A post-cyclotetramerization strategy towards novel binuclear phthalocyanine dimers-Reference-Cited by-同舟云学术

A post-cyclotetramerization strategy towards novel binuclear phthalocyanine dimers

Published:2017 Issue:1 Volume:4 Page:110-113
ISSN:2052-1553
Container-title:Inorganic Chemistry Frontiers
language:en
Short-container-title:Inorg. Chem. Front.

Author:

Wang Kang¹²³⁴⁵,Huang Chunhua¹²³⁴⁵,Pan Houhe¹²³⁴⁵,Kobayashi Nagao⁶⁷⁸⁹,Jiang Jianzhuang¹²³⁴⁵

Affiliation:

1. Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials

2. Department of Chemistry

3. University of Science and Technology Beijing

4. Beijing 100083

5. China

6. Faculty of Textile Science and Technology

7. Shinshu University

8. Ueda 386-8567

9. Japan

Abstract

A new and effective post-cyclotetramerization strategy was developed for the first time towards the synthesis and isolation of a new type of homo/heterodinuclear π-conjugated phthalocyanine dimer sharing one common pyrazine moiety.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QI/C6QI00408C

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3. Dimeric porphyrins linked by conjugated groups containing triple bonds: the crystal structure of the nickel octaethylporphyrin dimer bridged by 2,5-diethynylthiophene

4. Dimers and Model Monomers of Nickel(II) Octaethylporphyrin Substituted by Conjugated Groups Comprising Combinations of Triple Bonds with Double Bonds and Arenes. 1. Synthesis and Electronic Spectra

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