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Molecular self-assembly and nanochemistry: A chemical strategy for the synthesis of nanostructures

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TLDR
In this article, self-assembly is defined as the spontaneous association of molecules under equilibrium conditions into stable, structurally well-defined aggregates joined by noncovalent bonds.
Abstract
Molecular self-assembly is the spontaneous association of molecules under equilibrium conditions into stable, structurally well-defined aggregates joined by noncovalent bonds. Molecular self-assembly is ubiquitous in biological systems and underlies the formation of a wide variety of complex biological structures. Understanding self-assembly and the associated noncovalent interactions that connect complementary interacting molecular surfaces in biological aggregates is a central concern in structural biochemistry. Self-assembly is also emerging as a new strategy in chemical synthesis, with the potential of generating nonbiological structures with dimensions of 1 to 10(2) nanometers (with molecular weights of 10(4) to 10(10) daltons). Structures in the upper part of this range of sizes are presently inaccessible through chemical synthesis, and the ability to prepare them would open a route to structures comparable in size (and perhaps complementary in function) to those that can be prepared by microlithography and other techniques of microfabrication.

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Citations
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Folding DNA to create nanoscale shapes and patterns

TL;DR: This work describes a simple method for folding long, single-stranded DNA molecules into arbitrary two-dimensional shapes, which can be programmed to bear complex patterns such as words and images on their surfaces.
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Fabrication of novel biomaterials through molecular self-assembly.

TL;DR: Two complementary strategies can be used in the fabrication of molecular biomaterials as discussed by the authors : chemical complementarity and structural compatibility, both of which confer the weak and noncovalent interactions that bind building blocks together during self-assembly.
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Design and self-assembly of two-dimensional DNA crystals

TL;DR: The design and observation of two-dimensional crystalline forms of DNA that self-assemble from synthetic DNA double-crossover molecules that create specific periodic patterns on the nanometre scale are reported.
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Nanoparticles, Proteins, and Nucleic Acids: Biotechnology Meets Materials Science

TL;DR: This review is focused on current approaches emerging at the intersection of materials research, nanosciences, and molecular biotechnology, which is closely associated with both the physical and chemical properties of organic and inorganic nanoparticles.
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Self-assembly of DNA into nanoscale three-dimensional shapes

TL;DR: This work demonstrates the design and assembly of nanostructures approximating six shapes—monolith, square nut, railed bridge, genie bottle, stacked cross, slotted cross, and heterotrimeric wireframe icosahedra with precisely controlled dimensions.
References
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Hydrogen-bonded layers of hydrogentartrate anions: two-dimensional building blocks for crystal engineering

TL;DR: In this article, the authors investigated the properties of hydrogen-bond patterns in a family of ionic crystals and established the use of hydrogen bonding as a potential design strategy for crystal engineering.
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Coil-ring-coil block copolymers as building blocks for supramolecular hollow cylindrical brushes

TL;DR: Solvent-induced self-assembly of oligomer-substituted shape-persistent macrocycles leads to the formation of cylindrical aggregates, which have been fully characterized in solution and can be described as supramolecular hollow polymer brushes.
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Responsive helical self-assembly of AgNO3 and melamine through asymmetric coordination for Ag nanochain synthesis.

TL;DR: Responsive nanohelices can be self-assembled via asymmetric coordination bonding between AgNO3 and melamine and silver nanochains composed of nanoparticles can be synthesized simply by photo-reduction of the above complex.
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Design of rapidly assembling supramolecular systems responsive to synchronized stimuli

TL;DR: In this paper, a review of supramolecular self-assembling systems based on rapidly responsive hydrogels from polymeric hosts and low molecular weight guests is presented, showing that dual cooperative interactions, i.e. specific host-guest and intermolecular ionic interactions, play a dominant role in the fast aggregation process.
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Anthracene-Containing [2]Rotaxanes: Synthesis, Spectroscopic, and Electrochemical Properties

TL;DR: In this paper, two dumbbell-shaped compounds (8 and 11) were synthesized, each composed of two polyether chains intercepted by a 1,4-dioxybenzene recognition site, terminated by tetraarylmethane-based stoppers, and emanating from a central 9,10- or a 2,6-dioxyanthracene unit.
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