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      Self-assembly as a key player for materials nanoarchitectonics

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          ABSTRACT

          The development of science and technology of advanced materials using nanoscale units can be conducted by a novel concept involving combination of nanotechnology methodology with various research disciplines, especially supramolecular chemistry. The novel concept is called ‘nanoarchitectonics’ where self-assembly processes are crucial in many cases involving a wide range of component materials. This review of self-assembly processes re-examines recent progress in materials nanoarchitectonics. It is composed of three main sections: (1) the first short section describes typical examples of self-assembly research to outline the matters discussed in this review; (2) the second section summarizes self-assemblies at interfaces from general viewpoints; and (3) the final section is focused on self-assembly processes at interfaces. The examples presented demonstrate the strikingly wide range of possibilities and future potential of self-assembly processes and their important contribution to materials nanoarchitectonics. The research examples described in this review cover variously structured objects including molecular machines, molecular receptors, molecular pliers, molecular rotors, nanoparticles, nanosheets, nanotubes, nanowires, nanoflakes, nanocubes, nanodisks, nanoring, block copolymers, hyperbranched polymers, supramolecular polymers, supramolecular gels, liquid crystals, Langmuir monolayers, Langmuir–Blodgett films, self-assembled monolayers, thin films, layer-by-layer structures, breath figure motif structures, two-dimensional molecular patterns, fullerene crystals, metal–organic frameworks, coordination polymers, coordination capsules, porous carbon spheres, mesoporous materials, polynuclear catalysts, DNA origamis, transmembrane channels, peptide conjugates, and vesicles, as well as functional materials for sensing, surface-enhanced Raman spectroscopy, photovoltaics, charge transport, excitation energy transfer, light-harvesting, photocatalysts, field effect transistors, logic gates, organic semiconductors, thin-film-based devices, drug delivery, cell culture, supramolecular differentiation, molecular recognition, molecular tuning, and hand-operating (hand-operated) nanotechnology.

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          Most cited references351

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          Supramolecular polymerization.

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            Self-Assembly of Colloidal Nanocrystals: From Intricate Structures to Functional Materials.

            Chemical methods developed over the past two decades enable preparation of colloidal nanocrystals with uniform size and shape. These Brownian objects readily order into superlattices. Recently, the range of accessible inorganic cores and tunable surface chemistries dramatically increased, expanding the set of nanocrystal arrangements experimentally attainable. In this review, we discuss efforts to create next-generation materials via bottom-up organization of nanocrystals with preprogrammed functionality and self-assembly instructions. This process is often driven by both interparticle interactions and the influence of the assembly environment. The introduction provides the reader with a practical overview of nanocrystal synthesis, self-assembly, and superlattice characterization. We then summarize the theory of nanocrystal interactions and examine fundamental principles governing nanocrystal self-assembly from hard and soft particle perspectives borrowed from the comparatively established fields of micrometer colloids and block copolymer assembly. We outline the extensive catalog of superlattices prepared to date using hydrocarbon-capped nanocrystals with spherical, polyhedral, rod, plate, and branched inorganic core shapes, as well as those obtained by mixing combinations thereof. We also provide an overview of structural defects in nanocrystal superlattices. We then explore the unique possibilities offered by leveraging nontraditional surface chemistries and assembly environments to control superlattice structure and produce nonbulk assemblies. We end with a discussion of the unique optical, magnetic, electronic, and catalytic properties of ordered nanocrystal superlattices, and the coming advances required to make use of this new class of solids.
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              DNA origami with complex curvatures in three-dimensional space.

              We present a strategy to design and construct self-assembling DNA nanostructures that define intricate curved surfaces in three-dimensional (3D) space using the DNA origami folding technique. Double-helical DNA is bent to follow the rounded contours of the target object, and potential strand crossovers are subsequently identified. Concentric rings of DNA are used to generate in-plane curvature, constrained to 2D by rationally designed geometries and crossover networks. Out-of-plane curvature is introduced by adjusting the particular position and pattern of crossovers between adjacent DNA double helices, whose conformation often deviates from the natural, B-form twist density. A series of DNA nanostructures with high curvature--such as 2D arrangements of concentric rings and 3D spherical shells, ellipsoidal shells, and a nanoflask--were assembled.
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                Author and article information

                Journal
                Sci Technol Adv Mater
                Sci Technol Adv Mater
                TSTA
                tsta20
                Science and Technology of Advanced Materials
                Taylor & Francis
                1468-6996
                1878-5514
                2019
                31 January 2019
                : 20
                : 1
                : 51-95
                Affiliations
                [a ] WPI-MANA, National Institute for Materials Science (NIMS) , Ibaraki, Japan
                [b ] Department of Advanced Materials Science, Graduate School of Frontier Sciences, The University of Tokyo , Kashiwa, Japan
                Author notes
                CONTACT Katsuhiko Ariga ARIGA.Katsuhiko@ 123456nims.go.jp WPI-MANA, National Institute for Materials Science (NIMS) , 1-1 Namiki, Tsukuba, Ibaraki305-0044, Japan
                Article
                1553108
                10.1080/14686996.2018.1553108
                6374972
                30787960
                1186b194-2026-4d56-bdab-18c7a29fca24
                © 2019 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis Group

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 September 2018
                : 23 November 2018
                : 25 November 2018
                Page count
                Figures: 28, References: 349, Pages: 45
                Funding
                Funded by: Core Research for Evolutional Science and Technology 10.13039/501100003382
                Award ID: JPMJCR1665
                Funded by: Japan Society for the Promotion of Science 10.13039/501100001691
                Award ID: JP16H06518
                This work was supported by the Core Research for Evolutional Science and Technology [Grant Number JPMJCR1665] and Japan Society for the Promotion of Science [Grant Number JP16H06518].
                Categories
                Organic and Soft Materials (Colloids, Liquid Crystals, Gel, Polymers)

                nanoarchitectonics,self-assembly,interface,nanomaterial,20 organic and soft materials (colloids, liquid crystals, gel, polymers),101 self-assembly / self-organized materials

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