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.