Cation⋅⋅⋅anion and anion⋅⋅⋅anion interactions compete in hydrogen-bonded frameworks prepared using amidinium⋅⋅⋅phosphonate hydrogen bonding

01 August 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

We report the synthesis of hydrogen-bonded frameworks prepared from guanidinium, bis-amidinium or tetra-amidinium cations, and diphosphonate or tetraphosphonate anions. The frameworks are assembled by both charge-assisted amidinium⋅⋅⋅phosphonate and anti-electrostatic phosphonate⋅⋅⋅phosphonate hydrogen bonds, of which the phosphonate⋅⋅⋅phosphonate interactions are notably shorter. Frameworks prepared from the tetrahedral tetraphosphonate building block contain relatively large water-filled channels, but lose crystallinity upon drying. The crystal structure of a guanidinium⋅⋅⋅diphosphonate salt has an unusual structure related to classic Ward guanidinium⋅⋅⋅sulfonate frameworks but with an additional cation/solvent layer. This material includes toluene guests, which are held strongly within the crystal lattice.

Keywords

amidinium
phosphonate
crystal engineering
hydrogen bonded frameworks
hydrogen bonds
frameworks

Supplementary materials

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Description
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Supporting Information
Description
NMR and IR spectra, PXRD and TGA data, details of successful and unsuccessful crystallisations, details of X-ray crystallography including hydrogen bonding parameters.
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