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1 ing the photonic energy to the cleavage of a chemical bond.
2 nsidered to involve an intermediate-strength chemical bond.
3 the metal, resulting from the formation of a chemical bond.
4 driven by light without any rearrangement of chemical bonds.
5 appreciated processes that can make or break chemical bonds.
6 mall molecular objects containing only a few chemical bonds.
7 electrons can become the main components of chemical bonds.
8 nctions to store solar energy in the form of chemical bonds.
9 itor the intrinsic vibrational signatures of chemical bonds.
10 sociated without the cleavage of one or more chemical bonds.
11 center that stores energy from the photon in chemical bonds.
12 s no net change in the number of high-energy chemical bonds.
13 nit, held together by what are probably weak chemical bonds.
14 leading to storage of the energy of light in chemical bonds.
15 ersal symmetry, and possibly the weighing of chemical bonds.
16 metrology, fundamental physics, and weighing chemical bonds.
17 ule-like structures, each with two localized chemical bonds.
18 , which atomize the projectile and break all chemical bonds.
19 for the facile activation of otherwise inert chemical bonds.
20 are held together by mechanical rather than chemical bonds.
21 rks based on molecules containing reversible chemical bonds.
22 ategy for the storage of renewable energy in chemical bonds.
23 ology for the storage of renewable energy in chemical bonds.
24 H-X interactions in this broad range of weak chemical bonding.
25 the wettability is dominated by short-range chemical bonding.
26 discovery of novel molecular structures and chemical bonding.
27 Bipolar switching mode did not involve the chemical bonding.
28 s in the COOH and Si-O vibrations indicating chemical bonding.
29 ting the link between the topology and local chemical bonding.
30 structure and to elucidate the Au-O and Au-S chemical bonding.
31 ular orbital dichotomy present in studies of chemical bonding.
32 ence-region orbitals and the nature of their chemical bonding.
33 and experimentally studying a new regime of chemical bonding.
34 carrier-brush into the GO nanochannels with chemical bonding.
35 organic molecules) for examining delocalized chemical bonding.
36 nd a reset switching process disconnects the chemical bonding.
37 because of very subtle differences in local chemical bonding.
38 ls, making them energetically accessible for chemical bonding.
39 d had considerable impact on modern ideas of chemical bonding.
40 ays reduced dimensionality and rule-breaking chemical bonding.
42 t they continue to yield surprises and novel chemical bonding analogous to specific polycyclic aromat
53 ue even though the two species do not form a chemical bond and, therefore, the electronic coupling be
59 for maximum energy often results in unstable chemical bonds and causes safety problems in practical p
60 e aim of this study was to identify specific chemical bonds and characteristic structures in melanoid
61 that sigma stacking can reach the energy of chemical bonds and concludes that "sigma/sigma and pi/pi
62 lacticin 481 synthetase (LctM) cleaves eight chemical bonds and forms six new chemical bonds in a con
64 organizations intermediate between discrete chemical bonds and periodic crystalline lattices are pre
65 ombining with the stripped electrons to make chemical bonds and releasing O2 for powering respiratory
66 bricated so that it is sensitive to specific chemical bonds and the bond environment, but at the same
67 ent chemistry to prompt the disconnection of chemical bonds and the formation of new linkages in situ
68 rful reagents in the liquid phase that break chemical bonds and thereby create additional reactive sp
70 the application to DNA, whose basic kernels, chemical bonding, and overall molecular structure are qu
71 ue to weak physical interactions rather than chemical bonding, and that the strong adhesion forces of
72 rtant in developing our understanding of the chemical bonding, and therefore the reactivity, of actin
73 cellular ranges, interact destructively with chemical bonds, and are the most abundant product of ion
74 heres strongly to the surface, often through chemical bonds, and is therefore difficult to remove.
75 ing arises from the formation of interfacial chemical bonds, and the large magnitude of ageing at the
78 tal structure the hydration occurs and which chemical bonds are altered and weakened after hydration.
81 -defined chemical structure and well-defined chemical bonds, are of a great interest to the 2D materi
82 models, we show that those describing the OH chemical bond as rigid or harmonic greatly overpredict t
85 nversion of serine and glycine, changing the chemical bonding at the C(alpha)-C(beta) bond of the ser
88 thod for the measurement of the direction of chemical bonds at more than one molecular location withi
89 d that UV illumination alters the mixture of chemical bonds at the interface, permitting the formatio
90 mployed, yet debated, chemical concepts: the chemical bond, atomic charges, (hyper)conjugation, and m
92 hese data indicate the formation of a strong chemical bond between Cu and Mn atoms across the interfa
93 s is explained by the significantly stronger chemical bond between Cu and TCNQF(4) molecules than for
94 band are attributed to the development of a chemical bond between silver surface and uranyl species.
97 n hybrid materials are novel due to possible chemical bonding between inorganic nanoparticles and oxi
98 and structure, differences in structure and chemical bonding between native and technical lignins, e
100 usly obtained data, to assess the changes in chemical bonding between the allyl and benzyl radicals a
101 es, including x-ray crystallography, and the chemical bonding between the metal center and the nitrog
102 low for the identification of complexes with chemical bonds between the alkyl groups and the copper c
106 ere driven by electrostatic interactions and chemical bonding (bridge-coordination) between the COO(-
107 provides specific vibrational signatures of chemical bonds, but is often hindered by low sensitivity
108 organics via interactions that can resemble chemical bonds, but with much diminished bond energies.
109 n potentially provide control of the surface chemical bond by an external voltage, providing a new ap
111 stablish that binding forces due to discrete chemical bonds can be detected directly in AFM pull-off
113 onal flexibility about strategically located chemical bonds) can be a powerful drug design concept, e
117 s-liquid interface; and (3) in solutions via chemical bonding, depletion attraction forces and linker
118 yet the fleeting configuration when existing chemical bonds dissociate while new ones form is extreme
121 hemical formulas for fragment ions where the chemical bonding (e.g., Lewis structures) of the intact
125 Transduction of adenosine triphosphate (ATP) chemical-bond energy into work to drive large-scale conf
126 categories, catenation and interpenetration, chemical bonding enhancement, and electrostatic force in
127 metry-constrained, rigid-cluster, hybrid and chemical-bond ENMs have been developed and implemented a
131 parallels the order of the strengths of the chemical bonds expected to form by the respective monola
132 , there is generally a very similar level of chemical bonding for all M-C(ring) interactions, as expe
133 eveal that the 5f orbitals are active in the chemical bonding for uranium and neptunium, shown by sig
134 re trapped in appreciable potential wells by chemical bonding forces, despite powerful electrostatic
138 lts provide evidence for the early stages of chemical bond formation between H2O molecules and tetrah
139 barrier of 13 kcal mol(-1) was obtained for chemical bond formation between the di-iron active site
140 rene mutual orientation was achieved through chemical bond formation, in particular, by metal coordin
143 ing on states of atoms its connected to with chemical bonds (hard neighbours) and atoms being in phys
146 Selective cleavage and rearrangement of chemical bonds having dissociation energies up to approx
148 store solar-converted energy in the form of chemical bonds, i.e., in a photosynthetic process at a y
151 ationships between mechanical properties and chemical bonding in a dense inorganic-organic framework
153 ral assignments and provide insight into the chemical bonding in the AuX (-) and AuX 2 (-) molecules.
155 Related methods can be used to study the chemical bonding in the boron polyhedra found in other s
156 icity, antiaromaticity, and their effects on chemical bonding in the ground states (S0), lowest tripl
158 c band-structure analysis indicates that the chemical bonding in the structure is still optimized des
159 ry provides a more useful description of the chemical bonding in the studied crystals as compared to
160 e similar chemical makeup, the nature of the chemical bonding in the two compounds is subtly differen
162 ble the selective deformation of N-H and N-C chemical bonds in 2-thiopyridone in aqueous solution wit
163 eaves eight chemical bonds and forms six new chemical bonds in a controlled and ordered process.
164 ion and label-free vibrational signatures of chemical bonds in biomolecules, but the abundance of wat
165 Amide linkages are among the most important chemical bonds in living systems, constituting the conne
166 topological bond order and the nature of the chemical bonds in MA illustrates the fact that eliminati
167 second control of the breaking and making of chemical bonds in polyatomic molecules is poised to open
168 ing measured ORR activity with the change of chemical bonds in precursors during thermal activation u
169 entional knowledge that intrinsically strong chemical bonds in superhard materials should lead to hig
171 on methods, advances in the understanding of chemical bonding, in the development of force fields, an
172 The quantum mechanical description of the chemical bond is generally given in terms of delocalized
175 lexibility in enzyme-catalyzed activation of chemical bonds is an evolving perspective in enzymology.
176 ergy decomposition analysis (EDA) for single chemical bonds is presented within the framework of Kohn
177 th its ability to distort, bend, and stretch chemical bonds, is unique in the way it activates chemic
181 found changes in the properties of atoms and chemical bonding, leading to the formation of many unusu
182 he macroscale stretching of solids elongates chemical bonds, leading to the reduced overlap and deloc
184 are now focused on understanding the role of chemical bond manipulation to reversibly alter the free
189 isregard the tendency of carbon to form four chemical bonds, namely N-heterocyclic carbenes (NHCs) an
190 unt for the formation of discrete numbers of chemical bonds (nBonds) between the tip and substrate.
191 13C SSNMR was used to reveal details of the chemical bonding network, including the chemical groups
192 h, allows an in-depth investigation into the chemical-bonding network, as well as lone pairs, of the
193 itions to explore the nature of the covalent chemical bond, non-covalent interactions, bond formation
194 with the standard rule of three-dimensional chemical bonding nor with the maximum tetracoordination.
195 results have implications for understanding chemical bonding not only in organolanthanide complexes
196 lving dissociation and formation of multiple chemical bonds, occurring under strong laser fields.
197 calculations to elucidate the structure and chemical bonding of a series of MAl(6)(-) (M = Li, Na, K
198 d(5) in three-dimensional XeF(8) through the chemical bonding of all eight valence electrons in Xe an
200 ement in adsorption can be attributed to the chemical bonding of lithium ions by nitrogen functional
203 we investigated the electronic structure and chemical bonding of six anionic [Mo(V)O](3+) complexes,
204 pectedly high proclivity for two-dimensional chemical bonding of the carbon in D5h CAl5(+), the robus
206 the reaction mechanism, thermochemistry, and chemical bonding of the isoelectronic silaisocyanoacetyl
208 not readily react with H2 due to the strong chemical bonding of the thiolate to the Pd, which inhibi
210 We investigated the electronic structure and chemical bonding of two bimetallic clusters NaGa4- and N
211 ve investigated the electronic structure and chemical bonding of two isoelectronic Al-doped boron clu
212 s, were predicted to change the structure or chemical bonds of alphaMyHC, and were absent in at least
215 ation, enabling a hierarchical activation of chemical bonds on different length scales from the macro
218 physical processes such as the breaking of a chemical bond or the vibrational motion of atoms within
220 ith magic-angle spinning, we have identified chemical bonding patterns typical of alkane, alkene, alc
223 rgy and then store the energy in the form of chemical bonds, producing oxygen from water and a reduce
224 The EDA reveals distinguishing features of chemical bonds ranging across nonpolar, polar, ionic, an
225 investigation of the B cluster, which shows chemical bonding reminiscent of that in [10]annulene (CH
227 both the bulk components and identifies the chemical bonding requirements to connect distinct oxide
228 at the scaffold is stabilized by sulfilimine chemical bonds (S = N) that covalently cross-link methio
230 lysts that can selectively activate targeted chemical bonds, since the mechanism allows for tuning pl
231 el that incorporates the effects of discrete chemical bonds, solvent surface tensions, and random con
234 chemical concepts (e.g. atomic charges, the chemical bond, strain, aromaticity, branching, etc.), wh
235 l flexibility which arise due to its maximal chemical bond strength and minimal atomic thickness.
238 dation was attributed to the increase of the chemical bonding strength between the external screening
239 h tasks involve the cleavage or formation of chemical bonds, structural characterization at the atomi
240 xhibited higher beta-sheet contents and more chemical bonds such as hydrophobic interactions and disu
241 fied an enzyme that specifically cleaves the chemical bond that joins the active site tyrosine of top
242 extremely large electric field onto the C=O chemical bond that undergoes a charge rearrangement in K
243 bit intriguing size-dependent structures and chemical bonding that are different from bulk boron and
244 tures and from Pauling's resonance theory of chemical bonding that predicted planar peptide groups.
247 cation of these materials, the nature of the chemical bonds that enable the adaptable structure, how
248 matched and robust scandium telluride (ScTe) chemical bonds that stabilize crystal precursors in the
249 pulse was generated by ZIF-8 resulting from chemical bonds that were broken and subsequently reforme
251 of the capillaries are modified by covalent chemical bonds, the adsorption of peptides and proteins
252 ffects of aromaticity and antiaromaticity on chemical bonding, these can be viewed, arguably, as the
253 Besides the possible effect of the modified chemical bonding, this negative charge gives rise to an
255 unctionalized by Prussian blue nanocubes via chemical bonding to form a kind of interlocked microstru
258 t to compressive and tensile stresses due to chemical bonding to the substrate and island-like morpho
259 esents the balance between the much stronger chemical bonds to oxygen at the reactant formaldehyde hy
260 ylene C-H bonds are among the most difficult chemical bonds to selectively functionalize because of t
262 But none of them is known to form direct chemical bonds to the framework of these industrially im
263 nderlying such important ideas as Pauling's "chemical bond," "transferability," and Yang's computatio
266 itals of uranium, neptunium and plutonium in chemical bonding using advanced spectroscopies: actinide
269 ar stability of bare Ti8 O12 cluster: unique chemical bonding where eight electrons of Ti atoms inter
270 ternal structure of chemical gels is made of chemical bonds, while physical gels are characterized by
271 on by the parent radionuclide will break the chemical bond with its carrier molecule and that the res
272 aps water physically, which is stabilized by chemical bonding with protein within surimi gel matrix.
274 coating to the capillary wall resulting from chemical bonding with the silanol groups on the fused-si
275 ins, stabilized by the cooperative effect of chemical bonds with the substrate and hydrogen bonds.
276 trated that both Chelex-100 and Metsorb form chemical bonds with ZnO NP and Zn(2+), however the bindi
277 are shared or transferred between atoms in a chemical bond would greatly improve our understanding of
279 tion of the current density passing selected chemical bonds yields current pathways and the degree of
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