Issue 42, 2015

Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions

Abstract

Diphenylacetylene (tolan) derivatives with self-complementary aryl halides and halogen bond-accepting nitriles form 2D bricklayer packing motifs when halogen bonding occurs. When halogen bonding is absent, as occurred with fluorinated aryl bromides, the molecules adopt other packing motifs. These results suggest halogen bonding is potentially useful for producing rarely observed 2D bricklayer motifs in organic semiconductors.

Graphical abstract: Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions

Supplementary files

Article information

Article type
Communication
Submitted
16 Mar 2015
Accepted
22 Apr 2015
First published
29 Apr 2015

Chem. Commun., 2015,51, 8825-8828

Author version available

Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions

F. Frausto, Z. C. Smith, T. E. Haas and S. W. Thomas III, Chem. Commun., 2015, 51, 8825 DOI: 10.1039/C5CC02225H

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