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Pt(111) is unreactive at room temperature in UHV, while Pt(110) is quite reactive.
Iso-octane showed a small level of reactivity at 630 K and a weak NTC behavior starting at 665 K. Neat toluene was unreactive at these temperatures.
Specifically, the latter is unreactive at ≤25 mM with O2− within the timescale of cyclic voltammetry, while it reacts with HO2 at least an order of magnitude slower than all-trans-retinol.
While neat toluene was unreactive at these temperatures, in the mixture it reacted with the radical pool generated by the other surrogate components, forming benzaldehyde, benzene, phenol, and ethyl-benzene.
It is mostly unreactive at room temperature but is slowly attacked by hot concentrated sulfuric or nitric acid.
Alternatively, [E·acyl-ACP·SAM] could be unreactive at low SAM concentrations.
Similar(53)
Nucleotides in the anchoring helix became reactive only at 60% formamide, and nucleotides in the upper stem remained unreactive even at this high denaturant concentration.
The former gave high conversion, although the latter was unreactive even at elevated temperature (entries 3 and 8, Table 2).
Although relatively unreactive toward nonmetals at room temperature, it reacts with many at elevated temperatures.
The iodide 3 is unreactive towards PAr3 at 175 250 °C.
(xxvii) Linear alkynes are essentially unreactive with azides at physiological temperature, but OCT-biotin readily reacted with azide-labeled glycans on proteins, within cell lysates, and on live cultured cells.
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