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1.华东理工大学化学工程联合国家重点实验室 上海 200237
2.华南农业大学材料与能源学院 广州 510642
E-mail: rhcheng@ecust.edu.cn Rui-hua Cheng, E-mail: rhcheng@ecust.edu.cn
纸质出版日期:2019-11,
网络出版日期:2019-5-10,
收稿日期:2019-3-18,
修回日期:2019-4-9,
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于伶伶, 程瑞华, 童钰涛, 刘柏平. 紫外光照亲水性聚碳酸酯的合成及性能[J]. 高分子学报, 2019,50(11):1196-1201.
Ling-ling Yu, Rui-hua Cheng, Yu-tao Tong, Bo-ping Liu. Synthesis and Properties of Hydrophilic Poly(propylene carbonate) under UV Irradiation[J]. Acta Polymerica Sinica, 2019,50(11):1196-1201.
于伶伶, 程瑞华, 童钰涛, 刘柏平. 紫外光照亲水性聚碳酸酯的合成及性能[J]. 高分子学报, 2019,50(11):1196-1201. DOI: 10.11777/j.issn1000-3304.2019.19053.
Ling-ling Yu, Rui-hua Cheng, Yu-tao Tong, Bo-ping Liu. Synthesis and Properties of Hydrophilic Poly(propylene carbonate) under UV Irradiation[J]. Acta Polymerica Sinica, 2019,50(11):1196-1201. DOI: 10.11777/j.issn1000-3304.2019.19053.
采用2-{[(2-硝基苯基)甲氧基]甲基}环氧乙烷(单体
a
)与二氧化碳(CO
2
)、环氧丙烷(PO)在SalenCo
(III)
Cl/双(三苯基正膦基)氯化铵(PPNCl)催化下三元共聚,紫外(UV)光照脱除保护基,成功合成羟基官能化聚碳酸酯(PPC-OH). 采用红外光谱、核磁共振、凝胶渗透色谱、接触角测量仪等对产物表征,结果表明:单体
a
成功引入聚碳酸酯骨架;SalenCo
(III)
Cl催化剂表现出高催化活性、高选择性以及对第三单体良好的耐受性,聚合物碳酸酯单元含量
>
98%,首尾相连结构
>
99%,分子量分布极窄,CO
2
和环氧化物完美交替共聚. 通过UV光照成功脱除羟基保护基生成PPC-OH,主链骨架无降解;单体
a
加入量至6%时,PPC-OH羟基含量增加至19.4%,水接触角由78.3°减小至57.6°,亲水性得到明显改善.
To improve the hydrophilic properties of poly(propylene carbonate) (PPC)
hydroxyl-functionalized PPC (PPC-OH) were prepared by two steps. First
PPC containing
o
-nitrobenzyl (ONB) protecting groups (PPC-ONB) were synthesized by terpolymerization reactions of 2-{[(2-nitrophenyl)methoxy]-methyl}oxirane (monomer
a
)
propylene oxide (PO)
and CO
2
over SalenCo
(III)
Cl/bis(triphenylphosphine)iminium chloride (PPNCl) catalyst system.
1
H-NMR result showed that the PPC-ONB was a random copolymer with monomer
a
randomly inserted. Then PPC-OH were obtained with the removal of
o
-nitrobenzyl (ONB) protecting groups under ultraviolet (UV) irradiation. PPC-ONB were synthesized with various feed ratios of the monomer
a
and different reaction time. Based on the analysis of
1
H-NMR
13
C-NMR
gel permeation chromatography (GPC)
and differential scanning calorimeter (DSC)
SalenCo
(III)
Cl catalyst performed high reactivity and high selectivity (
>
94%). The polycarbonate exhibited excellent regioselectivity and perfect alternating copolymerization of CO
2
and PO with the carbonate linkages up to 98%
and the head-to-tail linkage (HT) up to 99%. With the increase of the feed ratios of the monomer
a
the polymer ratio of the monomer
a
increased to 19.4% without sacrificing the reactive activity
while the molecular weight (
M
n
) decreased slightly owing to the better reactivity of monomer
a
. The glass transition temperatures (
T
g
) were in the range of 35.7 − 38.9 °C. The kinetics of deprotection by UV irradiation proved that the ONB protecting groups could be carried out efficiently within minutes. And the characterization of polymer by
1
H-NMR
Fourier transform infrared spectrometer (FTIR) and GPC showed that the ONB protecting groups were removed and the ―OH was observed. Meanwhile
no degradation of polymer backbone occurred. The contact angle (CA) measurement of PPC-ONB and PPC-OH displayed a difference in hydrophilia. The hydrophilia of PPC-OH has been greatly improved compared with PPC-ONB due to the increase in polarity
and the CA of PPC-OH decreased from 78.3° to 58.6° when the molar ratio of ―OH increased to 19.4%.
羟基官能化聚碳酸酯二氧化碳亲水性三元共聚SalenCo(III)Cl催化剂
Hydroxyl-functionalized poly(propylene carbonate)Carbon dioxideHydrophilicTerpolymerizationSalenCo(III)Cl catalyst
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