The magnetic properties of two series of dinuclear complexes, and one trinuclear complex, have been examined as a function of the bridging pathway between the metal centers. The first series of dinuclear complexes is [{MoV(O)(Tp*)Cl}2(í-OO)], where “OO” is [1,4-O(C6H4)nO]2- (n ) 1, 1; n ) 2, 3), [4,4¢-O(C6H3-2-Me)2O]2- (4), or [1,3-OC6H4O]2- (2) [Tp* ) tris(3,5-dimethylpyrazolyl)hydroborate]. The second series of dinuclear complexes is [{MoI(NO)(Tp*)Cl}2(í-NN)], where “NN” is 4,4¢-bipyridyl (5), 3,3¢-dimethyl-4,4¢-bipyridine (6), 3,8-phenanthroline (7), or 2,7-diazapyrene (8). The trinuclear complex is [{MoV(O)(Tp*)Cl}3(1,3,5-C6H3O3)] (9), whose crystal structure was determined [9â5CH2Cl2: C56H81B3Cl13Mo3N18O6; monoclinic, P21/n; a ) 13.443, b ) 41.46(2), c ) 14.314(6) Å; â ) 93.21(3)°; V ) 7995(5) Å3; Z ) 4; R1 ) 0.106]. In these complexes, the sign and magnitude of the exchange coupling constant J is clearly related to both the topology and the conformation of the bridging ligand [where J is derived from H ) -J S1âS2 for 1-8 and H ) -J(S1âS2 + S2âS3 + S1âS3) for 9]. The values are as follows: 1, -80 cm-1; 2, +9.8 cm-1; 3, -13.2 cm-1; 4, -2.8 cm-1; 5, -33 cm-1; 6, -3.5 cm-1; 7, -35.6 cm-1; 8, -35.0 cm-1; 9, +14.4 cm-1. In particular the following holds: (1) J is negative (antiferromagnetic exchange) across the para-substituted bridges ligands of 1 and 3-8 but positive (ferromagnetic exchange) across the meta-substituted bridging ligands of 2 and 9. (2) J decreases in magnitude dramatically as the bridging ligand conformation changes from planar to twisted (compare 3 and 4, or 6 and 8). These observations are consistent with a spin-polarization mechanism for the exchange interaction, propagated across the ð-system of the bridging ligand by Via overlap of bridging ligand p(ð) orbitals with the d(ð) magnetic orbitals of the metals. The EPR spectrum of 9 is characteristic of a quartet species and shows weak ¢ms ) 2 and ¢ms ) 3 transitions at one-half and one-third, respectively, of the field strength of the principal ¢ms ) 1 component.

Roles of Bridging Ligand Topology and Conformation in Controlling Exchange Interactions between Paramagnetic Molybdenum Fragments in Dinuclear and Trinuclear Compounds / V. AN UNG; A. M. W. CARGILL THOMPSON; D. A. BARDWELL; D. GATTESCHI; J. C. JEFFERY; J. A. MACCLEVERTY; F. TOTTI; M. D. WARD. - In: INORGANIC CHEMISTRY. - ISSN 0020-1669. - STAMPA. - 36:(1997), pp. 3447-3454.

Roles of Bridging Ligand Topology and Conformation in Controlling Exchange Interactions between Paramagnetic Molybdenum Fragments in Dinuclear and Trinuclear Compounds

GATTESCHI, DANTE;TOTTI, FEDERICO;
1997

Abstract

The magnetic properties of two series of dinuclear complexes, and one trinuclear complex, have been examined as a function of the bridging pathway between the metal centers. The first series of dinuclear complexes is [{MoV(O)(Tp*)Cl}2(í-OO)], where “OO” is [1,4-O(C6H4)nO]2- (n ) 1, 1; n ) 2, 3), [4,4¢-O(C6H3-2-Me)2O]2- (4), or [1,3-OC6H4O]2- (2) [Tp* ) tris(3,5-dimethylpyrazolyl)hydroborate]. The second series of dinuclear complexes is [{MoI(NO)(Tp*)Cl}2(í-NN)], where “NN” is 4,4¢-bipyridyl (5), 3,3¢-dimethyl-4,4¢-bipyridine (6), 3,8-phenanthroline (7), or 2,7-diazapyrene (8). The trinuclear complex is [{MoV(O)(Tp*)Cl}3(1,3,5-C6H3O3)] (9), whose crystal structure was determined [9â5CH2Cl2: C56H81B3Cl13Mo3N18O6; monoclinic, P21/n; a ) 13.443, b ) 41.46(2), c ) 14.314(6) Å; â ) 93.21(3)°; V ) 7995(5) Å3; Z ) 4; R1 ) 0.106]. In these complexes, the sign and magnitude of the exchange coupling constant J is clearly related to both the topology and the conformation of the bridging ligand [where J is derived from H ) -J S1âS2 for 1-8 and H ) -J(S1âS2 + S2âS3 + S1âS3) for 9]. The values are as follows: 1, -80 cm-1; 2, +9.8 cm-1; 3, -13.2 cm-1; 4, -2.8 cm-1; 5, -33 cm-1; 6, -3.5 cm-1; 7, -35.6 cm-1; 8, -35.0 cm-1; 9, +14.4 cm-1. In particular the following holds: (1) J is negative (antiferromagnetic exchange) across the para-substituted bridges ligands of 1 and 3-8 but positive (ferromagnetic exchange) across the meta-substituted bridging ligands of 2 and 9. (2) J decreases in magnitude dramatically as the bridging ligand conformation changes from planar to twisted (compare 3 and 4, or 6 and 8). These observations are consistent with a spin-polarization mechanism for the exchange interaction, propagated across the ð-system of the bridging ligand by Via overlap of bridging ligand p(ð) orbitals with the d(ð) magnetic orbitals of the metals. The EPR spectrum of 9 is characteristic of a quartet species and shows weak ¢ms ) 2 and ¢ms ) 3 transitions at one-half and one-third, respectively, of the field strength of the principal ¢ms ) 1 component.
1997
36
3447
3454
V. AN UNG; A. M. W. CARGILL THOMPSON; D. A. BARDWELL; D. GATTESCHI; J. C. JEFFERY; J. A. MACCLEVERTY; F. TOTTI; M. D. WARD
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/256946
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