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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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Templated Hierarchical Self-Assembly of Poly(p-aryltriazole) Foldamers

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A Kind of Coordination Complex Cement for the Self-Assembly of Superstructure

TL;DR: A facile route of assembling particles into superstructures utilizing Mo-polydopamine complex as the binder and curing agent is established and a side-by-side adsorption and growth mechanism in a water/ethanol system is derived.
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Subtlety in the reactivity of a diketo phosphorus ylide towards mercuric halides: the unprecedented O-coordination of α-acetyl-α-benzoylmethylenetriphenylphosphorane to Hg(II)

TL;DR: In this article, the ylide with HgX2 (X = Cl, Br or I) leads to the regiospecific binding of the acetyl oxygen to soft Hg(II), producing a chloro complex with (2 + 2) coordination and isostructural dimeric bromo and iodo complexes containing halogen bridges with tetrahedral configurations around the metal centres.
Book ChapterDOI

Tissue P Systems with Contextual and Rewriting Rules

TL;DR: This paper uses string objects as the underlying data structure for tissue P systems, a restricted form of contextual rules and rewriting rules, and obtains two characterizations of recursively enumerable languages.
References
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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.
Journal ArticleDOI

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.
Journal ArticleDOI

Supramolecular Chemistry—Scope and Perspectives Molecules, Supermolecules, and Molecular Devices (Nobel Lecture)

TL;DR: Developments in molecular and supramolecular design and engineering open perspectives towards the realization of molecular photonic, electronic, and ionic devices that would perform highly selective recognition, reaction, and transfer operations for signal and information processing at the molecular level.
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