Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques

Racemization kinetics of the Ni2+- and Cu2+-complexes of three macrocyclic ligands with coordinated nitrogen as asymmetric centers have been measured. Reaction rates of all the complexes are first order in complex concentration and in hydroxide ion concentration. Arrhenius activation energies are i...

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Main Authors: E. Sledziewska, L. Plachta, D. VonderSchmitt, K. Bernauer
Format: Article
Language:deu
Published: Swiss Chemical Society 1971-10-01
Series:CHIMIA
Online Access:https://www.chimia.ch/chimia/article/view/8939
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author E. Sledziewska
L. Plachta
D. VonderSchmitt
K. Bernauer
author_facet E. Sledziewska
L. Plachta
D. VonderSchmitt
K. Bernauer
author_sort E. Sledziewska
collection DOAJ
description Racemization kinetics of the Ni2+- and Cu2+-complexes of three macrocyclic ligands with coordinated nitrogen as asymmetric centers have been measured. Reaction rates of all the complexes are first order in complex concentration and in hydroxide ion concentration. Arrhenius activation energies are in general smaller for the copper compounds. Deuteration rates were measured for the Ni2+-complexe–[Ni(CH3)6-1,7-CT](NCS)2 (structure I) in a mixture of D2O and d6-dimethyl-sulfoxide at low pD-values. These rates are found to be higher by a factor of 400 than racemization rates under the same conditions, indicating mainly retention of configuration about the nitrogen center, as is found for inert N-asymmetric CoIII- and PtII-complexes. 
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issn 0009-4293
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language deu
publishDate 1971-10-01
publisher Swiss Chemical Society
record_format Article
series CHIMIA
spelling doaj-art-1dca705db1b74732a9cb6f6cac3bf85d2025-08-20T01:47:41ZdeuSwiss Chemical SocietyCHIMIA0009-42932673-24241971-10-01251010.2533/chimia.1971.330Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliquesE. Sledziewska0L. Plachta1D. VonderSchmitt2K. Bernauer3Laboratoire de chimie inorganique et analytique Université de NeuchâtelLaboratoire de chimie inorganique et analytique Université de NeuchâtelLaboratoire de chimie inorganique et analytique Université de NeuchâtelLaboratoire de chimie inorganique et analytique, Université de Neuchâtel Racemization kinetics of the Ni2+- and Cu2+-complexes of three macrocyclic ligands with coordinated nitrogen as asymmetric centers have been measured. Reaction rates of all the complexes are first order in complex concentration and in hydroxide ion concentration. Arrhenius activation energies are in general smaller for the copper compounds. Deuteration rates were measured for the Ni2+-complexe–[Ni(CH3)6-1,7-CT](NCS)2 (structure I) in a mixture of D2O and d6-dimethyl-sulfoxide at low pD-values. These rates are found to be higher by a factor of 400 than racemization rates under the same conditions, indicating mainly retention of configuration about the nitrogen center, as is found for inert N-asymmetric CoIII- and PtII-complexes.  https://www.chimia.ch/chimia/article/view/8939
spellingShingle E. Sledziewska
L. Plachta
D. VonderSchmitt
K. Bernauer
Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques
CHIMIA
title Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques
title_full Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques
title_fullStr Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques
title_full_unstemmed Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques
title_short Azote asymétrique: racémisation et échange de deutérium dans des complexes macrocycliques
title_sort azote asymetrique racemisation et echange de deuterium dans des complexes macrocycliques
url https://www.chimia.ch/chimia/article/view/8939
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AT lplachta azoteasymetriqueracemisationetechangededeuteriumdansdescomplexesmacrocycliques
AT dvonderschmitt azoteasymetriqueracemisationetechangededeuteriumdansdescomplexesmacrocycliques
AT kbernauer azoteasymetriqueracemisationetechangededeuteriumdansdescomplexesmacrocycliques