ChemInform Abstract: Non-Biomimetic Route to Deoxyadenosine Adducts of Carcinogenic Polycyclic Aromatic Hydrocarbons.

ChemInform ◽  
2010 ◽  
Vol 23 (26) ◽  
pp. no-no
Author(s):  
S. J. KIM ◽  
C. M. HARRIS ◽  
K.-Y. JUNG ◽  
M. KOREEDA ◽  
T. M. HARRIS
1991 ◽  
Vol 32 (43) ◽  
pp. 6073-6076 ◽  
Author(s):  
Seong Jin Kim ◽  
Constance M. Harris ◽  
Kee-Yong Jung ◽  
Masato Koreeda ◽  
Thomas M. Harris

1995 ◽  
Vol 3 (6) ◽  
pp. 811-822 ◽  
Author(s):  
Seong Jin Kim ◽  
Hemant K. Jajoo ◽  
Hye-Young Kim ◽  
Liang Zhou ◽  
Pamela Horton ◽  
...  

1993 ◽  
Vol 34 (11) ◽  
pp. 1773-1774 ◽  
Author(s):  
Thomas Steinbrecher ◽  
Andreas Becker ◽  
John J. Stezowski ◽  
Franz Oesch ◽  
Albrecht Seidel

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>


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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