Source:http://linkedlifedata.com/resource/pubmed/id/15619727
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2005-2-24
|
pubmed:abstractText |
Three new unsymmetrical compartmental dinucleating ligands, 4-bromo-2-(4-methylpiperazin-1-ylmethyl)-6-[{2-(1-piperidyl)ethyl}aminomethyl]phenol (HL1), 4-bromo-2-(4-methylpiperazin-1-ylmethyl)-6-[{2-(morpholin-4-yl)ethyl}aminomethyl]phenol (HL2), and 4-bromo-2-(4-methylpiperazin-1-ylmethyl)-6-[{2-(thiomorpholin-4-yl)ethyl}aminomethyl]phenol (HL3), have been synthesized in order to model the active site of type 3 copper proteins. The dicopper(II) complexes of these ligands give first hints about the influence of a thioether group close to the metal site. The bromophenol-based ligands have one piperazine arm and one other bidentate arm in positions 2 and 6 of the phenolic ring, respectively. With each ligand a dinuclear copper(II) complex was prepared and structurally characterized. The copper ions were found to have square pyramidal environments and a mixture of endogenous phenoxo and exogenous acetate bridging. The influence of a heteroatom in one arm of the ligand on catecholase activity and speciation in solution was studied by UV/Vis spectroscopy, ESI-MS experiments and, DFT calculations.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Catechol Oxidase,
http://linkedlifedata.com/resource/pubmed/chemical/Copper,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Morpholines,
http://linkedlifedata.com/resource/pubmed/chemical/Organometallic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Phenols,
http://linkedlifedata.com/resource/pubmed/chemical/Piperidines,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfides
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0947-6539
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
4
|
pubmed:volume |
11
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1201-9
|
pubmed:dateRevised |
2009-8-4
|
pubmed:meshHeading |
pubmed-meshheading:15619727-Catechol Oxidase,
pubmed-meshheading:15619727-Copper,
pubmed-meshheading:15619727-Crystallography, X-Ray,
pubmed-meshheading:15619727-Enzyme Activation,
pubmed-meshheading:15619727-Kinetics,
pubmed-meshheading:15619727-Ligands,
pubmed-meshheading:15619727-Models, Chemical,
pubmed-meshheading:15619727-Models, Molecular,
pubmed-meshheading:15619727-Molecular Structure,
pubmed-meshheading:15619727-Morpholines,
pubmed-meshheading:15619727-Organometallic Compounds,
pubmed-meshheading:15619727-Phenols,
pubmed-meshheading:15619727-Piperidines,
pubmed-meshheading:15619727-Stereoisomerism,
pubmed-meshheading:15619727-Structure-Activity Relationship,
pubmed-meshheading:15619727-Sulfides
|
pubmed:year |
2005
|
pubmed:articleTitle |
Less symmetrical dicopper(II) complexes as catechol oxidase models--an adjacent thioether group increases catecholase activity.
|
pubmed:affiliation |
Institut für Anorganische und Analytische Chemie der Westfälischen Wilhelms-Universität, Wilhelm-Klemm-Strasse 8, 48149 Münster, Germany.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|