Structural diversity, magnetic properties, and luminescence sensing based Ni(II)/Zn(II) coordination polymers of the semirigid 3,3′-((5-carboxy-1,3-phenylene)bis(oxy))dibenzate ligand.

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Title: Structural diversity, magnetic properties, and luminescence sensing based Ni(II)/Zn(II) coordination polymers of the semirigid 3,3′-((5-carboxy-1,3-phenylene)bis(oxy))dibenzate ligand.
Authors: Yang, Dong-Dong1 (AUTHOR), Lu, Li-Ping1 (AUTHOR) luliping@sxu.edu.cn, Zhu, Miao-Li1,2 (AUTHOR) miaoli@sxu.edu.cn
Source: CrystEngComm. 8/21/2020, Vol. 22 Issue 31, p5207-5217. 11p.
Subjects: Zinc compounds synthesis, Coordination polymers, Magnetic properties, Luminescence, X-ray powder diffraction, Luminescence quenching, Aqueous solutions
Abstract: Two two-dimensional Ni(II) or Zn(II)-based coordination polymers, namely [[Ni3(μ4-cpboda)2(μ2-H2O)2(DMF)2(H2O)2]·3DMF·2HCOOH·2H2O]n (1) and [[Zn3(μ4-cpboda)2(μ2-H2O)2(DMF)2(H2O)2]·3DMF·3HCOOH·3H2O]n (2), a three-dimensional Ni(II)-based coordination polymer, namely [[Ni3(μ3-cpboda)2(1,4-bib)5(H2O)2]·DMF]n (3), and a dinuclear Zn(II) complex, namely [Zn (μ2-Hcpboda)(2,2-bipy)(H2O)]2 (4) (H3cpboda = 3,3′-((5-carboxy-1,3-phenylene)bis(oxy))dibenzoic acid, 2,2-bipy = 2,2-bipyridine, 1,4-bib = 1,4-di(1H-imidazol-1-yl)benzene), were successfully synthesized under solvothermal conditions and characterized via single-crystal X-ray and powder diffraction analyses, elemental analyses (EA), FT-IR spectroscopy, and thermogravimetric analysis (TGA). Complexes 1 and 2 show isomorphism and (3,4,6)-connected 2D sheet structures with the (32·4)2(32·83·9)2(34·4·282·94·103) topology. Complex 3 is a 4,4,7-connected 3D structure with the (42·52·62)2(46·5·614)2(54·6·8) topology. Complex 4 is only a simple dinuclear structure. Magnetization measurements disclose the weak ferromagnetic behavior between Ni(II) ions in the complexes 1 and 3. Fluorescence measurements indicate that 2 and 4 exhibit fast, sensitive, and selective luminescence quenching responses towards Cr2O72−/CrO42− in an aqueous solution. The limit of detection for Cr2O72−/CrO42− ions were estimated to be 0.51 and 0.60 ppm for 2 (0.89 and 1.03 ppm for 4), respectively, which are comparable to those reported for the CP-based fluorescent probes that can simultaneously detect Cr2O72−/CrO42− in aqueous environments. Moreover, 2 and 4 can be easily regenerated after the detection experiments, which is indicative of the excellent recyclability. All these results suggest that complexes 2 and 4 are highly selective and recyclable luminescence sensing materials for the quantitative detection of Cr2O72−/CrO42− anions in aqueous solutions. [ABSTRACT FROM AUTHOR]
Copyright of CrystEngComm 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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  Label: Title
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  Data: Structural diversity, magnetic properties, and luminescence sensing based Ni(II)/Zn(II) coordination polymers of the semirigid 3,3′-((5-carboxy-1,3-phenylene)bis(oxy))dibenzate ligand.
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  Data: <searchLink fieldCode="AR" term="%22Yang%2C+Dong-Dong%22">Yang, Dong-Dong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lu%2C+Li-Ping%22">Lu, Li-Ping</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> luliping@sxu.edu.cn</i><br /><searchLink fieldCode="AR" term="%22Zhu%2C+Miao-Li%22">Zhu, Miao-Li</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> miaoli@sxu.edu.cn</i>
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  Data: <searchLink fieldCode="JN" term="%22CrystEngComm%22">CrystEngComm</searchLink>. 8/21/2020, Vol. 22 Issue 31, p5207-5217. 11p.
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  Data: <searchLink fieldCode="DE" term="%22Zinc+compounds+synthesis%22">Zinc compounds synthesis</searchLink><br /><searchLink fieldCode="DE" term="%22Coordination+polymers%22">Coordination polymers</searchLink><br /><searchLink fieldCode="DE" term="%22Magnetic+properties%22">Magnetic properties</searchLink><br /><searchLink fieldCode="DE" term="%22Luminescence%22">Luminescence</searchLink><br /><searchLink fieldCode="DE" term="%22X-ray+powder+diffraction%22">X-ray powder diffraction</searchLink><br /><searchLink fieldCode="DE" term="%22Luminescence+quenching%22">Luminescence quenching</searchLink><br /><searchLink fieldCode="DE" term="%22Aqueous+solutions%22">Aqueous solutions</searchLink>
– Name: Abstract
  Label: Abstract
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  Data: Two two-dimensional Ni(II) or Zn(II)-based coordination polymers, namely [[Ni3(μ4-cpboda)2(μ2-H2O)2(DMF)2(H2O)2]·3DMF·2HCOOH·2H2O]n (1) and [[Zn3(μ4-cpboda)2(μ2-H2O)2(DMF)2(H2O)2]·3DMF·3HCOOH·3H2O]n (2), a three-dimensional Ni(II)-based coordination polymer, namely [[Ni3(μ3-cpboda)2(1,4-bib)5(H2O)2]·DMF]n (3), and a dinuclear Zn(II) complex, namely [Zn (μ2-Hcpboda)(2,2-bipy)(H2O)]2 (4) (H3cpboda = 3,3′-((5-carboxy-1,3-phenylene)bis(oxy))dibenzoic acid, 2,2-bipy = 2,2-bipyridine, 1,4-bib = 1,4-di(1H-imidazol-1-yl)benzene), were successfully synthesized under solvothermal conditions and characterized via single-crystal X-ray and powder diffraction analyses, elemental analyses (EA), FT-IR spectroscopy, and thermogravimetric analysis (TGA). Complexes 1 and 2 show isomorphism and (3,4,6)-connected 2D sheet structures with the (32·4)2(32·83·9)2(34·4·282·94·103) topology. Complex 3 is a 4,4,7-connected 3D structure with the (42·52·62)2(46·5·614)2(54·6·8) topology. Complex 4 is only a simple dinuclear structure. Magnetization measurements disclose the weak ferromagnetic behavior between Ni(II) ions in the complexes 1 and 3. Fluorescence measurements indicate that 2 and 4 exhibit fast, sensitive, and selective luminescence quenching responses towards Cr2O72−/CrO42− in an aqueous solution. The limit of detection for Cr2O72−/CrO42− ions were estimated to be 0.51 and 0.60 ppm for 2 (0.89 and 1.03 ppm for 4), respectively, which are comparable to those reported for the CP-based fluorescent probes that can simultaneously detect Cr2O72−/CrO42− in aqueous environments. Moreover, 2 and 4 can be easily regenerated after the detection experiments, which is indicative of the excellent recyclability. All these results suggest that complexes 2 and 4 are highly selective and recyclable luminescence sensing materials for the quantitative detection of Cr2O72−/CrO42− anions in aqueous solutions. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of CrystEngComm 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/c9ce01998g
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        Text: English
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    Subjects:
      – SubjectFull: Zinc compounds synthesis
        Type: general
      – SubjectFull: Coordination polymers
        Type: general
      – SubjectFull: Magnetic properties
        Type: general
      – SubjectFull: Luminescence
        Type: general
      – SubjectFull: X-ray powder diffraction
        Type: general
      – SubjectFull: Luminescence quenching
        Type: general
      – SubjectFull: Aqueous solutions
        Type: general
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      – TitleFull: Structural diversity, magnetic properties, and luminescence sensing based Ni(II)/Zn(II) coordination polymers of the semirigid 3,3′-((5-carboxy-1,3-phenylene)bis(oxy))dibenzate ligand.
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            NameFull: Yang, Dong-Dong
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            NameFull: Lu, Li-Ping
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            NameFull: Zhu, Miao-Li
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              Text: 8/21/2020
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              Y: 2020
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