Synthesis of cardanol-based photo-active SET-LRP initiator and its application to preparation of UV-cured resin
被引:5
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作者:
Cheng, Chuan-Jie
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机构:
Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R ChinaJiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
Cheng, Chuan-Jie
[1
]
Zhang, Xu
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Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R ChinaJiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
Zhang, Xu
[1
]
Bai, Xiong-Xiong
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机构:
Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R ChinaJiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
Bai, Xiong-Xiong
[1
]
Li, Jin
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Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R ChinaJiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
Li, Jin
[1
]
Cao, Xing-Xing
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Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R ChinaJiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
Cao, Xing-Xing
[1
]
Wang, Jing-Lan
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Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R ChinaJiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
Wang, Jing-Lan
[1
]
机构:
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
cardanol;
SET-LRP;
photo-active;
UV-cured resin;
TRANSFER RADICAL POLYMERIZATION;
ROOM-TEMPERATURE;
FACILE SYNTHESIS;
CLICK CHEMISTRY;
AGET ATRP;
POLYMERS;
COPOLYMERS;
CHEMICALS;
LIGAND;
FUTURE;
D O I:
10.1515/chempap-2015-0176
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A benzophenone-containing SET-LRP initiator based on renewable and abundant cardanol was synthesised in 71 % yield using the selective etherification reaction. Next, methyl methacrylate (MMA) as a monomer was polymerised under SET-LRP conditions using the newly prepared initiator to prepare cardanol-end poly(methyl methacrylate) (PMMA). The kinetic results of the polymerisation indicated that the reaction was controllable when the monomer conversion was lower than approximately 50 %, and the molecular masses of PMMA measured by GPC were higher than the theoretical values while the monomer conversion was more than 50 %. In addition, most of the carbon-carbon double bonds of the side hydrocarbon chain of the end-cardanol group in the PMMA were kept intact from H-1 NMR spectrum characterisation. Accordingly, when the cardanolend PMMA together with a tertiary amine-containing cardanol derivative was irradiated by UV light, the corresponding UV-cured resin was obtained. The chemical resistance and hardness of the UV-cured film were enhanced with the increasing irradiation time. (C) 2015 Institute of Chemistry, Slovak Academy of Sciences