Solitaire and gemini metallocene porphyrazines

Citation
Slj. Michel et al., Solitaire and gemini metallocene porphyrazines, J AM CHEM S, 123(20), 2001, pp. 4741-4748
Citations number
27
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
123
Issue
20
Year of publication
2001
Pages
4741 - 4748
Database
ISI
SICI code
0002-7863(20010523)123:20<4741:SAGMP>2.0.ZU;2-G
Abstract
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.