Synthesis and Structure of Tetraphenylstibonium Organosulfonates Ph4SbOSO2R, R = C10H15O, C10H4(OH-1)(NO2)2-2,4, C10H7-1, C6H4(COOH-2)

The reaction of equimolar amounts of pentaphenylantimony with camphor-10-sulfonic, 2,4-dinitro-1-naphthol-7-sulfonic (flavianic), 1-naphthalenesulfonic, and 2-sulfobenzoic acids in benzene resulted in the synthesis of tetraphenylstibonium organosulfonates Ph 4 SbOSO 2 C 10 H 15 O∙H 2 O ( I ), Ph 4 S...

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Veröffentlicht in:Russian journal of coordination chemistry 2023-05, Vol.49 (5), p.311-317
Hauptverfasser: Senchurin, V. S., Sharutin, V. V., Sharutina, O. K., Krasnoselskaya, V. V.
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Sprache:eng
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Zusammenfassung:The reaction of equimolar amounts of pentaphenylantimony with camphor-10-sulfonic, 2,4-dinitro-1-naphthol-7-sulfonic (flavianic), 1-naphthalenesulfonic, and 2-sulfobenzoic acids in benzene resulted in the synthesis of tetraphenylstibonium organosulfonates Ph 4 SbOSO 2 C 10 H 15 O∙H 2 O ( I ), Ph 4 SbOSO 2 C 10 H 4 (OH-1)(NO 2 ) 2 -2,4∙PhH ( II ), Ph 4 SbOSO 2 (C 10 H 7 -1)∙H 2 O ( III ), and Ph 4 SbOSO 2 C 6 H 4 (COOH-2) ( IV ). According to X-ray diffraction data (CCDC no. 2119791 ( I ), 2121381 ( II ), 2116582 ( III ), and 2123516 ( IV ), the crystal of I contains trigonal-bipyramidal sulfonate molecules (the axial Sb−C and Sb−O bond lengths are 2.130(3) and 2.565(2) Å, respectively) and hydration water molecules, which form a centrosymmetric eight-membered ring (the S=O∙∙∙H−O−H∙∙∙O=S distances are 2.06 and 2.21 Å). In the molecules of II , the metal atom geometry is a distorted trigonal bipyramid (the axial Sb−C and Sb−O bonds are 2.133(2) and 2.643(3) Å, respectively). The Sb−O distance (2.842(3) Å) is longer in III than in I or II ; the hydration water molecules form centrosymmetric twelve-membered rings with the anions (the S=O∙∙∙H−O−H∙∙∙O=S distances are 2.02 and 2.05 Å). Meanwhile, the crystal of compound IV consists of tetrahedral tetraphenylstibonium cations and (2-carboxy)benzenesulfonate anions with the intramolecular O−H∙∙∙O=S hydrogen bond (1.75 Å).
ISSN:1070-3284
1608-3318
DOI:10.1134/S1070328423700513