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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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Journal ArticleDOI

Peptide self-assembly in functional polymer science and engineering

TL;DR: Several types of self-assembling peptides have been engineered as discussed by the authors, which represent a significant advancement in the molecular engineering of protein fragments for diverse technological innovations and represent simple, versatile and easy to modify and to produce.
Journal ArticleDOI

Chromonic liquid crystals: properties and applications as functional materials

TL;DR: This review summarizes the research on chromonic liquid crystals in the last two decades, which embraced the studies of commercially available chromonic dyes and drugs, the syntheses and investigations of molecularly designed mesogens, the invention of novel processes for aligning chromonicLiquid crystals, and the development of new applications as functional materials and biosensors.
Journal ArticleDOI

Colloidal graphene quantum dots with well-defined structures.

TL;DR: Graphene QDs are synthesized through stepwise, well-controlled organic chemistry, achieving structures with an atomic precision that has not been possible for any other semiconductor materials, and extraordinarily slow "electron cooling"--the relaxation of electrons from high excited states to lower ones is observed.
Journal ArticleDOI

Hierarchical formation of helical supramolecular polymers via stacking of hydrogen-bonded pairs in water

TL;DR: Chiral side chains attached to the ureido-s-triazine units bias the helicity of these columns as concluded from CD spectroscopy and “Sergeants and Soldiers” experiments.
Proceedings ArticleDOI

Combinatorial optimization problems in self-assembly

TL;DR: Two combinatorial optimization problems related to efficient self-assembly of shapes in the Tile Assembly Model of self- assembly proposed by Rothemund and Winfree are studied, and it is proved that the first problem is NP-complete in general, and polynomial time solvable on trees and squares.
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