Literature DB >> 11091368

Artificial Molecular Machines.

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Abstract

The miniaturization of components used in the construction of working devices is being pursued currently by the large-downward (top-down) fabrication. This approach, however, which obliges solid-state physicists and electronic engineers to manipulate progressively smaller and smaller pieces of matter, has its intrinsic limitations. An alternative approach is a small-upward (bottom-up) one, starting from the smallest compositions of matter that have distinct shapes and unique properties-namely molecules. In the context of this particular challenge, chemists have been extending the concept of a macroscopic machine to the molecular level. A molecular-level machine can be defined as an assembly of a distinct number of molecular components that are designed to perform machinelike movements (output) as a result of an appropriate external stimulation (input). In common with their macroscopic counterparts, a molecular machine is characterized by 1) the kind of energy input supplied to make it work, 2) the nature of the movements of its component parts, 3) the way in which its operation can be monitored and controlled, 4) the ability to make it repeat its operation in a cyclic fashion, 5) the timescale needed to complete a full cycle of movements, and 6) the purpose of its operation. Undoubtedly, the best energy inputs to make molecular machines work are photons or electrons. Indeed, with appropriately chosen photochemically and electrochemically driven reactions, it is possible to design and synthesize molecular machines that do work. Moreover, the dramatic increase in our fundamental understanding of self-assembly and self-organizational processes in chemical synthesis has aided and abetted the construction of artificial molecular machines through the development of new methods of noncovalent synthesis and the emergence of supramolecular assistance to covalent synthesis as a uniquely powerful synthetic tool. 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. After analyzing a few important examples of natural molecular machines, the most significant developments in the field of artificial molecular machines are highlighted. The systems reviewed include 1) chemical rotors, 2) photochemically and electrochemically induced molecular (conformational) rearrangements, and 3) chemically, photochemically, and electrochemically controllable (co-conformational) motions in interlocked molecules (catenanes and rotaxanes), as well as in coordination and supramolecular complexes, including pseudorotaxanes. Artificial molecular machines based on biomolecules and interfacing artificial molecular machines with surfaces and solid supports are amongst some of the cutting-edge topics featured in this review. The extension of the concept of a machine to the molecular level is of interest not only for the sake of basic research, but also for the growth of nanoscience and the subsequent development of nanotechnology.

Entities:  

Year:  2000        PMID: 11091368     DOI: 10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-x

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  125 in total

1.  Supramolecular templating in thermodynamically controlled synthesis.

Authors:  Ricardo L E Furlan; Sijbren Otto; Jeremy K M Sanders
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-05       Impact factor: 11.205

2.  Unidirectional rotary motion in a liquid crystalline environment: color tuning by a molecular motor.

Authors:  Richard A van Delden; Nagatoshi Koumura; Noboyuki Harada; Ben L Feringa
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-02       Impact factor: 11.205

3.  Toward complex matter: supramolecular chemistry and self-organization.

Authors:  Jean-Marie Lehn
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-02       Impact factor: 11.205

4.  Entropically driven self-assembly of multichannel rosette nanotubes.

Authors:  Hicham Fenniri; Bo-Liang Deng; Alexander E Ribbe; Klaas Hallenga; Jaby Jacob; Pappannan Thiyagarajan
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

5.  Chemical synthesis gets a fillip from molecular recognition and self-assembly processes.

Authors:  J Fraser Stoddart; Hsian-Rong Tseng
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

6.  Controlled disassembling of self-assembling systems: toward artificial molecular-level devices and machines.

Authors:  Vincenzo Balzani; Alberto Credi; Margherita Venturi
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

7.  Dynamic chemical devices: modulation of contraction/extension molecular motion by coupled-ion binding/pH change-induced structural switching.

Authors:  Mihail Barboiu; Jean-Marie Lehn
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-09       Impact factor: 11.205

8.  Photoisomerization of a rotaxane hydrogen bonding template: light-induced acceleration of a large amplitude rotational motion.

Authors:  Francesco G Gatti; Salvador León; Jenny K Y Wong; Giovanni Bottari; Andrea Altieri; M Angeles Farran Morales; Simon J Teat; Céline Frochot; David A Leigh; Albert M Brouwer; Francesco Zerbetto
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-27       Impact factor: 11.205

9.  DNA duplex-quadruplex exchange as the basis for a nanomolecular machine.

Authors:  Patrizia Alberti; Jean-Louis Mergny
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-06       Impact factor: 11.205

10.  Thermal modulation of birefringence observed in a crystalline molecular gyrotop.

Authors:  Wataru Setaka; Kentaro Yamaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-29       Impact factor: 11.205

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