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1 indicator pKa (the negative logarithm of the acid dissociation constant).
2 d based on selected reduction potentials and acid dissociation constants.
3 Lewis-acid-containing organic salts with low acid dissociation constants and offers a universal appro
4 y based on solvent, pK(a) (where K(a) is the acid dissociation constant), and the samarium coordinati
5 lationships between reduction potentials and acid dissociation constants are presented to model n=1 a
6 ynamic quantities of ionization reaction for acid dissociation constants as a function of temperature
7 LC peak retention time-based method, the two acid dissociation constants associated with the carboxyl
9 to simultaneously measure the difference in acid dissociation constants (delta pKa) of two or more c
14 ized nucleophiles (pKa < 25, where Ka is the acid dissociation constant) in palladium-catalysed asymm
16 relationship between cofactor efficiency and acid dissociation constants is consistent with a mechani
17 he CPO-II ferryl [pKa > 8.2 (where Ka is the acid dissociation constant)] is attributable to strong e
18 (LAC for short) allows the estimation of the acid dissociation constant Ka(LAC) of diamagnetic transi
20 1.2 pH units higher, respectively, than the acid dissociation constants obtained for the phosphate g
22 om the ferric iron atom in metmyoglobin, the acid dissociation constant of HCN inside the protein (K*
23 We hypothesize that the reduction in the acid dissociation constant of the imidazolium ring resul
26 etermination of residue-specific, side-chain acid dissociation constants of peptides that contain mul
28 ted to increase the pK(a) (where K(a) is the acid dissociation constant) of compound II, an iron(IV)h
32 tructures suggest that Lys73 has a perturbed acid dissociation constant (pK(a)) compared with acyl-en
34 lability of SO(4)(2-) at pH values below the acid dissociation constant (pK(a)) of SO(4)(2-) and bisu
35 Here, we used NMR spectroscopy to determine acid dissociation constants (pK(a) ) for wild-type EmrE
36 fected by volume ratios, we use the apparent acid dissociation constant, pK', as a proxy for intersys
37 inally, theoretical results indicate aqueous acid dissociation constant (pKa) values of 1.5 +/- 1 for
38 he deprotonation of carboxyl groups with low acid dissociation constants (pKa) as the main contributo