scholarly journals Hierarchical self-assembly of polydisperse colloidal bananas into a two-dimensional vortex phase

2021 ◽  
Vol 118 (33) ◽  
pp. e2107241118
Author(s):  
Carla Fernández-Rico ◽  
Roel P. A. Dullens

Self-assembly of microscopic building blocks into highly ordered and functional structures is ubiquitous in nature and found at all length scales. Hierarchical structures formed by colloidal building blocks are typically assembled from monodisperse particles interacting via engineered directional interactions. Here, we show that polydisperse colloidal bananas self-assemble into a complex and hierarchical quasi–two-dimensional structure, called the vortex phase, only due to excluded volume interactions and polydispersity in the particle curvature. Using confocal microscopy, we uncover the remarkable formation mechanism of the vortex phase and characterize its exotic structure and dynamics at the single-particle level. These results demonstrate that hierarchical self-assembly of complex materials can be solely driven by entropy and shape polydispersity of the constituting particles.

ChemPhysChem ◽  
2020 ◽  
Vol 21 (10) ◽  
pp. 1044-1051 ◽  
Author(s):  
Diego Carnevale ◽  
Marcel Hollenstein ◽  
Geoffrey Bodenhausen

2013 ◽  
Vol 5 (3) ◽  
Author(s):  
Magesh Sadasivam ◽  
Pinar Avci ◽  
Gaurav K. Gupta ◽  
Shanmugamurthy Lakshmanan ◽  
Rakkiyappan Chandran ◽  
...  

AbstractPhotodynamic therapy (PDT) employs the combination of non-toxic photosensitizers (PS) together with harmless visible light of the appropriate wavelength to produce reactive oxygen species that kill unwanted cells. Because many PS are hydrophobic molecules prone to aggregation, numerous drug delivery vehicles have been tested to solubilize these molecules, render them biocompatible and enhance the ease of administration after intravenous injection. The recent rise in nanotechnology has markedly expanded the range of these nanoparticulate delivery vehicles beyond the well-established liposomes and micelles. Self-assembled nanoparticles are formed by judicious choice of monomer building blocks that spontaneously form a well-oriented 3-dimensional structure that incorporates the PS when subjected to the appropriate conditions. This self-assembly process is governed by a subtle interplay of forces on the molecular level. This review will cover the state of the art in the preparation and use of self-assembled liposomal nanoparticles within the context of PDT.


2015 ◽  
Vol 181 ◽  
pp. 481-487 ◽  
Author(s):  
David J. Schiffrin

Some four years ago, one of the participants in this Discussion (Prof. Nicholas Kotov) predicted that: “within five years we shall see multiple examples of electronic, sensor, optical and other devices utilizing self-assembled superstructures” (N. A. Kotov, J. Mater. Chem., 2011, 21, 16673–16674). Although this prediction came partially to fruition, we have witnessed an unprecedented interest in the properties of materials at the nanoscale. The point highlighted by Kotov, however, was the importance of self-assembly of structures from well characterised building blocks to yield hierarchical structures, hopefully with predictable properties, a concept that is an everyday pursuit of synthetic chemists. This Discussion has brought together researchers from a wide range of disciplines, i.e., colloid science, modelling, nanoparticle synthesis and organisation, magnetic and optical materials, and new imaging methods, within the excellent traditional Faraday Discussion format, to discuss advances in areas relevant to the main theme of the meeting.


2018 ◽  
Vol 6 (31) ◽  
pp. 8405-8410 ◽  
Author(s):  
Furkan H. Isikgor ◽  
Chilla Damodara Reddy ◽  
Mengsha Li ◽  
Hikmet Coskun ◽  
Bichen Li ◽  
...  

2D hybrid perovskites are formed through the self assembly of polyaniline with PbI6 octahedra.


2015 ◽  
Vol 6 ◽  
pp. 632-639 ◽  
Author(s):  
Ping Du ◽  
David Bléger ◽  
Fabrice Charra ◽  
Vincent Bouchiat ◽  
David Kreher ◽  
...  

Two-dimensional (2D), supramolecular self-assembly at surfaces is now well-mastered with several existing examples. However, one remaining challenge to enable future applications in nanoscience is to provide potential functionalities to the physisorbed adlayer. This work reviews a recently developed strategy that addresses this key issue by taking advantage of a new concept, Janus tecton materials. This is a versatile, molecular platform based on the design of three-dimensional (3D) building blocks consisting of two faces linked by a cyclophane-type pillar. One face is designed to steer 2D self-assembly onto C(sp2)-carbon-based flat surfaces, the other allowing for the desired functionality above the substrate with a well-controlled lateral order. In this way, it is possible to simultaneously obtain a regular, non-covalent paving as well as supramolecular functionalization of graphene, thus opening interesting perspectives for nanoscience applications.


2016 ◽  
Vol 72 (4) ◽  
pp. 285-290 ◽  
Author(s):  
Xiang-Wen Wu ◽  
Shi Yin ◽  
Wan-Fu Wu ◽  
Jian-Ping Ma

Bimetallic macrocyclic complexes have attracted the attention of chemists and various organic ligands have been used as molecular building blocks, but supramolecular complexes based on semi-rigid organic ligands containing 1,2,4-triazole have remained rare until recently. It is easier to obtain novel topologies by making use of asymmetric semi-rigid ligands in the self-assembly process than by making use of rigid ligands. A new semi-rigid ligand, 3-[(pyridin-4-ylmethyl)sulfanyl]-5-(quinolin-2-yl)-4H-1,2,4-triazol-4-amine (L), has been synthesized and used to generate two novel bimetallic macrocycle complexes, namely bis{μ-3-[(pyridin-4-ylmethyl)sulfanyl]-5-(quinolin-2-yl)-4H-1,2,4-triazol-4-amine}bis[(methanol-κO)(nitrato-κ2O,O′)nickel(II)] dinitrate, [Ni2(NO3)2(C17H14N6S)2(CH3OH)2](NO3)2, (I), and bis{μ-3-[(pyridin-4-ylmethyl)sulfanyl]-5-(quinolin-2-yl)-4H-1,2,4-triazol-4-amine}bis[(methanol-κO)(nitrato-κ2O,O′)zinc(II)] dinitrate, [Zn2(NO3)2(C17H14N6S)2(CH3OH)2](NO3)2, (II), by solution reactions with the inorganic saltsM(NO3)2(M= Ni and Zn, respectively) in mixed solvents. In (I), two NiIIcations with the same coordination environment are linked byLligands through Ni—N bonds to form a bimetallic ring. Compound (I) is extended into a two-dimensional network in the crystallographicacplaneviaN—H...O, O—H...N and O—H...O hydrogen bonds, and neighbouring two-dimensional planes are parallel and form a three-dimensional structureviaπ–π stacking. Compound (II) contains two bimetallic rings with the same coordination environment of the ZnIIcations. The ZnIIcations are bridged byLligands through Zn—N bonds to form the bimetallic rings. One type of bimetallic ring constructs a one-dimensional nanotubeviaO—H...O and N—H...O hydrogen bonds along the crystallographicadirection, and the other constructs zero-dimensional molecular cagesviaO—H...O and N—H...O hydrogen bonds. They are interlinked into a two-dimensional network in theacplane through extensive N—H...O hydrogen bonds, and a three-dimensional supramolecular architecture is formedviaπ–π interactions between the centroids of the benzene rings of the quinoline ring systems.


Author(s):  
Dong Liu ◽  
Ni-Ya Li

Colourless crystals of the title compound, [Cd2(C7H4IO2)4(C12H10N2)(H2O)2]n, were obtained by the self-assembly of Cd(NO3)2·4H2O, 1,2-bis(pyridin-4-yl)ethene (bpe) and 4-iodobenzoic acid (4-IBA). Each CdIIatom is seven-coordinated in a pentagonal–bipyramidal coordination environment by four carboxylate O atoms from two different 4-IBA ligands, two O atoms from two water molecules and one N atom from a bpe ligand. The CdIIcentres are bridged by the aqua molecules and bpe ligands, which lie across centres of inversion, to give a two-dimensional net. Topologically, taking the CdIIatoms as nodes and the μ-aqua and μ-bpe ligands as linkers, the two-dimensional structure can be simplified as a (6,3) network.


Science ◽  
2020 ◽  
Vol 369 (6506) ◽  
pp. 950-955
Author(s):  
Carla Fernández-Rico ◽  
Massimiliano Chiappini ◽  
Taiki Yanagishima ◽  
Heidi de Sousa ◽  
Dirk G. A. L. Aarts ◽  
...  

Understanding the impact of curvature on the self-assembly of elongated microscopic building blocks, such as molecules and proteins, is key to engineering functional materials with predesigned structure. We develop model “banana-shaped” colloidal particles with tunable dimensions and curvature, whose structure and dynamics are accessible at the particle level. By heating initially straight rods made of SU-8 photoresist, we induce a controllable shape deformation that causes the rods to buckle into banana-shaped particles. We elucidate the phase behavior of differently curved colloidal bananas using confocal microscopy. Although highly curved bananas only form isotropic phases, less curved bananas exhibit very rich phase behavior, including biaxial nematic phases, polar and antipolar smectic-like phases, and even the long-predicted, elusive splay-bend nematic phase.


MRS Bulletin ◽  
2004 ◽  
Vol 29 (2) ◽  
pp. 91-95 ◽  
Author(s):  
Vinothan N. Manoharan ◽  
David J. Pine

AbstractAn effective way to build ordered materials with micrometer- or submicrometer-sized features is to pack together monodisperse (equal-sized) colloidal particles. But most monodisperse particles in this size range are spheres, and thus one problem in building new micrometer-scale ordered materials is controlling how spheres pack. In this article, we discuss how this problem can be approached by constructing and studying packings in the few-sphere limit. Confinement of particles within containers such as micropatterned holes or spherical droplets can lead to some unexpected and diverse types of polyhedra that may become building blocks for more complex materials. The packing processes that form these polyhedra may also be a source of disorder in dense bulk suspensions.


Author(s):  
Kunal S. Mali ◽  
Steven De Feyter

Self-assembled physisorbed monolayers consist of regular two-dimensional arrays of molecules. Two-dimensional self-assembly of organic and metal–organic building blocks is a widely used strategy for nanoscale functionalization of surfaces. These supramolecular nanostructures are typically sustained by weak non-covalent forces such as van der Waals, electrostatic, metal–ligand, dipole–dipole and hydrogen bonding interactions. A wide variety of structurally very diverse monolayers have been fabricated under ambient conditions at the liquid–solid and air–solid interface or under ultra-high-vacuum (UHV) conditions at the UHV–solid interface. The outcome of the molecular self-assembly process depends on a variety of factors such as the nature of functional groups present on assembling molecules, the type of solvent, the temperature at which the molecules assemble and the concentration of the building blocks. The objective of this review is to provide a brief account of the progress in understanding various parameters affecting two-dimensional molecular self-assembly through illustration of some key examples from contemporary literature.


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