Synthesis and Reactivity of Iron- and Cobalt-Dinitrogen Complexes Bearing PSiP-Type Pincer Ligands toward Nitrogen Fixation

2017 ◽  
Vol 2017 (32) ◽  
pp. 3769-3778 ◽  
Author(s):  
Ryuji Imayoshi ◽  
Kazunari Nakajima ◽  
Jun Takaya ◽  
Nobuharu Iwasawa ◽  
Yoshiaki Nishibayashi

2017 ◽  
Vol 2017 (32) ◽  
pp. 3768-3768 ◽  
Author(s):  
Ryuji Imayoshi ◽  
Kazunari Nakajima ◽  
Jun Takaya ◽  
Nobuharu Iwasawa ◽  
Yoshiaki Nishibayashi


2020 ◽  
Author(s):  
Fanqiang Meng ◽  
Shogo Kuriyama ◽  
Hiromasa Tanaka ◽  
Akihito Egi ◽  
Kazunari Yoshizawa ◽  
...  

A series of rhenium complexes bearing a pyridine-based PNP-type pincer ligand are synthesized from rhenium phosphine complexes as precursors. A dinitrogen-bridged dirhenium complex bearing the PNP-type pincer ligands catalytically converts dinitrogen into ammonia in the reaction with KC<sub>8</sub> as a reductant and [HPCy<sub>3</sub>]BAr<sup>F</sup><sub>4</sub> (Cy = cyclohexyl, Ar<sup>F</sup> = 3,5-(CF<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>) as a proton source at –78 °C to afford 8.4 equiv of ammonia based on the rhenium atom of the catalyst. The rhenium-dinitrogen complex also catalyzes silylation of dinitrogen in the reaction with KC<sub>8</sub> as a reductant and Me<sub>3</sub>SiCl as a silylating reagent under ambient reaction conditions to afford 11.3 equiv of tris(trimethylsilyl)amine based on the rhenium atom of the catalyst. These results demonstrate the first successful example of catalytic nitrogen fixation under mild reaction conditions by using rhenium-dinitrogen complexes as catalysts.



2017 ◽  
Vol 2017 (32) ◽  
pp. 3767-3767
Author(s):  
Ryuji Imayoshi ◽  
Kazunari Nakajima ◽  
Jun Takaya ◽  
Nobuharu Iwasawa ◽  
Yoshiaki Nishibayashi


Author(s):  
Fanqiang Meng ◽  
Shogo Kuriyama ◽  
Hiromasa Tanaka ◽  
Akihito Egi ◽  
Kazunari Yoshizawa ◽  
...  

A series of rhenium complexes bearing a pyridine-based PNP-type pincer ligand are synthesized from rhenium phosphine complexes as precursors. A dinitrogen-bridged dirhenium complex bearing the PNP-type pincer ligands catalytically converts dinitrogen into ammonia in the reaction with KC<sub>8</sub> as a reductant and [HPCy<sub>3</sub>]BAr<sup>F</sup><sub>4</sub> (Cy = cyclohexyl, Ar<sup>F</sup> = 3,5-(CF<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>) as a proton source at –78 °C to afford 8.4 equiv of ammonia based on the rhenium atom of the catalyst. The rhenium-dinitrogen complex also catalyzes silylation of dinitrogen in the reaction with KC<sub>8</sub> as a reductant and Me<sub>3</sub>SiCl as a silylating reagent under ambient reaction conditions to afford 11.3 equiv of tris(trimethylsilyl)amine based on the rhenium atom of the catalyst. These results demonstrate the first successful example of catalytic nitrogen fixation under mild reaction conditions by using rhenium-dinitrogen complexes as catalysts.



2017 ◽  
Vol 53 (88) ◽  
pp. 12040-12043 ◽  
Author(s):  
Yoshiya Sekiguchi ◽  
Shogo Kuriyama ◽  
Aya Eizawa ◽  
Kazuya Arashiba ◽  
Kazunari Nakajima ◽  
...  

Newly designed and prepared iron–dinitrogen complex is found to work as a more effective catalyst toward catalytic nitrogen fixation.





2018 ◽  
Vol 47 (33) ◽  
pp. 11322-11326 ◽  
Author(s):  
Yoshiya Sekiguchi ◽  
Fanqiang Meng ◽  
Hiromasa Tanaka ◽  
Aya Eizawa ◽  
Kazuya Arashiba ◽  
...  

Dinitrogen-bridged dititanium and dizirconium complexes bearing anionic pyrrole-based PNP-type pincer ligands are prepared and characterized by X-ray analysis.



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).



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