Highly ordered Langmuir-Blodgett films of amphiphilic poly(propylene imine) dendrimers

被引:17
|
作者
Su, Aihua
Tan, Susheng
Thapa, Prem
Flanders, Bret N.
Ford, Warren T.
机构
[1] Oklahoma State Univ, Microscopy Lab, Stillwater, OK 74074 USA
[2] Oklahoma State Univ, Dept Chem, Stillwater, OK 74078 USA
[3] Oklahoma State Univ, Dept Phys, Stillwater, OK 74078 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2007年 / 111卷 / 12期
关键词
D O I
10.1021/jp0683566
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three amphiphilic poly(propylene imine) (PPI) dendrimers were synthesized by (1) attaching dodecanoyl chains to a PPI (DAB-dendr-(NH2)(8)) dendrimer core, (2) reducing the amide groups to secondary amines, and (3) methylating the secondary amines to tertiary amines. Monolayers of all three dendrimers on water were compressed to areas of 160 A(2)/molecule. The monolayers of the dendrimers were transferred to newly cleaved mica by the Langmuir-Blodgett method. Atomic force microscopy (AFM) measurements showed that the amphiphilic dendrimers formed stable homogeneous monolayers with surface roughness < 0.5 nm on mica. High-resolution AFM images displayed tetragonal order of a two-dimensional crystal with alkyl chain-to-chain spacing of 0.4-0.5 nm. Differential scanning calorimetry experiments detected glass transitions of the bulk dendrimers in the range of -12 to -60 degrees C and endothermic transitions from more ordered to less ordered molecular packing at higher temperatures.
引用
收藏
页码:4695 / 4701
页数:7
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