0000000001301387

AUTHOR

Erik Ekengard

Thiophene based imino-pyridyl palladium(II) complexes : Synthesis, molecular structures and Heck coupling reactions

Abstract The new compounds (5-methyl-2-thiophene-2-pyridyl(R))imine [R = methyl (L1); R = ethyl (L2)] and (5-bromo-2-thiophene-2-pyridyl(R)imine [R = methyl (L3); R = ethyl (L4)] were successfully synthesized via Schiff base condensation reaction and obtained in good yields. These potential ligands were reacted with [PdCl2(COD)] and [PdClMe(COD)] to give the corresponding complexes [PdCl2(L)] (L = L1-L4; 1–4) and [PdClMe(L)] (L = L1-L4; 5–8). All compounds were characterized by IR, 1H and 13C NMR spectroscopy, elemental analysis and mass spectrometry. The molecular structures of 1, 2, 6 and 8 were confirmed by X-ray crystallography. The complexes were evaluated as catalyst precursors for st…

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Pentamethylcyclopentadienyl-rhodium and iridium complexes containing (N^N and N^O) bound chloroquine analogue ligands: synthesis, characterization and antimalarial properties

The synthesis and characterization of twenty new pentamethylcyclopentadienyl-rhodium and iridium complexes containing N^N and N^O-chelating chloroquine analogue ligands are described. The in vitro antimalarial activity of the new ligands as well as the complexes was evaluated against the chloroquine sensitive (CQS) NF54 and the chloroquine resistant (CQR) Dd2 strains of Plasmodium falciparum. The antimalarial activity was found to be good to moderate; although all complexes are less active than artesunate, some of the ligands and complexes showed better activity than chloroquine (CQ). In particular, rhodium complexes were found to be considerably more active than iridium complexes against t…

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Thiophene based imino-pyridyl palladium(II) complexes : Synthesis, molecular structures and Heck coupling reactions

The new compounds (5-methyl-2-thiophene-2-pyridyl(R))imine [R = methyl (L1); R = ethyl (L2)] and (5-bromo-2-thiophene-2-pyridyl(R)imine [R = methyl (L3); R = ethyl (L4)] were successfully synthesized via Schiff base condensation reaction and obtained in good yields. These potential ligands were reacted with [PdCl2(COD)] and [PdClMe(COD)] to give the corresponding complexes [PdCl2(L)] (L = L1-L4; 1–4) and [PdClMe(L)] (L = L1-L4; 5–8). All compounds were characterized by IR, 1H and 13C NMR spectroscopy, elemental analysis and mass spectrometry. The molecular structures of 1, 2, 6 and 8 were confirmed by X-ray crystallography. The complexes were evaluated as catalyst precursors for standard He…

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CCDC 1426907: Experimental Crystal Structure Determination

Related Article: Erik Ekengard, Kamlesh Kumar, Thibault Fogeron, Carmen de Kock, Peter J. Smith, Matti Haukka, Magda Monari, Ebbe Nordlander|2016|Dalton Trans.|45|3905|doi:10.1039/C5DT03739E

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CCDC 1525885: Experimental Crystal Structure Determination

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

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CCDC 971206: Experimental Crystal Structure Determination

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

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CCDC 1426908: Experimental Crystal Structure Determination

Related Article: Erik Ekengard, Kamlesh Kumar, Thibault Fogeron, Carmen de Kock, Peter J. Smith, Matti Haukka, Magda Monari, Ebbe Nordlander|2016|Dalton Trans.|45|3905|doi:10.1039/C5DT03739E

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CCDC 971205: Experimental Crystal Structure Determination

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

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CCDC 1426906: Experimental Crystal Structure Determination

Related Article: Erik Ekengard, Kamlesh Kumar, Thibault Fogeron, Carmen de Kock, Peter J. Smith, Matti Haukka, Magda Monari, Ebbe Nordlander|2016|Dalton Trans.|45|3905|doi:10.1039/C5DT03739E

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CCDC 1510203: Experimental Crystal Structure Determination

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

research product

CCDC 1510204: Experimental Crystal Structure Determination

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

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