scholarly journals Synthesis and electronic properties of polycyclic aromatic hydrocarbons doped with phosphorus and sulfur

2016 ◽  
Vol 45 (5) ◽  
pp. 1896-1903 ◽  
Author(s):  
W. Delaunay ◽  
R. Szűcs ◽  
S. Pascal ◽  
A. Mocanu ◽  
P.-A. Bouit ◽  
...  

Synthesis and physical properties of polyaromatic hydrocarbons containing phosphole and thiophene rings at the edge.

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>


Molecules ◽  
2018 ◽  
Vol 24 (1) ◽  
pp. 118 ◽  
Author(s):  
Amber Senese ◽  
Wesley Chalifoux

The extension of π-conjugation of polycyclic aromatic hydrocarbons (PAHs) via alkyne benzannulation reactions has become an increasingly utilized tool over the past few years. This short review will highlight recent work of alkyne benzannulations in the context of large nanographene as well as graphene nanoribbon synthesis along with a brief discussion of the interesting physical properties these molecules display.


1981 ◽  
Vol 36 (3) ◽  
pp. 297-300 ◽  
Author(s):  
K. D. Gundermann ◽  
C. Lohberger ◽  
M. Zander

Good correlations exist between both the carbonyl stretching frequency and the carbonyl bond order of the monoaldehydes of polycyclic aromatic hydrocarbons and the HMO atom localisation energies or PMO reactivity numbers of the corresponding hydrocarbons at the carbon centres contiguous to the CHO group. Applications of these correlations are discussed


RSC Advances ◽  
2016 ◽  
Vol 6 (64) ◽  
pp. 59237-59241 ◽  
Author(s):  
Tandrima Chaudhuri ◽  
Neelam Shivran ◽  
Soumyaditya Mula ◽  
Animesh Karmakar ◽  
Soumi Chattopadhyay ◽  
...  

Polycyclic aromatic hydrocarbons (PAHs) demonstrated unusual weak C–H⋯F type H-bonding interaction with meso-substituted Bodipy dyes (1–3) in ethanol medium.


2021 ◽  
Author(s):  
Thomas Delouche ◽  
Ghizlene Taifour ◽  
Marie Cordier ◽  
Thierry Roisnel ◽  
Denis - Tondelier ◽  
...  

We report the straightforward synthesis of Si-containing PAHs (Polycyclic Aromatic Hydrocarbons). The impact of pi-extension and exocyclic modifications on both the optical and redox properties is investigated using a joint...


Author(s):  
Hajime Gotoh ◽  
Soichiro Nakatsuka ◽  
Hiroki Tanaka ◽  
Nobuhiro Yasuda ◽  
Yohei Haketa ◽  
...  

2021 ◽  
Author(s):  
Hajime Gotoh ◽  
Soichiro Nakatsuka ◽  
Hiroki Tanaka ◽  
Nobuhiro Yasuda ◽  
Yohei Haketa ◽  
...  

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