3,6-Dipyridyl-1,2,4,5-tetrazine in the Synthesis of Zinc and Cadmium Metal-Organic Frameworks with Anilate-Type Ligands

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New heteroleptic metal-organic frameworks (MOF) of zinc (3D MOF) and cadmium (2D MOF) are prepared by the two-stage synthesis: [Zn(pQ)(DPT)]·2DMF (I) and Cd2(NO3)2-(pQ)(DPT)3]·2DMF·2MeOH (II), where pQ is the 2,5-dihydroxy-3,6-di-tert-butyl-para-benzoquinone dianion, DPT is 3,6-di(pyridin-4-yl)-1,2,4,5-tetrazine, and DMF is N,N-dimethylformamide (DMF). The structures of the compounds are studied by XRD (CIF files CCDC nos. 2332754 (I) and 2332755 (II)). The thermal stability of the MOF is studied by thermogravimetry.

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O. Trofimova

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: olesya@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod

D. Kolevatov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

Email: olesya@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod

N. Druzhkov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

Email: olesya@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod

A. Maleeva

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

Email: olesya@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod

I. Yakushev

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Email: olesya@iomc.ras.ru
俄罗斯联邦, Moscow

P. Dorovatovskii

National Research Center Kurchatov Institute

Email: olesya@iomc.ras.ru
俄罗斯联邦, Moscow

A. Piskunov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

Email: olesya@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod

参考

  1. Kovalenko K.A., Potapov A.S., Fedin V.P. // Russ. Chem. Rev. 2022. V. 91. P. RCR5026. https://doi.org/10.1070/RCR5026
  2. Agafonov M.A., Alexandrov E.V., Artyukhova N.A. et al. // J. Struct. Сhem. 2022. V. 63. P. 671. https://doi.org/10.26902/JSC_id93211
  3. Monni N., Oggianu M., Sahadevan S.A. et al. // Magnetochemistry. 2021. V. 7. P. 109. https://doi.org/10.3390/magnetochemistry7080109
  4. Benmansour S., Gómez-García C.J. // Magnetochemistry. 2020. V. 6. P. 71. https://doi.org/10.3390/magnetochemistry6040071
  5. Liu K.-G., Sharifzadeh Z., Rouhani F. et al. // Coord. Chem. Rev. 2021. V. 436. P. 213827. https://doi.org/10.1016/j.ccr.2021.213827
  6. Wang C., Liao K. // ACS Appl. Mater. Interfaces. 2021. V. 13. P. 56752. https://doi.org/10.1021/acsami.1c13408
  7. Fasna F., Sasi S. // ChemistrySelect. 2021. V. 6. P. 6365. https://doi.org/doi.org/10.1002/slct.202101533
  8. Antipin I.S., Burilov V.A., Gorbatchuk V.V. et al. // Russ. Chem. Rev. 2021. V. 90. P. 895. https://doi.org/10.1070/RCR5011
  9. Kitagawa S., Matsuda R. // Coord. Chem. Rev. 2007. V. 251. P. 2490. https://doi.org/10.1016/j.ccr.2007.07.009
  10. Kingsbury C.J., Abrahams B.F., Auckett J.E. et al. // Chem. Eur. J. 2019. V. 25. P. 5222. https://doi.org/10.1002/chem.201805600
  11. Abrahams B.F., Dharma A.D., Dyett B. et al. // Dalton Trans. 2016. V. 45. P. 1339. https://doi.org/10.1039/c5dt04095g
  12. Adil K., Belmabkhout Y., Pillai R.S. et al. // Chem. Soc. Rev. 2017. V. 46. P. 3402. https://doi.org/10.1039/c7cs00153c
  13. Ezugwu C.I., Liu S., Li C., et al. // Coord. Chem. Rev. 2021. V. 450. P. 214245. https://doi.org/10.1016/j.ccr.2021.214245
  14. Hu Z., Zhao D. // CrystEngComm. 2017. V. 19. P. 4066. https://doi.org/10.1039/c6ce02660e
  15. Zhang X., Wang C., Wang L.Y. et al. // Appl Organomet Chem. 2022. V. e6603. P. 1. https://doi.org/10.1002/aoc.6603
  16. Artem′ev A.V., Fedin V.P. // Russian Journal of Organic Chemistry. 2019. V. 55. P. 800. https://doi.org/10.1134/S1070428019060101
  17. Wang Y., Liu X., Li X. et al. // J. Am. Chem. Soc. 2019. V. 141. P. 8030. 10.1021/jacs.9b01270
  18. Chang C.-H., Li A.-C., Popovs I. et al. // J. Mater. Chem. A. 2019. V. 7. P. 23770. https://doi.org/10.1039/c9ta05244e
  19. Chen H.-J., Chen L.-Q., Lin L.-R. et al. // Inorg. Chem. 2021. V. 60. P. 6986−6990. https://doi.org/10.1021/acs.inorgchem.1c00740
  20. Huangfu M., Wang M., Lin C. et al. // Dalton Trans. 2021. V. 50. P. 3429. https://doi.org/10.1039/D0DT04276E
  21. Li P., Zhou Z., Zhao Y.S. et al. // Chem. Commun. 2021. V. 57. P. 13678. https://doi.org/10.1039/d1cc05541k
  22. Gorai T., Schmitt W., Gunnlaugsson T. // Dalton Trans. 2021. V. 50. P. 770. https://doi.org/10.1039/d0dt03684f
  23. Rogovoy M.I., Frolova T.S., Samsonenko D.G. et al. // Eur. J. Inorg. Chem.. 2020. V. 2020. P. 1635. https://doi.org/10.1002/ejic.202000109
  24. Calbo J., Golomb M.J., Walsh A. // J. Mater. Chem. A. 2019. V. 7. P. 16571. https://doi.org/10.1039/c9ta04680a
  25. Wang M., Dong R. and Feng X. // Chem. Soc. Rev. 2021. V. 50. P. 2764. https://doi.org/10.1039/d0cs01160f
  26. Dong R., Feng X. // Nature Materials. 2021. V. 20. P. 122. https://doi.org/10.1038/s41563-020-00912-1
  27. Benmansour S., Gómez-García C.J. // Gen. Chem. 2020. V. 6. P. 190033. https://doi.org/10.21127/yaoyigc20190033
  28. Espallargas G.M., Coronado E. // Chem. Soc. Rev. 2018. V. 47. P. 533. https://doi.org/10.1039/c7cs00653e
  29. Gou X., Wu Y., Wang M. et al. // Dalton Trans. 2024. V. 53. P. 148. https://doi.org/10.1039/D3DT02714G
  30. Monni N., Baldoví J.J., García-López V. et al. // Chemical Science. 2022. V. 13. P. 7419. https://doi.org/10.1039/D2SC00769J
  31. Ovcharenko V., Fursova E., Letyagin G. et al. // CrystEngComm. 2023. V. 25. P. 6194. https://doi.org/10.1039/D3CE00912B
  32. Huang Z., Yu H., Wang L. et al. // Coord. Chem. Rev. 2021. V. 430. P. 213737. https://doi.org/10.1016/j.ccr.2020.213737
  33. Monni N., Angotzi M.S., Oggianu M. et al. // J. Mater. Chem. C. 2022. V. 10. P. 1548. https://doi.org/10.1039/d1tc05335c
  34. Kitagawa S., Kawata S. // Coord. Chem. Rev. 2002. V. 224. P. 11. https://doi.org/10.1016/S0010-8545(01)00369-1
  35. Kharitonov A.D., Trofimova O.Y., Meshcheryakova I.N. et al. // CrystEngComm. 2020. V. 22. P. 4675. https://doi.org/10.1039/d0ce00767f
  36. Trofimova O.Yu., Ershova I.V., Maleeva A.V. et al. // Russ. J. Coord. Chem. 2021. V. 47. P. 610. https://doi.org/10.1134/S1070328421090086
  37. Trofimova O.Yu., Maleeva A.V., Ershova I.V. et al. // Molecules. 2021. V. 26. P. 2486. https://doi.org/10.3390/molecules26092486
  38. Trofimova O.Yu., Maleeva A.V., Arsenyeva K.V. et al. // Crystals. 2022. V. 12. P. 370. https://doi.org/10.3390/cryst12030370
  39. Trofimova O.Yu., Maleeva A.V., Arsenyeva K.V., et al. // J. Struct. Сhem. 2023. Vol. 64. P. 1070. https://doi.org/10.1134/S0022476623060100
  40. Trofimova O.Yu., Maleeva A.V., Arsenyeva K.V., et al. // Russ. J. Coord. Chem. 2023. V. 49. P. 276. https://doi.org/10.1134/S1070328423600183
  41. Okhlopkova L.S., Poddel′sky A.I., Fukin G.K., et al. // Russ. J. Coord. Chem. 2020. V. 46. P. 386. https://doi.org/10.31857/S0132344X20050059
  42. Khamaletdinova N.M., Meshcheryakova I.N., Piskunov A.V., et al. // J. Struct. Сhem. 2015. V. 56. P. 233. https://doi.org/10.1134/S0022476615020055
  43. Min K.S., DiPasquale A.G., Rheingold A.L. et al. // J. Am. Chem. Soc. 2009. V. 131. P. 6229. https://doi.org/10.1021/ja900909u
  44. Min K.S., DiPasquale A., Rheingold A.L. et al. // Inorg. Chem. Com. 2007. V. 46. P. 1048. https://doi.org/10.1021/ic062400e
  45. Trofimova O.Y., Ershova I.V., Maleeva A.V. et al. // J. Inorg. Organomet. Polym. Materials. 2024. V.P. https://doi.org/10.1007/s10904-024-03013-7
  46. Withersby M.A., Blake A.J., Champness N.R. et al. // J. Am. Chem. Soc. 2000. V. 122. P. 4044. https://doi.org/10.1021/ja991698n
  47. Liu K., Han X., Zou Y. et al. // Inorg. Chem. Comm. 2014. V. 39. P. 131. https://doi.org/10.1016/j.inoche.2013.11.011
  48. Cepeda J., Pérez-Yáñez S., García J.Á. et al. // Dalton Trans. 2021. V. 50. P. 9269. https://doi.org/10.1039/D1DT01204E
  49. Li J., Peng Y., Liang H. et al. // Eur. J. Inorg. Chem. 2011. V. 2011. P. 2712. https://doi.org/10.1002/ejic.201100227
  50. Xue M., Ma S., Jin Z. et al. // Inorg. Chem. 2008. V. 47. P. 6825. https://pubs.acs.org/doi/10.1021/ic800854y
  51. Hijikata Y., Horike S., Sugimoto M. et al. // Chem. Eur. J. 2011. V. 17. P. 5138. https://doi.org/10.1002/chem.201003734
  52. Lee L.-W., Luo T.-T., Lo S.-H. et al. // CrystEngComm. 2015. V. 17. P. 6320. https://doi.org/10.1039/C5CE00923E
  53. Razavi S.A.A., Masoomi M.Y., Islamoglu T. et al. // Inorg. Chem. 2017. V. 56. P. 2581. https://doi.org/10.1021/acs.inorgchem.6b02758
  54. Zhang R., Huang J.-H., Meng D.-X. et al. // Dalton Trans. 2020. V. 49. P. 5618. https://doi.org/10.1039/D0DT00793E
  55. Hijikata Y., Horike S., Sugimoto M. et al. // Inorg. Chem. 2013. V. 52. P. 3634. https://doi.org/10.1021/ic302006x
  56. Fernández B., Seco J.M., Cepeda J. et al. // CrystEngComm. 2015. V. 17. P. 7636. https://doi.org/10.1039/C5CE01521A
  57. Seco J.M., Pérez-Yáñez S., Briones D., et al. // Cryst. Growth Des. 2017. V. 17. P. 3893. https://doi.org/10.1021/acs.cgd.7b00522
  58. Mulfort K.L., Wilson T.M., Wasielewski M.R. et al. // Langmuir. 2009. V. 25. P. 503. https://doi.org/10.1021/la803014k
  59. Dinolfo P.H., Williams M.E., Stern C.L. et al. // J. Am. Chem. Soc. 2004. V. 126. P. 12989. https://doi.org/10.1021/ja0473182
  60. Svetogorov R.D., Dorovatovskii P.V., Lazarenko V.A. //Cryst. Res. Technol. 2020. V. 55. P. 1900184. https://doi.org/10.1002/crat.201900184
  61. Kabsch W. // Acta Crystallogr. D. 2010. V. 66. P. 125. https://doi.org/10.1107/S0907444909047337
  62. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053273314026370
  63. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053229614024218
  64. Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339. https://doi.org/10.1107/S0021889808042726
  65. Blatov V.A., Shevchenko A.P., Proserpio D.M. // Cryst. Growth Des. 2014. V. 14. P. 3576. https://doi.org/10.1021/cg500498k
  66. Alexandrov E.V., Blatov V.A., Kochetkov A.V. et al. // CrystEngComm. 2011. V. 13. P. 3947. https://doi.org/10.1039/c0ce00636j
  67. Aleksandrov E.V., Shevchenko A.P., Nekrasova N.A. et al. // Russ. Chem. Rev. 2022. V. 91. P. Art. RCR5032. https://doi.org/10.1070/RCR5032
  68. Cordero B., Gomez V., Platero-Prats A.E. et al. // Dalton Trans. 2008. V.P. 2832. https://doi.org/10.1039/b801115j
  69. Batsanov S.S. // Russ. J. Inorg. Chem. 1991. V. 36. P. 1694.

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2. Scheme 1: Organic ligands used for the synthesis of zinc and cadmium MOCPs.

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3. Scheme 2: Synthesis of heteroleptic MOCPs I and II.

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4. Fig. 1. Molecular structure of the link and polyhedron of MOCP I. Thermal ellipsoids are given at 50% probability. Hydrogen atoms and “guest” DMF molecules are not depicted.

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5. Fig. 2. Molecular structure of the link and polyhedron of MOCP II. Thermal ellipsoids are given at 50% probability. Hydrogen atoms and “guest” molecules of DMF and MeOH are not depicted.

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6. Fig. 3. View of the MOCP I framework along vector (001) (a); location of interpenetrating MOCP I frameworks in the crystal along vector (001) (b); view of channels in I along vector (001) (c). The outer side of the channels is pink; the inner side is blue. “Guest” DMF molecules are not depicted.

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7. Fig. 4. View of a pair of interpenetrating MOCP II networks along vector (100) (a); layers formed by pairwise interpenetrating networks in the crystal along vector (010) (b); view of pores in II along vector (010) (c). The outer side of the pores is pink; the inner side is blue. “Guest” molecules of DMF and MeOH are not depicted.

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8. Fig. 5. Thermogravimetric curves for MOC I (red line) and II (blue line).

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