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Bromide Anation Kin...
Bromide Anation Kinetics of Some Platinum(IV) Bromo Aqua Complexes
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- Elding, Lars Ivar (författare)
- Lund University,Lunds universitet,Centrum för analys och syntes,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Centre for Analysis and Synthesis,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
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- Gustafson, Lena (författare)
- Lund University
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(creator_code:org_t)
- 1977
- 1977
- Engelska 7 s.
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Ingår i: Inorganica Chimica Acta. - 0020-1693. ; 22:2, s. 201-207
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Abstract
Ämnesord
Stäng
- 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.
- 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.
Ämnesord
- NATURVETENSKAP -- Kemi -- Oorganisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
Nyckelord
- Platinum(IV)
- Bromide anation
- Kinetics
- Reaction mechanism
- Bromide assisted substitution
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
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