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Title: Substituted angular bistetracenes and substituted angular bisoligoacenes and electronic devices made with same

Abstract

We report the synthesis and characterization of novel bistetracenes, an unconventional, linearly extended conjugated core with eight fused rings. Also described are bisoligoacenes. In general, the properties and stability of large polycyclic aromatic hydrocarbons (PAHs) strongly depend on the mode of ring annellation and the topology of their it-electron systems, which are usually associated with the resonance stabilization energy in large PAHs.

Inventors:
;
Issue Date:
Research Org.:
University of Massachusetts, Boston, MA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1460559
Patent Number(s):
10,005,796
Application Number:
15/307,968
Assignee:
University of Massachusetts (Boston, MA) EFRC
DOE Contract Number:  
SC0001087
Resource Type:
Patent
Resource Relation:
Patent File Date: 2015 May 01
Country of Publication:
United States
Language:
English

Citation Formats

Briseno, Alejandro L., and Zhang, Lei. Substituted angular bistetracenes and substituted angular bisoligoacenes and electronic devices made with same. United States: N. p., 2018. Web.
Briseno, Alejandro L., & Zhang, Lei. Substituted angular bistetracenes and substituted angular bisoligoacenes and electronic devices made with same. United States.
Briseno, Alejandro L., and Zhang, Lei. Tue . "Substituted angular bistetracenes and substituted angular bisoligoacenes and electronic devices made with same". United States. https://www.osti.gov/servlets/purl/1460559.
@article{osti_1460559,
title = {Substituted angular bistetracenes and substituted angular bisoligoacenes and electronic devices made with same},
author = {Briseno, Alejandro L. and Zhang, Lei},
abstractNote = {We report the synthesis and characterization of novel bistetracenes, an unconventional, linearly extended conjugated core with eight fused rings. Also described are bisoligoacenes. In general, the properties and stability of large polycyclic aromatic hydrocarbons (PAHs) strongly depend on the mode of ring annellation and the topology of their it-electron systems, which are usually associated with the resonance stabilization energy in large PAHs.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {2018},
month = {6}
}

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