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Journal ArticleDOI

(Nano)mechanical Motion Triggered by Metal Coordination: from Functional Devices to Networked Multicomponent Catalytic Machinery

TLDR
Metal coordination has a manifold of rewards, putting it primo loco in opportunities for putting nanomechanical systems into action, and its strength and dynamics can be properly modulated and fine-tuned by the choice of metal, redox state, and ligand.
Abstract
A look at the elegance and efficiency of biological machines readily reveals that Nature masters the full gamut of chemical interactions to compose masterpieces of the living world. The present analysis singles out metal coordination for the actuation of nanomechanical motion. According to our analysis, metal coordination has a manifold of rewards, putting it primo loco in opportunities for putting nanomechanical systems into action: (i) its strength and dynamics can be properly modulated and fine-tuned by the choice of metal, redox state, and ligand(s), (ii) the high directionality of the interaction allows reliable design, and (iii) the emergence of novel self-sorting algorithms allows multiple of these interactions to be working in parallel. On top of all these advantages, intermolecular metal-ion translocation is a well-known factor in biological signaling. These benefits have recently proven their usefulness in the operation of networked devices and in overcoming the limitations of traditional stand-alone molecular systems.

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Citations
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The Future of Molecular Machines.

TL;DR: This Outlook uses a bicycle as an analogy to explain what a molecular machine is, in my opinion, and works through a representative selection of case studies to specify the significant accomplishments made to date, and the obstacles that currently stand between these and the field’s fulfillment of its great potential.
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New horizons for catalysis disclosed by supramolecular chemistry

TL;DR: In this article, a review summarizes the main developments that have opened new frontiers, with the aim of providing a guide to researchers approaching the field of supramolecular catalysis.
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Towards artificial molecular factories from framework-embedded molecular machines

TL;DR: The prospects of assembling multiple molecular machines within ordered frameworks, with the goal of producing artificial molecular factories in which molecular motions are coupled, synchronized and amplified across multiple length scales, leading to robust and stimuli-responsive solids.
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Beyond Platonic: How to Build Metal–Organic Polyhedra Capable of Binding Low-Symmetry, Information-Rich Molecular Cargoes

TL;DR: The field of metallosupramolecular chemistry has advanced rapidly in recent years as discussed by the authors , and much work in this area has focused on the formation of hollow self-assembled metal-organic architectures and exploration of the applications of their confined nanospaces.
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Coordination-Assembled Water-Soluble Anionic Lanthanide Organic Polyhedra for Luminescent Labeling and Magnetic Resonance Imaging.

TL;DR: A series of water-stable anionic Ln2nL3n-type lanthanide organic polyhedra constructed by deprotonation self-assembly of three fully-conjugated ligands featuring a 2,6-pyridine bitetrazolate chelating moiety offer potential candidates of supramolecular-edifices for bioimaging and drug delivery.
References
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Journal ArticleDOI

Supramolecular coordination: self-assembly of finite two- and three-dimensional ensembles.

TL;DR: In the early 1960s, the discovery of crown ethers and spherands by Pedersen, Lehn, and Cram3 led to the realization that small, complementary molecules can be made to recognize each other through non-covalent interactions such as hydrogen-bonding, charge-charge, donor-acceptor, π-π, van der Waals, hydrophilic and hydrophobic interactions to achieve these highly complex and often symmetrical architectures as mentioned in this paper.
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Direct observation of the rotation of F1-ATPase

TL;DR: It is shown that a single molecule of F1-ATPase acts as a rotary motor, the smallest known, by direct observation of its motion by attaching a fluorescent actin filament to the γ-subunit as a marker, which enabled us to observe this motion directly.
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Kinesin and Dynein Superfamily Proteins and the Mechanism of Organelle Transport

TL;DR: This review focuses on the molecular mechanism of organelle transport in cells and describes kinesin and dynein superfamily proteins.
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Light-driven monodirectional molecular rotor

TL;DR: In this article, the authors report repetitive, monodirectional rotation around a central carbon-carbon double bond in a chiral, helical alkene, with each 360° rotation involving four discrete isomerization steps activated by ultraviolet light or a change in the temperature of the system.
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