RAS Chemistry & Material ScienceКоординационная химия Russian Journal of Coordination Chemistry

  • ISSN (Print) 0132-344X
  • ISSN (Online) 3034-5499

SOLVOTHERMAL SYNTHESIS, STRUCTURE, AND PROPERTIES OF CADMIUM(II)-ORGANIC COORDINATION POLYMER CONTAINING CARBOXYL GROUPS

PII
10.31857/S0132344X23600133-1
DOI
10.31857/S0132344X23600133
Publication type
Status
Published
Authors
Volume/ Edition
Volume 49 / Issue number 12
Pages
731-736
Abstract
Under the conditions of solvothermal synthesis, a new metal-organic coordination polymer of the composition Cd[H2L] (I, H4L = 4,4'-([2,2'-bipyridine]-6,6'-diylbis(oxy))diphthalic acid). According to X-ray diffraction analysis, each Cd(II) cation binds four organic ligands: one via the coordination of the chelate bipyridyl fragment, two via the bidentate coordination of deprotonated COO groups, and one more via the monodentate coordination of the protonated carboxylate group. The obtained three-dimensional metal-organic framework does not contain free space capable of including guest molecules. Compound I was characterized by powder X-ray diffraction, IR spectroscopy, elemental (C, H, N) and thermogravimetric analyses, and luminescence spectra were recorded for it.
Keywords
металл-органические координацинные полимеры синтез рентгеноструктурный анализ поликарбоксилатные лиганды комплексы кадмия(II) люминесценция
Date of publication
01.12.2023
Year of publication
2023
Number of purchasers
0
Views
13

References

  1. 1. Agafonov M.A., Alexandrov E.V., Artyukhova N.A. et al. // J. Struct. Chem. 2022. V. 63. P. 671.
  2. 2. Kirchon A., Feng L., Drake H.F. et al. // Chem. Soc. Rev. 2018. V. 47. P. 8611.
  3. 3. Bhadra B.N., Ahmed I., Lee H.J., Jhung S.H. // Coord. Chem. Rev. 2022. V. 450. Art. 214237.
  4. 4. Yin H.-Q., X.-B. Yin // Acc. Chem. Res. 2020. V. 53. P. 485.
  5. 5. Ji Z., Wang H., Canossa S. et al. // Adv. Funct. Mater. 2020. V. 30. Art. 2000238.
  6. 6. Mandal S., Natarajan S., Mani P., Pankajakshan A. // Adv. Funct. Mater. 2021. V. 31. Art. 2006291.
  7. 7. Razavi S.A.A., Morsali A. // Coord. Chem. Rev. 2019. V. 399. Art. 213023.
  8. 8. Bruker Apex3 Software Suite: Apex3, SADABS-2016/2 and SAINT. Version 2018.7-2. Madison (WI, USA): Bruker AXS Inc., 2017.
  9. 9. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. № 1. P. 3.
  10. 10. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. № 1. P. 3.
  11. 11. Llunell M., Casanova D., Cirera J. et al. SHAPE. Version 2.1. Program for the Stereochemical Analysis of Molecular Fragments by Means of Continuous Shape Measures and Associated Tools. Barcelona: Universitat de Barcelona, 2013.
  12. 12. Shigematsu A., Yamada T., Kitagawa H. // J. Am. Chem. Soc. 2011. V. 133. P. 2034.
  13. 13. He T., Zhang Y.Z., Wu H. et al. // ChemPhysChem. 2017. V. 18. P. 3245.
  14. 14. Sun Z., Yu S., Zhao L. et al. // Chem. Eur. J. 2018. V. 24. № 2018. P. 10829.
  15. 15. Qin Y., Xue M.-H., Dou B.-H. et al. // New J. Chem. 2020. V. 44. P. 2741.
  16. 16. Su J., He W., Li X.-M. et al. // Matter. 2020. V. 2. P. 711.
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