Works matching DE "TETRATHIAFULVALENE"
Results: 239
Integrating Tetrathiafulvalene and Nickel‐Bis(dithiolene) Units into Donor‐Acceptor Covalent Organic Frameworks for Stable and Efficient Photothermal Conversion.
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- Chemistry - A European Journal, 2023, v. 29, n. 34, p. 1, doi. 10.1002/chem.202301048
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On‐Demand Control of Short‐Wave Infrared Light Transparency Based on Stimuli‐Responsive Association of Tetrathiafulvalene Radical Cations.
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- Angewandte Chemie, 2023, v. 135, n. 35, p. 1, doi. 10.1002/ange.202308570
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Coordination‐Modulated Metal Tetrathiafulvalene Octacarboxylate Frameworks for High‐Performance Lithium‐Ion Battery Anodes.
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- Angewandte Chemie, 2023, v. 135, n. 27, p. 1, doi. 10.1002/ange.202304183
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Redox‐Active Mixed‐Linker Metal–Organic Frameworks with Switchable Semiconductive Characteristics for Tailorable Chemiresistive Sensing.
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- Angewandte Chemie, 2023, v. 135, n. 10, p. 1, doi. 10.1002/ange.202211850
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Oxidation‐Reduction Molecular Junction Covalent Organic Frameworks for Full Reaction Photosynthesis of H<sub>2</sub>O<sub>2</sub>.
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- Angewandte Chemie, 2023, v. 135, n. 9, p. 1, doi. 10.1002/ange.202218868
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TTF‐Annulated Silicon Phthalocyanine Oligomers and Their External‐Stimuli‐Responsive Orientational Ordering.
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- Angewandte Chemie, 2020, v. 132, n. 50, p. 22910, doi. 10.1002/ange.202011025
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Accordion‐Like Motion in Electrochemically Switchable Crown Ether/Ammonium Oligorotaxanes.
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- Angewandte Chemie, 2019, v. 131, n. 11, p. 3534, doi. 10.1002/ange.201813265
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Molecular Heterojunctions of Oligo(phenylene ethynylene)s with Linear to Cruciform Framework.
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- Advanced Functional Materials, 2015, v. 25, n. 11, p. 1700, doi. 10.1002/adfm.201404388
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Resonant Raman scattering and ESR study of ET salts with rhenium‐containing anions.
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- Journal of Raman Spectroscopy, 2018, v. 49, n. 2, p. 238, doi. 10.1002/jrs.5271
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Infrared and Raman spectroscopic studies of the charge localization in one-dimensional organic metals (DMtTTF)<sub>2</sub>X (X = ReO<sub>4</sub>, ClO<sub>4</sub>) with regular organic stacks.
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- Journal of Raman Spectroscopy, 2013, v. 44, n. 12, p. 1765, doi. 10.1002/jrs.4405
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Molecular Diodes With Tunable Threshold Voltage Based on π‐Extended Tetrathiafulvalene.
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- Advanced Materials Interfaces, 2022, v. 9, n. 27, p. 1, doi. 10.1002/admi.202201238
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Conjugated Tetrathiafulvalene Carboxylates for Stable Organic Lithium Batteries.
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- ChemElectroChem, 2022, v. 9, n. 6, p. 1, doi. 10.1002/celc.202200026
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Voltammetric, Spectroscopic, and Microscopic Investigation of the Oxidation of Solid and Solution Phases of Tetrathiafulvalene (TTF) to (TTF)<sub>2</sub>MO<sub>4</sub> (M=Mo, W).
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- ChemElectroChem, 2018, v. 5, n. 6, p. 885, doi. 10.1002/celc.201700463
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The Development and Evaluation of Reagentless Glucose Biosensors Using Dendritic Gold Nanostructures as a Promising Sensing Platform.
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- Biosensors (2079-6374), 2023, v. 13, n. 7, p. 727, doi. 10.3390/bios13070727
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π‐Extended 4,5‐Fused Bis‐Fluorene: Highly Open‐Shell Compounds and their Cationic Tetrathiafulvalene Derivatives.
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- Angewandte Chemie, 2024, v. 136, n. 49, p. 1, doi. 10.1002/ange.202410458
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Electrical properties of new organic composites obtained by mechanochemical synthesis.
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- Journal of Materials Science, 2001, v. 36, n. 5, p. 1227, doi. 10.1023/A:1004898329344
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Enantio‐Recognition and Charge Transfer Complex Formation Involving Tetrathiafulvalene‐Appended Chiral 1,2‐Cyclohexane‐Diamine: An Integrated Experimental and Theoretical Study.
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- Chirality, 2024, v. 36, n. 12, p. 1, doi. 10.1002/chir.70009
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Collimating the growth of twisted crystals of achiral compounds.
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- Chirality, 2023, v. 35, n. 7, p. 418, doi. 10.1002/chir.23558
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Tetrathiafulvalene‐[2.2]paracyclophanes: Synthesis, crystal structures, and chiroptical properties.
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- Chirality, 2018, v. 30, n. 5, p. 568, doi. 10.1002/chir.22831
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Recent advances in developing tetrathiafulvalene analogs of electrode materials: discovery of an in-cell polymerization technique.
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- Pure & Applied Chemistry, 2023, v. 95, n. 4, p. 431, doi. 10.1515/pac-2023-0302
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Tetrathiafulvalene vinylogues as versatile building blocks for new organic materials.
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- Pure & Applied Chemistry, 2012, v. 84, n. 4, p. 1005, doi. 10.1351/PAC-CON-11-09-22
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Molecular recognition and switching via radical dimerization*.
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- Pure & Applied Chemistry, 2010, v. 82, n. 12, p. 2281, doi. 10.1351/PAC-CON-10-08-03
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- Article
New routes to functionalized dihydroazulene photoswitches.
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- Pure & Applied Chemistry, 2010, v. 82, n. 4, p. 843, doi. 10.1351/PAC-CON-09-07-08
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Molecular tweezers for fullerenes.
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- Pure & Applied Chemistry, 2010, v. 82, n. 3, p. 523, doi. 10.1351/PAC-CON-09-09-27
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Theoretical investigation of different functional groups effect on the photophysical performance of tricarbonylrhenium(I) complexes with tetrathiafulvalene derivative as dyes in dye-sensitized solar cell.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2015, v. 134, n. 5, p. 1, doi. 10.1007/s00214-015-1665-z
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Theoretical study of the benzoquinone-tetrathiafulvalene-benzoquinone triad in neutral and oxidized/reduced states.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2013, v. 132, n. 3, p. 1, doi. 10.1007/s00214-013-1330-3
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Theoretical studies of COOH group effect on the performance of rhenium (I) tricarbonyl complexes with bispyridine sulfur-rich core ligand as dyes in DSSC.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2012, v. 131, n. 9, p. 1, doi. 10.1007/s00214-012-1266-z
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An ion-pair complex [TTF][Pd(mnt) 2 ]: synthesis, crystal structure, magnetic property, and electrical conductivity.
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- Journal of Coordination Chemistry, 2013, v. 66, n. 14, p. 2529, doi. 10.1080/00958972.2013.808337
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Threefold exTTF-based Buckycatcher.
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- Journal of Coordination Chemistry, 2010, v. 63, n. 14-16, p. 2939, doi. 10.1080/00958972.2010.500666
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(BEDT-TTF)<sub>2</sub>Cu<sub>2</sub>(HCOO)<sub>5</sub>: An Organic-Inorganic Hybrid Conducting Magnet.
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- ChemistryOpen, 2017, v. 6, n. 3, p. 320, doi. 10.1002/open.201700041
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Printed, Flexible Lactate Sensors: Design Considerations Before Performing On-Body Measurements.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49689-7
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Quasi-Two-Dimensional Organic Superconductors.
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- Journal of Low Temperature Physics, 2007, v. 146, n. 5/6, p. 641, doi. 10.1007/s10909-006-9282-9
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Thermoelectric Properties of Organic Charge-Transfer Compounds.
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- Journal of Electronic Materials, 2009, v. 38, n. 7, p. 1171, doi. 10.1007/s11664-009-0791-6
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A silver(I) coordination derivative of 2,3-dimethylthio-6-pyridyl tetrathiafulvalene, synthesis, crystal structure and electrochemical properties.
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- Journal of Coordination Chemistry, 2007, v. 60, n. 21, p. 2319, doi. 10.1080/00958970701261378
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Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand.
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- Inorganics, 2021, v. 9, n. 7, p. 50, doi. 10.3390/inorganics9070050
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Synthesis and Physical Properties of Tetrathiafulvalene-8-Quinolinato Zinc(II) and Nickel(II) Complexes.
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- Inorganics, 2021, v. 9, n. 2, p. 11, doi. 10.3390/inorganics9020011
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Field-Induced Dysprosium Single-Molecule Magnet Involving a Fused o-Semiquinone-Extended-Tetrathiafulvalene-o-Semiquinone Bridging Triad.
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- Inorganics, 2018, v. 6, n. 2, p. 45, doi. 10.3390/inorganics6020045
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Metal (Hg, Pt, Ru) Bisalkynyl Bridge between Tetrathiafulvalene Electrophores and Electronic Interplay.
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- Inorganics, 2018, v. 6, n. 2, p. 43, doi. 10.3390/inorganics6020043
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DFT study including NBO, NLO response and reactivity descriptor of bis and tris (1, 3-dithiole) tetrathiafulvalene.
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- Journal of Drug Delivery & Therapeutics, 2018, v. 8, n. 3, p. 96, doi. 10.22270/jddt.v8i3.1716
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Engineering spin-dependent catalysts: chiral covalent organic frameworks with tunable electroactivity for electrochemical oxygen evolution.
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- National Science Review, 2024, v. 11, n. 9, p. 1, doi. 10.1093/nsr/nwae332
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Spectrum of somatic EGFR, KRAS, BRAF, PTEN mutations and TTF-1 expression in Brazilian lung cancer patients.
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- Genetics Research, 2014, v. 96, p. 00, doi. 10.1017/S0016672314000032
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Time to first flare-up episode of GVHD can stratify patients according to their prognosis during clinical course of progressive- or quiescent-type chronic GVHD.
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- Bone Marrow Transplantation, 2007, v. 40, n. 8, p. 779, doi. 10.1038/sj.bmt.1705806
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Tetrathiafulvalenes as anchors for building highly conductive and mechanically tunable molecular junctions.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29483-2
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Charge-transfer regulated visible light driven photocatalytic H<sub>2</sub> production and CO<sub>2</sub> reduction in tetrathiafulvalene based coordination polymer gel.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27457-4
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Synthesis, Structure, Optical, and Electrochemical Properties of Triple- and Quadruple-Decker Co-facial Tetrathiafulvalene Arrays.
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- Chemistry - An Asian Journal, 2016, v. 6, p. 10090, doi. 10.1002/chem.201601785
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Bipyridinium Polymers That Dock Tetrathiafulvalene Guests in Water Driven by Donor-Acceptor and Ion Pair Interactions.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 7, p. 1065, doi. 10.1002/asia.201600017
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Dimerization of Conjugated Radical Cations: An Emerging Non-Covalent Interaction for Self-Assembly.
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- Chemistry - An Asian Journal, 2015, v. 10, n. 1, p. 56, doi. 10.1002/asia.201402805
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Unprecedented Sensitization of Visible and Near-Infrared Lanthanide Luminescence by Using a Tetrathiafulvalene-Based Chromophore.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 10, p. 2814, doi. 10.1002/asia.201402385
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Dimeric Tetrathiafulvalene Linked to pseudo-ortho-[2.2]Paracyclophane: Chiral Electrochromic Properties and Use as a Chiral Dopant.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 10, p. 2751, doi. 10.1002/asia.201402667
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Cover Picture: Hydrogen-Bonding Effect on Spin-Center Transfer of Tetrathiafulvalene-Linked 6-Oxophenalenoxyl Evaluated Using Temperature-Dependent Cyclic Voltammetry and Theoretical Calculations (Chem. Asian J. 2/2014).
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- Chemistry - An Asian Journal, 2014, v. 9, n. 2, p. 381, doi. 10.1002/asia.201490000
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