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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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Short to ultrashort peptide-based hydrogels as a platform for biomedical applications.

TL;DR: The progress of research in the rapidly expanding field of short to ultrashort peptide-based hydrogels and their possible applications is reviewed and special attention is paid to address and review this field with regard to the stability of peptides, particularly to enzymatic degradation.
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Highly controllable and green reduction of graphene oxide to flexible graphene film with high strength

TL;DR: Graphene film with high strength was fabricated by the assembly of graphene sheets derived from graphene oxide (GO) in an effective and environmentally friendly approach as discussed by the authors, which was achieved with sodium citrate as a facile reductant, in which the reduction process was monitored by XRD analysis and UV-vis absorption spectra.
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Time sensitive, temperature and pH responsive photoluminescence behaviour of a melamine containing bicomponent hydrogel

TL;DR: In this paper, the storage modulus (G′) is invariant with frequency supporting the formation of thermoreversible hydrogel and a probable cause is attributed to number of H-bonds, which follows the same order in nanofibers.
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Preparation of millimeter-sized chitosan/carboxymethyl cellulose hollow capsule and its dye adsorption properties

TL;DR: The CTS/CMC hollow capsule exhibited distinct removal performance for three typical dyes of methylene blue, methyl orange and acid blue-113 with different charged functional groups and might have potential applications in the dye removal, the mixed dye wastewater and drug release.
References
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Journal ArticleDOI

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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