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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2004 Volume 14, Issue 6, Pages 284–285 (Mi mendc3912)

This article is cited in 3 papers

Is the unexpected behaviour of the resolved K3[CrIII(C2O4)3] in aqueous solution responsible for the formation of pure chiral solid phase of a two-dimensional (2D) [MnIICrIII(C2O4)3 NEt(n-Pr)(n-Bu)(n-C5H11)] network?

M. Grusellea, C. Traina, N. S. Ovanesyanb, V. D. Makhaevb, Ch. Cordierc

a Laboratoire de Chimie Inorganique et Matériaux Moléculaires, CNRS, Université Pierre et Marie Curie, Paris, France
b Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
c Itodys, UMR CNRS 7086, Université Paris 7 - Denis Diderot, Paris, France

Abstract: Racemic and resolved [CrIII(C2O4)3]K3 dissolved in water were investigated by IR spectroscopy. Compared to the racemic compound, the spectrum of the resolved one exhibits additional peaks, which have a complex temporal evolution. These peaks are attributed to water molecules coordinated to the metal ion and tentatively related to the formation of a pure chiral solid phase of two-dimensional (2D) oxalate-based Mn–Cr networks starting from partially resolved CrIII(C2O4)3]3−.

Language: English

DOI: 10.1070/MC2004v014n06ABEH002035



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