Tri- and hexaferrocenyl-substituted subphthalocyanines in the quest for the optimum electron donor–acceptor distances-Reference-Cited by-同舟云学术

Tri- and hexaferrocenyl-substituted subphthalocyanines in the quest for the optimum electron donor–acceptor distances

Published:2017 Issue:61 Volume:53 Page:8525-8528
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Fernández-Ariza Javier¹²³⁴^ORCID,Krick Calderón Rafael M.⁵⁶⁷⁸,Perles Josefina⁹¹⁰¹¹³⁴^ORCID,Rodríguez-Morgade M. Salomé¹²³⁴¹²^ORCID,Guldi Dirk M.⁵⁶⁷⁸^ORCID,Torres Tomás¹²³⁴¹²^ORCID

Affiliation:

1. Departamento de Química Orgánica

2. Universidad Autónoma de Madrid (UAM)

3. 28049 Madrid

4. Spain

5. Department of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM)

6. University of Erlangen-Nuremberg

7. 91058 Erlangen

8. Germany

9. Laboratorio de DRX Monocristal

10. Servicio Interdepartamental de Investigación

11. UAM

12. Institute for Advanced Research in Chemical Sciences (IAdChem)

Abstract

Three and six ferrocenyl subunits have been attached to the periphery of subphthalocyanines (SubPcs).

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/CC/C7CC04726F

Reference36 articles.

1. Subphthalocyanines, Subporphyrazines, and Subporphyrins: Singular Nonplanar Aromatic Systems

2. Subphthalocyanines: Singular Nonplanar Aromatic CompoundsSynthesis, Reactivity, and Physical Properties

3. Chiral Self-Discrimination in a M3L2 Subphthalocyanine Cage

4. Pyrene-fused subphthalocyanine

5. Trapping fullerenes with jellyfish-like subphthalocyanines

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