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1 ative and positive ion mode laser/desorption ionization.
2 negative ionization modes using electrospray ionization.
3 s spectrometry (MS) assay using electrospray ionization.
4 pectrometry by atmospheric pressure chemical ionization.
5 ased on capillary vibrating sharp-edge spray ionization.
6 at fluorine gauche effects are a function of ionization.
7 metry signal suppression during electrospray ionization.
8 by the mass spectrometer after electrospray ionization.
9 into the mass spectrometer via electrospray ionization.
10 na will be unambiguously observable via high-ionization absorption lines in the ultraviolet spectra o
13 r two of the three sealants, indicating that ionization and hydrophilicity control partitioning betwe
14 negative and positive ion mode electrospray ionization and negative and positive ion mode laser/deso
15 near processes including Kerr self-focusing, ionization and plasma defocusing, and dynamic spatial re
16 abel-free MS methods, including electrospray ionization and solid state MALDI, as well as MS methods
17 ults strongly point towards the target field ionization and the outward expanding hot electron curren
18 the nucleophilic olefin facilitates chloride ionization and thereby circumvents simple elimination pa
19 of the valence hole created by strong-field ionization and to track the primary proton transfer reac
20 ic pressure matrix-assisted laser desorption/ionization (AP-MALDI) setup for high-throughput large-sc
22 the contained atmospheric pressure chemical ionization (APCI) source that enabled nonthermal, nonequ
25 hing between DESI, voltage-free EASI, or LTP ionization as well as to freely move the interface over
28 ISD MS data is complementary to electrospray ionization-based MS/MS sequencing readouts, providing kn
30 In this study, we comprehensively assess the ionization behavior of nanoporous polyamide selective la
38 direct complex mixture analysis via ambient ionization, chemical imaging and profiling, and systems
39 ore of trace gas analyses in modern chemical ionization (CI) mass spectrometer instruments, which are
40 we show that GC methods coupled to chemical ionization (CI) MS have a clear advantage over alternati
41 rs all the wavelengths of light required for ionization, cooling, coherent operations and quantum sta
42 urthermore, we report that interior carboxyl ionization could improve the water-salt permselectivity
43 lly resolved by low-fluence laser desorption ionization, coupled with high-resolution mass spectromet
45 ionization (MALDI), desorption electrospray ionization (DESI) and secondary ion mass spectrometry (S
46 HT platform based on desorption electrospray ionization (DESI) MS for the label-free study of enzymat
47 is method for online desorption electrospray ionization (DESI) MS imaging of FA isomers from human ti
48 maging capability in desorption electrospray ionization (DESI) MSI, which enables cell-type-specific
54 hromatography using a dual column/dual flame ionization detector (HS-GC-FID/FID), a technique routine
56 ct inlet probe-atmospheric pressure chemical ionization (DIP-APCI) analyses were performed on the sam
57 Ss were obtained using a native electrospray ionization drift tube ion mobility-Orbitrap mass spectro
58 zation capability of extractive electrospray ionization (EESI) and the ultrahigh mass resolution of O
59 the aid of in silico predicted electrospray ionization efficiencies and this allows direct compariso
63 e to matrix effects caused by changes in the ionization efficiency of an analyte, ion suppression, or
64 low abundance of native sulfoproteins, poor ionization efficiency of sulfopeptides in the positive m
65 s, early eluting peaks, ion suppression, low ionization efficiency), and issues related to software (
66 eV) and calculated (CCSD(T)/pVQZ) adiabatic ionization energies are the same; (2) the origin band ro
67 ctivity was switched to p-type with acceptor ionization energy of 42 meV by altering hydrogen incorpo
68 hotoluminescence spectroscopy revealed an Mg ionization energy of about 100 meV, which agrees quite w
69 late with stronger responses in electrospray ionization (ESI(-)) and longer retention times on a C18
72 sorption ionization (MALDI) and electrospray ionization (ESI) for both spatial imaging and solution-b
74 solution mass spectrometry with electrospray ionization (ESI) in negative mode for the comprehensive
80 ty of variable-temperature (vT) electrospray ionization (ESI) paired with ion mobility spectrometry (
81 he nonlinear signal response of electrospray ionization (ESI) presents a critical limitation for mass
82 ly process, we have used native electrospray ionization (ESI) together with ion mobility mass spectro
84 ree different ionization modes (electrospray ionization (ESI)(+), ESI(-), and atmospheric pressure ph
85 hen metabolites are analyzed by electrospray ionization (ESI)-mass spectrometry, they are usually det
87 cle tissue were conducted using electrospray ionization (ESI)-MS/MS in a triple quadrupole mass spect
90 lline order as damage progresses, but not if ionization events are spatially non-uniform due to under
91 n of fiber-based laser ablation electrospray ionization (f-LAESI) with 21 T Fourier transform ion cyc
92 ons (DIs) generated in positive electrospray ionization for 57 amino acid standard compounds using ca
94 ted in equilibration among up to 16 distinct ionization forms, including uncharged forms capable of d
96 ted the relativistic radial expansion of the ionization front, whose speed was determined to be 0.77c
99 zation sources, that is, heated electrospray ionization (HESI) and nano-ESI for the analysis of atmos
101 composition are subjected to either thermal/ionization-induced artifacts or limited mass resolving p
102 Q-TOF equipped with ETD and an electrospray ionization interface consisting of a glass transfer capi
105 g method based on vibrating sharp-edge spray ionization is presented in this work to overcome the cha
107 ared (IR) laser ablation-remote-electrospray ionization (LARESI) platform coupled to a tandem mass sp
108 r laser-desorption flexible microtube plasma ionization (LD-FmuTPi) setup, without sample manipulatio
110 rms such as matrix-assisted laser desorption ionization (MALDI) and electrospray ionization (ESI) for
111 of this is matrix-assisted laser desorption/ionization (MALDI) combined with in-source decay (ISD) f
112 ry imaging: Matrix Assisted Laser Desorption Ionization (MALDI) Imaging and Laser Ablation - Inductiv
114 gated using matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry (IMS) combi
116 surfaces by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) requi
117 ifunctional matrix-assisted laser desorption/ionization (MALDI) matrix for spatially resolved lipidom
119 tissue via matrix-assisted laser desorption/ionization (MALDI) with 1,4-phenylenedipropionic acid (P
120 chniques is matrix-assisted laser desorption/ionization (MALDI), combined with in-source decay (ISD)
121 s including matrix-assisted laser desorption ionization (MALDI), desorption electrospray ionization (
122 ysis (FIA), matrix assisted laser desorption ionization (MALDI), including MALDI-MS imaging and ion m
123 itional experiments revealed that laser post-ionization (MALDI-2) has great potential to overwrite ch
124 for GSLs for catch-and-release-electrospray ionization mass spectrometry (CaR-ESI-MS)-based screenin
125 ion of a customized F-TD inlet with chemical ionization mass spectrometry (CIMS) and ultraperformance
126 E, a versatile and quantitative electrospray ionization mass spectrometry (ESI-MS) assay for measurin
128 be capillary microsampling with electrospray ionization mass spectrometry (ESI-MS) for the in vivo an
129 electrophoresis (CE) coupled to electrospray ionization mass spectrometry (ESI-MS) is implemented to
131 ein, we describe the potency of electrospray ionization mass spectrometry (ESI-MS) to study molecular
132 ry (AEMS) setup for contactless electrospray ionization mass spectrometry (ESI-MS)-based sample injec
136 HiTES) with matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for the rapid id
138 to a detector (atmospheric pressure chemical ionization mass spectrometry (MS) or gas chromatography
139 same enriched pellets by nanoscale secondary ionization mass spectrometry (NanoSIMS), which reveals a
140 e coupled Raman spectroscopy and paper spray ionization mass spectrometry (PSI-MS) on a single instru
141 rmined the capacity of the rapid evaporative ionization mass spectrometry (REIMS), also known as inte
143 lts at neutral pH combined with electrospray-ionization mass spectrometry (SEC-ESI-MS) is a useful to
144 hroughput compared to an established thermal ionization mass spectrometry (TIMS) double-spike method
146 Liquid chromatography/negative electrospray ionization mass spectrometry [LC/(-)ESI-MS] is routinely
147 the deep-UV spectral region and electrospray ionization mass spectrometry after the first and second
148 application of a novel UV fs Laser Ablation Ionization Mass Spectrometry approach for chemical depth
149 ncements in matrix-assisted laser desorption/ionization mass spectrometry have enabled the high-throu
151 of refined matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI MSI) technol
153 oupled with matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) was dev
155 re obtained with ultraviolet (UV) desorption/ionization mass spectrometry imaging (UV-LDI-MSI) using
157 olution, month-long measurements by chemical ionization mass spectrometry in a previously unoccupied
158 peptides by matrix-assisted laser desorption ionization mass spectrometry of decalcified, formalin-fi
160 d consistent enhancement in the electrospray ionization mass spectrometry signal (ESI-MS) was observe
162 ed ferric particle-assisted laser desorption/ionization mass spectrometry within 1 s using only 50 nL
163 of EC-ESI/MS (Electrochemistry/ElectroSpray Ionization Mass Spectrometry) in the presence of (18)O(2
164 hydrogen evolution experiments, electrospray ionization mass spectrometry, nuclear magnetic resonance
167 , a compact and lightweight laser desorption ionization - mass spectrometer designed and developed fo
170 chromatography-atmospheric pressure chemical ionization-mass spectrometry (GC-APCI-MS) increases the
171 sis, we utilized laser ablation electrospray ionization-mass spectrometry (LAESI-MS) for in situ meta
173 e demonstrated that by utilizing paper spray ionization-mass spectrometry (PSI-MS) coupled with field
174 ecent development of desorption electrospray ionization-mass spectrometry imaging (DESI-MSI) facilita
175 filing with matrix-assisted laser desorption/ionization-mass spectrometry imaging to investigate accu
177 molecules follow a charged residue model of ionization mechanism, and at high flow rates-due to stru
179 ionization has been used as a fast sampling/ionization method for the direct mass spectrometric anal
180 cial attention is given to the soft chemical ionization method known as selected ion flow tube-mass s
181 trate a novel atmospheric-pressure elemental ionization method where fluorinated compounds separated
186 hree-way arrays have been generated for each ionization mode considering three dimensions: DBE relate
189 bovine tissue in both negative and positive ionization mode in one single run using a single CBS dev
191 standards were used for correction, one per ionization mode, excellent accuracy and precision were a
193 onsidering six replicates in three different ionization modes (electrospray ionization (ESI)(+), ESI(
194 light simultaneously the impact of the three ionization modes in order to explain the differences bet
198 ultracentrifugation, and native electrospray ionization MS, we show that LC8 forms a predominantly in
199 peptide arrays and nanoflow LC-electrospray ionization/MS of Nav1.6 reveal potential sites of CaMKII
201 lopment of nanospray desorption electrospray ionization (nano-DESI) has enabled the robust imaging of
202 nized by interaction with a nanoelectrospray ionization (nano-ESI) plume of sodium-containing aqueous
203 ple extracts analyzed using nanoelectrospray ionization (nano-ESI) show less adduct formation; howeve
204 tion of an excited atom or molecule leads to ionization of a neighboring one via Coulombic electron i
210 bmicrometer capillaries for nanoelectrospray ionization of native proteins and protein complexes effe
211 tory, lead to rapid vaporization/atomization/ionization of particles with minimized atom/ion cloud di
212 e that the mechanism proposed previously for ionization of saturated hydrocarbons upon APCI, hydride
215 ground-state complex shows substrate-induced ionization of the nucleophilic l-Tyr37, now H-bonded to
216 this complex mixture prevents the efficient ionization of the organic material by a single ionizatio
217 device for the sensitive and nonfragmenting ionization of volatile organic biomarkers relevant for c
222 ated oligomeric segment has its own discrete ionization potential, electron affinity, and optical ban
225 photoelectron mediated secondary collisional ionization processes upon the absorption of the incident
227 rly account for the temporal distribution of ionization products resulting from dilute contamination
229 stone H4 by matrix-assisted laser desorption/ionization-Q-MSI (MALDI-Q-MSI), using a mixture of three
230 y coupled to a unit-mass-resolution electron ionization quadrupole mass spectrometer (GC/EI-MS), a st
231 rformance liquid chromatography electrospray ionization quadrupole-Orbitrap (UHPLC/ESI Q-Orbitrap) ma
232 ispersion (DVUA-MSPD) and UHPLC-electrospray ionization (+)-quadrupole time-of-flight mass spectromet
233 ating a second field-free region between the ionization region and the drift region, shielding of the
235 ocation and spray stability in PS-MS and the ionization region humidity and analyte evaporation rate
236 egion and the drift region, shielding of the ionization region is significantly improved, even when u
237 e droplets are subsequently ejected into the ionization region of an ambient pressure inlet mass spec
238 ough a 2 + 1 resonantly-enhanced multiphoton ionization (REMPI) scheme targeting molecular oxygen (la
242 laser pulse efficiently creates initial gas ionization (seed electrons) through a 2 + 1 resonantly-e
243 on the application of a novel electric field-ionization setup for high-resolution laser spectroscopy
245 The versatility and ease of use of this ionization source is demonstrated using beta-blockers, p
246 d by analysis with a commercial electrospray ionization source that produces larger (~60 um) droplets
247 ressure glow discharge (LS-APGD) microplasma ionization source with an Orbitrap mass spectrometer to
248 nization of the organic material by a single ionization source, so the presence of uncharacterized ma
250 microtube plasma (FmuTP) was selected as the ionization source, this being the first time that laser
254 ry imaging (MSI), where the use of different ionization sources allows detection of different classes
258 setup was tested at the Collinear Resonance Ionization Spectroscopy experiment at ISOLDE-CERN to per
262 ed-phase LC columns and the resulting severe ionization suppression from coeluting matrix components.
264 glycerophospholipids via direct electrospray ionization tandem mass spectrometry (ESI-MS/MS) provides
266 lex biological samples prior to electrospray ionization-tandem mass spectrometry (ESI-MS/MS) at a rat
267 on efficiency and the fact that CI is a soft ionization technique that yields identifiable protonated
271 rovide enhanced fundamental understanding of ionization that could enable novel membrane design.
272 xidation by matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF M
273 pplied surface-enhanced laser desorption and ionization time of flight mass spectrometry technology t
274 hesized for matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry
276 oupled with matrix-assisted laser desorption/ionization time-of-flight mass spectrometer analyses.
277 termined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF M
278 s work, the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF M
279 conidia by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF M
280 nless-steel matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF M
281 , including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-M
282 dynamics by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analyses following
283 S-PAGE) and matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry.
284 ch included matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF M
285 ds included matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF M
286 A-FISH) and matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF M
287 entified by matrix-assisted laser desorption/ionization-time of flight mass spectrometry, antimicrobi
288 e propose a novel approach based on chemical ionization-time-of-flight (CI-TOF) mass spectrometry emp
289 using capillary electrophoresis-electrospray ionization-time-of-flight mass spectrometry (CE-ESI-TOF-
290 s diseases, matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF M
293 ionized using negative ion mode electrospray ionization, transferred into a linear quadrupole ion tra
294 ed using a variable temperature electrospray ionization (vt-ESI) technique in combination with ion mo
295 , precision, and kinetics of atomization and ionization were investigated with optical spectrometry.
296 dily reach their threshold energy for impact ionization while the holes experience the multiple valen
297 e neutral octamer (measured after its gentle ionization), while the smaller serine clusters are achir
298 CC extract was characterized by electrospray ionization with high-resolution time-of-flight mass spec
299 ion source to atmospheric-pressure chemical ionization with the exact same chromatographic method al