Synthesis and ring opening reaction of octaoctyl substituted [2.2.2.2](2,7)-fluorenophanetetraene by photooxidation-Reference-Cited by-同舟云学术

Synthesis and ring opening reaction of octaoctyl substituted [2.2.2.2](2,7)-fluorenophanetetraene by photooxidation

Published:2017 Issue:23 Volume:41 Page:14116-14121
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Yu Chin-Yang¹²³⁴^ORCID,Chen Yu-Chi¹²³⁴,Wang Chao-Chi¹²³⁴

Affiliation:

1. Department of Materials Science and Engineering

2. National Taiwan University of Science and Technology

3. Taipei

4. Taiwan

Abstract

Octaoctyl substituted fluorenophanetetraene has been synthesized and the photooxidation of the fluorenophanetetraene gives all trans linear fluorenevinylene with aldehyde end groups.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C7NJ02735D

Reference43 articles.

1. Enhanced light harvesting with π-conjugated cyclic aromatic hydrocarbons for porphyrin-sensitized solar cells

2. Organoplatinum-Mediated Synthesis of Cyclic π-Conjugated Molecules: Towards a New Era of Three-Dimensional Aromatic Compounds

3. Enhanced light harvesting with π-conjugated cyclic aromatic hydrocarbons for porphyrin-sensitized solar cells

4. Highly Flexible π-Expanded Cyclooctatetraenes: Cyclic Thiazole Tetramers with Head-to-Tail Connection

5. Discrete Cyclic Porphyrin Arrays as Artificial Light-Harvesting Antenna

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