학술논문

Structurally Diverse Dendritic Libraries:  A Highly Efficient Functionalization Approach Using Click Chemistry
Document Type
Article
Source
Macromolecules; May 2005, Vol. 38 Issue: 9 p3663-3678, 16p
Subject
Language
ISSN
00249297; 15205835
Abstract
The high fidelity and efficiency of Click chemistry are exploited in the synthesis of a library of chain end functionalized dendritic macromolecules. In this example, the selectivity of the Cu-catalyzed [3 + 2π] cycloaddition reaction of azides with terminal acetylenes, coupled with mild reaction conditions, permits unprecedented functional group tolerance during the derivatization of dendrimeric and hyperbranched scaffolds. The resulting dendritic libraries are structurally diverse, encompassing a variety of backbones/surface functional groups, and are prepared in almost quantitative yields under very mild conditions. The robust and simple nature of this procedure, combined with its applicability to many aspects of polymer synthesis and materials chemistry, demonstrates an evolving synergy between advanced organic chemistry and functional materials.