Ruthenium(II) bipyridine complexes bearing quinoline–azoimine (NN′N″) tridentate ligands : Synthesis, spectral characterization, electrochemical properties and single-crystal X-ray structure analysis
| dc.contributor.author | Al-Noaimi, Mousa | |
| dc.contributor.author | Abdel-Rahman, Obadah S. | |
| dc.contributor.author | Fasfous, Ismail I. | |
| dc.contributor.author | El-khateeb, Mohammad | |
| dc.contributor.author | Awwadi, Firas A. | |
| dc.contributor.author | Warad, Ismail | |
| dc.date.accessioned | 2015-03-19T12:24:07Z | |
| dc.date.available | 2015-03-19T12:24:07Z | |
| dc.date.issued | 2014 | eng |
| dc.description.abstract | Four octahedral ruthenium(II) azoimine–quinoline complexes having the general molecular formula [RuII(Lsingle bondY)(bpy)Cl](PF6) {Lsingle bondY = YC6H4Ndouble bond; length as m-dashNC(COCH3)double bond; length as m-dashNC9H6N, Y = H (1), CH3 (2), Br (3), NO2 (4) and bpy = 2,2′-bipyrdine} were synthesized. The azoimine–quinoline based ligands behave as NN′N″ tridentate donors and coordinated to ruthenium via azo-N′, imine-N′ and quinolone-N″ nitrogen atoms. The composition of the complexes has been established by elemental analysis, spectral methods (FT-IR, electronic, 1H NMR, UV/Vis and electrochemical (cyclic voltammetry) techniques. The crystal structure of complex 1 is reported. The Ru(II) oxidation state is greatly stabilized by the novel tridentate ligands, showing Ru(III/II) couples ranging from 0.93–1.27 V vs. Cp2Fe/Cp2Fe+. The absorption spectrum of 1 in dichloromethane was modeled by time-dependent density functional theory (TD-DFT). | eng |
| dc.description.version | published | |
| dc.identifier.doi | 10.1016/j.saa.2014.01.075 | eng |
| dc.identifier.uri | http://kops.uni-konstanz.de/handle/123456789/30426 | |
| dc.language.iso | eng | eng |
| dc.subject.ddc | 540 | eng |
| dc.title | Ruthenium(II) bipyridine complexes bearing quinoline–azoimine (NN′N″) tridentate ligands : Synthesis, spectral characterization, electrochemical properties and single-crystal X-ray structure analysis | eng |
| dc.type | JOURNAL_ARTICLE | eng |
| dspace.entity.type | Publication | |
| kops.citation.bibtex | @article{AlNoaimi2014Ruthe-30426,
year={2014},
doi={10.1016/j.saa.2014.01.075},
title={Ruthenium(II) bipyridine complexes bearing quinoline–azoimine (NN′N″) tridentate ligands : Synthesis, spectral characterization, electrochemical properties and single-crystal X-ray structure analysis},
volume={125},
issn={1386-1425},
journal={Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy},
pages={375--383},
author={Al-Noaimi, Mousa and Abdel-Rahman, Obadah S. and Fasfous, Ismail I. and El-khateeb, Mohammad and Awwadi, Firas A. and Warad, Ismail}
} | |
| kops.citation.iso690 | AL-NOAIMI, Mousa, Obadah S. ABDEL-RAHMAN, Ismail I. FASFOUS, Mohammad EL-KHATEEB, Firas A. AWWADI, Ismail WARAD, 2014. Ruthenium(II) bipyridine complexes bearing quinoline–azoimine (NN′N″) tridentate ligands : Synthesis, spectral characterization, electrochemical properties and single-crystal X-ray structure analysis. In: Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy. 2014, 125, pp. 375-383. ISSN 1386-1425. eISSN 1873-3557. Available under: doi: 10.1016/j.saa.2014.01.075 | deu |
| kops.citation.iso690 | AL-NOAIMI, Mousa, Obadah S. ABDEL-RAHMAN, Ismail I. FASFOUS, Mohammad EL-KHATEEB, Firas A. AWWADI, Ismail WARAD, 2014. Ruthenium(II) bipyridine complexes bearing quinoline–azoimine (NN′N″) tridentate ligands : Synthesis, spectral characterization, electrochemical properties and single-crystal X-ray structure analysis. In: Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy. 2014, 125, pp. 375-383. ISSN 1386-1425. eISSN 1873-3557. Available under: doi: 10.1016/j.saa.2014.01.075 | eng |
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<dcterms:abstract xml:lang="eng">Four octahedral ruthenium(II) azoimine–quinoline complexes having the general molecular formula [RuII(Lsingle bondY)(bpy)Cl](PF<sub>6</sub>) {Lsingle bondY = YC<sub>6</sub>H<sub>4</sub>Ndouble bond; length as m-dashNC(COCH<sub>3</sub>)double bond; length as m-dashNC<sub>9</sub>H<sub>6</sub>N, Y = H (1), CH<sub>3</sub> (2), Br (3), NO<sub>2</sub> (4) and bpy = 2,2′-bipyrdine} were synthesized. The azoimine–quinoline based ligands behave as NN′N″ tridentate donors and coordinated to ruthenium via azo-N′, imine-N′ and quinolone-N″ nitrogen atoms. The composition of the complexes has been established by elemental analysis, spectral methods (FT-IR, electronic, <sup>1</sup>H NMR, UV/Vis and electrochemical (cyclic voltammetry) techniques. The crystal structure of complex 1 is reported. The Ru(II) oxidation state is greatly stabilized by the novel tridentate ligands, showing Ru(III/II) couples ranging from 0.93–1.27 V vs. Cp<sub>2</sub>Fe/Cp<sub>2</sub>Fe<sup>+</sup>. The absorption spectrum of 1 in dichloromethane was modeled by time-dependent density functional theory (TD-DFT).</dcterms:abstract>
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| kops.sourcefield | Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy. 2014, <b>125</b>, pp. 375-383. ISSN 1386-1425. eISSN 1873-3557. Available under: doi: 10.1016/j.saa.2014.01.075 | deu |
| kops.sourcefield.plain | Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy. 2014, 125, pp. 375-383. ISSN 1386-1425. eISSN 1873-3557. Available under: doi: 10.1016/j.saa.2014.01.075 | deu |
| kops.sourcefield.plain | Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy. 2014, 125, pp. 375-383. ISSN 1386-1425. eISSN 1873-3557. Available under: doi: 10.1016/j.saa.2014.01.075 | eng |
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| source.bibliographicInfo.fromPage | 375 | eng |
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| source.bibliographicInfo.volume | 125 | eng |
| source.identifier.eissn | 1873-3557 | eng |
| source.identifier.issn | 1386-1425 | eng |
| source.periodicalTitle | Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy | eng |
| temp.internal.duplicates | <p>Keine Dubletten gefunden. Letzte Überprüfung: 30.01.2015 10:23:47</p> | deu |