In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction 499-40-1, Name is (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal, molecular formula is C12H22O11. In a Article,once mentioned of 499-40-1, category: Tetrahydropyrans
[Ru(II)(hedta)L]- complexes (hedta3- = N-hydroxyethylethylenediamine-N,N,N’-triacetate); L = dpaH (2,2′-dipyridylamine) and tpada (N,N,N’,N’-tetrakis(2-pyridyl)adipamide)) have been studied by 1H NMR and electrochemical methods in aqueous solution. The bidentate rings of dpaH and tpada are differentiated as shown by NMR upon coordination to Ru(II) due to differences in the local environment. The dpa-R headgroup of each ligand binds ‘in-plane’ with the en backbone of hedta3- and with one pyridyl ring being nearer the amine of hedta3- having the pendant glycinato group (matching the known arrangement with bpy (2,2′-bipyridine)). Ru(II/III) E(1/2) values follow the order dpaH (0.32 V) < tpada (0.47 V) < bpy (0.54 V), showing that dpaH is a weaker pi-acceptor ligand than bpy, and that the withdrawing carbonyl functionality enhances the pi-acceptor capacity for the tpada ligand, approaching the stability imparted by bpy. Only the 1:1 [Ru(II)(hedta)(dpaH)]- complex forms even in the presence of excess dpaH. [Ru(II)(hedta)(dpaH)] has a pK(a) of the dipyridylamine proton of approximately 5.0 with [Ru(II)(hedta)(dpa-)] undergoing aquation (k(H2O)= 1.4
The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 499-40-1 is helpful to your research., category: Tetrahydropyrans
Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics