Rapid UV Light-Triggered Macromolecular Click Conjugations via the Use of o-Quinodimethanes

被引:98
作者
Gruendling, Till [1 ]
Oehlenschlaeger, Kim K. [1 ]
Frick, Elena [1 ]
Glassner, Mathias [1 ]
Schmid, Christina [1 ]
Barner-Kowollik, Christopher [1 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
关键词
diblock copolymer; electrospray ionization mass spectrometry (SEC/ESI-MS); ortho-quinodimethanes; photoconjugation; photo Diels-Alder; MOLECULAR-WEIGHT DISTRIBUTIONS; RADICAL POLYMERIZATION; BLOCK-COPOLYMERS; RAFT; CHEMISTRY; POLYMERS; CYCLOADDITION; COMBINATION; NETWORKS; DESIGN;
D O I
10.1002/marc.201100159
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Shining a light on click chemistry: The use of UV-radiation as trigger signal provides a facile means to obtain spatial and temporal control over polymer conjugation reactions in addition to providing a further means of achieving orthogonality in click transformations. In the current contribution, UV-radiation was employed to induce a highly efficient Diels-Alder conjugation of polymeric building blocks via the photo-induced in situ formation of highly reactive cis-dienes from a 2-methylbenzophenone precursor.
引用
收藏
页码:807 / 812
页数:6
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