Mechanistic insights into the reactions of hydride transfer versus hydrogen atom transfer by a trans-dioxoruthenium(vi) complex

2015 ◽  
Vol 44 (16) ◽  
pp. 7634-7642 ◽  
Author(s):  
Sunder N. Dhuri ◽  
Yong-Min Lee ◽  
Mi Sook Seo ◽  
Jaeheung Cho ◽  
Dattaprasad D. Narulkar ◽  
...  

Valuable insights into the hydride-transfer mechanism and C–H bond activation reactions by high-valent trans-dioxoruthenium(vi) species is provided.

1966 ◽  
Vol 19 (1) ◽  
pp. 59 ◽  
Author(s):  
Souza BC de ◽  
JH Green

Mass-spectrometric studies of ion-molecule reactions in acetone-water mixtures at 70 eV and 20 eV electron energies are described. The results provide evidence in favour of the proton transfer mechanism rather than for a hydrogen atom transfer process for the production of M + 1 ions.


ChemInform ◽  
2004 ◽  
Vol 35 (20) ◽  
Author(s):  
Elisabetha Shandalov ◽  
Israel Zilbermann ◽  
Eric Maimon ◽  
Yeoshua Nahmani ◽  
Haim Cohen ◽  
...  

2020 ◽  
Vol 739 ◽  
pp. 137030
Author(s):  
Yelechakanahalli Lingaraju Ramu ◽  
Kandigowda Jagadeesha ◽  
Tavarekere Shivalingaswamy ◽  
Mariyappa Ramegowda

2020 ◽  
Vol 11 (22) ◽  
pp. 5790-5796
Author(s):  
Xin-Ran Chen ◽  
Shuo-Qing Zhang ◽  
Tjark H. Meyer ◽  
Chun-Hui Yang ◽  
Qin-Hao Zhang ◽  
...  

A formal Co(iv) intermediate in electrochemical cobalt-catalyzed C–H oxygenation allows pivalate to break the arene C–H bond via a hydrogen-atom-transfer mechanism.


2021 ◽  
Author(s):  
Tarali Devi ◽  
Yong-Min Lee ◽  
Shunichi Fukuzumi ◽  
Wonwoo Nam

Acid-promoted hydride transfer from an NADH analogue to a Cr(iii)–superoxo complex in the presence of acid proceeds via the full formation of the NADH analogue radical cation, followed by the decay of the radical, and accompanied then by the formation of NAD+.


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