ライフサイエンスコーパス: hydronium ion

1 rst order in nitrite, carbamate species, and hydronium ion.

2 n nitrite, piperazine carbamate species, and hydronium ion.

3 on-specific effects are here overshadowed by hydronium ions.

4 c protons both able to generate the hydrated hydronium ions.

5 by forming a narrow double-charge layer with hydronium ions.

6 ion and ejection of excess charge, primarily hydronium ions.

7 ionization generates catalytic hydroxide and hydronium ions, (2) hydroxide and hydronium ions rapidly

8 l discharge of water (alkaline solutions) or hydronium ions (acid solutions).

9 tling) proton and a classical (nonshuttling) hydronium ion along two aquaporin channels, Aqp1 and Glp

10 tion of ring-substituted -methoxystyrenes by hydronium ion and by carboxylic acids to form the corres

11 h cases the average O-O distance between the hydronium ion and its nearest neighbor water molecule wa

12 used by the enhanced association between the hydronium ion and the alcohol, as well as a higher intri

13 Subsequently, a bonded complex of a hydronium ion and the nearest backbone phosphate group f

14 ignificantly enhance the association between hydronium ions and alcohols in a steric environment rese

15 The H(+),K(+)-ATPase pumps protons or hydronium ions and is responsible for the acidification

16 k that is collapsed owing to the presence of hydronium ions and weak base cations.

17 ts of approximately 2400 water molecules, 22 hydronium ions, and 10 chloride and contains a single Su

18 tate, MV(2+) reacts with water to generate a hydronium ion approximately 1.5 ps after excitation.

19 This confirms that hydronium ions are in exchange with protons in the His37

20 ther water to stabilize the bridge through a hydronium ion as well as to produce the hydroxide anion

21 at hydrogen ions do not pass through M(2) as hydronium ions, but instead must interact with titratabl

22 We demonstrate for the first time that hydronium ions can be reversibly stored in an electrode

23 Here we show that hydronium ion catalysis, exemplified by intramolecular d

24 The hydronium ion-catalyzed hydrolyses of 5-methoxyindene 1,

25 tion reaction, a real-time monitoring of the hydronium ions concentration, a byproduct of this reacti

26 Here we demonstrate that hydronium ions confined in the nanopores of zeolite HBEA

27 The correctness of the hydronium ion formulation in crystalline H(3)O(+)A(-) sa

28 The effects of the hydronium ion, H(3)0+, on the structure of the ion chann

29 Salts of the C(3v) symmetric hydronium ion, H(3)O(+), have been obtained in the weakl

30 urface potential leads to an accumulation of hydronium ions, H(3)O(+), in the electrical double layer

31 ere found to interact with the charge on the hydronium ion, helping in its stabilization.

32 The presence of the hydronium ion in the channel also inhibits to some degre

33 s initiated by electrogenerated hydroxide or hydronium ions in water under reductive and oxidative co

34 ohexanol at a rate significantly higher than hydronium ions in water.

35 The higher activity of hydronium ions in zeolites is caused by the enhanced ass

36 c electrolyte, which can only be ascribed to hydronium-ion intercalation.

37 The electrode's response to the hydronium ion is a particular concern because its voltam

38 n of the scissile peptide bond nitrogen by a hydronium ion is an important first step in the reaction

39 which water is inaccessible or hydroxide or hydronium ion is not even momentarily stable.

40 After the hydronium ion is produced, the corresponding hydroxide i

41 Acid catalysis by hydronium ions is ubiquitous in aqueous-phase organic re

42 Although the hydronium ion itself did not cross the channel gate by t

43 ecular dynamics simulations of hydroxide and hydronium ions near a hydrophobic interface, indicating

44 The catalytically active hydronium ions originate from Bronsted acid sites (BAS)

45 We found clear evidence that hydronium ions prefer to emerge at interfaces.

46 clic polyether hosts form 1:1 complexes with hydronium ion, producing large enhancements in luminesce

47 ophobic paste environment, to the barrier to hydronium ions provided by the pasting liquid and to dec

48 roxide and hydronium ions, (2) hydroxide and hydronium ions rapidly convert donor aldehyde or ketone

49 ntagonal dodecahedron H-bonded cage with the hydronium ion residing on the surface.

50 All hydronium ions were equally active for the acid-catalyze

51 Hydronium ions were soft-landed at 1 electron volt on co

52 ing to be converted into an ionically bonded hydronium ion, while a second water molecule bonded to M

53 We have characterized the binding of hydronium ion within these host molecules and have synth