Higher-order organization by mesoscale self-assembly and transformation of hybrid nanostructures

被引:1644
作者
Cölfen, H
Mann, S
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TH, Avon, England
[2] Univ Bristol, Ctr Organized Matter Chem, Bristol BS8 1TH, Avon, England
[3] Max Planck Inst Colloids & Interfaces, Potsdam, Germany
关键词
biomineralization; crystal growth; materials science; self-assembly; solid-state chemistry;
D O I
10.1002/anie.200200562
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The organization of nanostructures across extended length scales is a key challenge in the design of integrated materials with advanced functions. Current approaches tend to be based on physical methods, such as patterning, rather than the spontaneous chemical assembly and transformation of building blocks across multiple length scales. It should be possible to develop a chemistry of organized matter based on emergent processes in which time- and scale-dependent coupling of interactive components generate higher-order architectures with embedded structure. Herein we highlight how the interplay between aggregation and crystallization can give rise to mesoscale self-assembly and cooperative transformation and reorganization of hybrid inorganic-organic building blocks to produce single-crystal mosaics, nanoparticle arrays, and emergent nanostructures with complex form and hierarchy. We propose that similar mesoscale processes are also relevant to models of matrix-mediated nucleation in biomineralization.
引用
收藏
页码:2350 / 2365
页数:16
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