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Hand-foot skin reaction (HFSR) is the most debilitating and prevalent side effect caused by multikinase inhibitors (MKIs) that share vascular endothelial growth factor receptor (VEGFR) as the common inhibition target, such as sorafenib, regorafenib, axitinib, etc. Though not life-threatening, HFSR can significantly deteriorate patients' quality of life and jeopardize the continuity of cancer therapy. Despite years of efforts, there are no FDA-approved treatments for HFSR and the understanding of the precise pathogenic mechanism is still limited. In this study, we hypothesized that nitric oxide has the potential therapeutic effect to reverse the toxicity caused by MKI through upregulation of several VEGF/VEGFR downstream signaling pathways. We found that glyceryl trinitrate (GTN), a nitric oxide donor, could stimulate cell proliferation, migration, and protect cells from apoptosis induced by MKIs in vitro. Local application of GTN mitigated tissue damage in a rat model, while not impacting the anti-tumor effect of the MKI in HepG2 tumor-bearing mice. Finally, GTN ointment alleviated cutaneous damages and improved quality of life in 6 HFSR patients. Our study proposed and validated the mechanism to counteract VEGFR inhibition, providing GTN as the potential treatment to MKI-induced HFSR, which may further improve the therapeutic window of various MKI based cancer therapies.

Graphite as a competitive anode material of potassium-ion batteries (KIBs) is currently frustrated by the poor cycling stability and rate performance. In this study, high-performance activated graphite that derives from low-grade microcrystalline graphite ore is fabricated through a facile KOH activation method and the following HF leaching. The effect of activation temperature (from 450 to 650 °C) on the physical parameters and K-storage performance of the activated graphite materials (AMGs) is systematically investigated. The material characterization results demonstrate the activation temperature imposes distinct influence on the morphology, interlayer distance (d002), crystalline size (Lc), specific surface area and surface functional groups of the AMGs. At the optimized activation temperature of 550 °C, the activated graphite (AMG-55) presents enlarged d002 of 0.3451 nm, small Lc of 14.61 nm and lowest surface oxygen content (1.79%). Moreover, the moderate etching reactions of KOH at 550 °C results in the highest specific surface area (11.91 m2 g−1) and the creation of abundant of nanosheets which construct rich mesopores for convenient K+ diffusion. Benefitted from the high purity, increased activated sites for K+ association as well as the accelerated charge transfer/ion diffusion kinetics, the AMG-55 electrode exhibits high reversible capacity (262.3 mAh g−1), superior cycling ability and best rate performance among the activated samples. A stable charge capacity of 171.9 mAh g−1 still can be maintained after 200 discharge/charge cycles at 0.1 A g−1 with a favorable capacity retention of 65.5%. Moreover, the electrode releases a high reversible capacity of 162.1 mAh g−1 at the large current density of 0.6 A g−1, suggesting the promising application potential of activated graphite for high-performance KIBs.

The practical application of the state-of-art graphite anode materials for potassium ion batteries (KIBs) is currently frustrated by their poor cycling life and unsatisfactory rate performance. Her...

Graphite has been considered as promising anode material of potassium-ion batteries (KIBs), which however the practical applications are frustrated due to the unsatisfactory cycling stability and p...

Carbon nanotubes (CNTs) as superior support materials for functional nanoparticles (NPs) have been widely demonstrated. Nevertheless, the homogeneous loading of these NPs is still frustrated due to the inert surface of CNTs. In this work, a facile gas-phase pyrolysis strategy that the mixture of ferrocene and CNTs are confined in an isolated reactor with rising temperature is developed to fabricate a carbon-coated Fe3O4 nanoparticle/carbon nanotube (Fe3O4@C/CNT) composite. It is found the ultra-small Fe3O4 NPs (

A plasma wave device model for THz non-resonant detection is proposed in this paper. The recessed gate (RE) enhanced AlGaN/GaN HEMT structure is adopted for enhancing the detection responsivity with its excellent 2DEG channel controlling. The detector is worked at Dyakonov-Shur instability condition and the radiation frequency detected is in the range of THz. Hydrodynamic equations and asymmetric B.C. are modeled for the plasma device while detection responsivity $(R_{\mathrm{v}})$ and noise equivalent power (NEP) are modeled by channel conductance. The numerical results in TCAD show the detection responsivity is 1.3 times higher than conventional single-channel (SC) AlGaN/GaN HEMT with keeping a low NEP of 60 pW/Hz0.5, which indicates potential of RE _ HEMT devices in THz detectors.

RATIONALE The biggest obstacle in the rational conversion of biomass into aromatic chemicals is the identification of unknown compounds in lignin degradation mixtures that are highly complex. As opposed to lignin degradation products with β-O-4 linkages, very little is known about the mass spectrometric analysis of lignin degradation products with α-O-4 linkages. METHODS Lignin model compounds with an α-O-4 and another linkage, as well as lignin model compounds with only β-O-4 linkages, were ionized by attachment of lithium or sodium cations under positive-ion mode electrospray ionization (ESI) or by deprotonation in negative-ion mode ESI in a linear quadrupole ion trap mass spectrometer. The ions were subjected to collision-activated dissociation in multiple-stage tandem mass spectrometry experiments to characterize their fragmentation patterns. RESULTS All studied compounds formed abundant sodium and lithium cation adducts in positive-ion mode ESI with no fragmentation. Model compounds with β-O-4 linkages displayed stable [M - H]- ions in negative-ion mode ESI whereas compounds with α-O-4 linkages only showed fragment ions. CAD of the lithiated α-O-4 compounds provided more structural information than CAD of sodiated compounds. However, both sodiated and lithiated compounds with α-O-4 linkages showed losses of monomer units at the MS2 stage, which is useful for sequencing of lignins with this type of linkage. CONCLUSIONS An ionization and sequencing method has been developed for lignin model compounds with α-O-4 linkages that spontaneously fragment upon ionization via (-)ESI.

Seven synthesized G-lignin oligomer model compounds (ranging in size from dimers to an octamer) with 5-5 and/or β-O-4 linkages, and three synthesized S-lignin model compounds (a dimer, trimer, and tetramer) with β-O-4 linkages, were evaporated and deprotonated using negative-ion mode ESI in a linear quadrupole ion trap/Fourier transform ion cyclotron resonance mass spectrometer. The collision-activated dissociation (CAD) fragmentation patterns (obtained in MS2 and MS3 experiments, respectively) for the negative ions were studied to develop a procedure for sequencing unknown lignin oligomers. On the basis of the observed fragmentation patterns, the measured elemental compositions of the most abundant fragment ions, and quantum chemical calculations, the most important reaction pathways and likely mechanisms were delineated. Many of these reactions occur via charge-remote fragmentation mechanisms. Deprotonated compounds with only β-O-4 linkages, or both 5-5 and β-O-4 linkages, showed major 1,2-eliminations ...

As a promising cathode for sodium ion batteries, polyanion-type phosphate compounds are considered as a potential candidate of the next-generation sodium storage materials for the three-dimensional (3D) structure and open pathways. However, several intrinsic faults, such as low electrical conductivity seriously prevent their practical application in broader fields. Herein, the nitrogen and sulfur co-doped carbon layer coated Na2VTi(PO4)3 nanocomposites have been synthesized by a facile sol-gel method. The crystal structure, surface morphology and charge-discharge performance were investigated to confirm the successful preparation of target particles and the substitution of nitrogen and sulfur elements. Among these prepared materials, the optimal sample can display a satisfactory discharge capacity of 164.85 mAh g−1 and high capacity retention of 96.5% after thirty cycles. Meanwhile, the superior rate properties and rapid reaction kinetics are achieved as a result of high electrical conductivity and fast ion diffusion coefficient, resulting in an enhanced electrochemical performance. The route in this paper may provide guidance to a large-scale commercial production of energy storage devices.

A fast pyrolysis probe/linear quadrupole ion trap mass spectrometer combination was used to study the primary fast pyrolysis products (those that first leave the hot pyrolysis surface) of cellulose, cellobiose, cellotriose, cellotetraose, cellopentaose, and cellohexaose, as well as of cellobiosan, cellotriosan, and cellopentosan, at 600°C. Similar products with different branching ratios were found for the oligosaccharides and cellulose, as reported previously. However, identical products (with the exception of two) with similar branching ratios were measured for cellotriosan (and cellopentosan) and cellulose. This result demonstrates that cellotriosan is an excellent small-molecule surrogate for studies of the fast pyrolysis of cellulose and also that most fast pyrolysis products of cellulose do not originate from the reducing end. Based on several observations, the fast pyrolysis of cellulose is suggested to initiate predominantly via two competing processes: the formation of anhydro-oligosaccharides, such as cellobiosan, cellotriosan, and cellopentosan (major route), and the elimination of glycolaldehyde (or isomeric) units from the reducing end of oligosaccharides formed from cellulose during fast pyrolysis.

Cellulose, a major component of renewable biomass, is a polymer of glucose. Abundant and cheap iron salts promote the conversion of glucose to 5-hydroxymethylfurfural (HMF) and levulinic acid (LA). In this study, glucose transformations catalyzed by iron(III) chloride (FeCl3) in aqueous and in biphasic media (water and 2-methyltetrahydrofuran (MeTHF)) were investigated. Speciation via mass spectrometry (MS), UV-Vis, and X-ray absorption spectroscopy (XAS) show that FeIII is reduced to FeII (over 95%) readily in the early stage of carbohydrate conversion. The reaction time profiles of reactants (glucose and fructose) as well as products (HMF and LA) were modeled using MATLAB to obtain reaction rate constants. The contributions of iron and the intrinsic Bronsted acidity of iron salts in the sugar conversion are discussed. The kinetic study of sugar conversion indicated that the water–MeTHF biphasic system hinders the conversion of sugars to humins and unknown byproducts and increases the yields of HMF and LA. By adjusting concentrations of FeII and Bronsted acidity, yields of 88% LA (FeCl3, pH = 1) or 56% HMF (FeSO4, pH = 2) from glucose in a water–MeTHF biphasic system are achieved. The optimized reaction conditions proved effective in the conversion of milled poplar biomass to LA (53% yield based on glucose content) and furfural (64% yield based on xylan content) using iron salt, outperforming aluminum and chromium salts.

Mass spectrometric methodology was developed for the determination and manipulation of the primary products of fast pyrolysis of carbohydrates. To determine the true primary pyrolysis products, a very fast heating pyroprobe was coupled to a linear quadrupole ion trap mass spectrometer through a custom-built adaptor. A home-built flow tube that simulates pyrolysis reactor conditions was used to examine the secondary reactions of the primary products. Depending on the experiment, the pyrolysis products were either evaporated and quenched or allowed to react for a period of time. The quenched products were ionized in an atmospheric pressure chemical ionization (APCI) source infused with one of two ionization reagents, chloroform or ammonium hydroxide, to aid in ionization. During APCI in negative ion mode, chloroform produces chloride anions that are known to readily add to carbohydrates with little bias and little to no fragmentation. On the other hand, in positive ion mode APCI, ammonium hydroxide forms ammonium adducts with carbohydrates with little to no fragmentation. The latter method ionizes compounds that are not readily ionized upon negative ion mode APCI, such as furan derivatives. Six model compounds were studied to verify the ability of the ionization methods to ionize known pyrolysis products: glycolaldehyde, hydroxyacetone, furfural, 5-hydroxymethylfurfural, levoglucosan, and cellobiosan. The method was then used to examine fast pyrolysis of cellobiose. The primary fast pyrolysis products were determined to consist of only a handful of compounds that quickly polymerize to form anhydro-oligosaccharides when allowed to react at high temperatures for an extended period of time.

A negatively charged biradical intermediate was successfully generated in the gas phase via cyclization of the deprotonated bicyclo[8.3.0]trideca-12-ene-2,7-diyn-1-one precursor. The inherent negative charge of this biradical allows its characterization via collision-activated dissociation and reactions with a variety of neutral substrates in an FT-ICR mass spectrometer. Although the biradical is unreactive toward reagents that usually react rapidly with positively charged biradicals, such as dimethyl disulfide, it reacts with the halogen-containing substrates carbon tetrachloride, carbon tetrabromide, and bromotrichloromethane via bromine or chlorine atom abstraction, which supports its biradical structure. The results presented in this study indicate that cyclizations commonly used in solution to form biradical intermediates from enediyne compounds may also occur in the gas phase.

Klf4 is a transcription factor of the family of Kruppel-like factors and plays important roles in stem cell biology; however, its function during embryogenesis is unknown. Here, we report the characterization of a Klf4 homologue in Xenopus laevis during embryogenesis. Klf4 is transcribed both maternally and zygotically and the transcript is ubiquitous in embryos during germ-layer formation. Klf4 promotes endoderm differentiation in both Nodal/Activin-dependent and -independent manners. Moreover, Klf4 regulates anteroposterior body axis patterning via activation of a subset of genes in the Spemann organizer, such as Noggin, Dkk1 and Cerberus, which encode Nodal, Wnt and BMP antagonists. Loss of Klf4 function leads to the failure of germ-layer differentiation, the loss of responsiveness of early embryonic cells to inducing signals, e.g. Nodal/Activin, and the loss of transcription of genes involved in axis patterning. We conclude that Klf4 is required for germ-layer differentiation and body axis patterning by means of rendering early embryonic cells competent to differentiation signals.

Experimental studies have demonstrated that a typical investor derives utility of the gain and loss, relative to certain reference point, realized at each sale of a stock, and that the reference point adapts asymmetrically to the stock's prior gains and losses in that the adaptation to a gain is more substantial than to a comparable loss. This empirical finding motivates us to consider a dynamic trading problem in which an agent decides when to sequentially sell and buy a stock in order to maximize her utility of terminal wealth and realized gains and losses based on a reference point that adapts asymmetrically to the stock's prior gains and losses. We show that this agent is more reluctant to sell the stock at a loss than another agent whose reference point does not adapt to the stock gain or loss at all, leading to a higher percentage of gains realized (PGR) and a lower percentage of losses realized (PLR). We also show that when the agent weighs the utility of realized gains and losses more heavily in her investment criteria, she trades the stock more frequently, the PGR becomes lower, and the PLR becomes higher.

A credit valuation adjustment (CVA) is an adjustment applied to the value of a derivative contract or a portfolio of derivatives to account for counterparty credit risk. Measuring CVA requires combining models of market and credit risk to estimate a counterparty's risk of default together with the market value of exposure to the counterparty at default. Wrong-way risk refers to the possibility that a counterparty's likelihood of default increases with the market value of the exposure. We develop a method for bounding wrong-way risk, holding fixed marginal models for market and credit risk and varying the dependence between them. Given simulated paths of the two models, a linear program computes the worst-case CVA. We analyze properties of the solution and prove convergence of the estimated bound as the number of paths increases. The worst case can be overly pessimistic, so we extend the procedure by constraining the deviation of the joint model from a baseline reference model. Measuring the deviation through relative entropy leads to a tractable convex optimization problem that can be solved through the iterative proportional fitting procedure. Here, too, we prove convergence of the resulting estimate of the penalized worst-case CVA and the joint distribution that attains it. We consider extensions with additional constraints and illustrate the method with examples.

Counterparty risk measurement integrates two sources of risk: market risk, which determines the size of a firm’s exposure to a counter party, and credit risk, which reflects the likelihood that the counterparty will default on its obligations. Wrong-way risk refers to the possibility that a counterparty’s default risk increases with the market value of the exposure. We investigate the potential impact of wrong-way risk in calculating a credit valuation adjustment (CVA) to a derivatives portfolio: CVA has become a standard tool for pricing counterparty risk and setting associated capital requirements. We present a method, introduced in our earlier work, for bounding the impact of wrong-way risk on CVA. The method holds fixed marginal models for market and credit risk while varying the dependence between them. Given simulated paths of the two models, we solve a linear program to find the worst-case CVA resulting from wrong way risk. The worst case can be overly conservative, so we extend the procedure by penalizing deviations of the joint model from a baseline model. By varying the penalty for deviations, we can sweep out the full range of possible CVA values for different degrees of wrong-way risk. Our method addresses an important source of model risk in counterparty risk measurement.

The synthesis of furoins from biomass-derived furfural and 2-methylfurfural is demonstrated in high yields in green and renewable solvents using N-heterocyclic carbene organocatalysts. The resulting furoin molecules are used as precursors for fuels using cascade catalysis, first by using Pd/C with acidic co-catalysts under very mild conditions to yield oxygenated C12 molecules. Two main products were formed, which we identified as 1,2-bis(5-methyltetrahydrofuran-2-yl)ethane and 1-(5-methyltetrahydrofuran-2-yl)heptanol. The use of a Pd/Zeolite-β catalyst under more extreme conditions resulted in the complete hydrodeoxygenation of 5,5'-dimethylfuroin to dodecanes in high yields (76%) and exceptional selectivity (94%) for n-dodecane.

The reactivity of carbon-centered distonic radical ions has been of interest for decades. The existence of distonic radical ions was first postulated by Gross and McLafferty in the early 1970’s.1,2 In 1978, Bouma, MacLeod and Radom reported experimental results that supported theoretical predictions of the existence of a stable ring-opened ethylene oxide distonic radical cation.3 Ions with spatially separated charge and radical sites were coined as “distonic ions” by Yates, Bouma, and Radom4 in 1984. They later refined this definition5 to correspond to radical ions generated by ionization of a zwitterion, ylide, or diradical. Eberlin and co-workers later introduced the term “distonoid”, meaning distonic like, to encompass any radical ion that displays distonic “character” (i.e., ions with a high degree of discrete (non-mandatory) charge-spin separation) and is over-looked as a result of the strict distonic ion definition.6 However, the “distonoid” classification is not commonly used by the scientific community. Currently, the term “distonic” is widely accepted and used to denote ions with formally separated charge and radical sites even if they do not fall into the formal definition.7 According to the conventional valence bond description, the charge and radical sites are on adjacent atoms in α-distonic ions while they are separated by one and two atoms in β- and γ-distonic ions, respectively. A vast amount of experimental and theoretical studies were dedicated to distonic ions from the 1980’s to 1990’s, which have been previously reviewed separately by Hammerum and Kenttamaa.8,9,10 The focus of this review is on gaseous ions with one or more aryl radical sites, a subgroup of distonic radical cations. The interest in these distonic ions was initially sparked by the limited knowledge on the reactivity of neutral phenyl radicals and their diradical counterparts in spite of the vast amount of research dedicated to these reactive intermediates.11–70 Many such mono- and diradicals have been investigated as they are thought to play a vital role in numerous fields, including combustion,11–13 polymerization,14–16 atmospheric chemistry,17–19 interstellar chemistry,20 organic synthesis8 and the biological activity of certain drugs.21–33 In the 1990’s, the formation of such aromatic diradicals in naturally occurring anti-tumor antibiotics was associated with their DNA-cleaving ability.21–33 The two radical sites are thought to abstract a hydrogen atom from each strand of double stranded DNA, thus causing irreversible DNA cleavage. Since then, theoretical and experimental research on aryl mono- and diradicals has boomed. An area of special interest has been the mechanistic understanding of hydrogen atom abstraction by these radicals from small organic and biological molecules both in solution34–45 and in the gas phase.46–70 However, the ability to predict the rates of such seemingly simple reactions has proven challenging due to a poor understanding of the nature of the transition states for these reactions. Further, the examination of the chemical properties of neutral radicals is a challenge due to the difficulty to cleanly generate them both in solution and in the gas phase. In order to address the above difficulties, studies were carried out in the early 1990’s on distonic radical cations’ ion-molecule reactions inside mass spectrometers as ions can be easily manipulated in this environment.46–70 Distonic radical cations that have a phenyl radical site spatially separated from a chemically inert charge site were found to almost exclusively undergo radical reactions at the radical site(s) in the gas phase46–70 and lately also in solution.45 Hence, examination of these distonic ions will provide information on the properties of phenyl mono- and diradicals. A special benefit of using mass spectrometry to study above species is that the desired charged radical can be isolated before examining its reactivity. Hence, the precursors to any products formed in these gas-phase experiments are known, which is not always true for solution experiments wherein highly reactive molecules cannot be isolated. The chemical properties of many aryl mono-, di- and triradicals have been successfully examined in mass spectrometers by using this ‘distonic ion approach’.49,50,52 The results obtained in these studies provide valuable information on the relative reactivities of mono- and polyradicals, which would otherwise not be available. This paper reviews the current knowledge of the properties and reactivity of distonic radical ions with aryl radical sites and the mechanisms of these reactions. Distonic phenyl radical ions generated within peptides are not included due to space limitations and also since these radicals are usually generated as precursors to less reactive nonaromatic peptide radicals that are the true interest of the researchers. However, this is an important and exciting new field of distonic ion research that should be reviewed separately.

The reactivity of carbon-centered distonic radical ions has been of interest for decades. The existence of distonic radical ions was first postulated by Gross and McLafferty in the early 1970’s.1,2 In 1978, Bouma, MacLeod and Radom reported experimental results that supported theoretical predictions of the existence of a stable ring-opened ethylene oxide distonic radical cation.3 Ions with spatially separated charge and radical sites were coined as “distonic ions” by Yates, Bouma, and Radom4 in 1984. They later refined this definition5 to correspond to radical ions generated by ionization of a zwitterion, ylide, or diradical. Eberlin and co-workers later introduced the term “distonoid”, meaning distonic like, to encompass any radical ion that displays distonic “character” (i.e., ions with a high degree of discrete (non-mandatory) charge-spin separation) and is over-looked as a result of the strict distonic ion definition.6 However, the “distonoid” classification is not commonly used by the scientific community. Currently, the term “distonic” is widely accepted and used to denote ions with formally separated charge and radical sites even if they do not fall into the formal definition.7 According to the conventional valence bond description, the charge and radical sites are on adjacent atoms in α-distonic ions while they are separated by one and two atoms in β- and γ-distonic ions, respectively. A vast amount of experimental and theoretical studies were dedicated to distonic ions from the 1980’s to 1990’s, which have been previously reviewed separately by Hammerum and Kenttamaa.8,9,10 The focus of this review is on gaseous ions with one or more aryl radical sites, a subgroup of distonic radical cations. The interest in these distonic ions was initially sparked by the limited knowledge on the reactivity of neutral phenyl radicals and their diradical counterparts in spite of the vast amount of research dedicated to these reactive intermediates.11–70 Many such mono- and diradicals have been investigated as they are thought to play a vital role in numerous fields, including combustion,11–13 polymerization,14–16 atmospheric chemistry,17–19 interstellar chemistry,20 organic synthesis8 and the biological activity of certain drugs.21–33 In the 1990’s, the formation of such aromatic diradicals in naturally occurring anti-tumor antibiotics was associated with their DNA-cleaving ability.21–33 The two radical sites are thought to abstract a hydrogen atom from each strand of double stranded DNA, thus causing irreversible DNA cleavage. Since then, theoretical and experimental research on aryl mono- and diradicals has boomed. An area of special interest has been the mechanistic understanding of hydrogen atom abstraction by these radicals from small organic and biological molecules both in solution34–45 and in the gas phase.46–70 However, the ability to predict the rates of such seemingly simple reactions has proven challenging due to a poor understanding of the nature of the transition states for these reactions. Further, the examination of the chemical properties of neutral radicals is a challenge due to the difficulty to cleanly generate them both in solution and in the gas phase. In order to address the above difficulties, studies were carried out in the early 1990’s on distonic radical cations’ ion-molecule reactions inside mass spectrometers as ions can be easily manipulated in this environment.46–70 Distonic radical cations that have a phenyl radical site spatially separated from a chemically inert charge site were found to almost exclusively undergo radical reactions at the radical site(s) in the gas phase46–70 and lately also in solution.45 Hence, examination of these distonic ions will provide information on the properties of phenyl mono- and diradicals. A special benefit of using mass spectrometry to study above species is that the desired charged radical can be isolated before examining its reactivity. Hence, the precursors to any products formed in these gas-phase experiments are known, which is not always true for solution experiments wherein highly reactive molecules cannot be isolated. The chemical properties of many aryl mono-, di- and triradicals have been successfully examined in mass spectrometers by using this ‘distonic ion approach’.49,50,52 The results obtained in these studies provide valuable information on the relative reactivities of mono- and polyradicals, which would otherwise not be available. This paper reviews the current knowledge of the properties and reactivity of distonic radical ions with aryl radical sites and the mechanisms of these reactions. Distonic phenyl radical ions generated within peptides are not included due to space limitations and also since these radicals are usually generated as precursors to less reactive nonaromatic peptide radicals that are the true interest of the researchers. However, this is an important and exciting new field of distonic ion research that should be reviewed separately.

Catalytic deoxydehydration (DODH) of vicinal diols is carried out employing methyltrioxorhenium (MTO) as the catalyst and a sacrificial alcohol as the reducing agent. The reaction kinetics feature an induction period when MTO is added last and show zero-order in [diol] and half-order dependence on [catalyst]. The rate-determining step involves reaction with alcohol, as evidenced by a KIE of 1.4 and a large negative entropy of activation (Delta S-double dagger = -154 +/- 33 J mol(-1) K-1). The active form of the catalyst is methyldioxorhenium(V) (MDO), which is formed by reduction of MTO by alcohol or via a novel C-C bond cleavage of an MTO-diolate complex. The majority of the MDO-diolate complex is present in dinuclear form, giving rise to the [Re](1/2) dependence. The MDO-diolate complex undergoes further reduction by alcohol in the rate-determining step to give rise to a putative rhenium(III) diolate. The latter is the active species in DODH extruding stereoselectively trans-stilbene from (R,R)-(+)-hydrobenzoin to regenerate MDO and complete the catalytic cycle.

In order to improve the understanding of the interactions of aromatic sigma,sigma-biradicals with DNA, the reactivity of three isomeric sigma,sigma-biradicals toward four dinucleoside phosphates was studied in a mass spectrometer. The dinucleoside phosphates were evaporated into the mass spectrometer by using laser-induced acoustic desorption (LIAD). The results demonstrate that the structure of the sigma,sigma-biradical and the base sequence of the dinucleoside phosphate can have a major influence on these reactions.

The gas-phase reactions of sugars with aromatic, carbon-centered sigma,sigma-biradicals with varying polarities [as reflected by their calculated electron affinities (EA)] and extent of spin-spin coupling [as reflected by their calculated singlet-triplet (S-T) gaps] have been studied. The biradicals are positively charged, which allows them to be manipulated and their reactions to be studied in a Fourier-transform ion cyclotron resonance mass spectrometer. Hydrogen atom abstraction from sugars was found to be the dominant reaction for the biradicals with large EA values, while the biradicals with large S-T gaps tend to form addition/elimination products instead. Hence, not all sigma, sigma-biradicals may be able to damage DNA by hydrogen atom abstraction. The overall reaction efficiencies of the biradicals towards a given substrate were found to be directly related to the magnitude of their EA values, and inversely related to their S-T gaps. The EA of a biradical appears to be a very important rate-controlling factor, and it may even counterbalance the reduced radical reactivity characteristic of singlet biradicals that have large S-T gaps.

After publication of the paper, the authors realized that the affiliation of the fourth author (Tiberiu Esanu) was given incorrectly. Its correct version appears above. Moreover, a second funding grant was missed in the acknowledgements. We give their complete correct version below.

The gas-phase reactions of sugars with aromatic, carbon-centered σ,σ-biradicals with varying polarities [as reflected by their calculated electron affinities (EA)] and extent of spin-spin coupling [as reflected by their calculated singlet-triplet (S-T) gaps] have been studied. The biradicals are positively charged, which allows them to be manipulated and their reactions to be studied in a Fourier-transform ion cyclotron resonance mass spectrometer. Hydrogen atom abstraction from sugars was found to be the dominant reaction for the biradicals with large EA values, while the biradicals with large S-T gaps tend to form addition/elimination products instead. Hence, not all σ,σ-biradicals may be able to damage DNA by hydrogen atom abstraction. The overall reaction efficiencies of the biradicals towards a given substrate were found to be directly related to the magnitude of their EA values, and inversely related to their S-T gaps. The EA of a biradical appears to be a very important rate-controlling factor, and it may even counterbalance the reduced radical reactivity characteristic of singlet biradicals that have large S-T gaps.