Compounds > tetrathiafulvalene
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tetrathiafulvalene and calixarenes

tetrathiafulvalene has been researched along with calixarenes in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (12.50)29.6817
2010's7 (87.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cho, WS; Jeppesen, JO; Levillain, E; Lynch, VM; Lyskawa, J; Nielsen, KA; Sessler, JL1
Bejger, CM; Jeppesen, JO; Johnsen, C; Le Derf, F; Lynch, VM; Nielsen, KA; Park, JS; Sessler, JL1
Cao, QY; Kim, JS; Kim, SK; Lee, MH; Sessler, JL1
Fukuzumi, S; Jana, A; Kawashima, Y; Kim, D; Kim, DS; Lynch, VM; Ohkubo, K; Park, JS; Sessler, JL1
Hu, F; Sun, F; Zhang, D; Zhang, G1
Bielawski, CW; Johnston, KP; Kim, DS; Lynch, VM; Park, JS; Sessler, JL; Yoon, KY1
Bähring, S; Kongsted, J; Nielsen, KA; Olsen, G; Stein, PC1
Azov, VA; Düker, MH; Schäfer, H; Zeller, M1

Other Studies

8 other study(ies) available for tetrathiafulvalene and calixarenes

ArticleYear
Tetrathiafulvalene-calix[4]pyrroles: synthesis, anion binding, and electrochemical properties.
    Journal of the American Chemical Society, 2006, Feb-22, Volume: 128, Issue:7

    Topics: Anions; Calixarenes; Crystallography, X-Ray; Electrochemistry; Heterocyclic Compounds; Kinetics; Magnetic Resonance Spectroscopy; Mass Spectrometry; Porphyrins; Titrimetry

2006
Positive homotropic allosteric receptors for neutral guests: annulated tetrathiafulvalene-calix[4]pyrroles as colorimetric chemosensors for nitroaromatic explosives.
    Chemistry (Weinheim an der Bergstrasse, Germany), 2010, Jan-18, Volume: 16, Issue:3

    Topics: Calixarenes; Colorimetry; Crystallography, X-Ray; Cyclization; Explosive Agents; Heterocyclic Compounds; Molecular Conformation; Porphyrins

2010
Anion responsive TTF-appended calix[4]arenes. Synthesis and study of two different conformers.
    The Journal of organic chemistry, 2011, Feb-04, Volume: 76, Issue:3

    Topics: Anions; Calixarenes; Heterocyclic Compounds; Magnetic Resonance Spectroscopy; Molecular Conformation; Molecular Structure; Phenols

2011
Ion-controlled on-off switch of electron transfer from tetrathiafulvalene calix[4]pyrroles to Li+@C60.
    Journal of the American Chemical Society, 2011, Oct-12, Volume: 133, Issue:40

    Topics: Calixarenes; Crystallography, X-Ray; Electron Transport; Fullerenes; Heterocyclic Compounds; Ions; Lithium; Models, Molecular; Porphyrins

2011
Metal-ion-promoted electron transfer between tetrathiafulvalene and quinone units within a calix[4]arene framework and tuning through coordination of the neighboring crown ether with a sodium cation.
    Chemistry, an Asian journal, 2012, Jan-02, Volume: 7, Issue:1

    Topics: Calixarenes; Cations; Crown Ethers; Electron Transport; Heterocyclic Compounds; Ions; Metals, Heavy; Molecular Structure; Phenols; Quinones; Sodium

2012
Chemoresponsive alternating supramolecular copolymers created from heterocomplementary calix[4]pyrroles.
    Proceedings of the National Academy of Sciences of the United States of America, 2011, Dec-27, Volume: 108, Issue:52

    Topics: Calixarenes; Chemistry, Physical; Crystallography, X-Ray; Dinitrobenzenes; Heterocyclic Compounds; Hydrogen Bonding; Magnetic Resonance Spectroscopy; Microscopy, Electron, Scanning; Molecular Conformation; Polymers; Porphyrins

2011
Coordination-driven switching of a preorganized and cooperative calix[4]pyrrole receptor.
    Chemistry (Weinheim an der Bergstrasse, Germany), 2013, Feb-18, Volume: 19, Issue:8

    Topics: Allosteric Site; Calixarenes; Heterocyclic Compounds; Hydrogen Bonding; Magnetic Resonance Spectroscopy; Molecular Structure; Porphyrins; Pyridines; Trinitrobenzenes; Zinc

2013
Rationally designed calix[4]arene-pyrrolotetrathiafulvalene receptors for electron-deficient neutral guests.
    The Journal of organic chemistry, 2013, May-17, Volume: 78, Issue:10

    Topics: Calixarenes; Electrons; Heterocyclic Compounds; Models, Molecular; Molecular Structure; Phenols

2013