Chiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivities

dc.contributor.authorVedder, Christophdeu
dc.contributor.authorSchaper, Frankdeu
dc.contributor.authorBrintzinger, Hans-Herbert
dc.contributor.authorKettunen, Mikadeu
dc.contributor.authorBabik, Sebastiandeu
dc.contributor.authorFink, Gerharddeu
dc.date.accessioned2013-07-11T08:04:21Zdeu
dc.date.available2013-07-11T08:04:21Zdeu
dc.date.issued2005
dc.description.abstractA new class of iron(II) and cobalt(II) complexes with neutral, tetradentate bis(pyridylimine) chelate ligands bridged by a chiral 6,6′-dimethylbiphenyl backbone has been synthesized. Their dihalogen derivatives gave spectral, magnetic and X-ray diffraction results in agreement with a C2-symmetric, approximately octahedral geometry with cis-positioned halide ligands and high-spin d-electron configuration. 1H NMR signals of these paramagnetic complexes were assigned by correlating line widths with reciprocal proton-metal distances. Methyl substitution in 6-position of the pyridyl rings lead to a different, presumably square-pyramidal coordination geometry under dissociation of one chloride ion. FeII dimethyl and diisocyanide derivatives were shown to have low-spin configuration and C1-symmetric geometry. With respect to MAO-activated olefin polymerization, significant catalytic activities were reproducibly obtained only under conditions, where the original complex structure was degraded.eng
dc.description.versionpublished
dc.identifier.citationEuropean Journal of Inorganic Chemistry ; (2005), 6. - S. 1071-1080deu
dc.identifier.doi10.1002/ejic.200400912deu
dc.identifier.ppn390810347deu
dc.identifier.urihttp://kops.uni-konstanz.de/handle/123456789/23698
dc.language.isoengdeu
dc.legacy.dateIssued2013-07-11deu
dc.rightsterms-of-usedeu
dc.rights.urihttps://rightsstatements.org/page/InC/1.0/deu
dc.subjectIron(II)deu
dc.subjectcobalt(II)deu
dc.subjectbianilinedeu
dc.subjectpyridyliminedeu
dc.subject.ddc540deu
dc.titleChiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivitieseng
dc.typeJOURNAL_ARTICLEdeu
dspace.entity.typePublication
kops.citation.bibtex
@article{Vedder2005Chira-23698,
  year={2005},
  doi={10.1002/ejic.200400912},
  title={Chiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivities},
  number={6},
  volume={2005},
  issn={1434-1948},
  journal={European Journal of Inorganic Chemistry},
  pages={1071--1080},
  author={Vedder, Christoph and Schaper, Frank and Brintzinger, Hans-Herbert and Kettunen, Mika and Babik, Sebastian and Fink, Gerhard}
}
kops.citation.iso690VEDDER, Christoph, Frank SCHAPER, Hans-Herbert BRINTZINGER, Mika KETTUNEN, Sebastian BABIK, Gerhard FINK, 2005. Chiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivities. In: European Journal of Inorganic Chemistry. 2005, 2005(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912deu
kops.citation.iso690VEDDER, Christoph, Frank SCHAPER, Hans-Herbert BRINTZINGER, Mika KETTUNEN, Sebastian BABIK, Gerhard FINK, 2005. Chiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivities. In: European Journal of Inorganic Chemistry. 2005, 2005(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912eng
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    <dcterms:abstract xml:lang="eng">A new class of iron(II) and cobalt(II) complexes with neutral, tetradentate bis(pyridylimine) chelate ligands bridged by a chiral 6,6′-dimethylbiphenyl backbone has been synthesized. Their dihalogen derivatives gave spectral, magnetic and X-ray diffraction results in agreement with a C&lt;sub&gt;2&lt;/sub&gt;-symmetric, approximately octahedral geometry with cis-positioned halide ligands and high-spin d-electron configuration. &lt;sup&gt;1&lt;/sup&gt;H NMR signals of these paramagnetic complexes were assigned by correlating line widths with reciprocal proton-metal distances. Methyl substitution in 6-position of the pyridyl rings lead to a different, presumably square-pyramidal coordination geometry under dissociation of one chloride ion. FeII dimethyl and diisocyanide derivatives were shown to have low-spin configuration and C&lt;sub&gt;1&lt;/sub&gt;-symmetric geometry. With respect to MAO-activated olefin polymerization, significant catalytic activities were reproducibly obtained only under conditions, where the original complex structure was degraded.</dcterms:abstract>
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kops.description.openAccessopenaccessgreen
kops.identifier.nbnurn:nbn:de:bsz:352-236980deu
kops.sourcefieldEuropean Journal of Inorganic Chemistry. 2005, <b>2005</b>(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912deu
kops.sourcefield.plainEuropean Journal of Inorganic Chemistry. 2005, 2005(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912deu
kops.sourcefield.plainEuropean Journal of Inorganic Chemistry. 2005, 2005(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912eng
kops.submitter.emailoleg.kozlov@uni-konstanz.dedeu
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source.bibliographicInfo.volume2005
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source.periodicalTitleEuropean Journal of Inorganic Chemistry

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