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Electrochemical and spectroelectrochemical characterization show that this compound undergoes a two-electron reduction mechanism.
The compound undergoes a structural transformation upon dehydration and the structure can be switched back through reabsorbing water.
This latter compound undergoes a [2+2] photocycloaddition reaction yielding the tetraphosphane all-trans-1,2,3,4-tetrakis all-trans-1,2,3,4-tetrakis all-trans-1,2,3,4-tetrakis all-trans-1,2,3,4-tetrakis
When a large proton concentration is imposed, as well as using an aqueous buffered solution, the compound undergoes a hydrolysis reaction submitted to an equilibrium and giving rise to a thienophenone derivative.
This compound undergoes a spontaneous cyclization to 1-pyrroline-5-carboxylate which is next finally converted to l-proline by a δ-pyrroline-5-carboxylate reductase Pro3p.
The compound undergoes a phase transition, and the authors of the original paper searched for a subgroup of Pbnm (a non-standard setting of Pnma) that allows for a doubling of the a-axis.
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The applicability of the approach is demonstrated for the transport of compounds undergoing a second-order irreversible bimolecular reaction.
All compounds undergo a reductive cleavage of their IO bonds which yields the corresponding I(I) derivatives.
While all compounds undergo a sluggish transformation to a defect cotunnite-like phase for a certain range of pressures, an intermediate metastable phase (P21am) is found when A2TiO5 has an initial orthorhombic structure (Pnma).
All of the compounds undergo a reversible oxidation, and the formal potentials are sensitive to the R groups on the phenyl rings.
The compounds undergo a rapid interaction with amines followed by the resulting weakened electron withdrawing ability to yield florescent products with either hypochromatic shift or decrease in the emission intensity.
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