Abstract
Ionic palladium complexes with mononuclear anions [Ph3PCH2C(O)Me][PdCl3(Dmso-S)] (I) and [Ph4Sb(Dmso-O)][PdBr3(Dmso-S)] (II) are synthesized from tetraorganylphosphonium or tetraorganylstibonium halide and palladium dihalide in the presence of hydrochloric or hydrobromic acid. The structures of complexes I and II are determined by X-ray diffraction (XRD) (CIF files CCDC nos. 1907718 (I) and 1979208 (II)). The complexes contain tetrahedral tetraorganylphosphonium or tetraorganylstibonium cations and square anions [PdHal3(Dmso-S)]−. According to the XRD data, the phosphorus and antimony atoms in the cations have a slightly distorted tetrahedral coordination with the CPC (105.76(7)°−110.31(7)°) and CSbC (100.03(16)°−117.62(15)°) bond angles slightly differed from the theoretical value and close P−C (1.7903(15)−1.8037(16) Å) and Sb−C (2.061(5)−2.100(4) Å) bond lengths. The P−CAlk bonds are longer (1.8037(16) Å) than the P−CPh bonds. In the square planar anions [PdHal3(Dmso-S)]−, the Pd−Cl and Pd−Br bond lengths vary in ranges of 2.2918(7)−2.3012(8) and 2.371(3)−2.403(2) Å, respectively, and the S−Pd distances (2.2492(6) and 2.237(2) Å) are less than the sum of covalent radii of palladium and sulfur atoms (2.44 Å). The cis-ClPdCl (89.88(3)°) and cis-BrPdBr (88.93(4)°, 89.59(4)°) angles do not almost differ from the theoretical value (90°). The trans-ClPdCl and trans-SPdCl angles are comparable and equal to 178.15(2)° and 178.714(19)°. The corresponding values for complex II are 174.22(3)° and 177.53(4)°. The deviations of the palladium atom from the Cl3S and Br3S planes are insignificant (0.019 and 0.033 Å). The structural organization in the crystals of the complexes is formed by interionic contacts S=O···H–C (2.56−2.72 Å (I) and 2.44−2.62 Å (II)), Pd–Cl···H–C (2.83−2.93 Å), and Br···H (2.86−3.04 Å).
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REFERENCES
Meyer, D., Taige, M.A., Zeller, A., et al., Organometallics, 2009, vol. 28, no. 7, p. 2142. https://doi.org/10.1021/om8009238
Gardiner, M.G., Ho, C.C., McGuinness, D.S., and Liu, Y.L., Aust. J. Chem., 2020, vol. 73, p. 1158. https://doi.org/10.1071/CH20194
Gacal, E., Denizalti, S., Kinal, A., et al., Tetrahedron, 2018, vol. 74, no. 47, p. 6829. https://doi.org/10.1016/j.tet.2018.10.003
Mansour, W., Fettouhi, M., and El Ali, B., ACS Omega, 2020, vol. 5, no. 50, p. 32515. https://doi.org/10.1021/acsomega.0c04706
Mansour, W., Suleiman, R., and Fettouhi, M., ACS Omega, 2020, vol. 5, no. 50, p. 23687. https://doi.org/10.1021/acsomega.0c02413
Trofimov, B.A., Vasilevsky, S.F., Gusarova, N.K., et al., Mendeleev Commun., 2008, vol. 18, no. 6, p. 318. https://doi.org/10.1016/j.mencom.2008.11.010
Bykov, M.V., Abramov, Z.D., Orlov, T.S., et al., J. Struct. Chem., 2021, vol. 62, no. 8, p. 1218. https://doi.org/10.1134/S0022476621080072
Artem’ev, A.V., Malysheva, S.F., Gusarova, N.K., et al., Tetrahedron, 2016, vol. 72, no. 4, p. 443. https://doi.org/10.1016/j.tet.2015.11.009
Artem’ev, A.V., Kuimov, V.A., Matveeva, E.A., et al., Inorg. Chem. Commun., 2017, vol. 86, p. 94. https://doi.org/10.1016/j.inoche.2017.09.008
Adamson, A., Budiman, Y.P., Mkhalid, I., et al., J. Struct. Chem., 2020, vol. 61, p. 466. https://doi.org/10.1134/S0022476620030130
Wolfe, M.M.W., Shanahan, J.P., Kampf, J.W., et al., J. Am. Chem. Soc., 2020, vol. 142, no. 43, p. 18698. https://doi.org/10.1021/jacs.0c09505
Mori, M., Sunatsuki, Y., and Suzuki, T., Inorg. Chem., 2020, vol. 59, no. 24, p. 18225. https://doi.org/10.1021/acs.inorgchem.0c02706
Behnia, A., Fard, M.A., Blacquiere, J.M., et al., Organometallics, 2020, vol. 39, no. 22, p. 4037. https://doi.org/10.1021/acs.organomet.0c00615
Materne, K., Braun-Cula, B., Herwig, C., et al., Chem.-Eur. J., 2017, vol. 23, p. 11797. https://doi.org/10.1002/chem.201703489
Lin, T.-P., Ke, I.-Sh., and Gabbai, F.P., Angew. Chem., Int. Ed. Engl., 2012, vol. 51, p. 4985. https://doi.org/10.1002/anie.201200854
Cambridge Crystallographic Data Center, 2022. http://www.ccdc.cam.ac.uk.
Sharutin, V.V., Sharutina, O.K., Senchurin, V.S., et al., Russ. J. Gen. Chem., 2017, vol. 87, no. 1, p. 122. https://doi.org/10.1134/S1070363217010194
Sharutin, V.V., Senchurin, V.S., and Sharutina, O.K., Russ. J. Inorg. Chem., 2013, vol. 58, no. 5, p. 543. https://doi.org/10.1134/S0036023613050203
Sharutin, V.V., Sharutina, O.K., Senchurin, V.S., et al., Russ. J. Coord. Chem., 2015, vol. 41, no. 7, p. 462. https://doi.org/10.1134/S1070328415070088
Sharutin, V.V., Sharutina, O.K., Senchurin, V.S., et al., Vest. YuUrGU. Ser. Khim., 2015, vol. 7, no. 2, p. 11.
Yarygina, D.M., Batalov A.E., and Senchurin V.S., Vestn. YuUrGU. Ser. Khim., 2018, vol. 10, no. 3, p. 51. https://doi.org/10.14529/chem180306
Sharutin, V.V., Sharutina, O.K., Senchurin, V.S., et al., Russ. J. Inorg. Chem., 2018, vol. 63, no. 6, p. 747. https://doi.org/10.1134/S0036023618060220
Denisov, M.S., Dmitriev, M.V., Eroshenko, D.V., et al., Russ. J. Inorg. Chem., 2019, vol. 64, no. 1, p. 56. https://doi.org/10.1134/S0036023619010054
Gupta, A., Deka, R., Butcher, R.J., and Singh, H.B., Acta Crystallog., Sect. E: Crystallogr. Commun., 2020, vol. 76, p. 1520. https://doi.org/10.1107/S2056989020011482
Hazell, A., McKenzie, C.J., and Nielsen, L.P., Dalton Trans., 1998, p. 1751. https://doi.org/10.1039/A800602D
Geary, W.J., Mason, N.J., Nixon, L.A., and Nowell, I.W., Chem. Commun., 1980, no. 22, p. 1064. https://doi.org/10.1039/c39800001064
Schroeter, F., Soellner, J., and Strassner, T., Chem.-Eur. J., 2019, vol. 25, p. 2527. https://doi.org/10.1002/chem.201804431
Lang, C., Pahnke, K., Kiefer, C., et al., Polym. Chem., 2013, vol. 4, no. 21, p. 5456. https://doi.org/10.1039/C3PY00648D
Kocheshkov, K.A., Skoldinov, A.P., and Zemlyanskii, N.N. Metody elementoorganicheskii khimii. Sur’ma, vismut (Methods of Organoelement Chemistry. Antimony, Bismuth), Moscow: Nauka, 1976.
SMART and SAINT-Plus. Version 5.0. Data Collection and Processing Software for the SMART System, Madison: Bruker AXS Inc., 1998.
SHELXTL/PC. Version 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data, Madison: Bruker AXS Inc., 1998.
Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., et al., J. Appl. Crystallogr., 2009, vol. 42, p. 339. https://doi.org/10.1107/S0021889808042726
Kazitsyna, L.A. and Kupletskaya, N.B., Primenenie UF-, IK- i YaMR-spektroskopii v organicheskoi khimii (Application of UV, IR, and NMR Spectroscopy in Organic Chemistry), Moscow: Vyssh. shkola, 1971, p. 50.
Kukushkin, Yu.N., Koord. Khim., 1997, vol. 23, no. 3, p. 163.
Cordero, B., Gómez, V., Platero-Prats, A.E., et al., Dalton Trans., 2008, vol. 21, p. 2832. https://doi.org/10.1039/B801115J
Mantina, M., Chamberlin, A.C., Valero, R., et al., J. Phys. Chem. A, 2009, vol. 113, no. 19, p. 5806. https://doi.org/10.1021/jp8111556
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Translated by E. Yablonskaya
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Sharutin, V.V., Senchurin, V.S. Palladium Complexes [Ph3PCH2C(O)Me][PdCDmso-S)] and [Ph4Sb(Dmso-O)][PdBr3(Dmso-S)]: Synthesis and Structures. Russ J Coord Chem 49, 453–457 (2023). https://doi.org/10.1134/S107032842360033X
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DOI: https://doi.org/10.1134/S107032842360033X