Self-Assembled Heterometallic Complexes by Incorporation of Calcium or Strontium Ion into a Manganese(II) 12-Metallacrown-3 Framework Supported by a Tripodal Ligand with Pyridine-Carboxylate Motifs: Stability in Their Manganese(III) Oxidized Form.

We report on the isolation of a new family of µ-carboxylato-bridged metallocrown (MC) compounds by self-assembly of the recently isolated hexadentate tris(2-pyridylmethyl)amine ligand tpada2- incorporating two carboxylate units with metal cations. Twelve-membered MCs of manganese of the type 12-MC-3, namely, [{MnII(tpada)}3(M)(H2O)n]2+ (Mn3M) (M = Mn2+ (n = 0), Ca2+ (n = 1), or Sr2+ (n = 2)), were structurally characterized. The metallamacrocycles connectivity consisting in three -[Mn-O-C-O]- repeating units is provided by one carboxylate unit of the three tpada2- ligands, while the second carboxylate coordinated a fourth cation in the central cavity of the MC, Mn2+ or an alkaline earth metal, Ca2+ or Sr2+. Mn3Ca and {Mn3Sr}2 join the small family of heterometallic manganese-calcium complexes and even rarer manganese-strontium complexes as models of the OEC of photosystem II (PSII). A 8-MC-4 of strontium of the molecular wheel type with four -[Sr-O]- repeating unit was also isolated by self-assembly of the tpada2- ligand with Sr2+. This complex, namely, [Sr(tpada)(OH2)]4 (Sr4), does not incorporate any cation in the central cavity but instead four water molecules coordinated to each Sr2+. Electrochemical investigations coupled to UV-visible absorption and EPR spectroscopies as well as electrospray mass spectrometry reveal the stability of the 12-MC-3 tetranuclear structures in solution, both in the initial oxidation state, MnII3M, as well as in the three-electrons oxidized state, MnIII3M. Indeed, the cyclic voltammogram of all these complexes exhibits three-successive reversible oxidation waves between +0.5 and +0.9 V corresponding to the successive one-electron oxidation of the Mn(II) ion into Mn(III) of the three {Mn(tpada)} units constituting the ring, which are fully maintained after bulk electrolysis.

Seven Reversible Redox Processes in a Self-Assembled Cobalt Pentanuclear Bis(triple-stranded helicate): Structural, Spectroscopic, and Magnetic Characterizations in the CoICoII4, CoII5, and CoII3CoIII2 Redox States.

We report on the synthesis and structural characterization of the cobalt pentanuclear helicate complex from the rigid tetradentate bis(2-pyridyl)-3,5-pyrazolate ligand bpp-, namely, [{CoII(µ-bpp)3}2CoII3(µ3-OH)]3+ (13+), in which a trinuclear {CoII3(µ3-OH)} core is wrapped by two {CoII(µ-bpp)3} units. The cyclic voltammogram of 13+ in CH3CN revealed seven successive reversible one-electron waves, in the 0 and -3.0 V potential range, highlighting the remarkable stability of such architecture in several redox states. Two mixed-valent states of this complex, the two-electron-oxidized CoII3CoIII2 (15+) and the one-electron-reduced species CoICoII4 (12+), were generated by bulk electrolyses and successfully characterized by single-crystal X-ray diffraction among the eight redox levels between CoI5 and CoII3CoIII2 that can be accessed under electrochemical conditions. Because of the crystallographic characterization of 15+ and 12+, the five reduction processes located at E1/2 values of -1.63 (13+/2+), -1.88 (12+/+), -2.14 (1+/0), -2.40 (10/-), and -2.60 V (1-/2-) versus Ag/AgNO3 were unambiguously assigned to the successive reduction of each of the five Co(II) ions to Co(I), starting with the three ions located in the central core followed by the two apical ions. The two other redox events at E1/2 values of -0.21 (14+/3+) and -0.11 V (15+/4+) are assigned to the successive oxidation of the apical Co(II) ions to Co(III). The Co(I) complexes are rare, and the stabilization of a Co(I) within a trinuclear µ-hydroxo core in the reduced species, 12+, 1+, 10, 1-, and 12-, is probably the result of the particular structure of this complex in the presence of the two apical sites that maintain the trinuclear core through the six bridging bpp- ligands. The spectroscopic characteristics of 12+, 13+, and 15+ (ultraviolet-visible and X-band electron paramagnetic resonance) are also described as well as their magnetic properties in the solid state.

Redox Self-Adaptation of a Nitrene Transfer Catalyst to the Substrate Needs.

The development of iron catalysts for carbon-heteroatom bond formation, which has attracted strong interest in the context of green chemistry and nitrene transfer, has emerged as the most promising way to versatile amine synthetic processes. A diiron system was previously developed that proved efficient in catalytic sulfimidations and aziridinations thanks to an FeIII FeIV active species. To deal with more demanding benzylic and aliphatic substrates, the catalyst was found to activate itself to a FeIII FeIV L. active species able to catalyze aliphatic amination. Extensive DFT calculations show that this activation event drastically enhances the electron affinity of the active species to match the substrates requirements. Overall this process consists in a redox self-adaptation of the catalyst to the substrate needs.

Intramolecular Electron Transfers Thwart Bistability in a Pentanuclear Iron Complex.

With the intention to investigate the redox properties of polynuclear complexes as previously reported for the pentamanganese complex [{Mn(II)(µ-bpp)3}2Mn(III)Mn(II)2(µ3-O)](3+) (2(3+)), we focused on the analogous pentairon complex that was previously isolated as all-ferrous. As Masaoka and co-workers recently published, aerobic synthesis leads to the [{Fe(II)(µ-bpp)3}2Fe(III)Fe(II)2(µ3-O)](3+) complex (1(3+)). This species exhibits in acetonitrile solution four reversible one-electron oxidation waves. Accordingly, the three oxidized species 1(4+), 1(5+), and 1(6+) with a 3Fe(II)2Fe(III), 2Fe(II)3Fe(III), and 1Fe(II)4Fe(III) composition, respectively, were generated by bulk electrolysis and isolated. Mössbauer spectroscopy allowed us to determine the spin states of all the iron ions and to unambiguously locate the sites of the successive oxidations. They all occur in the µ3-oxo core except for the 1(4+) to 1(5+) process that presents a striking electronic rearrangement, with both metals in axial position being oxidized while the core is reduced to the [Fe(III)Fe(II)2(µ3-O)](5+) oxidation level. This strongly differs from the redox behavior of the Mn5 system. The origin of this electronic switch is discussed.

Reaction of PerR with Molecular Oxygen May Assist H2O2 Sensing in Anaerobes.

PerR is the peroxide resistance regulator found in several pathogenic bacteria and governs their resistance to peroxide stress by inducing enzymes that destroy peroxides. However, it has recently been implicated as a key component of the aerotolerance in several facultative or strict anaerobes, including the highly pathogenic Staphylococcus aureus. By combining (18)O labeling studies to ESI- and MALDI-TOF MS detection and EMSA experiments, we demonstrate that the active form of PerR reacts with dioxygen, which leads ultimately to disruption of the PerR/DNA complex and is thus physiologically meaningful. Moreover, we show that the presence of O2 assists PerR sensing of H2O2, another feature likely to be important for anaerobic organisms. These results allow one to envisage different scenarios for the response of anaerobes to air exposure.

Hydrazine N-N Bond Cleavage over Silica-Supported Tantalum-Hydrides.

Hydrazine reacts with silica-supported tantalum-hydrides [(≡SiO)2TaHx] (x = 1, 3), 1, under mild conditions (100 °C). The IR in situ monitoring of the reaction with N2H4 or (15)N2H4, and the solid-state MAS NMR spectra of the fully (15)N labeled compounds (CP (15)N, (1)H-(15)N HETCOR, (1)H-(1)H double-quantum, and (1)H-(1)H triple-quantum spectra) were used to identify stable intermediates and products. DFT calculations were used for determining the reaction pathway and calculating the (15)N and (1)H NMR chemical shifts. Combining the experimental and computational studies led to the following results. At room temperature, only hydrazine adducts, 1-N2H4, are formed. Upon heating at 100 °C, the hydrazine adducts are converted to several species among which [(≡SiO)2Ta(═NH)(NH2)], 2, [(≡SiO)2TaH(NH2)2], 3, and [(≡SiO)2TaH2(NH-NH2)], 4, were identified. The final product 2 is also formed in the reaction of N2 with the same silica-supported tantalum-hydride complexes, and the species identified as 3 and 4 had been previously suggested by DFT studies as intermediates on the reaction pathway for N-N cleavage in N2. The present computational studies (cluster models with M06 functional complemented by selected calculations with periodic calculations) show that 2 is formed via 3 and 4, with either N2 or N2H4. This strengthens the previous proposal of the existence of 3 and 4 as intermediates in the reaction of N2 with the tantalum-hydrides. However, the reaction of N2 does not imply the formation of N2H4 or its hydrazido monoanionic or dianionic ligand as an intermediate. For this reason, this study informs both on the similarities and differences of the reaction pathways involving N2 and N2H4 with tantalum-hydrides.

Calcium and heterometallic manganese-calcium complexes supported by tripodal pyridine-carboxylate ligands: structural, EPR and theoretical investigations.

Carboxylate-bridged Mn(II)-Ca(II) complexes are potentially relevant for mimicking the first stages of the Oxygen-Evolving Complex (OEC) assembly process. Here, we report on new homonuclear Ca(II) and heteronuclear Mn(II)­Ca(II) complexes with carboxylate-functionalized tripodal tris(2-pyridylmethyl)amine ligands, the heptadentate H3tpaa, previously reported, and the new hexadentate H2tpada, containing respectively three and two carboxylate units. The mononuclear [Ca(Htpaa)(OH2)] (Ca1) and dinuclear [Ca(tpada)(OH2)2]2 (Ca2) calcium complexes, as well as the tetranuclear [{Mn(tpaa)}2{Ca(OH2)5(µ-OH2)}2][Mn(tpaa)]2 (Mn2Ca2·2Mn) and dinuclear [Mn(tpada)ClCa(OH2)2.67(MeOH)2.33]Cl (MnCa) heterometallic species have been structurally characterized; the syntheses of Ca1 and Mn2Ca2·2Mn being previously reported by us (Inorg. Chem., 2015, 54, 1283). The Mn(II) and Ca(II) are linked by two µ1,1-bridging carboxylates in MnCa, while only one µ1,3-carboxylate bridge connects each Ca2+ ion to each Mn(II) in Mn2Ca2. A variable number of water molecules (n = 1 to 7) are coordinated to Ca in all complexes, most of them being involved in hydrogen-bond networks, in analogy to what occurs in the photosystem II. All donor atoms of the tpaa3- and tpada2- ligands are coordinated to the Mn2+ ions, despite the unusually long distance between the Mn2+ ion and the tertiary amine imposed by the constraining nature of the ligands, as supported by theoretical calculations. Solid state EPR spectroscopy, in combination with DFT calculations, has also shown that the Ca2+ ion has an effect on the electronic parameters (zero field splitting) of the linked Mn(II) in the case of MnCa (µ1,1-carboxylate bridges). In Mn2Ca2 (µ1,3-carboxylate bridge) the Ca2+ ion induces only slight structural changes in the Mn coordination sphere.

Deprotonation in Mixed-Valent Diiron(II,III) Complexes with Aniline or Benzimidazole Ligands.

We have previously investigated cis/trans isomerization processes in phenoxido-bridged mixed-valent Fe(II)Fe(III) complexes that contain either one aniline or one anilide ligand. In this work, we compare the properties of similar complexes bearing one terminal protic ligand, either aniline or 1H-benzimidazole. Whatever the ligand, (1)H NMR spectroscopy clearly evidences that the complexes are present in CH3CN as a mixture of cis- and trans-isomers in a close to 1:1 ratio. We show here that addition of NEt3 indeed allows the deprotonation of these ligands, the resulting complexes bearing either anilide or benzimidazolide that are coordinated to the ferric site. The latter are singular examples of a high-spin ferric ion coordinated to a benzimidazolide ligand. Whereas the trans-isomer of the anilide complex is the overwhelming species, benzimidazolide species are mixtures of cis- and trans-isomers in equal proportions. Moreover, cyclic voltammametry studies show that Fe(III)Fe(III) complexes with 1H-benzimidazole are more stable than their aniline counterparts, whereas the reverse is observed for the deprotonated species.

Phosphoester hydrolysis: the incoming substrate turns the bridging hydroxido nucleophile into a terminal one.

Identifying the active nucleophile in hydrolysis reactions catalyzed by binuclear hydrolases is a recurrent problem and a matter of intense debate. We report on the phosphate ester hydrolysis by a Fe(III)Fe(II) complex of a binucleating ligand. This complex presents activities in the range of those observed for similar biomimetic compounds in the literature. The specific electronic properties of the Fe(III)Fe(II) complex allowed us to use (1)H NMR and Mössbauer spectroscopies to investigate the nature of the various species present in the solution in the pH range of 5-10. Both techniques showed that the hydrolysis activity is associated to a µ-hydroxido Fe(III)Fe(II) species. Further (1)H NMR experiments show that binding of anions or the substrate changes this bonding mode suggesting that a terminal hydroxide is the likely nucleophile in these hydrolysis reactions. This view is further supported by the structure determination of the hydrolysis product.

Ca K-edge XAS as a probe of calcium centers in complex systems.

Herein, Ca K-edge X-ray absorption spectroscopy (XAS) is developed as a means to characterize the local environment of calcium centers. The spectra for six, seven, and eight coordinate inorganic and molecular calcium complexes were analyzed and determined to be primarily influenced by the coordination environment and site symmetry at the calcium center. The experimental results are closely correlated to time-dependent density functional theory (TD-DFT) calculations of the XAS spectra. The applicability of this methodology to complex systems was investigated using structural mimics of the oxygen-evolving complex (OEC) of PSII. It was found that Ca K-edge XAS is a sensitive probe for structural changes occurring in the cubane heterometallic cluster due to Mn oxidation. Future applications to the OEC are discussed.

Cis/trans isomerizations in diiron complexes involving aniline or anilide ligands.

We have recently reported a deprotonation-induced valence inversion within a phenoxido-bridged mixed-valent diiron(II,III) complex. The initial aniline coordinated to the Fe(II) site reacts with triethylamine, and the resulting complex contains an anilide ligand coordinated to the Fe(III) ion. The behavior of these complexes in acetonitrile is indeed more intricate. Owing to the very distinctive spectroscopic signatures of the complexes, the conjunction of NMR, Mössbauer, and UV-visible absorption spectroscopies allows one to evidence two isomerization reactions, one involving the aniline linked to Fe(II) and the other the anilide on Fe(III). Theoretical calculations sustain this conclusion. Aniline in the cis position versus the bridging phenoxide is shown to be the most stable isomer while the anilide trans to the phenoxido bridge is favored. The trans isomer of the aniline complex is more acidic than the cis one by 1 pKa unit. Isomerization of the anilide complex is 10 times faster than the analogous isomerization of the aniline complex. Both reactions are proposed to proceed through a unique mechanism. This is the first time that such isomerization reactions are evidenced in dinuclear complexes.

A diiron(III,IV) imido species very active in nitrene-transfer reactions.

Metal-catalyzed nitrene transfer reactions arouse intense interest as clean and efficient procedures for amine synthesis. Efficient Rh- and Ru-based catalysts exist but Fe alternatives are actively pursued. However, reactive iron imido species can be very short-lived and getting evidence of their occurrence in efficient nitrene-transfer reactions is an important challenge. We recently reported that a diiron(III,II) complex is a very efficient nitrene-transfer catalyst to various substrates. We describe herein how, by combining desorption electrospray ionization mass spectrometry, quantitative chemical quench experiments, and DFT calculations, we obtained conclusive evidence for the occurrence of an {Fe(III) Fe(IV) NTosyl} intermediate that is very active in H-abstraction and nitrene-transfer reactions. DFT calculations revealed a strong radical character of the tosyl nitrogen atom in very low-lying electronic configurations of the Fe(IV) ion which are likely to confer its high reactivity.

Successive heterolytic cleavages of H2 achieve N2 splitting on silica-supported tantalum hydrides: a DFT proposed mechanism.

DFT(B3PW91) calculations have been carried out to propose a pathway for the N(2) cleavage by H(2) in the presence of silica-supported tantalum hydride complexes [(≡SiO)(2)TaH(x)] that forms [(≡SiO)(2)Ta(NH)(NH(2))] (Science 2007, 317, 1056). The calculations, performed on the cluster models {µ-O[(HO)(2)SiO](2)}TaH(1) and {µ-O[(HO)(2)SiO](2)}TaH(3), labelled as (≡SiO)(2)TaH(x) (x = 1, 3), show that the direct hydride transfers to coordinated N-based ligands in (≡SiO)(2)TaH(η(2)-N(2)) and (≡SiO)(2)TaH(η(2)-HNNH) have high energy barrier barriers. These high energy barriers are due in part to a lack of energetically accessible empty orbitals in the negatively charged N-based ligands. It is shown that a succession of proton transfers and reduction steps (hydride transfer or 2 electron reduction by way of dihydride reductive coupling) to the nitrogen-based ligands leads to more energetically accessible pathways. These proton transfers, which occur by way of heterolytic activation of H(2), increase the electrophilicity of the resulting ligand (diazenido, N(2)H(-), and hydrazido, NHNH(2)(-), respectively) that can thus accept a hydride with a moderate energy barrier. In the case of (≡SiO)(2)TaH(η(2)-HNNH), the H(2) molecule that is adding across the Ta-N bond is released after the hydride transfer step by heterolytic elimination from (≡SiO)(2)TaH(NH(2))(2), suggesting that dihydrogen has a key role in assisting the final steps of the reaction without itself being consumed in the process. This partly accounts for the experimental observation that the addition of H(2) is needed to convert an intermediate, identified as a diazenido complex [(≡SiO)(2)TaH(η(2)-HNNH)] from its ν(N-H) stretching frequency of 3400 cm(-1), to the final product. Throughout the proposed mechanism, the tantalum remains in its preferred high oxidation state and avoids redox-type reactions, which are more energetically demanding.

Shifting from Ziegler-Natta to Philips-type catalyst? A simple and safe access to reduced titanium systems for ethylene polymerization.

Silica-supported titanium(IV) chloride is readily reduced by Mashima and co-workers' reagent (1-methyl-3,6-bis(trimethylsilyl)-1,4-cyclohexadiene) to afford materials active in ethylene polymerisation without need of aluminum alkyl cocatalyst.

Reversible (de)protonation-induced valence inversion in mixed-valent diiron(II,III) complexes.

The coupling of electron and proton transfers is currently under intense scrutiny. This Communication reports a new kind of proton-coupled electron transfer within a homodinuclear first-row transition-metal complex. The triply-bridged complex [Fe(III)(µ-OPh)(µ(2)-mpdp)Fe(II)(NH(2)Bn)] (1; mpdp(2-) = m-phenylenedipropionate) bearing a terminal aminobenzyl ligand can be reversibly deprotonated to the anilinate complex 2 whose core [Fe(II)(µ-OPh)(µ(2)-mpdp)Fe(III)(NHBn)] features an inversion of the iron valences. This observation is supported by a combination of UV-visible, (1)H NMR, and Mössbauer spectroscopic studies.