Electron transfer, bond breaking, and bond formation

1993 ◽  
Vol 26 (9) ◽  
pp. 455-461 ◽  
Author(s):  
Jean Michel Saveant



2020 ◽  
Vol 8 (42) ◽  
pp. 14939-14947
Author(s):  
So Yokomori ◽  
Shun Dekura ◽  
Tomoko Fujino ◽  
Mitsuaki Kawamura ◽  
Taisuke Ozaki ◽  
...  

A novel vapochromic mechanism by intermolecular electron transfer coupled with hydrogen-bond formation was realized in a zinc dithiolene complex crystal.





2000 ◽  
Vol 104 (32) ◽  
pp. 7492-7501 ◽  
Author(s):  
Cyrille Costentin ◽  
Marc Robert ◽  
Jean-Michel Savéant


Synthesis ◽  
2021 ◽  
Author(s):  
Bin Dai ◽  
Ping Liu ◽  
Jing He ◽  
Yueting Wei ◽  
Xuezhen Li

AbstractA TBAI-mediated sulfenylation of N,3-diaryl-1-arylsulfonyl-1H-pyrazol-5-amines with arylsulfonyl hydrazides has been established, and an expanded inventory of N,5-diaryl-4-(arylthio)-1H-pyrazol-3-amines was constructed through C–S bond formation and N–S bond breaking. Mechanistic investigations suggest thiosulfonate as a key intermediate in the sulfenylation, and the detosylation is promoted by the generated arylsulfinic acid. The method is characterized by simple operating conditions, broad substrate range as well as gram-scale reaction.



2018 ◽  
Vol 42 (9) ◽  
pp. 481-485
Author(s):  
Xiulian Zhang ◽  
Zhicheng Zhang ◽  
Yongbin Xie ◽  
Yujie Jiang ◽  
Ruibo Xu ◽  
...  

A simple and efficient access to arylboronates was achieved with methanol-initiated borylation of aryldiazonium salts. Reduction of aryldiazonium ions by single electron transfer from methanol affords aryl radical species, which undergo a subsequent C–B bond formation with bis(pinacolato)diboron. This highly practical borylation process, which can be carried out on the gram-scale, enjoys operational simplicity as well as mild and catalyst-free conditions.



2003 ◽  
pp. 391-398
Author(s):  
Eva Åkesson ◽  
Alexander N. Tarnovsky ◽  
Gabor Benkö ◽  
Arkady Yartsev ◽  
Villy Sundström


1996 ◽  
Vol 7 (6) ◽  
pp. 481-502 ◽  
Author(s):  
Daniel T. Stoelting ◽  
Richard T. Ludwig ◽  
Edward M. Arnett


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