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The viscous monomers (Bis-GMA or UDMA) were found to be less reactive than the diluent comonomer (TEGDMA) at nearly all stages of the photopolymerization process.
Fe3+OH−cdta4−, being the dominating iron III -cdta speciron III -cdtawaspecies to be less reattive than Fe3+cdta4− towards the pH>10ulfides (Sn2-;n="2–8).
Fe3+OH−cdta4−, being the dominating iron III) product at pH>10, was found to be less reactive than Fe3+cdta4− with the superoxide intermediate (O⋅−2), thus reducing the effect of the reverse step at higher pH.
Consequently, ethylene-derived soot is shown to be less reactive than n-heptane-derived soot under the same carbon flow rate and the same adiabatic flame temperature, because soot is formed at an earlier stage with ethylene than with n-heptane.
Hence, the most stable oxidation state of ununtrium is predicted to be the +1 state, and ununtrium is expected to be less reactive than thallium.
This result was not completely unexpected as it has been shown[ 17] that conformational restraints imposed by these type of trans-fused bicyclic systems can disfavor the formation of oxacarbenium ions, and thus such substrates tend to be less reactive than the noncyclic derivatives.
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Although 1,4-divinylbenzene is a styrene derivative, it was higher in monomer reactivity than styrene, but its chain-end anion was less reactive than that generated from styrene.
When the halogen acts as a functional group, aryl halides are less reactive than alkyl halides and more closely resemble vinylic halides in their reactivity.
Results from real-time FTIR spectroscopic studies indicated that ethoxy was less reactive than methoxy substituent.
Crystalline silicon is less reactive than finely divided and, possibly, amorphous silicon.
Initially, clean Pt(111) is less reactive than clean Pt(110) even in the electrochemical environment.
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