A theoretical study on quasi-one-dimensional open-shell singlet ladder oligomers: multi-radical nature, aromaticity and second hyperpolarizability-Reference-Cited by-同舟云学术

A theoretical study on quasi-one-dimensional open-shell singlet ladder oligomers: multi-radical nature, aromaticity and second hyperpolarizability

Published:2017 Issue:5 Volume:4 Page:779-789
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Fukuda Kotaro¹²³⁴⁵,Fujiyoshi Jun-ya¹²³⁴⁵,Matsui Hiroshi¹²³⁴⁵,Nagami Takanori¹²³⁴⁵,Takamuku Shota¹²³⁴⁵,Kitagawa Yasutaka¹²³⁴⁵,Champagne Benoît⁶⁷⁸⁹,Nakano Masayoshi¹²³⁴⁵

Affiliation:

1. Department of Materials Engineering Science

2. Graduate School of Engineering Science

3. Osaka University

4. Toyonaka

5. Japan

6. Laboratoire de Chimie Théorique

7. University of Namur

8. B-5000 Namur

9. Belgium

Abstract

Quasi-one-dimensional open-shell singlet ladder oligomers composed of indenofluorene-like units show strong correlation between multiradical nature, aromaticity and second hyperpolarizability.

Funder

Japan Society for the Promotion of Science

King Khalid University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C7QO00108H

Reference61 articles.

1. Indeno[1,2-b]fluorenes: Fully Conjugated Antiaromatic Analogues of Acenes

2. Indeno[2,1-a]fluorene: An Air-Stable ortho-Quinodimethane Derivative