Layered Coordination Polymers Based on the Cluster Complexes [Re6Q8(CN)6]4– (Q = S or Se) and Dimeric Cations {(Ag(Dppe))2(μ-Dppe)}2+

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Resumo

The reactions of salts of cluster anions [Re6Q8(CN)6]4– with the [Ag(CN)2]– dicyanoargentate anion in the presence of 1,2-bis(diphenylphosphino)ethane are studied. Two new coordination polymers, [{(Ag(Dppe))2 (µ-Dppe)}2{Re6S8(CN)6}]⋅H2O (I) and [{(Ag(Dppe))2(µ-Dppe)}2{Re6Se8(CN)6}]0,85[{(Ag(Dppe))(Ag(DppeSe))(µ-Dppe)}2{Re6Se8(CN)6}]0,15 (II), are prepared by the solvothermal synthesis. The XRD study of single crystals of the compounds (CIF files CCDC nos. 2341356 (I) and 2341355 (II)) shows their layered structures. The XRD study of crystalline powders of the compounds shows that the synthesis of compound II leads to the formation of two crystalline phases, one of which is isostructural to compound I. The luminescence parameters of the solid-state compounds (quantum yields, emission lifetimes) resemble the parameters of other coordination polymers based on the [Re6Q8(CN)6]4– ions.

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Sobre autores

Yu. Litvinova

Nikolaev Institute of Inorganic Chemistry of the Siberian Branch of the Russian Academy of Sciences

Email: yuri@niic.nsc.ru
Rússia, Novosibirsk

Ya. Gaifulin

Nikolaev Institute of Inorganic Chemistry of the Siberian Branch of the Russian Academy of Sciences

Email: yuri@niic.nsc.ru
Rússia, Novosibirsk

T. Sukhikh

Nikolaev Institute of Inorganic Chemistry of the Siberian Branch of the Russian Academy of Sciences

Email: yuri@niic.nsc.ru
Rússia, Novosibirsk

K. Brylev

Nikolaev Institute of Inorganic Chemistry of the Siberian Branch of the Russian Academy of Sciences

Email: yuri@niic.nsc.ru
Rússia, Novosibirsk

Yu. Mironov

Nikolaev Institute of Inorganic Chemistry of the Siberian Branch of the Russian Academy of Sciences

Autor responsável pela correspondência
Email: yuri@niic.nsc.ru
Rússia, Novosibirsk

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2. Fig. 1. Fragment of the structure of compound I with numbering of symmetrically independent atoms (thermal ellipsoids of 75% probability are given, hydrogen atoms are not shown)

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3. Fig. 2. Coordination environment of Ag(1), Ag(2), Ag(4) and Ag(5) atoms

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4. Fig. 3. Structure of the dimeric fragment [{Ag(Dppe)}2µ-Dppe]2+ in compound I. Hydrogen atoms as well as phenyl rings of the bridging molecule Dppe are not shown

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5. Fig. 4. Fragment of the layered structure of compound I. S atoms, Dppe phenyl ring molecules and H2O solvate molecules are not shown

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6. Fig. 5. Independent fragment of the structure of compound II with numbering of heavy symmetrically independent atoms showing the ligands Dppe (a) and DppeSe (b) coordinated to the disordered Ag(2) (a) or Ag(2B) (b) atom, respectively. Thermal ellipsoids of 75% probability are given. Hydrogen atoms are not shown

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7. Fig. 6. Coordination environment of Ag(1), Ag(2A) and Ag(2B) atoms in compound II

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8. Fig. 7. Structure of the dimeric fragment {(Ag(Dppe))2(µ-Dppe)}2+ in compound II. Hydrogen atoms are not shown

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9. Fig. 8. Fragment of the layered structure of compound II. Se atoms, phenyl rings of Dppe molecules and hydrogen atoms are not shown

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10. Fig. 9. Experimental powder diffractogram of compound I in a polycrystalline sample (bottom) in comparison with the calculated one based on the structure of a single crystal (top)

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11. Fig. 10. Experimental powder diffractogram of compound II in a polycrystalline sample (bottom) in comparison with the calculated structures of single crystals of compounds I (top, solid line) and II (top, dotted line)

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12. Fig. 11. Photoluminescence spectra of compounds I and II

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