Colloids with valence and specific directional bonding
Author(s) -
Yufeng Wang,
Yu Wang,
Dana R. Breed,
Vinothan Manoharan,
Lang Feng,
Andrew D. Hollingsworth,
Marcus Weck,
David J. Pine
Publication year - 2012
Publication title -
nature
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 15.993
H-Index - 1226
eISSN - 1476-4687
pISSN - 0028-0836
DOI - 10.1038/nature11564
Subject(s) - colloid , colloidal particle , valence (chemistry) , chemical physics , nanotechnology , molecule , materials science , tetrahedron , atomic orbital , crystallography , chemistry , physics , organic chemistry , electron , quantum mechanics
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.
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