A family of tetrahedral coordination cages with different symmetries by assembly of bis-bidentate bridging ligands with first-row transition metal dications

2012 ◽  
Vol 24 (7) ◽  
pp. 499-507 ◽  
Author(s):  
Benjamin R. Hall ◽  
Harry Adams ◽  
Michael D. Ward
2003 ◽  
Vol 6 (9) ◽  
pp. 1224-1227 ◽  
Author(s):  
Garikoitz Beobide ◽  
Oscar Castillo ◽  
Antonio Luque ◽  
Urko Garcı́a-Couceiro ◽  
Juan P. Garcı́a-Teran ◽  
...  

1983 ◽  
Vol 38 (11) ◽  
pp. 1392-1398 ◽  
Author(s):  
Wolfgang A. Herrmann ◽  
Johann Plank ◽  
John L. Hubbard ◽  
Gangolf W. Kriechbaum ◽  
Willibald Kalcher ◽  
...  

Abstract Carbene transfer from aliphatic diazoalkanes upon coordinatively unsaturated metal centers is a general synthetic concept that provides straight-forward routes into organo-metallic hydrocarbon chemistry. A comparison focussing on several key reactions of general applicability demonstrates that mononuclear organometal substrates add carbenes that may act as bridging ligands (e.g., compound 6) if they arise from ω,ω'-bisdiazoalkanes. By way of contrast, metal-metal double bonds cleanly form dimetallacyclo-propane-type derivatives under very mild conditions (7-9). The broadest variety of structures is finally encountered with metal-metal triply bonded precursors such as the molybdenum compounds 3: here, the initial diazoalkane adducts are subject to further rearrangement processes commonly leading to metal-metal single bonds (11) or causing irreversible cleavage of the dinuclear metal systems (10).


2018 ◽  
Vol 537 ◽  
pp. 184-187 ◽  
Author(s):  
Filomena Forte ◽  
Delia Guerra ◽  
Carmine Autieri ◽  
Alfonso Romano ◽  
Canio Noce ◽  
...  

2016 ◽  
Vol 3 (10) ◽  
pp. 1272-1279 ◽  
Author(s):  
Jordi Cirera ◽  
Yuan Jiang ◽  
Lei Qin ◽  
Yan-Zhen Zheng ◽  
Guanghua Li ◽  
...  

Design of new polynuclear transition metal complexes showing ferromagnetic interactions to achieve high spin values is an important challenge due to the scarcity of bridging ligands that provide such coupling.


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