Monotelechelic Poly(oxa)norbornenes by Ring-Opening Metathesis Polymerization Using Direct End-Capping and Cross-Metathesis

被引:51
|
作者
Matson, John B. [1 ]
Grubbs, Robert H. [1 ]
机构
[1] CALTECH, NanoSyst Biol Canc Ctr, Div Chem & Chem Engn, Pasadena, CA 91125 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
TRANSFER RADICAL POLYMERIZATION; LIVING ANIONIC-POLYMERIZATION; BLOCK-COPOLYMERS; OLEFIN-METATHESIS; TELECHELIC POLYMERS; DIBLOCK COPOLYMERS; CLICK CYCLIZATION; SYNTHETIC ROUTE; CHAIN-TRANSFER; ROMP;
D O I
10.1021/ma9019366
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two different methodologies for the synthesis of monotelechelic poly(oxa)norbornenes prepared by living ring-opening metathesis polymerization (ROMP) are presented. The First met hod, termed direct end-capping, is carried Out by adding an internal cis-olefin terminating agent (TA) to the reaction mixture immediately after the completion of the living ROMP reaction. The second method relics oil cross-metathesis (CM) between a methylene-terminated poly(oxa)norbornene and a cis-olefin TA mediated by the ruthenium olefin metathesis catalyst (H(2)IMes)(Cl)(2)Ru(CH-o-OiPrC(6)H(4)) (H(2)IMes = 1,3-dimesitylimidazolidine-2-ylidene). TAs containing various functional groups, including alcohols, acetates, bromides, alpha-bromoesters, thioacetates, N-hydroxysuccinimidyl esters, and Boc-amines, as well as fluorescein and biotin groups, were synthesized and tested, The direct end-capping method typically resulted ill > 90% end-functionalization efficiency, while the CM method was nearly as effective for TAs Without polar functional groups or significant steric bulk. End-functionalization efficiency values were determined by H-1 NMR spectroscopy.
引用
收藏
页码:213 / 221
页数:9
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