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Insight from Electrochemical Analysis in the Radical Cation State of a Monopyrrolotetrathiafulvalene‐Based [2]Rotaxane.
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- Chemistry - A European Journal, 2024, v. 30, n. 55, p. 1, doi. 10.1002/chem.202402377
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Two-Dimensional Molecular Electronics Circuits.
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- ChemPhysChem, 2002, v. 3, n. 6, p. 519, doi. 10.1002/1439-7641(20020617)3:6<519::AID-CPHC519>3.0.CO;2-2
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Cover Picture: ChemPhysChem 6/2002.
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- ChemPhysChem, 2002, v. 3, n. 6, p. 467, doi. 10.1002/1439-7641(20020617)3:6<467::AID-CPHC467>3.0.CO;2-V
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- Article
Synthesis and Complexation Studies between Trifluoromethylammonium Threads and Dibenzo[24]Crown-8.
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- European Journal of Organic Chemistry, 2011, v. 2011, n. 4, p. 759, doi. 10.1002/ejoc.201001277
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Acid/Base Controllable Molecular Recognition.
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- Chemistry - A European Journal, 2011, v. 17, n. 39, p. 11001, doi. 10.1002/chem.201101266
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- Article
Positive Homotropic Allosteric Receptors for Neutral Guests: Annulated Tetrathiafulvalene-Calix[4]pyrroles as Colorimetric Chemosensors for Nitroaromatic Explosives.
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- Chemistry - A European Journal, 2010, v. 16, n. 3, p. 848, doi. 10.1002/chem.200902924
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Self-Assembled Monolayers of Mono-Tetrathiafulvalene Calix[4]pyrroles and Their Electrochemical Sensing of Chloride.
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- Chemistry - A European Journal, 2009, v. 15, n. 33, p. 8128, doi. 10.1002/chem.200901394
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- Article
Tetrathiafulvalene Porphyrins.
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- Chemistry - A European Journal, 2009, v. 15, n. 2, p. 506, doi. 10.1002/chem.200801636
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The Introduction of Pyrrolotetrathiafulvalene into Conjugated Architectures: Synthesis and Electronic Properties.
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- Macromolecular Rapid Communications, 2008, v. 29, n. 14, p. 1226, doi. 10.1002/marc.200800154
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Characterization of a Byproduct in the Alkylation of DMIT: Alkylation on the Least Nucleophilic Sulfur Atom.
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- European Journal of Inorganic Chemistry, 2006, v. 2006, n. 15, p. 3099
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- Article
Cover Picture: Ground-State Equilibrium Thermodynamics and Switching Kinetics of Bistable [2]Rotaxanes Switched in Solution, Polymer Gels, and Molecular Electronic Devices (Chem. Eur. J. 1/2006).
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- Chemistry - A European Journal, 2006, v. 12, n. 1, p. 3, doi. 10.1002/chem.200690000
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Ground-State Equilibrium Thermodynamics and Switching Kinetics of Bistable [2]Rotaxanes Switched in Solution, Polymer Gels, and Molecular Electronic Devices.
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- Chemistry - A European Journal, 2006, v. 12, n. 1, p. 261, doi. 10.1002/chem.200500934
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- Article
Redox-Controllable Amphiphilic [2]Rotaxanes.
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- Chemistry - A European Journal, 2004, v. 10, n. 1, p. 155, doi. 10.1002/chem.200305204
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In the Twilight Zone between [2]Pseudorotaxanes and [2]Rotaxanes.
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- Chemistry - A European Journal, 2003, v. 9, n. 19, p. 4611, doi. 10.1002/chem.200304798
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- Article
Amphiphilic Bistable Rotaxanes.
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- Chemistry - A European Journal, 2003, v. 9, n. 13, p. 2982, doi. 10.1002/chem.200204589
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- Article
Preparation of Cyclobis(paraquat- p-phenylene)-Based [2]Rotaxanes Without Flexible Glycol Chains.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 32, p. 6093, doi. 10.1002/anie.200701722
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Supramolecular Receptor Design: Anion-Triggered Binding of C.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 41, p. 6848, doi. 10.1002/anie.200602724
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Molecular-Mechanical Switch-Based Solid-State Electrochromic DevicesThis research was funded by the Office of Naval Research, the National Science Foundation, and the Moletronics Program of the Defense Advanced Research Projects Agency, the Microelectronics Advanced Research Corporation, its Focus Centers on Functional Engineered NanoArchitectonics and Advanced Materials and Devices, and the Center for Nanoscale Innovation for Defense.
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- Angewandte Chemie International Edition, 2004, v. 43, n. 47, p. 6486, doi. 10.1002/anie.200461723
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Cover Feature: Probing the Electrostatic Barrier of Tetrathiafulvalene Dications using a Tetra‐stable Donor–Acceptor [2]Rotaxane (Chem. Eur. J. 28/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 28, p. 6087, doi. 10.1002/chem.202000973
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- Article
Probing the Electrostatic Barrier of Tetrathiafulvalene Dications using a Tetra‐stable Donor–Acceptor [2]Rotaxane.
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- Chemistry - A European Journal, 2020, v. 26, n. 28, p. 6165, doi. 10.1002/chem.202000302
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- Article
Molecular-Mechanical Switch-Based Solid-State Electrochromic DevicesThis research was funded by the Office of Naval Research, the National Science Foundation, and the Moletronics Program of the Defense Advanced Research Projects Agency, the Microelectronics Advanced Research Corporation, its Focus Centers on Functional Engineered NanoArchitectonics and Advanced Materials and Devices, and the Center for Nanoscale Innovation for Defense.
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- Angewandte Chemie, 2004, v. 116, n. 47, p. 6648, doi. 10.1002/ange.200461723
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- Article
Pyrrolo-Tetrathiafulvalenes and Their Applications in Molecular and Supramolecular Chemistry.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 17, p. 3245, doi. 10.1002/ejoc.200300078
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Cover Picture: Pyrrolo-Tetrathiafulvalenes and Their Applications in Molecular and Supramolecular Chemistry (Eur. J. Org. Chem. 17/2003).
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 17, p. 3235, doi. 10.1002/ejoc.200390238
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A chloride-anion insensitive colorimetric chemosensor for trinitrobenzene and picric acid.
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- Analytical & Bioanalytical Chemistry, 2009, v. 395, n. 2, p. 393, doi. 10.1007/s00216-009-2819-4
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Cover Picture: Design and Sensing Properties of a Self-Assembled Supramolecular Oligomer (Chem. Eur. J. 6/2016).
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- Chemistry - A European Journal, 2016, v. 22, n. 6, p. 1865, doi. 10.1002/chem.201504887
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Design and Sensing Properties of a Self-Assembled Supramolecular Oligomer.
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- Chemistry - A European Journal, 2016, v. 22, n. 6, p. 1958, doi. 10.1002/chem.201503701
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Design and Sensing Properties of a Self-Assembled Supramolecular Oligomer.
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- Chemistry - A European Journal, 2016, v. 22, n. 6, p. 1869, doi. 10.1002/chem.201504920
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- Article
Self-Assembled Architectures with Segregated Donor and Acceptor Units of a Dyad Based on a Monopyrrolo-Annulated TTF-PTM Radical.
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- Chemistry - A European Journal, 2015, v. 21, n. 24, p. 8816, doi. 10.1002/chem.201500497
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Robust Inclusion Complexes of Crown Ether Fused Tetrathiafulvalenes with Li<sup>+</sup>@C<sub>60</sub> to Afford Efficient Photodriven Charge Separation.
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- Chemistry - A European Journal, 2014, v. 20, n. 43, p. 13976, doi. 10.1002/chem.201402449
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Mono- and Bis(pyrrolo)tetrathiafulvalene Derivatives Tethered to C<sub>60</sub>: Synthesis, Photophysical Studies, and Self-Assembled Monolayers.
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- Chemistry - A European Journal, 2014, v. 20, n. 32, p. 9918, doi. 10.1002/chem.201402623
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Chromo-Fluorogenic Detection of Nitroaromatic Explosives by Using Silica Mesoporous Supports Gated with Tetrathiafulvalene Derivatives.
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- Chemistry - A European Journal, 2014, v. 20, n. 3, p. 855, doi. 10.1002/chem.201302461
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Cover Feature: Naphtho[1,2‐b:5,6‐b′]dithiophene Building Blocks and their Complexation with Cyclobis(paraquat‐p‐phenylene) (Eur. J. Org. Chem. 46/2019).
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 46, p. 7512, doi. 10.1002/ejoc.201901757
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Naphtho[1,2‐b:5,6‐b′]dithiophene Building Blocks and their Complexation with Cyclobis(paraquat‐p‐phenylene).
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 46, p. 7532, doi. 10.1002/ejoc.201901161
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- Article
Redox‐Active Monopyrrolotetrathiafulvalene‐Based Rotaxane Incorporating the Dihydroazulene/Vinylheptafulvene Photo/Thermoswitch.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5532, doi. 10.1002/ejoc.201900690
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Mono-Tetrathiafulvalene Calix[4]pyrrole in the Electrochemical Sensing of Anions.
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- Angewandte Chemie International Edition, 2003, v. 42, n. 2, p. 187, doi. 10.1002/anie.200390074
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Tetrathiafulvaleno-Annelated Porphyrins.
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- Angewandte Chemie International Edition, 2001, v. 40, n. 13, p. 2497, doi. 10.1002/1521-3773(20010702)40:13<2497::AID-ANIE2497>3.0.CO;2-F
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Slow Shuttling in an Amphiphilic Bistable [2]Rotaxane Incorporating a Tetrathiafulvalene Unit.
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- Angewandte Chemie International Edition, 2001, v. 40, n. 7, p. 1216, doi. 10.1002/1521-3773(20010401)40:7<1216::AID-ANIE1216>3.0.CO;2-W
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