Synthesis and electrochromic properties of epoxy materials containing triphenylamine units
Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorpti...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Hao, Liping [verfasserIn] Wang, Wen [verfasserIn] Sun, Yan [verfasserIn] Niu, Haijun [verfasserIn] Ji, Yan [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2015 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of polymer research - Dordrecht : Springer Science + Business Media B.V., 1994, 22(2015), 5 vom: 28. Apr. |
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| Übergeordnetes Werk: |
volume:22 ; year:2015 ; number:5 ; day:28 ; month:04 |
| Links: |
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| DOI / URN: |
10.1007/s10965-015-0715-5 |
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| Katalog-ID: |
SPR01513492X |
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| 520 | |a Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. | ||
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| 650 | 4 | |a Electrochromic properties |7 (dpeaa)DE-He213 | |
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| 650 | 4 | |a Epoxy resins |7 (dpeaa)DE-He213 | |
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| 700 | 1 | |a Sun, Yan |e verfasserin |4 aut | |
| 700 | 1 | |a Niu, Haijun |e verfasserin |4 aut | |
| 700 | 1 | |a Ji, Yan |e verfasserin |4 aut | |
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10.1007/s10965-015-0715-5 doi (DE-627)SPR01513492X (SPR)s10965-015-0715-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Hao, Liping verfasserin aut Synthesis and electrochromic properties of epoxy materials containing triphenylamine units 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. Triphenylamines (dpeaa)DE-He213 Electrochromic properties (dpeaa)DE-He213 Photoelectro conversions (dpeaa)DE-He213 Epoxy resins (dpeaa)DE-He213 Wang, Wen verfasserin aut Sun, Yan verfasserin aut Niu, Haijun verfasserin aut Ji, Yan verfasserin aut Enthalten in Journal of polymer research Dordrecht : Springer Science + Business Media B.V., 1994 22(2015), 5 vom: 28. Apr. (DE-627)340872098 (DE-600)2065616-6 1572-8935 nnns volume:22 year:2015 number:5 day:28 month:04 https://dx.doi.org/10.1007/s10965-015-0715-5 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_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_206 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_2056 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 35.00 ASE AR 22 2015 5 28 04 |
| spelling |
10.1007/s10965-015-0715-5 doi (DE-627)SPR01513492X (SPR)s10965-015-0715-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Hao, Liping verfasserin aut Synthesis and electrochromic properties of epoxy materials containing triphenylamine units 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. Triphenylamines (dpeaa)DE-He213 Electrochromic properties (dpeaa)DE-He213 Photoelectro conversions (dpeaa)DE-He213 Epoxy resins (dpeaa)DE-He213 Wang, Wen verfasserin aut Sun, Yan verfasserin aut Niu, Haijun verfasserin aut Ji, Yan verfasserin aut Enthalten in Journal of polymer research Dordrecht : Springer Science + Business Media B.V., 1994 22(2015), 5 vom: 28. Apr. (DE-627)340872098 (DE-600)2065616-6 1572-8935 nnns volume:22 year:2015 number:5 day:28 month:04 https://dx.doi.org/10.1007/s10965-015-0715-5 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_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_206 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_2056 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 35.00 ASE AR 22 2015 5 28 04 |
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10.1007/s10965-015-0715-5 doi (DE-627)SPR01513492X (SPR)s10965-015-0715-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Hao, Liping verfasserin aut Synthesis and electrochromic properties of epoxy materials containing triphenylamine units 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. Triphenylamines (dpeaa)DE-He213 Electrochromic properties (dpeaa)DE-He213 Photoelectro conversions (dpeaa)DE-He213 Epoxy resins (dpeaa)DE-He213 Wang, Wen verfasserin aut Sun, Yan verfasserin aut Niu, Haijun verfasserin aut Ji, Yan verfasserin aut Enthalten in Journal of polymer research Dordrecht : Springer Science + Business Media B.V., 1994 22(2015), 5 vom: 28. Apr. (DE-627)340872098 (DE-600)2065616-6 1572-8935 nnns volume:22 year:2015 number:5 day:28 month:04 https://dx.doi.org/10.1007/s10965-015-0715-5 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_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_206 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_2056 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 35.00 ASE AR 22 2015 5 28 04 |
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10.1007/s10965-015-0715-5 doi (DE-627)SPR01513492X (SPR)s10965-015-0715-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Hao, Liping verfasserin aut Synthesis and electrochromic properties of epoxy materials containing triphenylamine units 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. Triphenylamines (dpeaa)DE-He213 Electrochromic properties (dpeaa)DE-He213 Photoelectro conversions (dpeaa)DE-He213 Epoxy resins (dpeaa)DE-He213 Wang, Wen verfasserin aut Sun, Yan verfasserin aut Niu, Haijun verfasserin aut Ji, Yan verfasserin aut Enthalten in Journal of polymer research Dordrecht : Springer Science + Business Media B.V., 1994 22(2015), 5 vom: 28. Apr. (DE-627)340872098 (DE-600)2065616-6 1572-8935 nnns volume:22 year:2015 number:5 day:28 month:04 https://dx.doi.org/10.1007/s10965-015-0715-5 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_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_206 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_2056 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 35.00 ASE AR 22 2015 5 28 04 |
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10.1007/s10965-015-0715-5 doi (DE-627)SPR01513492X (SPR)s10965-015-0715-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Hao, Liping verfasserin aut Synthesis and electrochromic properties of epoxy materials containing triphenylamine units 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. Triphenylamines (dpeaa)DE-He213 Electrochromic properties (dpeaa)DE-He213 Photoelectro conversions (dpeaa)DE-He213 Epoxy resins (dpeaa)DE-He213 Wang, Wen verfasserin aut Sun, Yan verfasserin aut Niu, Haijun verfasserin aut Ji, Yan verfasserin aut Enthalten in Journal of polymer research Dordrecht : Springer Science + Business Media B.V., 1994 22(2015), 5 vom: 28. Apr. (DE-627)340872098 (DE-600)2065616-6 1572-8935 nnns volume:22 year:2015 number:5 day:28 month:04 https://dx.doi.org/10.1007/s10965-015-0715-5 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_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_206 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_2056 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 35.00 ASE AR 22 2015 5 28 04 |
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Hao, Liping @@aut@@ Wang, Wen @@aut@@ Sun, Yan @@aut@@ Niu, Haijun @@aut@@ Ji, Yan @@aut@@ |
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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">SPR01513492X</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519175050.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201006s2015 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10965-015-0715-5</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR01513492X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s10965-015-0715-5-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="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.00</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Hao, Liping</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis and electrochromic properties of epoxy materials containing triphenylamine units</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015</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 series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Triphenylamines</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Electrochromic properties</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Photoelectro conversions</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Epoxy resins</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wang, Wen</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sun, Yan</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Niu, Haijun</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ji, Yan</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">Journal of polymer research</subfield><subfield code="d">Dordrecht : Springer Science + Business Media B.V., 1994</subfield><subfield code="g">22(2015), 5 vom: 28. 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Hao, Liping |
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Hao, Liping ddc 540 bkl 35.00 misc Triphenylamines misc Electrochromic properties misc Photoelectro conversions misc Epoxy resins Synthesis and electrochromic properties of epoxy materials containing triphenylamine units |
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540 ASE 35.00 bkl Synthesis and electrochromic properties of epoxy materials containing triphenylamine units Triphenylamines (dpeaa)DE-He213 Electrochromic properties (dpeaa)DE-He213 Photoelectro conversions (dpeaa)DE-He213 Epoxy resins (dpeaa)DE-He213 |
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Synthesis and electrochromic properties of epoxy materials containing triphenylamine units |
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synthesis and electrochromic properties of epoxy materials containing triphenylamine units |
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Synthesis and electrochromic properties of epoxy materials containing triphenylamine units |
| abstract |
Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. |
| abstractGer |
Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. |
| abstract_unstemmed |
Abstract A series of novel aromatic epoxy resins are prepared from the epichlorohydrin (ECH) and di(4-hydroxybenzylideneamino) triphenylamine (DHB-TPA) monomers, which are synthesized from different triphenylamine (TPA)-containing diamines and p-hydroxybenzaldehyde. FT-IR, 1H NMR and UV–Vis absorption spectra are employed to characterize the chemical structures of the polymers. All the polymers are amorphous, soluble in a variety of common organic solvents. The thermal properties of the polymers are investigated by thermogravimetric analysis (TGA) indicating good thermal stabilities compared with conventional epoxy resins on behalf of the introduction of aromatic TPA groups. All the polymers exhibit excellent reversibility of electrochromic characteristics by continuous cyclic scans between 0 and 2.0 V with the color changing from green to blue. The polymers also display photoelectrical response. The above properties prove that the series of polymers exhibit high thermal stability, excellent reversibility of electrochromic characteristics and photoelectric behaviours, which can be prospective candidates as electrochromic materials and photoelectrical conversion materials. |
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5 |
| title_short |
Synthesis and electrochromic properties of epoxy materials containing triphenylamine units |
| url |
https://dx.doi.org/10.1007/s10965-015-0715-5 |
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| author2 |
Wang, Wen Sun, Yan Niu, Haijun Ji, Yan |
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Wang, Wen Sun, Yan Niu, Haijun Ji, Yan |
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| doi_str |
10.1007/s10965-015-0715-5 |
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2024-07-03T14:08:44.282Z |
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| score |
7.402316 |