Polycyclic aromatic hydrocarbons (PAHs) in yerba maté ( Ilex paraguariensis St. Hil) traditional infusions ( mate and tereré )

Food Control ◽  
2016 ◽  
Vol 60 ◽  
pp. 215-220 ◽  
Author(s):  
Ana Eugenia Thea ◽  
Darío Ferreira ◽  
Luis Alberto Brumovsky ◽  
Miguel Eduardo Schmalko
2012 ◽  
Vol 46 (24) ◽  
pp. 13488-13493 ◽  
Author(s):  
Asieh Golozar ◽  
Renato B. Fagundes ◽  
Arash Etemadi ◽  
Michele M. Schantz ◽  
Farin Kamangar ◽  
...  

2010 ◽  
Vol 27 (6) ◽  
pp. 776-782 ◽  
Author(s):  
Manoela Alano Vieira ◽  
Marcelo Maraschin ◽  
Ângela Angeloni Rovaris ◽  
Renata Dias de Mello Castanho Amboni ◽  
Cristiane Manfé Pagliosa ◽  
...  

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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