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1 ires knowing the entropy and enthalpy of the adsorbed molecule.
2 irections and the C-H bond directions in the adsorbed molecule.
3 dressable gate electrode and the presence of adsorbed molecules.
4 hanical sensitivity as well as the number of adsorbed molecules.
5 rp lasing emission that is ultrasensitive to adsorbed molecules.
6 gies often lack sufficient interactions with adsorbed molecules.
7 e (S/N) spectra from femtomole quantities of adsorbed molecules.
8 quilibrium constants for reactions involving adsorbed molecules.
9 ive to both the amount and the energetics of adsorbed molecules.
10 ical intermediates produced by photolysis of adsorbed molecules.
11 mal coupling between the laser pulse and the adsorbed molecules.
12 d to amplify the spectroscopic signatures of adsorbed molecules.
14 t more than one molecular location within an adsorbed molecule and the new method is named electron s
15 edicted to show no diffusion limitations for adsorbed molecules and extremely high CO(2)/N(2) adsorpt
16 NMR techniques to measure and assess dilute adsorbed molecules and their molecular interactions on l
17 all and we have to reckon with the motion of adsorbed molecules, and there is no "bulk" fluid region.
19 ange of molecular structure of catalysts and adsorbed molecules as the reactions proceed with changes
22 strate that the faster the AFM tip displaces adsorbed molecules in a monolayer, the more heterogeneou
24 hindrance effect exerted on the neighboring adsorbed molecules increases, and the geometrical packin
25 nd then back to large pore) as the number of adsorbed molecules increases, which is explained in term
26 nergy, and the LUMO density extends onto the adsorbed molecule, increasing the donor-acceptor interac
27 -dependent in situ spectra indicate that the adsorbed molecule is the benzotriazole anion (BTA-) at a
28 t electron transfer between the TiO2 and the adsorbed molecules is governed by competition between el
30 ric repulsion resulting in area exclusion by adsorbed molecules is taken into account by treating the
31 ssibility of attractive interactions between adsorbed molecules is taken into account in a limited fa
34 rgely focused on model systems consisting of adsorbed molecules on flat metallic surfaces with minima
36 measurements of the nonlocal manipulation of adsorbed molecules on the Si(111)-7 x 7 surface in the s
38 ical response due to radial diffusion of the adsorbed molecules outward from the microspots onto the
39 led understanding of the conformation of the adsorbed molecule relative to the Cu(110) crystal lattic
40 w way to determine the standard entropies of adsorbed molecules (S(ad)(0)) on single crystal surfaces
41 Importantly, the smallest concentration of adsorbed molecules shows the largest Raman enhancements
42 ch other, despite the fact that the directly adsorbed molecules take up less than 10% of the silica s
43 ron-acceptor molecule and as an irreversibly adsorbed molecule that heals natural oxygen vacancy defe
46 ver, with glutaraldehyde fixation of already adsorbed molecules, the resolution of both GroEL and Gro
47 because they are not wide enough to host non-adsorbed molecules; this is the case for samples with le
52 ely on the ability to tune the properties of adsorbed molecules, we anticipate that the ability to sy
53 ect this conclusion to apply to all types of adsorbed molecules where van der Waals interactions gove
55 e the local potential energy landscape of an adsorbed molecule with a carbon monoxide (CO)-terminated
56 l matching of the rotational symmetry of the adsorbed molecule with that of the underlying metal surf
57 milarly, selective vibrational excitation of adsorbed molecules with an STM tip to induce motion or d
58 dependence of the amount of adsorbed and non-adsorbed molecules within micropores, which experience s
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