71 research outputs found

    Reduction of CO\u3csub\u3e2\u3c/sub\u3e By a Masked Two-Coordinate Cobalt(I) Complex and Characterization of a Proposed Oxodicobalt(II) Intermediate

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    Fixation and chemical reduction of CO2 are important for utilization of this abundant resource, and understanding the detailed mechanism of C-O cleavage is needed for rational development of CO2 reduction methods. Here, we describe a detailed analysis of the mechanism of the reaction of a masked two-coordinate cobalt(i) complex, LtBuCo (where LtBu = 2,2,6,6-tetramethyl-3,5-bis[(2,6-diisopropylphenyl)imino]hept-4-yl), with CO2, which yields two products of C-O cleavage, the cobalt(i) monocarbonyl complex LtBuCo(CO) and the dicobalt(ii) carbonate complex (LtBuCo)2(μ-CO3). Kinetic studies and computations show that the κN,η6-arene isomer of LtBuCo rearranges to the κ2N,N′ binding mode prior to binding of CO2, which contrasts with the mechanism of binding of other substrates to LtBuCo. Density functional theory (DFT) studies show that the only low-energy pathways for cleavage of CO2 proceed through bimetallic mechanisms, and DFT and highly correlated domain-based local pair natural orbital coupled cluster (DLPNO-CCSD(T)) calculations reveal the cooperative effects of the two metal centers during facile C-O bond rupture. A plausible intermediate in the reaction of CO2 with LtBuCo is the oxodicobalt(II) complex LtBuCoOCoLtBu, which has been independently synthesized through the reaction of LtBuCo with N2O. The rapid reaction of LtBuCoOCoLtBu with CO2 to form the carbonate product indicates that the oxo species is kinetically competent to be an intermediate during CO2 cleavage by LtBuCo. LtBuCoOCoLtBu is a novel example of a thoroughly characterized molecular cobalt-oxo complex where the cobalt ions are clearly in the +2 oxidation state. Its nucleophilic reactivity is a consequence of high charge localization on the μ-oxo ligand between two antiferromagnetically coupled high-spin cobalt(ii) centers, as characterized by DFT and multireference complete active space self-consistent field (CASSCF) calculations

    Ru(II)-diimine complexes and cytochrome P450 working hand-in-hand

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    With a growing interest in utilizing visible light to drive biocatalytic processes, several light-harvesting units and approaches have been employed to harness the synthetic potential of heme monooxygenases and carry out selective oxyfunctionalization of a wide range of substrates. While the fields of cytochrome P450 and Ru(II) photochemistry have separately been prolific, it is not until the turn of the 21st century that they converged. Non-covalent and subsequently covalently attached Ru(II) complexes were used to promote rapid intramolecular electron transfer in bacterial P450 enzymes. Photocatalytic activity with Ru(II)-modified P450 enzymes was achieved under reductive conditions with a judicious choice of a sacrificial electron donor. The initial concept of Ru(II)-modified P450 enzymes was further improved using protein engineering, photosensitizer functionalization and was successfully applied to other P450 enzymes. In this review, we wish to present the recent contributions from our group and others in utilizing Ru(II) complexes coupled with P450 enzymes in the broad context of photobiocatalysis, protein assemblies and chemoenzymatic reactions. The merging of chemical catalysts with the synthetic potential of P450 enzymes has led to the development of several chemoenzymatic approaches. Moreover, strained Ru(II) compounds have been shown to selectively inhibit P450 enzymes by releasing aromatic heterocycle containing molecules upon visible light excitation taking advantage of the rapid ligand loss feature in those complexes

    Methyl Complexes of the Transition Metals

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    Organometallic chemistry can be considered as a wide area of knowledge that combines concepts of classic organic chemistry, that is, based essentially on carbon, with molecular inorganic chemistry, especially with coordination compounds. Transition-metal methyl complexes probably represent the simplest and most fundamental way to view how these two major areas of chemistry combine and merge into novel species with intriguing features in terms of reactivity, structure, and bonding. Citing more than 500 bibliographic references, this review aims to offer a concise view of recent advances in the field of transition-metal complexes containing M-CH fragments. Taking into account the impressive amount of data that are continuously provided by organometallic chemists in this area, this review is mainly focused on results of the last five years. After a panoramic overview on M-CH compounds of Groups 3 to 11, which includes the most recent landmark findings in this area, two further sections are dedicated to methyl-bridged complexes and reactivity.Ministerio de Ciencia e Innovación Projects CTQ2010–15833, CTQ2013-45011 - P and Consolider - Ingenio 2010 CSD2007 - 00006Junta de Andalucía FQM - 119, Projects P09 - FQM - 5117 and FQM - 2126EU 7th Framework Program, Marie Skłodowska - Curie actions C OFUND – Agreement nº 26722

    Methyl Complexes of the Transition Metals

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    The coordination chemistry and reactivity of organometallic cobalt, iron, and manganese complexes

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    Thesis (Ph. D.)--University of Rochester. Department of Chemistry, 2016.First-row transition metal complexes are less toxic, less expensive, and more sustainable than precious metals. Yet complexes of precious metals are widely used by the chemical industry as catalysts. An understanding of the electronic structure and reactivity of first-row transition metals is crucial to the development of earth-abundant metal catalysts to rival precious metal-based systems. In this thesis, the fundamental coordination chemistry of some manganese, iron, and cobalt complexes is investigated. In chapter 2 we explore a β-diketiminate supported cobalt(I) complex that can rapidly interconvert between different spin states with different structures ("spin isomers"). The new cobalt(I) monocarbonyl complex LtBuCo(CO) is a singlet in the solid state, with an unprecedented binding mode where one of the C-C double bonds of an aromatic ring completes a pseudo-square planar coordination. Dissolving the compound gives substantial population of the triplet state. The interconversion of the two spin isomers is rapid at low temperature, and temperature-dependent NMR and electronic absorption spectroscopy studies show the energy differences quantitatively. Spectroscopically validated computations elucidate the detailed pathway through which the β-diketiminate ligand can "slip" between bidentate and arene-bound forms. These results show that multiple spin states are easily accessible in this hemilabile system. In chapter 3 we report the synthesis of the homoleptic tetralkyliron(III) ferrate complex [MgCl(THF)₅][FeMe₄] from the reaction of iron(III)chloride with methylmagnesium bromide in THF. Upon warming, this distorted square-planar spin quartet species converts to the spin doublet species originally observed by Kochi and coworkers with concomitant formation of ethane, consistent with its intermediacy in the reduction pathway of iron(III) chloride to generate the reduced iron species involved in catalysis. In chapter 4 we report the synthesis and characterization of manganese complexes supported by N-heterocyclic carbene (NHC) ligands. These complexes were prepared in straightforward fashion by direct carbene addition to MnCl₂(THF)₁.₆. The complex [Mn₂Cl₂(µ-Cl)₂(IPr)₂] serves as a precursor to dimeric alkyl and aryl compounds of Mn(II) including [Mn₂R₂(µ-Cl)₂(NHC)₂] (R = Bn, o-tolyl, and Ph) and the bridging methyl complex, [Mn₂Me₂(µ-Me)₂(IPr)₂]. Stoichiometric reactions of these hydrocarbyl species with cyclohexyl bromide demonstrate that they are not chemically competent in C-C coupling reactions involving alkyl electrophiles

    Spatio-Temporal Sentiment Mining of COVID-19 Arabic Social Media

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    Since the recent outbreak of COVID-19, many scientists have started working on distinct challenges related to mining the available large datasets from social media as an effective asset to understand people’s responses to the pandemic. This study presents a comprehensive social data mining approach to provide in-depth insights related to the COVID-19 pandemic and applied to the Arabic language. We first developed a technique to infer geospatial information from non-geotagged Arabic tweets. Secondly, a sentiment analysis mechanism at various levels of spatial granularities and separate topic scales is introduced. We applied sentiment-based classifications at various location resolutions (regions/countries) and separate topic abstraction levels (subtopics and main topics). In addition, a correlation-based analysis of Arabic tweets and the official health providers’ data will be presented. Moreover, we implemented several mechanisms of topic-based analysis using occurrence-based and statistical correlation approaches. Finally, we conducted a set of experiments and visualized our results based on a combined geo-social dataset, official health records, and lockdown data worldwide. Our results show that the total percentage of location-enabled tweets has increased from 2% to 46% (about 2.5M tweets). A positive correlation between top topics (lockdown and vaccine) and the COVID-19 new cases has also been recorded, while negative feelings of Arab Twitter users were generally raised during this pandemic, on topics related to lockdown, closure, and law enforcement

    Spin Isomers and Ligand Isomerization in a Three-Coordinate Cobalt(I) Carbonyl Complex

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    Hemilabile ligands, which have one donor that can reversibly bind to a metal, are widely used in transition-metal catalysts to create open coordination sites. This change in coordination at the metal can also cause spin-state changes. Here, we explore a cobalt(I) system that is poised on the brink of hemilability and of a spin-state change and can rapidly interconvert between different spin states with different structures (“spin isomers”). The new cobalt(I) monocarbonyl complex LtBuCo(CO) (2) is a singlet (12) in the solid state, with an unprecedented diketiminate binding mode where one of the C═C double bonds of an aromatic ring completes a pseudo-square-planar coordination. Dissolving the compound gives a substantial population of the triplet (32), which has exceptionally large uniaxial zero-field splitting due to strong spin–orbit coupling with a low-lying excited state. The interconversion of the two spin isomers is rapid, even at low temperature, and temperature-dependent NMR and electronic absorption spectroscopy studies show the energy differences quantitatively. Spectroscopically validated computations corroborate the presence of a low minimum-energy crossing point (MECP) between the two potential energy surfaces and elucidate the detailed pathway through which the β-diketiminate ligand “slips” between bidentate and arene-bound forms: rather than dissociation, the cobalt slides along the aromatic system in a pathway that balances strain energy and cobalt–ligand bonding. These results show that multiple spin states are easily accessible in this hemilabile system and map the thermodynamics and mechanism of the transition
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