ライフサイエンスコーパス: aqua

1 s axial diaqua species [FeL(H 2O) 2] (-) ( 1 aqua) which are deprotonated to afford [FeL(OH)(H 2O)] (

2 The pathways 1 aqua + H 2O 2 ( k 1), 1 OH + H 2O 2 ( k 2), and 1 OH + H

3 m based on the [Mo(2)O(2)S(2)(OH(2))(6)](2+) aqua cation (noted L) and the trivacant [AsW(9)O(33)](9-

4 was converted into the catalytically active aqua counterpart by a ligand exchange process.

5 r drug, and its related biologically active "aqua" compounds in biofluid samples is described.

6 es using a lithium borate fusion although an aqua regia leachate is also effective in many instances.

7 ter activation with light, the release of an aqua ruthenium(II) complex is observed.

8 ich forms a hydrogen-bonding network with an aqua ligand on iron and the pterin cofactor.

9 n atom transfer from a W(IV) species with an aqua ligand, yielding W(V)-[OH(-)] and a substrate radic

10 Monodentate acetate and aqua ligands lend the flexible environment of 1 closest

11 hich can substitute components of animal and aqua feeds.

12 nalyses were consistent with cysteinate- and aqua-ligated heme iron in CYP51.

13 enes (Bmal1, Clock, Per1, and Per2), ion and aqua channel genes (Ae2a, Car2, and Aqp5), and salivary

14 A weakly associated S-Met and aqua are likely axial ligands.

15 stems thus far, as they retain their form as aqua complexes.

16 dinated Fe(III)-TAML complexes with an axial aqua ligand ([PPh(4)]1-H(2)O, tetraamidato macrocyclic F

17 conditions to produce the corresponding bis-aqua-iron(III) porphyrin cation radicals.

18 8)F-FPMA for coordination with the cisplatin-aqua complex.

19 eling agent to coordinate with the cisplatin-aqua complex.

20 indicates the presence of a solvent-derived aqua/hydroxo ligand bound either terminally or in a brid

21 Here we show with three-dimensional aqua-planet simulations that CO2-induced forcing as read

22 NWs screening platform in real environmental aqua system.

23 as the processes that govern the equilibrium aqua-hydroxo (O2H3)(-)<-->hydroxyl (OH) in Sc-MOFs, are

24 edox-inactive Ca(2+) analogues with flexible aqua-/acetate ligands into active and stable WOCs (max.

25 or monitoring non-ruminant PAPs intended for aqua feed.

26 2 cores having one single atom bridge (e.g., aqua or hydroxo) together with one or two carboxylate br

27 of NU-1000-supported bimetallic-oxo,hydroxo,aqua clusters.

28 Even with the less stable hydroxo/aqua complex [Cp*(2)Ir(2)(mu-OH)(3)]OH, nanoparticle for

29 structure of the axial region of the Pd(II) aqua ion in solution using a combination of neutron and

30 The six-coordinate Fe(III)-aqua complex [Fe(III)(dpaq)(H2O)](2+) (1, dpaq is 2-[bis

31 rmore, in some cases, gene annotation and in aqua assays disagree by describing gene annotation witho

32 ruminant processed animal proteins (PAPs) in aqua feed, two immunoassays have been tested in an inter

33 decomposition by means of solubilisation in aqua regia or tetramethyl ammonium hydroxide and simple

34 O2, partial decomposition (solubilisation in aqua regia), 1:1 dilution with 2% (v/v) HNO3 and direct

35 y porous MOF material reported to survive in aqua regia.

36 be the iron photoreactivity in terms of iron-aqua and oxalate complexes, are not in accordance with o

37 Using the pKa of the M-aqua complex as a measure of Lewis acidity, these compou

38 drogen bonding interaction between the metal aqua and boron hydroxide moieties.

39 With the pKa of the redox-inactive metal-aqua complex as a measure of Lewis acidity, these compou

40 (2) Proton transfer from the terminal MnA-aqua ligand to the substrate Ndelta-guanidino atom forms

41 accompanied by protonations to afford the Mo-aqua complex, [(PY5Me(2))Mo(OH(2))](+).

42 (1)H ENDOR measurements indicate there is no aqua (HxO) ligand bound to the Cu(II), either terminally

43 zolyl)alkane ligands on the rate constant of aqua ligand substitution of ruthenium(II) complexes with

44 roton-coupled electron transfer oxidation of aqua precursors, but access at inert electrodes is kinet

45 process, specifically the transformation of aqua cobalt (II) complexes to their fully halogenated sp

46 igand environment of three nitrogens and one aqua ligand "in the plane".

47 sfer follows to yield a Ru(V)/Ru(III) peroxo/aqua mixed valence complex, which performs the third red

48 istidine and is likely trans to the in-plane aqua ligand.

49 ed water in any system, including the simple aqua ion.

50 cob(III)alamins bound to MetH, specifically aqua-, methyl-, and n-propylcobalamin, show a correlatio

51 magnetically coupled Ru(IV)/Ru(III) superoxo/aqua species is predicted, which will then promote the l

52 he third redox reaction to give the superoxo/aqua complex.

53 Thus, we confirm that X contains a terminal aqua (most likely hydroxo) ligand to Fe(III) in addition

54 ambiguous for Mn(IV)PFOM where both terminal aqua and hydroxo ligands can be rationalized, but the re

55 rm that X contains an Fe(III)-bound terminal aqua ligand (H(x)O), but the spectra contain none of the

56 hat Mn(II)PFOM and Mn(III)PFOM have terminal aqua ligands and Mn(V)PFOM has a terminal hydroxo ligand

57 The aqua complexes [[Tp(Bu)t(,Me)]M(OH(2))][HOB(C(6)F(5))(3)

58 A metal-organic framework (MOF) bearing the aqua-hydroxo species (O2H3)(-) in the framework, as well

59 y be viewed as analogous to that between the aqua ligand and Thr-199 at the active site of carbonic a

60 als; Ln(solv)n3+, where in 1:9 D2O-CD3CN the aqua complexes are the predominant species, Ln = lanthan

61 chemically functionalized; for example, the aqua ligands can be replaced by pyridines.

62 films of TiO(2) nanoparticles on glass, the aqua complex [Ru(II)(tpy)(bpy(PO(3)H(2))(2))(OH(2))](2+)

63 t irradiation enhances the production of the aqua adducts in which eq CH3CN is replaced by H2O molecu

64 determine the relative MS/MS response of the aqua compounds for the first time.

65 l ions studied, we identify the pK(a) of the aqua ion as the factor that determines the functional co

66 H2O molecules, whereas the formation of the aqua species for cis-[Rh2(fhp)2(CH3CN)6][BF4]2 (7) is on

67 ither can be prepared by pretreatment of the aqua-coordinated polyoxometalates (L = H2O) with NO2 or

68 thermodynamically easier to oxidize than the aqua precursor, [Mn(2+)(OH(2))].

69 that an intramolecular hydrogen bond to the aqua ligand can reduce this internal rotation and increa

70 onated by (C(6)F(5))(3)B(OH(2)) to yield the aqua derivative [[Tp(Bu)t(,Me)]Co(OH(2))][HOB(C(6)F(5))(

71 onated by (C(6)F(5))(3)B(OH(2)) to yield the aqua derivative [[Tp(Bu)t(,Me)]Zn(OH(2))][HOB(C(6)F(5))(

72 ctivity of 1 increases with pH value through aqua ligand deprotonation.

73 udies, and the latter confirms oxo and trans aqua (H2O) ligands on Au.

74 minent sites of reactivity by the Cp*Rh tris aqua complex.

75 The metal is coordinated by two aqua ligands, two histidines (5 and 74), and two glutama

76 mples between 101% and 106% were found using aqua regia treatment.

77 It was found that the extraction with aqua regia provides the best results, i.e., limits of de