Iron-Catalyzed Parahydrogen Induced Polarization.

Parahydrogen induced polarization (PHIP) can address the low sensitivity problem intrinsic to nuclear magnetic resonance spectroscopy. Using a catalyst capable of reacting with parahydrogen and substrate in either a hydrogenative or nonhydrogenative manner can result in signal enhancement of the substrate. This work describes the development of a rare example of an iron catalyst capable of reacting with parahydrogen to hyperpolarize olefins. Complexes of the form (MesCCC)Fe(H)(L)(N2) (L = Py (Py = pyridine), PMe3, PPh3) were synthesized from the reaction of the parent complexes (MesCCC)FeMes(L) (Mes = mesityl) with H2. The isolated low-spin iron(II) hydride compounds were characterized via multinuclear NMR spectroscopy, infrared spectroscopy, and single crystal X-ray diffraction. (MesCCC)Fe(H)(Py)(N2) is competent in the hydrogenation of olefins and demonstrated high activity toward the hydrogenation of monosubstituted terminal olefins. Reactions with p-H2 resulted in the first PHIP effect mediated by iron which requires diamagnetism throughout the reaction sequence. This work represents the development of a new PHIP catalyst featuring iron, unlocking potential to develop more PHIP catalysts based on first-row transition metals.

Formation of Red Elemental Selenium from Seleniferous Oxyanions: Deoxygenation by a Homogeneous Iron Catalyst.

Seleniferous oxyanions are groundwater contaminants from both anthropogenic and natural sources, while pure amorphous selenium nanoparticles have a variety of industrial applications. Biology can achieve the multicomponent 6 e-/8 H+ reduction of selenate to amorphous selenium using multiple metalloenzymes, like selenate and selenite reductase. Inspired by biology, we developed a new homogeneous system that can generate pure elemental selenium with no caustic waste. The stoichiometric reductions of selenate, selenite, and selenium dioxide with an iron(II) complex produced an iron(III)-oxo and red elemental selenium, the latter of which has been characterized by a variety of spectroscopic techniques. The catalytic reduction of SeO42- and SeO32- directly to amorphous Se and isolated as Se=PPh3 is reported with a turnover number of 12 and 7, respectively.

Secondary Coordination Sphere Influences the Formation of Fe(III)-O or Fe(III)-OH in Nitrite Reduction: A Synthetic and Computational Study.

The reduction of nitrite (NO2-) to generate nitric oxide (NO) is a significant area of research due to their roles in the global nitrogen cycle. Here, we describe various modifications of the tris(5-cyclohexyliminopyrrol-2-ylmethyl)amine H3[N(piR)3] ligand where the steric bulk and acidity of the secondary coordination sphere were explored in the non-heme iron system for nitrite reduction. The cyclohexyl and 2,4,6-trimethylphenyl variants of the ligand were used to probe the mechanism of nitrite reduction. While previously stoichiometric addition of nitrite to the iron(II)-species generated an iron(III)-oxo complex, changing the secondary coordination sphere to mesityl resulted in an iron(III)-hydroxo complex. Subsequent addition of an electron and two protons led to the release of water and regeneration of the starting iron(II) catalyst. This sequence mirrored the proposed mechanism of nitrite reduction in biological systems, where the distal histidine residue shuttles protons to the active site. Computational studies aimed at interrogating the dissimilar behavior of the cyclohexyl and mesityl ligand systems resulting in Fe(III)-oxo and Fe(III)-hydroxo complexes, respectively, shed light on the key role of H-bonds involving the secondary coordination sphere in the relative stability of these species.

Effects of a Tridentate Pincer Ligand on Parahydrogen Induced Polarization.

The role of ligands in rhodium- and iridium-catalyzed Parahydrogen Induced Polarization (PHIP) and SABRE (signal amplification by reversible exchange) chemistry has been studied in the benchmark systems, [Rh(diene)(diphos)]+ and [Ir(NHC)(sub)3 (H)2 ]+ , and shown to have a great impact on the degree of hyperpolarization observed. Here, we examine the role of the flanking moieties in the electron-rich monoanionic bis(carbene) aryl pincer ligand, Ar CCC (Ar=Dipp, 2,6-diisopropyl or Mes, 2,4,6-trimethylphenyl) on the cobalt-catalyzed PHIP and PHIP-IE (PHIP via Insertion and Elimination) chemistry that we have previously reported. The mesityl groups were exchanged for diisopropylphenyl groups to generate the (Dipp CCC)Co(N2 ) catalyst, which resulted in faster hydrogenation and up to 390-fold 1 H signal enhancements, larger than that of the (Mes CCC)Co-py (py=pyridine) catalyst. Additionally, the synthesis of the (Dipp CCC)Rh(N2 ) complex is reported and applied towards the hydrogenation of ethyl acrylate with parahydrogen to generate modest signal enhancements of both 1 H and 13 C nuclei. Lastly, the generation of two (Mes CCC)Ir complexes is presented and applied towards SABRE and PHIP-IE chemistry to only yield small 1 H signal enhancements of the partially hydrogenated product (PHIP) with no SABRE hyperpolarization.

Radical Rebound Hydroxylation Versus H-Atom Transfer in Non-Heme Iron(III)-Hydroxo Complexes: Reactivity and Structural Differentiation.

The characterization of high-valent iron centers in enzymes has been aided by synthetic model systems that mimic their reactivity or structural and spectral features. For example, the cleavage of dioxygen often produces an iron(IV)-oxo that has been characterized in a number of enzymatic and synthetic systems. In non-heme 2-oxogluterate dependent (iron-2OG) enzymes, the ferryl species abstracts an H-atom from bound substrate to produce the proposed iron(III)-hydroxo and caged substrate radical. Most iron-2OG enzymes perform a radical rebound hydroxylation at the site of the H-atom abstraction (HAA); however, recent reports have shown that certain substrates can be desaturated through the loss of a second H atom at a site adjacent to a heteroatom (N or O) for most native desaturase substrates. One proposed mechanism for the removal of the second H-atom  involves a polar-cleavage mechanism (electron transfer-proton transfer) by the iron(III)-hydroxo, as opposed to a second HAA. Herein we report the synthesis and characterization of a series of iron complexes with hydrogen bonding interactions between bound aquo or hydroxo ligands and the secondary coordination sphere in ferrous and ferric complexes. Interconversion among the iron species is accomplished by stepwise proton or electron addition or subtraction, as well as H-atom transfer (HAT). The calculated bond dissociation free energies (BDFEs) of two ferric hydroxo complexes, differentiated by their noncovalent interactions and reactivity, suggest that neither complex is capable of activating even weak C-H bonds, lending further support to the proposed mechanism for desaturation in iron-2OG desaturase enzymes. Additionally, the ferric hydroxo species are differentiated by their reactivity toward performing a radical rebound hydroxylation of triphenylmethylradical. Our findings should encourage further study of the desaturase systems that may contain unique H-bonding motifs proximal to the active site that help bias substrate desaturation over hydroxylation.

Characterization of Terminal Iron(III)-Oxo and Iron(III)-Hydroxo Complexes Derived from O2 Activation.

O2 activation at nonheme iron centers is a common motif in biological systems. While synthetic models have provided numerous insights into the reactivity of high-valent iron-oxo complexes related to biological processes, the majority of these complexes are synthesized using alternative oxidants. This report describes O2 activation by an iron(II)-triflate complex of the imino-functionalized tris(pyrrol-2-ylmethyl)amine ligand framework, H3[N(piCy)3]. Initial reaction conditions result in the formation of a mixture of oxidation products including terminal iron(III)-oxo and iron(III)-hydroxo complexes. The relevance of these species to the O2 activation process is demonstrated through reactivity studies and electrochemical analysis of the iron(III)-oxo complex.

13C NMR Signal Enhancement Using Parahydrogen-Induced Polarization Mediated by a Cobalt Hydrogenation Catalyst.

The use of a cobalt-based catalyst for the generation of hyperpolarized 13C NMR resonances by parahydrogenation of ethyl acrylate is presented herein. Comparisons of the carboxylate 13C NMR signal enhancement factor of ethyl propionate between using (MesCCC)Co-py and a commonly utilized cationic diphosphine rhodium complex demonstrates that the cobalt system is a viable PHIP catalyst alternative. Furthermore, the operative hydrogenation mechanism of the cobalt system was examined by using 1H, 13C, and parahydrogen-induced polarization NMR spectroscopies to elucidate reaction intermediates affiliated with the observed 1H and 13C NMR signal enhancements in ethyl propionate.

Cobalt-Catalyzed and Lewis Acid-Assisted Nitrile Hydrogenation to Primary Amines: A Combined Effort.

The selective hydrogenation of nitriles to primary amines using a bench-stable cobalt precatalyst under 4 atm of H2 is reported herein. The catalyst precursor was reduced in situ using NaHBEt3, and the resulting Lewis acid formed, BEt3, was found to be integral to the observed catalysis. Mechanistic insights gleaned from para-hydrogen induced polarization (PHIP) transfer NMR studies revealed that the pairwise hydrogenation of nitriles proceeded through a Co(I/III) redox process.

Tuning the Fe(II/III) Redox Potential in Nonheme Fe(II)-Hydroxo Complexes through Primary and Secondary Coordination Sphere Modifications.

The derivatization of the imino-functionalized tris(pyrrolylmethyl)amine ligand framework, N(XpiR)3 (XLR; X = H, Br; R = cyclohexyl (Cy), phenyl (Ph), 2,6- diisopropylphenyl (DIPP)), is reported. Modular ligand synthesis allows for facile modification of both the primary and secondary coordination sphere electronics. The iron(II)-hydroxo complexes, N(XpiR)(XafaR)2Fe(II)OH (XLRFeIIOH), are synthesized to establish the impact of the ligand modifications on the complexes' electronic properties, including their chemical and electrochemical oxidation. Cyclic voltammetry demonstrates that the Fe(II/III) redox couple spans a 400 mV range across the series. The origin of the shifted potential is explained based on spectroscopic, structural, and theoretical analyses of the iron(II) and iron(III) compounds.

Alkyne Semihydrogenation with a Well-Defined Nonclassical Co-H2 Catalyst: A H2 Spin on Isomerization and E-Selectivity.

The reactivity of a CoI-H2 complex was extended toward the semihydrogenation of internal alkynes. Under ambient temperatures and moderate pressures of H2, a broad scope of alkynes were semihydrogenated using a CoI-N2 precatalyst, resulting in the formation of trans-alkene products. Furthermore, mechanistic studies using 1H, 2H, and para-hydrogen induced polarization (PHIP) transfer NMR spectroscopy revealed cis-hydrogenation of the alkyne occurs first. The Co-mediated alkene isomerization afforded the E-selective products from a broad group of alkynes with good yields and E/Z selectivity.

Well-Defined Cobalt(I) Dihydrogen Catalyst: Experimental Evidence for a Co(I)/Co(III) Redox Process in Olefin Hydrogenation.

The synthesis of a cobalt dihydrogen Co(I)-(H2) complex prepared from a Co(I)-(N2) precursor supported by a monoanionic pincer bis(carbene) ligand, (Mes)CCC ((Mes)CCC = bis(mesityl-benzimidazol-2-ylidene)phenyl), is described. This species is capable of H2/D2 scrambling and hydrogenating alkenes at room temperature. Stoichiometric addition of HCl to the Co(I)-(N2) cleanly affords the Co(III) hydridochloride complex, which, upon the addition of Cp2ZrHCl, evolves hydrogen gas and regenerates the Co(I)-(N2) complex. Furthermore, the catalytic olefin hydrogenation activity of the Co(I) species was studied by using multinuclear and parahydrogen (p-H2) induced polarization (PHIP) transfer NMR studies to elucidate catalytically relevant intermediates, as well as to establish the role of the Co(I)-(H2) in the Co(I)/Co(III) redox cycle.

Accessing Pincer Bis(carbene) Ni(IV) Complexes from Ni(II) via Halogen and Halogen Surrogates.

This communication describes the two-electron oxidation of ((DIPP)CCC)NiX ((DIPP)CCC = bis(diisopropylphenyl-benzimidazol-2-ylidene)phenyl); X = Cl or Br) with halogen and halogen surrogates to form ((DIPP)CCC)NiX3. These complexes represent a rare oxidation state of nickel, as well as an unprecedented reaction pathway to access these species through Br2 and halogen surrogate (benzyltrimethylammonium tribromide). The Ni(IV) complexes have been characterized by a suite of spectroscopic techniques and can readily reduce to the Ni(II) counterpart, allowing for cycling between the Ni(II)/Ni(IV) oxidation states.

Facile nitrite reduction in a non-heme iron system: formation of an iron(III)-oxo.

Reaction of tetrabutylammonium nitrite with [N(afa(Cy))3Fe(OTf)](OTf) cleanly resulted in the formation of an iron(III)-oxo species, [N(afa(Cy))3Fe(O)](OTf), and NO(g). Formation of NO(g) as a byproduct was confirmed by reaction of the iron(II) starting material with half an equivalent of nitrite, resulting in a mixture of two products, the iron-oxo and an iron-NO species, [N(afa(Cy))3Fe(NO)](OTf)2. Formation of the latter was confirmed through independent synthesis. The results of this study provide insight into the role of hydrogen bonding in the mechanism of nitrite reduction and the binding mode of nitrite in biological heme systems.

Isolation of iron(II) aqua and hydroxyl complexes featuring a tripodal H-bond donor and acceptor ligand.

A tripodal ligand platform, tris(5-cycloiminopyrrol-2-ylmethyl)amine (H3[N(pi(Cy))3]), that features a hydrogen bond-accepting secondary coordination sphere when bound anionically to an iron center is reported. Neutral coordination to iron affords ligand tautomerization, resulting in a hydrogen bond-donating secondary coordination sphere, and formation of the tris(5-cyclohexyl-amineazafulvene-2-methyl)amine, H3[N(afa(Cy))3], scaffold. Both binding motifs result in formation of stable, high-spin iron(II) complexes featuring ancillary water, triflate, or hydroxo ligands. Structural analysis reveals that these complexes exhibit distorted trigonal-bipyramidal geometries with coordination of the apical nitrogen to iron as well as three equatorial amine or imine nitrogens, depending on the axial ancillary ligand. Formation of the aqua complex K[(N(pi(Cy))3)Fe(OH2)] (3) illustrated the propensity of the ligand to be hydrogen bond-accepting, whereas the iron triflate species [N(afa(Cy))3Fe](OTf)2 (4) features a hydrogen bond-donating secondary coordination sphere. The ability of each of the three arms of the ligand to tautomerize independently was observed during the formation of the iron-hydroxyl species [N(afa(Cy))2(pi(Cy))]FeOH (5) and characterized by X-ray crystallography and IR spectroscopy. The combined data for the iron complexes established that each arm of the tripodal ligand can tautomerize independently and is likely dependent on the electronic needs of the iron center when binding various substrates.

Synthesis of open-shell, bimetallic Mn/Fe trinuclear clusters.

Concomitant deprotonation and metalation of hexadentate ligand platform (tbs)LH6 ((tbs)LH6 = 1,3,5-C6H9(NHC6H4-o-NHSiMe2(t)Bu)3) with divalent transition metal starting materials Fe2(Mes)4 (Mes = mesityl) or Mn3(Mes)6 in the presence of tetrahydrofuran (THF) resulted in isolation of homotrinuclear complexes ((tbs)L)Fe3(THF) and ((tbs)L)Mn3(THF), respectively. In the absence of coordinating solvent (THF), the deprotonation and metalation exclusively afforded dinuclear complexes of the type ((tbs)LH2)M2 (M = Fe or Mn). The resulting dinuclear species were utilized as synthons to prepare bimetallic trinuclear clusters. Treatment of ((tbs)LH2)Fe2 complex with divalent Mn source (Mn2(N(SiMe3)2)4) afforded the bimetallic complex ((tbs)L)Fe2Mn(THF), which established the ability of hexamine ligand (tbs)LH6 to support mixed metal clusters. The substitutional homogeneity of ((tbs)L)Fe2Mn(THF) was determined by (1)H NMR, (57)Fe Mössbauer, and X-ray fluorescence. Anomalous scattering measurements were critical for the unambiguous assignment of the trinuclear core composition. Heating a solution of ((tbs)LH2)Mn2 with a stoichiometric amount of Fe2(Mes)4 (0.5 mol equiv) affords a mixture of both ((tbs)L)Mn2Fe(THF) and ((tbs)L)Fe2Mn(THF) as a result of the thermodynamic preference for heavier metal substitution within the hexa-anilido ligand framework. These results demonstrate for the first time the assembly of mixed metal cluster synthesis in an unbiased ligand platform.

Synthesis and Characterization of Palladium Pincer Bis(carbene) CCC Complexes.

The metalation of the DIPPCCC (DIPPCCC = bis(diisopropylphenyl-imidazol-2-ylidene)phenyl) ligand platform with Pd was achieved under mild conditions by reacting [H3(DIPPCCC)]Cl2 with Pd(OAc)2 at room temperature in the presence of 3.1 equiv of LiN(SiMe3)2. The resulting complexes (DIPPCCC)PdX (X = Cl or Br) were oxidized by two-electron oxidants PhICl2, Br2, and BTMABr3. All the complexes were crystallographically characterized, and analysis of structural parameters around the ligand scaffold show no evidence of a ligand-centered radical, rendering the metal center in the oxidized species, (DIPPCCC)PdX3 (X = Cl or Br), a formal PdIV oxidation state. Unlike their NiIV analogues, these PdIV complexes are stable to air and moisture. The addition of styrene to (DIPPCCC)PdBr3 resulted in the clean reduction of PdIV to PdII, along with the formation of the halogenated alkane. The oxidation to PdIV and subsequent return to PdII upon reduction, as opposed to formation of PdIII species, showcases the accessibility of high-valent palladium DIPPCCC complexes.

Trigonal Mn3 and Co3 clusters supported by weak-field ligands: a structural, spectroscopic, magnetic, and computational investigation into the correlation of molecular and electronic structure.

Transamination of divalent transition metal starting materials (M(2)(N(SiMe(3))(2))(4), M = Mn, Co) with hexadentate ligand platforms (R)LH(6) ((R)LH(6) = MeC(CH(2)NPh-o-NR)(3) where R = H, Ph, Mes (Mes = Mesityl)) or (H,Cy)LH(6) = 1,3,5-C(6)H(9)(NHPh-o-NH(2))(3) with added pyridine or tertiary phosphine coligands afforded trinuclear complexes of the type ((R)L)Mn(3)(py)(3) and ((R)L)Co(3)(PMe(2)R')(3) (R' = Me, Ph). While the sterically less encumbered ligand varieties, (H)L or (Ph)L, give rise to local square-pyramidal geometries at each of the bound metal atoms, with four anilides forming an equatorial plane and an exogenous pyridine or phosphine in the apical site, the mesityl-substituted ligand ((Mes)L) engenders local tetrahedral coordination. Both the neutral Mn(3) and Co(3) clusters feature S = (1)/(2) ground states, as determined by direct current (dc) magnetometry, (1)H NMR spectroscopy, and low-temperature electron paramagnetic resonance (EPR) spectroscopy. Within the Mn(3) clusters, the long internuclear Mn-Mn separations suggest minimal direct metal-metal orbital overlap. Accordingly, fits to variable-temperature magnetic susceptibility data reveal the presence of weak antiferromagnetic superexchange interactions through the bridging anilide ligands with exchange couplings ranging from J = -16.8 to -42 cm(-1). Conversely, the short Co-Co interatomic distances suggest a significant degree of direct metal-metal orbital overlap, akin to the related Fe(3) clusters. With the Co(3) series, the S = (1)/(2) ground state can be attributed to population of a single molecular orbital manifold that arises from mixing of the metal- and o-phenylenediamide (OPDA) ligand-based frontier orbitals. Chemical oxidation of the neutral Co(3) clusters affords diamagnetic cationic clusters of the type [((R)L)Co(3)(PMe(2)R)(3)](+). Density functional theory (DFT) calculations on the neutral (S = (1)/(2)) and cationic (S = 0) Co(3) clusters reveal that oxidation occurs at an orbital with contributions from both the Co3 core and OPDA subunits. The predicted bond elongations within the ligand OPDA units are corroborated by the ligand bond perturbations observed by X-ray crystallography.

γ-Agostic interactions in (MesCCC)Fe-Mes(L) complexes.

Agostic interactions were observed in the bound mesityl group in a series of iron compounds bearing a bis(NHC) pincer CCC ligand. The L-type ligand on [(CCC)FeIIMes(L)] complexes influences the strength of the agostic interaction and is manifested in the upfield shift of the 1H NMR resonance for the mesityl methyl resonances. The nature of the interaction was further investigated by density functional theory calculations, allowing rationalization of some unexpected trends and proving to be a powerful predictive tool.

Oxidative atom-transfer to a trimanganese complex to form Mn6(µ6-E) (E = O, N) clusters featuring interstitial oxide and nitride functionalities.

Utilizing a hexadentate ligand platform, a trinuclear manganese complex of the type ((H)L)Mn(3)(thf)(3) was synthesized and characterized ([(H)L](6-) = [MeC(CH(2)N(C(6)H(4)-o-NH))(3)](6-)). The pale-orange, formally divalent trimanganese complex rapidly reacts with O-atom transfer reagents to afford the µ(6)-oxo complex ((H)L)(2)Mn(6)(µ(6)-O)(NCMe)(4), where two trinuclear subunits bind the central O-atom and the ((H)L) ligands cooperatively bind both trinuclear subunits. The trimanganese complex ((H)L)Mn(3)(thf)(3) rapidly consumes inorganic azide ([N(3)]NBu(4)) to afford a dianionic hexanuclear nitride complex [((H)L)(2)Mn(6)(µ(6)-N)](NBu(4))(2), which subsequently can be oxidized with elemental iodine to ((H)L)(2)Mn(6)(µ(6)-N)(NCMe)(4). EPR and alkylation of the interstitial light atom substituent were used to distinguish the nitride from the oxo complex. The oxo and oxidized nitride complexes give rise to well-defined Mn(II) and Mn(III) sites, determined by bond valence summation, while the dianionic nitride shows a more symmetric complex, giving rise to indistinguishable ion oxidation states based on crystal structure bond metrics.