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Synthesis and characterization of [PtMe3L(H2O)]BF4·H2O (L=3-O-acetyl-1,2-O-isopropylidene-α-D-glucofuranose)

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Reaction of [PtMe3(Me2CO)3]BF4 (1) with 3-O-acetyl-1,2;5,6-di-O-isopropylidene-α-D-glucofuranose in acetone affords [PtMe3L]BF4 (2) (L=3-O-acetyl-1,2-O-isopropylidene-α-D-glucofuranose). In wet methylene chloride, complex2 transforms to [PtMe3L(H2O)]BF4·H2O (3). Complex3 was characterized by microanalysis and NMR spectroscopy (1H,13C,195Pt). The X-ray structure analysis (monoclinic, P21, a=10.529(3) Å, b=7.322(2) Å, c=14.668(4) Å, Z=2) reveals that 3-O-acetyl-1,2-O-isopropylidene-α-D-glucofuranose acts as a neutral bidentate ligand which is coordinated via two hydroxyl groups (κ2O5,6 coordination). The five-membered 1,3,2-dioxaplatina rings exhibit an envelope conformation. The coordination sphere of platinum is completed by H2O ligand.

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Authors
  1. Henrik Junicke
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  2. Clemens Bruhn
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  3. Christoph Wagner
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  4. Dirk Steinborn
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Additional information

Institut für Anorganische Chemie, Martin-Luther-Universität; Halle-Wittenberg, Kurt-Mothes Str. 2, D-06120 Halle/Saale, Germany. Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1119–1126, August, 1999.

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Junicke, H., Bruhn, C., Wagner, C. et al. Synthesis and characterization of [PtMe3L(H2O)]BF4·H2O (L=3-O-acetyl-1,2-O-isopropylidene-α-D-glucofuranose). Chem Heterocycl Compd 35, 984–991 (1999). https://doi.org/10.1007/BF02252168

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  • DOI: https://doi.org/10.1007/BF02252168

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