Octahedral metal carbonyls. 54. Rates of chelate ring closure in five-coordinate metal carbonyl intermediates

1983 ◽  
Vol 105 (16) ◽  
pp. 5505-5506 ◽  
Author(s):  
Gerard R. Dobson ◽  
Saber E. Mansour ◽  
D. Eric Halverson ◽  
Erika S. Erikson
1992 ◽  
Vol 31 (16) ◽  
pp. 3482-3488 ◽  
Author(s):  
Shulin Zhang ◽  
I Hsiung Wang ◽  
Paul H. Wermer ◽  
Charles B. Dobson ◽  
Gerard R. Dobson

1974 ◽  
Vol 13 (3) ◽  
pp. 627-631 ◽  
Author(s):  
William J. Knebel ◽  
Robert J. Angelici

1975 ◽  
Vol 30 (3-4) ◽  
pp. 229-234 ◽  
Author(s):  
Wolfgang Malisch ◽  
Peter Panster

The reaction of SbBr3 with the complex metal carbonyl anions [π-C5H6(CO)3M]Na (M = Mo, W) leads to the formation of transition metal antimony bromides π-C5H5(CO)3M-Sb̅-Br2, which can be further metallated, yielding the stable species [XXX]All bromine substituted transition metal stibines prove to be excellent coordinating ligands and can easily be introduced into activated metal carbonyls. The interaction of π-C5H5(CO)3M-Sb̅Br2, with bromine results in a quantitative Sb-M bond cleavage, presumably via primary formation of pentavalent intermediates. All new compounds are fully characterized by means of IR, 1H NMR and mass spectroscopy.


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