SYNTHESIS, CHARACTERIZATION, AND ELECTROCHEMISTRY OF HETEROMETALLIC DENDRIMERS

A method for the synthesis of new heterometallic dendritic molecules c ontaining organoplatinum centers is reported. Reaction of Pt2Me4(mu-SM e2)(2) with bpy-Fc(2) (1) (bpy-Fc(2) = 4,4'-bis (ferrocenylvinyl)-2,2' -bipyridine) gave the platinum(II) complex PtMe2(bpy-Fc(2)) (2). Compl ex 2 undergoes oxidative addition with iodomethane to yield PtMe3I(bpy -Fc(2)) (3) and with bis(bromomethyl)benzenes to yield complexes of th e type [PtMe2Br(bpy-Fc(2))-CH2-](2)R (4, R = 1,2-C6H4; 5, R = 1,3-C6H4 ; 6, R = 1,4-C6H4). 1, 3, and 4 were characterized by X-ray structure determinations. For 1, a = 11.780(3) Angstrom, b = 10.662(3) Angstrom, c = 11.642(3) Angstrom, beta = 118.61(2)degrees, and V = 1283.7(6) An gstrom(3) while, for 2, a = 11.497(2) Angstrom, b = 22.796(6) Angstrom , c = 15.801(3) Angstrom, beta = 106.08(1)degrees, and V = 3979(2) Ang strom(3). Only poor quality crystals of 4 could be obtained resulting in a partial structure refinement with a = 14.46(1) Angstrom, b = 15.1 4(1) Angstrom, c = 21.32(2) Angstrom, alpha = 69.45(4)degrees, beta = 71.14(5)degrees, gamma = 81.86(5)degrees and V = 4140(6) Angstrom(3). The preferred conformation for 1 places the the bipyridine groups anti with respect to each other. However, as a consequence of the coordina tion to the metal centers in 3 and 4, they are located cis to each oth er, and the cyclopentadienyl rings attached directly to the vinyl grou ps lie on the same plane. In compound 4 the planes containing the plat inum bipyridine units lie above and below the plane of the benzene rin g, presumably to minimize steric hindrance. 2 also reacts with 1,3,5-t ris(bromomethyl)mesitylene, 1,2,4,5-tetrakis(bromomethyl)benzene, and 1,2,3,4,5,6-hexakis(bromomethyl)benzene in 3:1, 4:1, and 6:1 molar rat ios to yield the dendritic molecules [PtMe2Br(bpy-Fc(2))CH2-](n)R [7, n = 3, R = 1,3,5-C-6(CH3)(3); 8, n = 4, R = 1,2,4,5-C6H2; 9, n = 6, R = 1,2,3,4,5,6-C-6], respectively. The largest dendrimer 9 contains six platinum and 12 ferrocene centers. Each complex undergoes a single 2n -electron electrochemical oxidation (corresponding to the ferrocenium/ ferrocene couple of the bpy-Fc(2) ligands), confirming that the pendan t ferrocenyl units are noninteracting. The number of ferrocene centers for each complex was determined both by exhaustive electrolysis and b y a chronocoulometric/voltammetric assay.