Document Detail


An expedient synthesis of fused heteroacenes bearing a pyrrolo[3,2-b]pyrrole core.
MedLine Citation:
PMID:  23152957     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Two linear fused heteroacenes bearing a pyrrolo[3,2-b]pyrrole core have been synthesized via a novel reductive ring closure methodology in three steps and in good overall yield. Preliminary OFET results showed that dinaphtho[2,3-b:2',3'-f]pyrrolo[3,2-b]pyrrole (DNPP) is a potential candidate for organic electronics.
Authors:
Li Qiu; Chunmeng Yu; Na Zhao; Weichao Chen; Yunlong Guo; Xiaobo Wan; Renqiang Yang; Yunqi Liu
Related Documents :
21744887 - Accurate explicitly correlated wave functions for two electrons in a square.
22086617 - Chemistry and physics of a single atomic layer: strategies and challenges for functiona...
9878497 - A high-resolution analysis of the nu3 and nu9 absorption bands of difluoromethane.
2404757 - Lumo energies and hydrophobicity as determinants of mutagenicity by nitroaromatic compo...
19274677 - Using hyperbolic secant pulses to assist characterization of chemical shift tensors for...
22894347 - Transition metal phthalocyanines: insight into the electronic structure from soft x-ray...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-11-14
Journal Detail:
Title:  Chemical communications (Cambridge, England)     Volume:  -     ISSN:  1364-548X     ISO Abbreviation:  Chem. Commun. (Camb.)     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-11-15     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9610838     Medline TA:  Chem Commun (Camb)     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Qingdao Institute of Bioenergy & Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Road, Qingdao, Shandong Province, 266101, P. R. China. wanxb@qibebt.ac.cn.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Metabolomics study on the hepatoprotective effect of scoparone using ultra-performance liquid chroma...
Next Document:  Nickel-catalyzed decyanation of inert carbon-cyano bonds.