Reactivity of a New Zirconium Phosphonate Phase, Zr2(O3P-CH2CH2-bipyridinium-CH2CH2-PO3)X6·2H2O, Toward Organic and Inorganic Monophosphonates
✍ Scribed by Lori A. Vermeulen; Scott J. Burgmeyer
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 289 KB
- Volume
- 147
- Category
- Article
- ISSN
- 0022-4596
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✦ Synopsis
We report that zirconium viologen diphosphonate, (Zr 2 (O 3 P-CH 2 CH 2 -bipyridinium-CH 2 CH 2 -PO 3 )X 6 ' 2H 2 O), where X ؍ halide ion, ZrVP, will react with a variety of phosphonates (H 2 O 3 P-R, where R ؍ OH, H, CH 3 , C 6 H 5 ) under mild conditions, producing a disordered porous phase. This is in sharp contrast to the observed reactivity of the more common zirconium phosphonate phases: the -phase group (IVB) layered phosphonates Zr(O 3 PR) 2 (whose structures are based upon -(Zr(O 3 POH) 2 ' H 2 O), -ZrP) are resistant to reaction with monophosphonates while -Zr(O 4 P)(O 2 P(OH) 2 ) ' 2H 2 O, -ZrP, undergoes topotactic ligand exchange with mono-and di-phosphonates to form ordered porous materials. We follow the reaction by X-ray powder di4raction and IR and UV spectroscopies and investigate the porous nature of the resulting solids through ion-exchange and N 2 adsorption experiments.
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A nickel molybdenum phosphate, (NH 3 CH 2 CH 2 NH 3 ) 4 ' (NH 3 CH 2 CH 2 NH 2 ) ' Na ' [Ni 2 Mo 12 O 30 (PO 4 ) (HPO 4 ) 4 (H 2 PO 4 ) 3 ] ' 6H 2 O, involving molybdenum present in V oxidation, has been hydrothermally synthesized and structurally characterized by single crystal X-ray di4raction. De