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1 into 5 subfractions (L1-L5) with increasing electronegativity.
2 OSoxy, indicating it decreased heme-thiolate electronegativity.
3 ydroxylating species by tuning heme-thiolate electronegativity.
4 reduction in T1/2 for increasing substituent electronegativity.
5 rt of the C-terminal domain, diminishing its electronegativity.
6 ing monomers times the square of the Pauling electronegativity.
7 nts yielded subfractions L1-L5 in increasing electronegativity.
8 y not be the same because of their different electronegativity.
9 lence and, less strongly, on ionic radius or electronegativity.
10 ically with leaving group hydrophobicity and electronegativity.
11 to oxygen ranking high in both abundance and electronegativity amongst the stable elements of the uni
12 n of K in PbTe as a result of the balance of electronegativity and also lowers the lattice thermal co
14 cture but strongly dependent on the absolute electronegativity and hardness of the interacting metal
15 he nature of pucker is dependent on both the electronegativity and stereochemistry of the substituent
16 nergy band is likely the result of a loss of electronegativity and the acceptor unit's ability to sep
17 ibutions one can judge when more traditional electronegativity arguments can be justifiably invoked i
18 vealed that those bearing groups with strong electronegativity at the R1 position (i.e., CHD-5, CHD-1
21 mple approaches for quantitatively assessing electronegativity, chemical hardness, and ionicity, whil
22 he dominant (if not sole) contributor to the electronegativity chi, one is led to assume that P depen
23 tion initiated the idea to derive the "true" electronegativity chiSIMS from the measured ion yields P
25 d here is counterintuitive based upon simple electronegativity considerations, but this finding is un
28 erage electron binding energy, a generalized electronegativity, DeltaVNN is the change in nuclear rep
29 nsfer in these oxides, suggesting that large electronegativity difference and high pressure are the k
30 er effect, rationalizes the influence of the electronegativity difference between A and Y in (AY)4 on
32 in a complex metallic alloy, even though the electronegativity differences within the unit cell are l
36 to other recent reports, Pauling's original electronegativity equation, applied as Pauling specified
38 due to its similar size but vastly different electronegativity has been substituted for hydrogen as a
39 ode in a rechargeable battery due to its low electronegativity (high cell voltage), double valence, e
40 r ability of sigma bonds being controlled by electronegativity in periods and by sigma orbital energy
41 rt the discovery of an important role of the electronegativity in the nanowire growth on arbitrary su
42 retained even with significant reduction of electronegativity in the selectivity filter, and that co
43 tor desensitization, whereas the substituent electronegativity is correlated with ligand potency.
45 substitution, and the effect of substituent electronegativity is opposite of the effect on the therm
46 tumor effect(s) of substituents of differing electronegativities, located at the several sites compri
48 indicates that 113 variables including size, electronegativity, number of valence electrons, and posi
49 west occupied Kohn-Sham levels and elemental electronegativities of the constituent atomic species as
51 ectrostatic model and not with one involving electronegativities of the ligated phenoxide oxygens.
52 '-F should closely imitate the atom size and electronegativity of a 2'-OH, demonstrates low levels of
54 the combination of the electron affinity and electronegativity of doping elements, which serves as an
56 on varied from 0.57 to 35 h depending on the electronegativity of the 2-substituents and the size of
58 that the "stickiness" of this pin (i.e., the electronegativity of the anion) contributes to the energ
59 or the zinc increased monotonically with the electronegativity of the bound substituent X, e.g., Br <
60 oupling constants ((3)JHalpha,Hbeta) and the electronegativity of the Cgamma-substituents by chemical
64 chemists and biologists because the size and electronegativity of the fluorine atom can be used to ma
67 eometric arrangement of the heteroatoms, the electronegativity of the heteroatoms, and the electronic
70 exploits establishing a balance between the electronegativity of the materials' constituents and the
71 dine, pyrazine, pyrimidine), indicating that electronegativity of the nitrogen can change regioselect
72 es and the reaction energies with increasing electronegativity of the substituent (F > OH > NH2, Cl >
73 in monosubstituted ethenes where the role of electronegativity of the substituent X becomes more impo
76 H, its phenoxide anion strongly reducing the electronegativity of the sulfonyl group, thereby inhibit
78 lity in groups is opposite to the changes in electronegativity of X and in the C-X bond polarization,
79 p(pi) orbital on boron is correlated to the electronegativity of X, and the competition between the
80 eption of C-C, the order corresponded to the electronegativity of X, suggesting that the differences
81 o right in periods parallels the increase in electronegativity of X, whereas augmentation of acceptor
82 lls' internal bioactivity, (iii) cell-wall's electronegativity or dipole moment and their relaxation
83 a given type of annelation, such as strain, electronegativity, or cyclic electron count, can be sort
84 imal widening exhibit significantly enhanced electronegativity, ranging from 0.8 to 2.5 kT/e, dependi
85 endent; the former correlated very well with electronegativity scales, whereas the latter correlated
86 ppropriate value of chi is selected from the electronegativity tables of Pauling (read in eV), Mullik
89 he reduction of elements with lower relative electronegativity, the highly reducing nature of the B-B
90 y that correlated strongest was the ratio of electronegativity to hardness, chi2/eta, a quantity rela
92 by relating the central chemical concept of electronegativity with the average binding energy of ele
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