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1 due to the distinct electronic structure and ionic radius.
2 metal ions with the same charge and similar ionic radius.
3 complexes with cations (bK(AIB)) varies with ionic radius.
4 0-fold higher than alkali cations of similar ionic radius.
5 ared to monovalent alkali cations of similar ionic radius.
6 ty irrespective of cation, charge density or ionic radius.
7 inity for the lanthanide ions with a smaller ionic radius.
8 l ions decreases linearly with an increasing ionic radius.
9 d the smallest for cadmium, with the largest ionic radius.
11 s due to its relatively small six-coordinate ionic radius, 0.89 angstroms, vs 1.09 angstroms for Cd2+
12 finity supported by these ions suggests that ionic radius and charge are not critical to the promotio
17 l and theoretical results reveal that dopant ionic radius and electronic structure have a significant
19 dependent on small variations in lanthanide ionic radius and occurs despite identical coordination-l
20 The considerable adjustments incurred to ionic radius and resultant cation charge density also pr
21 s proposed which predicts effects of charge, ionic radius and temperature on counterion-induced RNA f
22 monovalent cation depends on its unhydrated ionic radius, and at a low monovalent cation concentrati
23 es synergistic contributions from S(config), ionic radius, and electronegativity, enabling screening
25 can be fulfilled by other cations of similar ionic radius, and that the functional role of Ca2+ to ac
26 is the largest for nickel, with the smallest ionic radius, and the smallest for cadmium, with the lar
27 lanthanide trisamides scales with the Ln(3+) ionic radius, and this process is effective with post-co
28 ice formation enthalpy (DeltaH(L)) and metal ionic radius are the best predictors of IXZO oxygen gett
32 has a higher affinity for metal ions with an ionic radius close to 1.0 A, particularly Cd(II), Gd(III
34 ture is still monovalent-cation specific and ionic-radius dependent, but a larger number of cations (
36 ion fields by tailoring chemical bonds using ionic radius differences, strains, doping and lattice di
38 This contribution probes mechanism and metal ionic radius effects in the catalytic lanthanide triflat
43 thanide complexes, namely one with a similar ionic radius (i.e., Nd(III) ) and an isoelectronic one (
47 ure, A-site cation size or decreasing halide ionic radius is found principally in the strengthening o
50 than that for lanthanides with most similar ionic radius, Nd(3+) and Sm(3+), and making LanM the str
51 respectively. Li(+) is a lighter ion with an ionic radius of 0.76 angstrom compared to the Zn(2+) ion
53 e in a novel structure type due to the small ionic radius of Ca and the strong Jahn-Teller effect of
55 th the larger amount of iron and the smaller ionic radius of Fe(2+) as a result of an electronic spin
57 erovskite framework facilitated by the large ionic radius of K(+) enhances the local polarity of Bi-O
61 d cyclability is difficult because the large ionic radius of potassium-ions causes structural distort
62 ally longer than would be predicted from the ionic radius of Ra(2+) and by analogy with Ba(2+), suppo
65 monoclinic lattice parameters to the average ionic radius of the cations (Ga(3+), Al(3+), In(3+)) ena
66 enthalpy at the Cu(I) sites according to the ionic radius of the central metal ion of the pentanuclea
74 s activated by cations of varying charge and ionic radius, such as Li+, A13+, Tb3+, and Eu3+, as well
76 rimary storage sites for elements with large ionic radius--that is, incompatible elements in the Eart
77 an oligomeric state sensitive to rare-earth ionic radius, the lanthanum(III)-induced dimer being >10
79 onfirm that adsorption energy increases with ionic radius, while being highly dependent on the pore s