Photoexcitation of iron-allyl complexes (η5: η1-C5H4CH2CH2PPh2Fe(CO)(η1-CH2CR=CH2) (R = H, CH3) which contains a tethered phosphine ligand
摘要:
Photoexcitation of the phosphino ligand chelated iron-allyl complexes (eta(5):eta'-C5H4CH2CH2PPh2)Fe(CO)(eta'-CH2CR=CH2) (1a: R=H; 1b: R=CH3) gives a mixture of Fe-CO bond cleavaged compound (eta(5):eta(1)-C5H4CH2CH2PPh2)Fe(eta(3)-CH2CRCH2) (2) and Fe-allyl bond homolysis compounds [eta(4):eta(1)-(1-CH2CR=CH2)C5H4CH2CH2PPh2]Fe(CO)(2) (3) and [eta(4):eta(1)-(3-CH2CR=CH2)C5H4CH2CH2PPh2]Fe(CO)(2) (4) in a ratio of 20:5:1. Their structures were determined spectroscopically. No phosphine exchange products were observed when the reaction was conducted in the presence of triphenylphosphine. (C) 1997 Elsevier Science S.A.
Preparations of novel half-sandwich iron carbonyl phosphine complexes: Intramolecular link between the cyclopentadienyl and the phosphine ligand
摘要:
The novel iron half-sandwich complex (eta(5):eta(1)-C(5)H(4)CH(2)CH(2)PPh(2))Fe(CO)Cl (4), in which the ligating phosphine was connected to the cyclopentadienyl ring, was prepared by reacting the LiC(5)H(4)CH(2)CH(2)PPh(2) (2) with FeCl2 followed by CO bubbling. Reaction of 4 with sp-, sp(2)- and sp(3)-hybridized carbon nucleophiles provided formal substitution product (eta(5):eta(1)-C(5)H(4)CH(2)CH(2)PPh(2))Fe(CO)R (5). Solid state structures of the methyl complex 5a, phenylacetylide 5g and trimethylsilylacetylide 5j were characterized by single-crystal X-ray analyses.