RESUMEN
Extensive high-level quantum-chemical calculations reveal that the rod-shaped molecule BeOBeC, which was recently generated in matrix experiments, exists in two nearly isoenergetic states, the 5 Σ quintet (5 6) and the 3 Σ triplet (3 6). Their IR features are hardly distinguishable at finite temperature. The major difference concerns the mode of spin coupling between the terminal beryllium and carbon atoms. Further, the ground-state potential-energy surface of the [2Be,C,O] system at 4â K is presented and differences between the photochemical and thermal behaviors are highlighted. Finally, a previously not considered, so far unknown C2v -symmetric rhombus-like four-membered ring 3 [Be(O)(C)Be] (3 5) is predicted to represent the global minimum on the potential-energy surface.
RESUMEN
Presented here is that isolated, long-lived electronic states of ReC+ serve as the root cause for distinctly different reactivities of this diatomic ion in the thermal activation of dihydrogen. Detailed high-level quantum chemical calculations support the experimental findings obtained in the highly diluted gas phase using FT-ICR mass spectrometry. The origin for the existence of these long-lived excited electronic states and the resulting implications for the varying mechanisms of dihydrogen splitting are addressed.
RESUMEN
[V2 O]+ remains "invisible" in the thermal gas-phase reaction of bare [V2 ]+ with CO2 giving rise to [V2 O2 ]+ ; this is because the [V2 O]+ intermediate is being consumed more than 230â times faster than it is generated. However, the fleeting existence of [V2 O]+ and its involvement in the [V2 ]+ â [V2 O2 ]+ chemistry are demonstrated by a cross-over labeling experiment with a 1:1 mixture of C16 O2 /C18 O2 , generating the product ions [V2 16 O2 ]+ , [V2 16 O18 O]+ , and [V2 18 O2 ]+ in a 1:2:1 ratio. Density functional theory (DFT) calculations help to understand the remarkable and unexpected reactivity differences of [V2 ]+ versus [V2 O]+ towards CO2 .
RESUMEN
An unprecedented, spontaneous, and complete cleavage of the triple bond of N2 in the thermal reaction of 15N2 with Ta214N+ was observed experimentally by Fourier transform ion cyclotron resonance mass spectrometry; mechanistic aspects of the degenerate ligand exchange were addressed by high-level quantum chemical calculations. The "hidden" dis- and reassembly of N2, mediated by Ta2N+, constitutes a full catalytic cycle. A frontier orbital analysis reveals that the scission of the N2 triple bond is essentially governed by the donation of d-electrons from the 2 metal centers into antibonding π*-orbitals of N2 and by the concurrent migration of electrons from bonding π- and σ-orbitals of N2 into empty d-orbitals of the metals. This work may contribute to a rational design of catalysts in order to reduce the still enormous energy demand required for an artificial dinitrogen activation.
RESUMEN
The gas-phase reaction of the heteronuclear oxide cluster [VPO4 ].+ with C2 H4 is studied under multiple collision conditions at 150â K using cryogenic ion-trap vibrational spectroscopy combined with electronic structure calculations. The exclusive formation of acetaldehyde is directly identified spectroscopically and discussed in the context of the underlying reaction mechanism. In line with computational predictions it is the terminal P=O and not the V=O unit that provides the oxygen atom in the barrier-free thermal C2 H4 âCH3 CHO conversion. Interestingly, in the course of the reaction, the emerging CH3 CHO product undergoes a rather complex intramolecular migration, coordinating eventually to the vanadium center prior to its liberation. Moreover, the spectroscopic structural characterization of neutral C2 H4 O deserves special mentioning as in most, if not all, ion/molecule reactions, the neutral product is usually only indirectly identified.
RESUMEN
The reactivity of the cationic metal-carbon cluster FeC4 + towards methane has been studied experimentally using Fourier-transform ion cyclotron resonance mass spectrometry and computationally by high-level quantum chemical calculations. At room temperature, FeC4 H+ is formed as the main ionic product, and the experimental findings are substantiated by labeling experiments. According to extensive quantum chemical calculations, the C-H bond activation step proceeds through a radical-based hydrogen-atom transfer (HAT) mechanism. This finding is quite unexpected because the initial spin density at the terminal carbon atom of FeC4 + , which serves as the hydrogen acceptor site, is low. However, in the course of forming an encounter complex, an electron from the doubly occupied sp-orbital of the terminal carbon atom of FeC4 + migrates to the singly occupied π*-orbital; the latter is delocalized over the entire carbon chain. Thus, a highly localized spin density is generated in situ at the terminal carbon atom. Consequently, homolytic C-H bond activation occurs without the obligation to pay a considerable energy penalty that is usually required for HAT involving closed-shell acceptor sites. The mechanistic insights provided by this combined experimental/computational study extend the understanding of methane activation by transition-metal carbides and add a new facet to the dizzying mechanistic landscape of hydrogen-atom transfer.
RESUMEN
The mechanisms of the thermal reactions of the two iconic magnesium oxide cations MgO.+ and Mg2 O2.+ with methane have been re-evaluated at the CCSD(T)/CBS//CCSD/def2-TZVP level of theory. For the reaction of MgO.+ with CH4 , only the classical hydrogen-atom transfer (HAT) was found; in contrast, for the Mg2 O2.+ /CH4 couple, both HAT and proton-coupled electron-transfer (PCET) exist as mechanistic variants. In order to evaluate the suitability of density functional theory (DFT) methods, the reactions were computed by using 27 density functionals. The results obtained demonstrate that the various DFT methods often deliver rather different results for both geometric and energetic features. As to the prediction of the apparent barriers, pure functionals give the largest mean absolute errors. BMK, ωB97XD, and the double-hybrid functional mPW2PLYP were confirmed to come closest to the results provided by CCSD(T)/CBS. Thus, mechanistic conclusions based on a single DFT method should be viewed with great caution. In summary, this study may assist in the selection of a suitable quantum chemical method to unravel the mechanistic details of C-H bond activation by charged metal oxides.
RESUMEN
The thermal gas-phase reactions of [Al2 VO5 ]+ and [AlV2 O6 ]+ with methane have been explored by using Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry complemented by high-level quantum chemical calculations. Both cluster ions chemisorbed methane as the major reaction channels at room temperature. [Al2 VO5 ]+ could break only one C-H bond to liberate CH3 , whereas [AlV2 O6 ]+ exhibited higher oxidizing ability such that it brings about the selective generation of formaldehyde. Mechanistic aspects are revealed and the crucial roles of the metal centers are discussed.
RESUMEN
Thermal gas-phase reactions of the ruthenium-oxide clusters [RuOx ]+ (x=1-3) with methane and dihydrogen have been explored by using FT-ICR mass spectrometry complemented by high-level quantum chemical calculations. For methane activation, as compared to the previously studied [RuO]+ /CH4 couple, the higher oxidized Ru systems give rise to completely different product distributions. [RuO2 ]+ brings about the generations of [Ru,O,C,H2 ]+ /H2 O, [Ru,O,C]+ /H2 /H2 O, and [Ru,O,H2 ]+ /CH2 O, whereas [RuO3 ]+ exhibits a higher selectivity and efficiency in producing formaldehyde and syngas (CO+H2 ). Regarding the reactions with H2 , as compared to CH4 , both [RuO]+ and [RuO2 ]+ react similarly inefficiently with oxygen-atom transfer being the main reaction channel; in contrast, [RuO3 ]+ is inert toward dihydrogen. Theoretical analysis reveals that the reduction of the metal center drives the overall oxidation of methane, whereas the back-bonding orbital interactions between the cluster ions and dihydrogen control the H-H bond activation. Furthermore, the reactivity patterns of [RuOx ]+ (x=1-3) with CH4 and H2 have been compared with the previously reported results of Groupâ 8 analogues [OsOx ]+ /CH4 /H2 (x=1-3) and the [FeO]+ /H2 system. The electronic origins for their distinctly different reaction behaviors have been addressed.
RESUMEN
Cryogenic ion trap vibrational spectroscopy paired with quantum chemistry currently represents the most generally applicable approach for the structural investigation of gaseous cluster ions that are not amenable to direct absorption spectroscopy. Here, we give an overview of the most popular variants of infrared action spectroscopy and describe the advantages of using cryogenic ion traps in combination with messenger tagging and vibrational predissociation spectroscopy. We then highlight a few recent studies that apply this technique to identify highly reactive ionic intermediates and to characterize their reactive sites. We conclude by commenting on future challenges and potential developments in the field.
RESUMEN
The thermal gas-phase catalytic reduction of N2 O by CO, mediated by the transition-metal nitride cluster ion [NbN]+ , has been explored by using FT-ICR mass spectrometry and complemented by high-level quantum chemical calculations. In contrast to the [Nb]+ /[NbO]+ and [NbO]+ /[Nb(O)2 ]+ systems, in which the oxidation of [Nb]+ and [NbO]+ with N2 O is facile, but in which neither [NbO]+ nor [Nb(O)2 ]+ react with CO at room temperature, the [NbN]+ /[ONbN]+ system at ambient temperature mediates the catalytic oxidation of CO. The origins of the distinctly different reactivities upon nitrogen ligation are addressed by quantum chemical calculations.
RESUMEN
N-Heterocyclic carbenes (NHCs, :C) can interact with azolium salts (C-H+ ) by either forming a hydrogen-bonded aggregate (CHC+ ) or a covalent C-C bond (CCH+ ). In this study, the intramolecular NHC-azolium salt interactions of aromatic imidazolin-2-ylidenes and saturated imidazolidin-2-ylidenes have been investigated in the gas phase by traveling wave ion mobility mass spectrometry (TW IMS) and DFT calculations. The TW IMS experiments provided evidence for the formation of these important intermediates in the gas phase, and they identified the predominant aggregation mode (hydrogen bond vs. covalent C-C) as a function of the nature of the interacting carbene-azolium pairs.
RESUMEN
Mechanistic aspects of the C-H bond activation of methane by metal-carbide cations MC+ of the 3d transition-metals Sc-Zn were elucidated by NEVPT2//CASSCF quantum-chemical calculations and verified experimentally for M = Ti, V, Fe, and Cu by using Fourier transform ion-cyclotron resonance mass spectrometry. While MC+ species with M = Sc, Ti, V, Cr, Cu, and Zn activate CH4 at ambient temperature, this is prevented with carbide cations of M = Mn, Fe, and Co by high apparent barriers; NiC+ has a small apparent barrier. Hydrogen-atom transfers from methane to metal-carbide cations were found to proceed via a proton-coupled electron transfer mechanism for M = Sc-Co; wherein the doubly occupied πxz/yz-orbitals between metal and carbon at the carbon site serve as electron donors and the corresponding metal-centered vacant π*xz/yz-orbitals as electron acceptors. Classical hydrogen-atom transfer transpires only in the case of NiC+, while ZnC+ follows a mechanistic scenario, in which a formally hydridic hydrogen is transferred. CuC+ reacts by a synchronous activation of two C-H bonds. While spin density is often so crucial for the reactions of numerous MO+/CH4 couples, it is much less important for the C-H bond activation by carbide cations of the 3d transition-metals, in which one notes large changes in bond dissociation energies, spin states, number of d-electrons, and charge distributions. All these factors jointly affect both the reactivity of the metal carbides and their mechanisms of C-H bond activation.
RESUMEN
In a full catalytic cycle, bare Ta2+ in the highly diluted gas phase is able to mediate the formation of ammonia in a Haber-Bosch-like process starting from N2 and H2 at ambient temperature. This finding is the result of extensive quantum chemical calculations supported by experiments using Fourier transform ion cyclotron resonance MS. The planar Ta2N2+, consisting of a four-membered ring of alternating Ta and N atoms, proved to be a key intermediate. It is formed in a highly exothermic process either by the reaction of Ta2+ with N2 from the educt side or with two molecules of NH3 from the product side. In the thermal reaction of Ta2+ with N2, the N≡N triple bond of dinitrogen is entirely broken. A detailed analysis of the frontier orbitals involved in the rate-determining step shows that this unexpected reaction is accomplished by the interplay of vacant and doubly occupied d-orbitals, which serve as both electron acceptors and electron donors during the cleavage of the triple bond of N≡N by the ditantalum center. The ability of Ta2+ to serve as a multipurpose tool is further shown by splitting the single bond of H2 in a less exothermic reaction as well. The insight into the microscopic mechanisms obtained may provide guidance for the rational design of polymetallic catalysts to bring about ammonia formation by the activation of molecular nitrogen and hydrogen at ambient conditions.
RESUMEN
The thermal gas-phase reactions of [CeON]+ with methane have been explored by FT-ICR mass spectrometry and high-level quantum-chemical calculations. Nitrogen-atom transfer from the cluster ion to methane was observed as the only reaction channel. Based on computational work, the neutral molecule formed corresponds to either CH2 NH2 or CH3 NH. In addition to a rather weak OCe+ -N bond, this reaction benefits from a highly efficient intersystem crossing. Mechanistic aspects and the associated electronic origins are discussed, and a detailed comparison of [CeON]+ , [CeO]+ , [CeN]+ , [CeO2 ]+ , and atomic N in their reactions with CH4 is given.
RESUMEN
In the course of combined computational and mass spectrometry-based mechanistic studies, recently we came across rather unusual, if not unprecedented, effects of transition-metal ions and ligands when simple metal oxides or carbides are subjected to thermal gas-phase reactions with methane. Interestingly, "Gedankenexperiments" demonstrate how these effects can be modeled using oriented external electric fields (OEEFs), thus expanding their predicted role as "smart reagents" (Shaik et al., Nat. Chem., 2016, 8, 1091), and further suggesting that the OEEFs may be used in controlling the adsorption/desorption behavior of methane as well as serving as a tool to explore mechanistic features.
RESUMEN
The thermal gas-phase reaction of [Al2 CuO5 ]+ with methane has been explored by using FT-ICR mass spectrometry complemented by high-level quantum chemical calculations. The generation of atomic [Cu]+ from the [Al2 CuO5 ]+ /CH4 couple corresponds to the only reaction channel. Labeling experiments and computational studies strongly suggest that methane activation is indeed involved in the production of [Cu]+ , and generation of CH2 O prevails. Mechanistic aspects and the associated doping effects are discussed.
RESUMEN
Mechanistic insight into the thermal O-H bond activation of water by the cubane-like, prototypical heteronuclear oxide cluster [Al2Mg2O5]â¢+ has been derived from a combined experimental/computational study. Experiments in the highly diluted gas phase using Fourier transform ion-cyclotron resonance mass spectrometry show that hydrogen-atom abstraction from water by the cluster cation [Al2Mg2O5]â¢+ occurs at ambient conditions accompanied by the liberation of an OH⢠radical. Because of a complete randomization of all oxygen atoms prior to fragmentation, about 83% of the oxygen atoms of the hydroxyl radical released originate from the oxide cluster itself. The experimental findings are supported by detailed high-level quantum chemical calculations. The theoretical analysis reveals that the transfer of a formal hydrogen atom from water to the metal-oxide cation can proceed mechanistically via proton- or hydrogen-atom transfer exploiting different active sites of the cluster oxide. In addition to the unprecedented oxygen-atom scrambling, one of the more general and quite unexpected findings concerns the role of spin density at the hydrogen-acceptor oxide atom. While this feature is crucial for [M-O]+/CH4 couples, it is much less important in the O-H bond activation of water.