Chiral sulfur diphosphazanes derived from S-(Ph<sub>2</sub>P)<sub>2</sub>N(CHMePh) and its rhodium(I), (III) and iridium(III) complexes. Crystal structures of Ph<sub>2</sub>P(S)N(CHMePh)PPh<sub>2</sub>, {Ph<sub>2</sub>P(S)}<sub>2</sub>N(CHMePh) and [(Cp*)MCl{η<SUP>2</SUP>-P,S-Ph<sub>2</sub>PNHP(S)Ph<sub>2</sub>}]BF<sub>4</sub>, Cp* = η<SUP>5</SUP>-C<sub>5</sub>Me<sub>5</sub>; M = Rh, Ir
dc.contributor.author | Simón-Manso, E | |
dc.contributor.author | Valderrama, M | |
dc.contributor.author | Gantzel, P | |
dc.contributor.author | Kubiak, CP | |
dc.date.accessioned | 2025-01-21T01:30:25Z | |
dc.date.available | 2025-01-21T01:30:25Z | |
dc.date.issued | 2002 | |
dc.description.abstract | The reaction of S-(Ph2P)(2)N(CHMePh) with sulfur (1:1 molar ratio) in diethyl ether solution leads to S-Ph2P(S)N(CHMePh)PPh2 (1). The disulphide S-{Ph2P(S)}(2)N(CHMePh) (2), was obtained when the reaction was carried out in tetrahydrofuran with an excess of sulfur (1:5 molar ratio). 1 reacts with the solvated rhodium. (I) complex [Rh(cod)S-x]BF4 to afford the cationic complex [Rh(cod){eta(2)-S,P-Ph2P(S)N(CHMePh)PPh2}]BF4 (3). However, when the above reaction was carried out with 2, cleavage of the C-N bond of the ligand occurred, to yield the complex [Ph(cod)(eta(2)-S,S-{Ph2P(S)}(2)NH)]BF4 (4). Reactions of I with the fragments of Rh (III) and Ir (III) [Cp*MClSx]BF4 lead to cleavage of the C-N bond of the ligand yielding cationic complexes, [(Cp*)MCl{eta(2)- P,S-Ph2PNHP(S)Ph-2}]BF4 (M = Rh, 5; Ir, 6]. Crystal structures of 1, 2, 5 and 6 have beet determined by X-ray diffraction methods. Compounds 1 and 1 crystallize in the same space group P2(1)2(1)2(1). The molecular structure of 1 shows a nearly trigonal planar nitrogen atom bound to two different phosphorus atoms and to the chiral carbon atom. Compound 2 acquires a twisted conformation with the two sulfur atoms adopting mutually trans positions with respect to the PNP backbone. (C) 2002 Elsevier Science B.V. All rights reserved. | |
dc.fuente.origen | WOS | |
dc.identifier.eissn | 1872-8561 | |
dc.identifier.issn | 0022-328X | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/96749 | |
dc.identifier.wosid | WOS:000176048900012 | |
dc.issue.numero | 1-2 | |
dc.language.iso | en | |
dc.pagina.final | 97 | |
dc.pagina.inicio | 90 | |
dc.revista | Journal of organometallic chemistry | |
dc.rights | acceso restringido | |
dc.subject | chiral diphosphazanes | |
dc.subject | chalcogenide compounds | |
dc.subject | rhodium and iridium complexes | |
dc.subject | synthesis | |
dc.subject | crystal structures | |
dc.subject.ods | 12 Responsible Consumption and Production | |
dc.subject.odspa | 12 Producción y consumo responsable | |
dc.title | Chiral sulfur diphosphazanes derived from S-(Ph<sub>2</sub>P)<sub>2</sub>N(CHMePh) and its rhodium(I), (III) and iridium(III) complexes. Crystal structures of Ph<sub>2</sub>P(S)N(CHMePh)PPh<sub>2</sub>, {Ph<sub>2</sub>P(S)}<sub>2</sub>N(CHMePh) and [(Cp*)MCl{η<SUP>2</SUP>-P,S-Ph<sub>2</sub>PNHP(S)Ph<sub>2</sub>}]BF<sub>4</sub>, Cp* = η<SUP>5</SUP>-C<sub>5</sub>Me<sub>5</sub>; M = Rh, Ir | |
dc.type | artículo | |
dc.volumen | 651 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |