4.8 Article

Orthogonal Functionalization of Cyclopenta[hi]aceanthrylenes

Journal

ORGANIC LETTERS
Volume 15, Issue 6, Pages 1202-1205

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol400093g

Keywords

-

Funding

  1. Southern Illinois University

Ask authors/readers for more resources

A synthetic strategy to prepare 2,7- or 4,9-functionalized cyclopenta[hi]aceanthrylenes that are capable of Suzuki cross-coupling reactions is demonstrated. This method has been utilized to create a series of thiophene derivatized compounds that were subsequently used to Investigate the role of substitution pattern on the photophysical and electronic properties of cyclopenta[hi]aceanthrylenes. The orthogonal functionalization provides access to unique substitution patterns (e.g., cruciform-like architectures) and materials with small optical band gaps (1.22-1.97 eV).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available