Artigo Revisado por pares

Structure, Electrochemistry and Hydroformylation Catalytic Activity of the Bis(pyrazolylborato)rhodium( I ) Complexes [RhBp(CO)P] [P = P(NC 4 H 4 ) 3 , PPh 3 , PCy 3 , P(C 6 H 4 OMe‐4) 3 ]

2004; Wiley; Volume: 2004; Issue: 7 Linguagem: Inglês

10.1002/ejic.200300517

ISSN

1099-0682

Autores

Anna M. Trzeciak, Beata Borak, Z. Ciunik, Józef J. Ziółkowski, M. Fátima C. Guedes da Silva, Armando J. L. Pombeiro,

Tópico(s)

Magnetism in coordination complexes

Resumo

Abstract Rhodium complexes of formula [RhBp(CO)P] [Bp = bis(pyrazolylborate), P = P(NC 4 H 4 ) 3 1 , PPh 3 2 , PCy 3 3 , P(C 6 H 4 OMe‐4) 3 4 ] have been prepared by exchange of the acetylacetonate (acac − ) ligand in [Rh(acac)(CO)P] complexes. The spectroscopic and electrochemical properties as well as X‐ray data of [Rh(acac)(CO)P] and [RhBp(CO)P] complexes have been compared with the aim to estimate the relative donor properties of both anionic ligands (acac − and Bp − ). The cyclic voltammetric results indicate that the Bp − ligand behaves as a much stronger electron donor than acac − and a value of the Lever E L ligand parameter identical to that of the pyrazolate ligand (−0.24 V vs. NHE for each coordinating arm) is proposed for the bis‐ and tris(pyrazolyl)borate ligands, whereas P(C 6 H 4 OMe‐4) 3 is also shown to have an identical E L value (0.69 V) to that of P(NC 4 H 4 ) 3 . An improved linear relationship between the oxidation potential and the sum of the ligand E L values for square‐planar Rh I complexes is also obtained and adjusted values for the Lever S M and I M parameters for the Rh I /Rh II redox couple are given. The trans influence of phosphanes was not observed in crystals of complexes 2 and 3 , in contrast to analogous acetylacetonato complexes in which the Rh−O bonds differ by ca. 0.04−0.06 Å. Complexes 1 − 4 are very attractive precursors for hydroformylation catalysts and yields of aldehydes of 80−87% have been obtained with all complexes without extra phosphane as co‐catalyst. During the hydroformylation reaction, however, small amounts of a catalytically inactive [RhBp(CO) 2 ] complex were formed. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

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