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1.中国科学院长春应用化学研究所 高分子物理与化学国家重点实验室 长春 130022
2.中国科学技术大学应用化学与工程学院 合肥 230026
E-mail: shihui-li@ciac.ac.cn;
E-mail: dmcui@ciac.ac.cn
纸质出版日期:2022-05-20,
网络出版日期:2022-03-08,
收稿日期:2021-10-15,
录用日期:2022-01-12
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汪骐远,黄建铭,李世辉等.羟基功能化高顺1,4-共轭双烯橡胶的合成[J].高分子学报,2022,53(05):474-481.
Wang Qi-yuan,Huang Jian-ming,Li Shi-hui,et al.Preparation of Hydroxyl Functionalized Cis-1,4 Polydienes[J].ACTA POLYMERICA SINICA,2022,53(05):474-481.
汪骐远,黄建铭,李世辉等.羟基功能化高顺1,4-共轭双烯橡胶的合成[J].高分子学报,2022,53(05):474-481. DOI: 10.11777/j.issn1000-3304.2021.21312.
Wang Qi-yuan,Huang Jian-ming,Li Shi-hui,et al.Preparation of Hydroxyl Functionalized Cis-1,4 Polydienes[J].ACTA POLYMERICA SINICA,2022,53(05):474-481. DOI: 10.11777/j.issn1000-3304.2021.21312.
将对异戊二烯聚合具有高选择性的稀土催化剂
1
~
5
,在助催化剂有机硼盐和烷基铝的作用下,用于催化硅烷基保护的极性共轭双烯单体IP-OTBS均聚合,制得了顺式1
4-结构单元含量最高为98.5%和3
4-结构含量最高达82.2%的聚(IP-OTBS). PNP-型稀土钇催化剂
2
催化IP-OTBS与1
3-丁二烯(BD)、异戊二烯(IP)无规共聚合,制备出了极性基团含量分别为10.2%和16.7%的顺丁橡胶和异戊橡胶. 这些极性聚合物在四丁基氟化铵的作用下脱除硅烷基保护基团,制得醇羟基功能化的顺丁橡胶和异戊橡胶.
Random incorporation of polar groups into polyolefins
via
coordination copolymerization has made a great progress in the past decades. In contrast
the preparation of polar functionalized conjugated diene rubbers receives less attention
although the polar groups play an important role in improving the mechanical properties of green tire. In this work
one kind of polar conjugated diene mononer IP-OTBS is prepared. Then
a series of rare-earth metal complexes
1‒5
which show different selectivities for isoprene polymerization
are utilized to initiate the homopolymerization of IP-OTBS in the presence of cocatalysts [Ph
3
C
]
[B(C
6
F
5
)
4
]
and Al
i
Bu
3
. Among them
complexes
1
and
2
still show high
cis
-1
4 selectivity (
>
98%) for IP-OTBS polymerization and
in contrast
the maximum value of 3
4 selectivity is 82.2% achieved by complex
3
. Complexes
4
and
5
which show higher 3
4 selectivity (
>
98%) for isoprene polymerization
show moderate 3
4 selectivity (67.6%) and inert
respectively
under the same conditions. The copolymerizations of IP-OTBS with isoprene and butadiene using complex
2
generate the functional polybutadiene and polyisopene with
cis
-1
4 content of 10.2 mol% and 16.7 mol%
respectively. The bulky tert-butyldimethylsilane masked polybutadienes are readily transformed into the hydroxyl group functionalized polybutadienes or polyisoprene
via
the reaction with Bu
4
NF. Finally
we demonstrate that the p
olar group functionalized conjugated diene rubbers could be obtained
via
the stereoselective (co)polymerization of IP-OTBS by using rare-earth metal catalysts.
醇羟基功能化聚共轭双烯高顺式14-选择性稀土催化剂丁二烯异戊二烯
Hydroxyl-functionalized polybutadieneCis-14 selectivityRare-earth metal catalystsButadieneIsoprene
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