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Woodall, Christopher H.

Publications and source records attributed to Woodall, Christopher H..

Observation of a re-entrant phase transition in the molecular complex tris(μ 2 -3,5-diisopropyl-1,2,4-triazolato-κ 2 N 1 : N 2 )trigold(I) under high pressure

We report a molecular crystal that exhibits four successive phase transitions under hydro­static pressure, driven by aurophilic interactions, with the ground-state structure re-emerging at high pressure. The effect of pressure on two polytypes of tris(μ 2 -3,5-diiso­propyl-1,2,4-triazolato-κ 2 N 1 : N 2 )trigold(I) (denoted Form-I and Form-II) has been analysed using luminescence spectroscopy, single-crystal X-ray diffraction and first-principles computation. A unique phase behaviour was observed in Form-I, with a complex sequence of phase transitions between 1 and 3.5 GPa. The ambient C 2/c mother cell transforms to a P 2 1 /n phase above 1 GPa, followed by a P 2 1 /a phase above 2 GPa and a large-volume C 2/c supercell at 2.70 GPa, with the previously observed P 2 1 /n phase then reappearing at higher pressure. The observation of crystallographically identical low- and high-pressure P 2 1 /n phases makes this a rare example of a re-entrant phase transformation. The phase behaviour has been characterized using detailed crystallographic theory and modelling, and rationalized in terms of molecular structural distortions. The dramatic changes in conformation are correlated with shifts of the luminescence maxima, from a band maximum at 14040 cm –1 at 2.40 GPa, decreasing steeply to 13550 cm –1 at 3 GPa. A similar study of Form-II displays more conventional crystallographic behaviour, indicating that the complex behaviour observed in Form-I is likely to be a direct consequence of the differences in crystal packing between the two polytypes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Tunable trimers: Using temperature and pressure to control luminescent emission in gold(I) pyrazolate-based trimers

A systematic investigation into the relationship between the solid-state luminescence and the intermolecular Au∙∙∙Au interactions in a series of pyrazolate-based gold(I) trimers; tris(μ 2 -pyrazolato-N,N')-tri-gold(I) (1), tris(μ 2 -3,4,5-trimethylpyrazolato-N,N')-tri-gold(I) (2), tris(μ 2 -3-methyl-5-phenylpyrazolato-N,N')-tri-gold(I) (3) and tris(μ 2 -3,5-diphenylpyrazolato-N,N')-tri-gold(I) (4) has been carried out using variable temperature and high pressure X-ray crystallography, solid-state emission spectroscopy, Raman spectroscopy and computational techniques. Single-crystal X-ray studies show that there is a significant reduction in the intertrimer Au∙∙∙Au distances both with decreasing temperature and increasing pressure. In the four complexes, the reduction in temperature from 293 to 100 K is accompanied by a reduction in the shortest intermolecular Au∙∙∙Au contacts of between 0.04 and 0.08 Å. The solid-state luminescent emission spectra of 1 and 2 display a red shift with decreasing temperature or increasing pressure. Compound 3 does not emit under ambient conditions but displays increasingly red-shifted luminescence upon cooling or compression. Compound 4 remains emissionless, consistent with the absence of intermolecular Au∙∙∙Au interactions. The largest pressure induced shift in emission is observed in 2 with a red shift of approximately 630 cm -1 per GPa between ambient and 3.80 GPa. The shifts in all the complexes can be correlated with changes in Au∙∙∙Au distance observed by diffraction.

74 ATOMIC AND MOLECULAR PHYSICS↗

Solid-State Interconversions: Unique 100 % Reversible Transformations between the Ground and Metastable States in Single-Crystals of a Series of Nickel(II) Nitro Complexes

The solid-state, low-temperature linkage isomerism in a series of five square planar group 10 phosphino nitro complexes have been investigated by a combination of photocrystallographic experiments, Raman spectroscopy and computer modelling. The factors influencing the reversible solid-state interconversion between the nitro and nitrito structural isomers have also been investigated, providing insight into the dynamics of this process. The cis-[Ni(dcpe)- (NO 2 ) 2 ] (1) and cis-[Ni(dppe)(NO 2 ) 2 ] (2) complexes show reversible 100% interconversion between the h 1 -NO 2 nitro isomer and the h 1 -ONO nitrito form when single-crystals are irradiated with 400 nm light at 100 K. Variable temperature photocrystallographic studies for these complexes established that the metastable nitrito isomer reverted to the ground-state nitro isomer at temperatures above 180 K. By comparison, the related trans complex [Ni(PCy 3 ) 2 (NO 2 ) 2 ] (3) showed 82% conversion under the same experimental conditions at 100 K. The level of conversion to the metastable nitrito isomers is further reduced when the nickel centre is replaced by palladium or platinum. Prolonged irradiation of the trans-[Pd(PCy 3 ) 2 (NO 2 ) 2 ] (4) and trans-[Pt(PCy 3 ) 2 (NO 2 ) 2 ] (5) with 400 nm light gives reversible conversions of 44 and 27%, respectively, consistent with the slower kinetics associated with the heavier members of group 10. The mechanism of the interconversion has been investigated by theoretical calculations based on the model complex [Ni(dmpe)Cl(NO 2 )].

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗