The two rhodium complexes [Rh(acac)(LR)] (LR = (S,S)-5,11,17,23-tetra-tert-butyl-25,27-di(OR)-26,28-bis(1,1'-binaphthyl-2,2'-dioxyphosphanyloxy)-calix[4]arene (6: R = benzyl; 7: R = fluorenyl), each based on a hemispherical chelator forming a pocket about the metal centre upon chelation, are active in the hydroformylation of 1-octene and styrene. As expected for this family of diphosphanes, both complexes resulted in remarkably high selectivities towards the linear aldehyde in the hydroformylation of 1-octene (l:b ~ 15 for both complexes). Linear aldehyde selectivity was also observed when using styrene, but surprisingly only 6 displayed a marked preference for the linear product (l:b = 12.4 (6) vs. 1.9 (7)). A detailed study of the structure of the complexes under CO or CO/H2 in toluene was performed by high-pressure NMR (HP-NMR) and high pressure FT-IR (HP-IR) spectroscopy. The spectroscopic data revealed that reaction of 6 with CO gave [Rh(acac)(CO)(?1-Lbenzyl)] (8), in which the diphosphite behaves as a unidentate ligand. Subsequent addition of H2 to the solution resulted in a well-defined chelate complex having the formula [RhH(CO)2(Lbenzyl)] (9). Unlike 6, complex 7, led with CO alone, to ligand dissociation and concomitant formation of [Rh(acac)(CO)2], but upon addition of H2 a chelate complex analogue to 9 was formed quantitatively. In both [RhH(CO)2(LR)] complexes the diphosphite adopts the bis-equatorial coordination mode, a structural feature known to favour the formation of linear aldehydes. As revealed by variable temperature NMR studies, these complexes show the typical fluxionality of trigonal bipyramidal [RhH(CO)2(diphosphane)] complexes. The lower linear selectivity of 7 vs. 6 in the hydroformylation of styrene was assigned to steric effects, the pocket in which the catalysis takes place being less adapted to accommodate CO or larger olefins, and therefore possibly leading to facile ligand decoordination. This interpretation was corroborated by an X-ray structure determination carried out for 7.

High Pressure Investigation under CO/H2 of Rhodium Complexes containing Hemispherical Diphosphites

Oberhauser W;Bianchini C
2010

Abstract

The two rhodium complexes [Rh(acac)(LR)] (LR = (S,S)-5,11,17,23-tetra-tert-butyl-25,27-di(OR)-26,28-bis(1,1'-binaphthyl-2,2'-dioxyphosphanyloxy)-calix[4]arene (6: R = benzyl; 7: R = fluorenyl), each based on a hemispherical chelator forming a pocket about the metal centre upon chelation, are active in the hydroformylation of 1-octene and styrene. As expected for this family of diphosphanes, both complexes resulted in remarkably high selectivities towards the linear aldehyde in the hydroformylation of 1-octene (l:b ~ 15 for both complexes). Linear aldehyde selectivity was also observed when using styrene, but surprisingly only 6 displayed a marked preference for the linear product (l:b = 12.4 (6) vs. 1.9 (7)). A detailed study of the structure of the complexes under CO or CO/H2 in toluene was performed by high-pressure NMR (HP-NMR) and high pressure FT-IR (HP-IR) spectroscopy. The spectroscopic data revealed that reaction of 6 with CO gave [Rh(acac)(CO)(?1-Lbenzyl)] (8), in which the diphosphite behaves as a unidentate ligand. Subsequent addition of H2 to the solution resulted in a well-defined chelate complex having the formula [RhH(CO)2(Lbenzyl)] (9). Unlike 6, complex 7, led with CO alone, to ligand dissociation and concomitant formation of [Rh(acac)(CO)2], but upon addition of H2 a chelate complex analogue to 9 was formed quantitatively. In both [RhH(CO)2(LR)] complexes the diphosphite adopts the bis-equatorial coordination mode, a structural feature known to favour the formation of linear aldehydes. As revealed by variable temperature NMR studies, these complexes show the typical fluxionality of trigonal bipyramidal [RhH(CO)2(diphosphane)] complexes. The lower linear selectivity of 7 vs. 6 in the hydroformylation of styrene was assigned to steric effects, the pocket in which the catalysis takes place being less adapted to accommodate CO or larger olefins, and therefore possibly leading to facile ligand decoordination. This interpretation was corroborated by an X-ray structure determination carried out for 7.
2010
calixarenes
NMR spectroscopy
hydroformylation
bite angle
rhodium
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/165177
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact