Issue 13, 2008

Central-ring functionalization and application of the rigid, aromatic, and H-shaped pentiptycene scaffold

Abstract

The progress of pentiptycene chemistry is reviewed. Pentiptycene belongs to the iptycene family and possesses a rigid, aromatic, and H-shaped scaffold. An important feature for pentiptycene vs. triptycene is the presence of a ‘sterically shielded’ central benzene ring. Such a feature has led to the use of pentiptycene as a conformational regulator and in the formation of functional molecules, including fluorescent chemosensors, molecular machines, low dielectric constant materials, and porous solids. The synthesis of these materials relies on central-ring prefunctionalized pentiptycene building blocks. A useful approach toward the preparation of these building blocks is the derivatization of pentiptycene quinone.

Graphical abstract: Central-ring functionalization and application of the rigid, aromatic, and H-shaped pentiptycene scaffold

Article information

Article type
Feature Article
Submitted
31 Aug 2007
Accepted
22 Nov 2007
First published
14 Feb 2008

Chem. Commun., 2008, 1501-1512

Central-ring functionalization and application of the rigid, aromatic, and H-shaped pentiptycene scaffold

J. Yang and J. Yan, Chem. Commun., 2008, 1501 DOI: 10.1039/B713428M

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