Role of architecture and molecular weight in the formation of tailor-made ultrathin multilayers using dendritic macromolecules and click chemistry

被引:107
作者
Vestberg, Robert
Malkoch, Michael
Kade, Matthew
Wu, Peng
Fokin, Valery V.
Sharpless, K. Barry
Drockenmuller, Eric
Hawker, Craig J. [1 ]
机构
[1] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
[2] Royal Inst Technol, SE-10044 Stockholm, Sweden
[3] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[4] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[5] Univ Lyon 1, CNRS, UMR 5627, Lab Mat Polymeres & Biomat, F-69365 Lyon, France
关键词
dendrimers; functionalization of polymers; layer growth; thin films;
D O I
10.1002/pola.22178
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The high efficiency and mild reaction conditions associated with the Cu(I) catalyzed cycloaddition of azides and alkynes were exploited for the covalent layer-by-layer synthesis of dendritic thin films on silicon wafers. The preparation of azide and alkyne-terminated dendrimers based on bisMPA was accomplished by a divergent strategy; combinations of these monodisperse building blocks from the 2nd to the 5th generation were used for construction of the thin films. The layer-by-layer self assembly process proceeds under ambient conditions and was monitored by ellipsometry, XPS, and ATR-IR, which showed extremely regular growth of the dendritic thin films. Film thickness could be accurately controlled by both the size/generation number of the dendrimers as well as the number of layers. In comparison with linear analogues, the growth of the dendritic films was significantly more controlled and defect-free with each layer being thinner than the corresponding films prepared from the isomeric linear polymers, demonstrating the well-defined, three-dimensional nature of the dendritic architecture. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:2835 / 2846
页数:12
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