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These two polymers reacted via Schiff-base reaction to form hydrozone linkages as cross-linking sites.
Pentachloroethane (PCA) reacted via concurrent reductive β-elimination (93%) and hydrolysis (7%).
At higher temperatures, therefore, larger, better-developed crystals reacted via an oriented aggregation mechanism, requiring a larger degree of order.
Esterification of the oligomer end groups with methacryloyl chloride led to divinyl terminated macromers that were reacted via photoinitiated polymerizations to produce crosslinked networks.
We observed clear effects of feature-based response retrieval on performance when the features were relatively complex, while participants reacted via foot pedals as well as while driving a car.
To obtain "active surfaces" for detecting sugar alcohols, the nanoreactors optimized in solution were then immobilized on a solid support: aldehyde groups exposed at the compartment external surface reacted via an aldehyde-amino reaction with glass surfaces chemically modified with amino groups.
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The pyruvate so formed can then react via either step [50] or [50a].
Although both inner and loop primers react via the loops, they do so by different mechanisms.
These comonomers react via free radical copolymerization to yield void-free thermosets.
As reactions involving radicals typically react via the radical, it is assumed that these mappings are incorrect.
In the simulations fuel and oxidant react via a one-step, isothermal reaction (activation energy is set to zero).
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