A Focus on Triazolium as a Multipurpose Molecular Station for pH-Sensitive Interlocked Crown-Ether-Based Molecular Machines
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[1] Zheng Meng,et al. A molecular pulley based on a triply interlocked [2]rotaxane. , 2015, Chemical communications.
[2] Wei Jiang,et al. A double plug-socket system capable of molecular keypad locks through controllable photooxidation. , 2009, Chemistry.
[3] Chuan-feng Chen. Novel triptycene-derived hosts: synthesis and their applications in supramolecular chemistry. , 2011, Chemical communications.
[4] J. F. Stoddart,et al. Supramolecular daisy chains. , 2001, The Journal of organic chemistry.
[5] A. Credi,et al. Light to investigate (read) and operate (write) molecular devices and machines. , 2014, Chemical Society reviews.
[6] N. Giuseppone,et al. pH and light-controlled self-assembly of bistable [c2] daisy chain rotaxanes. , 2015, Chemical communications.
[7] Jean-Pierre Sauvage,et al. Towards artificial muscles at the nanometric level. , 2003, Chemical communications.
[8] Chuan-Feng Chen,et al. A new [3]rotaxane molecular machine based on a dibenzylammonium ion and a triazolium station. , 2010, Organic letters.
[9] J. Sauvage,et al. Transition-metal template synthesis of a rotaxane incorporating two different coordinating units in its thread , 1997 .
[10] Severin T. Schneebeli,et al. An electrochemically and thermally switchable donor-acceptor [c2]daisy chain rotaxane. , 2014, Angewandte Chemie.
[11] K. Sharpless,et al. Click-Chemie: diverse chemische Funktionalität mit einer Handvoll guter Reaktionen , 2001 .
[12] C. Dietrich-Buchecker,et al. Shuttles and muscles: linear molecular machines based on transition metals. , 2001, Accounts of chemical research.
[13] H. Ågren,et al. A switchable bis-branched [1]rotaxane featuring dual-mode molecular motions and tunable molecular aggregation. , 2014, ACS applied materials & interfaces.
[14] D. H. Busch,et al. Gaining control over molecular threading: benefits of second coordination sites and aqueous–organic interfaces in rotaxane synthesis , 1995 .
[15] J. Fraser Stoddart,et al. The Self‐Assembly of a Switchable [2]Rotaxane , 1997 .
[16] F. Coutrot,et al. A strategy utilizing a recyclable macrocycle transporter for the efficient synthesis of a triazolium-based [2]rotaxane. , 2014, Angewandte Chemie.
[17] 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.
[18] T. Takata,et al. Selective transformation of a crown ether/sec-ammonium salt-type rotaxane to N-alkylated rotaxanes. , 2010, Organic letters.
[19] J. Jiménez-Barbero,et al. Tightening or loosening a pH-sensitive double-lasso molecular machine readily synthesized from an ends-activated [c2]daisy chain , 2012 .
[20] R. Huisgen. 1,3-Dipolar Cycloadditions. Past and Future† , 1963 .
[21] Francesco Zerbetto,et al. Entropy-driven translational isomerism: a tristable molecular shuttle. , 2003, Angewandte Chemie.
[22] M. Jiménez,et al. Towards Synthetic Molecular Muscles: Contraction and Stretching of a Linear Rotaxane Dimer , 2000 .
[23] Chi-Ming Che,et al. Self‐Assembled Electroluminescent Polymers Derived from Terpyridine‐Based Moieties , 2003 .
[24] D. Leigh,et al. A switchable [2]rotaxane asymmetric organocatalyst that utilizes an acyclic chiral secondary amine. , 2014, Journal of the American Chemical Society.
[25] C. Enjalbal,et al. Straightforward synthesis of a double-lasso macrocycle from a nonsymmetrical [c2]daisy chain. , 2013, Organic letters.
[26] Heng-Yi Zhang,et al. A double-leg donor-acceptor molecular elevator: new insight into controlling the distance of two platforms. , 2013, Organic letters.
[27] J. F. Stoddart,et al. Acid-base actuation of [c2]daisy chains. , 2009, Journal of the American Chemical Society.
[28] Ying Ma,et al. A novel pentiptycene bis(crown ether)-based [2](2)rotaxane whose two DB24C8 rings act as flapping wings of a butterfly. , 2014, Organic letters.
[29] J. F. Stoddart,et al. Supramolecular polymers: Molecular machines muscle up. , 2013, Nature nanotechnology.
[30] T. Takata,et al. Sequential O- and N-acylation protocol for high-yield preparation and modification of rotaxanes: synthesis, functionalization, structure, and intercomponent interaction of rotaxanes. , 2006, The Journal of organic chemistry.
[31] D. Qu,et al. A Perylene‐Bridged Switchable [3]Rotaxane Molecular Shuttle with a Fluorescence Output , 2015 .
[32] Kevin D. Haenni,et al. A rotaxane-based switchable organocatalyst. , 2012, Angewandte Chemie.
[33] M. W. Hosseini,et al. Porphyrin-based switchable molecular turnstiles. , 2011, Chemistry.
[34] J. F. Stoddart,et al. The master of chemical topology. , 2009, Chemical Society reviews.
[35] J. Fraser Stoddart,et al. Künstliche molekulare Maschinen , 2000 .
[36] J. Sauvage,et al. Molecular Muscles: From Species in Solution to Materials and Devices , 2014 .
[37] D. Qu,et al. A bis-spiropyran-containing multi-state [2]rotaxane with fluorescence output , 2013 .
[38] Emilie Moulin,et al. Muscle-like supramolecular polymers: integrated motion from thousands of molecular machines. , 2012, Angewandte Chemie.
[39] J. F. Stoddart,et al. On the thermodynamic and kinetic investigations of a [c2]daisy chain polymer , 2010 .
[40] Euan R Kay,et al. Electrochemically switchable hydrogen-bonded molecular shuttles. , 2003, Journal of the American Chemical Society.
[41] Benoit Colasson,et al. Towards molecular machines and motors based on transition metal complexes , 2002 .
[42] Stoddart,et al. Artificial Molecular Machines. , 2000, Angewandte Chemie.
[43] Francesco Zerbetto,et al. Unidirectional rotation in a mechanically interlocked molecular rotor , 2003, Nature.
[44] Vincenzo Balzani,et al. Operating molecular elevators. , 2006, Journal of the American Chemical Society.
[45] Francesco Zerbetto,et al. Remarkable positional discrimination in bistable light- and heat-switchable hydrogen-bonded molecular shuttles. , 2003, Angewandte Chemie.
[46] Laurence Raehm,et al. A Transition Metal Containing Rotaxane in Motion: Electrochemically Induced Pirouetting of the Ring on the Threaded Dumbbell , 1999 .
[47] J. F. Stoddart,et al. A chemically and electrochemically switchable molecular shuttle , 1994, Nature.
[48] R. Huisgen. Kinetik und Mechanismus 1.3‐Dipolarer Cycloadditionen , 1963 .
[49] R. Huisgen. Kinetics and reaction mechanisms: selected examples from the experience of forty years , 1989 .
[50] Jean-Pierre Sauvage,et al. Chemically induced contraction and stretching of a linear rotaxane dimer. , 2002, Chemistry.
[51] J. Fraser Stoddart,et al. Selbstaufbau eines schaltbaren [2]Rotaxans , 1997 .
[52] Günter Szeimies,et al. 1.3-Dipolare Cycloadditionen, XXXII. Kinetik der Additionen organischer Azide an CC-Mehrfachbindungen , 1967 .
[53] U. Schubert,et al. High molecular weight supramolecular polymers containing both terpyridine metal complexes and ureidopyrimidinone quadruple hydrogen-bonding units in the main chain. , 2005, Journal of the American Chemical Society.
[54] F. Coutrot,et al. A new glycorotaxane molecular machine based on an anilinium and a triazolium station. , 2008, Chemistry.
[55] D. Leigh,et al. Exploring the activation modes of a rotaxane-based switchable organocatalyst. , 2014, Journal of the American Chemical Society.
[56] David J. Williams,et al. Acid−Base Controllable Molecular Shuttles† , 1998 .
[57] Harald Hofmeier,et al. Recent developments in the supramolecular chemistry of terpyridine-metal complexes. , 2004, Chemical Society reviews.
[58] M. Finn,et al. Click Chemistry: Diverse Chemical Function from a Few Good Reactions. , 2001 .
[59] Alberto Credi,et al. Shuttling dynamics in an acid-base-switchable [2]rotaxane. , 2005, Chemphyschem : a European journal of chemical physics and physical chemistry.
[60] F. Coutrot,et al. N-benzyltriazolium as both molecular station and barrier in [2]rotaxane molecular machines. , 2013, The Journal of organic chemistry.
[61] M. W. Hosseini,et al. A platinum turnstile with a palladium lock. , 2013, Dalton transactions.
[62] Pablo Gaviña,et al. Electrochemically induced molecular motions in a copper(I) complex pseudorotaxane , 1996 .
[63] J. Fraser Stoddart,et al. A Molecular Elevator , 2004, Science.
[64] Jean-Pierre Sauvage,et al. Transition‐Metal‐Complexed Molecular Machine Prototypes , 2006 .
[65] David J. Williams,et al. Dialkylammonium Ion/Crown Ether Complexes: The Forerunners of a New Family of Interlocked Molecules , 1995 .
[66] Huibiao Liu,et al. Synthesis of a [2]rotaxane operated in basic environment. , 2011, Organic & biomolecular chemistry.
[67] M. W. Hosseini,et al. A molecular gate based on a porphyrin and a silver lock. , 2007, Chemical communications.
[68] F. Coutrot,et al. Bistable or oscillating state depending on station and temperature in three-station glycorotaxane molecular machines. , 2010, Chemistry.
[69] F. Coutrot,et al. Controlling the chair conformation of a mannopyranose in a large-amplitude [2]rotaxane molecular machine. , 2009, Chemistry.
[70] R. Grubbs,et al. Switching and extension of a [c2]daisy-chain dimer polymer. , 2009, Journal of the American Chemical Society.
[71] D. Qu,et al. Dual-mode operation of a bistable [1]rotaxane with a fluorescence signal. , 2013, Organic letters.
[72] Euan R. Kay,et al. Synthetische molekulare Motoren und mechanische Maschinen , 2007 .
[73] M. W. Hosseini,et al. Open and closed states of a porphyrin based molecular turnstile. , 2011, Dalton transactions.
[74] Jeffrey S. Moore,et al. Design and Synthesis of a “Molecular Turnstile” , 1995 .
[75] David J. Williams,et al. DIALKYLAMMONIUM-IONEN/KRONENETHER-KOMPLEXE : VORLAUFER EINER NEUEN FAMILIE MECHANISCH VERKNUPFTER MOLEKULE , 1995 .
[76] Yu Liu,et al. pH-Controlled intramolecular charge-transfer behavior in bistable [3]rotaxane. , 2010, Organic letters.
[77] Pablo Gaviña,et al. Rotaxanes Incorporating Two Different Coordinating Units in Their Thread: Synthesis and Electrochemically and Photochemically Induced Molecular Motions , 1999 .
[78] Emile Brabet,et al. A pH-sensitive lasso-based rotaxane molecular switch. , 2013, Chemistry.
[79] M. W. Hosseini,et al. Strapped-porphyrin-based molecular turnstiles. , 2012, Chemistry.
[80] V. Balzani,et al. Ruthenium(II) and Osmium(II) Bis(terpyridine) Complexes in Covalently-Linked Multicomponent Systems: Synthesis, Electrochemical Behavior, Absorption Spectra, and Photochemical and Photophysical Properties , 1994 .
[81] Maurizio Prato,et al. Hydrogen bond-assembled fullerene molecular shuttle. , 2003, Organic letters.
[82] Frédéric Coutrot,et al. Recent Advances in the Chemical Synthesis of Lasso Molecular Switches , 2015 .
[83] Lei Fang,et al. An acid-base-controllable [c2]daisy chain. , 2008, Angewandte Chemie.
[84] Euan R Kay,et al. Beyond switches: ratcheting a particle energetically uphill with a compartmentalized molecular machine. , 2006, Journal of the American Chemical Society.
[85] M. Mayor,et al. Molecular daisy chains. , 2013, Chemical Society reviews.
[86] Frédéric Coutrot,et al. A new pH-switchable dimannosyl[c2]daisy chain molecular machine. , 2008, Organic letters.
[87] J. F. Stoddart,et al. Rotaxane-based molecular muscles. , 2014, Accounts of chemical research.
[88] Jean-Pierre Sauvage,et al. Transition metal-complexed catenanes and rotaxanes in motion: Towards molecular machines , 2005 .
[89] F. Coutrot,et al. A pH-Sensitive Peptide-Containing Lasso Molecular Switch , 2013, Molecules.
[90] Raluca M. Fratila,et al. Triazolium cations: from the “click” pool to multipurpose applications , 2014 .
[91] T. Takata,et al. Fluorescence control of boron enaminoketonate using a rotaxane shuttle. , 2013, Organic letters.
[92] R. Huisgen. 1.3‐Dipolare Cycloadditionen Rückschau und Ausblick , 1963 .
[93] S. Lincoln,et al. The foundation of a light driven molecular muscle based on stilbene and alpha-cyclodextrin. , 2008, Chemical communications.
[94] Morten Meldal,et al. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. , 2002, The Journal of organic chemistry.
[95] R. Huisgen. Kinetics and Mechanism of 1,3‐Dipolar Cycloadditions , 1963 .
[96] Feihe Huang,et al. A solvent-driven molecular spring , 2012 .
[97] D. Leigh,et al. A three-compartment chemically-driven molecular information ratchet. , 2012, Journal of the American Chemical Society.
[98] A. Slawin,et al. A chemically-driven molecular information ratchet. , 2008, Journal of the American Chemical Society.
[99] Severin T. Schneebeli,et al. Redox switchable daisy chain rotaxanes driven by radical-radical interactions. , 2014, Journal of the American Chemical Society.
[100] F. Paolucci,et al. Photoinduction of Fast, Reversible Translational Motion in a Hydrogen-Bonded Molecular Shuttle , 2001, Science.
[101] M. F. Mayer,et al. Actuator prototype: capture and release of a self-entangled [1]rotaxane. , 2010, Journal of the American Chemical Society.
[102] H. Ågren,et al. Two switchable star-shaped [1](n)rotaxanes with different multibranched cores. , 2014, Organic letters.
[103] Francesco Zerbetto,et al. Synthetic molecular motors and mechanical machines. , 2007, Angewandte Chemie.