Your browser doesn't support javascript.
loading
Innocent BN bond substitution in anthracene derivatives.
van de Wouw, H L; Lee, J Y; Siegler, M A; Klausen, R S.
Affiliation
  • van de Wouw HL; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. klausen@jhu.edu.
  • Lee JY; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. klausen@jhu.edu.
  • Siegler MA; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. klausen@jhu.edu.
  • Klausen RS; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. klausen@jhu.edu.
Org Biomol Chem ; 14(12): 3256-63, 2016 Mar 28.
Article in En | MEDLINE | ID: mdl-26928939
ABSTRACT
Extended azaborine heterocycles are promising biomedical and electronic materials. Herein we report the synthesis of a novel family of azaborine anthracene derivatives and their structural, electrochemical and spectroscopic characterization. We observe that the properties of these materials are remarkably similar to the parent hydrocarbons, suggesting the innocence of the CC to BN bond substitution. Our results support the prospective stability to long-term usage of extended azaborines and the feasibility of using such materials in device applications.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2016 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2016 Document type: Article Affiliation country: