Metal-free hydrogenation catalysis of polycyclic aromatic hydrocarbons

2012 ◽  
Vol 48 (98) ◽  
pp. 11963 ◽  
Author(s):  
Yasutomo Segawa ◽  
Douglas W. Stephan
2015 ◽  
Vol 6 (1) ◽  
pp. 436-441 ◽  
Author(s):  
Reinhard Berger ◽  
Manfred Wagner ◽  
Xinliang Feng ◽  
Klaus Müllen

Based on polycyclic aromatic azomethine ylides, a metal-free “cycloaddition-planarization-sequence” is proposed, providing a unique entry to nitrogen-containing polycyclic aromatic hydrocarbons.


2018 ◽  
Vol 54 (74) ◽  
pp. 10415-10418 ◽  
Author(s):  
Hong-Kai Sha ◽  
Ting Xu ◽  
Feng Liu ◽  
Bu-Zheng Tang ◽  
Wen-Juan Hao ◽  
...  

The first metal-free base-promoted naphthannulation reactions of yne-allenone esters were developed for the direct assembly of a wide range of polycyclic aromatic hydrocarbons with generally good yields.


2017 ◽  
Vol 53 (11) ◽  
pp. 1904-1907 ◽  
Author(s):  
Chada Raji Reddy ◽  
Uredi Dilipkumar ◽  
Ravula Shravya

A novel [4+2]-benzannulation approach to substituted polycyclic aromatic hydrocarbons has been developed under atom-economical, mild and metal-free reaction conditions.


2021 ◽  
Author(s):  
Daqian Zhu ◽  
Hui Peng ◽  
Yameng Sun ◽  
Zhouming Wu ◽  
Yun Wang ◽  
...  

Tert-butylamine-catalyzed free radical annulations with cyclic diaryliodoniums occur in environmentally friendly ethyl acetate and do not require transition metal, providing diversified polycyclic aromatic hydrocarbons by modulating substituents.


2019 ◽  
Vol 64 (1) ◽  
pp. 55-67
Author(s):  
Vlad Pӑnescu ◽  
◽  
Mihaela Cӑtӑlina Herghelegiu ◽  
Sorin Pop ◽  
Mircea Anton ◽  
...  

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>


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