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Combining ring-opening metathesis polymerization (ROMP) with sharpless-type 'click' reactions: An easy method for the preparation of side chain functionalized poly(oxynorbornenes)

机译:结合开环易位聚合(ROMP)与无尖锐型“喀哒”反应:制备侧链官能化聚降冰片烯的简便方法

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摘要

Sharpless 1,3-dipolar cycloadditions ("click reactions") between azides and acetylenes were used to prepare functional poly(oxynorbornenes) within their side chains. Two different strategies were applied to combine the preparation of ROMP polymers with the 1,3-dipolar cycloaddition approach: (a) the attachment of functional groups (i.e., hydrophobic and hydrogen bonding units) by 1,3-dipolar cycloaddition reactions to 7-oxynorbornenes bearing acetylenes and subsequent ROMP yielding the final polymers; (b) the ROMP polymerization furnishing first poly(oxynorbornenes) bearing acetylenic and azido moieties and subsequently attaching the functional units by use of the "click" reactions onto the modified polymers. Both strategies show efficient functionalization behavior with a high tolerance of functional groups with respect to the functional units attached as demonstrated by H-1 and C-13 NMR spectroscopy, opening the possibility to prepare a large variety of functionalized poly(oxynorbornenes) by use of only few starting materials.
机译:叠氮化物和乙炔之间的无尖锐的1,3-偶极环加成反应(“点击反应”)用于制备侧链内的功能性聚氧降冰片烯。应用了两种不同的策略将ROMP聚合物的制备与1,3-偶极环加成方法结合起来:(a)通过1,3-偶极环加成反应将官能团(即疏水和氢键合单元)与7-带有乙炔的氧降冰片烯和随后的ROMP产生最终聚合物; (b)ROMP聚合反应首先提供带有炔和叠氮基部分的聚(氧降冰片烯),然后通过“点击”反应将官能团连接到改性聚合物上。两种策略均显示出有效的官能化行为,相对于H-1和C-13 NMR光谱所显示的官能团,对官能团具有高度的耐受性,这为通过使用H2O3制备各种官能化的聚氧降冰片烯开辟了可能性只有很少的起始材料。

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