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Unusual cationic rhodathiaboranes: synthesis and characterization of [8,8,8-(H)(PR3)2-9-(Py)-nido-8,7-RhSB9H 10]+ and [1,3-μ-(H)-1,1-(PR3) 2-3-(Py)-isonido-1,2-RhSB9H8]+

AutorCalvo, Beatriz ; Macías, Ramón ; Artigas, María José ; Lahoz, Fernando J. ; Oro, Luis A.
Fecha de publicación2014
EditorRoyal Society of Chemistry (Great Britain)
CitaciónDalton Transactions 43(13): 5121-5133 (2014)
ResumenThe treatment of the hydridorhodathiaboranes, [8,8,8-(H)(PR 3)2-9-(Py)-nido-8,7-RhSB9H9], where PR3 = PPh3 (2), PMePh2 (3), PPh3 and PMe2Ph (4), or PMe3 and PPh3 (5), and [8,8,8-(H)(PMePh2)2-9-(PMePh2)-nido-8,7- RhSB9H9] (6), with TfOH affords [8,8,8-(H)(PR 3)2-9-(Py)-nido-8,7-RhSB9H10] + cations, where PR3 = PPh3 (12), PMePh 2 (13), PPh3 and PMe2Ph (14), or PMe 3 and PPh3 (15), and [8,8,8-(H)(PMePh2) 2-9-(PMePh2)-nido-8,7-RhSB9H10] + (16). Compounds 13 and 14 lose H2 to give [1,3-μ-(H)-1,1-(PR3)2-3-(Py)-isonido-1,2-RhSB 9H8]+, where PR3 = PMe2Ph (18), PPh3 and PMe2Ph (21), or PMePh2 (22). Similarly, the 11-vertex rhodathiaboranes, [1,1-(PR3) 2-3-(Py)-1,2-RhSB9H8], where PR3 = PPh3 (7), PMe2Ph (8), PMe3 (9), or PPh 3 and PMe3 (10), react with TfOH to give the corresponding cations, [1,3-μ-(H)-1,1-(PR3)2-3-(Py)-isonido-1,2- RhSB9H8]+, where PR3 = PPh 3 (17), PMe2Ph (18), PMe3 (19), or PPh 3 and PMe3 (20). Four conformers of 20 are studied by X-ray diffraction methods and DFT-calculations, identifying packing motifs that stabilize different metal-thiaborane linkages, and energy variations that are involved in these conformational changes. It is demonstrated that the proton induces nonrigidity on these clusters as well as an enhancement of their Lewis acidity. © 2014 The Royal Society of Chemistry.
Versión del editorhttp://dx.doi.org/10.1039/C3DT52018H
URIhttp://hdl.handle.net/10261/111578
DOI10.1039/C3DT52018H
Identificadoresdoi: 10.1039/C3DT52018H
issn: 1477-9226
e-issn: 1477-9234
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