Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor
Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the chara...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Zheng, Jian [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2016 |
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| Schlagwörter: |
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| Anmerkung: |
© The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 |
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| Übergeordnetes Werk: |
Enthalten in: Macromolecular research - Heidelberg : Springer, 2010, 24(2016), 5 vom: Mai, Seite 409-414 |
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| Übergeordnetes Werk: |
volume:24 ; year:2016 ; number:5 ; month:05 ; pages:409-414 |
| Links: |
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| DOI / URN: |
10.1007/s13233-016-4061-1 |
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| Katalog-ID: |
SPR030967678 |
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| 100 | 1 | |a Zheng, Jian |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor |
| 264 | 1 | |c 2016 | |
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| 520 | |a Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. | ||
| 650 | 4 | |a phthalonitrile |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a polybenzoxazine |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a main-chain |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a high-performance |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Zhang, Yan |4 aut | |
| 700 | 1 | |a Wang, Ying |4 aut | |
| 700 | 1 | |a Gan, Jianqun |4 aut | |
| 700 | 1 | |a Shen, Lu |4 aut | |
| 700 | 1 | |a Luo, FuBin |4 aut | |
| 700 | 1 | |a Liang, Liyan |4 aut | |
| 700 | 1 | |a Wu, Kun |4 aut | |
| 700 | 1 | |a Lu, Mangeng |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Macromolecular research |d Heidelberg : Springer, 2010 |g 24(2016), 5 vom: Mai, Seite 409-414 |w (DE-627)618327576 |w (DE-600)2537708-5 |x 2092-7673 |7 nnns |
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10.1007/s13233-016-4061-1 doi (DE-627)SPR030967678 (SPR)s13233-016-4061-1-e DE-627 ger DE-627 rakwb eng Zheng, Jian verfasserin aut Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. phthalonitrile (dpeaa)DE-He213 polybenzoxazine (dpeaa)DE-He213 main-chain (dpeaa)DE-He213 high-performance (dpeaa)DE-He213 Zhang, Yan aut Wang, Ying aut Gan, Jianqun aut Shen, Lu aut Luo, FuBin aut Liang, Liyan aut Wu, Kun aut Lu, Mangeng aut Enthalten in Macromolecular research Heidelberg : Springer, 2010 24(2016), 5 vom: Mai, Seite 409-414 (DE-627)618327576 (DE-600)2537708-5 2092-7673 nnns volume:24 year:2016 number:5 month:05 pages:409-414 https://dx.doi.org/10.1007/s13233-016-4061-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_2008 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 24 2016 5 05 409-414 |
| spelling |
10.1007/s13233-016-4061-1 doi (DE-627)SPR030967678 (SPR)s13233-016-4061-1-e DE-627 ger DE-627 rakwb eng Zheng, Jian verfasserin aut Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. phthalonitrile (dpeaa)DE-He213 polybenzoxazine (dpeaa)DE-He213 main-chain (dpeaa)DE-He213 high-performance (dpeaa)DE-He213 Zhang, Yan aut Wang, Ying aut Gan, Jianqun aut Shen, Lu aut Luo, FuBin aut Liang, Liyan aut Wu, Kun aut Lu, Mangeng aut Enthalten in Macromolecular research Heidelberg : Springer, 2010 24(2016), 5 vom: Mai, Seite 409-414 (DE-627)618327576 (DE-600)2537708-5 2092-7673 nnns volume:24 year:2016 number:5 month:05 pages:409-414 https://dx.doi.org/10.1007/s13233-016-4061-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_2008 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 24 2016 5 05 409-414 |
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10.1007/s13233-016-4061-1 doi (DE-627)SPR030967678 (SPR)s13233-016-4061-1-e DE-627 ger DE-627 rakwb eng Zheng, Jian verfasserin aut Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. phthalonitrile (dpeaa)DE-He213 polybenzoxazine (dpeaa)DE-He213 main-chain (dpeaa)DE-He213 high-performance (dpeaa)DE-He213 Zhang, Yan aut Wang, Ying aut Gan, Jianqun aut Shen, Lu aut Luo, FuBin aut Liang, Liyan aut Wu, Kun aut Lu, Mangeng aut Enthalten in Macromolecular research Heidelberg : Springer, 2010 24(2016), 5 vom: Mai, Seite 409-414 (DE-627)618327576 (DE-600)2537708-5 2092-7673 nnns volume:24 year:2016 number:5 month:05 pages:409-414 https://dx.doi.org/10.1007/s13233-016-4061-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_2008 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 24 2016 5 05 409-414 |
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10.1007/s13233-016-4061-1 doi (DE-627)SPR030967678 (SPR)s13233-016-4061-1-e DE-627 ger DE-627 rakwb eng Zheng, Jian verfasserin aut Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. phthalonitrile (dpeaa)DE-He213 polybenzoxazine (dpeaa)DE-He213 main-chain (dpeaa)DE-He213 high-performance (dpeaa)DE-He213 Zhang, Yan aut Wang, Ying aut Gan, Jianqun aut Shen, Lu aut Luo, FuBin aut Liang, Liyan aut Wu, Kun aut Lu, Mangeng aut Enthalten in Macromolecular research Heidelberg : Springer, 2010 24(2016), 5 vom: Mai, Seite 409-414 (DE-627)618327576 (DE-600)2537708-5 2092-7673 nnns volume:24 year:2016 number:5 month:05 pages:409-414 https://dx.doi.org/10.1007/s13233-016-4061-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_2008 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 24 2016 5 05 409-414 |
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10.1007/s13233-016-4061-1 doi (DE-627)SPR030967678 (SPR)s13233-016-4061-1-e DE-627 ger DE-627 rakwb eng Zheng, Jian verfasserin aut Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. phthalonitrile (dpeaa)DE-He213 polybenzoxazine (dpeaa)DE-He213 main-chain (dpeaa)DE-He213 high-performance (dpeaa)DE-He213 Zhang, Yan aut Wang, Ying aut Gan, Jianqun aut Shen, Lu aut Luo, FuBin aut Liang, Liyan aut Wu, Kun aut Lu, Mangeng aut Enthalten in Macromolecular research Heidelberg : Springer, 2010 24(2016), 5 vom: Mai, Seite 409-414 (DE-627)618327576 (DE-600)2537708-5 2092-7673 nnns volume:24 year:2016 number:5 month:05 pages:409-414 https://dx.doi.org/10.1007/s13233-016-4061-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_2008 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 24 2016 5 05 409-414 |
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English |
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Enthalten in Macromolecular research 24(2016), 5 vom: Mai, Seite 409-414 volume:24 year:2016 number:5 month:05 pages:409-414 |
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Enthalten in Macromolecular research 24(2016), 5 vom: Mai, Seite 409-414 volume:24 year:2016 number:5 month:05 pages:409-414 |
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phthalonitrile polybenzoxazine main-chain high-performance |
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Zheng, Jian @@aut@@ Zhang, Yan @@aut@@ Wang, Ying @@aut@@ Gan, Jianqun @@aut@@ Shen, Lu @@aut@@ Luo, FuBin @@aut@@ Liang, Liyan @@aut@@ Wu, Kun @@aut@@ Lu, Mangeng @@aut@@ |
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2016-05-01T00:00:00Z |
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| author |
Zheng, Jian |
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Zheng, Jian misc phthalonitrile misc polybenzoxazine misc main-chain misc high-performance Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor |
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Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor phthalonitrile (dpeaa)DE-He213 polybenzoxazine (dpeaa)DE-He213 main-chain (dpeaa)DE-He213 high-performance (dpeaa)DE-He213 |
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misc phthalonitrile misc polybenzoxazine misc main-chain misc high-performance |
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Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor |
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Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor |
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Zheng, Jian |
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Zheng, Jian Zhang, Yan Wang, Ying Gan, Jianqun Shen, Lu Luo, FuBin Liang, Liyan Wu, Kun Lu, Mangeng |
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Zheng, Jian |
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10.1007/s13233-016-4061-1 |
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synthesis and characterization of a lateral phthalonitrile functionalized main-chain polybenzoxazine precursor |
| title_auth |
Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor |
| abstract |
Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 |
| abstractGer |
Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 |
| abstract_unstemmed |
Abstract A lateral phthalonitrile functionalized main-chain polybenzoxazine precursor has been successfully synthesized. The structure was characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FTIR). The formation of benzoxazine rings were confirmed by the characteristic resonances observed at about 4.55 (C-$ CH_{2} $-N) and 5.30 ppm (N-$ CH_{2} $-O) and the absorbance at 950 $ cm^{-1} $ of benzene attached with an oxazine ring. The curing behavior was monitored by differential scanning calorimetry (DSC) and in situ FTIR. The completion of polymerization was proved by the disappearance of the band located at 950 $ cm^{-1} $ in FTIR. Thermogravimetric analysis (TGA) was used to investigate the thermal stability, and the results indicated that the thermal stability of the cured polymer gained significant improvement than that without phthalonitrile functionalization. © The Polymer Society of Korea and Springer Sciene+Business Media Dordrecht 2016 |
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Synthesis and Characterization of a Lateral Phthalonitrile Functionalized Main-Chain Polybenzoxazine Precursor |
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https://dx.doi.org/10.1007/s13233-016-4061-1 |
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Zhang, Yan Wang, Ying Gan, Jianqun Shen, Lu Luo, FuBin Liang, Liyan Wu, Kun Lu, Mangeng |
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Zhang, Yan Wang, Ying Gan, Jianqun Shen, Lu Luo, FuBin Liang, Liyan Wu, Kun Lu, Mangeng |
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| doi_str |
10.1007/s13233-016-4061-1 |
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2024-07-03T21:12:51.709Z |
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| score |
7.3996134 |