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Polymorphic (NH): As Polyimidogen and Ammonium Azide Structure-types
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  • Published: 21 November 2008

Polymorphic (NH): As Polyimidogen and Ammonium Azide Structure-types

  • Michael Bucknum PhD1 

Nature Precedings (2008)Cite this article

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Abstract

This paper reports a productive discussion of bonding principles in the non-metallic 2nd row hydrides. It suggests the inversion of a bonding character, potentially from hydrides of B & C, which may display unsaturation and electronic deficiency accompanied by electronic delocalization in 1D or 2D or 3D. Contrasted with the opposite possibility, within the finite number of hydrides of N, O and F, that display apparently extensive H-bonding and subsequently proton delocalization in 1D and 2D (in HF & ice polymorphs, respectively), and now potentially in 3D in a corresponding hydride of N called Rice's blue material, or perhaps polyimidogen. Where polyimidogen is a crystalline NH lattice that is a polymorph of the ammonium azide structure-type thus.

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  1. Hexagonite, 3380 Harding Street, 14A, Carlsbad, CA, 92008, USA & Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET), Buenos Aires, Republica Argentina

    Michael Bucknum PhD

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  1. Michael Bucknum PhD
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Correspondence to Michael Bucknum PhD.

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Bucknum, M. Polymorphic (NH): As Polyimidogen and Ammonium Azide Structure-types. Nat Prec (2008). https://doi.org/10.1038/npre.2008.2541.1

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  • Received: 19 November 2008

  • Accepted: 21 November 2008

  • Published: 21 November 2008

  • DOI: https://doi.org/10.1038/npre.2008.2541.1

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Keywords

  • delocalization in 1D, 2D & 3D
  • hydrides
  • H-bonding
  • resonance
  • Discussion
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