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

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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Strategies to utilize naturally occurring protein architectures as nanovehicles for hydrophobic nutraceuticals

TL;DR: Reassembled casein micelles, ferritin (or apoferritin) and legume oligomeric protein nanoparticles are demonstrated to perform as outstanding nanovehicles for improving water dispersion, stability and bioactivities of many nutraceuticals or drugs.
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Self-assembled cyclic oligothiophene nanotubes: Electronic properties from a dispersion-corrected hybrid functional

TL;DR: The band structure and size scaling of electronic properties in self-assembled cyclic oligothiophene nanotubes are investigated using density functional theory in this article, where a dispersion-corrected Becke three-parameter Lee-Yang-Parr-D (B3LYP-D) hybrid functional in conjunction with all-electron basis sets and one-dimensional periodic boundary conditions are used to simultaneously describe both the π-π stacking interactions and the global electronic band structure.
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Hierarchical Assembly of Organic/Inorganic Building Molecules with π–π Interactions

TL;DR: In this paper, hierarchical assemblies of perylenetetracarboxylic diimide bridged silsesquioxane (PDBS) with controlled structure at multi-length scale are studied using both experimental and computational methods.
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Cyano-Functionalized Triarylamines on Coinage Metal Surfaces: Interplay of Intermolecular and Molecule-Substrate Interactions.

TL;DR: The significant variety in the molecular self-assembly of the cyano-functionalized triarylamine derivatives on these coinage metal surfaces is explained by differences in molecular mobility and the subtle interplay between intermolecular and molecule-substrate interactions.
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Orthogonal Recognition Processes Drive the Assembly and Replication of a [2]Rotaxane.

TL;DR: The interplay between the recognition and reaction processes in this reaction network results in the formation of undesirable pseudorotaxane complexes, causing thread formation to exceed rotaxane formation in the current experimental system.
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