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1 ured human lung A549 cells directly from the gas phase.
2 nt for delivering membrane proteins into the gas phase.
3 stinct from the underlying bulk or overlying gas phase.
4  reactions that ultimately yield HOMs in the gas phase.
5 g peptide containing up to five units in the gas phase.
6 s are energetically nearly degenerate in the gas phase.
7 ions released from the target protein in the gas phase.
8 iranium ion 5 and cycloalkenes occurs in the gas phase.
9 arged negative ions are seldom stable in the gas phase.
10 order of magnitude lower in MeCN than in the gas phase.
11 m from solution studies, but a few also from gas phase.
12 ional chemicals either in solution or in the gas phase.
13 cts directly with water to form H2SO3 in the gas phase.
14  in the solid state, in solution, and in the gas phase.
15 hat McjD in complex with MccJ25 survives the gas phase.
16  about the shape of an ionic molecule in the gas phase.
17  how this alters with increasing time in the gas phase.
18  presence of heterometallic fragments in the gas phase.
19 ntaining a tetraazamacrocyclic ligand in the gas phase.
20 occur upon charge reduction reactions in the gas phase.
21 ich are detected as single conformers in the gas phase.
22 s carefully transferred from solution to the gas phase.
23 d with octadecyldimethylmethoxysilane in the gas phase.
24 lopentamerization to form naphthalene in the gas phase.
25 l adsorption of heavy isotopologues from the gas phase.
26 to the pentameric self-assembly, even in the gas phase.
27 d for the detection of hydrazine even in the gas phase.
28 sistent loss or accumulation of (222)Rn in a gas phase.
29 zed diamondoids is shown to fluoresce in the gas phase.
30 in trap adducts with alpha-pinene CIs in the gas phase.
31 o oligomeric species both in solution and in gas phase.
32  gas-phase analogs or not even stable in the gas phase.
33 onse when compared to water molecules in the gas phase.
34 fter transfer from the solution phase to the gas phase?
35 complexes are collisionally activated in the gas phase, a larger proportion of the product ions produ
36 e that enables the separation of ions in the gas phase according to their charge, shape and size.
37                                  Herein, the gas phase acidities have been measured and calculated fo
38             We find correlations between the gas phase acidity and selectivity in two Umpolung reacti
39                   Emission factors for these gas-phase acids varied from 0.3-8.4 mg kg(-1) fuel.
40 tion structures are largely preserved in the gas phase, although the lipids do not maintain regular b
41 either higher in energy than the most stable gas-phase analogs or not even stable in the gas phase.
42                                              Gas phase analyses revealed that two were complete denit
43 e gas phase and, in some cases, trapping the gas-phase analytes into sorbents or containers.
44 latile ring-opened species are formed in the gas phase and assist particle formation through condensa
45 ynamics (BOMD) simulation shows that, in the gas phase and at a temperature of 300 K, the dominant in
46 ed species are in quasi-equilibrium with the gas phase and can be used in an approximate manner to pr
47 takes place through a concerted mechanism in gas phase and in apolar solvents but a stepwise mechanis
48 ociation of proton-bound dimers, both in the gas phase and in dichloromethane solution, showing that
49      Computational analysis performed in the gas phase and in MeCN solution shows that the free energ
50 end of predominance of Phax conformer in the gas phase and of Pheq in solution.
51 S=O and O=C=N-S=O, has been generated in the gas phase and subsequently characterized in cryogenic ma
52 ducts with alpha-pinene CIs also form in the gas phase and that they are stable enough to be detected
53 raction of a SO2 with water molecules in the gas phase and with the surface of various sized water na
54 lies only on noninvasive measurements of the gas phase and, given its simplicity, indicates the poten
55 g the samples to release the analytes to the gas phase and, in some cases, trapping the gas-phase ana
56 s at the surface of fuel droplet, liquid and gas phases and then show how experimental observations f
57  4.0, a photochemical box model that couples gas-phase and aqueous-phase aerosol chemistry, along wit
58 chanistic point of view, with the support of gas-phase and computational studies.
59  and reaction intermediates were observed by gas-phase and electrospray ionization mass spectrometry,
60 rplay among electrolyte, solid catalyst, and gas-phase and liquid-phase reactants and products.
61        EID allowed for the comparison of the gas-phase and the solution-phase structural stability an
62 ism for multidomain protein unfolding in the gas phase, and highlights key similarities and differenc
63 ge states of denatured ubiquitin ions in the gas phase, and ion mobility to probe their structures.
64 gh-valent compound could be generated in the gas phase, and its reactivity against olefins, sulfides,
65  the pH, the concentration of mercury in the gas phase, and the enhancement of mercury in the slurry
66 oping analytical methods for both liquid and gas phases, and integrating different units to quantitat
67 s regarding the unfolding of albumins in the gas phase, as well as more general inferences regarding
68 pectroscopic evidence for H-tunneling in the gas phase at temperatures around 320-350 K observed in t
69 ) as well as mustard (HD) in both liquid and gas phases at ambient temperature and in the absence of
70 ere formed by the CPA oxidation by OH in the gas-phase, at the air-water interface as well as in the
71 0) surface, including studies of the role of gas-phase atomic hydrogen, surface hydrogen, and subsurf
72                                              Gas-phase autoxidation-regenerative peroxy radical forma
73 rometry (IM-MS), which separates ions in the gas phase based on their size, charge and shape, offers
74 structures that is supported by experimental gas-phase basicities.
75 aper presents an analysis of the exceptional gas-phase basicity, mostly in terms of experimental data
76       However, they are rarely stable in the gas phase because of strong electrostatic repulsion betw
77            Further, the relationship between gas-phase behavior, lipid composition, and instrumental
78 eties of FBDSA and basic sites to facilitate gas-phase bioconjugation and to reduce charge sequestrat
79                                       In the gas phase, both the CH...O and OH...O hydrogen bonds are
80 ine changes in both individual molecules and gas-phase bulk properties of oxidation products as a fun
81 lifetimes at near-ambient temperature in the gas phase but that gas-phase dynamics should be consider
82  treated with reactive metal reagents in the gas phase by ALD to form an outer metal ion bridging gro
83 ain interface protect the native fold in the gas phase by mediating contacts between the mobile prote
84 stable GTP analogue) were transferred to the gas phase by nano-electrospray ionization and characteri
85 single-crystal X-ray diffraction, and in the gas phase by quantum-chemical calculations.
86  relevant Criegee intermediates (CIs) in the gas phase by stabilization with spin traps and analysis
87 hat govern complex formation in solution and gas phases by comparing nonselective lipid binding with
88            Investigations of proteins in the gas phase can be used to selectively decouple factors af
89                                              Gas-phase carboxylic acids are ubiquitous in ambient air
90                To fill this gap, we measured gas-phase carboxylic acids in real-time inside and outsi
91          This is well known in heterogeneous gas-phase catalysis but much less discussed for electroc
92 the basis of the empirical difference in the gas-phase CCS and a CCS-based resolving power definition
93 which involved the use of ethanol as a polar gas-phase chemical modifier.
94 high-NOx conditions was caused by changes in gas-phase chemistry that led to the formation of organon
95 sed in higher-scale models, which only treat gas-phase chemistry.
96 ion catalyst achieved using high-temperature gas-phase chlorine and hydrogen treatments.
97 th approximately 20% of its mass detected as gas-phase CO2, CO, and H2O.
98 somer identification by measurement of their gas phase collision cross sections (CCSs).
99 h ion assemblies that have undergone minimal gas-phase collisional "clean-up" to retain native-like s
100                    This is done thanks to a "gas-phase collisional purification" inside an ion trap m
101 f water, solar wind-surface interactions and gas-phase collisions.
102 tical standard free energies of formation in gas phase combined with quantum chemical estimates of He
103 these sensing materials for broad classes of gas-phase compounds such as condensable vapors and non-c
104                     An estimation of the OPE gas phase concentration and gross absorption fluxes by u
105 pace, has thus far only been observed at low gas phase concentrations or in inert gas matrices.
106 es but are also observed to have substantial gas-phase concentrations contrary to many models that tr
107 wing frequency response performed at varying gas-phase concentrations gives diffusion coefficients th
108                            This is the first gas-phase confirmation that the markedly elongated C-C b
109                                     Here the gas phase conformational space of drug and drug-like mol
110 play quite different physical properties and gas-phase conformations from lipids, which could lead to
111 llowing electrospray into kinetically stable gas-phase conformations).
112 n inert vaporization surface speeding up the gas-phase conversion of large molecules while lessening
113 etics steps and an activation energy for the gas-phase cycloaddition of two hexafluoropropene molecul
114 to assign each unfolded form observed in our gas-phase data set to the disruption of specific domains
115 vity over lyophilized enzyme powders for the gas-phase dehalogenation of 1-bromopropane.
116  supports the idea that interactions between gas-phase DEHP and soiled surfaces have been reduced to
117 nd Ag9 Pt3 clusters are size-selected in the gas phase, deposited on an ultrathin amorphous alumina s
118 a C horizontal lineC in FAs and a subsequent gas-phase detagging via tandem (neutral loss scan) mass
119 ize the significance of packing effects; the gas-phase dimer structure at the same level shows a 1.63
120 uridine-specific chemical derivatization and gas phase dissociation of RNA during liquid chromatograp
121 ric fragment ions, in turn shedding light on gas-phase dissociation mechanisms of glycosidic linkages
122    The complex mass spectra that result from gas-phase dissociation were assigned using a Bayesian de
123 ons generated by electrospray ionization and gas-phase dissociation.
124                            Here we show that gas phase DMS concentrations (DMSgas) increased by an or
125 significant influence over structures in the gas phase due to strong Coulombic and hydrogen-bonding i
126 mbient temperature in the gas phase but that gas-phase dynamics should be considered when interpretin
127    A nanowire bonding process referred to as gas-phase electrodeposition is reported to form nanobrid
128 ding single-crystal X-ray diffraction (XRD), gas-phase electron diffraction (GED), a combined GED/mic
129                      A historical challenge: Gas-phase electron diffraction and single-crystal X-ray
130                                          The gas-phase electron diffraction parameters are in good ag
131 Si(Ph,X) (X = F (3), Cl (4)) were studied by gas-phase electron diffraction, low-temperature NMR spec
132                                     IMS is a gas-phase electrophoretic technique that enables the sep
133 onsiderable uncertainty in how anthropogenic gas phase emissions alter the oxidative aging of organic
134 ors and the detailed chemical composition of gas phase emissions from a broad variety of cooking styl
135  organic aerosol production potential of the gas-phase emissions was determined by smog chamber aging
136                           The interaction of gas phase endohedral fullerene Ho3N@C80 with intense (0.
137 ology, medicine, nutrition, and in industry, gas phase enthalpies of formation of many long chain sat
138 ering and Raman spectroscopy in a controlled gas-phase environment.
139                      The fast release of the gas-phase extract gives rise to a high signal recorded b
140 d to liberate the sampled materials into the gas phase for atmospheric pressure chemical ionization a
141 es of approximately 95% were measured in the gas phase for oxygen evolution in alkaline media at an I
142 ovitamin A, vitamin E, and vitamin K1 in the gas phase for the first time.
143 entified 27 different reaction routes in the gas phase, forming a complex interlinked reaction networ
144 sine or cysteine residues, identification of gas-phase fragmentation patterns of endogenous dityrosin
145        The potential of copper(II) to induce gas-phase fragmentation reactions in macrotetrolides, a
146 anomeric configuration is retained following gas-phase glycosidic bond fragmentation during tandem ma
147                                In studies of gas-phase H atoms impinging on a CO-adsorbed Ni(110) sur
148 beyond the atomic limit of the corresponding gas-phase harmonics measured under similar conditions.
149 nic acid (HMSA) in particle formation in the gas phase has been extensively studied, the details of t
150 ry (bimolecular) polyatomic reactions in the gas-phase have occurred.
151  states of matter (for instance solid/liquid/gas phases) have different symmetries, the phase transit
152 ion has shown potential to contribute to the gas-phase HONO levels during the morning, which accounts
153  C, and these species are useful for various gas-phase hydrocarbon reactions, including the selective
154 terestingly, the particle formation from the gas-phase hydrogen-bonded complexes of HMSA with (R1)(R2
155 n proof-of-principle experiments, the use of gas-phase hydrogen/deuterium exchange (HDX) combined wit
156 ety of protonated carbohydrate structures by gas-phase hydrogen/deuterium exchange (HDX) to discover
157           Propylene oxide is detected in the gas phase in a cold, extended molecular shell around the
158 ulfinylnitrene CF3S(O)N was generated in the gas phase in its singlet ground state and was characteri
159 unds (ELVOCs) that have been detected in the gas phase in previous studies and linked to SOA particle
160 ides by analyzing the N-H stretching mode in gas phase infrared (IR) spectroscopy, and then observing
161            Other powerful techniques such as gas-phase infrared (IR) spectroscopy have been limited t
162 ture and purity of which were verified using gas-phase infrared spectroscopy coupled to mass spectrom
163  mobility spectrometry-mass spectrometry and gas-phase infrared spectroscopy.
164 ing, we illustrate the capacity of selective gas-phase interactions using neutral gas vapors to yield
165 how that the unfolding of the protein in the gas phase involves the disruption of inter-domain contac
166 s vapors to yield an additional dimension of gas-phase ion mobility separation.
167 ional selectivity provided by a postsampling gas-phase ion mobility separation.
168  report an approach for spatial and temporal gas-phase ion population manipulation, wherein we collap
169 pectroscopy coupled to mass spectrometry and gas-phase ion-mobility measurements.
170                                              Gas-phase ion/ion reactions of (13)C-TrEnDi-modified pho
171 zation (ESI) allows the production of intact gas-phase ions from proteins in solution.
172 V spectroscopy of cold ( approximately 10 K) gas-phase ions, we probe the inherent conformational pre
173 w-in contrast-several advantages compared to gas phase IRMS.
174 ructural characterization of proteins in the gas phase is becoming increasingly popular, highlighting
175  drug molecules and their metabolites in the gas phase is poorly understood.
176 rpentinization environments where a separate gas phase is present may be more favorable for abiotic s
177 n isolated and cold molecular complex in the gas-phase is a fundamental measure of the strength of th
178 using a multicollector magnetic sector field gas-phase isotope ratio mass spectrometer.
179  and (La0.8 Sr0.2 )0.95 MnO3+/-delta , using gas-phase isotope-exchange with a 1:1 (16) O2 :(18) O2 r
180  spectrometry provides ion separation in the gas phase mainly based on differing ion-neutral collisio
181                   Comparison of solution and gas phase measurements on a doubly tagged tripeptide sho
182           Despite the growing application of gas-phase measurements in structural biology and drug di
183  we use ab initio methods to investigate the gas-phase mechanisms governing the reactions of amines,
184 ferent dependence from the well-known one in gas-phase media is observed.
185 nd unique control of the emission, absent in gas-phase media.
186 xidative intramolecular electron transfer in gas-phase metal complexes.
187 are synthesized as films on substrates using gas-phase methods at high temperatures.
188                            This implies that gas-phase methods such as polarization gating for attose
189 ayers with respect to the composition of the gas-phase mixtures: a kinetic effect dominant during the
190 on of ultrafast 2D terahertz spectroscopy of gas-phase molecular rotors at room temperature.
191 o otherwise identical enantiomers of a large gas-phase molecule using resonant microwave fields are h
192 te combustion (associated with less oxidized gas-phase molecules) correlated to higher primary organi
193                                       In the gas phase, most of the so-called push-pull nitrogen base
194 n NMR data and help in the assignment of the gas-phase MW data to individual diastereomers.
195   Moreover, a strong correlation between the gas-phase NHC-CO2 bond distance and the Gibbs free energ
196                    Molecular interactions of gas-phase nonylphenols (NPs) with the surfaces of two co
197 e form of nanoparticles should be related to gas-phase nucleation procedure.
198 incorporated a substantial fraction (70%) of gas-phase O2 More oxygenated products were formed than t
199                             We evaluated how gas-phase O3 interacts with residual petroleum hydrocarb
200 etailed reaction mechanisms and kinetics for gas-phase O3, NO3, and OH when they impinge on organic s
201                              Purification in gas phase of PLA mixtures was established based on SY cu
202 of high harmonic generation in the solid and gas phases of argon and krypton.
203 s grow past it by direct condensation of the gas phase on their surface, driving liquid evaporation,
204                                       In the gas phase only three (3) and two (4) stable conformers d
205                                       In the gas phase, only 10% of the reactive trajectories undergo
206       This is one of the few basepairs whose gas-phase-optimized isolated geometry is inconsistent wi
207  been spectroscopically characterized in the gas phase or in matrices at very low temperatures.
208 o underestimates of both organic aerosol and gas-phase organic acids.
209          Exploring, exposing, and exploiting gas-phase organic chemistry at temperatures of 1000 degr
210  is formed from the atmospheric oxidation of gas-phase organic compounds leading to the formation of
211 ming an evaluation of a comprehensive set of gas-phase organic compounds present in gasoline motor ve
212                They emit complex mixtures of gas-phase organic compounds that vary in volatility and
213                              Partitioning of gas-phase organic compounds to the walls of Teflon envir
214 nic radicals have played a central role in a gas-phase organosynthesis.
215                                The selective gas-phase oxidation of disulfide bonds to their thiosulf
216 b) occur on similar time scales as analogous gas-phase oxidation reactions.
217 scopy to quantify SOx and NOx emissions from gas-phase oxy-combustion systems.
218 istry, the surface reaction of squalene with gas-phase ozone has been investigated.
219 ation of mainly secondary CI, in contrast to gas-phase ozonolysis mechanisms.
220 egee intermediates (CIs), mainly formed from gas-phase ozonolysis of alkenes, are considered as atmos
221 action products and kinetics differ from the gas-phase ozonolysis of alpha-terpineol.
222                                              Gas phase particle formation mechanisms and the effect o
223  have been shown to function as an effective gas-phase photocatalyst for the reduction of CO2 to CO v
224                            Ozonolysis of the gas phase photochemical products in the dark or under co
225 of forming methylcyanoacetylene and MeC5N by gas-phase photolysis was evaluated from relevant acetyle
226                                  A one-step, gas-phase photothermocatalytic process for the synthesis
227 erry juice was subjected to cold atmospheric gas phase plasma and changes in hydroxycinnamic acids, f
228 m of the study was to evaluate the effect of gas phase plasma on phenolic compounds in pomegranate ju
229 re is no statistical difference of regulated gas-phase pollutant emissions between PFIs and GDIs.
230 tyrene (BTEXS) because of their toxicity and gas-phase prevalence, where exposure is typically by inh
231  that self-quenching is a sensitive and fast gas-phase probe of biomolecular structure that can be di
232 um interfacial phenomena and the equilibrium gas phase processes, respectively.
233 ex in either the electrospray droplet or the gas phase produced c-type fragment ions.
234 O2, a mixture of CO and H2 was produced as a gas-phase product (syngas).
235     The relative molar ratio of the produced gas-phase product was controllable by the reduction temp
236                     We have investigated the gas-phase production of isoquinoline by performing colli
237 produces a very fast burst of low-volatility gas-phase products, which are competitively taken up by
238 rometry (DART-MS), and transmission FTIR for gas-phase products.
239 e strength of dispersive interactions in the gas phase properly, the importance of inter- and intramo
240 ltaneous detection of these molecules in the gas phase provides direct evidence for their gas-to-part
241 tionalisation with two different approaches, gas phase radical grafting and liquid phase reductive gr
242  polycyclic aromatic hydrocarbons (PAHs) via gas phase radical mediated aromatization reactions.
243  ion activation technology that exploits the gas-phase reaction between mass-selected ions and ozone
244 ry base) is known to drive the reaction, the gas-phase reaction follows the "mobile proton model" to
245 he complex [Ru(tpy)(bpy)(O2)](2+), formed by gas-phase reaction of [Ru(tpy)(bpy)](2+) with molecular
246 H2 )Si) isomers, was initially formed in the gas-phase reaction of ground-state atomic silicon (Si) w
247  for the very first time via the bimolecular gas-phase reaction of ground-state carbon atoms with 1,3
248                    The rate coefficients for gas-phase reaction of trifluoroacetic acid (TFA) with tw
249 phenols, cresols, and methoxyphenols by fast gas-phase reaction with hydroxyl radicals (HO(*)).
250                                              Gas phase reactions between PtHn (-) cluster anions and
251  of predictions derived from computations on gas-phase reactivity of carbocations.
252                           In this paper, the gas-phase reactivity of HFC-1447fz with OH radicals is p
253                                              Gas-phase reactivity of protonated model compounds with
254 the solution state or post-ionization in the gas phase, respectively.
255 tein oligomers ejected from nanodiscs in the gas phase retain large numbers of lipid interactions.
256 ty of defected indium oxide surfaces for the gas-phase reverse water gas shift reaction, CO2 + H2 + h
257                        Partitioning into the gas phase seems to be determined by an octanol-air parti
258         Ion mobility spectrometry (IMS) is a gas phase separation technique, which relies on differen
259  dissociation, we demonstrate rapid baseline gas-phase separation and identification of tails involvi
260                           With this combined gas-phase separation and subsequent fragmentation, we co
261                       Ion mobility (IM) is a gas-phase separation technique that is used to determine
262 ltrasound (US), undergo an ensuing liquid-to-gas phase shift and transiently deposit 20-30mum large b
263                                              Gas-phase single-conformation spectroscopy is used to st
264 rier were determined computationally for the gas-phase SN2 reaction between the acetaldehyde enolate
265 onversion of the dominant interaction in the gas phase (SO2)S...O(H2O) to the dominant interaction on
266 tives to be promising precursors for further gas-phase spectroscopic studies of phosphinidenes; in pa
267 the utility of this technique for analytical gas phase spectroscopy.
268 Cr(H2O)4Cl2](+), difficult to be observed by gas-phase spectroscopy, are detected easily with carbon
269                                    The known gas-phase spectrum, including its vibronic structure, is
270 ht mass spectrometer was used to examine the gas-phase structures of a set of glycopeptides resulting
271                        Their solid-state and gas-phase structures were studied using a multitechnique
272     These observations, however, are made on gas-phase structures.
273                          The solid-state and gas-phase studies of the icosahedral Sb@M12@Sb20(n-/n+)
274  study reports a modified hydrogen-assisted, gas-phase synthesis for facile, scalable production of s
275                Our approach provides a clean gas-phase synthesis of this hitherto elusive cyclic radi
276 ly on collision with a third molecule in the gas-phase systems of combustion and planetary atmosphere
277 es high-temperature thermal reactions in the gas phase that are generally difficult to achieve in sol
278              Both in the solid state and the gas phase the central C-C bond is of similar length for
279                            Compared with the gas phase, the enzyme lowers the Diels-Alder barrier sig
280 olecular oxygen under mild conditions in the gas phase, the process is either stoichiometric (and the
281                         When compared to the gas phase, the trans to cis isomerization of glyoxal at
282 adium, PtC3 and PdC3 , were generated in the gas phase through laser vaporization of a metal target i
283 ne cross-section at this wavelength based on gas phase titration (GPT) measurements.
284 ination with limited charge reduction in the gas phase to obtain meaningful information on noncovalen
285 gen bond dissociation free energy from 99.5 (gas phase) to an experimentally measured value of 45.8 k
286 sities, heliotropic COD growth, solid-liquid-gas phase transformations, strong longitudinal phonon co
287  opposed to the distinct transitions through gas-phase unfolding intermediates observed of K6-, K11-,
288 have elucidated the reaction pathways in the gas phase using tandem mass spectrometry.
289 inker that can be selectively cleaved in the gas phase using two differential tandem mass-spectrometr
290  cm(-1) red-shifted with respect to unbiased gas-phase values.
291      The stability of the XB capsules in the gas phase was confirmed by electrospray ionization mass
292 vidin, transthyretin, and hemoglobin) in the gas phase was undertaken by 193 nm ultraviolet photodiss
293  zwitterionic pairs are rarely stable in the gas phase, we now demonstrate that charge-separated stat
294 methyl-benzene (m-C8H8I2) produces m-C8H8 in gas phase; we used photoelectron spectroscopy to probe t
295 hich are highly reactive with O((3)P) in the gas phase, were not previously investigated.
296 eby increasing the intrinsic basicity in the gas phase, while the bulk prevents efficient cation solv
297 es and dynamics of these biomolecules in the gas phase with beta-carotene as a particularly interesti
298 ore compact molecules were discovered in the gas phase with thus far unknown structures.
299 N, SCN, BO) trianions is demonstrated in the gas phase, with BeB11 (CN)12(3-) exhibiting colossal sta
300 ions of nanoscale vent holes on each chip by gas-phase Xenon difluoride etching.

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