Bromide Anation Kinetics of Some Platinum(IV) Bromo Aqua Complexes
(1977) In Inorganica Chimica Acta 22(2). p.201-207- Abstract (Swedish)
- Bromide anations of PtBr5H2O− in the presence of PtBr42− or bromine, of trans-PtBr4(H2O)2 in the presence of PtBr42− and of cis-PtBr4(H2O)2 in the presence of bromine have been studied in 0.50 M perchloric acid medium at 25 °C.
The rate law for the bromide anation of PtBr5H2O−indicates two parallel reaction paths. The term k′Br−2 corresponds to a bromide assisted mechanism. The second term in the rate expression can be accounted for by assuming that a dimeric intermediate is formed from the platinum(IV) substrate and hydrated PtBr42−. The formation of the reaction product PtBr62− is preceded by a substitution of water by bromide in this dimer.
A bromide assisted mechanism can also describe the bromide anation kinetics of... (More) - Bromide anations of PtBr5H2O− in the presence of PtBr42− or bromine, of trans-PtBr4(H2O)2 in the presence of PtBr42− and of cis-PtBr4(H2O)2 in the presence of bromine have been studied in 0.50 M perchloric acid medium at 25 °C.
The rate law for the bromide anation of PtBr5H2O−indicates two parallel reaction paths. The term k′Br−2 corresponds to a bromide assisted mechanism. The second term in the rate expression can be accounted for by assuming that a dimeric intermediate is formed from the platinum(IV) substrate and hydrated PtBr42−. The formation of the reaction product PtBr62− is preceded by a substitution of water by bromide in this dimer.
A bromide assisted mechanism can also describe the bromide anation kinetics of cis-PtBr4(H2O)2, the rate law determined. The bromide anation of trans-PtBr4(H2O)2 in the presence of PtBr42− occurs by a two-term rate law, indicating two parallel paths, k′ corresponding to formation of PtBr5H2O− and k″ to formation of PtBr62−.
Trans-PtBr4(H2O)2 reacts so slowly with bromide in the absence of PtBr42− that no reaction can be observed. The large difference in bromide anation rates for PtBr5H2O− and cis-PtBr4(H2O)2 compared to trans-PtBr4(H2O)2 might indicate that halide assisted anations are possible only for complexes having a halide (or some other effective bridging group) in trans-position to the aqua ligand to be replaced. (Less) - Abstract
- Bromide anations of PtBr5H2O− in the presence of PtBr42− or bromine, of trans-PtBr4(H2O)2 in the presence of PtBr42− and of cis-PtBr4(H2O)2 in the presence of bromine have been studied in 0.50 M perchloric acid medium at 25 °C.
The rate law for the bromide anation of PtBr5H2O−indicates two parallel reaction paths. The term k′Br−2 corresponds to a bromide assisted mechanism. The second term in the rate expression can be accounted for by assuming that a dimeric intermediate is formed from the platinum(IV) substrate and hydrated PtBr42−. The formation of the reaction product PtBr62− is preceded by a substitution of water by bromide in this dimer.
A bromide assisted mechanism can also describe the bromide anation kinetics... (More) - Bromide anations of PtBr5H2O− in the presence of PtBr42− or bromine, of trans-PtBr4(H2O)2 in the presence of PtBr42− and of cis-PtBr4(H2O)2 in the presence of bromine have been studied in 0.50 M perchloric acid medium at 25 °C.
The rate law for the bromide anation of PtBr5H2O−indicates two parallel reaction paths. The term k′Br−2 corresponds to a bromide assisted mechanism. The second term in the rate expression can be accounted for by assuming that a dimeric intermediate is formed from the platinum(IV) substrate and hydrated PtBr42−. The formation of the reaction product PtBr62− is preceded by a substitution of water by bromide in this dimer.
A bromide assisted mechanism can also describe the bromide anation kinetics of cis-PtBr4(H2O)2, the rate law determined. The bromide anation of trans-PtBr4(H2O)2 in the presence of PtBr42− occurs by a two-term rate law, indicating two parallel paths, k′ corresponding to formation of PtBr5H2O− and k″ to formation of PtBr62−.
Trans-PtBr4(H2O)2 reacts so slowly with bromide in the absence of PtBr42− that no reaction can be observed. The large difference in bromide anation rates for PtBr5H2O− and cis-PtBr4(H2O)2 compared to trans-PtBr4(H2O)2 might indicate that halide assisted anations are possible only for complexes having a halide (or some other effective bridging group) in trans-position to the aqua ligand to be replaced. (Less)
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- author
- Elding, Lars Ivar LU and Gustafson, Lena
- organization
- publishing date
- 1977
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Platinum(IV), Bromide anation, Kinetics, Reaction mechanism, Bromide assisted substitution
- in
- Inorganica Chimica Acta
- volume
- 22
- issue
- 2
- pages
- 7 pages
- publisher
- Elsevier
- external identifiers
-
- scopus:4243404116
- ISSN
- 0020-1693
- DOI
- 10.1016/S0020-1693(00)90919-8
- language
- English
- LU publication?
- yes
- id
- b3f84f25-a447-4bd0-8c67-b34c9825ae38
- date added to LUP
- 2017-02-19 16:51:58
- date last changed
- 2019-01-06 12:57:57
@article{b3f84f25-a447-4bd0-8c67-b34c9825ae38,
abstract = {Bromide anations of PtBr5H2O− in the presence of PtBr42− or bromine, of trans-PtBr4(H2O)2 in the presence of PtBr42− and of cis-PtBr4(H2O)2 in the presence of bromine have been studied in 0.50 M perchloric acid medium at 25 °C.<br/> The rate law for the bromide anation of PtBr5H2O−indicates two parallel reaction paths. The term k′Br−2 corresponds to a bromide assisted mechanism. The second term in the rate expression can be accounted for by assuming that a dimeric intermediate is formed from the platinum(IV) substrate and hydrated PtBr42−. The formation of the reaction product PtBr62− is preceded by a substitution of water by bromide in this dimer.<br/> A bromide assisted mechanism can also describe the bromide anation kinetics of cis-PtBr4(H2O)2, the rate law determined. The bromide anation of trans-PtBr4(H2O)2 in the presence of PtBr42− occurs by a two-term rate law, indicating two parallel paths, k′ corresponding to formation of PtBr5H2O− and k″ to formation of PtBr62−.<br/> Trans-PtBr4(H2O)2 reacts so slowly with bromide in the absence of PtBr42− that no reaction can be observed. The large difference in bromide anation rates for PtBr5H2O− and cis-PtBr4(H2O)2 compared to trans-PtBr4(H2O)2 might indicate that halide assisted anations are possible only for complexes having a halide (or some other effective bridging group) in trans-position to the aqua ligand to be replaced.},
author = {Elding, Lars Ivar and Gustafson, Lena},
issn = {0020-1693},
keyword = {Platinum(IV),Bromide anation,Kinetics,Reaction mechanism,Bromide assisted substitution},
language = {eng},
number = {2},
pages = {201--207},
publisher = {Elsevier},
series = {Inorganica Chimica Acta},
title = {Bromide Anation Kinetics of Some Platinum(IV) Bromo Aqua Complexes},
url = {http://dx.doi.org/10.1016/S0020-1693(00)90919-8},
volume = {22},
year = {1977},
}