Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator

Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purp...
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Gespeichert in:

Autor*in:	Göktaş, Melahat [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2020

Schlagwörter:	Reversible addition-fragmentation chain transfer Redox polymerization Macromonomeric initiator (macro-CTA) -isopropylacrylamide 2-(Dimethyl amino)ethyl methacrylate

Übergeordnetes Werk:	Enthalten in: Chemical papers - Wien : Springer Vienna, 1947, 74(2020), 7 vom: 03. Feb., Seite 2297-2307
Übergeordnetes Werk:	volume:74 ; year:2020 ; number:7 ; day:03 ; month:02 ; pages:2297-2307

Links:	Volltext

DOI / URN:	10.1007/s11696-020-01074-9

Katalog-ID:	SPR039500632

Internformat


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245	1	0	\|a Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
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520			\|a Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis.
650		4	\|a Reversible addition-fragmentation chain transfer \|7 (dpeaa)DE-He213
650		4	\|a Redox polymerization \|7 (dpeaa)DE-He213
650		4	\|a Macromonomeric initiator (macro-CTA) \|7 (dpeaa)DE-He213
650		4	\|a -isopropylacrylamide \|7 (dpeaa)DE-He213
650		4	\|a 2-(Dimethyl amino)ethyl methacrylate \|7 (dpeaa)DE-He213
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912			\|a GBV_ILN_23
912			\|a GBV_ILN_24
912			\|a GBV_ILN_31
912			\|a GBV_ILN_32
912			\|a GBV_ILN_39
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_73
912			\|a GBV_ILN_74
912			\|a GBV_ILN_90
912			\|a GBV_ILN_95
912			\|a GBV_ILN_100
912			\|a GBV_ILN_101
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_120
912			\|a GBV_ILN_138
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_152
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_171
912			\|a GBV_ILN_187
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_250
912			\|a GBV_ILN_266
912			\|a GBV_ILN_281
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_636
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2031
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2039
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2056
912			\|a GBV_ILN_2057
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2065
912			\|a GBV_ILN_2068
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2093
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2107
912			\|a GBV_ILN_2108
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2113
912			\|a GBV_ILN_2118
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2144
912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2188
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2232
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2446
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2472
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_2548
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4046
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4126
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4246
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4328
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4335
912			\|a GBV_ILN_4336
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
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Indexfelder

author_variant	m g mg
matchkey_str	article:13369075:2020----::yteiadhrceiainfeprtrrsosvbokooyess
hierarchy_sort_str	2020
bklnumber	35.00
publishDate	2020
allfields	10.1007/s11696-020-01074-9 doi (DE-627)SPR039500632 (SPR)s11696-020-01074-9-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Göktaş, Melahat verfasserin aut Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis. Reversible addition-fragmentation chain transfer (dpeaa)DE-He213 Redox polymerization (dpeaa)DE-He213 Macromonomeric initiator (macro-CTA) (dpeaa)DE-He213 -isopropylacrylamide (dpeaa)DE-He213 2-(Dimethyl amino)ethyl methacrylate (dpeaa)DE-He213 Enthalten in Chemical papers Wien : Springer Vienna, 1947 74(2020), 7 vom: 03. Feb., Seite 2297-2307 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307 https://dx.doi.org/10.1007/s11696-020-01074-9 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_266 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_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_2118 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_4126 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_4328 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 74 2020 7 03 02 2297-2307
spelling	10.1007/s11696-020-01074-9 doi (DE-627)SPR039500632 (SPR)s11696-020-01074-9-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Göktaş, Melahat verfasserin aut Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis. Reversible addition-fragmentation chain transfer (dpeaa)DE-He213 Redox polymerization (dpeaa)DE-He213 Macromonomeric initiator (macro-CTA) (dpeaa)DE-He213 -isopropylacrylamide (dpeaa)DE-He213 2-(Dimethyl amino)ethyl methacrylate (dpeaa)DE-He213 Enthalten in Chemical papers Wien : Springer Vienna, 1947 74(2020), 7 vom: 03. Feb., Seite 2297-2307 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307 https://dx.doi.org/10.1007/s11696-020-01074-9 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_266 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_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_2118 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_4126 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_4328 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 74 2020 7 03 02 2297-2307
allfields_unstemmed	10.1007/s11696-020-01074-9 doi (DE-627)SPR039500632 (SPR)s11696-020-01074-9-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Göktaş, Melahat verfasserin aut Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis. Reversible addition-fragmentation chain transfer (dpeaa)DE-He213 Redox polymerization (dpeaa)DE-He213 Macromonomeric initiator (macro-CTA) (dpeaa)DE-He213 -isopropylacrylamide (dpeaa)DE-He213 2-(Dimethyl amino)ethyl methacrylate (dpeaa)DE-He213 Enthalten in Chemical papers Wien : Springer Vienna, 1947 74(2020), 7 vom: 03. Feb., Seite 2297-2307 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307 https://dx.doi.org/10.1007/s11696-020-01074-9 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_266 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_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_2118 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_4126 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_4328 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 74 2020 7 03 02 2297-2307
allfieldsGer	10.1007/s11696-020-01074-9 doi (DE-627)SPR039500632 (SPR)s11696-020-01074-9-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Göktaş, Melahat verfasserin aut Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis. Reversible addition-fragmentation chain transfer (dpeaa)DE-He213 Redox polymerization (dpeaa)DE-He213 Macromonomeric initiator (macro-CTA) (dpeaa)DE-He213 -isopropylacrylamide (dpeaa)DE-He213 2-(Dimethyl amino)ethyl methacrylate (dpeaa)DE-He213 Enthalten in Chemical papers Wien : Springer Vienna, 1947 74(2020), 7 vom: 03. Feb., Seite 2297-2307 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307 https://dx.doi.org/10.1007/s11696-020-01074-9 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_266 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_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_2118 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_4126 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_4328 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 74 2020 7 03 02 2297-2307
allfieldsSound	10.1007/s11696-020-01074-9 doi (DE-627)SPR039500632 (SPR)s11696-020-01074-9-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Göktaş, Melahat verfasserin aut Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis. Reversible addition-fragmentation chain transfer (dpeaa)DE-He213 Redox polymerization (dpeaa)DE-He213 Macromonomeric initiator (macro-CTA) (dpeaa)DE-He213 -isopropylacrylamide (dpeaa)DE-He213 2-(Dimethyl amino)ethyl methacrylate (dpeaa)DE-He213 Enthalten in Chemical papers Wien : Springer Vienna, 1947 74(2020), 7 vom: 03. Feb., Seite 2297-2307 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307 https://dx.doi.org/10.1007/s11696-020-01074-9 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_266 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_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_2118 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_4126 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_4328 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 74 2020 7 03 02 2297-2307
language	English
source	Enthalten in Chemical papers 74(2020), 7 vom: 03. Feb., Seite 2297-2307 volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307
sourceStr	Enthalten in Chemical papers 74(2020), 7 vom: 03. Feb., Seite 2297-2307 volume:74 year:2020 number:7 day:03 month:02 pages:2297-2307
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topic_facet	Reversible addition-fragmentation chain transfer Redox polymerization Macromonomeric initiator (macro-CTA) -isopropylacrylamide 2-(Dimethyl amino)ethyl methacrylate
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container_title	Chemical papers
authorswithroles_txt_mv	Göktaş, Melahat @@aut@@
publishDateDaySort_date	2020-02-03T00:00:00Z
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author	Göktaş, Melahat
spellingShingle	Göktaş, Melahat ddc 540 bkl 35.00 misc Reversible addition-fragmentation chain transfer misc Redox polymerization misc Macromonomeric initiator (macro-CTA) misc -isopropylacrylamide misc 2-(Dimethyl amino)ethyl methacrylate Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
authorStr	Göktaş, Melahat
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topic_title	540 ASE 35.00 bkl Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator Reversible addition-fragmentation chain transfer (dpeaa)DE-He213 Redox polymerization (dpeaa)DE-He213 Macromonomeric initiator (macro-CTA) (dpeaa)DE-He213 -isopropylacrylamide (dpeaa)DE-He213 2-(Dimethyl amino)ethyl methacrylate (dpeaa)DE-He213
topic	ddc 540 bkl 35.00 misc Reversible addition-fragmentation chain transfer misc Redox polymerization misc Macromonomeric initiator (macro-CTA) misc -isopropylacrylamide misc 2-(Dimethyl amino)ethyl methacrylate
topic_unstemmed	ddc 540 bkl 35.00 misc Reversible addition-fragmentation chain transfer misc Redox polymerization misc Macromonomeric initiator (macro-CTA) misc -isopropylacrylamide misc 2-(Dimethyl amino)ethyl methacrylate
topic_browse	ddc 540 bkl 35.00 misc Reversible addition-fragmentation chain transfer misc Redox polymerization misc Macromonomeric initiator (macro-CTA) misc -isopropylacrylamide misc 2-(Dimethyl amino)ethyl methacrylate
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title	Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
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title_full	Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
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title_sort	synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
title_auth	Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
abstract	Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis.
abstractGer	Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis.
abstract_unstemmed	Abstract Temperature-responsive block copolymers, poly(2-(dimethyl amino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) [PDMAEMA-b-PNIPAM], have been prepared by a combination of the redox polymerization and the reversible addition-fragmentation chain transfer (RAFT) polymerization. For this purpose, poly-N-isopropylacrylamide (PNIPAM-Cl) was acquired by redox polymerization of N-isopropylacrylamide (NIPAM) using 2-(2-chloroethoxy)ethanol and Ce($ NH_{4} $)2($ NO_{3} $)6 was used as a catalyst. Poly(DMAEMA-b-NIPAM) temperature-responsive copolymers were prepared via RAFT of 2-(dimethyl amino)ethyl methacrylate) (DMAEMA) in the presence of macromonomeric initiator (macro-CTA) which was obtained via the reaction of PNIPAM-Cl with the potassium salt of ethyl xanthogenate. The synthesized temperature-responsive block copolymer was characterized using multi-instruments and methods such as nuclear magnetic resonance spectroscopy, F(f)ourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, differential scanning calorimetry, scanning electron microscope and UV–Vis.
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container_issue	7
title_short	Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator
url	https://dx.doi.org/10.1007/s11696-020-01074-9
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doi_str	10.1007/s11696-020-01074-9
up_date	2024-07-04T00:12:59.750Z
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Synthesis and characterization of temperature-responsive block copolymers using macromonomeric initiator

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