Publications 2015
8498180
2015
1
american-chemical-society
50
creator
asc
929
https://www0.sun.ac.za/chemistry/wp-content/plugins/zotpress/
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Eddaoudi, M.; Barbour, L. J. CO2 Separation, Capture and Reuse: A Web Themed Issue. Chem. Commun. (Cambridge, U. K.) 2015, 51 (26), 5554–5555. https://doi.org/10.1039/C5CC90085A.
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Ekengard, E.; Glans, L.; Cassells, I.; Fogeron, T.; Govender, P.; Stringer, T.; Chellan, P.; Lisensky, G. C.; Hersh, W. H.; Doverbratt, I.; Lidin, S.; de Kock, C.; Smith, P. J.; Smith, G. S.; Nordlander, Ebbe. Antimalarial Activity of Ruthenium(II) and Osmium(II) Arene Complexes with Mono- and Bidentate Chloroquine Analogue Ligands. Dalton Trans. 2015, 44 (44), 19314–19329. https://doi.org/10.1039/C5DT02410B.
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Engelbrecht, L.; Murray, P.; Koch, K. R. Isotope Effects in 195Pt NMR Spectroscopy: Unique 35/37Cl- and 16/18O-Resolved “Fingerprints” for All [PtCl6-n(OH)n]2- (n = 1-5) Anions in an Alkaline Solution and the Implications of the Trans Influence. Inorg. Chem. 2015, 54 (6), 2752–2764. https://doi.org/10.1021/ic502901d.
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Gerber, W. J.; van Wyk, P.-H.; van Niekerk, D. M. E.; Koch, K. R. The Fundamental Flaw of the HSAB Principle Is Revealed by a Complete Speciation Analysis of the [PtCl6-NBrn]2- (n = 0-6) System. Phys. Chem. Chem. Phys. 2015, 17 (8), 5712–5724. https://doi.org/10.1039/C4CP05294C.
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Gildenhuys, J.; Sammy, C. J.; Muller, R.; Streltsov, V. A.; le Roex, T.; Kuter, D.; de Villiers, K. A. Alkoxide Coordination of Iron(III) Protoporphyrin IX by Antimalarial Quinoline Methanols: A Key Interaction Observed in the Solid-State and Solution. Dalton Trans. 2015, 44 (38), 16767–16777. https://doi.org/10.1039/C5DT02671G.
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Govender, D.; Islam, R. U.; De Koning, C. B.; van Otterlo, W. A. L.; Arbuthnot, P.; Ariatti, M.; Singh, Moganavelli. Stealth Lipoplex Decorated with Triazole-Tethered Galactosyl Moieties: A Strong Hepatotropic Gene Vector. Biotechnol. Lett. 2015, 37 (3), 567–575. https://doi.org/10.1007/s10529-014-1729-5.
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Greyling, G.; Pasch, Harald. Fractionation of Poly(Butyl Methacrylate) by Molecular Topology Using Multidetector Thermal Field-Flow Fractionation. Macromol. Rapid Commun. 2015, 36 (24), 2143–2148. https://doi.org/10.1002/marc.201500429.
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Greyling, G.; Pasch, Harald. Multidetector Thermal Field-Flow Fractionation as a Unique Tool for the Tacticity-Based Separation of Poly(Methyl Methacrylate)-Polystyrene Block Copolymer Micelles. J. Chromatogr. A 2015, 1414 (Copyright (C) 2021 American Chemical Society (ACS). All Rights Reserved.), 163–172. https://doi.org/10.1016/j.chroma.2015.08.023.
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Greyling, G.; Pasch, Harald. Tacticity Separation of Poly(Methyl Methacrylate) by Multidetector Thermal Field-Flow Fractionation. Anal. Chem. (Washington, DC, U. S.) 2015, 87 (5), 3011–3018. https://doi.org/10.1021/ac504651p.
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Hehn, M.; Sinha, P.; Pasch, H.; Hiller, Wolf. Onflow Liquid Chromatography at Critical Conditions Coupled to 1H and 2H Nuclear Magnetic Resonance as Powerful Tools for the Separation of PMMA According to Isotopic Composition. J. Chromatogr. A 2015, 1387 (Copyright (C) 2021 American Chemical Society (ACS). All Rights Reserved.), 69–74. https://doi.org/10.1016/j.chroma.2015.02.012.
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Jacobs, L.; de Kock, C.; de Villiers, K. A.; Smith, P. J.; Smith, V. J.; van Otterlo, W. A. L.; Blackie, M. A. L. Design, Synthesis, and Evaluation of Novel Ferroquine and Phenylequine Analogues as Potential Antiplasmodial Agents. ChemMedChem 2015, 10 (12), 2099–2110. https://doi.org/10.1002/cmdc.201500349.
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Kornienko, A.; Evidente, A.; Vurro, M.; Mathieu, V.; Cimmino, A.; Evidente, M.; van Otterlo, W. A. L.; Dasari, R.; Lefranc, F.; Kiss, Robert. Toward a Cancer Drug of Fungal Origin. Med. Res. Rev. 2015, 35 (5), 937–967. https://doi.org/10.1002/med.21348.
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Maiko, K.; Pasch, Harald. Comprehensive Microstructure and Molar Mass Analysis of Polybutadiene by Multidimensional Liquid Chromatography. Macromol. Rapid Commun. 2015, 36 (24), 2137–2142. https://doi.org/10.1002/marc.201500381.
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Malgas-Enus, R.; Mapolie, S. F. Nickel Metallodendrimers as Catalyst Precursors in the Tandem Oligomerization of Ethylene and Friedel-Crafts Alkylation of Its Olefinic Products [Erratum to Document Cited in CA160:035396]. Inorg. Chim. Acta 2015, 428 (Copyright (C) 2021 American Chemical Society (ACS). All Rights Reserved.), 212. https://doi.org/10.1016/j.ica.2015.02.015.
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Matsinha, L. C.; Mao, J.; Mapolie, S. F.; Smith, G. S. Water-Soluble Palladium(II) Sulfonated Thiosemicarbazone Complexes: Facile Synthesis and Preliminary Catalytic Studies in the Suzuki-Miyaura Cross-Coupling Reaction in Water. Eur. J. Inorg. Chem. 2015, 2015 (24), 4088–4094. https://doi.org/10.1002/ejic.201500588.
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Matsinha, L. C.; Mapolie, S. F.; Smith, G. S. Recoverable and Recyclable Water-Soluble Sulphonated Salicylaldimine Rh(I) Complexes for 1-Octene Hydroformylation in Aqueous Biphasic Media. Dalton Trans. 2015, 44 (3), 1240–1248. https://doi.org/10.1039/C4DT02740J.
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Ndiripo, A.; Pasch, Harald. On the Multimodality of Preparative TREF Fractionation as Detected by Advanced Analytical Methods. Anal. Bioanal. Chem. 2015, 407 (21), 6493–6503. https://doi.org/10.1007/s00216-015-8814-z.
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Ngaza, N.; Brand, M.; Pasch, Harald. Multidetector-ThF3 as a Novel Tool for the Investigation of Solution Properties of Amphiphilic Block Copolymers. Macromol. Chem. Phys. 2015, 216 (12), 1355–1364. https://doi.org/10.1002/macp.201500070.
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Pasch, Harald. Polymer Science Education - A (Southern) African Perspective. Macromol. Symp. 2015, 355 (1), 96–103. https://doi.org/10.1002/masy.201500029.
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Pasch, Harald. Advanced Fractionation Methods for the Microstructure Analysis of Complex Polymers. Polym. Adv. Technol. 2015, 26 (7), 771–784. https://doi.org/10.1002/pat.3479.
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Pelly, S. C.; Van Otterlo, W. A. L.; Muller, R.; Basson, Adriaan. Trisubstituted Indoles and Their Use as Non-Nucleoside Reverse Transcriptase Inhibitors for Treatment of HIV Infection or AIDS., April 2, 2015.
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Phiri, M. J.; Dimeska, A.; Pasch, Harald. On the Homogeneity of Metallocene Ethylene-Propylene Copolymers as Investigated by Multiple Fractionation Techniques. Macromol. Chem. Phys. 2015, 216 (15), 1619–1628. https://doi.org/10.1002/macp.201500135.