Formation of Bromocarbenium Bromide Ion Pairs in the Electrophilic Bromination of Highly Reactive Olefins in Chlorinated Aprotic Solvents†

1997 ◽  
Vol 62 (10) ◽  
pp. 3176-3182 ◽  
Author(s):  
Giuseppe Bellucci ◽  
Cinzia Chiappe ◽  
Giacomo Lo Moro
1966 ◽  
Vol 19 (1) ◽  
pp. 43 ◽  
Author(s):  
WA Millen ◽  
DW Watts

Ion association constants at 30� have been determined for the cis-[Co en, Cl2]+Cl- ion pair in NN-dimethylformamide (DMF), NN-dimethylacetamide (DMA), and at 20.0�, 25.0�, and 30.0� in dimethyl sulphoxide (DMSO), by a spectrophotometric method. Association constants for the cis-[Co en2 Cl2]+Br- and the trans- [Co en2 Cl2]+Cl- ion pairs have also been determined in DMF at 30�.


1967 ◽  
Vol 20 (12) ◽  
pp. 2623 ◽  
Author(s):  
IR Lantzke ◽  
DW Watts

The anation of the cis-chlorodimethylformamidebisethylenediaminecobalt(III) ion (cis- [CoCl(DMF) en2]2+) by bromide ion in N,N-dimethylformamide (DMF) has been studied. The reaction has an SNIIP1 mechanism, and when due allowance is made for ion association its activation parameters closely parallel those of other SNIIP anation reactions in DMF. The solvolysis and isomerization of the dichlorobisethylenediaminecobalt(III) ions (cis- and trans-[CoCl2 en2]+) and the bromochlorobisethylenediaminecobalt(III) ions (cis- and trans- CoBrCl en2]+) in DMF have been examined over a range of anion concentration. In all cases solvolysis reactions are important, although direct isomerization appears to become an important path for the reaction of the trans complexes at high anion concentrations. Solvolysis of the cis-[CoCl2 en2]+ ion involves an SN2 mechanism.1 The cis-[CoBrClen2]+, trans-[CoCl2 en2]+, and trans-[CoBrCl en2]+ ions all react by an SN1 mechanism.


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