DNA Cleaving "Tandem-Array" Metallopeptides Activated With KHSO: Towards the Development of Multi-Metallated Bioactive Conjugates and Compounds.

Amino terminal peptides of the general form Gly-Gly-His have been used to introduce single sites of metal binding and redox activity into a wide range of biomolecules to create bioactive compounds and conjugates capable of substrate oxidation. We report here that Gly-Gly-His-like peptides linked in a tandem fashion can also be generated leading to multi-metal binding arrays. While metal binding by the native Gly-Gly-His motif (typically to Cu, Ni, or Co) requires a terminal peptide amine ligand, previous work has demonstrated that an ornithine (Orn) residue can be substituted for the terminal Gly residue to allow solid-phase peptide synthesis to continue via the side chain -δ.

Understanding intrinsically irreversible, non-Nernstian, two-electron redox processes: a combined experimental and computational study of the electrochemical activation of platinum(IV) antitumor prodrugs.

Six-coordinate Pt(IV)-complexes are prominent prodrug candidates for the treatment of various cancers where, upon two-electron reduction and loss of two axial ligands, they form more familiar, pharmacologically active four-coordinate Pt(II) drugs. A series of electrochemical experiments coupled with extensive density functional calculations has been employed to elucidate the mechanism for the two-electron reduction of Pt(IV)(NH3)2Cl2L2 to Pt(II)(NH3)2Cl2 (L = CH3COO(-), 1; L = CHCl2COO(-), 2; L = Cl(-), 3). A reliable estimate for the normal reduction potential E(o) is derived for the electrochemically irreversible Pt(IV) reduction and is compared directly to the quantum chemically calculated reduction potentials.

Ring-slippage and multielectron redox properties of Fe/Ru/Os-bis(arene) complexes: does hapticity change really cause potential inversion?

Bis(hexamethylbenzene) complexes of the group 8 metals (Fe, Ru, Os) show surprising diversity in their electron-transfer mechanisms and associated thermodynamics for the M(II) → M(I) → M(0) redox series. In electrochemical experiments, the Fe complex exhibits normally ordered potentials separated by ∼1 V, the Ru system shows nearly overlapping one-electron redox events, and Os demonstrates a one-step, two-electron transfer with a peak potential separation suggestive of highly inverted potentials. It has been conjectured that the sequential one-electron transfers observed for Fe are due to the lack of an accessible η(4):η(6) Fe(0) state, destabilizing the fully reduced species.

Two-electron redox energetics in ligand-bridged dinuclear molybdenum and tungsten complexes.

Electron-transfer energetics of bridged dinuclear compounds of the form [(CO)(4)M(mu-L)](2)(0/1-/2-) (M = Mo, W; L = PPh(2)(-), SPh(-)) were explored using density functional theory coupled to a continuum solvation model. The experimentally observed redox potential inversion, a situation where the second of two electron transfers is more thermodynamically favorable than the first, was reproduced within this model. This nonclassical energy ordering is a prerequisite for the apparent transfer of two electrons at one potential, as observed in many biologically and technologically important systems.

Spin crossover-coupled electron transfer of [M(tacn)(2)](3+/2+) complexes (tacn = 1,4,7-triazacyclononane; M = Cr, Mn, Fe, Co, Ni).

The role of spin state equilibria on the thermodynamics of electron transfer in [M(tacn)(2)](3+/2+) complexes (tacn = 1,4,7-triazacyclononane; M = Cr, Mn, Fe, Co, Ni) was examined using density functional theory at the B3LYP*/cc-pVTZ(-f) level coupled to a continuum solvation model to afford excellent agreement between computed and experimental redox properties. An intuitive explanation of the previously observed nonperiodic trend in reduction potentials, which display a sawtooth pattern along the first-row transition metal series, is offered utilizing a novel diagrammatic illustration of the relationship between spin state energetics and reduction potentials. This representation leads to a generalized proposal for analyzing and designing nearly isoenergetic spin states of transition metals in a given ligand environment.

Synthesis, structure, and properties of low-spin manganese(III)-poly(pyrazolyl)borate complexes.

The manganese(III)-bis[poly(pyrazolyl)borate] complexes, Mn(pzb)2SbF6, where pzb- = tetrakis(pyrazolyl)borate (pzTp) (1), hydrotris(pyrazolyl)borate (Tp) (2), or hydrotris(3,5-dimethylpyrazolyl)borate (Tp*) (3), have been synthesized by oxidation of the corresponding Mn(pzb)2 compounds with NOSbF6. The Mn(III) complexes are low-spin in solution and the solid state (microeff = 2.9-3.

Modulation of molybdenum-centered redox potentials and electron-transfer rates by sulfur versus oxygen ligation.

Temperature-dependent measurements of potential, E degrees', and electron-transfer rate constant, k(s,h), are reported for electrochemical reduction (in 0.3 M TBAPF(6)/CH(3)CN) of a series of oxomolybdenum(V) complexes, [(Tp)MoO(X,Y)], where Tp = hydrotris(3,5-dimethyl-1-pyrazolyl)borate and X,Y is a series of bidentate 1,2-disubstituted aliphatic or aromatic ligands in which oxygen donors are replaced sequentially by sulfur. E degrees' values shift in the positive direction, and k(s,h) values increase as O is replaced by S and as the framework of the ligand is changed from aliphatic to aromatic.

Metal-bis[poly(pyrazolyl)borate] complexes. Electrochemical, magnetic, and spectroscopic properties and coupled electron-transfer and spin-exchange reactions.

Electrochemical, magnetic, and spectroscopic properties are reported for homoleptic divalent (M = Mn, Fe, Co, Ni, Ru) and trivalent (M = Cr, Mn, Fe, Co) metal-bis[poly(pyrazolyl)borate] complexes, [M(pzb)(2)](+/0), where pzb(-) = hydrotris(pyrazolyl)borate (Tp), hydrotris(3,5-dimethylpyrazolyl)borate (Tp), or tetrakis(pyrazolyl)borate (pzTp). Ligand field strengths in metal-pzb complexes increase as Tp < Tp < pzTp, which reflects the importance of steric rather than electronic effects on spectroscopic properties. However, metal-centered redox potentials become more negative as pzTp < Tp < Tp, which follows the electron-donating ability of the ligands.

Ligand Structural Effects on the Electrochemistry of Chromium(III) Amino Carboxylate Complexes.

The aqueous electrochemical behavior of 10 Cr(III) complexes with potentially tri- and hexadentate amino carboxylate ligands is reported and is shown to depend on the composition and spatial arrangement of the donor atom set. Complexes with two amine and four carboxylate donors (N(2)O(4)) and two amine, one aquo, and three carboxylate donors (N(2)O(3)O') in which the N atoms are coordinated cis to one another undergo chemically and electrochemically reversible reduction at ca. -1.