Chiral redox-Active isosceles triangles

Siva Krishna Mohan Nalluri, Zhichang Liu, Yilei Wu, Keith R. Hermann, Avik Samanta, Dong Jun Kim, Matthew D. Krzyaniak, Michael R. Wasielewski, J. Fraser Stoddart

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Designing small-molecule organic redox-active materials, with potential applications in energy storage, has received considerable interest of late. Herein, we report on the synthesis, characterization, and application of two rigid chiral triangles, each of which consist of non-identical pyromellitic diimide (PMDI) and naphthalene diimide (NDI)-based redox-active units. 1H and 13C NMR spectroscopic investigations in solution confirm the lower symmetry (C2 point group) associated with these two isosceles triangles. Single-crystal X-ray diffraction analyses reveal their rigid triangular prism-like geometries. Unlike previously investigated equilateral triangle containing three identical NDI subunits, both isosceles triangles do not choose to form one-dimensional supramolecular nanotubes by dint of [C-H···O] interaction-driven columnar stacking. The rigid isosceles triangle, composed of one NDI and two PMDI subunits, forms in the presence of N,N-dimethylformamidetwo different types of intermolecular NDI-NDI and NDI-PMDI stacked dimers with opposite helicities in the solid state. Cyclic voltammetry reveals that both isosceles triangles can accept reversibly up to six electrons. Continuous-wave electron paramagnetic resonance and electron-nuclear double-resonance spectroscopic investigations, supported by density functional theory calculations, on the single-electron reduced radical anions of the isosceles triangles confirm the selective sharing of unpaired electrons among adjacent redox-active NDI subunit(s) within both molecules. The isosceles triangles have been employed as electrode-active materials in organic rechargeable lithium-ion batteries. The evaluation of the structure-performance relationships of this series of diimide-based triangles reveals that the increase in the number of NDI subunits, replacing PMDI ones, within the molecules improves the electrochemical cell performance of the batteries.

Original languageEnglish
Pages (from-to)5968-5977
Number of pages10
JournalJournal of the American Chemical Society
Volume138
Issue number18
DOIs
Publication statusPublished - May 11 2016

Fingerprint

Naphthalene
Oxidation-Reduction
Electrons
Electron Spin Resonance Spectroscopy
Molecules
Point groups
Nanotubes
Electrochemical cells
naphthalenediimide
Crystal symmetry
Prisms
Lithium
X-Ray Diffraction
Dimers
Energy storage
Cyclic voltammetry
Density functional theory
Anions
Paramagnetic resonance
Electrodes

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Nalluri, S. K. M., Liu, Z., Wu, Y., Hermann, K. R., Samanta, A., Kim, D. J., ... Stoddart, J. F. (2016). Chiral redox-Active isosceles triangles. Journal of the American Chemical Society, 138(18), 5968-5977. https://doi.org/10.1021/jacs.6b02086

Chiral redox-Active isosceles triangles. / Nalluri, Siva Krishna Mohan; Liu, Zhichang; Wu, Yilei; Hermann, Keith R.; Samanta, Avik; Kim, Dong Jun; Krzyaniak, Matthew D.; Wasielewski, Michael R.; Stoddart, J. Fraser.

In: Journal of the American Chemical Society, Vol. 138, No. 18, 11.05.2016, p. 5968-5977.

Research output: Contribution to journalArticle

Nalluri, SKM, Liu, Z, Wu, Y, Hermann, KR, Samanta, A, Kim, DJ, Krzyaniak, MD, Wasielewski, MR & Stoddart, JF 2016, 'Chiral redox-Active isosceles triangles', Journal of the American Chemical Society, vol. 138, no. 18, pp. 5968-5977. https://doi.org/10.1021/jacs.6b02086
Nalluri SKM, Liu Z, Wu Y, Hermann KR, Samanta A, Kim DJ et al. Chiral redox-Active isosceles triangles. Journal of the American Chemical Society. 2016 May 11;138(18):5968-5977. https://doi.org/10.1021/jacs.6b02086
Nalluri, Siva Krishna Mohan ; Liu, Zhichang ; Wu, Yilei ; Hermann, Keith R. ; Samanta, Avik ; Kim, Dong Jun ; Krzyaniak, Matthew D. ; Wasielewski, Michael R. ; Stoddart, J. Fraser. / Chiral redox-Active isosceles triangles. In: Journal of the American Chemical Society. 2016 ; Vol. 138, No. 18. pp. 5968-5977.
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