Alkyl side-chain branching point effects in thieno[3,4-c]pyrrole-4,6-dione copolymers

2013 ◽  
Vol 1 (1) ◽  
pp. 30-35 ◽  
Author(s):  
Joseph W. Rumer ◽  
Christine K.L. Hor ◽  
Iain Meager ◽  
Chin P. Yau ◽  
Zhenggang Huang ◽  
...  
2010 ◽  
Vol 5 (3) ◽  
pp. 486-496 ◽  
Author(s):  
Richard J Johnson ◽  
Ben E Smith ◽  
Paul A Sutton ◽  
Terry J McGenity ◽  
Steven J Rowland ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (61) ◽  
pp. 55946-55952 ◽  
Author(s):  
Cheng Zeng ◽  
Chengyi Xiao ◽  
Rui Xin ◽  
Wei Jiang ◽  
Yafei Wang ◽  
...  

4CldiPDIs with different side-chain lengths and positions of the branching point was designed, synthesized, and characterized to study how the electron transporting properties vary with the branching point away from the perylene backbone.


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.


2019 ◽  
Vol 43 (8) ◽  
pp. 3556-3564 ◽  
Author(s):  
Vinay S. Sharma ◽  
Akshara P. Shah ◽  
Anuj S. Sharma

A new class of bowl-shaped supramolecular liquid crystals (LCs) is described derived from calix[4]arene substituted with 1,3,4-thiadiazole derivatives, inbuilt with Schiff base and ester on the lower rim and with an azo group on the upper rim with an alkyl side chain (–OC3H7, –OC8H17).


Sign in / Sign up

Export Citation Format

Share Document