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31P NMR Studies on (β-Naphthoxy)Cyclotriphosphazene Derivatives with Various Degree of Substitution

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25th Congress Ampere on Magnetic Resonance and Related Phenomena
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Abstract

The application of 1H broadband decoupling has greatly improved the quality and usefulness of 131P NMR data, in particular for cyclophosphazenes1,2. In most cases 121 MHz 131P NMR appears convenient for unambiguous structural assignments of various derivatives of parent hexachlorocyclo- triphosphazene, N3,P3,Cl6(I)3. In this work we have applied 131P NMR data for studying the course of substitution of (I) with β-naphtol residues.

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References

  1. R. Keat and R. A. Shaw, Organic Phosphorus Compounds, eds. G. M. Kosolapoff and L. Meier, Inter science, New York 1973, vol.6, ch.17.

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© 1990 Springer-Verlag Berlin Heidelberg

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Brandt, K., Kupka, T. (1990). 31P NMR Studies on (β-Naphthoxy)Cyclotriphosphazene Derivatives with Various Degree of Substitution. In: Mehring, M., von Schütz, J.U., Wolf, H.C. (eds) 25th Congress Ampere on Magnetic Resonance and Related Phenomena. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76072-3_314

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  • DOI: https://doi.org/10.1007/978-3-642-76072-3_314

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-53136-4

  • Online ISBN: 978-3-642-76072-3

  • eBook Packages: Springer Book Archive

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