Search PubMed⌕ Search

Biomedical subjects

Santiago Herrero

Publications and source records attributed to Santiago Herrero.

7 recordsLinked to original sources

Equatorially connected diruthenium(II,III) units toward paramagnetic supramolecular structures with singular magnetic properties.

The reaction of Ru2Cl(O2CMe)(DPhF)3 (DPhF = N,N'-diphenylformamidinate) with mono- and polycarboxylic acids gives a clean substitution of the acetate ligand, leading to the formation of complexes Ru2Cl(O2CC6H5)(DPhF)3 (1), Ru2Cl(O2CC6H4-p-CN)(DPhF)3 (2), [Ru2Cl(DPhF)3(H2O)]2(O2C)2 (3), [Ru2Cl(DPhF)3]2[C6H4-p-(CO2)2] (4), and [Ru2Cl(DPhF)3]3[C6H3-1,3,5-(CO2)3] (5). The preparation of [Ru2(NCS)(DPhF)3]3[C6H3-1,3,5-(CO2)3] (6) and {[Ru2(DPhF)3(H2O)]3[C6H3-1,3,5-(CO2)3]}(SO3CF3)3 (7) from 5 is also described. All complexes are characterized by elemental analysis, IR and electronic spectroscopy, mass spectrometry, cyclic voltammetry, and variable-temperature magnetic measurements. The crystal structure determinations of complexes 2.0.5THF and 3.THF.4H2O (THF = tetrahydrofuran) are reported. The reactions carried out demonstrate the high chemical stability of the fragment [Ru2(DPhF)3]2+, which is preserved in all tested experimental conditions. The stability of this fragment is also corroborated by the mass spectra. Electrochemical measurements reveal in all complexes one redox process due to the equilibrium Ru2(5+) <--> Ru2(6+). In the polynuclear complex 7, some additional oxidation processes are also observed that have been ascribed to the presence of two types of dimetallic units rather than two consecutive reversible oxidations. The magnetic behavior toward temperature for complexes 1-7 from 300 to 2 K is analyzed. Complexes 1-7 show low values of antiferromagnetic coupling in accordance with the molecular nature in 1 and 2 and the absence of important antiferromagnetic interaction through the carboxylate bridging ligands in 3-7, respectively. In addition, the magnetic properties of complex 7 do not correspond to any magnetic behavior described for diruthenium(II,III) complexes. The experimental data of compound 7 are simulated considering a physical mixture of S = 1/2 and 3/2 spin states. This magnetic study demonstrates the high sensitivity of the electronic configuration of the unit [Ru2(DPhF)3]2+ to small changes in the nature of the axial ligands. Finally, the energy gap between the pi and delta orbitals in these types of compounds allows the tentative assignment of the transition pi --> delta.

Journal Article↗

Mixed Chloride/Amine Complexes of Dimolybdenum(II,II). 4. Rotational Isomers of Mo(2)Cl(4)(R-py)(4) (R-py = 4-Picoline, 3,5-Lutidine, and 4-tert-Butylpyridine).

The quadruply bonded dimolybdenum complexes with alkyl-substituted pyridines of the formula Mo(2)Cl(4)(R-py)(4) (R-py = 4-pic (4-methylpyridine) (1), 3,5-lut (3,5-dimethylpyridine) (2), and 4-Bu(t)-py (4-tert-butylpyridine) (3)) have been prepared. Nine different compounds, in which there are 11 independent molecules, have been obtained in crystalline form, and their crystal structures have been investigated by X-ray diffraction. Three types of geometric isomers which differ by the angle of internal rotation about the Mo-Mo axis have been recognized in these structures. The eclipsed structures 1-3a display pyridine ligands opposite to each other across the metal-metal bond and have a virtual symmetry D(2)(h)(). The noncentrosymmetric D(2)(d)() structures 1-3b have each pyridine ligand opposite to a Cl atom. The molecules 3c-f have a partially staggered D(2) geometry with N-Mo-Mo-N torsion angles ranging from 10.4 degrees to 25.2 degrees. As a result of this work it is now clear that Mo(2)Cl(4)(R-py)(4) compounds do not show a preference for D(2)(h)() conformation rather than D(2)(d)() conformation. In fact, they seem unusually unrestricted in their rotational conformation, and packing forces appear to have a major influence on the conformation adopted. Further clarification of this question will require spectroscopic study of solutions.

Journal Article↗

Mixed Chloride/Amine Complexes of Dimolybdenum(II,II). 2. Reactions of Mo(2)Cl(4)(NHEt(2))(4) with Monodentate and Bidentate Phosphines. New Type of Compounds Mo(2)Cl(4)(diphosphine)(4).

The complex Mo(2)Cl(4)(NHEt(2))(4) (1) undergoes facile substitution reactions of the amine ligands by phosphines to give compounds with the same core structure, Mo(2)Cl(4)(phosphine)(4), where the phosphine is PMe(3) (2), PMe(2)Ph (3), PHEt(2) (4), dmpm (bis(dimethylphosphino)methane) (5), or dmpe (1,2-bis(dimethylphosphino)ethane) (6). Complexes of the type M(2)X(4)L(4) are well-known with monodentate ligands, but there is no previous crystallographically verified example of the M(2)X(4)L(4) type of compound in which L is a potentially bidentate ligand acting as a unidentate ligand. Mo(2)Cl(4)(eta(1)-dmpm)(4) (5) can be isolated in good yield as the kinetic product of the substitution reaction at room temperature. When a solution of 5 in THF is heated, transformation into the more stable compound Mo(2)Cl(4)(&mgr;-dmpm)(2) (7) takes place. Mo(2)Cl(4)(eta(1)-dmpe)(4) (6) is stable in solution in the presence of free phosphine and can be detected by NMR. Over time it converts to a polymeric material which precipitates from the solution. For dppm (bis(diphenylphosphino)methane) (8) and dppa (bis(diphenylphosphino)amine) (9), only products of the stoichiometry Mo(2)Cl(4)(diphosphine)(2) were obtained. The crystal structures of the complexes 4 and 5 have been investigated by X-ray diffraction. The crystallographic parameters for them are as follows: for 4, orthorhombic space group Pbcn with a = 7. 6015(8) Å, b = 20.120(8) Å, c = 19.070(6) Å, and Z = 4; for 5, hexagonal space group P6(4)22 with a = 12.396(1) Å, c = 21.960(2) Å, and Z = 3. Both structures have a Mo(2)Cl(4)P(4) core where the phosphorus atoms are trans one to another on each metal center. The Mo-Mo distances of 2.137(1) Å (4) and 2.137(1) Å (5) are consistent with quadruple bonding.

Journal Article↗

Reactions of {[Pd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd](&mgr;-SC(6)F(5))}(4).2O(C(2)H(5))(2). Crystal Structures of the Complexes [(Ph(3)P)Pd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd(SC(6)F(5))].1.4CH(2)Cl(2) and [(Ph(3)P)Pd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd(PPh(3))]SO(3)CF(3).2CH(2)Cl(2) and ab Initio MO Calculations on the Model Systems [(H(3)P)Pd(&mgr;-H(2)PCH(2)PH(2))(&mgr;-SH)Pd(PH(3))](+) and [(H(3)P)Pd(&mgr;-H(2)PCH(2)PH(2))Pd(PH(3))](2+).

{[Pd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd](&mgr;-SC(6)F(5))}(4) reacts 1:4 with neutral ligands L to give [LPd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd(SC(6)F(5))] or 1:8 to form [LPd(&mgr;-SC(6)F(5))(&mgr;-dppm)PdL](+) (dppm = bis(diphenylphosphino)methane). These binuclear complexes retain the palladium-palladium bond and the two dissimilar bridging ligands, as demonstrated by the X-ray structural determinations carried out on [(Ph(3)P)Pd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd(SC(6)F(5))].1.4CH(2)Cl(2) and [(Ph(3)P)Pd(&mgr;-SC(6)F(5))(&mgr;-dppm)Pd(PPh(3))]SO(3)CF(3).2CH(2)Cl(2). Ab initio calculations on the model systems [(H(3)P)Pd(&mgr;-H(2)PCH(2)PH(2))(&mgr;-SH)Pd(PH(3))](+) and [(H(3)P)Pd(&mgr;-H(2)PCH(2)PH(2))Pd(PH(3))](2+) show that the metal-metal bond arises mainly from interactions between palladium sp orbitals, which also play a predominant role in the binding with the sulfur bridge.

Journal Article↗