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M.T. Pope

Publications and source records attributed to M.T. Pope.

2 recordsLinked to original sources

Polyoxometalates from heteropoly "brown" precursors. A new structural class of mixed valence heteropolytungstates, [(XO4)W3IVW17VIO 62Hx]n-

Reduction of the α-Keggin anion [X n + O 4 W 12 O 36 ] [8 − n]− (X = H 2 2+ , B 3+ , Si 4+ ) by six electrons results in the known tungsten “brown” species [X n + O 4 (H 2 O) 3 W IV 3 W VI 9 O 33 ] [8 − n ]− in which three W atoms have been reduced from W VI to W IV , forming a metal–metal bonded triad. The W IV atoms have terminal water coordinated in place of terminal oxo groups. Additional tungstate can condense onto these water molecules in aqueous solution between pH = 4 and 6.5 to form the species reported here, [(XO 4 )W IV 3 W VI 17 O 62 H x ] y − . The boron derivative (X = B 3+ ) is more stable than the metatungstate (X = H 2 2+ ), both of which have been characterized by elemental analysis, 183 W NMR and X-ray crystal structure analysis. Eight additional tungstate groups condense in the form of a partial Keggin structure containing two triads and one dyad which is rotated 60° relative to a hypothetical α-isomer.

Journal of the Chemical Society, Dalton Transactio↗

Tungstorhenate heteropolyanions. 2. Synthesis and characterization of enneatungstorhenates(V), -(VI), and -(VII)

The tungstorhenate(V) heteropolyanion [W 9 ReO 32 ] 5 - has been isolated as guanidinium and cesium salts from reaction of [ReO 2 (PPh 3 )(py) 3 ] + with sodium tungstate. Crystallographic analysis of black Cs 5 [W 9 ReO 32 ]·3H 2 O [triclinic, P 1 or P 1̄; a = 10.194(1), b = 11.503(2), c = 9.682(1) Å; α = 100.55(1), β = 115.81(1), γ = 99.13(1)°; Z = 1], based on 3743 reflections, shows the anion to be isostructural with decatungstate, [W 10 O 32 ] 4 - . Refinement in P 1̄ led to reliability indices R = 0.084, R w = 0.046. Electrochemical investigation revealed the existence of Re VI and Re VII analogues, which were hydrolytically unstable in aqueous solution but which were isolated as crystalline tetra- n -butylammonium and tetra- n -heptylammonium salts, respectively, from nonaqueous solvents. The tetra- n -butylammonium salts of [W 9 Re VI O 32 ] 4 - and [W 10 O 32 ] 4 - were shown to be isomorphous by X-ray powder diffraction. Simulation of the Q-band ESR spectrum of [W 9 Re VI O 32 ] 4 - (polycrystalline solid solution in [W 10 O 32 ] 4 - ) gave g x = 1.69(1), g y = 1.66(1), g z = 1.730(2) and 10 4 A x ( 185,187 Re, I = 5 / 2 ) = (−)252(10), 10 4 A y = (−)398(10), 10 4 A z = (−)653(5) cm - 1 . The orthorhombic ESR spectrum proves that the Re atom occupies one of the eight equivalent “equatorial” sites in the decatungstate structure.

Inorganic Chemistry↗