Howard G. Harvey
Royal Institution
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Featured researches published by Howard G. Harvey.
Journal of Materials Chemistry | 2000
Howard G. Harvey; Simon J. Teat; Martin P. Attfield
The synthesis and crystal structure of the novel aluminium diphosphonate Al2[O3PC2H4PO3](H2O)2F2·H2O is described; the material consists of chains of AlO4F2 octahedra linked together by ethylenediphosphonate units to form a structure with channels running parallel to the a axis which contain extra-framework water molecules that can be desorbed.
Inorganic Chemistry | 2010
Martin P. Attfield; Zhanhui Yuan; Howard G. Harvey; William Clegg
Three new gallium diphosphonates: Ga(3)(OH)(O(3)PC(3)H(6)PO(3))(2) (1), Ga(4)(O(3)PC(5)H(10)PO(3))(3)(C(5)H(5)N)(2) (2), and Ga(HO(3)PC(10)H(20)PO(3)) (3), in which the diphosphonate bridging ligands have 3, 5, and 10 methylene units, respectively, have been synthesized using solvothermal methods and their structures determined using single-crystal laboratory and synchrotron X-ray diffraction data. All three materials contain Ga-centered tetrahedra and octahedra linked together through the -PO(3) groups of the diphosphonate ligands to form two-dimensional pillared slab (1) and three-dimensional pillared (2 and 3) materials. Compound 1 contains bridging hydroxide anions that connect Ga-centered octahedra and tetrahedra, and contains pillared slabs in which one side of the Ga-P-O/OH/CH hybrid layers are connected by the propylenediphosphonate groups only. This slab also contains propylenediphosphonate groups arranged orthogonally to the pillaring direction in the outermost layer of the Ga-P-O/OH/CH hybrid layers. Compound 2 is a framework structure that contains framework pyridine molecules between alternate layers of diphosphonate-pillared Ga-P-O layers and is structurally stable to loss of 1 equiv of pyridine molecules from the structure. Compound 3 is a partially condensed pillared framework structure with one P-O-H bond per diphosphonate group remaining in the resulting material. The structural changes observed as the alkylene chain in the diphosphonate ligand is increased in these compounds is compared to other members of the gallium diphosphonate family synthesized in a similar manner, and other metal diphosphonate series, to gain some general oversight of the structural trends observed in series of metal diphosphonate materials in which the alkylene chain length is varied systematically.
MRS Proceedings | 2000
Martin P. Attfield; Howard G. Harvey
The gallium diphosphonate, Ga 2 [O 3 PC 2 H 4 PO 3 ](H 2 O) 2 F 2 ·H 2 O, has been prepared under solvothermal conditions from a HF/ pyridine solvent system. The structure of the material was determined by Rietveld refinement using the isostructural aluminium compound as the starting model for refinement. The structure consists of chains of corner sharing GaO 4 F 2 octahedra with bridging F atoms linking the octahedra. The chains of octahedra are linked together in two directions perpendicular to the chain direction by the ethylenediphosphonate groups. The resulting structure contains a one-dimensional channel system in which extra-framework water molecules reside. Thermal gravimetric analysis of the material shows that 40 % of the extra- framework water can be reversibly absorbed. Thermodiffraction studies show that the material retains its structural integrity until all the extra-framework water is lost and then undergoes a considerable loss in crystallinity as the framework water molecules are lost. The crystallinity of the material then progressively decreases as the temperature is increased.
Chemistry: A European Journal | 2004
Howard G. Harvey; Ben Slater; Martin P. Attfield
Chemistry of Materials | 2004
Howard G. Harvey; Anne C. Herve; Helen C. Hailes; Martin P. Attfield
Chemistry of Materials | 2003
Howard G. Harvey; Jerry Hu; Martin P. Attfield
Inorganic Chemistry | 2003
Howard G. Harvey; Simon J. Teat; Chiu C. Tang; Lachlan M. D. Cranswick; Martin P. Attfield
Chemistry of Materials | 2004
Howard G. Harvey; Martin P. Attfield
Journal of Solid State Chemistry | 2004
Martin P. Attfield; Howard G. Harvey; Simon J. Teat
Solid State Sciences | 2006
Howard G. Harvey; Martin P. Attfield