Results 231 to 236 of about 1,615,291 (236)
[Hologram quantitative structure-activity relationship on the gas chromatographic retention index of plant essential oil constituents]. [PDF]
Guo R +5 more
europepmc +1 more source
Role of Histidine‐Containing Peptoids in Accelerating the Kinetics of Calcite Growth
Amphiphilic histidine‐containing peptoids mimic carbonic anhydrase (CA) to accelerate calcite step growth. In the presence of Zn2+, they promote the deprotonation of HCO3−, the desolvation of Ca2+, and the reorganization of interfacial hydration layers, thereby reducing the activation barrier for calcite growth.
Mingyi Zhang +5 more
wiley +1 more source
Rational halogen mixing strategy was employed to shift the bandgap of Cs2PbBr2I2 from ultraviolet to visible region, enabling first realization of a visible‐light photodetector with this 2D layered Ruddlesden‐Popper perovskite material. Under illumination, light‐induced internal field forms and drives trap‐mediated persistent photoconductivity ...
Md Fahim Al Fattah +11 more
wiley +1 more source
Lipid nanoparticles containing messenger RNA are characterized by sedimentation velocity analytical ultracentrifugation using UltraScan's new Custom Grid algorithm to provide multi‐dimensional distributions for partial specific volume (particle density), molar mass, sedimentation, diffusion, and hydrodynamic radius.
Sophia Bird +8 more
wiley +1 more source
Multi‐metal Cu─Ce─Ag nanoparticles harness synergistic interactions to drive efficient electrochemical CO2 reduction reaction toward C2+ products at high current densities. Ag enhances CO production, Ce modulates Cu oxidation states, and together they boost *CO coverage and local pH to enhance C─C coupling, enabling record C2+ yields with suppressed ...
Nini Zhang +9 more
wiley +1 more source
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TrAC Trends in Analytical Chemistry, 1999
Abstract Molecular descriptors represent important tools for predicting properties of chemicals, for classifying chemical structures, and for seeking similarities among them. A class of molecular descriptors is described which views a molecule as a whole, and leads to codes of uniform length, irrespective of the size of the molecule.
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Abstract Molecular descriptors represent important tools for predicting properties of chemicals, for classifying chemical structures, and for seeking similarities among them. A class of molecular descriptors is described which views a molecule as a whole, and leads to codes of uniform length, irrespective of the size of the molecule.
openaire +1 more source

