Is the unexpected behaviour of the resolved K 3[Cr III(C 2O 4) 3] in aqueous solution responsible for the formation of pure chiral solid phase of a two-dimensional (2D) [Mn IICr III(C 2O 4) 3 NEt( n-Pr)( n-Bu)( n-C 5H 11)] network?
Racemic and resolved [Cr III(C 2O 4) 3]K 3 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...
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Veröffentlicht in: | Mendeleev communications 2004-11, Vol.14 (6), p.284-285 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Racemic and resolved [Cr
III(C
2O
4)
3]K
3 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 Cr
III(C
2O
4)
3]
3−. |
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ISSN: | 0959-9436 |
DOI: | 10.1070/MC2004v014n06ABEH002035 |