The dominance of sulfate over two organic ligands in the solvothermal assembly of an undecanuclear cobaltous cluster: crystallography and mass spectrometry.

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Title: The dominance of sulfate over two organic ligands in the solvothermal assembly of an undecanuclear cobaltous cluster: crystallography and mass spectrometry.
Authors: Jiang, Li-Ping1,2 (AUTHOR), Kurmoo, Mohamedally3 (AUTHOR) kurmoo@unistra.fr, Zeng, Ming-Hua1,4 (AUTHOR) zmh@mailbox.gxnu.edu.cn
Source: Dalton Transactions: An International Journal of Inorganic Chemistry. 12/28/2020, Vol. 49 Issue 48, p17683-17688. 6p.
Subjects: Mass spectrometry, Ligands (Chemistry), Crystallography, Sulfates, Social dominance
Abstract: An unexpected dominance of the coordination affinity of the sulfate anion over those of two organic chelating ligands, (1-methyl-1H-benzo[d]imidazol-2-yl)methanol (Hmbm) and pyridin-2-ylmethanamine (pma), was observed during the study of the solvothermal assembly of [Co11(mbm)6(pma)2(SO4)8(H2O)6(CH3OH)6]·5CH3OH (1), from CoSO4·7H2O at 100 °C in methanol. ESI-MS of solutions at different periods of the assembly reveal a hierarchical sequence, [Co1] → [Co2] → [Co3] → [Co4] → [Co5] → [Co9], where the lower nuclearity species are richer in Co2+ and SO42− before the inclusion of more mbm ligands at the last step. Its crystal structure consists of an almost symmetrical wheel of nine cobalt atoms, [Co9(mbm)6(SO4)8(H2O)6] in edge-sharing octahedral coordination arranged in triangles with two peripheral dangling [Co(pma)(CH3OH)3]. The sulfate ions exhibit three different coordination modes, two in μ6-, two in μ3- and four as μ2-bridging. Its thermal, optical and magnetic properties are also reported. [ABSTRACT FROM AUTHOR]
Copyright of Dalton Transactions: An International Journal of Inorganic Chemistry is the property of Royal Society of Chemistry and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: The dominance of sulfate over two organic ligands in the solvothermal assembly of an undecanuclear cobaltous cluster: crystallography and mass spectrometry.
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  Data: <searchLink fieldCode="DE" term="%22Mass+spectrometry%22">Mass spectrometry</searchLink><br /><searchLink fieldCode="DE" term="%22Ligands+%28Chemistry%29%22">Ligands (Chemistry)</searchLink><br /><searchLink fieldCode="DE" term="%22Crystallography%22">Crystallography</searchLink><br /><searchLink fieldCode="DE" term="%22Sulfates%22">Sulfates</searchLink><br /><searchLink fieldCode="DE" term="%22Social+dominance%22">Social dominance</searchLink>
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  Data: An unexpected dominance of the coordination affinity of the sulfate anion over those of two organic chelating ligands, (1-methyl-1H-benzo[d]imidazol-2-yl)methanol (Hmbm) and pyridin-2-ylmethanamine (pma), was observed during the study of the solvothermal assembly of [Co11(mbm)6(pma)2(SO4)8(H2O)6(CH3OH)6]·5CH3OH (1), from CoSO4·7H2O at 100 °C in methanol. ESI-MS of solutions at different periods of the assembly reveal a hierarchical sequence, [Co1] → [Co2] → [Co3] → [Co4] → [Co5] → [Co9], where the lower nuclearity species are richer in Co2+ and SO42− before the inclusion of more mbm ligands at the last step. Its crystal structure consists of an almost symmetrical wheel of nine cobalt atoms, [Co9(mbm)6(SO4)8(H2O)6] in edge-sharing octahedral coordination arranged in triangles with two peripheral dangling [Co(pma)(CH3OH)3]. The sulfate ions exhibit three different coordination modes, two in μ6-, two in μ3- and four as μ2-bridging. Its thermal, optical and magnetic properties are also reported. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
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  Group: Ab
  Data: <i>Copyright of Dalton Transactions: An International Journal of Inorganic Chemistry is the property of Royal Society of Chemistry and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1039/d0dt02880k
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        Text: English
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      – SubjectFull: Mass spectrometry
        Type: general
      – SubjectFull: Ligands (Chemistry)
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      – SubjectFull: Crystallography
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      – SubjectFull: Sulfates
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      – SubjectFull: Social dominance
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      – TitleFull: The dominance of sulfate over two organic ligands in the solvothermal assembly of an undecanuclear cobaltous cluster: crystallography and mass spectrometry.
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              Text: 12/28/2020
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              Y: 2020
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