Synthesis and Structure of Bismuth Complexes [Ph<sub>4</sub>P]<sup>+</sup><sub>2</sub>[Bi<sub>2</sub>I<sub>8</sub>(μ<sub>2</sub>-Et<sub>2</sub>SO-O)]<sup>2–</sup> и [Ph<sub>4</sub>P]<sup>+</sup><sub>2</sub><i>trans</i>-[Bi<sub>2</sub>I<sub>8</sub>(dmso-O)<sub>2</sub>]<sup>2-</sup>
DOI:
https://doi.org/10.14529/chem200107Keywords:
tetraphenylphosphonium iodide, bismuth (III) iodide, synthesis, structure, X-ray analysisAbstract
The interaction of bismuth (III) iodide with tetraphenylphosphonium iodide in dimethylsulfoxide and diethylsolfoxide have synthesized bismuth complexes [Ph4P]+2[Bi2I8(m2-Et2SO-O)]2– (1) и [Ph4P]+2trans-[Bi2I8(dmso-O)2]2- (2). They have been structurally characterized. The X-ray diffraction pattern has been obtained at 293 K on an automatic diffractometer D8 Quest Bruker (MoKα-radiation, λ = 0.71073 Å, graphite monochromator) of crystals 1 [C26H24O0.5SI4BiP, M 1124.06, the monoclinic syngony, the symmetry group С2/с; cell parameters: а = 27.563(15) Å, b = 9.140(7) Å, с =28.978(17) Å; α = 90.00 degrees, β =119.069(17) degrees, γ = 90.00 degrees; V = 6381(7) Å3; the crystal size 0.43×0.35×0.19 mm; intervals of reflection indexes are –41 ≤ h ≤ 41, –13 ≤ k ≤ 13, –43 ≤ l ≤ 42; total reflections 124163; independent reflections 11658; Rint 0.0708; GOOF 1.025; R1 = 0.0852, wR2 = 0.1380; residual electron density –3.19/2.61 e/Å3][C28H32O2PS2BiI4, M 1212.21; the triclinic syngony, the symmetry group Р-1; cell parameters: а = 9.409(10) Å, b = 14.149(16) Å, с =15.745(15) Å; α = 113.85 degrees, β =92.50(4) degrees, γ = 104.05 degrees; V = 1836(3) Å3; the crystal size 0.64×0.43×0.4 mm; intervals of reflection indexes are –15 ≤ h ≤ 15, –23 ≤ k ≤ 24, –25 ≤ l ≤ 26; total reflections 117427; independent reflections 18300; Rint 0.0927; GOOF 1.006; R1 = 0.1366, wR2 = 0.1369; residual electron density –2.99/2.59 e/Å3] the phosphor atoms have a distorted tetrahedral coordination (the CPC angles are 107.7(3)–112.8(4)° (1), 107.2(3)–111.2(3)° (2); the Р–С bond lengths are 1.771(7)–1.823(8) Å (1), 1.786(6)–1.804(5) Å (2)). The equatorial angles IBiI are 86.22(3)–92.87(3)° (1), 80.43(8)–95.86(8)° (2), the axial angles OBiI are 162.71(11)° (1), и 174.34(11)° (2); the equatorial Bi–I bond lengths are 2.8882(14)–3.2829(18) Å (1), 2.928(2)–3.364(3) Å (2), the axial Bi–I bond lengths are 2.9156(17) Å (1), 2.928(2) Å (2), the axial Bi–O bond lengths are 2.747(5)Å (1), 2.572(5) Å (2). Complete tables of coordinates of atoms, bond lengths and valence angles for structures 1 and 2 are deposited at the Cambridge Structural Data Bank (no. 1969793, 1969795; deposit@ccdc.cam.ac.uk; https://www.ccdc.cam.ac.uk).
References
Elfaleh, N. Structural Characterization, Vibrational Studies and Optical Properties of a New Lu-minescent Organic-Inorganic Material / N. Elfaleh, S. Kamoun // J. Organomet. Chem. – 2016. – V. 819. – P. 95–102. DOI: 10.1016/j.jorganchem.2016.06.029
Structural Diversity and Thermochromic Properties of Iodobismuthate Materials Containing d-Metal Coordination Cations: Observation of a High Symmetry [Bi3I11]2− Anion and of Isolated I− Anions / A.M. Goforth, M.A. Tershansy, M.D. Smith et al. // J. Am. Chem. Soc. – 2010. – V. 133, № 3. – P. 305–313. DOI: 10.1021/ja108278j
α- to β-[C6H4(NH3)2]2Bi2I10 Reversible Solid-State Transition, Thermochromic and Optical Studies in the p-Phenylenediamine-Based Iodobismuthate (III) Material / C. Hrizi, A. Trigui, Y. Abid et al. // J. of Solid State Chem. – 2011. – V. 58, № 4. – P. 3336–3344. DOI: 10.1016/j.jssc.2011.10.004
Синтез и строение фосфорсодержащих комплексов: [Ph4P]2+[Hg4I10]2– и [Ph4P]2+[BiI5(Me2S=O]2– / В.В. Шарутин, И.В. Егорова, О.К. Шарутина и др. // Коорд. химия.
– 2005. – Т. 31, № 10. – С. 791–795.
Syntheses, Structures and Vibrational Spectra of Some Dimethyl Sulfoxide Solvates of Bis-muth(III) Bromide and Iodide / G.A. Bowmaker, J.M. Harrowfield, P.C. Junk et al. // Aust. J. Chem. – 1998. – V. 51, № 4. – P. 285–292. DOI: 10.1071/C97035
Lindqvist, O. The Crystal Structure of Caesium Bismuth Iodide, Cs3Bi2I9 / O. Lindqvist // Acta Chemica Scandinavica. – 1968. – V. 22, № 9. – P. 2943–2952. DOI: 10.3891/acta.chem.scand.22-2943.
Chabot, B. Cs3Sb2I9 and Cs3Bi2I9 with the Hexagonal Cs3Cr2Cl9 Structure Type / B. Chabot, E. Parthe // Acta Cryst. – 1978. – V. B 34, № 2. – P. 645–648. DOI: 10.1107/S0567740878003684
Tris(ethyldimethylphenylammonium) Nonahalogenodibismuthates (III) / H. Eickmeier, B. Jaschinski, A. Hepp et al. // Z. Naturforsch. B. – 1999. – V. 54, № 3. – P. 305–313. DOI: 10.1515/znb-1999-0303
Effect of Mono-Versus Di-ammonium Cation of 2,2'-Bithiophene Derivatives on the Structure of Organic-Inorganic Hybrid Materials Based on Iodometallates / X.H. Zhu, N. Mercier, P. Frere et al. // Inorg. Chem. – 2003. – V. 42, № 17. – P. 5330–5339. DOI: 10.1021/ic034235y
Реакции иодида висмута с солями аммония, фосфония и висмутония / В.В. Шарутин,
И.В. Егорова, Е.А. Бояркина и др. // Журн. общ. химии. – 2008. – Т. 78, № 7. – С. 1083–1088.
Синтез и строение комплексов висмута [Bu4P]+2[Bi2I8·2Me2S=O]2–, [(Me2S=O)8BI]3+[Bi2I9]3– / В.В. Шарутин, О.К. Шарутина, В.С. Сенчурин, Р.М. Хисамов // Бутлеровские сообщения. – 2013. – Т. 36, № 11. – С. 78–82.
Synthesis and Structure of Bismuth Complexes [pTol4E]+3 [Bi3I12]3– ∙HOCH2CH2OC2H5
E=P, Sb / V.V. Sharutin, O.K. Sharutina, V.S. Senchurin et al. // Вестник ЮУрГУ. Серия «Химия». – 2015. – Т. 7, № 4. – С. 44–51. DOI: 10.14529/chem150406
Mitzi D.B. Structure and Optical Properties of Several Organic-Inorganic Hybrids Containing Corner-Sharing Chains of Bismuth Iodide Octahedra / D.B. Mitzi, P. Brock // Inorg. Chem. – 2001. – V. 40, № 9. – P. 2096–2104. DOI: 10.1021/ic000622l
Синтез и строение комплекса висмута [n-Bu4N]2+[Bi2I8•2Me2S=O]2− / В.В. Шарутин,
В.С. Сенчурин, О.К. Шарутина и др. // Журн. неорг. химии. – 2011. – Т. 56, № 8. – С. 1342–1345.
Clegg, W. Synthesis and Structure of [SMe3]2[Bi2I8(SMe2)2]: a Dimethylsulphide Complex of Bismuth (III) / W. Clegg, N.C. Norman, N.L. Pickett // Polyhedron. – 1993. – V. 12, № 10. – P. 1251–1252. DOI: 10.1016/S0277-5387(00)88219-4
Синтез и кристаллическая структура соединений висмута [Ph3BuP]+I−, [Ph3BuP]2+[Bi2I8• 2Me2C=O]2−, и [Ph3BuP]2+[Bi2I8•2Me2S=O]2− / В.В. Шарутин, И.В. Егорова, Н.Н. Клепиков и др. // Коорд. химия. – 2009. – Т. 35, № 3. – С. 188–192.
A Double Salt of Iodobismuthate: cis-Aquaiodidobis (1, 10-phenanthroline) Cobalt (II) tris(1,10-phenanthroline) Cobalt (II) Trans-hexa-μ2-iodido-hexaiodidotribismuthate (III) / J. Chen, W. Chai, L. Song et al. // Acta Crystallogr., Sect. E: Struct. Rep. Online. – 2011. – V. 67, № 9. – P. m1284–m1285. DOI:
1107/S1600536811033460
Синтез и строение комплексов висмута [Ph4P]4[Bi8I28], [Ph4P]2[Bi2I8•2Me2S=O]•2Me2S=O, [(Me2S=O)8Bi][Bi2I9] / В.В. Шарутин, В.С. Сенчурин, О.К. Шарутина, О.А. Давыдова // Журн. общ. химии. – 2012. – Т. 82, № 2. – С. 197–201.
Синтез и строение комплексов висмута [p-Tol4P]2[Bi2I8(THF)2]2–, [p-Tol4Sb]2[Bi2I8(THF)2]2–, [p-Tol4P]2[Bi2I8(DMSO)2]2–, [Bu4P] [(Bi2I7)n]n–, [p-Tol4P] [(Bi2I7)n]n–, [p-Tol4Sb] [(Bi2I7)n]n– / В.В. Ша-рутин, О.К. Шарутина, Р.М. Хисамов, В.С. Сенчурин // Журн. неорг. химии. – 2017. – Т. 62, № 6. – С. 782–793.
Bruker. SMART and SAINT-Plus. Versions 5.0. Data Collection and Processing Software for the SMART System. Bruker AXS Inc., Madison, Wisconsin, USA, 1998.
Bruker. SHELXTL/PC. Versions 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures From Diffraction Data. Bruker AXS Inc., Madison, Wisconsin, USA, 1998.
OLEX2: Complete Structure Solution, Refinement and Analysis Program / O.V. Dolomanov, L.J. Bourhis, R.J. Gildea et al. // J. Appl. Cryst. – 2009. – V. 42. – P. 339–341. DOI: 10.1107/S0021889808042726
Covalent Radii Revisited / B. Cordero, V. Gómez, A.E. Platero-Prats et al. // Dalton Trans. – 2008. – Iss. 21. – P. 2832–2838. DOI: 10.1039/B801115J
Consistent Van der Waals Radii for the Whole Main Group / M. Mantina, A.C. Chamberlin, R. Valero et al. // J. Phys. Chem. A. – 2009. – V. 113, iss. 19. – P. 5806–5812. DOI: 10.1021/jp8111556
Бацанов, С.С. Атомные радиусы элементов / С.С. Бацанов // Журн. неорган. химии. – 1991. – Т. 36, № 12. – С. 3015–3037.





