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2,318 results for “Synthesis”
Raw data for the article "Synthesis of Fluorescent Cyclic Peptides via Gold(I)-Catalyzed Macrocyclization"
<p>Raw NMR, IR, MS fluorescence and imaging data for the article "Synthesis of Fluorescent Cyclic Peptides via Gold(I)-Catalyzed Macrocyclization" published in the Journal of the American Chemical Society, DOI: </p><p><a href="https://doi.org/10.1021/jacs.3c09261">https://doi.org/10.1021/jacs.3c09261</a></p><p>The number of the folders either correspond to compounds numbers in the article or the name of the folder is self-describing. All details concerning conditions and equipment for measurements can be found in the supporting information of the article. For convenience, the word file version of the supporting information can be found on the top of the raw data folder.</p>
Aza-Claisen rearrangement as a key step in synthesis of specialised anilines used in the production of efficient ethenolysis catalysts
<p>Data confirming the structure of the new compounds obtained within the project, published in <br><i><strong>Catal. Sci. Technol.</strong></i>, 2023,<strong>13</strong>, 3682-3688, https://pubs.rsc.org/en/content/articlelanding/2023/cy/d3cy00395g</p><p>The research was supported by the National Science Centre, Poland (OPUS grant DEC-2017/27/B/ST5/02563).</p>
Inovis: Instant Novel-view Synthesis
<p><strong>Abstract:</strong> Novel-view synthesis is an ill-posed problem in that it requires inference of previously unseen information. Recently, reviving the traditional field of image-based rendering, neural methods proved particularly suitable for this interpolation/extrapolation task; however, they often require a-priori scene-completeness or costly preprocessing steps and generally suffer from long (scene-specific) training times. Our work draws from recent progress in neural spatio-temporal supersampling to enhance a state-of-the-art neural renderer's ability to infer novel-view information at inference time. We adapt a supersampling architecture~\cite{xiao2020neural}, which resamples previously rendered frames, to instead recombine nearby camera images in a multi-view dataset. These input frames are warped into a joint target frame, guided by the most recent (point-based) scene representation, followed by neural interpolation. The resulting architecture gains sufficient robustness to significantly improve transferability to previously unseen datasets. In particular, this enables novel applications for neural rendering where dynamically streamed content is directly incorporated in a (neural) image-based reconstruction of a scene. As we will show, our method reaches state-of-the-art performance when compared to previous works that rely on static and sufficiently densely sampled scenes; in addition, we demonstrate our system's particular suitability for dynamically streamed content, where our approach is able to produce high-fidelity novel-view synthesis even with significantly fewer available frames than competing neural methods.</p>
The nature and extent of bomb tritium remaining in deep vadose zones: A synthesis and prognosis
<p>Tritium present in deep vadose zones is a useful tracer for estimating groundwater recharge, but its full utility is constrained by not knowing where and for how long the tritium tracing method remains applicable. We obtained 44 tritium profiles from 17 globally distributed sites with vadose zone thicknesses of 13−624 m and used transport models to estimate the number of years that tritium may still be useful. Results show that the method may still be usable for 26 of 44 soil profiles surveyed, mainly in China, Australia, USA, South Africa, and Senegal, with a remaining useful period of between 6 and 83 years. We also developed a statistical model that uses outputs from a hydrological model to predict the applicability of the tritium tracing method. Global implementation of the statistical model showed that the method remains usable at 20% of Earth's land mass (excluding Antarctica and Greenland) over the next few decades.</p>
Detailed Controller Synthesis and Laboratory Verification of a Matching-Controlled Grid-Forming Inverter for Microgrid Applications
<p><strong>Figure5 Blackstart:</strong><br>BS->blackstart<br>noload/min/inter->Initial load<br>U4 -> Voltage waveforms<br>Udq-> Voltage dq values</p> <p><strong>Figure6 Stat<br></strong>data_sati_voltage3 -> Current and voltage waveforms<br>THD -> THD values<br><br><strong>Figure7 Trans:</strong></p> <p>Trans4to7kwdq-> dq values<br>Trans4to7kwPower->P and Q values<br>Trans4to7kwUI->Waveforms</p> <p><strong>Figure8 DCSens:</strong><br>Test1-14 -> Tests corresponding to DC bus sensitivity<br>p/i min/max -> identifier wether p or i value were increased/decreased</p> <p><strong>Figure9 ACsens:</strong><br>AC0-22 -> Tests corresponding to AC sensitivity</p> <p> </p>
Spatial data of Synthesis of the land carbon fluxes of the Amazon region between 2010 and 2020
<p>Spatial data used in the main figures of the manuscript Synthesis of the land carbon fluxes of the Amazon region between 2010 and 2020. </p> <p>To reproduce Figure 4b sum the maps of Figure 2c+2e and Figure 4c sum the maps of Figure 2d+2e. </p> <p>To reproduce Figure 5b sum the maps of Figure 3c+3d. </p> <p>The shapefiles with the Brazilian Amazon and biogeographical Amazon are also provided. </p>
Bacterial zoonoses impacts to conservation of wildlife populations: A global synthesis
<p>Emerging infectious diseases have significantly increased in recent years; approximately 60% of these emerging diseases are of zoonotic origin, and of those, around 70% were identified to start with wild animals. To better understand the impacts of zoonotic diseases on wildlife, there is a need to identify the distribution and impact of zoonotic pathogens in wildlife, particular those species with threatened populations. To investigate this question, we constructed a zoonotic disease database identifying wildlife hosts for each bacterial zoonotic disease and recorded clinical signs of disease for each host-pathogen relationship if found. Species of least concern were found to have a significantly higher prevalence and richness of zoonotic bacterial diseases (n= 0.0608, x<sup>2</sup>= 5.898, p=0.01516). The taxonomic level Order was found to be the best predictor for pathogen richness, and the Artiodactyla and Carnivora contain a significantly higher pathogen richness than other vertebrate Orders. Species with the greatest pathogen richness include the wild boar (<em>Sus scrofa</em>, n=66), Northern raccoon (<em>Procyon lotor</em>, n=16) and the red fox (<em>Vulpes vulpes</em>, n=41). Our results indicate bacterial zoonoses are not likely to be a driving factor of species population declines, and future zoonotic disease surveillance efforts should target species in the Artiodactyla and Carnivora families. The wild boar (<em>Sus scrofa</em>) in particular may be a good candidate for zoonotic disease monitoring due to its high pathogen richness, wide range, and large population. Understanding the impacts and distribution of bacterial zoonoses in wildlife populations can help in planning for future wildlife management efforts, particularly in species of conservation concern and wildlife disease monitoring.</p>
Heterotelechelic silicones: Facile synthesis and functionalization using silane-based initiators
<p><span>The synthetic utility of heterotelechelic polydimethylsiloxane (PDMS) derivatives is limited due to challenges in preparing materials with high chain-end fidelity. In this study, anionic ring-opening polymerization (AROP) of hexamethylcyclotrisiloxane (D<sub>3</sub>) monomer using a specifically designed silyl hydride (Si–H)-based initiator provides a versatile approach towards a library of heterotelechelic PDMS polymers. A novel initiator, where the Si–H terminal group is connected to a C atom (H</span><span>–</span><span>Si–C) and not an O atom (H–Si–O) as in traditional systems, suppresses intermolecular transfer of the Si–H group, leading to heterotelechelic PDMS derivatives with a high degree of control over chain-ends. <em>In-situ</em> termination of the D<sub>3</sub> propagating chain end with commercially available chlorosilanes (alkyl chlorides, methacrylates, and norbornenes) yields an array of chain-end functionalized PDMS derivatives. This diversity can be further increased by hydrosilylation with functionalized alkenes </span><span>(alcohols, esters, and epoxides) to </span><span>generate a library of heterotelechelic PDMS polymers. Due to the living nature of ring opening polymerization and efficient initiation, narrow-dispersity (<em>Đ</em> < 1.2) polymers spanning a wide range of molar masses (2 – 11 kg mol<sup>−1</sup>) were synthesized. With facile access to <em>α</em>-Si–H and <em>ω</em>-norbornene functionalized PDMS macromonomers (H–PDMS–Nb), the synthesis of well-defined super-soft (<em>G</em>ʹ = 30 kPa) PDMS bottlebrush networks, which are difficult to prepare using established strategies, was demonstrated</span><span>.</span></p>
Lichen biomass for green synthesis of silver nanocolloids
<p>Lichen is one of the most abundant non-vascular biomasses, however, a systematic study on application of the biomass in nanomaterial synthesis is very limited. In this study, aqueous lichen extract was obtained from <em>Hypotrachyna cirrhata, </em>one of the most abundant Himalayan Lichen biomass,<em> </em>following a simple cold percolation method. The effect of extract to silver nitrate mixing ratio, pH, and waiting time in growth and stability of nanoparticle was systematically explored. The rate constant for bio-reduction was found to be 5.3×10<sup>-3</sup> min<sup>-1</sup>. Transmission electron microscopy (TEM) showed a narrow particle size distribution with mean particle size of 11.1±3.6 nm (n=200) The X-ray diffraction (XRD) and selected area electron diffraction (SAED) techniques confirmed the formation of cubic crystals. The synthesized colloidal solution showed excellent response for Hg<sup>2+</sup> and Cu<sup>2+</sup> ions in spiked water samples. The limit of detection and calibration sensitivity for Hg<sup>2+</sup> and Cu<sup>2+</sup> ions were found to be 1 mg/L and 5 mg/L, and 2.9×10<sup>-3</sup> units/ppm and 1.6×10<sup>-3</sup> units/ppm; respectively. These findings suggested that green synthesis of spherical silver nanoparticles having narrow size distribution is possible using the aqueous lichen extract and the nanoparticles can be used for detection of selected heavy metals.</p>
DCASE 2024 Challenge Task 7 Development Dataset : Environmental Sound Scene Synthesis
<h1><strong>Description</strong></h1> <p>This dataset comprises embeddings and captions utilized as the development dataset for <a href="https://dcase.community/challenge2024/task-sound-scene-synthesis"><strong>DCASE 2024 Challenge Task 7</strong></a>, focusing on 'Environmental Sound Scene Synthesis.' The embeddings are derived from 60 different 4-second audio files formatted as mono 32-bit 32kHz, and are contained in the 'embeddings.tar.xz' file. Captions corresponding to each audio file can be found in 'caption.csv'. This dataset does not comprise the audio files, only the embeddings. Three different types of embeddings are provided: VGGish (vggish), MS-CLAP (clap-2023), and PANNs CNN14 Wavegram-Logmel (panns-wavegram-logmel). Only PANNs CNN14 Wavegram-Logmel (panns-wavegram-logmel) embeddings are used for evaluation in the challenge. For further details, please refer to the challenge website.</p> <p><strong>Contact</strong></p> <ul> <li>Modan Tailleur, modan.tailleur@ls2n.fr</li> <li>Mathieu Lagrange, mathieu.lagrange@ls2n.fr</li> </ul>
Direct synthesis, characterization, in vitro and in silico studies of simple chalcones as potential antimicrobial and antileishmanial agents
<p>Chalcone represents a vital biosynthetic scaffold owing to its numerous therapeutic effects. The present study was intended to synthesize seventeen chalcone derivatives <strong>(3a-q)</strong> by direct coupling of substituted acetophenones and benzaldehyde. The target chalcones were characterized by spectroscopic analyses followed by their <em>in vitro</em> antimicrobial, and antileishmanial investigations with reference to standard drugs. The majority of the chalcones displayed good to excellent biological activities. Chalcone <strong>3q</strong> (1000 μg/mL) exhibited the most potent antibacterial effect with its zone of inhibition values of 30, 33, and 34 mm versus <em>Staphylococcus aureus,</em> <em>Escherichia coli, and Pseudomonas aeruginosa </em>respectively. The results also confirmed chalcone <strong>3q</strong> to be the most potent versus <em>Leishmania major </em>with the lowest IC<sub>50</sub> value of 0.59±0.12 μg/mL.<em> </em>Chalcone <strong>3i</strong> (500 μg/mL) was noticed to be the most potent antifungal agent with its zone of inhibition being 29 mm against <em>Candida albicans</em>. Computational studies of chalcones <strong>3i </strong>and<strong> 3q</strong> supported the preliminary <em>in vivo</em> results. The existence of the amino moiety and bromine atom on ring-A and methoxy moieties on ring-B caused better biological effects of the chalcones. In brief, the investigations reveal that chalcones (<strong>3i </strong>and<strong> 3q) </strong>can be employed as building blocks<strong> </strong>to discover novel antimicrobial agents.</p>
Videos accompanying article "Facial Expressions for Sign Language Synthesis using FACSHuman and AZee"
<p>Accompanying videos for the article "Facial Expressions for Sign Language Synthesis using FACSHuman and AZee".</p> <ul> <li>all_action_units.mp4 - Shows mesh deformations for all the action units used.</li> <li>all_expressions.mp4 - Shows all the expressions synthesized using the study.</li> <li>big_threatening_hot.mp4 - Shows comparison of a sign with and without facial expressions.</li> </ul>
IntelliMan_WP5_Grasping, Manipulationand Arm-Hand Coordination_T5.4_Experience-and Model-Based Grasp Synthesis and Manipulation_Pushing_v0
<p>The dataset provides the data recorded during the experiments described in the paper “Costanzo, M.; De Simone, M.; Federico, S.; Natale, C. Non-Prehensile Manipulation Actions and Visual 6D Pose Estimation for Fruit Grasping Based on Tactile Sensing. Robotics 2023, 12, 92. https://doi.org/10.3390/robotics12040092”</p>
Continuous-Flow Synthesis of BiVO4 Nanoparticles: From laboratory scale to practical systems
<p>#Data set of "Continuous-Flow Synthesis of BiVO4 Nanoparticles: From laboratory scale to practical systems"</p> <p>---</p> <p>## GENERAL INFORMATION</p> <p>1. Data set title: "Continuous-Flow Synthesis of BiVO4 Nanoparticles: From laboratory scale to practical systems"</p> <p>2.Authorship: <br> Name: Christian Robles<br> Institution: Institute of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0003-1166-2950</p> <p> Name: Laura Montañés<br> Institution: Institute of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0002-1076-013X <br> <br> Name: Camilo A. Mesa<br> Institution: Institute of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0002-8450-2563</p> <p> Name:Diego Iglesias <br> Institution: institute of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0002-4030-5816</p> <p> Name: Helena Rabelo<br> Institution: Catalan Institute of Nanoscience and Nanotechnology (ICN2) and BIST, Campus UAB, Ballaterra, 08193, Barcelona, Spain<br> ORCID: 0000-0002-7773-3929</p> <p> Name: Maria Chiara Spadaro<br> Institution: Catalan Institute of Nanoscience and Nanotechnology (ICN2) and BIST, Campus UAB, Ballaterra, 08193, Barcelona, Spain. Department SIMAU, Marche Polytechnic University, 60131, Ancona, Italy.<br> ORCID: 0000-0002-6540-0377<br> <br> Name: Jordi Arbiol<br> Institution: Catalan Institute of Nanoscience and Nanotechnology (ICN2) and BIST, Campus UAB, Ballaterra, 08193, Barcelona, Spain ICREA, 08010, Barcelona, Spain<br> ORCID: 0000-0002-0695-1726</p> <p> Name: Jesús Redondo<br> Institution: Department of Polymers and Advanced Materials, Centro de Física de Materiales CFM (UPV/EHU-CSIC), University of the Basque Country UPV/EHU, 20018, San Sebastián Spain. Department of Surface and Plasma Science, Faculty of Mathematics and Physics, Charles University, 180 00 Prague 8, Czech Republic<br> ORCID: 0000-0002-8147-689X</p> <p> Name: F.Schiller<br> Institution: Department of Polymers and Advanced Materials, Centro de Física de Materiales CFM (UPV/EHU-CSIC), University of the Basque Country UPV/EHU, 20018, San Sebastián Spain. Donostia International Physics Center DIPC, 20018 San Sebastián, Spain<br> ORCID: 0000-0003-1727-3542</p> <p> Name:Sara Barja<br> Institution: Department of Polymers and Advanced Materials, Centro de Física de Materiales CFM (UPV/EHU-CSIC), University of the Basque Country UPV/EHU, 20018, San Sebastián Spain. Donostia International Physics Center DIPC, 20018 San Sebastián, Spain. IKERBASQUE, Basque Foundation for Science, 48009 Bilbao, Spain</p> <p> Name: Beatriz Julián-López<br> Institution: Institude of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0003-1019-776X</p> <p> Name: Ana Gutiérrez-Blanco<br> Institution: Institude of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0001-9412-2321<br> Email: <angutier@uji.es></p> <p> Name: Victor Sans<br> Institution: Institude of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0001-7045-5244<br> Email: <sans@uji.es></p> <p> Name: Sixto Giménez<br> Institution: Institude of Advanced Materials (INAM), Universitat Jaume I, 12006, Castelló, Spain<br> ORCID: 0000-0002-4522-3174<br> Email: <sjulia@uji.es></p> <p>## FILE DESCRIPTION<br>----------------<br>### Figure 1<br>-Fig1b.txt : Distribution hystogram of the BiVO4 NPs after the synthetic procedure.</p> <p>### Figure 3 (All measurements were carried out in 0.1 M potassium phosphate buffer (pH 7), containing 0.1 M Na2SO3 as hole scavenger.)<br>-Fig3a.txt : LSVs under chopped illumination conditions, scan rate, 10 mV·s-1, simulated solar light (AM 1.5 G, 100 mW·cm-2), back illumination.<br>-Fig3b.txt : Chronoamperometries at 1.23 V vs. RHE.<br>-Fig3c.txt : IPCE measurements and integrated photocurrent at 1.23 V vs. RHE</p> <p>### Figure 4<br>-Fig4c.txt : LSV of the measured photoanode (the electrolyte consisted on 0.5 M KPi at a constant pH of 7 and 0.5 M Na2SO3 as hole scavenger) with back illumination configuration.</p> <p>### Figure S4<br>-FigS4a.txt : Absorbance spectra of the different BiVO4 colloidal suspension alliquots taken for reproducibility studies.Seven consecutive synthetic runs were carried out and an aliquot was taken from each run, always under identical conditions regarding the collection time of the sample (30 minutes after starting the reaction).<br>-FigS4b.txt : Transmittance spectra of the different BiVO4 colloidal suspension alliquots taken for reproducibility studies.Seven consecutive synthetic runs were carried out and an aliquot was taken from each run, always under identical conditions regarding the collection time of the sample (30 minutes after starting the reaction).<br>-FigS4c.txt : Absorbance mean + error or the different BiVO4 colloidal suspension alliquots taken for reproducibility studies.<br>-FigS4d.txt : Transmittance at the selcted wavelength (400 nm) for the different BiVO4 colloidal suspension alliquots taken for reproducibility studies.</p> <p>## Figure S6<br>-FigS6.txt : Thermogravimetric analysis (TGA) curve of the BiVO4 NPs from room temperature to 500 ºC.</p> <p>### Figure S7<br>-FigS7.txt : XRD patterns of the FTO/BiVO4 photoanodes before and after thermal annealing. </p> <p>### Figure S8<br>-FigS8a.txt : Raman spectra of the FTO/BiVO4/Al2O3 based films before and after annealing. <br>-FigS8b.txt : FT-IR spectra of the FTO/BiVO4/Al2O3 based films before and after annealing. </p> <p>### Figure S9<br>-FigS9a.txt : Absorptance spectra of the FTO/BiVO4/Al2O3 samples before and after the annealing process.<br>-FigS9b.txt : Tauc plot of the FTO/BiVO4/Al2O3 samples before and after the annealing process. </p> <p>### Figure S11<br>-Fig11a.txt : LSV of the FTO/BiVO4/Al2O3 films in 0.1 M potassium phosphate buffer (pH 7) containing 0.1 M Na2SO3 as hole scavenger under AM 1.5 G, 100 mW·cm-2 back side illumination (scan rate, 10 mV·s-1) for the deposition reproducibility studies.<br>-Fig11b takes the same data contained in Fig11a.txt</p> <p>### Figure S12 (Measurements in 0.1 M phosphate buffer (pH 7) containing 0.1 M Na2SO3 as hole scavenger under AM 1.5 G, 100 mW·cm-2 back side illumination.)<br>-FigS12a.txt : Consecutive LSVs (LSV1, LSV2 LSV3) and LSV after 2 hours testing for the FTO/BiVO4 (area 5 cm2).<br>-FigS12b.txt : Consecutive LSVs (LSV1, LSV2 LSV3) and LSV after 2 hours testing for the FTO/BiVO4/Al2O3 films (area 5 cm2) showing the enhanced stability after deposition of the Al2O3 layer.</p> <p> </p>
E/Z Switchable Ring-closing Metathesis in 1,1′-Bis(but-3-enyl)ferrocenes: Synthesis and Characterization of Axially Chiral ansa[6]-Ferrocenes. Raw Diffraction Data.
<p>Diffraction data for article <em>E</em>/<em>Z</em> Switchable Ring-Closing Metathesis in 1,1′-Bis(but-3-enyl)ferrocenes: Synthesis and Characterization of Axially Chiral <em>ansa</em>[6]-Ferrocenes doi: <a href="https://doi.org/10.1021/acs.organomet.2c00163">10.1021/acs.organomet.2c00163</a>. The crystal structures have been deposited in CSD with CCDC numbers 2093772-2093775, 2094024-2094027 and 2119739.</p>
Metadata of " Synthesis of (poly)gallic acid in a bacterial growth medium"
<p>Metadata of " Synthesis of (poly)gallic acid in a bacterial growth medium"</p>
Continuous Flow Synthesis of Iron Oxide Nanoparticles Using Water-in-Oil Microemulsion_experimental_dataset
<p>This dataset contains the raw experimental data to the article Sopoušek et al., Continuous Flow Synthesis of Iron Oxide Nanoparticles<br> Using Water-in-Oil Microemulsion, Colloid Journal, 2020, Vol. 82, No. 6, pp. 727–734. </p>
Metadata of "Solvent-free Reactions for the Synthesis of Indolenine-based Squaraines and Croconaines: Comparison of Thermal Heating, Mechanochemical Milling, and IR Irradiation"
<p>Metadata of "Solvent-free Reactions for the Synthesis of Indolenine-based Squaraines and Croconaines: Comparison of Thermal Heating, Mechanochemical Milling, and IR Irradiation"</p>
Impact of synthesis routes of metal-oxide photoanodes on the oxygen evolution reaction kinetics
<p>Reducir las emisiones de CO2 es fundamental en la lucha contra el cambio climático y para ello, el uso y almacenamiento de energías renovables juega un papel importante. La fotosíntesis artificial, inspirados en la fotosíntesis natural, ha surgido como una de las soluciones más prometedoras para lograr este propósito. Tal y como lo hace una planta, esta tecnología apunta a almacenar energías alternativas, como la solar, eólica, geotérmica, etc., en forma de combustibles o enlaces químicos, como el hidrógeno verde, a través de la electrólisis de agua. Este proceso consiste en pasar una corriente eléctrica, proveniente de energías renovables, desde el cátodo hasta el ánodo a través del agua. Para que este proceso sea económicamente viable, es necesario que el cátodo, donde se produce el hidrógeno verde, y el ánodo, donde se produce oxígeno, estén fabricados de catalizadores económicos, abundantes y eficientes. Dentro de este grupo de catalizadores, aquellos basados en metales de transición tienen a ser los más estudiados por su abundancia y estabilidad. Sin embargo, las reacciones de evolución de hidrógeno y oxígeno presentan una cinética lenta, de manera que entender los mecanismos de reacción de dichos catalizadores es crucial para aumentar su eficiencia. En esta charla presentaré un resumen de las acciones que Colombia esta tomado frente al cambio climático, así como los avances más recientes en la producción de hidrógeno verde. Posteriormente, enfocaré la charla en los avances en investigación que he desarrollado en conjunto con mis colaboradores. En particular, explicaré los avances en el diseño e implementación de un sistema automatizado de ‘spray coating’ para producir materiales nanoestructurados de manera económica. Así mismo, explicaré con dos ejemplos los avances para producir nanomateriales y elucidar sus mecanismos de reacción para producir hidrógeno verde en un cátodo de Cu2S y oxígeno en un ánodo de α-Fe2O3.</p>
Hydrogen-bonded xanthones as potential UV absorbers. The synthesis of xanthones from bio-renewable cardanol utilizing a ceric ammonium sulfate (CAS) mediated oxidation reaction
<p>The synthesis of hydrogen-bonded xanthones using the bio-renewable phenol, cardanol is described. Cardanol was initially converted into hydroxy-benzophenones. These benzophenones were converted into xanthones utilizing an oxidative ceric ammonium sulfate (CAS) mediated reaction. Subsequent ruthenium-mediated late-stage oxidation of the xanthones provided hydrogen-bonded xanthones, which displayed good UVA and UVB absorbing properties.</p>
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.