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RAS Chemistry & Material ScienceКоординационная химия Russian Journal of Coordination Chemistry

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

Synthesis and Luminescent Properties of the Carbonyl-Isonitrile Re(I) Complex Based on Menthol-Modified Phenanthroline

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PII
S0132344X25070036-1
DOI
10.31857/S0132344X25070036
Publication type
Article
Status
Published
Authors
V. Artem'ev
  • Affiliation: Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences
Volume/ Edition
Volume 52 / Issue number 7
Pages
449-455
Abstract
A carbonyl-isonitrile complex of [Re(CO)₃(L)(m-XylylNC)]OTf formulation (-XylylNC - 2,6-dimethyl- phenyl isocyanide) was synthesized based on the 1,10-phenanthroline ligand (L) containing a menthol fragment (MtO-) in position 2. The Re(I) atom in the cationic part of this complex has a distorted octahedral environment formed by the N,N′-chelate ligand L, one isonitrile ligand, and three CO ligands. The resulting compound exhibits bright green phosphorescence at room temperature in both the solid state and solution, with quantum yields of 15% and 10%, respectively.
Keywords
трикарбонильные комплексы рения(I) изонитрилы фосфоресценция синтез кристаллическая структура
Date of publication
28.04.2025
Year of publication
2025
Number of purchasers
0
Views
3

References

  1. 1. Kirgan R.A., Sullivan B.P., Rillema D.P. // Photochemistry and photophysics of coordination compounds II / Eds. Balzani V., Campagna S. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. P. 45.
  2. 2. Abramov P.A., Dmitriev A.A., Kholin K.V. et al. // Electrochim. Acta. 2018, V. 270. P. 526. https://doi.org/10.1016/j.electacta.2018.03.111
  3. 3. Abramov P.A., Brylev K.A., Vorob’ev A.Y. et al. // Polyhedron. 2017. V. 137. P. 231. https://doi.org/10.1016/j.poly.2017.08.046
  4. 4. Абрамов П.А. // Журн. структур. химии. 2021 V. 62. P. 1513. https://doi.org/10.26902/JSC_id79933
  5. 5. Abramov P.A. // J. Struct. Chem. 2021. V. 62. P. 1416. https://doi.org/10.1134/S0022476621090109.
  6. 6. Abramov P.A., Gritsan N.P., Suturina E. A. et al. // Inorg. Chem. 2015. V. 54. P. 6727. https://doi.org/10.1021/acs.inorgchem.5b00407
  7. 7. Nayeri S., Jamali S., Pavlovskiy V.V. et al. // Eur. J. Inorg. Chem. 2019. V. 2019. P. 4350. https://doi.org/10.1002/ejic.201900617
  8. 8. Shakirova J.R., Nayeri S., Jamali S. et al. // ChemPlusChem. 2020. V. 85. P. 2518. https://doi.org/10.1002/cplu.202000597
  9. 9. Kisel K.S., Baigildin V.A., Solomatina A.I. et al. // Molecules. 2023. V. 28. P. 348. https://doi.org/10.3390/molecules28010348
  10. 10. Kisel K.S., Shakirova J.R., Pavlovskiy V.V. et al. // Inorg. Chem. 2023. V. 62. P. 18625. https://doi.org/10.1021/acs.inorgchem.3c02915
  11. 11. Kisel K.S., Eskelinen T., Zafar W. et al. // Inorg. Chem. 2018. V. 57. P. 6349. https://doi.org/10.1021/acs.inorgchem.8b00422
  12. 12. Kalyanasundaram K. // Faraday Trans. 2. 1986. V. 82. P. 2401. https://doi.org/10.1039/F29868202401
  13. 13. Yu T., Tsang D.P.-K., Au V. K.-M. et al. // Chem. Eur. J. 2013. V. 19. P. 13418. https://doi.org/10.1002/chem.201301841
  14. 14. Sacksteder L., Lee M., Demas J. et al. // J. Am. Chem. Soc. 1993. V. 115. P. 8230. https://doi.org/10.1021/ja00071a036
  15. 15. Villegas J.M., Stoyanov S.R., Huang W. et al. // Inorg. Chem. 2005 V. 44. P. 2297. https://doi.org/10.1021/ic048786f
  16. 16. Favale J.M., Jr., Danilov E.O., Yarnell J E. et al. // Inorg. Chem. 2019 V. 58. P. 8750. https://doi.org/10.1021/acs.inorgchem.9b01155
  17. 17. Klemens T., Świtlicka A., Szlapa-Kula A. et al. // Organometallics. 2019. V. 38. P. 4206. https://doi.org/10.1021/acs.organomet.9b00517
  18. 18. Taydakov I.V., Vashchenko A.A., Lyssenko K.A. et al. // ARKIVOC. 2017. V. 2017, P. 205. https://doi.org/10.24820/ark.5550190.p010.130
  19. 19. Hostachy S., Policar C., Delsuc N. // Coord. Chem. Rev. 2017. V. 351. P. 172. https://doi.org/10.1016/j.ccr.2017.05.004
  20. 20. Chelushkin P.S., Shakirova J.R., Kritchenkov I.S. et al. // Dalton Trans. 2022 V. 51. P. 1257. https://doi.org/10.1039/D1DT03077A
  21. 21. Leonidova A., Gasser G. // ACS Chem. Biol. 2014. V.9. P. 2180. https://doi.org/10.1021/cb500528c
  22. 22. Lee L.C.-C., Leung K.-K., Lo K.K.-W. // Dalton Trans. 2017. V. 46. P. 16357. https://doi.org/10.1039/C7DT03465B
  23. 23. Kuninobu Y., Takai K. // Chem. Rev. 2011. V. 111. P. 1938. https://doi.org/10.1021/cr100241u
  24. 24. Kisel K.S., Samandarsangari M., Sokolov V.V. et al. // Opt. Mater. 2025. V. 159. P. 116589. https://doi.org/10.1016/j.optmat.2024.116589
  25. 25. Saleh N., Srebro M., Reynaldo T. et al. // Chem. Commun. 2015. V. 51. P. 3754. https://doi.org/10.1039/C5CC00453E
  26. 26. Gauthier E.S., Abella L., Hellou N. et al. // Angew. Chem. Int. Ed. 2020. V. 59 P. 8394. https://doi.org/10.1002/anie.202002387
  27. 27. Saleh N., Kundu D., Vanthuyne N. et al. // ChemPlusChem. 2020, Vol. 85, P. 2446. https://doi.org/10.1002/cplu.202000559
  28. 28. Gauthier E.S., Abella L., Caytan E. et al. // Chem. Eur. J. 2023, Vol. 29, P. e202203477. https://doi.org/10.1002/chem.202203477
  29. 29. Giuso V., Gourlaouen C., Delporte-Pébay M. et al. // Phys. Chem. Chem. Phys. 2024. V. 26. P. 4855. https://doi.org/10.1039/D3CP04300B
  30. 30. Kundu D., Jelonek D., Del Rio N. et al. // Chem. Asian J. год ? V. n/a. Аrt. e202401735. https://doi.org/10.1002/asia.202401735
  31. 31. Davydova M.P., Xu T., Agafontsev A.M. et al. // Angew. Chem. Int. Ed. 2025. V. 64. Аrt. e202419788. https://doi.org/10.1002/anie.202419788
  32. 32. Bruker Apex3 Software Suite: Apex3, SADABS-2016/2 and SAINT 8.40a. 2017. V. ? Bruker AXS Inc., Madison, WI, USA.
  33. 33. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053273314026370
  34. 34. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053229614024218
  35. 35. Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Crystallogr. 2009. V. 42, P. 339. https://doi.org/10.1107/S0021889808042726
  36. 36. van der Sluis P., Spek A.L. // Acta Crystallogr. A. 1990. V. 46. P. 194. https://doi.org/10.1107/S0108767389011189
  37. 37. Ortega J.V., Khin K., van der Veer W.E. et al. // Inorg. Chem. 2000. V. 39. P. 3038. https://doi.org/10.1021/ic0006910
  38. 38. Aechter B., Knizek J., Nöth H. et al. // Z. Kristallogr. NCS. 2005. V. 220. P. 107. https://doi.org/10.1524/ncrs.2005.220.14.107
  39. 39. King A.P., Marker S.C., Swanda R.V. et al. // Chem. Eur. J. 2019. V. 25. P. 9206. https://doi.org/10.1002/chem.201902223
  40. 40. Ko C.-C., Ng C.-O., Yiu S.-M. // Organometallics. 2012. V. 31. P. 7074. https://doi.org/10.1021/om300526e
  41. 41. Marker S.C., King A.P., Granja S. et al. // Inorg. Chem. 2020. V. 59. P. 10285. https://doi.org/10.1021/acs.inorgchem.0c01442
  42. 42. Тюпина М.Ю., Мирославов А.Е., Сидоренко Г.В. и др. // Журн. общ. химии. 2022. V. 92. P. 110. https://doi.org/10.31857/S0044460X22010127
  43. 43. Tyupina M.Y., Miroslavov A.E., Sidorenko G.V. et al. // Russ. J. Gen. Chem. 2022, V. 92. P. 69. https://doi.org/10.1134/S1070363222010108.
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