Issue 5, 2017

The effect of a highly twisted C[double bond, length as m-dash]C double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states

Abstract

We synthesized methyl-substituted 9,9′-bifluorenylidene (9,9′-BF) derivatives in which two planar fluorene units are connected through a C[double bond, length as m-dash]C double bond. The C[double bond, length as m-dash]C double bond is twisted owing to the steric crowding between the fluorene units, and by introducing substituents at 1,1′-positions (inner space of 9,9′-BF) it becomes more twisted. Indeed, single crystal X-ray structural analysis and theoretical calculation reveal that the dihedral angle between two fluorene π-planes of a 1,1′-dimethyl-substituted 9,9′-BF is 56°, which is clearly larger than those of pristine 9,9′-BF (42°) and 1-methyl-substituted 9,9′-BF (50°). The twisted conformation of 1,1′-dimethyl-substituted 9,9′-BF facilitates the cistrans isomerization process which we assessed quantitatively by variable-temperature NMR measurements. The 9,9′-BF derivatives with different numbers of methyl groups also exhibit remarkable changes in optoelectronic properties, primarily because of the change in the twisting angle of the central C[double bond, length as m-dash]C double bond. Theoretical calculation further indicates that the electronic structures of methyl-substituted 9,9′-BF derivatives in the excited states are considerably different from those of pristine 9,9′-BF.

Graphical abstract: The effect of a highly twisted C [[double bond, length as m-dash]] C double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states

Supplementary files

Article information

Article type
Research Article
Submitted
14 фев 2017
Accepted
09 мар 2017
First published
16 мар 2017

Org. Chem. Front., 2017,4, 650-657

The effect of a highly twisted C[double bond, length as m-dash]C double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states

A. Takai, D. J. Freas, T. Suzuki, M. Sugimoto, J. Labuta, R. Haruki, R. Kumai, S. Adachi, H. Sakai, T. Hasobe, Y. Matsushita and M. Takeuchi, Org. Chem. Front., 2017, 4, 650 DOI: 10.1039/C7QO00125H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements