NEW ADDUCTS OF DIRHODIUM(II) FORMAMIDINATE COMPLEXES WITH POLYCYANO ACCEPTOR MOLECULES - X-RAY CRYSTAL-STRUCTURE OF THE TRICYANOMETHANIDE COMPLEX RH-2(FORM)(4)[C(CN)(3)] (FORM EQUALS N,N'-DI-P-TOLYLFORMAMIDINATE)

Citation
S. Loschiavo et al., NEW ADDUCTS OF DIRHODIUM(II) FORMAMIDINATE COMPLEXES WITH POLYCYANO ACCEPTOR MOLECULES - X-RAY CRYSTAL-STRUCTURE OF THE TRICYANOMETHANIDE COMPLEX RH-2(FORM)(4)[C(CN)(3)] (FORM EQUALS N,N'-DI-P-TOLYLFORMAMIDINATE), Inorganic chemistry, 36(6), 1997, pp. 1004-1012
Citations number
57
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
36
Issue
6
Year of publication
1997
Pages
1004 - 1012
Database
ISI
SICI code
0020-1669(1997)36:6<1004:NAODFC>2.0.ZU;2-5
Abstract
The dirhodium(II) formamidinate complexes Rh-2(form)(2)(O2CCF3)(2)(H2O )(2) (I) and Rh-2(form)(4) (II, form = N,N'-di-p-tolylformamidinate) r eact with the polycyano acceptor molecules tetracyanoethylene (TCNE), tetracyano-p-quinodimethane (TCNQ), 2,5-dimethyl-N,N'-dicyano-p-quinon ediimine (2,5-DMDCNQI), and N,N'-naphthocyano-p-quinonediimine (NCNQI) giving species whose nature is critically dependent on the redox pote ntials of the two parent complexes. Complex I reacts via axial coordin ation with negligible charge transfer (CT) from the dimetal unit to th e ligand. With TCNE, it gives the labile monoaxial adduct Rh-2(form)(2 )(O2CCF3)(2)(TCNE) (1), which easily loses the cyano ligand restoring the parent complex. TCNQ, 2,5-DMDCNQI, and NCNQI react with I giving p olymeric materials of composition {[Rh-2(form)(2)(O2CCF3)(2)](2)TCNQ)} (n) (2) and [Rh-2(form)(2)(O2CCF3)(2)X](n) (X = 2,5-DMDCNQI (3), NCNQI (4)). The reaction of II with TCNE, TCNQ, and 2,5-DMDCNQI proceeds vi a a single electron transfer from the dimetal unit to the cyano ligand to form the CT species [Rh-2(form)(4)X] (X = TCNE (5), TCNQ (6), 2,5- DMDCNQI (7)). Electrochemical and EPR measurements suggest a different extent of coordination between the polycyano fragment and the dirhodi um unit, depending upon the polarity of the solvents. Attempts to crys tallize complex 5 from acetonitrile unexpectedly led to the formation of the tricyanomethanide complex Rh-2(form)(4)[C(CN)(3)] (5A), arising from the unprecedented transformation of the tetracyanoethylenide ion into the tricyanomethanide anion. The complex crystallizes in the tet ragonal P4/ncc space group with a = 14.169(6) Angstrom, c = 29.20(2) A ngstrom, V = 5863(5) Angstrom(3), and Z = 4. The molecule consists of a dirhodium unit symmetrically bridged by four formamidinate ligands a nd one tricyanomethanide anion N-coordinated at the axial position of Rh(2).