913095-15-5Relevant articles and documents
Synthesis and coordination behavior of planar-chiral ferrocene alkenylphosphines
Stepnicka, Petr,Cisarova, Ivana
, p. 8785 - 8798 (2008/10/09)
A series of planar-chiral ferrocene alkenylphosphines, (S p)-2-(diphenylphosphino)-1-vinylferrocene (2), (Sp)-2- (diphenylphosphino)-1-(prop-1-en-1-yl)ferrocene (3; as a mixture of Z and E isomers in ca. 5:1 ratio), and (E,Sp)-2-(diphenylphosphina)-1-(2- phenylethen-1-yl)ferrocene ((E)-4), was obtained by Wittig and Horner-Wadsworth-Emmons reactions from the common precursor, (S p)-2-(diphenylphosphino)ferrocene-1-carboxaldehyde (1). Coordination properties of these novel ferrocene donors were studied in their palladium(II) and tungsten(0)-carbonyl complexes. The reaction between 2 and [{Pd(μ-Cl)(LNC)}2] (5, LNC = 2-{(dimethylamino)methyl-κN}phenyl-κC1) gave the bridge-cleavage product [PdCl(LNC)(2-κP)] (6) while the reaction with [Pd(LNC)(MeCN)2]ClO4 (7) yielded the cationic bis(chelate) [Pd(LNC)(2-η2:κP)] ClO4 (8). Chelate complexes of the type [W(CO)4(L- η2:κP)] (9 with L = 2; (Z/E)-10 with L = (Z/E)-3) were obtained by reacting [W(CO)4(cod)] (cod = η2: η2-cycloocta-1,5-diene) with the appropriate phosphinoalkene in refluxing toluene while a similar reaction with (E)-4 yielded mixtures of [W(CO)5-(4-κP)] ((E)-11) and [W(CO)4(4- η2:κP)] ((E)-12). All compounds were characterized by spectral methods (multinuclear NMR, IR, MS, and CD), and the structures of 1, 2, 8, 9, (Z/E)-10, and (E)-11 were corroborated by X-ray diffraction analysis. Ligands 2 and (E)-4 as well as their complexes 6, 8, 9, (E)-11, and (E)-12 were further studied by electrochemical methods.
