Micelle-Enabled Suzuki–Miyaura Cross-Coupling of Heteroaryl Boronate Esters

2018 ◽  
Vol 83 (14) ◽  
pp. 7523-7527 ◽  
Author(s):  
Pengfei Guo ◽  
Hao Zhang ◽  
Jianguang Zhou ◽  
Fabrice Gallou ◽  
Michael Parmentier ◽  
...  
2016 ◽  
Vol 81 (13) ◽  
pp. 5789-5794 ◽  
Author(s):  
Jing Zhou ◽  
Johannes H. J. Berthel ◽  
Maximilian W. Kuntze-Fechner ◽  
Alexandra Friedrich ◽  
Todd B. Marder ◽  
...  

2020 ◽  
Vol 1 ◽  
Author(s):  
Josue Ayuso-Carrillo

AbstractCyclopentadithiophene (CPDT), a Csp3-bridged bithiophene heteroaromatic unit, displays interesting properties when it is embedded in the repeating units of π-conjugated polymers, and they are applied in organic electronics devices. Common synthetic routes to CPDT-derived polymers rely on toxic methodologies whilst alternative non-toxic strategies such as the Suzuki-Miyaura reaction have been less studied. In this report we demonstrate that the use of a N-methyliminodiacetic acid (MIDA) boronate ester-derived CPDT monomer allows the efficient formation of poly(cyclopentadithiophene) homopolymer under Suzuki-Miyaura cross-coupling reaction conditions. Thus, the use of MIDA boronate esters might be extended to other organic units to design and construct a plethora of π-conjugated polymers.


2017 ◽  
Vol 55 (17) ◽  
pp. 2798-2806 ◽  
Author(s):  
Andrew B. Foster ◽  
Viktor Bagutski ◽  
Josue I. Ayuso-Carrillo ◽  
Martin J. Humphries ◽  
Michael J. Ingleson ◽  
...  

2020 ◽  
Author(s):  
Logan Forshee ◽  
Kaitie Cartwright ◽  
Jon Tunge ◽  
Megan Hegarty
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