Monodisperse, sequence-defined macromolecules as a tool to evaluate the limits of ring-closing metathesis

被引:7
|
作者
Wetzel, Katharina S. [1 ]
Meier, Michael A. R. [1 ]
机构
[1] Karlsruhe Inst Technol, Inst Organ Chem, Mat Wissensch Zentrum Energiesyteme MZE, Str Forum 7, D-76131 Karlsruhe, Germany
关键词
MULTICOMPONENT REACTIONS; OLEFIN ISOMERIZATION; POLYMER CHEMISTRY; DRUG DISCOVERY; OLIGOMERS; STRATEGY; ROUTE; CONVENIENT; GROWTH;
D O I
10.1039/c9py00438f
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Sequence-defined macromolecules of uniform size unlock the door to many new applications in polymer chemistry, such as structure/property or structure/activity relationship investigations, which cannot be conducted accurately, if the investigated macromolecules exhibit dispersity. We herein demonstrate a first example by reporting the efficient and template-free synthesis of monodisperse, sequence-defined cyclic oligomers that are significantly larger than conventional large macrocycles (here > 150 backbone atoms). Linear monodisperse precursors were utilized to evaluate the limits of ring-closing metathesis (RCM), manifesting clear trends depending on the ring size and introduced side chains. Furthermore, this work is the first example of a sequence-defined synthesis of a polymer architecture other than linear macromolecules.
引用
收藏
页码:2716 / 2722
页数:7
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