Electrochemical Activation of TTF-Based Halogen Bond Donors: A Powerful, Selective and Sensitive Analytical Tool for Probing a Weak Interaction in Complex Media
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F. Barrière | M. Fourmigué | B. Schöllhorn | E. Maisonhaute | C. Fave | A. Vacher | S. Groni | D. Lorcy | R. Oliveira | Sihem Groni
[1] M. Branca,et al. Comparative study of non-covalent interactions between cationic N-phenylviologens and halides by electrochemistry and NMR: the halogen bonding effect. , 2017, Faraday discussions.
[2] F. Mavré,et al. Electrochemical activation of a tetrathiafulvalene halogen bond donor in solution. , 2016, Physical chemistry chemical physics : PCCP.
[3] Pierangelo Metrangolo,et al. The Halogen Bond , 2016, Chemical reviews.
[4] Jason Y. C. Lim,et al. Halogen bonding-enhanced electrochemical halide anion sensing by redox-active ferrocene receptors. , 2015, Chemical communications.
[5] Pierre Kennepohl,et al. Evidence for Halogen Bond Covalency in Acyclic and Interlocked Halogen-Bonding Receptor Anion Recognition , 2014, Journal of the American Chemical Society.
[6] Lise‐Marie Chamoreau,et al. Directed synthesis of a halogen-bonded open porphyrin network , 2014 .
[7] M. Branca,et al. Electrochemical controlling and monitoring of halogen bond formation in solution. , 2014, Chemical communications.
[8] P. Beer,et al. Halogen- and hydrogen-bonding triazole-functionalised porphyrin-based receptors for anion recognition. , 2013, Dalton transactions.
[9] Pierangelo Metrangolo,et al. Definition of the halogen bond (IUPAC Recommendations 2013) , 2013 .
[10] O. Jeannin,et al. Toward chiral conductors: combining halogen bonding ability and chirality within a single tetrathiafulvalene molecule , 2013 .
[11] O. Jeannin,et al. Expanded halogen-bonded anion organic networks with star-shaped iodoethynyl-substituted molecules: from corrugated 2D hexagonal lattices to pyrite-type 2-fold interpenetrated cubic lattices. , 2013, Journal of the American Chemical Society.
[12] P. Dubois,et al. Halogen bonding at work: recent applications in synthetic chemistry and materials science , 2013 .
[13] M. Chudziński,et al. Halogen bonding in solution: thermodynamics and applications. , 2013, Chemical Society reviews.
[14] M. Erdélyi,et al. Halogen bonding in solution. , 2012, Chemical Society reviews.
[15] G. Cavallo,et al. Halogen bonding: a general route in anion recognition and coordination. , 2010, Chemical Society reviews.
[16] M. Nielsen,et al. Tetrathiafulvalenes as building blocks in supramolecular chemistry II , 2010 .
[17] Mohammed G. Sarwar,et al. Thermodynamics of halogen bonding in solution: substituent, structural, and solvent effects. , 2010, Journal of the American Chemical Society.
[18] Marc Fourmigué,et al. Halogen bonding: Recent advances , 2009 .
[19] C. Amatore,et al. Direct Monitoring of Ultrafast Redox Commutation at the Nanosecond and Nanometer Scales by Ultrafast Voltammetry: From Molecular Wires to Cation Releasing Systems , 2008 .
[20] G. Bodenhausen,et al. Revealing molecular self-assembly and geometry of non-covalent halogen bonding by solid-state NMR spectroscopy. , 2008, Chemical communications.
[21] P. Beer,et al. Halogen Bonding in Supramolecular Chemistry. , 2008, Chemical reviews.
[22] N. Raouafi,et al. Electrochemically driven release of picomole amounts of calcium ions with temporal and spatial resolution. , 2008, Angewandte Chemie.
[23] L. Brammer,et al. Metal fluorides form strong hydrogen bonds and halogen bonds: measuring interaction enthalpies and entropies in solution. , 2008, Journal of the American Chemical Society.
[24] J. G. Vinter,et al. Solvent effects on hydrogen bonding. , 2007, Angewandte Chemie.
[25] Timothy Clark,et al. Halogen bonding: the σ-hole , 2007 .
[26] T. Imakubo,et al. Supramolecular organic conductors based on diiodo-TTFs and spherical halide ion X−(X = Cl, Br) , 2006 .
[27] F. Barrière,et al. Use of weakly coordinating anions to develop an integrated approach to the tuning of deltaE(1/2) values by medium effects. , 2006, Journal of the American Chemical Society.
[28] K. Boubekeur,et al. Self-assembly of nitroxide radicals via halogen bonding—directional NO⋯I interactions , 2006 .
[29] M. Kaupp,et al. 13C NMR study of halogen bonding of haloarenes: measurements of solvent effects and theoretical analysis. , 2004, Journal of the American Chemical Society.
[30] M. Prato,et al. Cyclic voltammetry and bulk electronic properties of soluble carbon nanotubes. , 2004, Journal of the American Chemical Society.
[31] P. Metrangolo,et al. Perfluorocarbon–hydrocarbon self-assembly: Part 16. 19F NMR study of the halogen bonding between halo-perfluorocarbons and heteroatom containing hydrocarbons , 2002 .
[32] T. Ouimet,et al. Electrochemically controlled hydrogen bonding. o-Quinones as simple redox-dependent receptors for arylureas. , 2000, The Journal of organic chemistry.
[33] Anthony C. Legon. Präreaktive Komplexe der Dihalogene XY mit Lewis‐Basen B in der Gasphase: eine systematische Studie der Halogen‐Analoga B⋅⋅⋅XY der Wasserstoffbrückenbindungen B⋅⋅⋅HX , 1999 .
[34] Anthony C. Legon,et al. Prereactive Complexes of Dihalogens XY with Lewis Bases B in the Gas Phase: A Systematic Case for the Halogen Analogue B⋅⋅⋅XY of the Hydrogen Bond B⋅⋅⋅HX , 1999 .
[35] Philip A. Gale,et al. Mechanisms of electrochemical recognition of cations, anions and neutral guest species by redox-active receptor molecules , 1999 .
[36] A. Kaifer. Interplay Between Molecular Recognition and Redox Chemistry , 1999 .
[37] Frank H. Allen,et al. The Nature and Geometry of Intermolecular Interactions between Halogens and Oxygen or Nitrogen , 1996 .
[38] J. Siegel,et al. Polar Interactions between Stacked π Systems in Fluorinated 1,8-Diarylnaphthalenes: Importance of Quadrupole Moments in Molecular Recognition† , 1995 .
[39] Franco Cozzi,et al. Polare Wechselwirkungen zwischen gestapelten π‐Systemen in fluorierten 1,8‐Diarylnaphthalinen: Bedeutung des Quadrupolmoments für die molekulare Erkennung , 1995 .
[40] A. Jentzsch. Applications of halogen bonding in solution , 2015 .
[41] Hiroshi M. Yamamoto,et al. Supramolecular insulating networks sheathing conducting nanowires based on organic radical cations. , 2008, ACS nano.