Sentence examples for much more reactivity from inspiring English sources

The former has much more reactivity than the other sulfuric compounds while the latter, particularly benzothiophenic and dibenzothiphenic derivatives, are difficult to desulfurize.

However, in the FCR3 parasite that has more than 10 copies of the PfRh1 gene, there is much more reactivity against the unprocessed form (Fig. 1C).

When the recombinant fibrillin-1 polypeptides rF16 and rF6H were tested in this assay, they showed much more reactivity in the non-reduced conformation than in the reduced conformation, showing that the corresponding epitopes are present in the same correct conformation as in native fibrillin-1.

It was found that acrylate is much more reactive than methacrylate; the reactivity ratios are quite different from unity and show a high similarity in GTP and anionic polymerization.

At low concentrations (<50 nM), Cu and 1,2-NQN have very similar reactivities, while at higher concentrations 1,2-NQN is much more reactive than Cu.

More specifically, the intensity map in Fig. 30h reveals the presence of zeolite aggregate domains, which have almost no reactivity towards furfuryl alcohol, whereas other zeolite aggregate domains are much more reactive.

Aziridines are inherently much more reactive to opportunistic biological nucleophiles than oxiranes; however, incorporation of N in an amide functionality attenuates this electrophilic reactivity.

Relative to the reference ENHS core, the molten-salt cooled cores require significantly tighter lattice, have softer neutron spectra, significantly more negative Doppler reactivity effect, much more positive coolant temperature and void reactivity effect and smaller reactivity worth of the control elements.

From the experimental results, it is found that a catalyst with high reactivity is much more preferable for reducing not only rising time but also tail-off time.

(15) Examples of X-N(O)=NO– ions for which X is carbon, oxygen, sulfur, or a primary amino group were also studied; they showed very similar structural and ultraviolet spectral characteristics, 9) though their reactivity patterns were much more diverse than those of the well-behaved secondary amine analogues, often generating little to no NO on hydrolysis, for example.

For a set of Treg epitopes that were previously defined in HCV disease, HG cross-reactivity appears to be much more extensive than HM.