scholarly journals Reassessing Alkyne Coupling Reactions While Studying the Electronic Properties of Diverse Pyrene Linkages at Surfaces

ACS Nano ◽  
2021 ◽  
Author(s):  
James Lawrence ◽  
Mohammed S. G. Mohammed ◽  
Dulce Rey ◽  
Fernando Aguilar-Galindo ◽  
Alejandro Berdonces-Layunta ◽  
...  
1997 ◽  
Vol 16 (12) ◽  
pp. 2698-2708 ◽  
Author(s):  
Wen-Yann Yeh ◽  
Chi-Lin Ho ◽  
Michael Y. Chiang ◽  
I-Ting Chen

ChemInform ◽  
2004 ◽  
Vol 35 (31) ◽  
Author(s):  
Karen M. Miller ◽  
Torsak Luanphaisarnnont ◽  
Carmela Molinaro ◽  
Timothy F. Jamison

1993 ◽  
Vol 12 (5) ◽  
pp. 1623-1628 ◽  
Author(s):  
Richard D. Adams ◽  
Linfeng Chen ◽  
Wengan Wu

2016 ◽  
Vol 2016 ◽  
pp. 1-14 ◽  
Author(s):  
E. F. Damit ◽  
N. Nordin ◽  
A. Ariffin ◽  
K. Sulaiman

A series of carbazole-thiophene dimers,P1–P9, were synthesized using Suzuki-Miyaura and Ullmann coupling reactions. InP1–P9, carbazole-thiophenes were linked at the N-9 position for different core groups via biphenyl, dimethylbiphenyl, and phenyl. Electronic properties were evaluated by UV-Vis, cyclic voltammogram, and theoretical calculations. Particularly, the effects of conjugation connectivity on photophysical and electrochemical properties, as well as the correlation between carbazole-thiophene and the core, were studied. Carbazole connecting with thiophenes at the 3,6-positions and the phenyl group as a core group leads to increased stabilization of HOMO and LUMO energy levels where the bandgap (ΔE) is significantly reduced.


2004 ◽  
Vol 126 (13) ◽  
pp. 4130-4131 ◽  
Author(s):  
Karen M. Miller ◽  
Torsak Luanphaisarnnont ◽  
Carmela Molinaro ◽  
Timothy F. Jamison

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