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Journal articleSung S, Braddock DC, Armstrong A, et al., 2015,
Synthesis, Characterisation and Reactivity of Copper(I) Amide Complexes and Studies on Their Role in the Modified Ullmann Amination Reaction
, CHEMISTRY-A EUROPEAN JOURNAL, Vol: 21, Pages: 7179-7192, ISSN: 0947-6539- Author Web Link
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- Citations: 18
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Journal articleCampbell J, Davies RP, Braddock DC, et al., 2015,
Improving the permeance of hybrid polymer/metal-organic framework (MOF) membranes for organic solvent nanofiltration (OSN) - development of MOF thin films via interfacial synthesis
, JOURNAL OF MATERIALS CHEMISTRY A, Vol: 3, Pages: 9668-9674, ISSN: 2050-7488- Author Web Link
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- Citations: 105
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Journal articleCampbell J, Szekely G, Davies RP, et al., 2014,
Fabrication of hybrid polymer/metal organic framework membranes: mixed matrix membranes versus in situ growth
, Journal of Materials Chemistry A, Vol: 2, Pages: 9260-9271, ISSN: 2050-7488Hybrid polymer/metal organic framework (MOF) membranes have been prepared using either a mixed matrix membrane (MMM) or in situ growth (ISG) approach and were evaluated for application in organic solvent nanofiltration (OSN). MMMs were produced by dispersing pre-formed particles of the MOF HKUST-1 in polyimide P84 dope solutions. MMMs demonstrated both (i) higher rejections of styrene oligomers and (ii) lower flux decline than the polymeric control membranes. Furthermore, an alternative hybrid membrane fabrication methodology – in situ growth (ISG) of HKUST-1 in integrally skinned asymmetric polymer membrane supports – has been successfully demonstrated. Ultrafiltration support membranes were submerged in HKUST-1 precursor solutions in order to promote the growth of MOF within the porous structure of the polymer membranes. The presence of HKUST-1 in the membranes was proven with X-ray powder diffraction (XRPD). Energy-dispersive X-ray spectroscopy (EDX) was used to reveal the distribution of HKUST-1 throughout the ISG membranes, and was found to be even across the surface and throughout the cross-section. The ISG membranes also had higher solute rejections and lower flux decline than the MMMs.
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Journal articleKim M-S, Buisson LA, Heathcote DA, et al., 2014,
Approaches to design non-covalent inhibitors for human granzyme B (hGrB)
, ORGANIC & BIOMOLECULAR CHEMISTRY, Vol: 12, Pages: 8952-8965, ISSN: 1477-0520- Author Web Link
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- Citations: 7
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Journal articleBraddock DC, Gao AX, White AJP, et al., 2014,
Studies towards the synthesis of halomon: asymmetric hexafunctionalisation of myrcene
, CHEMICAL COMMUNICATIONS, Vol: 50, Pages: 13725-13728, ISSN: 1359-7345- Author Web Link
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- Citations: 6
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Journal articleBraddock DC, Sbircea D-T, 2014,
Proof-of-principle direct double cyclisation of a linear C-15-precursor to a dibrominated bicyclic medium-ring ether relevant to Laurencia species
, CHEMICAL COMMUNICATIONS, Vol: 50, Pages: 12691-12693, ISSN: 1359-7345- Author Web Link
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- Citations: 11
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Journal articleArmstrong A, Braddock DC, Jones AX, et al., 2013,
Catalytic asymmetric bromolactonization reactions using (DHQD)(2)PHAL-benzoic acid combinations
, TETRAHEDRON LETTERS, Vol: 54, Pages: 7004-7008, ISSN: 0040-4039- Author Web Link
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- Citations: 43
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Journal articleBraddock DC, Marklew JS, Foote KM, et al., 2013,
An Enantiospecific Polyene Cyclization Initiated by an Enantiomerically Pure Bromonium Ion
, CHIRALITY, Vol: 25, Pages: 692-700, ISSN: 0899-0042- Author Web Link
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- Citations: 14
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Journal articleBraddock DC, Clarke J, Rzepa HS, 2013,
Epoxidation of bromoallenes connects red algae metabolites by an intersecting bromoallene oxide - Favorskii manifold
, CHEMICAL COMMUNICATIONS, Vol: 49, Pages: 11176-11178, ISSN: 1359-7345- Author Web Link
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- Citations: 7
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Journal articleBonney KJ, Braddock DC, 2012,
A Unifying Stereochemical Analysis for the Formation of Halogenated C-15-Acetogenin Medium-Ring Ethers From Laurencia Species via Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening and Experimental Corroboration with a Model Epoxide
, JOURNAL OF ORGANIC CHEMISTRY, Vol: 77, Pages: 9574-9584, ISSN: 0022-3263- Author Web Link
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- Citations: 30
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