Institute of Polymer Chemistry, University of Stuttgart, Stuttgart, Germany.
Macromol Rapid Commun. 2012 Aug 28;33(16):1399-403. doi: 10.1002/marc.201200247. Epub 2012 Jun 5.
Monolithic polymeric materials are prepared via ring-opening metathesis copolymerization of norborn-2-ene with 1,4,4a,5,8,8a-hexahydro-1,4,5,8-exo,endo-dimethanonaphthalene in the presence of macro- and microporogens, that is, of n-hexane and 1,2-dichloroethane, using the Schrock catalyst Mo(N-2,6-(2-Pr)(2) -C(6) H(3) )(CHCMe(2) Ph)(OCMe(3) )(2) . Functionalization of the monolithic materials is accomplished by either terminating the living metal alkylidenes with various functional aldehydes or by post-synthesis grafting with norborn-5-en-2-ylmethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate. Finally, boronate-grafted monolithic columns (100 × 3 mm i.d.) are successfully applied to the affinity chromatographic separation of cis-diol-based biomolecules.
通过在 Schrock 催化剂 Mo(N-2,6-(2-Pr)(2) -C(6) H(3) )(CHCMe(2) Ph)(OCMe(3) )(2) 的存在下,使用大孔和微孔引发剂正己烷和 1,2-二氯乙烷,使降冰片-2-烯与 1,4,4a,5,8,8a-六氢-1,4,5,8-内, 外-二甲酰基萘开环易位共聚,制备了整体聚合材料。通过用各种官能醛终止活的金属亚烷基,或者通过后合成接枝降冰片-5-烯-2-基甲基-4-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)苯甲酸酯,对整体聚合材料进行了功能化。最后,硼酸酯接枝整体柱(100×3mm id)成功应用于基于顺二醇的生物分子的亲和色谱分离。