Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
62
datasets available to search
ShareScore release 0.9.0
Dataset results
62 results for “supramolecular”
Mechanically Resistant Poly(N-vinylcaprolactam) Microgels with Sacrificial Supramolecular Catechin Hydrogen Bonds
<p>Original data corresponding to the plots of Figures 2, 4, 5 of the manuscript and S1-S16 of the Supporting Information in *.csv format and raw data for NMR measurements.</p>
Dataset supporting the paper "Supramolecular chemistry based on 4-acetylbiphenyl on Au(111). Phys. Chem. Chem. Phys. 22: 15208 (2020)"
<p>Dataset corresponding to theoretical calculations in the paper "Supramolecular chemistry based on 4-acetylbiphenyl on Au(111)" Phys. Chem. Chem. Phys. 22: 15208 (2020), <a href="http://dx.doi.org/10.1039/d0cp01657h">http://dx.doi.org/10.1039/d0cp01657h</a></p> <p>List of files:</p> <p>Several folders corresponding to the figures of the paper. They contain:</p> <ul> <li>.siesta files: STM images in WsXM format (<a href="http://www.wsxm.eu/">http://www.wsxm.eu/</a>) simulated using STMpw (<a href="https://doi.org/10.5281/zenodo.3581159">https://doi.org/10.5281/zenodo.3581159</a>).</li> <li>CONTCAR and POSCAR files: relaxed structures in VASP format. They can be visualized with VESTA (<a href="https://jp-minerals.org/vesta/en/">https://jp-minerals.org/vesta/en/</a>)</li> <li>.agr: grace files (<a href="https://plasma-gate.weizmann.ac.il/Grace/">https://plasma-gate.weizmann.ac.il/Grace/</a>).</li> </ul>
Research data supporting: "Self-assembly of cyclic peptide monolayers by hydrophobic supramolecular hinges"
<p>This repository contains the set of modelling data shown in the paper:<strong> "Self-assembly of cyclic peptide monolayers by hydrophobic supramolecular hinges"</strong>, published on Chemical Science (DOI: 10.1039/d3sc03930g)</p>
Growth of Merocyanine Dye J-Aggregate Nanosheets by Living Supramolecular Polymerization
<p>Data to report <a href="https://doi.org/10.1002/ange.202314667">https://doi.org/10.1002/ange.202314667</a>:</p><p>J-aggregates are highly desired dye aggregates but so far there has been no general concept how to accomplish the required slip-stacked packing arrangement for dipolar merocyanine (MC) dyes whose aggregation commonly affords one-dimensional aggregates composed of antiparallel, co-facially stacked MCs with H-type coupling. Herein we describe a strategy for MC J-aggregates based on our results for an amphiphilic MC dye bearing alkyl and oligo(ethylene glycol) side chains. In an aqueous solvent mixture, we observe the formation of two supramolecular polymorphs for this MC dye, a metastable off-pathway nanoparticle showing H-type coupling and a thermodynamically favored nanosheet showing J-type coupling. Detailed studies concerning the self-assembly mechanism by UV-Vis spectroscopy and the packing structure by atomic force microscopy and wide-angle X-ray scattering show how the packing arrangement of such amphiphilic MC dyes can afford slip-stacked two-dimensional nanosheets whose macrodipole is compensated by the formation of a bilayer structure. As an additional feature we demonstrate how the size of the nanosheets can be controlled by seeded living supramolecular polymerization.</p>
Supramolecular Self-Healing Sensor Fiber Composites for Damage Detection in Piezoresistive Electronic Skin for Soft Robots
<p>Self-healing materials can prolong the lifetime of structures and products by enabling the repairing of damage. However, detecting the damage and the progress of the healing process remains an important issue. In this study, self-healing, piezoresistive strain sensor fibers (ShSFs) are used for detecting strain deformation and damage in a self-healing elastomeric matrix. The ShSFs were embedded in the self-healing matrix for the development of self-healing sensor fiber composites (ShSFC) with elongation at break values of up to 100%. A quadruple hydrogen-bonded supramolecular elastomer was used as a matrix material. The ShSFCs exhibited a reproducible and monotonic response. The ShSFCs were investigated for use as sensorized electronic skin on 3D-printed soft robotic modules, such as bending actuators. Depending on the bending actuator module, the electronic skin was loaded under either compression (pneumatic-based module) or tension (tendon-based module). In both configurations, the ShSFs could be successfully used as deformation sensors, and in addition, detect the presence of damage based on the sensor signal drift. The sensor under tension showed better recovery of the signal after healing, and smaller signal relaxation. Even with the complete severing of the fiber, the piezoresistive properties returned after the healing, but in that case, thermal heat treatment was required. With their resilient response and self-healing properties, the supramolecular fiber composites can be used for the next generation of soft robotic modules</p>
Pyrene-Based Macrocrosslinkers with Supramolecular Mechanochromism for Elastic Deformation Sensing in Hydrogel Networks
<p>Primary data used in the manuscript (NMR, MS, fluorescence, GPC) sorted after Figure and associated panel in manuscipt and supporting information.</p>
Panchromatic Light-Harvesting Antenna by Supramolecular Exciton Band Engineering for Heteromeric Dye Foldamer
<p>Data to report <a href="https://doi.org/10.1016/j.chempr.2024.05.023">https://doi.org/10.1016/j.chempr.2024.05.023</a>:</p> <p>Natural photosystems accomplish panchromatic light absorption by different chromophores that are non-covalently embedded in protein matrices and mostly lack close dye-dye interactions. In this article, we introduce a light-harvesting (LH) system established by four different merocyanine dyes that are co-facially stacked by dipole-dipole interactions and a peptide-like backbone in a folded heteromer architecture to afford a panchromatic absorption band consisting of several strongly coupled exciton states. This exciton manifold allows for ultrafast and efficient energy transport in the artificial antenna. Furthermore, due to the tight stacking of the dyes in their folded state, non-radiative processes are slowed down, thereby increasing the lifetime of the excited state and the fluorescence quantum yield from <3% for the individual dyes up to 38% for the folda-heteromer. Together with the panchromatic absorption, this leads to a substantial improvement of the fluorescence brightness upon broadband excitation in comparison with its constituent chromophores.</p>
The Delayed Box: Biphenyl Bisimide Cyclophane, a Supramolecular Nano‒environment for Efficient Generation of Delayed Fluorescence
<p>Additional data to report <a title="DOI URL" href="https://doi.org/10.1021/jacs.4c07730">https://doi.org/10.1021/jacs.4c07730</a>:</p> <p>Activating delayed fluorescence emission in a dilute solution via a non-covalent approach is a formidable challenge. In this report, we propose a strategy for efficient delayed fluorescence generation in dilute solution using a non-covalent approach via supramolecularly engineered cyclophane-based nanoenvironments that provide sufficient binding strength to π-conjugated guests and that can stabilize triplet excitons by reducing vibrational dissipation and lowering the singlet–triplet energy gap for efficient delayed fluorescence emission. Toward this goal, a novel biphenyl bisimide-derived cyclophane is introduced as an electron-deficient and efficient triplet-generating host. Upon encapsulation of various carbazole-derived guests inside the nanocavity of this cyclophane, emissive charge transfer (CT) states close to the triplet energy level of the biphenyl bisimide are generated. The experimental results of host–guest studies manifest high association constants up to 10<sup>4</sup> M<sup>–1</sup> as the prerequisite for inclusion complex formation, the generation of emissive CT states, and triplet-state stabilization in a diluted solution state. By means of different carbazole guest molecules, we could realize tunable delayed fluorescence emission in this carbazole-encapsulated biphenyl bisimide cyclophane in methylcyclohexane/carbon tetrachloride solutions with a quantum yield (QY) of up to 15.6%. Crystal structure analyses and solid-state photophysical studies validate the conclusions from our solution studies and provide insights into the delayed fluorescence emission mechanism.</p>
Controlling the Supramolecular Polymerization of Squaraine Dyes by a Molecular Chaperone Analogue
<p>ABSTRACT: Molecular chaperones are proteins that assist in the (un)folding and (dis)assembly of other macromolecular structures toward their biologically functional state in a non-covalent manner. Transferring this concept from nature to artificial self-assembly processes, here, we show a new strategy to control supramolecular polymerization via a chaperone-like two-component system. A new kinetic trapping method was developed that enables efficient retardation of the spontaneous self-assembly of a squaraine dye monomer. The suppression of supramolecular polymerization could be regulated with a cofactor, which precisely initiates self-assembly. The presented system was investigated and characterized by ultraviolet–visible, Fourier transform infrared, and nuclear magnetic resonance spectroscopy, atomic force microscopy, isothermal titration calorimetry, and single-crystal X-ray diffraction. With these results, living supramolecular polymerization and block copolymer fabrication could be realized, demonstrating a new possibility for effective control over supramolecular polymerization processes.</p>
Research data supporting "Plasmonic chirality imprinting on nucleobase-displaying supramolecular nanohelices via metal-nucleobase recognition"
<p>This file contains the raw research data supporting the publication:</p> <p>Y. Lin<em> et al</em>., Plasmonic chirality imprinting on nucleobase-displaying supramolecular nanohelices via metal-nucleobase recognition, Angew. Chem. Int. Ed. 2017, DOI: 10.1002/anie.201610976.</p> <p> </p>
Dataset for "Exploring the Potential of Various Cyclodextrin-based Derivatives in Enzyme Supramolecular Engineering" research article
<p>The dataset for the paper titled "Exploring the Potential of Various Cyclodextrin-based Derivatives in Enzyme Supramolecular Engineering".<br>The dataset includes the following items:<br><br>1. "alpha-CD-TES_Characterization" xls file (1 file) including 5 datasheets;<br>These data sheets provide raw characterization data regarding the synthesis of the alpha-CD-TES molecule including 1H NMR, 13C NMR, FTIR, ESI-MS, and MALDI.</p> <p>2. "beta-CD-TES_Characterization" xls file (1 file) including 5 datasheets;<br>These data sheets provide raw characterization data regarding the synthesis of the beta-CD-TES molecule including 1H NMR, 13C NMR, FTIR, ESI-MS, and MALDI.</p> <p>3. "gamma-CD-TES_Characterization" xls file (1 file) including 5 datasheets;<br>These data sheets provide raw characterization data regarding the synthesis of the gamma-CD-TES molecule including 1H NMR, 13C NMR, FTIR, ESI-MS, and MALDI.<br><br>4. "Activities" xls file (1 file) including 6 datasheets;<br>These datasheets contain the raw data of the enzymatic activities measured for both LipMRD9 and A50 enzymes for each set of stability experiments reported in the manuscript or the supporting information documents.</p> <p>5. "Layer growth - A50" zip file including 5 files:<br>The unprocessed SEM micrographs of A50 enzyme shielding with alpha/beta/gamma-CD-TES building blocks (after 75 min reaction) and the corresponding size measurements in an xls file.</p> <p>6. "Layer growth - LipMRD9" zip file including 15 files:<br>The unprocessed SEM micrographs of the shielded LipMRD9 enzyme with α-, β-, and γ-CD-TES building blocks (after 30, 60, 90, and 120 min reaction) and the corresponding size measurements (using ImageJ software) saved in separate xls files.</p>
Support Data to "Interface flexibility controls the nucleation and growth of supramolecular networks"
<p><strong>Overview</strong></p> <p>This repository contains the inputs and support data for the publication "Interface Flexibility Controls the Nucleation and Growth of Supramolecular Networks," which is currently under review in Nature Chemistry.</p> <p><strong>Folder Structure</strong><br>Each subfolder is named after the primary method used to obtain the data. The internal structure may vary depending on whether it was more convenient to organize the data by the figure they were used for or by the structures analyzed. Each folder includes a detailed README.md file providing further information.<br><br><strong>Notes<br></strong>In the second version we added the data for Figure S27, which was not uploaded before due oversight.</p>
Research Data Supporting "Controlling Exchange Pathways in Dynamic Supramolecular Polymers by Controlling Defects"
<p>This repository contains the set of data shown in the paper "<strong>Controlling Exchange Pathways in Dynamic Supramolecular Polymers by Controlling Defects</strong>", published on <strong>ACS Nano</strong> (DOI: 10.1021/acsnano.1c01398).</p> <p>The data stored in this section is organized as follow:</p> <p><strong>supervisedClustering/ :</strong> folder containing scripts for carrying out the supervised analysis as discussed in the main paper. Subfolders are divided in <strong><code>kmeans</code></strong><code><strong>/</strong></code> and <strong><code>spectral</code></strong><code>/</code> contain the different analysis as explained in the paper.</p> <p><strong>unbiasMD/ : </strong>folder containing the Gromacs input files for reproducing the unbias MD trajectories of the 3 types of fiber, as explained in the paper.</p> <p><strong>biasMD/</strong> <strong>:</strong> folder containing the PLUMED input files for reproducing enhanced sampling dynamics as discussed in the paper.</p> <p><strong>unsupervisedClustering/ : </strong>folder containing the directions and the original files to reproduce the unsupervised clustering results.</p>
Which bridge to cross, which mountain to climb – supramolecular photocatalysis outpacing conventional catalysis
<p>The file contains all raw data for the manuscript entitled "Which bridge to cross, which mountain to climb – supramolecular photocatalysis outpacing conventional catalysis" (i.e. Figs. 3-10).</p>
Research data supporting "Fate of Liposomes in Presence of Phospholipase C and D: From Atomic to Supramolecular Lipid Arrangement"
<p>Raw research data for experimental work supporting the publication above.</p> <p>Raw data for MD simulation is available upon reasonable request from Irene Yarovsky (irene.yarovsky@rmit.edu.au).</p>
Research data supporting "Multiscale Molecular Modelling of ATP-Fueled Supramolecular Polymerisation and Depolymerisation"
<p>Raw research data supporting the publication Perego C. et al., <em>ChemSystemsChem</em> <strong>2021</strong>, DOI: <a href="https://doi.org/10.1002/syst.202000038">https://doi.org/10.1002/syst.202000038</a></p>
Research data supporting: "Toward Chemotactic Supramolecular Nanoparticles: From Autonomous Surface Motion Following Specific Chemical Gradients to Multivalency-Controlled Disassembly"
<p>This repository contains the set of data shown in the paper "<em>Toward Chemotactic Supramolecular Nanoparticles: From Autonomous Surface Motion Following Specific Chemical Gradients to Multivalency-Controlled Disassembly</em>", published on <em>ACS Nano</em> (DOI: 10.1021/acsnano.1c0500).</p> <p>All the input data needed to run the simulations and get the results are organized in 5 different folders:</p> <ul> <li> <p><code>1-MinimlisticCGModel/</code></p> <p>in this folder there are the Gromacs and PLUMED input files for reproducing the minimalistic coarse-grained model shown in the article.</p> </li> <li> <p><code>2-AAandFineCGModels/</code></p> <p>the folder contains the atomistic (<code>monomerAA/</code>) and the coarse-grained Martini "wet" (<code>monomerGCWet/</code>) input files for modelling the Original monomer with one carboxyl group. The coarse-grained Martini "dry" (<code>monomerCGDry/</code>) model is reported for the Original monomer at the three different charged states.</p> </li> <li> <p><code>3-UnbiasedMD/</code></p> <p>this folder includes the Gromacs input files needed to reproduce the Unbiased simulations as shown in the article.</p> </li> <li> <p><code>4-MetaD/</code></p> <p>this folder incorporates the Gromacs and PLUMED input files necessary to reproduce both the Infrequent CG Metadynamics simulations (<code>InfrequentMetaD/</code>) and the Multiple-walker CG Metadynamics simulations (<code>MultipleWalkerMetaD/</code>)</p> </li> <li> <p><code>5-InSilico/</code></p> <p>in this folder all the files used to run the simulations about the exoliation experiments (<code>Original/</code>, <code>Type-1/</code>, <code>Type-2/</code>, <code>Type-3/</code>, <code>Type-4/</code>) are reported. Every subfolder contains all input files for the three different charged monomers (<code>Olig1-/</code>, <code>Olig2-/</code>, <code>Olig3-/</code>).</p> </li> </ul>
Supramolecular cages benchmark datasets
<p>Two benchmark datasets, comprising 22 well-known supramolecular cages, have been selected from the supramolecular chemistry literature to evaluate cavity detection and volume characterization.</p> <p>All supramolecular cage structures were prepared in the following way: the original CIF files were downloaded from the Cambridge Structural Database (CSD) and atoms and molecular fragments, that are not part of the cage-framework, were removed from the structures, using Diamond Crystal and Molecular Structure Visualization software and saved in a PDB format.</p> <ul> <li><strong>Benchmark dataset 1:</strong> host-guest pairs</li> </ul> <p>For benchmark dataset 1, the guest structures were obtained, from the corresponding CIF files, by removing the supramolecular cage and other molecular fragments that are not part of the guest. </p> <table> <tbody> <tr> <td> <p><strong>Supramolecular Cage Identifier </strong></p> </td> <td> <p><strong>Guest </strong></p> </td> <td> <p><strong>CSD Identifier </strong></p> </td> <td> <p><strong>DOI </strong></p> </td> </tr> <tr> <td> <p><strong>B1</strong> </p> </td> <td> <p>Et4N+ </p> </td> <td> <p>718468 </p> </td> <td> <p><a href="https://doi.org/10.1021/ic8012848">10.1021/ic8012848</a></p> </td> </tr> <tr> <td> <p><strong>B2</strong> </p> </td> <td> <p>BnNMe3+ </p> </td> <td> <p>718469 </p> </td> <td> <p><a href="https://doi.org/10.1021/ic8012848">10.1021/ic8012848</a></p> </td> </tr> <tr> <td> <p><strong>B3</strong> </p> </td> <td> <p>(Cp)2Co+ </p> </td> <td> <p>718470 </p> </td> <td> <p><a href="https://doi.org/10.1021/ic8012848">10.1021/ic8012848</a></p> </td> </tr> <tr> <td> <p><strong>B4</strong> </p> </td> <td> <p>(Cp*)2Co+ </p> </td> <td> <p>718471 </p> </td> <td> <p><a href="https://doi.org/10.1021/ic8012848">10.1021/ic8012848</a></p> </td> </tr> <tr> <td> <p><strong>B5</strong> </p> </td> <td> <p>BF4- </p> </td> <td> <p>1862753 </p> </td> <td> <p><a href="https://doi.org/10.1002/asia.201801262">10.1002/asia.201801262</a></p> </td> </tr> <tr> <td> <p><strong>B6</strong> </p> </td> <td> <p>ClO4- </p> </td> <td> <p>1862752 </p> </td> <td> <p><a href="https://doi.org/10.1002/asia.201801262">10.1002/asia.201801262</a></p> </td> </tr> <tr> <td> <p><strong>B7</strong> </p> </td> <td> <p>C60 </p> </td> <td> <p>942782 </p> </td> <td> <p><a href="https://doi.org/10.1021/ja4110446">10.1021/ja4110446</a></p> </td> </tr> <tr> <td> <p><strong>B8</strong> </p> </td> <td> <p>C60 </p> </td> <td> <p>1872778 </p> </td> <td> <p><a href="https://doi.org/10.1002/chem.201805353">10.1002/chem.201805353</a></p> </td> </tr> <tr> <td> <p><strong>B9</strong> </p> </td> <td> <p>Adamantane-2,6-dione </p> </td> <td> <p>183906 </p> </td> <td> <p><a href="https://doi.org/10.1002/1521-3757(20021018)114:20<3947::AID-ANGE3947>3.0.CO;2-X">10.1002/1521-3757(20021018)114:20<3947::AID-ANGE3947>3.0.CO;2-X</a></p> </td> </tr> <tr> <td> <p><strong>B10</strong> </p> </td> <td> <p>Et4N+ </p> </td> <td> <p>100947 </p> </td> <td> <p><a href="https://doi.org/10.1002/(SICI)1521-3773(19980803)37:13/14<1840::AID-ANIE1840>3.0.CO;2-D">10.1002/(SICI)1521-3773(19980803)37:13/14<1840::AID-ANIE1840>3.0.CO;2-D</a></p> </td> </tr> <tr> <td> <p><strong>B11</strong> </p> </td> <td> <p>Corannulene and Cyclohexane </p> </td> <td> <p>2068665 </p> </td> <td> <p><a href="https://doi.org/10.1038/s41467-021-24344-w">10.1038/s41467-021-24344-w</a></p> </td> </tr> <tr> <td> <p><strong>B12</strong> </p> </td> <td> <p>C60 </p> </td> <td> <p>2068666 </p> </td> <td> <p><a href="https://doi.org/10.1038/s41467-021-24344-w">10.1038/s41467-021-24344-w</a></p> </td> </tr> <tr> <td> <p><strong>B13</strong> </p> </td> <td> <p>C70 </p> </td> <td> <p>2068667 </p> </td> <td> <p><a href="https://doi.org/10.1038/s41467-021-24344-w">10.1038/s41467-021-24344-w</a></p> </td> </tr> </tbody> </table> <p> </p> <p><strong>Benchmark dataset 2: </strong>topologically and morphologically distinct supramolecular cages</p> <p>The single resorcin[4]arene ligand (O2) was prepared from the corresponding resorcin[4]arene-cage (A1) by removing 5 ligands. In the cyclotricatechylene cage (C1), the outward-pointing phenyl groups (that do not affect the cavity calculations) were removed.</p> <table> <tbody> <tr> <td> <p><strong>Supramolecular Cage Identifier </strong></p> </td> <td> <p><strong>CSD Identifier </strong></p> </td> <td> <p><strong>DOI </strong></p> </td> </tr> <tr> <td> <p><strong>A1</strong> </p> </td> <td> <p>1207879 </p> </td> <td> <p><a href="https://doi.org/10.1038/38985">10.1038/38985</a></p> </td> </tr> <tr> <td> <p><strong>C1</strong> </p> </td> <td> <p>1892128 </p> </td> <td> <p><a href="https://doi.org/10.1039/C9CC02103E">10.1039/C9CC02103E</a></p> </td> </tr> <tr> <td> <p><strong>F1</strong> </p> </td> <td> <p>293777 </p> </td> <td> <p><a href="https://doi.org/10.1126/science.1124985">10.1126/science.1124985</a></p> </td> </tr> <tr> <td> <p><strong>F2</strong> </p> </td> <td> <p>1831430 </p> </td> <td> <p><a href="https://doi.org/10.1038/nature20771">10.1038/nature20771</a></p> </td> </tr> <tr> <td> <p><strong>H1</strong> </p> </td> <td> <p>768969 </p> </td> <td> <p><a href="https://doi.org/10.1039/C0CC00234H">10.1039/C0CC00234H</a></p> </td> </tr> <tr> <td> <p><strong>N1</strong> </p> </td> <td> <p>1541839 </p> </td> <td> <p><a href="https://doi.org/10.1021/jacs.7b05202">10.1021/jacs.7b05202</a></p> </td> </tr> <tr> <td> <p><strong>O1</strong> </p> </td> <td> <p>2074472 </p> </td> <td> <p><a href="https://doi.org/10.1021/acs.joc.1c00794">10.1021/acs.joc.1c00794</a></p> </td> </tr> <tr> <td> <p><strong>O2</strong> </p> </td> <td> <p>1207879 </p> </td> <td> <p><a href="https://doi.org/10.1038/38985">10.1038/38985</a></p> </td> </tr> <tr> <td> <p><strong>W1</strong> </p> </td> <td> <p>1416694 </p> </td> <td> <p><a href="https://doi.org/10.1038/nchem.2452">10.1038/nchem.2452</a></p> </td> </tr> </tbody> </table>
Research data supporting: "Non-trivial stimuli-responsive collective behaviours emerging from microscopic dynamic complexity in supramolecular polymer systems"
<p>Contains the relevant simulation data and input files. See "readme.txt" for information.</p>
Dataset for "Mechanically robust supramolecular polymer co-assemblies"
<p>Source data of the study reported in the publication entitled "Mechanically robust supramolecular polymer co-assemblies". The data should be considered together with the published manuscript and the supplementary information file.</p>
ScienceDex guides
Understand access before you commit
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.