4.6 Article

Naphthalimide-Based Triptycenes: Synthesis and Optoelectronic Properties

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 10, Issue 3, Pages 602-607

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201403302

Keywords

Diels-Alder reaction; naphthalimide; optoelectronic properties; triptycenes

Funding

  1. National Natural Science Foundation of China [21272088, 21472059, 21402057]
  2. Program for Academic Leader in Wuhan Municipality [201271130441]
  3. Scientific Research Foundation for the Returned Overseas Chinese Scholars, Ministry of Education
  4. Natural Science Foundation of Hubei Province [2013CFB207]
  5. CCNU from the colleges' basic research and operation of MOE [CCNU14A05009, CCNU14F01003]

Ask authors/readers for more resources

In the past decades, the naphthalimide structure has found application in many areas of chemistry due to its unique photophysical properties. Naphthalimide has two isomers, 1,8-naphthalimide containing a six-membered imide ring and 2,3-naphthalimide containing a five-membered imide ring. The former has been widely investigated while studies on the latter are considerably more rare. On the other hand, naphthalimide can also be regarded as a building block to construct polycyclic aromatic hydrocarbons (PAHs), which have found wide applications in optical materials. Here we report the synthesis and optoelectronic properties of three 2,3-naphthalimide-based triptycenes. These three triptycene derivatives enrich the family of triptycenes.

Authors

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

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available