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Winterfeld KA, Lavarda G, Guilleme J, et al. Subphthalocyanines Axially Substituted with a Tetracyanobuta-1,3-diene-Aniline Moiety: Synthesis, Structure, and Physicochemical Properties. J Am Chem Soc. 2017;139(15):5520-5529doi: 10.1021/jacs.7b01460.
Winterfeld, K. A., Lavarda, G., Guilleme, J., Sekita, M., Guldi, D. M., Torres, T., & Bottari, G. (2017). Subphthalocyanines Axially Substituted with a Tetracyanobuta-1,3-diene-Aniline Moiety: Synthesis, Structure, and Physicochemical Properties. Journal of the American Chemical Society, 139(15), 5520-5529. https://doi.org/10.1021/jacs.7b01460
Winterfeld, Kim A, et al. "Subphthalocyanines Axially Substituted with a Tetracyanobuta-1,3-diene-Aniline Moiety: Synthesis, Structure, and Physicochemical Properties." Journal of the American Chemical Society vol. 139,15 (2017): 5520-5529. doi: https://doi.org/10.1021/jacs.7b01460
Winterfeld KA, Lavarda G, Guilleme J, Sekita M, Guldi DM, Torres T, Bottari G. Subphthalocyanines Axially Substituted with a Tetracyanobuta-1,3-diene-Aniline Moiety: Synthesis, Structure, and Physicochemical Properties. J Am Chem Soc. 2017 Apr 19;139(15):5520-5529. doi: 10.1021/jacs.7b01460. Epub 2017 Apr 06. PMID: 28322560.
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J Am Chem Soc. 2017 Apr 19;139(15):5520-5529. doi: 10.1021/jacs.7b01460. Epub 2017 Apr 06.

Subphthalocyanines Axially Substituted with a Tetracyanobuta-1,3-diene-Aniline Moiety: Synthesis, Structure, and Physicochemical Properties.

Journal of the American Chemical Society

Kim A Winterfeld, Giulia Lavarda, Julia Guilleme, Michael Sekita, Dirk M Guldi, Tomás Torres, Giovanni Bottari

Affiliations

  1. Department of Chemistry and Pharmacy, Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-Universität Erlangen-Nürnberg , Egerlandstr. 3, 91058 Erlangen, Germany.
  2. Departamento de Química Orgánica, Universidad Autónoma de Madrid , 28049 Madrid, Spain.
  3. IMDEA-Nanociencia , Campus de Cantoblanco, 28049 Madrid, Spain.
  4. Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid , 28049 Madrid, Spain.

PMID: 28322560 DOI: 10.1021/jacs.7b01460

Abstract

A 1,1,4,4-tetracyanobuta-1,3-diene (TCBD)-aniline moiety has been introduced, for the first time, at the axial position of two subphthalocyanines (SubPcs) peripherally substituted with hydrogen (H

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