AI Article Synopsis

  • The (S,S,S,S) and (R,R,R,R) enantiomers of TM-BEDT-TTF have been found to adopt an equatorial conformation in solid-state structures as confirmed by single-crystal X-ray analyses.
  • Theoretical calculations suggest that the axial conformer is more stable in gas phase than the equatorial conformer, providing insights into their UV-vis and circular dichroism properties.
  • Electrocrystallization produced a series of radical cation salts with triiodide anions, revealing that while organized dimers facilitate interactions among donors, the racemic mixture shows lower conductivity and higher activation energy due to structural disorder.

Article Abstract

The (S,S,S,S) and (R,R,R,R) enantiomers of tetramethyl-bis(ethylenedithio)-tetrathiafulvalene (TM-BEDT-TTF) show equatorial conformation for the four methyl groups in the solid state, according to the single-crystal X-ray analyses. Theoretical calculations at the Density Functional Theory (DFT) and time-dependent (TD) DFT levels indicate higher gas phase stability for the axial conformer than the equatorial one by 1.25 kcal ∙ mole⁻¹ and allow the assignment of the UV-vis and circular dichroism transitions. A complete series of radical cation salts of 1:1 stoichiometry with the triiodide anion I₃⁻ was obtained by electrocrystallization of both enantiopure and racemic forms of the donor. In the packing the donors are organized in dimers that further interact through S ∙ ∙ ∙ S intermolecular contacts and the triiodide anions lie parallel to pairs of oxidized donors. The conductivity of the racemate, which adopts the same, but disordered, structural type, is considerably lower, with much higher activation energy.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chir.22210DOI Listing

Publication Analysis

Top Keywords

tetramethyl-bisethylenedithio-tetrathiafulvalene tm-bedt-ttf
8
theoretical calculations
8
complete series
8
radical cation
8
cation salts
8
∙ ∙
8
tm-bedt-ttf revisited
4
revisited crystal
4
crystal structures
4
structures chiroptical
4

Similar Publications

Enantio-discrimination and spin-dependent electrochemistry (SDE), as a manifestation of the chirality-induced spin selectivity (CISS) effect, are important phenomena that can be probed by "chiral" electrochemistry. Here, we prepared chiralized surfaces of gold and nickel, to serve as working electrodes, through effective chemisorption of enantiopure dimethyl-bis(ethylenedithio)-tetrathiafulvalene (DM-BEDT-TTF) 1, tetramethyl-bis(ethylenedithio)-tetrathiafulvalene (TM-BEDT-TTF) 2, and their capped silver nanoparticle (AgNPs) aggregate by simple incubation of the metallic substrates. The effective chemisorption was checked by means of ultrahigh vacuum x-ray photoelectron spectroscopy (XPS) and by electro-desorption experiments, i.

View Article and Find Full Text PDF

Electrocrystallization of enantiopure (S,S,S,S)- and (R,R,R,R)-tetramethyl-bis(ethylenedithio)-tetrathiafulvalene (TM-BEDT-TTF) donors, as well as the racemic mixture, in the presence of potassium cations and the tris(chloranilato)ferrate(III) [Fe(Cl2An)3](3-) paramagnetic anion afforded a complete series of chiral magnetic molecular conductors formulated as β-[(S,S,S,S)-TM-BEDT-TTF]3PPh4[K(I)Fe(III)(Cl2An)3]·3H2O (1), β-[(R,R,R,R)-TM-BEDT-TTF]3PPh4[K(I)Fe(III)(Cl2An)3]·3H2O (2), and β-[(rac)-TM-BEDT-TTF]3PPh4[K(I)Fe(III)(Cl2An)3]·3H2O (3). Compounds 1-3 are isostructural and crystallize in triclinic space groups (P1 for 1 and 2, P-1 for 3) showing a segregated organic-inorganic crystal structure, where anionic honeycomb layers obtained by self-assembling of the Λ and Δ enantiomers of the paramagnetic complex with potassium cations alternate with organic layers where the chiral donors are arranged in the β packing motif. Compounds 1-3 show a molecular packing strongly influenced by the topology of the inorganic layers and behave as molecular semiconductors with room-temperature conductivity values of ca.

View Article and Find Full Text PDF
Article Synopsis
  • The (S,S,S,S) and (R,R,R,R) enantiomers of TM-BEDT-TTF have been found to adopt an equatorial conformation in solid-state structures as confirmed by single-crystal X-ray analyses.
  • Theoretical calculations suggest that the axial conformer is more stable in gas phase than the equatorial conformer, providing insights into their UV-vis and circular dichroism properties.
  • Electrocrystallization produced a series of radical cation salts with triiodide anions, revealing that while organized dimers facilitate interactions among donors, the racemic mixture shows lower conductivity and higher activation energy due to structural disorder.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!