We report the synthesis and physical characterization of a series of periph
erally functionalized porphyrazines (pzs) of the forms Hr[pz(A;B-3)] and tr
ans-H-2[pz(A(2);B-2)], where A is a dithiolene chelate of molybdocene or va
nadocene and B is a solublizing group. The precursor pz's 8 and 9, of the f
orm H-2[pz(A;B-3)], where A = (4-(butyloxycarbonyl)-S-benzyl)(2) and B = di
-tert-butylphenyl (8) or di-n-propyl (9), have been prepared, deprotected,
and peripherally metalated with molybdocene and vanadocene to form 1(Mo-IV)
and 1(V-IV), prepared from 8, and 2(Mo-IV) from 9, respectively. Likewise,
the protected trans-H-2[pz(A(2);B-2)]. where A = (S-benzyl)(2) and B = 3,6
-butyloxybenzene (12) or A = (S-benzyl)(2) and B = (tert-butylphenyl)(2) (1
3), have been prepared and peripherally metalated with molybdocene and vana
docene to give the trans dinuclear complexes, 3(Mo-IV,Mo-IV), 3(V-IV,V-IV)
(from 12), and 4(V-IV,V-IV) (from 13). A crystal structure of the trans van
adocene pz 4(V-IV,V-IV) is presented; the distance between the two vanadium
atoms is 14.5 Angstrom. The molybdocene-appended pz's are highly redox act
ive and exhibit cyclic voltammograms that are more than just the sum of the
metallocene and the parent pz's. Chemical oxidation with FcPF(6) gives the
Mo-V species 1(Mo-V), 2(Mo-V), 3(Mo-V,Mo-IV), and 3(Mo-V,Mo-V). Their EPR
spectra are indicative of extensive delocalization from the MoV into the di
thiolato-pz. The EPR spectrum of the mononuclear paramagnetic vanadocene pz
, 1(V-IV), shows an expected 8-line pattern for an S = 2 system with hyperf
ine coupling to a single V-51 (I = 7/2) nucleus, but the dinuclear vanadoce
ne pz's, 3(V-IV,V-IV) and 4(V-IV,V-IV), exhibit a striking 15-line pattern
of the same breadth from the S = 1 state formed by exchange coupling betwee
n the S = 2 vanadium centers of a dinuclear complex. Thus, the porphyrazine
macrocycle is capable of mediating magnetic exchange interactions between
metal ions bound to the periphery, separated by 14.5 Angstrom.