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1 the metal, resulting from the formation of a chemical bond.
2 ing the photonic energy to the cleavage of a chemical bond.
3 nsidered to involve an intermediate-strength chemical bond.
4 leading to storage of the energy of light in chemical bonds.
5 for the facile activation of otherwise inert chemical bonds.
6 are held together by mechanical rather than chemical bonds.
7 hains and a following formation of new Fe-Fe chemical bonds.
8 rks based on molecules containing reversible chemical bonds.
9 ategy for the storage of renewable energy in chemical bonds.
10 are necessary for activations of most stable chemical bonds.
11 ology for the storage of renewable energy in chemical bonds.
12 driven by light without any rearrangement of chemical bonds.
13 appreciated processes that can make or break chemical bonds.
14 mall molecular objects containing only a few chemical bonds.
15 electrons can become the main components of chemical bonds.
16 nctions to store solar energy in the form of chemical bonds.
17 itor the intrinsic vibrational signatures of chemical bonds.
18 sociated without the cleavage of one or more chemical bonds.
19 center that stores energy from the photon in chemical bonds.
20 ficiently convert light from the sun to form chemical bonds.
21 y by storing electrons in the form of stable chemical bonds.
22 energy through the breaking or formation of chemical bonds.
23 of intermittent solar energy in the form of chemical bonds.
24 s is a powerful tool for the construction of chemical bonds.
25 and store solar energy in the form of stable chemical bonds.
26 ttice, implying the breaking of the original chemical bonds.
27 ce of the perovskite films by forming strong chemical bonds.
28 sts to provide swift exchange of the dynamic chemical bonds.
29 n and fundamental insight into the nature of chemical bonds.
30 Bipolar switching mode did not involve the chemical bonding.
31 ting the link between the topology and local chemical bonding.
32 carrier-brush into the GO nanochannels with chemical bonding.
33 nd a reset switching process disconnects the chemical bonding.
34 because of very subtle differences in local chemical bonding.
35 ls, making them energetically accessible for chemical bonding.
36 d had considerable impact on modern ideas of chemical bonding.
37 ays reduced dimensionality and rule-breaking chemical bonding.
38 H-X interactions in this broad range of weak chemical bonding.
39 interference (or resonance) as the origin of chemical bonding.
40 the wettability is dominated by short-range chemical bonding.
41 discovery of novel molecular structures and chemical bonding.
42 s in the COOH and Si-O vibrations indicating chemical bonding.
43 of the organic host, and embodies guest-host chemical bonding.
44 stood through the long-established schema of chemical bonding.
46 t they continue to yield surprises and novel chemical bonding analogous to specific polycyclic aromat
63 86 mg/g) and pH 7.0 (3.12 mg/g) owing to the chemical bonding and entrapment of cholesterol molecules
64 tal understanding of the correlation between chemical bonding and lattice dynamics in intrinsically l
69 hanism that correlates phonon transport with chemical bonding and solid-state structure is the key to
70 as epitaxial growth, usually involve strong chemical bonds and are typically limited to materials wi
71 for maximum energy often results in unstable chemical bonds and causes safety problems in practical p
72 e aim of this study was to identify specific chemical bonds and characteristic structures in melanoid
73 that sigma stacking can reach the energy of chemical bonds and concludes that "sigma/sigma and pi/pi
74 trate the nearly equivalent tradeoff between chemical bonds and entropic bonds in the colloidal cryst
75 lacticin 481 synthetase (LctM) cleaves eight chemical bonds and forms six new chemical bonds in a con
76 quire harsh conditions to collectively break chemical bonds and overcome the stress caused to the ori
77 ombining with the stripped electrons to make chemical bonds and releasing O2 for powering respiratory
78 bricated so that it is sensitive to specific chemical bonds and the bond environment, but at the same
79 ent chemistry to prompt the disconnection of chemical bonds and the formation of new linkages in situ
80 rful reagents in the liquid phase that break chemical bonds and thereby create additional reactive sp
82 about a Renaissance in the mental map of the chemical bond, and to contribute to productive chemical
84 rtant in developing our understanding of the chemical bonding, and therefore the reactivity, of actin
85 cellular ranges, interact destructively with chemical bonds, and are the most abundant product of ion
86 heres strongly to the surface, often through chemical bonds, and is therefore difficult to remove.
88 ing arises from the formation of interfacial chemical bonds, and the large magnitude of ageing at the
91 tal structure the hydration occurs and which chemical bonds are altered and weakened after hydration.
94 conversion and storage of solar energy into chemical bonds are rare, inefficient and do not use sign
95 -defined chemical structure and well-defined chemical bonds, are of a great interest to the 2D materi
97 models, we show that those describing the OH chemical bond as rigid or harmonic greatly overpredict t
98 erties because of the exotic nature of their chemical bonding as they contain both metal-metal and me
100 methods, we reconstructed the nature of the chemical bonds as well as the influence of the increasin
101 ork sheds light on the orbitalwise nature of chemical bonding at adsorption sites with d-states chara
105 PIR cross-linkers are designed to contain chemical bonds at specific locations within the cross-li
106 d that UV illumination alters the mixture of chemical bonds at the interface, permitting the formatio
107 mployed, yet debated, chemical concepts: the chemical bond, atomic charges, (hyper)conjugation, and m
108 cited as the primary origin of the covalent chemical bond based on Ruedenberg's pioneering analysis
109 s is explained by the significantly stronger chemical bond between Cu and TCNQF(4) molecules than for
110 band are attributed to the development of a chemical bond between silver surface and uranyl species.
113 tallinity of curcumin and did not create any chemical bonding between curcumin nanoparticles and the
114 n hybrid materials are novel due to possible chemical bonding between inorganic nanoparticles and oxi
115 and structure, differences in structure and chemical bonding between native and technical lignins, e
118 usly obtained data, to assess the changes in chemical bonding between the allyl and benzyl radicals a
120 low for the identification of complexes with chemical bonds between the alkyl groups and the copper c
121 and summarized: macromolecular deformation, chemical bond breakage, and biomineral crystal imperfect
125 ere driven by electrostatic interactions and chemical bonding (bridge-coordination) between the COO(-
126 provides specific vibrational signatures of chemical bonds, but is often hindered by low sensitivity
128 organics via interactions that can resemble chemical bonds, but with much diminished bond energies.
129 n potentially provide control of the surface chemical bond by an external voltage, providing a new ap
131 reaction involves the formation of five new chemical bonds by concatenating three distinct chemical
133 hemical rules, based on atomic distances and chemical bond character, which predict topological mater
138 it is possible that the hallmark features of chemical bonding could arise through local gradients res
139 s-liquid interface; and (3) in solutions via chemical bonding, depletion attraction forces and linker
142 hemical formulas for fragment ions where the chemical bonding (e.g., Lewis structures) of the intact
143 f charge density in materials dictates their chemical bonding, electronic transport, and optical and
144 st through its unique capability of sampling chemical bonding element-specifically ((1/2)H, (13)C, (1
147 categories, catenation and interpenetration, chemical bonding enhancement, and electrostatic force in
151 parallels the order of the strengths of the chemical bonds expected to form by the respective monola
152 eveal that the 5f orbitals are active in the chemical bonding for uranium and neptunium, shown by sig
153 re trapped in appreciable potential wells by chemical bonding forces, despite powerful electrostatic
155 sible for energy loss generally include both chemical bond formation (chemisorption) and nonbonding i
157 lts provide evidence for the early stages of chemical bond formation between H2O molecules and tetrah
158 barrier of 13 kcal mol(-1) was obtained for chemical bond formation between the di-iron active site
159 rene mutual orientation was achieved through chemical bond formation, in particular, by metal coordin
161 ects in oils are produced during frying, the chemical bonds forming these polymers are not well under
163 ing on states of atoms its connected to with chemical bonds (hard neighbours) and atoms being in phys
165 t lattice dynamics associated with the local chemical bonding hierarchy in Zintl compound TlInTe(2) ,
169 ationships between mechanical properties and chemical bonding in a dense inorganic-organic framework
171 icity, antiaromaticity, and their effects on chemical bonding in the ground states (S0), lowest tripl
173 ing from the structure models, the nature of chemical bonding in the molybdates is explained by molec
174 e similar chemical makeup, the nature of the chemical bonding in the two compounds is subtly differen
175 ble the selective deformation of N-H and N-C chemical bonds in 2-thiopyridone in aqueous solution wit
176 eaves eight chemical bonds and forms six new chemical bonds in a controlled and ordered process.
177 ion and label-free vibrational signatures of chemical bonds in biomolecules, but the abundance of wat
178 Amide linkages are among the most important chemical bonds in living systems, constituting the conne
179 topological bond order and the nature of the chemical bonds in MA illustrates the fact that eliminati
180 second control of the breaking and making of chemical bonds in polyatomic molecules is poised to open
181 ing measured ORR activity with the change of chemical bonds in precursors during thermal activation u
182 entional knowledge that intrinsically strong chemical bonds in superhard materials should lead to hig
185 on methods, advances in the understanding of chemical bonding, in the development of force fields, an
187 t be representative, and they provide little chemical bonding information with low contrast of light
188 A less-explored approach is to modulate the chemical bonding interactions within a material to promo
190 table is widely recognized, its influence on chemical-bonding interactions, and on consequent materia
191 The quantum mechanical description of the chemical bond is generally given in terms of delocalized
194 lexibility in enzyme-catalyzed activation of chemical bonds is an evolving perspective in enzymology.
195 ergy decomposition analysis (EDA) for single chemical bonds is presented within the framework of Kohn
196 th its ability to distort, bend, and stretch chemical bonds, is unique in the way it activates chemic
200 found changes in the properties of atoms and chemical bonding, leading to the formation of many unusu
201 he macroscale stretching of solids elongates chemical bonds, leading to the reduced overlap and deloc
202 to drive the formation or the degradation of chemical bonds, leading to unprecedented spatiotemporal
204 tting edge of characterisation at the single chemical bond level, and have revolutionised our underst
205 are now focused on understanding the role of chemical bond manipulation to reversibly alter the free
208 isregard the tendency of carbon to form four chemical bonds, namely N-heterocyclic carbenes (NHCs) an
209 rystalline phases, but also the very similar chemical-bonding nature between crystalline PCMs and one
210 h, allows an in-depth investigation into the chemical-bonding network, as well as lone pairs, of the
211 itions to explore the nature of the covalent chemical bond, non-covalent interactions, bond formation
212 with the standard rule of three-dimensional chemical bonding nor with the maximum tetracoordination.
213 results have implications for understanding chemical bonding not only in organolanthanide complexes
214 lving dissociation and formation of multiple chemical bonds, occurring under strong laser fields.
215 d(5) in three-dimensional XeF(8) through the chemical bonding of all eight valence electrons in Xe an
217 ement in adsorption can be attributed to the chemical bonding of lithium ions by nitrogen functional
220 pectedly high proclivity for two-dimensional chemical bonding of the carbon in D5h CAl5(+), the robus
222 the reaction mechanism, thermochemistry, and chemical bonding of the isoelectronic silaisocyanoacetyl
223 al pore environment but also from asymmetric chemical bonding of the target molecules with the framew
224 an analysis of the electronic structures and chemical bonding of these compounds in comparison with o
225 ve investigated the electronic structure and chemical bonding of two isoelectronic Al-doped boron clu
226 cess of transduction of energy stored within chemical bonds of ground-state reactants into light via
229 ation, enabling a hierarchical activation of chemical bonds on different length scales from the macro
236 reveal more interesting structures and novel chemical bonding, paving the foundation for new boron-ba
240 duced spin selectivity effect, which induces chemical bond polarization in the J-coupling, is the mec
241 e electron spin spatial asymmetry induced by chemical bond polarization involving a chiral center.
242 o acquire a fundamental understanding of the chemical bonding properties of such long-time elusive co
243 The EDA reveals distinguishing features of chemical bonds ranging across nonpolar, polar, ionic, an
244 investigation of the B cluster, which shows chemical bonding reminiscent of that in [10]annulene (CH
246 both the bulk components and identifies the chemical bonding requirements to connect distinct oxide
247 at the scaffold is stabilized by sulfilimine chemical bonds (S = N) that covalently cross-link methio
249 lysts that can selectively activate targeted chemical bonds, since the mechanism allows for tuning pl
251 superior electrochemical performance of the chemical bonding-stabilized C/S composite renders it a p
253 chemical concepts (e.g. atomic charges, the chemical bond, strain, aromaticity, branching, etc.), wh
254 l flexibility which arise due to its maximal chemical bond strength and minimal atomic thickness.
257 dation was attributed to the increase of the chemical bonding strength between the external screening
258 h tasks involve the cleavage or formation of chemical bonds, structural characterization at the atomi
259 xhibited higher beta-sheet contents and more chemical bonds such as hydrophobic interactions and disu
260 apable of the activation of relatively inert chemical bonds, such as those found in dihydrogen and ca
261 extremely large electric field onto the C=O chemical bond that undergoes a charge rearrangement in K
262 bit intriguing size-dependent structures and chemical bonding that are different from bulk boron and
265 heir constituting building blocks, while the chemical bonds that connect the individual subunits have
266 cation of these materials, the nature of the chemical bonds that enable the adaptable structure, how
268 matched and robust scandium telluride (ScTe) chemical bonds that stabilize crystal precursors in the
269 pulse was generated by ZIF-8 resulting from chemical bonds that were broken and subsequently reforme
270 ffects of aromaticity and antiaromaticity on chemical bonding, these can be viewed, arguably, as the
271 Besides the possible effect of the modified chemical bonding, this negative charge gives rise to an
273 unctionalized by Prussian blue nanocubes via chemical bonding to form a kind of interlocked microstru
274 noscale (~40 nm) diffusion distances and C S chemical bonding to minimize cycling capacity decay and
277 t to compressive and tensile stresses due to chemical bonding to the substrate and island-like morpho
278 tures and compare them to those exhibited by chemical bonds to argue for the existence of entropic bo
279 rength and three-dimensional organization of chemical bonds to be used as handles to manipulate how a
280 ylene C-H bonds are among the most difficult chemical bonds to selectively functionalize because of t
281 But none of them is known to form direct chemical bonds to the framework of these industrially im
284 samples based on vibrational transitions of chemical bonds upon interaction with infrared light.
285 itals of uranium, neptunium and plutonium in chemical bonding using advanced spectroscopies: actinide
287 Nature is capable of storing solar energy in chemical bonds via photosynthesis through a series of C-
290 ar stability of bare Ti8 O12 cluster: unique chemical bonding where eight electrons of Ti atoms inter
291 ternal structure of chemical gels is made of chemical bonds, while physical gels are characterized by
293 aps water physically, which is stabilized by chemical bonding with protein within surimi gel matrix.
295 y has become a powerful modality for imaging chemical bonds with high sensitivity, resolution, speed
296 ins, stabilized by the cooperative effect of chemical bonds with the substrate and hydrogen bonds.
297 trated that both Chelex-100 and Metsorb form chemical bonds with ZnO NP and Zn(2+), however the bindi
298 to study the effects of mechanical force on chemical bonds within a polymer backbone or to generate
299 are shared or transferred between atoms in a chemical bond would greatly improve our understanding of
300 tion of the current density passing selected chemical bonds yields current pathways and the degree of