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Controlling molecular deposition and layer structure with supramolecular surface assemblies

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TLDR
This work uses hydrogen bonding to guide the assembly of two types of molecules into a two-dimensional open honeycomb network that then controls and templates new surface phases formed by subsequently deposited fullerene molecules, and finds that the open network acts as aTwo-dimensional array of large pores of sufficient capacity to accommodate several large guest molecules.
Abstract
Selective non-covalent interactions have been widely exploited in solution-based chemistry to direct the assembly of molecules into nanometre-sized functional structures such as capsules, switches and prototype machines1,2,3,4,5. More recently, the concepts of supramolecular organization have also been applied to two-dimensional assemblies on surfaces6,7 stabilized by hydrogen bonding8,9,10,11,12,13,14, dipolar coupling15,16,17 or metal co-ordination18. Structures realized to date include isolated rows8,13,14,15, clusters9,10,18 and extended networks10,11,12,17, as well as more complex multi-component arrangements16. Another approach to controlling surface structures uses adsorbed molecular monolayers to create preferential binding sites that accommodate individual target molecules19,20. Here we combine these approaches, by using hydrogen bonding to guide the assembly of two types of molecules into a two-dimensional open honeycomb network that then controls and templates new surface phases formed by subsequently deposited fullerene molecules. We find that the open network acts as a two-dimensional array of large pores of sufficient capacity to accommodate several large guest molecules, with the network itself also serving as a template for the formation of a fullerene layer.

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Perylene bisimide dyes as versatile building blocks for functional supramolecular architectures

TL;DR: Perylene bisimide dyes and their organization into supramolecular architectures through hydrogen-bonding, metal ion coordination and pi-pi-stacking is discussed; further self-assembly leading to nano- and meso-scopic structures and liquid-crystalline compounds is also addressed.
Journal ArticleDOI

Engineering atomic and molecular nanostructures at surfaces

TL;DR: This work presents an autonomous ordering and assembly of atoms and molecules on atomically well-defined surfaces that combines ease of fabrication with exquisite control over the shape, composition and mesoscale organization of the surface structures formed.
Journal ArticleDOI

Nano-architectures by covalent assembly of molecular building blocks

TL;DR: It is shown that covalently bound molecular nanostructures can be formed on a gold surface upon thermal activation of porphyrin building blocks and their subsequent chemical reaction at predefined connection points, and it is demonstrated that the topology of these nanostructure can be precisely engineered by controlling the chemical structure of the building blocks.
Journal ArticleDOI

Molecular architectonic on metal surfaces.

TL;DR: This review delineates the principles of noncovalent synthesis on metal substrates under ultrahigh vacuum conditions and briefly assesses the pertaining terminology-self-assembly, self-organization, and self-organized growth.
References
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Journal ArticleDOI

Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model

TL;DR: In this paper, a new parametric quantum mechanical molecular model, AM1 (Austin Model l), based on the NDDO approximation, is described, in which the major weaknesses of MNDO, in particular failure to reproduce hydrogen bonds, have been overcome without any increase in computing time.
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DNA in a material world

TL;DR: The specific bonding of DNA base pairs provides the chemical foundation for genetics and this powerful molecular recognition system can be used in nanotechnology to direct the assembly of highly structured materials with specific nanoscale features, as well as in DNA computation to process complex information.
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Artificial Molecular Machines.

TL;DR: The aim of this review is to present a unified view of the field of molecular machines by focusing on past achievements, present limitations, and future perspectives.
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Toward complex matter: supramolecular chemistry and self-organization.

TL;DR: As the wind of time blows into the sails of space, the unfolding of the universe nurtures the evolution of matter under the pressure of information.
Journal ArticleDOI

Noncovalent synthesis using hydrogen bonding

TL;DR: Noncovalent synthesis based on the reversible formation of multiple hydrogen bonds is described and the development of novel materials (nanotubes, liquid crystals, polymers, etc.) and principles that recently have emanated from this intriguing field of research are summarized.
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