The Living ROMP of trans-Cyclooctene

被引:111
|
作者
Walker, Ron [1 ]
Conrad, Rosemary M. [1 ]
Grubbs, Robert H. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Arnold & Mabel Beckman Labs Chem Synth, Pasadena, CA 91125 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
OPENING METATHESIS POLYMERIZATION; BLOCK-COPOLYMERS; FUNCTIONALIZED CYCLOOCTENES; DOUBLE-BONDS; POLYMERS; HYDROGENATION; POLYETHYLENE; POLYNORBORNENE; INITIATORS; CATALYST;
D O I
10.1021/ma801693q
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The living ring-opening metathesis polymerization (ROMP) of trans-cyclooctene (tCO) was investigated. ROMP of tCO in the presence of PPh3 in THF leads to the formation of narrowly dispersed polycyclooctene (PCO). The presence of PPh4 as in additive and the use of THF as a solvent were demonstrated to be necessary to suppress competing secondary metathesis processes in the ROMP of tCO. Under optimal conditions, narrowly dispersed PCO was achieved without high molecular Weight contaminates. The PCO was then hydrogenated to form linear, narrowly dispersed polyethylene with a melting temperature Of 139 degrees C. Protected, hydroxy-functionalized tCO was polymerized by this method to afford narrowly dispersed, hydroxylated PCO, Block copolymers containing polynorbornene and PCO or containing differentially functionalized PCO were also synthesized and hydrogenated to form block copolymers containing blocks of linear, narrowly dispersed polyethylene.
引用
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页码:599 / 605
页数:7
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