Protonation reactions of molybdenum and tungsten dinitrogen complexes with halogen acids. Hydride hydrazido(2-) and diazenido complexes as intermediate stages of reduction

1980 ◽  
Vol 102 (25) ◽  
pp. 7461-7467 ◽  
Author(s):  
Tamotsu Takahashi ◽  
Yasushi Mizobe ◽  
Maki Sato ◽  
Yasuzo Uchida ◽  
Masanobu Hidai
2012 ◽  
Vol 31 (5) ◽  
pp. 2035-2041 ◽  
Author(s):  
Kazuya Arashiba ◽  
Kouitsu Sasaki ◽  
Shogo Kuriyama ◽  
Yoshihiro Miyake ◽  
Haruyuki Nakanishi ◽  
...  

2001 ◽  
Vol 73 (2) ◽  
pp. 261-263 ◽  
Author(s):  
Masanobu Hidai ◽  
Yasushi Mizobe

Dinitrogen complex cis-[W (N2) 2 (PMe2Ph) 4] reacts with an excess of acidic dihydrogen complexes such as trans-[RuCl (h2-H2) (dppe) 2]BF4 (dppe = 1,2-bis (diphenylphosphino) ethane) at 55 °C under 1 atm of H2 to form ammonia in moderate yield. The reaction is presumed to proceed through nucleophilic attack of the remote nitrogen of the coordinated dinitrogen on the dihydrogen ligand. The coordinated dinitrogen is also protonated by treatment with hydrosulfido-bridged dinuclear complexes such as [Cp*Ir (m-SH) 3IrCp*]Cl (Cp* = h5-C5Me5) to afford ammonia. On the other hand, the synthetic cycle for the formation of pyrrole and N-aminopyrrole from dinitrogen and 2,5-dimethoxytetrahydrofuran has been established starting from dinitrogen complexes of the type trans-[M (N2) 2 (dppe) 2 ] (M = Mo, W).


1982 ◽  
Vol 238 (4) ◽  
pp. C63-C66 ◽  
Author(s):  
Ernesto Carmona ◽  
Jose M. Marin ◽  
Manuel L. Poveda ◽  
Robin D. Rogers ◽  
Jerry L. Atwood

1993 ◽  
Vol 456 (2) ◽  
pp. 213-220 ◽  
Author(s):  
Hiroyuki Oshita ◽  
Yasushi Mizobe ◽  
Masanobu Hidai

1993 ◽  
Vol 461 (1-2) ◽  
pp. 43-49 ◽  
Author(s):  
Hiroyuki Oshita ◽  
Yasushi Mizobe ◽  
Masanobu Hidai

1994 ◽  
Vol 13 (12) ◽  
pp. 5062-5071 ◽  
Author(s):  
Youichi Ishii ◽  
Masayuki Kawaguchi ◽  
Yukiatsu Ishino ◽  
Takanori Aoki ◽  
Masanobu Hidai

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