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9 results for “Schiff base”
Data for: "Carbon dioxide reduction by lanthanide(III) complexes supported by redox-active Schiff base ligands"
<p>RAW DATA FOR ARTICLE</p> <p>DATE: NOVEMBER 2022</p> <p>TITLE: Carbon dioxide reduction by lanthanide(III) complexes supported by redox-active Schiff base ligands</p> <p>AUTHORS: Nadir Jori, Davide Toniolo, Bang C. Huynh, Rosario Scopelliti, and Marinella Mazzanti*</p> <p>JOURNAL: Inorganic Chemistry Frontiers (RSC) 2020</p> <p>DOI: <a href="https://doi.org/10.1039/D0QI00801J">10.1039/D0QI00801J</a> </p> <p> </p>
Data for "Mechanically-Sensitive Fluorochromism by Molecular Domino Transformation in a Schiff Base Crystal"
<p>The dataset contains input and output files of computational chemistry by Quantum ESPRESSO and Gaussian softwares conducted on two polymorphic crystal structures of 4-nitro-N-salicylideneaniline.</p>
Dataset of the publication: Dataset of the publication: Chiral spin-crossover complexes based on an enantiopure Schiff base ligand with three chiral carbon centers. Dalton Trans. 2024, 53, 10637.
<p><span><span><span>Dataset of the publication: Chiral spin-crossover complexes based on an enantiopure Schiff base ligand with three chiral carbon centers<br></span></span></span></p> <p><span><span> A. Regueiro, V. García-López, A. Forment-Aliaga, M. Clemente-León, <em>Dalton Trans.</em> <strong>2024</strong>, <em>53</em>, 10637. </span> </span></p> <p><span><span>doi: 10.1039/d4dt00924j</span></span></p>
Computational Data for "Synthesis, Structures and Photophysical Properties of Tetra- and Hexanuclear Zinc Complexes Supported by Tridentate Schiff Base Ligands"
<p>Computational data used for the article "Synthesis, Structures and Photophysical Properties of Tetra- and Hexanuclear Zinc Complexes Supported by Tridentate Schiff Base Ligands". This Includes the geometries, optimizations, and the TD-DFT calculations of all mentioned structures and simulated UV-Vis spectra.</p>
Schiff Base Crosslinked Hyaluronic Acid Hydrogels with Tunable and Cell Instructive Time-Dependent Mechanical Properties
<p>This folder contains raw data for the paper titled "<strong>Schiff Base Crosslinked Hyaluronic Acid Hydrogels</strong><strong> with Tunable and Cell Instructive Time-Dependent Mechanical Properties</strong>" authored by Taha Behroozi Kohlan, Yanru Wen, Carina Milena Mini, and Anna Finne-Wistrand, published in <em>Carbohydrate Polymers</em> journal. The raw data presented here contains NMR, FTIR, SEC, swelling and stability, and rheology data used to create figures.</p> <p><strong>Abstract:</strong></p> <p>The dynamic interplay between cells and their native extracellular matrix (ECM) influences cellular behavior, imposing a challenge in biomaterial design. Dynamic covalent hydrogels are viscoelastic and show self-healing ability, making them a potential scaffold for recapitulating native ECM properties. We aimed to implement kinetically and thermodynamically distinct crosslinkers to prepare self-healing dynamic hydrogels to explore the arising properties and their effects on cellular behavior. To do so, aldehyde-substituted hyaluronic acid (HA) was synthesized to generate imine, hydrazone, and oxime crosslinked dynamic covalent hydrogels. Differences in equilibrium constants of these bonds yielded distinct properties including stiffness, stress relaxation, and self-healing ability. The effects of degree of substitution (DS), polymer concentration, crosslinker to aldehyde ratio, and crosslinker functionality on hydrogel properties were evaluated. The self-healing ability of hydrogels was investigated on samples of the same and different crosslinkers and DS to obtain hydrogels with gradient properties. Subsequently, human dermal fibroblasts were cultured in 2D and 3D to assess the cellular response considering the dynamic properties of the hydrogels. Moreover, assessing cell spreading and morphology on hydrogels having similar modulus but different stress relaxation rates showed the effects of matrix viscoelasticity with higher cell spreading in slower relaxing hydrogels.</p>
Data from: Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship
Cinnamaldehyde amino acid Schiff base (CAAS) is a new class of safe, bioactive compounds which could be developed as potential antifungal agents for fungal infections. To design new cinnamaldehyde amino acid Schiff base compounds with high bioactivity, the quantitative structure–activity relationships (QSARs) for CAAS compounds against Aspergillus niger (A. niger) and Penicillium citrinum (P. citrinum) were analysed. The QSAR models (R2 = 0.9346 for A. niger, R2 = 0.9590 for P. citrinum,) were constructed and validated. The models indicated that the molecular polarity and the Max atomic orbital electronic population had a significant effect on antifungal activity. Based on the best QSAR models, two new compounds were designed and synthesized. Antifungal activity tests proved that both of them have great bioactivity against the selected fungi.
Data from: Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship
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Supplementary data from: Green synthesis, characterization, antileishmanial activity, and in silico investigations of Hydrazone Schiff Bases
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Output files of the theoretical calculation done for Cis/Trans-Retinal and its Schiff base with Lysine residue
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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.
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DANDI Archive for NWB datasets
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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.