Combined UHV and ambient pressure studies of 1,3-butadiene adsorption and reaction on Pd(1 1 1) by GC, IRAS and XPS

Abstract The hydrogenation of 1,3-butadiene on Pd(1 1 1) at 300 K was studied at atmospheric pressure by infrared reflection absorption spectroscopy (IRAS) and gas chromatography (GC). Kinetic measurements showed 1-butene, trans-2-butene and cis-2-butene as primary products. Once 1,3-butadiene had been completely consumed, 1-butene was re-adsorbed on the surface producing trans-/cis-2-butene through isomerization and n-butane through hydrogenation. These results were corroborated by in situ IRAS spectroscopy. Post-reaction analysis by X-ray photoelectron spectroscopy (XPS) in the C1s region revealed a band at 284.2 eV, corresponding to adsorbed butadiene and/or carbonaceous deposits. Quantification of this peak revealed a total carbon coverage of 0.3 ML. Nevertheless, deactivation due to carbon deposition was a minor effect under our reaction conditions, as indicated by the kinetics of the subsequent butene hydrogenation reaction. Temperature-dependent XPS experiments after butadiene adsorption at 100 K indicated a high stability of the diene molecule with hardly any desorption and/or decomposition up to 500 K. Above this temperature, butadiene decomposed to carbon species that eventually dissolved in the Pd bulk above 700 K

Design of a Functionalized Metal-Organic Framework System for Enhanced Targeted Delivery to Mitochondria.

Mitochondria play a key role in oncogenesis and constitute one of the most important targets for cancer treatments. Although the most effective way to deliver drugs to mitochondria is by covalently linking them to a lipophilic cation, the in vivo delivery of free drugs still constitutes a critical bottleneck. Herein, we report the design of a mitochondria-targeted metal-organic framework (MOF) that greatly increases the efficacy of a model cancer drug, reducing the required dose to less than 1% compared to the free drug and ca. 10% compared to the nontargeted MOF. The performance of the system is evaluated using a holistic approach ranging from microscopy to transcriptomics. Super-resolution microscopy of MCF-7 cells treated with the targeted MOF system reveals important mitochondrial morphology changes that are clearly associated with cell death as soon as 30 min after incubation. Whole transcriptome analysis of cells indicates widespread changes in gene expression when treated with the MOF system, specifically in biological processes that have a profound effect on cell physiology and that are related to cell death. We show how targeting MOFs toward mitochondria represents a valuable strategy for the development of new drug delivery systems

Design of a functionalized metal-organic framework system for enhanced targeted delivery to mitochondria

Mitochondria play a key role in oncogenesis and constitute one of the most important targets for cancer treatments. Although the most effective way to deliver drugs to mitochondria is by covalently linking them to a lipophilic cation, the in vivo delivery of free drugs still constitutes a critical bottleneck. Herein, we report the design of a mitochondria-targeted metal-organic framework (MOF) that greatly increases the efficacy of a model cancer drug, reducing the required dose to less than 1% compared to the free drug and ca. 10% compared to the non-targeted MOF. The performance of the system is evaluated using a holistic approach ranging from microscopy to transcriptomics. Super-resolution microscopy of MCF-7 cells treated with the targeted MOF system reveals important mitochondrial morphology changes that are clearly associated with cell death as soon as 30 minutes after incubation. Whole transcriptome analysis of cells indicated widespread changes in gene expression when treated with the MOF system, specifically in biological processes that have a profound effect on cell physiology and that are related to cell death. We show how targeting MOFs towards mitochondria represents a valuable strategy for the development of new drug delivery systems

Methane hydrate formation in confined nanospace can surpass nature

Natural methane hydrates are believed to be the largest source of hydrocarbons on Earth. These structures are formed in specific locations such as deep-sea sediments and the permafrost based on demanding conditions of high pressure and low temperature. Here we report that, by taking advantage of the confinement effects on nanopore space, synthetic methane hydrates grow under mild conditions (3.5 MPa and 2 degrees C), with faster kinetics (within minutes) than nature, fully reversibly and with a nominal stoichiometry that mimics nature. The formation of the hydrate structures in nanospace and their similarity to natural hydrates is confirmed using inelastic neutron scattering experiments and synchrotron X-ray powder diffraction. These findings may be a step towards the application of a smart synthesis of methane hydrates in energy-demanding applications (for example, transportation).We acknowledge UK Science and Technlology Facilities Council for the provision of beam time on the TOSCA spectrometer (Projects RB1410624 and RB122099) and financial support from the European Commission under the 7th Framework Programme through the 'Research Infrastructures' action of the 'Capacities' Programme (NMI3-II Grant number 283883). J.S.-A. and F.R. acknowledges the financial support from MINECO: Strategic Japanese-Spanish Cooperation Program (PLE2009-0052), Concert Project-NASEMS (PCIN-2013-057) and Generalitat Valenciana (PROMETEO/2009/002). F.R. and J.L.J. thank the financial support from MINECO (MAT2012-38567-C02-01, Consolider Ingenio 2010-Multicat CSD-2009-00050 and SEV-2012-0267). K.K. thanks Grant-in-Aid for Scientific Research (A) (2424-1038), Japan. 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CH₄/H₂O Competitive adsorption in Nano porous materials under clathrate hydrate formation conditions

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From Pd nanoparticles to single crystals: 1,3-butadiene hydrogenation on well-defined model catalysts

Although 1,3-butadiene hydrogenation is known to be a structure-sensitive reaction, correlation of the catalytic activity with the exact Pd particle surface structure shows that the reaction is in fact particle size independent

Micro/Mesoporous Activated Carbons Derived from Polyaniline: Promising Candidates for CO₂ Adsorption

A series of activated carbons were prepared by carbonization of polyaniline at different temperatures, using KOH or K₂CO₃ as activating agent. Pure microporous or micro/mesoporous activated carbons were obtained depending on the preparation conditions. Carbonization temperature has been proven to be a key parameter to define the textural properties of the carbon when using KOH. Low carbonization temperatures (400–650 °C) yield materials with a highly developed micro- and mesoporous structure, whereas high temperatures (800 °C) yield microporous carbons. Some of the materials prepared using KOH exhibit a BET surface area superior to 4000 m²/g, with total pore volume exceeding 2.5 cm³/g, which are among the largest found for activated carbons. On the other hand, microporous materials are obtained when using K₂CO₃, independently of carbonization temperature. Some of the materials were tested for CO₂ capture due to their high microporosity and N content. The adsorption capacity for CO₂ at atmospheric pressure and 0 °C achieves a value of ∼7.6 mmol CO₂/g, which is among the largest reported in the literature. This study provides guidelines for the design of activated carbons with a proper N/C ratio for CO₂ capture at atmospheric pressure