Structural tuning of quinoxaline-benzodithiophene copolymers via alkyl side chain manipulation: synthesis, characterization and photovoltaic properties

2014 ◽  
Vol 2 (29) ◽  
pp. 11162-11170 ◽  
Author(s):  
Marta Tessarolo ◽  
Desta Gedefaw ◽  
Margherita Bolognesi ◽  
Fabiola Liscio ◽  
Patrik Henriksson ◽  
...  

Effect of the alkyl side chain(s) on the optical, electronic, morphological and photovoltaic properties.

2016 ◽  
Vol 4 (30) ◽  
pp. 11747-11753 ◽  
Author(s):  
J. Zhang ◽  
X. W. Zhu ◽  
C. He ◽  
H. J. Bin ◽  
L. W. Xue ◽  
...  

Two new compounds with alkyl side chains at different positions have a similar structure, but exhibit different photovoltaic properties.


Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3440
Author(s):  
Thanh-Danh Nguyen ◽  
Van-Hai Nguyen ◽  
Jongwoo Song ◽  
Jongdeok An ◽  
Ngoc-Thuan Truong ◽  
...  

A series of poly-3-alkylthiophenes (P3ATs) with butyl (P3BT), hexyl (P3HT), and octyl (P3OT) sidechains and well-defined molecular weights (MWs) were synthesized using Grignard metathesis polymerization. The MWs of P3HTs and P3OTs obtained via gel permeation chromatography agreed well with the calculated MWs ranging from approximately 10 to 70 kDa. Differential scanning calorimetry results showed that the crystalline melting temperature increased with increasing MWs and decreasing alkyl side-chain length, whereas the crystallinity of the P3ATs increased with the growth of MWs. An MW-dependent red shift was observed in the UV–Vis and photoluminiscence spectra of the P3ATs in solution, which might be a strong evidence for the extended effective conjugation occurring in polymers with longer chain lengths. The photoluminescence quantum yields of pristine films in all polymers were lower than those of the diluted solutions, whereas they were higher than those of the phenyl-C61-butyric acid methyl ester-blended films. The UV–Vis spectra of the films showed fine structures with pronounced red shifts, and the interchain interaction-induced features were weakly dependent on the MW but significantly dependent on the alkyl side-chain length. The photovoltaic device performances of the P3BT and P3HT samples significantly improved upon blending with a fullerene derivative and subsequent annealing, whereas those of P3OTs mostly degraded, particularly after annealing. The optimal power conversion efficiencies of P3BT, P3HT, and P3OT were 2.4%, 3.6%, and 1.5%, respectively, after annealing with MWs of ~11, ~39, and ~38 kDa, respectively.


2011 ◽  
Vol 115 (36) ◽  
pp. 18002-18009 ◽  
Author(s):  
Zhao Li ◽  
Yanguang Zhang ◽  
Sai-Wing Tsang ◽  
Xiaomei Du ◽  
Jiayun Zhou ◽  
...  

2009 ◽  
Vol 19 (20) ◽  
pp. 3300-3306 ◽  
Author(s):  
Abay Gadisa ◽  
Wibren D. Oosterbaan ◽  
Koen Vandewal ◽  
Jean-Christophe Bolsée ◽  
Sabine Bertho ◽  
...  

2021 ◽  
Vol 5 (7) ◽  
pp. 3050-3060 ◽  
Author(s):  
Chenyu Han ◽  
Huanxiang Jiang ◽  
Pengchao Wang ◽  
Lu Yu ◽  
Jianxiao Wang ◽  
...  

An alkyl isomerization strategy is reported to finely modulate the crystallinity of nonfullerene acceptors as well as their photovoltaic responses to post-treatments.


2021 ◽  
Vol 22 (12) ◽  
pp. 6400
Author(s):  
Joseph Breheny ◽  
Cian Kingston ◽  
Robert Doran ◽  
Joao Anes ◽  
Marta Martins ◽  
...  

Herein, we report antibacterial and antifungal evaluation of a series of previously prepared (+)-tanikolide analogues. One analogue, (4S,6S)-4-methyltanikolide, displayed promising anti-methicillin-resistant Staphylococcus aureus activity with a MIC of 12.5 µg/mL. Based on the antimicrobial properties of the structurally related (−)-malyngolide, two further analogues (4S,6S)-4-methylmalyngolide and (4R,6S)-4-methylmalyngolide bearing a shortened n-nonyl alkyl side chain were prepared in the present study using a ZrCl4-catalysed deprotection/cyclisation as the key step in their asymmetric synthesis. When these were tested for activity against anti-methicillin-resistant Staphylococcus aureus, the MIC increased to 50 µg/mL.


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