Heterodinuclear PtRh and PtIr complexes with phosphinite groups as bridging ligands
dc.contributor.author | Contreras, R | |
dc.contributor.author | Valderrama, M | |
dc.contributor.author | Moscoso, R | |
dc.date.accessioned | 2025-01-21T01:32:34Z | |
dc.date.available | 2025-01-21T01:32:34Z | |
dc.date.issued | 1998 | |
dc.description.abstract | Compounds of the general formula [Pt(eta(2)-L) {P(O)Ph-2}{P(OH)Ph-2}], where eta(2)-L = {eta(2)-S2P(OEt)(2)}(-) (I) and {eta(2)-(SCNEt2)-C-2}(-) (2), react in THF solution with the dinuclear complex [{(cod)M(mu-OMe)}(2)] (M = Rh-I or Ir-I) to give new heterodinuclear compounds of the type [(eta(2)-L)Pt{mu-P(O)Ph-2}(2)M(cod)], where eta(2)-L = {eta(2)-S2P(OEt)(2)}(-); M = Rh-I (3), Ir-I (4) and eta(2)-L = {eta(2)-S2C-NEt2}(-); M = Rh-I (5) and Ir-I (6). Compounds (3) and (4) react with an excess of CO, leading to displacement of the coordinated pi-diolefin (cod) and the formation of the dicarbonyl derivatives [{eta(2)-S2P(OEt)(2)}Pt{mu-P(O)-Ph-2}(2)M(CO)(2)] [M = Rh-I (7), Ir-I (8)]. | |
dc.description.abstract | All products were characterized by carbon and hydrogen microanalysis and by i.r, and n.m.r. spectroscopy {H-1 and P-31(H-1)}. | |
dc.fuente.origen | WOS | |
dc.identifier.issn | 0340-4285 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/97284 | |
dc.identifier.wosid | WOS:000076269300008 | |
dc.issue.numero | 4 | |
dc.language.iso | en | |
dc.pagina.final | 359 | |
dc.pagina.inicio | 357 | |
dc.revista | Transition metal chemistry | |
dc.rights | acceso restringido | |
dc.subject.ods | 12 Responsible Consumption and Production | |
dc.subject.odspa | 12 Producción y consumo responsable | |
dc.title | Heterodinuclear PtRh and PtIr complexes with phosphinite groups as bridging ligands | |
dc.type | artículo | |
dc.volumen | 23 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |