about
Estimation of the proton affinity values of fifteen matrix-assisted laser desorption/ionization matrices under electrospray ionization conditions using the kinetic method.4-Chloro-alpha-cyanocinnamic acid is an advanced, rationally designed MALDI matrix.Alternative CHCA-based matrices for the analysis of low molecular weight compounds by UV-MALDI-tandem mass spectrometry.Collision cell pressure effect on CID spectra pattern using triple quadrupole instruments: a RRKM modeling.Selective detection of specific protein-ligand complexes by electrosonic spray-precursor ion scan tandem mass spectrometry.The applicability of the kinetic method for measuring relative affinities of macromolecules for polyatomic substrates.On-line chiral analysis using the kinetic method.Gas-Phase Studies of Formamidopyrimidine Glycosylase (Fpg) Substrates.Acid-catalyzed carboxylic acid esterification and ester hydrolysis mechanism: acylium ion as a sharing active intermediate via a spontaneous trimolecular reaction based on density functional theory calculation and supported by electrospray ionizatioRecognition and quantification of binary and ternary mixtures of isomeric peptides by the kinetic method: metal ion and ligand effects on the dissociation of metal-bound complexes.Ion-molecule reactions as probes of gas-phase structures of peptides and proteins.Isomeric discrimination and quantification of thyroid hormones, T3 and rT3, by the single ratio kinetic method using electrospray ionization mass spectrometry.Stereochemical effects during [M-H]- dissociations of epimeric 11-OH-17beta-estradiols and distant electronic effects of substituents at C(11) position on gas phase acidity.Interaction of the cesium cation with mono-, di-, and tricarboxylic acids in the gas phase. A Cs+ affinity scale for cesium carboxylates ion pairs.Estimation of proton affinity of proline and tryptophan under electrospray ionization conditions using the extended kinetic method.Primary and secondary kinetic isotope effects in proton (H(+)/D(+)) and chloronium ion ((35)Cl(+)/(37)Cl(+)) affinities.Electrospray ionization mass spectrometric investigation of ammonium ion complexes with anomeric 2,3-O-isopropylidene-1alpha- and -1beta-D-ribofuranosyl azides: anomeric and kinetic isotope effects in ammonium affinities.The proton affinity of proline analogs using the kinetic method with full entropy analysis.The unusually high proton affinity of aza-18-crown-6 ether: implications for the molecular recognition of lysine in peptides by lariat crown ethers.Proton bound homodimers and heterodimers of amides and amines in the gas phase. Equilibrium studies by Fourier transform ion cyclotron resonance spectrometry.Effects of internal hydrogen bonds between amide groups: protonation of alicyclic diamides.The kinetic method as a structural diagnostic tool: ionized alpha-diketones as loosely one-electron bonded diacylium ion dimers.Isomeric discrimination of arginine-containing dipeptides using electrospray ionization-ion trap mass spectrometry and the kinetic method.Proton affinity of beta-oxalylaminoalanine (BOAA): incorporation of direct entropy correction into the single-reference kinetic method.A reevaluation of computed proton affinities for the common alpha-amino acids.A comprehensive evaluation of the kinetic method applied in the determination of the proton affinity of the nucleic acid molecules.Electronic effects of 11β substituted 17β-estradiol derivatives and instrumental effects on the relative gas phase acidity.Vitamin C: an experimental and theoretical study on the gas-phase structure and ion energetics of protonated ascorbic acid.Stereoselective discrimination and quantification of arginine and N-blocked arginine enantiomers by formation and dissociation of calcium-mediated diastereomeric trimer complexes with a chiral reference compound using electrospray ionization-ion traCritical evaluation of kinetic method measurements: possible origins of nonlinear effects.Experimental versus Calculated Proton Affinities for Aromatic Carboxylic Acid Anions and Related Phenide Ions.Solution and gas-phase acidities of all-trans (all-E) retinoic acid: an experimental and computational study.Kinetic energy release of protonated methanol clusters using the low-temperature fast-atom bombardment: experiment and theory combined.Mononucleotide gas-phase proton affinities as determined by the kinetic method.Polar [4+2(+)] diels-alder cycloaddition to nitrilium and immonium ions in the gas phase: Applications of multiple stage mass spectrometry in a pentaquadrupole instrument.A comparison of the gas phase acidities of phospholipid headgroups: Experimental and computational studiesRelative silver(I) ion binding energies of α-amino acids: A determination by means of the kinetic method
P2860
Q30758341-F617FB8B-68D7-4E27-B958-4B5E67669C59Q33362852-268DFDDD-0F7B-4004-A604-5A5BFF3A3453Q33801272-5E86D5D9-B208-4B13-800A-6F745442B74BQ34573360-CB4D0BEE-C2DB-4986-85F5-A2E8ED49EBEBQ34870263-BC8748D7-D805-415E-8A42-CB0741E32A1CQ38014036-3E7E7A3C-4ED0-47E8-A34A-6400747C5AD7Q39918886-6530BEC0-A8E2-49DB-8BCC-4C4B349C41B5Q39984643-E667BCBA-4E33-4035-A834-6CB0B5DD01A3Q40456522-1367FB2B-0618-4059-A2F1-9A99ED02625DQ40605224-08CF0327-259B-49DB-9DDE-ADA8023DB724Q41671174-865BC566-9512-4276-B7B1-9B47DBCECD5EQ43255814-1DF2B0D4-3FEA-473F-B303-5C7A37F9F0F4Q43264248-4B2E68C6-0EEA-41AF-9DEC-56E69C9D0792Q43292909-36D3B09D-B652-447E-9C7A-83FA3BC1E390Q43635721-9C9B4C33-29FB-4D5F-8A2C-B45561F96A21Q43826027-F7C3596C-0340-417F-AC89-3EEE17FA530BQ43831378-8449AB41-E4FF-4E9E-B91E-0602BC72BC8AQ43845290-7D88E953-032F-400E-9F1E-D10A77CB6154Q43999669-F22D82D6-5524-43C6-BF72-4BF4CDCE67A4Q44223335-D6EF31B5-ED0F-418D-AFFD-F21DEE71797FQ44441976-24D03651-248C-473F-B5D2-0ADA16CC61E3Q44562314-3EE45344-5771-4D03-BF7D-F77D351FD105Q44897218-29249C89-A97D-4A50-AF9B-D3D54628A9B2Q44910903-D5F47F08-CDE9-437D-AC2F-660E1441FE17Q44949836-9BAEC20A-F6F2-4D6D-A206-E9A19027A151Q44964029-8BDCA765-8584-4297-AB19-780547EC4A83Q45388940-BDD141AD-FD27-4300-8FF1-86A653665BFEQ46492911-5826E6FD-FF3A-4F1E-896D-39ED12B3A7D2Q46501897-6EB33836-9B93-432F-8E26-C426202C0BA5Q46646813-806D865C-4E85-4C77-97ED-F4AE27D0B357Q48270098-9D21BC60-A8C3-4067-B72C-79F4747C4C93Q51842915-4CE1F6A9-93FA-4162-9C49-8B5F7F550E97Q51998907-40A443B0-DE8C-45E1-9153-0B41344C2290Q52083034-C791088D-3409-4B26-8BA9-79299011FED5Q54015569-15546675-1249-4470-847F-F415E5EFCC69Q57360998-0448780B-5087-49EC-A23F-A221387F06D2Q59165854-606D1FEE-DF5D-43A6-B1E9-879886654218
P2860
description
1977 nî lūn-bûn
@nan
1977 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1977 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
name
Intrinsic basicity determination using metastable ions
@ast
Intrinsic basicity determination using metastable ions
@en
type
label
Intrinsic basicity determination using metastable ions
@ast
Intrinsic basicity determination using metastable ions
@en
prefLabel
Intrinsic basicity determination using metastable ions
@ast
Intrinsic basicity determination using metastable ions
@en
P356
P1476
Intrinsic basicity determination using metastable ions
@en
P2093
R. G. Cooks
T. L. Kruger
P304
P356
10.1021/JA00446A059
P407
P577
1977-02-01T00:00:00Z