Rotaxane-based molecular muscles.
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[1] J. Sauvage,et al. Molecular Muscles: From Species in Solution to Materials and Devices , 2014 .
[2] Severin T. Schneebeli,et al. Redox switchable daisy chain rotaxanes driven by radical-radical interactions. , 2014, Journal of the American Chemical Society.
[3] J. Cornelissen,et al. Conversion of light into macroscopic helical motion. , 2014, Nature chemistry.
[4] Severin T. Schneebeli,et al. An electrochemically and thermally switchable donor-acceptor [c2]daisy chain rotaxane. , 2014, Angewandte Chemie.
[5] J. Sauvage,et al. Cyclic [4]rotaxanes containing two parallel porphyrinic plates: toward switchable molecular receptors and compressors. , 2014, Accounts of chemical research.
[6] Tsuneomi Kawasaki,et al. Five-state molecular switching of a [3]rotaxane in response to weak and strong acid and base stimuli. , 2013, Chemical communications.
[7] Yu Liu,et al. A double-leg donor-acceptor molecular elevator: new insight into controlling the distance of two platforms. , 2013, Organic letters.
[8] M. Mayor,et al. Molecular daisy chains. , 2013, Chemical Society reviews.
[9] Emilie Moulin,et al. Muscle-like supramolecular polymers: integrated motion from thousands of molecular machines. , 2012, Angewandte Chemie.
[10] Feihe Huang,et al. A solvent-driven molecular spring , 2012 .
[11] Nan Chen,et al. A controllable chiral molecular machine: movement on molecular level. , 2012, Small.
[12] Yanlei Yu,et al. Photodeformable polymer gels and crosslinked liquid-crystalline polymers , 2012 .
[13] Kentaro Tanaka,et al. Switchable intermolecular communication in a four-fold rotaxane. , 2012, Angewandte Chemie.
[14] J. F. Stoddart,et al. Great expectations: can artificial molecular machines deliver on their promise? , 2012, Chemical Society reviews.
[15] Y. Takashima,et al. Expansion–contraction of photoresponsive artificial muscle regulated by host–guest interactions , 2012, Nature Communications.
[16] Anne-Sophie Duwez,et al. A single synthetic small molecule that generates force against a load. , 2011, Nature nanotechnology.
[17] J. Sauvage,et al. A cyclic [4]rotaxane that behaves as a switchable molecular receptor: formation of a rigid scaffold from a collapsed structure by complexation with copper(I) ions. , 2010, Angewandte Chemie.
[18] T. Takata,et al. Neutralization of a sec-ammonium group unusually stabilized by the "rotaxane effect": synthesis, structure, and dynamic nature of a "free" sec-amine/crown ether-type rotaxane. , 2010, Chemistry.
[19] A. Hashidzume,et al. Light-switchable Janus [2]rotaxanes based on α-cyclodextrin derivatives bearing two recognition sites linked with oligo(ethylene glycol). , 2010, Chemistry, an Asian journal.
[20] Chuan-Feng Chen,et al. A new [3]rotaxane molecular machine based on a dibenzylammonium ion and a triazolium station. , 2010, Organic letters.
[21] F. Coutrot,et al. Very contracted to extended co-conformations with or without oscillations in two- and three-station [c2]daisy chains. , 2010, The Journal of organic chemistry.
[22] K. Rissanen,et al. Templated synthesis of cyclic [4]rotaxanes consisting of two stiff rods threaded through two bis-macrocycles with a large and rigid central plate as spacer. , 2010, Journal of the American Chemical Society.
[23] J. F. Stoddart,et al. On the thermodynamic and kinetic investigations of a [c2]daisy chain polymer , 2010 .
[24] Yu Liu,et al. pH-Controlled intramolecular charge-transfer behavior in bistable [3]rotaxane. , 2010, Organic letters.
[25] Q. Pei,et al. Advances in dielectric elastomers for actuators and artificial muscles. , 2010, Macromolecular rapid communications.
[26] R. Grubbs,et al. Switching and extension of a [c2]daisy-chain dimer polymer. , 2009, Journal of the American Chemical Society.
[27] Vincenzo Balzani,et al. Light powered molecular machines. , 2009, Chemical Society reviews.
[28] J. F. Stoddart,et al. The chemistry of the mechanical bond. , 2009, Chemical Society reviews.
[29] Ying-Wei Yang,et al. Acid-base actuation of [c2]daisy chains. , 2009, Journal of the American Chemical Society.
[30] J. Sauvage,et al. Adjustable receptor based on a [3]rotaxane whose two threaded rings are rigidly attached to two porphyrinic plates: synthesis and complexation studies. , 2009, Journal of the American Chemical Society.
[31] B. K. Juluri,et al. A mechanical actuator driven electrochemically by artificial molecular muscles. , 2009, ACS nano.
[32] Yi‐Hung Liu,et al. A molecular cage-based [2]rotaxane that behaves as a molecular muscle. , 2009, Organic letters.
[33] Lei Fang,et al. An acid-base-controllable [c2]daisy chain. , 2008, Angewandte Chemie.
[34] S. Lincoln,et al. The foundation of a light driven molecular muscle based on stilbene and alpha-cyclodextrin. , 2008, Chemical communications.
[35] M. Irie. Photochromism and Molecular Mechanical Devices , 2008 .
[36] F. Coutrot,et al. A new pH-switchable dimannosyl[c2]daisy chain molecular machine. , 2008, Organic letters.
[37] T. Ikeda,et al. Photomobile polymer materials: towards light-driven plastic motors. , 2008, Angewandte Chemie.
[38] D. Tuncel,et al. pH-Triggered dethreading-rethreading and switching of cucurbit[6]uril on bistable [3]pseudorotaxanes and [3]rotaxanes. , 2008, Chemistry.
[39] J. Sauvage,et al. A [3]rotaxane with two porphyrinic plates acting as an adaptable receptor. , 2008, Journal of the American Chemical Society.
[40] J. Madden,et al. Polymer artificial muscles , 2007 .
[41] B. Salih,et al. Molecular switch based on a cucurbit[6]uril containing bistable [3]rotaxane. , 2007, Chemical communications.
[42] Francesco Zerbetto,et al. Synthetic molecular motors and mechanical machines. , 2007, Angewandte Chemie.
[43] Y. Takashima,et al. Contraction of supramolecular double-threaded dimer formed by alpha-cyclodextrin with a long alkyl chain. , 2007, Organic letters.
[44] Yanlei Yu,et al. Photomechanics of liquid-crystalline elastomers and other polymers. , 2007, Angewandte Chemie.
[45] Wesley R Browne,et al. Making molecular machines work , 2006, Nature nanotechnology.
[46] Susumu Tsuda,et al. Linear oligomers composed of a photochromically contractible and extendable Janus [2]rotaxane. , 2006, Chemical communications.
[47] Chih-Ming Ho,et al. Evaluation of synthetic linear motor-molecule actuation energetics. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[48] Nathalie Katsonis,et al. Molecular machines: Nanomotor rotates microscale objects , 2006, Nature.
[49] Vincenzo Balzani,et al. Operating molecular elevators. , 2006, Journal of the American Chemical Society.
[50] Francesco Zerbetto,et al. Macroscopic transport by synthetic molecular machines , 2005, Nature materials.
[51] Chih-Ming Ho,et al. Linear artificial molecular muscles. , 2005, Journal of the American Chemical Society.
[52] Chih-Ming Ho,et al. A nanomechanical device based on linear molecular motors , 2004 .
[53] Nancy R Forde,et al. Mechanical processes in biochemistry. , 2004, Annual review of biochemistry.
[54] J. Fraser Stoddart,et al. A Molecular Elevator , 2004, Science.
[55] Z. Oltvai,et al. Network biology: understanding the cell's functional organization , 2004, Nature Reviews Genetics.
[56] Jean-Pierre Sauvage,et al. Towards artificial muscles at the nanometric level. , 2003, Chemical communications.
[57] Jean-Pierre Sauvage,et al. Chemically induced contraction and stretching of a linear rotaxane dimer. , 2002, Chemistry.
[58] M Venturi,et al. Artificial molecular-level machines: which energy to make them work? , 2001, Accounts of chemical research.
[59] Stoddart,et al. Artificial Molecular Machines. , 2000, Angewandte Chemie.
[60] M. Jiménez,et al. Towards Synthetic Molecular Muscles: Contraction and Stretching of a Linear Rotaxane Dimer , 2000 .
[61] B. Alberts. The Cell as a Collection of Protein Machines: Preparing the Next Generation of Molecular Biologists , 1998, Cell.
[62] R. Baughman. Conducting polymer artificial muscles , 1996 .
[63] J. F. Stoddart,et al. Supramolecular polymers: Molecular machines muscle up. , 2013, Nature nanotechnology.
[64] Kohzo Ito,et al. Novel entropic elasticity of polymeric materials: why is slide-ring gel so soft? , 2012 .