Three-dimensional self-assembly of millimetre-scale components

被引:231
作者
Terfort, A [1 ]
Bowden, N [1 ]
Whitesides, GM [1 ]
机构
[1] HARVARD UNIV, DEPT CHEM & CHEM BIOL, CAMBRIDGE, MA 02138 USA
关键词
D O I
10.1038/386162a0
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 spontaneous association of molecules, termed molecular self-assembly, is a successful strategy for the generation of large, structured molecular aggregates(1). The most important source of inspiration for this strategy is the biological world, in which many processes involve interfacial interactions and shape selectivity that guide the formation of complex, multicomponent three-dimensional structures. The success of molecular self-assembly notwithstanding, many objectives in science and technology require the assembly of components that are much larger than molecules: examples include microelectronic and microelectromechanical systems, sensors and microanalytical and microsynthetic devices(2). Photolithography, the principal technique used to make such microstructures, has certain limitations: it cannot easily form non-planar or three-dimensional structures; it generates structures that are metastable; and it can be used only for a Limited set of materials(3), Here we describe an approach for the self-assembly of millimetre-scale components that uses two concepts to direct the assembly process: shape recognition and the minimization of liquid-liquid interfacial free energies(4). These play a role in other spontaneous self-assembly phenomena, such as the formation of bubble rafts(5,6), the patterned dewetting of surfaces(7,8), and the coalescence of liquid drops(9). We apply self-assembled monolayer molecular films(10) to the surfaces of shaped macroscopic objects to render them hydrophilic or hydrophobic, depending on the terminal groups of the bound molecules. In aqueous solution, hydrophobic surfaces bearing a thin film of a hydrophobic, lubricating liquid adhere to similar surfaces with complementary shapes, while being able to adjust their relative alignment to ensure a good fit. In this way, the components assemble into well defined aggregates, which can be bound permanently when the hydrophobic liquid films consist of a polymerizable adhesive.
引用
收藏
页码:162 / 164
页数:3
相关论文
共 10 条
[1]   SELF-ORGANIZATION OF ORGANIC LIQUIDS ON PATTERNED SELF-ASSEMBLED MONOLAYERS OF ALKANETHIOLATES ON GOLD [J].
BIEBUYCK, HA ;
WHITESIDES, GM .
LANGMUIR, 1994, 10 (08) :2790-2793
[2]   FORMATION AND COALESCENCE OF BUBBLES AND DROPLETS [J].
BLASS, E .
CHEMIE INGENIEUR TECHNIK, 1988, 60 (12) :935-947
[3]   USE OF A PATTERNED SELF-ASSEMBLED MONOLAYER TO CONTROL THE FORMATION OF A LIQUID RESIST PATTERN ON A GOLD SURFACE [J].
GORMAN, CB ;
BIEBUYCK, HA ;
WHITESIDES, GM .
CHEMISTRY OF MATERIALS, 1995, 7 (02) :252-254
[4]  
Harrison DJ, 1996, SENSOR ACTUAT B-CHEM, V33, P105, DOI 10.1016/0925-4005(96)01932-6
[5]   USE OF MINIMAL FREE-ENERGY AND SELF-ASSEMBLY TO FORM SHAPES [J].
KIM, E ;
WHITESIDES, GM .
CHEMISTRY OF MATERIALS, 1995, 7 (06) :1257-1264
[6]  
Moreau W.M., 1988, SEMICONDUCTOR LITHOG
[7]   FORMATION OF SELF-ASSEMBLED MONOLAYERS BY CHEMISORPTION OF DERIVATIVES OF OLIGO(ETHYLENE GLYCOL) OF STRUCTURE HS(CH2)11(OCH2CH2)META-OH ON GOLD [J].
PALEGROSDEMANGE, C ;
SIMON, ES ;
PRIME, KL ;
WHITESIDES, GM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (01) :12-20
[8]   Self-assembly in natural and unnatural systems [J].
Philp, D ;
Stoddart, JF .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1996, 35 (11) :1154-1196
[9]   PROTON IMPLANTATION INTO GAAS - TRANSMISSION ELECTRON-MICROSCOPY RESULTS [J].
SCHOBER, T ;
FRIEDRICH, J ;
ALTMANN, A .
JOURNAL OF APPLIED PHYSICS, 1992, 71 (05) :2206-2210
[10]   BUBBLE RAFT MODEL FOR AN AMORPHOUS ALLOY [J].
SIMPSON, AW ;
HODKINSO.PH .
NATURE, 1972, 237 (5354) :320-+