Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)2XF6 (X = P, As, Sb).
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[1] N. Avarvari,et al. Enantiopure Radical Cation Salt Based on Tetramethyl-Bis(ethylenedithio)-Tetrathiafulvalene and Hexanuclear Rhenium Cluster , 2016 .
[2] N. Avarvari,et al. Complete series of chiral paramagnetic molecular conductors based on tetramethyl-bis(ethylenedithio)-tetrathiafulvalene (TM-BEDT-TTF) and Chloranilate-bridged heterobimetallic honeycomb layers. , 2015, Inorganic chemistry.
[3] D. Amabilino,et al. Hierarchical self-assembly of supramolecular helical fibres from amphiphilic C3-symmetrical functional tris(tetrathiafulvalenes). , 2014, Chemistry.
[4] H. Matsuzawa,et al. Dimeric tetrathiafulvalene linked to pseudo-ortho-[2.2]paracyclophane: chiral electrochromic properties and use as a chiral dopant. , 2014, Chemistry, an Asian journal.
[5] N. Avarvari,et al. Enantiopure Conducting Salts of Dimethylbis(ethylenedithio)tetrathiafulvalene (DM-BEDT-TTF) with the Hexachlororhenate(IV) Anion: Conducting Salts of Dimethylbis(ethylenedithio)tetrathiafulvalene , 2014 .
[6] N. Avarvari,et al. Electrical magnetochiral anisotropy in a bulk chiral molecular conductor , 2014, Nature Communications.
[7] N. Avarvari,et al. Charge transfer complexes and radical cation salts of chiral methylated organosulfur donors , 2014 .
[8] N. Avarvari,et al. Chirality driven metallic versus semiconducting behavior in a complete series of radical cation salts based on dimethyl-ethylenedithio-tetrathiafulvalene (DM-EDT-TTF). , 2013, Journal of the American Chemical Society.
[9] F. Pelletier,et al. Synthesis of new chiral organosulfur donors with hydrogen bonding functionality and their first charge transfer salts , 2013 .
[10] N. Avarvari,et al. Ethylenedithio-tetrathiafulvalene-helicenes: electroactive helical precursors with switchable chiroptical properties. , 2013, Chemistry.
[11] N. Avarvari,et al. Tetramethyl-bis(ethylenedithio)-tetrathiafulvalene (TM-BEDT-TTF) revisited: crystal structures, chiroptical properties, theoretical calculations, and a complete series of conducting radical cation salts. , 2013, Chirality.
[12] Takehiko Mori,et al. Structural transitions from triangular to square molecular arrangements in the quasi-one-dimensional molecular conductors (DMEDO-TTF)2XF6 (X = P, As, and Sb). , 2012, Journal of the American Chemical Society.
[13] Yasuto Sone,et al. Tetrathiafulvalenylallene: a new class of donor molecules having strong chiroptical properties in neutral and doped states. , 2011, Organic letters.
[14] E. Levillain,et al. Persistent mixed-valence [(TTF)2]+* dyad of a chiral bis(binaphthol)-tetrathiafulvalene (TTF) derivative. , 2010, Chemistry.
[15] E. Coronado,et al. A chiral ferromagnetic molecular metal. , 2010, Journal of the American Chemical Society.
[16] N. Avarvari,et al. Order versus disorder in chiral tetrathiafulvalene-oxazoline radical-cation salts: structural and theoretical investigations and physical properties. , 2010, Chemistry.
[17] N. Avarvari,et al. C(2)-symmetric chiral tetrathiafulvalene-bis(oxazolines) (TTF-BOX): new precursors for organic materials and electroactive metal complexes. , 2009, Chemical communications.
[18] N. Avarvari,et al. Strategies towards chiral molecular conductors , 2009 .
[19] L. Male,et al. Novel enantiopure bis(pyrrolo)tetrathiafulvalene donors exhibiting chiral crystal packing arrangements , 2009 .
[20] N. Avarvari,et al. Chemo- and enantioselective sulfoxidation of bis(ethylenedithio)-tetrathiafulvalene (BEDT-TTF) into chiral BEDT-TTF-sulfoxide. , 2008, Chemical communications.
[21] T. Imakubo,et al. New unsymmetrical donor dimethyl(ethylenedioxy)tetraselenafulvalene (DMEDO-TSeF): Structures and properties of its cation radical salts , 2005 .
[22] Huifen Nie,et al. Synthetic strategies to chiral organosulfur donors related to bis(ethylenedithio)tetrathiafulvalene. , 2005, Organic & biomolecular chemistry.
[23] N. Avarvari,et al. Chiral molecular metals: syntheses, structures, and properties of the AsF(6)(-) salts of racemic (+/-)-, (R)-, and (S)-tetrathiafulvalene-oxazoline derivatives. , 2005, Journal of the American Chemical Society.
[24] S. Roth,et al. Magneto-chiral anisotropy in charge transport through single-walled carbon nanotubes , 2002 .
[25] Gautam R Desiraju,et al. Hydrogen bridges in crystal engineering: interactions without borders. , 2002, Accounts of chemical research.
[26] P. Wyder,et al. Electrical magnetochiral anisotropy. , 2001, Physical review letters.
[27] Segura,et al. New chiral binaphthyl building blocks: synthesis of the first optically active tetrathiafulvalene and 11,11,12,12-tetracyano-9, 10-anthraquinodimethane dimers , 2000, The Journal of organic chemistry.
[28] Gautam R. Desiraju,et al. The Weak Hydrogen Bond: In Structural Chemistry and Biology , 1999 .
[29] Shu-Kun Lin. The Weak Hydrogen Bond: Applications to Structural Chemistry and Biology(International Union of Crystallography Monographs on Crystallography, 9). By Gautam R. Desiraju , 1999 .
[30] Gautam R. Desiraju,et al. The C-h···o hydrogen bond: structural implications and supramolecular design. , 1996, Accounts of chemical research.
[31] C. Rovira,et al. A new family of molecular metals based on bis(ethylenethio)tetrathiafulvalene (BET-TTF) and octahedral counterions , 1995 .
[32] M. Tokumoto,et al. Crystal Structure and Conductivity of Chiral Radical Ion Salts (Me2ET)2X , 1993 .
[33] A. Kobayashi,et al. Dimensionality Examination of Cation Radical Salts Based on EDT-TTF (EDT-TTF = Ethylenedithiotetrathiafulvalene) , 1989 .
[34] J. Dunitz,et al. Chiral metals? A chiral substrate for organic conductors and superconductors , 1986 .
[35] T. Emge,et al. Role of the intermolecular interactions in the two-dimensional ambient-pressure organic superconductors. beta. -(ET)/sub 2/I/sub 3/ and. beta. -(ET)/sub 2/IBr/sub 2/ , 1985 .