Hydrolysis of PhTeI in the presence of sodium phenylseleninate and M ions (M = Y, Nd, Ce) gives well-defined, bowl-shaped telluroxane clusters. Each of the two half-spheres of the compositions [(PhTe){ML}O] ({ML} = {Y(NO)(HO)} (), {Nd(NO)(HO)} (), or {Ce(NO)} ()) are connected by two (compound ) or four (compounds and ) PhSeO bridges. The resulting chalcogenoxane spheres have internal volumes of approximately 1500 Å. Charge compensation is provided by nitrate ions and/or [Na(NO)] clusters, which are located inside and surrounding these spheres.
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http://dx.doi.org/10.1021/acs.inorgchem.4c02274 | DOI Listing |
Inorg Chem
September 2024
Departamento de Química, Universidade Federal de Santa Maria - UFSM, Laboratório de Materiais Inorgânicos - LMI, 97105-900, Santa Maria, RS Brazil.
Hydrolysis of PhTeI in the presence of sodium phenylseleninate and M ions (M = Y, Nd, Ce) gives well-defined, bowl-shaped telluroxane clusters. Each of the two half-spheres of the compositions [(PhTe){ML}O] ({ML} = {Y(NO)(HO)} (), {Nd(NO)(HO)} (), or {Ce(NO)} ()) are connected by two (compound ) or four (compounds and ) PhSeO bridges. The resulting chalcogenoxane spheres have internal volumes of approximately 1500 Å.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2021
Institute of Chemistry and Biochemistry, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.
Phenyltelluroxane clusters of the composition [{(PhTe) O } I (solv)] (1) are formed during the hydrolysis of [PhTeI ] or the oxidation of various phenyltellurium(II) compounds with iodine under hydrolytic conditions. The compounds consist of two half-spheres with a {(PhTe) O } network, which are connected by 18 iodine atoms. The spherical clusters can accommodate solvent molecules such as pyridine or methanol in the center of two rings formed by iodine atoms.
View Article and Find Full Text PDFChemistry
January 2011
Institut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstrasse 34-36, 14195 Berlin, Germany.
The stoichiometrically controlled chlorination of the diarylditelluride (8-Me(2) NC(10) H(6) Te)(2) with SO(2) Cl(2) afforded the aryltellurinyl chloride 8-Me(2) NC(10) H(6) TeCl (1) and the aryltellurium trichloride 8-Me(2) NC(10) H(6) TeCl(3) (2). Alternatively, 1 was obtained by the reaction of the aryltellurenyl diethyldithiacarbamate 8-Me(2) NC(10) H(6) Te(S(2) CNEt(2) ) with hydrochloric acid. The base hydrolysis of 2 provided the novel telluroxanes (8-Me(2) NC(10) H(6) Te)(2) OCl(4) (3), (8-Me(2) NC(10) H(6) Te)(6) O(5) Cl(8) (4), (8-Me(2) NC(10) H(6) Te)(6) O(8) Cl(2) (5), [(8-Me(2) NC(10) H(6) Te)(2) O(3) ](n) (6) and (8-Me(2) NC(10) H(6) Te)(6) O(8) (OH)(2) (7) depending on the reaction conditions applied.
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