009 33(2014), 1 vom: 25. Nov., Seite 23-35 (DE-627)356885143 (DE-600)2093161-X 1439-6203 nnns volume:33 year:2014 number:1 day:25 month:11 pages:23-35 https://dx.doi.org/10.1007/s10118-015-1571-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 33 2014 1 25 11 23-35 |
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10.1007/s10118-015-1571-9 doi (DE-627)SPR009227458 (SPR)s10118-015-1571-9-e DE-627 ger DE-627 rakwb eng Guo, An-ru verfasserin aut Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. Cationic ring-opening polymerization (dpeaa)DE-He213 Living polymerization (dpeaa)DE-He213 Tetrahydrofuran (dpeaa)DE-He213 Equilibrium (dpeaa)DE-He213 Kinetics (dpeaa)DE-He213 Yang, Fan verfasserin aut Yu, Rui verfasserin aut Wu, Yi-xian verfasserin aut Enthalten in Chinese Journal of Polymer Science Chinese Chemical Society and Institute of Chemistry, CAS, 2009 33(2014), 1 vom: 25. Nov., Seite 23-35 (DE-627)356885143 (DE-600)2093161-X 1439-6203 nnns volume:33 year:2014 number:1 day:25 month:11 pages:23-35 https://dx.doi.org/10.1007/s10118-015-1571-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 33 2014 1 25 11 23-35 |
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10.1007/s10118-015-1571-9 doi (DE-627)SPR009227458 (SPR)s10118-015-1571-9-e DE-627 ger DE-627 rakwb eng Guo, An-ru verfasserin aut Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. Cationic ring-opening polymerization (dpeaa)DE-He213 Living polymerization (dpeaa)DE-He213 Tetrahydrofuran (dpeaa)DE-He213 Equilibrium (dpeaa)DE-He213 Kinetics (dpeaa)DE-He213 Yang, Fan verfasserin aut Yu, Rui verfasserin aut Wu, Yi-xian verfasserin aut Enthalten in Chinese Journal of Polymer Science Chinese Chemical Society and Institute of Chemistry, CAS, 2009 33(2014), 1 vom: 25. Nov., Seite 23-35 (DE-627)356885143 (DE-600)2093161-X 1439-6203 nnns volume:33 year:2014 number:1 day:25 month:11 pages:23-35 https://dx.doi.org/10.1007/s10118-015-1571-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 33 2014 1 25 11 23-35 |
allfieldsSound |
10.1007/s10118-015-1571-9 doi (DE-627)SPR009227458 (SPR)s10118-015-1571-9-e DE-627 ger DE-627 rakwb eng Guo, An-ru verfasserin aut Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. Cationic ring-opening polymerization (dpeaa)DE-He213 Living polymerization (dpeaa)DE-He213 Tetrahydrofuran (dpeaa)DE-He213 Equilibrium (dpeaa)DE-He213 Kinetics (dpeaa)DE-He213 Yang, Fan verfasserin aut Yu, Rui verfasserin aut Wu, Yi-xian verfasserin aut Enthalten in Chinese Journal of Polymer Science Chinese Chemical Society and Institute of Chemistry, CAS, 2009 33(2014), 1 vom: 25. Nov., Seite 23-35 (DE-627)356885143 (DE-600)2093161-X 1439-6203 nnns volume:33 year:2014 number:1 day:25 month:11 pages:23-35 https://dx.doi.org/10.1007/s10118-015-1571-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 33 2014 1 25 11 23-35 |
language |
English |
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Enthalten in Chinese Journal of Polymer Science 33(2014), 1 vom: 25. Nov., Seite 23-35 volume:33 year:2014 number:1 day:25 month:11 pages:23-35 |
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Enthalten in Chinese Journal of Polymer Science 33(2014), 1 vom: 25. Nov., Seite 23-35 volume:33 year:2014 number:1 day:25 month:11 pages:23-35 |
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topic_facet |
Cationic ring-opening polymerization Living polymerization Tetrahydrofuran Equilibrium Kinetics |
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Chinese Journal of Polymer Science |
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Guo, An-ru @@aut@@ Yang, Fan @@aut@@ Yu, Rui @@aut@@ Wu, Yi-xian @@aut@@ |
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2014-11-25T00:00:00Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR009227458</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20201124063837.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201005s2014 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10118-015-1571-9</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR009227458</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s10118-015-1571-9-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Guo, An-ru</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2014</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cationic ring-opening polymerization</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Living polymerization</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Tetrahydrofuran</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Equilibrium</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Kinetics</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yang, Fan</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yu, Rui</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wu, Yi-xian</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Chinese Journal of Polymer Science</subfield><subfield code="d">Chinese Chemical Society and Institute of Chemistry, CAS, 2009</subfield><subfield code="g">33(2014), 1 vom: 25. Nov., Seite 23-35</subfield><subfield code="w">(DE-627)356885143</subfield><subfield code="w">(DE-600)2093161-X</subfield><subfield code="x">1439-6203</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:33</subfield><subfield code="g">year:2014</subfield><subfield code="g">number:1</subfield><subfield code="g">day:25</subfield><subfield code="g">month:11</subfield><subfield code="g">pages:23-35</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://dx.doi.org/10.1007/s10118-015-1571-9</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_SPRINGER</subfield></datafield><datafield tag="912" 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author |
Guo, An-ru |
spellingShingle |
Guo, An-ru misc Cationic ring-opening polymerization misc Living polymerization misc Tetrahydrofuran misc Equilibrium misc Kinetics Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF |
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Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF Cationic ring-opening polymerization (dpeaa)DE-He213 Living polymerization (dpeaa)DE-He213 Tetrahydrofuran (dpeaa)DE-He213 Equilibrium (dpeaa)DE-He213 Kinetics (dpeaa)DE-He213 |
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Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF |
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Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF |
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Chinese Journal of Polymer Science |
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real-time monitoring of living cationic ring-opening polymerization of thf and direct prediction of equilibrium molecular weight of polythf |
title_auth |
Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF |
abstract |
Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. |
abstractGer |
Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. |
abstract_unstemmed |
Abstract A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]e) via in situ FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]0-[M]e)/([M]-[M]e) versus polymerization time at different temperatures in various solvents. [M]e decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (te) decreased with increasing solvent polarity and decreased linearly with increasing [M]0 in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of Mn,e = 72.1/(0.14-0.04[M]e) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C. |
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container_issue |
1 |
title_short |
Real-time monitoring of living cationic ring-opening polymerization of THF and direct prediction of equilibrium molecular weight of polyTHF |
url |
https://dx.doi.org/10.1007/s10118-015-1571-9 |
remote_bool |
true |
author2 |
Yang, Fan Yu, Rui Wu, Yi-xian |
author2Str |
Yang, Fan Yu, Rui Wu, Yi-xian |
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hochschulschrift_bool |
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doi_str |
10.1007/s10118-015-1571-9 |
up_date |
2024-07-04T01:12:34.676Z |
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score |
7.3999624 |