Colloids with valence and specific directional bonding

被引:910
作者
Wang, Yufeng [3 ,4 ]
Wang, Yu [3 ,4 ]
Breed, Dana R. [5 ]
Manoharan, Vinothan N. [6 ,7 ]
Feng, Lang [1 ,2 ]
Hollingsworth, Andrew D. [1 ,2 ]
Weck, Marcus [3 ,4 ]
Pine, David J. [1 ,2 ]
机构
[1] NYU, Ctr Soft Matter Res, New York, NY 10003 USA
[2] NYU, Dept Phys, New York, NY 10003 USA
[3] NYU, Inst Mol Design, New York, NY 10003 USA
[4] NYU, Dept Chem, New York, NY 10003 USA
[5] Dow Chem Co USA, Freeport, TX 77541 USA
[6] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[7] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
ASYMMETRIC FUNCTIONALIZATION; CLUSTERS; NANOPARTICLES; PARTICLES; ANISOTROPY;
D O I
10.1038/nature11564
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to design and assemble three-dimensional structures from colloidal particles is limited by the absence of specific directional bonds. As a result, complex or low-coordination structures, common in atomic and molecular systems, are rare in the colloidal domain. Here we demonstrate a general method for creating the colloidal analogues of atoms with valence: colloidal particles with chemically distinct surface patches that imitate hybridized atomic orbitals, including sp, sp(2), sp(3), sp(3)d, sp(3)d(2) and sp(3)d(3). Functionalized with DNA with single-stranded sticky ends, patches on different particles can form highly directional bonds through programmable, specific and reversible DNA hybridization. These features allow the particles to self-assemble into 'colloidal molecules' with triangular, tetrahedral and other bonding symmetries, and should also give access to a rich variety of new microstructured colloidal materials.
引用
收藏
页码:51 / U61
页数:6
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