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Self-assembling wholly synthetic systems

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TLDR
The idea of synthesizing, efficiently and precisely, large and complex artificial molecular assemblies and supramolecular arrays from simple modular components has resulted in some chemical scientists using self-assembly in chemical synthesis, thus mimicking the many and beautiful examples in nature as mentioned in this paper.
Abstract
The idea of synthesizing, efficiently and precisely, large and complex artificial molecular assemblies and supramolecular arrays from simple modular components has resulted in some chemical scientists using self-assembly in chemical synthesis, thus mimicking the many and beautiful examples of this paradigm in nature. Coordination of organic ligands around metal centres, hydrogen bonding interactions, and donor/acceptor π-π-stacking interactions have been employed to self-assemble numerous structures and superstructures, such as double and triple helices, grids, cages, and square-like networks, two- and three-dimensional aggregates, tubular ensembles, as well as a large number of mechanically interlocked molecular compounds, such as catenanes, rotaxanes, and knots.

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

TL;DR: 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.
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Synthetic supramolecular chemistry

TL;DR: For many decades, the construction of organic compounds in the laboratory has relied on the remarkable abilities of the 20th century "alchemists" to make and break covalent bonds as discussed by the authors.
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Self-Assembly, Spectroscopic, and Electrochemical Properties of [n]Rotaxanes1

TL;DR: In this article, the authors developed an approach to self-assembling [n] rotaxanes incorporating πelectron deficient bipyridinium-based dumbbell-shaped components and π-electron rich hydroquinone-based macrocycles.
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Controlling Self-Assembly

TL;DR: In this paper, the stereoelectronic information imprinted in the components is crucial in controlling the extent of the formation of the complexes and compounds in the first place; moreover, it has a very significant influence on the relative orientations and motions of the components.
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The Mechanism of the Slippage Approach to Rotaxanes. Origin of the “All-or-Nothing” Substituent Effect†

TL;DR: In this article, the AMBER* force field was simulated by the passage of the bis-p-phenylene-34-crown-10 macrocycle over four 4-R-phenyl-bis(4-tert-butyl-pharmyl)-methane model stoppers.
References
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Book

Principles of Nucleic Acid Structure

TL;DR: The goal of this series is to pinpoint areas of chemistry where recent progress has outpaced what is covered in any available textbooks, and then seek out and persuade experts in these fields to produce relatively concise but instructive introductions to their fields.
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Molecular self-assembly and nanochemistry: a chemical strategy for the synthesis of nanostructures.

TL;DR: The ability to prepare structures in the upper part of this range of sizes 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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Perspectives in Supramolecular Chemistry—From Molecular Recognition towards Molecular Information Processing and Self‐Organization

TL;DR: In this article, the authors proposed a self-assembly approach for the generation of a well-defined supramolecular architecture by self-assembling from their components under a given set of conditions.

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

TL;DR: 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.
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