Late-transition-metal .mu.-oxo and .mu.-imido complexes. 8. Rhodium imido/amido coupling reactions with carbon monoxide

1992 ◽  
Vol 31 (3) ◽  
pp. 379-384 ◽  
Author(s):  
Yuan Wen Ge ◽  
Paul R. Sharp
Keyword(s):  
Carbon Monoxide ◽  
Transition Metal ◽  
Late Transition Metal ◽  
Coupling Reactions ◽  
Imido Complexes ◽  
Late Transition

Late transition metal oxo and imido complexes. 11. Gold(I) oxo complexes

1993 ◽  
Vol 32 (10) ◽  
pp. 1946-1950 ◽  
Author(s):  
Yi Yang ◽  
Visalakshi Ramamoorthy ◽  
Paul R. Sharp
Keyword(s):  
Transition Metal ◽  
Late Transition Metal ◽  
Oxo Complexes ◽  
Imido Complexes ◽  
Late Transition

Late-transition-metal .mu.-oxo and .mu.-imido complexes. 6. Gold(I) imido complexes

1990 ◽  
Vol 29 (18) ◽  
pp. 3336-3339 ◽  
Author(s):  
Visalakshi Ramamoorthy ◽  
Paul R. Sharp
Keyword(s):  
Transition Metal ◽  
Late Transition Metal ◽  
Imido Complexes ◽  
Late Transition

Synthesis of late transition-metal nanoparticles by Na naphthalenide reduction of salts and their catalytic efficiency

2017 ◽  
Vol 4 (12) ◽  
pp. 2037-2044 ◽  
Author(s):  
Fangyu Fu ◽  
Angel M. Martinez-Villacorta ◽  
Ane Escobar ◽  
Joseba Irigoyen ◽  
Sergio Moya ◽  
...  
Keyword(s):  
Transition Metal ◽  
Metal Nanoparticles ◽  
Catalytic Efficiency ◽  
Late Transition Metal ◽  
Coupling Reactions ◽  
Salting Out ◽  
Transition Metal Nanoparticles ◽  
Late Transition

Late transition-metal nanoparticles were synthesized using Na naphthalenide reduction of salts followed by salting-out purification catalyse click, redox and coupling reactions.

scholarly journals Magnesium-Stabilised Transition Metal Formyl Complexes: Structures, Bonding, and Ethenediolate Formation

2021 ◽  
Author(s):  
Joe Parr ◽  
Andrew J. P. White ◽  
Mark Crimmin
Keyword(s):  
Carbon Monoxide ◽  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Late Transition Metal ◽  
Late Transition ◽  
Bonding Mode

Herein we report the first comprehensive series of crystallographically characterised transition metal formyl complexes. In these complexes, the formyl ligand is trapped as part of a chelating structure between a transition metal (Cr, Mn, Fe, Co, Rh, W, and Ir) and a magnesium (Mg) cation. Calculations suggest that this bonding mode results in significant oxycarbene-character of the formyl ligand. Electron-rich late-transition metal complexes have the highest oxycarbene-character to the bonding and are the most stable in solution. Further reaction of a heterometallic Cr---Mg formyl complex results in a rare example of C–C coupling and formation of an ethenediolate complex. These results show that well-defined transition metal formyl complexes are potential intermediates in the homologation of carbon monoxide.

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