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In order to validate the calculation method, mixtures of homologue model compounds with low molar-masses were also examined.
Three model compounds with different lipid chain lengths (n = 8, 12 and 18) were designed and synthesized.
The dual-function sensor detected both toxic and genotoxic model compounds with no interference from the co-immobilized member.
In this model, compounds with high inhibitory activity were generally larger, more lipophilic, more flexible and had a lower HOMO.
Furthermore, two kinds of model compounds with and without ZnO and a HBPI film blended with ZnO microparticles were prepared to clarify the fluorescence mechanism in the pristine HBPI and in situ hybrid films.
Model compounds with phenolic hydroxyl groups, amine structures and both of them were blended with bisphenol A phthalonitrile monomers and their curing behaviors were investigated by DSC and FTIR.
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The reactivity of the star core was demonstrated using a model compound with FTIR, 1H and 13C NMR spectroscopy.
The reaction kinetics are shown to be first order in model compound with the methylene-arene carbon-carbon bond adjacent to the most substituted arene being selectively cleaved.
The synthesis of such a model compound with different end-groups is presented that allows for assignment of degradation products from different parts of the molecule.
Reactions of the model compound with deuterated biphenyl indicated that the reactive intermediates formed from the phenylethynyl moiety are able to abstract aromatic deuterium atoms in the presence of aromatic protons.
Formic acid has been chosen as a model compound with the lowest decomposition energy (ΔH ∼ 32 kJ mole−1) compared to that needed for water decomposition (ΔH ∼ 286 kJ mole−1).
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