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M

Mary F. Mahon

Researcher at University of Bath

Publications -  563
Citations -  15395

Mary F. Mahon is an academic researcher from University of Bath. The author has contributed to research in topics: Catalysis & Crystal structure. The author has an hindex of 59, co-authored 539 publications receiving 14258 citations. Previous affiliations of Mary F. Mahon include University of Wales & Heriot-Watt University.

Papers
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Dipyridyl β-diketonate complexes and their use as metalloligands in the formation of mixed-metal coordination networks.

Andrew D. Burrows, +6 more
- 14 Mar 2012 - 
TL;DR: The iron( III) and aluminium(III) complexes of 1,3-di(4-pyridyl)propane-1, 3-dionato (dppd) and 1,2-di (3-p Pyridyl), [Fe( dppd)(3)], [Al(dppD)(3)] 1, [Fe (dmppd(3)] 2, [Al (dippd) 3)],
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C–F bond activation of perfluoroalkenes by ruthenium phosphine hydride complexes: X-ray crystal structures of cis-Ru(dmpe)2F(F⋯HF) and [Ru(dcpe)2H]+[(CF3)2CC(O)CF2CF3]−

Matthew S. Kirkham, +2 more
- 01 Jan 2001 - 
TL;DR: The reaction of (CF3)2CC(F)CF2CF3 or CF3CFCF2 with Ru(DMpe)2H2 affords the bifluoride fluoride complex cis-Ru(dmpe) 2F(F⋯HF) as mentioned in this paper.
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Aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole and vorozole templates.

Paul M. Wood, +5 more
- 01 Aug 2011 - 
TL;DR: A new series of letrozole‐derived sulfamates and a vorozole‐based sulfamate were designed and biologically evaluated in JEG‐3 cells to reveal structure–activity relationships and the S‐(+)‐enantiomer was found to inhibit aromatase and sulfatase most potently.
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Synthesis, characterisation and reaction chemistry of organotin-substituted bis(thiotetrazoles): supramolecular metallotetrazole structures containing hard and soft donors

Sonali Bhandari, +4 more
- 01 Jan 1998 - 
TL;DR: In this article, the supramolecular structure of 1,4-(Bu3SnSCN4)2C6H4 has been found to consist of a 2-D sheet arrangement containing 32-membered (C4NCSSnN2CSSnN3)2 rings.
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5-Nitroisocoumarins from tandem Castro–Stephens coupling—6-endo-dig cyclisation of 2-iodo-3-nitrobenzoic acid and arylethynes and ring-closure of methyl 2-alkynyl-3-nitrobenzoates with electrophiles

Esther C. Y. Woon, +3 more
- 15 May 2006 - 
TL;DR: 1H NMR and X-ray crystallography showed the cyclisations to be 6-endo, contrasting with reports of 5-exo cyclisation of analogous 2-iodobenzoate esters with alkynes, and the nitro group tends to direct these electrophile-driven cyclisations towards the 6-END mode.