Chiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivities
| dc.contributor.author | Vedder, Christoph | deu |
| dc.contributor.author | Schaper, Frank | deu |
| dc.contributor.author | Brintzinger, Hans-Herbert | |
| dc.contributor.author | Kettunen, Mika | deu |
| dc.contributor.author | Babik, Sebastian | deu |
| dc.contributor.author | Fink, Gerhard | deu |
| dc.date.accessioned | 2013-07-11T08:04:21Z | deu |
| dc.date.available | 2013-07-11T08:04:21Z | deu |
| dc.date.issued | 2005 | |
| dc.description.abstract | 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 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.version | published | |
| dc.identifier.citation | European Journal of Inorganic Chemistry ; (2005), 6. - S. 1071-1080 | deu |
| dc.identifier.doi | 10.1002/ejic.200400912 | deu |
| dc.identifier.ppn | 390810347 | deu |
| dc.identifier.uri | http://kops.uni-konstanz.de/handle/123456789/23698 | |
| dc.language.iso | eng | deu |
| dc.legacy.dateIssued | 2013-07-11 | deu |
| dc.rights | terms-of-use | deu |
| dc.rights.uri | https://rightsstatements.org/page/InC/1.0/ | deu |
| dc.subject | Iron(II) | deu |
| dc.subject | cobalt(II) | deu |
| dc.subject | bianiline | deu |
| dc.subject | pyridylimine | deu |
| dc.subject.ddc | 540 | deu |
| dc.title | Chiral iron(II) and cobalt(II) complexes with biphenyl-bridged bis(pyridylimine) ligands : syntheses, structures and reactivities | eng |
| dc.type | JOURNAL_ARTICLE | deu |
| dspace.entity.type | Publication | |
| 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.iso690 | VEDDER, 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.200400912 | deu |
| kops.citation.iso690 | VEDDER, 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.200400912 | eng |
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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<sub>2</sub>-symmetric, approximately octahedral geometry with cis-positioned halide ligands and high-spin d-electron configuration. <sup>1</sup>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<sub>1</sub>-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.openAccess | openaccessgreen | |
| kops.identifier.nbn | urn:nbn:de:bsz:352-236980 | deu |
| kops.sourcefield | European Journal of Inorganic Chemistry. 2005, <b>2005</b>(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912 | deu |
| kops.sourcefield.plain | European Journal of Inorganic Chemistry. 2005, 2005(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912 | deu |
| kops.sourcefield.plain | European Journal of Inorganic Chemistry. 2005, 2005(6), pp. 1071-1080. ISSN 1434-1948. eISSN 1099-0682. Available under: doi: 10.1002/ejic.200400912 | eng |
| kops.submitter.email | oleg.kozlov@uni-konstanz.de | deu |
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| source.bibliographicInfo.toPage | 1080 | |
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| source.identifier.eissn | 1099-0682 | deu |
| source.identifier.issn | 1434-1948 | |
| source.periodicalTitle | European Journal of Inorganic Chemistry |
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