scholarly journals Synthesis and Properties of NitroHPHAC: The First Example of Substitution Reaction on HPHAC

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2486
Author(s):  
Yoshiki Sasaki ◽  
Masayoshi Takase ◽  
Shigeki Mori ◽  
Hidemitsu Uno

Hexapyrrolohexaazacoronene (HPHAC) is one of the N-containing polycyclic aromatic hydrocarbons in which six pyrroles are fused circularly around a benzene. Despite the recent development of HPHAC analogues, there is no report on direct introduction of functional groups into the HPHAC skeleton. This work reports the first example of nitration reaction of decaethylHPHAC. The structures of nitrodecaethylHPHAC including neutral and two oxidized species (radical cation and dication), intramolecular charge transfer (ICT) character, and global aromaticity of the dication are discussed.

1973 ◽  
Vol 26 (1) ◽  
pp. 221 ◽  
Author(s):  
JL Garnett ◽  
KJ Nicol ◽  
A Rainis

Experimental conditions are reported for resolving the hyperfine splitting of e.p.r. spectra obtained from the interaction of polycyclic aromatic hydrocarbons with platinum oxide. By contrast with earlier interpretations where only a singlet was obtained even with perylene, the present results indicate that the adsorbed species are radical cations.


2020 ◽  
Vol 16 ◽  
pp. 530-536 ◽  
Author(s):  
Anping Luo ◽  
Min Zhang ◽  
Zhangyi Fu ◽  
Jingbo Lan ◽  
Di Wu ◽  
...  

The regioselective C–H arylation of substituted polycyclic aromatic hydrocarbons (PAHs) is a desired but challenging task. A copper-catalyzed C7–H arylation of 1-naphthamides has been developed by using aryliodonium salts as arylating reagents. This protocol does not need to use precious metal catalysts and tolerates wide variety of functional groups. Under standard conditions, the remote C–H arylation of other PAHs including phenanthrene-9-carboxamide, pyrene-1-carboxamide and fluoranthene-3-carboxamide has also accomplished, which provides an opportunity for the development of diverse organic optoelectronic materials.


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