Dielectric barrier discharge ionization in characterization of organic compounds separated on thin-layer chromatography plates.Flowing atmospheric pressure afterglow combined with laser ablation for direct analysis of compounds separated by thin-layer chromatographyMagnetic scavengers as carriers of analytes for flowing atmospheric pressure afterglow mass spectrometry (FAPA-MS).FAPA mass spectrometry of designer drugs.Molecularly imprinted polymers as selective adsorbents for ambient plasma mass spectrometry.Laser desorption/ionization mass spectrometric analysis of surfactants on functionalized carbon nanotubes.Immobilization of Zidovudine Derivatives on the SBA-15 Mesoporous Silica and Evaluation of Their Cytotoxic Activity.SBA-15 Mesoporous Silica Modified with Gallic Acid and Evaluation of Its Cytotoxic Activity.Effect of Solvent Variations in the Alcothermal Synthesis of Template-Free Mesoporous Titania for Dye-Sensitized Solar Cells Applications.Physico-chemical characterization of formulations containing endomorphin-2 derivatives.Determination of conditional stability constants for phytic acid complexes with Mg2+, Ca2+ and Zn2+ ions using electrospray ionization mass spectrometry.Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies.Halloysite nanotubes as carriers of vancomycin in alginate-based wound dressing.Determination of Hexapeptide ALA-ASP-LEU-LYS-PRO-THR by MALDI MS.Unexpected formation of complexes between protonated organic ligand and neutral salt molecule studied by electrospray ionization mass spectrometry.Self-assembly of quaterpyridine ligands and Cu+ cation into helical complexes of 2:2 stoichiometry under electrospray ionisation conditions.A study of the possible and preferred site of protonation in 7-methyl-1,5,7-triazabicyclo[4,4,0]dec-5-ene by vibrational spectroscopic methods.7Li-NMR and FTIR studies of lithium, potassium, rubidium, and cesium complexes with ionophore lasalocid in solution.Multinuclear NMR and FTIR studies of new polyoxaalkyl esters of lasalocid and their complexes with lithium and sodium cations.Reaction of some strong N-bases with chloropentafluorobenzene in the presence of water molecules.Schiff base of gossypol with 3,6,9-trioxa-decylamine complexes with monovalent cations studied by mass spectrometry, (1)H-NMR, FTIR, and PM5 semiempirical methods.Influence of mobile phase composition on the high-performance liquid chromatographic/electrospray ionization mass spectrometric analysis of 11-nor-9-carboxy-delta9-tetrahydrocannabinol (THC-COOH) and its glucuronide in urine.Loss of isocyanic acid from the internal oxadiazole ring of protonated molecules of some 2,5-diaryl-1,3,4-oxadiazoles.Influence of fluorine substituents on the NMR properties of phenylboronic acids.Antifungal activity of alkyl and heterocyclic aza-derivatives of gossypol as well as their complexes with NaClO4 against Fusarium oxysporum f. sp. lupini.Electrospray ionization mass spectrometric study of purine base-cisplatin complexes.Mass spectrometric decompositions of cationized beta-cyclodextrin.The tetrapeptide N-acetyl-Pro-Pro-Tyr-Leu in skin care formulations-Physicochemical and release studies.Will the use of double barrier result in sustained release of vancomycin? Optimization of parameters for preparation of a new antibacterial alginate-based modern dressing.Complexes between some lysine-containing peptides and crown ethers--electrospray ionization mass spectrometric study.Valuable natural products from marine and freshwater macroalgae obtained from supercritical fluid extracts.Synthesis of G0 aminopolyol and aminosugar dendrimers, controlled by NMR and MALDI TOF mass spectrometry.Molecular Structures and Stability Constants of Gossypol and Its Aza-Derivative Complexes with Silver(I) Cations Studied by Potentiometric, ESI MS, NMR, and AM1d Semiempirical MethodsFluorescence properties of riboflavin-functionalized mesoporous silica SBA-15 and riboflavin solutions in presence of different metal and organic cationsDouble barrier as an effective method for slower delivery rate of ibuprofenElectro-oxidation of diclofenac in methanol as studied by high-performance liquid chromatography/electrospray ionization mass spectrometryUnexpected formation of [M]2+ from [M+CuCl+H]2+ ions under CID conditions, where M is a molecule of 3,5-bis(2,2’-bipyridin-4-ylethynyl)benzoic acid or its methyl esterThe influence of fluorine position on the properties of fluorobenzoxaborolesFormation of the [M+Cu+4Cl]+ion under laser desorption ionization conditions as a result of Cl addition to a C≡C bond (M - methyl or ethyl ester of 3,5-bis(2,2'-bipyridin-4-ylethynyl)benzoic acid)The diffusion NMR studies of crown ethers-cyclodextrin complexation process
P50
Q28542667-39774163-002E-4EA2-8D54-796AAAC86A10Q30393481-687FC908-9CF0-43AC-813C-F5C4F2A73923Q33465723-B0FBA939-3C6C-4153-94E1-E6BBA425377BQ33466786-3D5917F9-1A2C-4735-845E-6B71EF368D57Q33470100-18EED4A3-14FB-403D-9395-3F14AC83CE75Q34511994-2E9D0EB5-CC59-4C2B-BB45-6AEFD08819BCQ35571174-E8992EF8-0BB8-45CC-A1D8-AD3BB7045E48Q35685323-91F832F3-997C-4AC1-AF8D-06E7F758C341Q36163977-834A805F-A055-4F57-AAF2-527795CA0BF8Q38656037-BB96E967-7FBF-4533-8F47-FFCD11D8084CQ39156899-44C1210C-F9C3-496A-85EF-BC6ED6EE944AQ41266062-FC12A56C-3A49-4C5A-91C8-56313A03842FQ41690420-70C2E522-9AB7-4F61-AB4C-F3F37E0512B9Q41979070-C93BC39E-04A7-496A-82B3-74462FA93CD5Q42918944-BB5A6C18-6828-4ED4-A686-79B2D30FE32EQ43197247-881A76F8-FB2E-4A3A-A655-84500D2BAD6AQ43573639-5A144FC8-FDA5-45A9-AD31-291CB6BBA0FBQ43601262-E861AEC5-67E3-43FF-9933-7A99EB726882Q44124026-E122552C-800A-492B-B94C-58E54BAEEBF1Q44399303-AA20C6E6-BB1B-4351-A8D2-527A70E8C2F5Q44781074-5FF7E899-39D1-4F74-92AA-0477683FCF28Q44855386-DA362349-E43B-4C02-83C8-E85089A24CC0Q45714627-8126B7FE-EBF1-45CA-B989-BF954DDF3C95Q45973906-F2D719E1-5177-4618-B01D-476FE5151566Q46098950-1674A258-4A7A-4AD7-920B-F64F18359619Q46368880-1743D398-614B-46AE-A1C9-2F3470F411F1Q46476493-6E7A869A-C89C-4419-9AE2-B7F1CD02C7E0Q50880917-8A44F9E7-BE14-4984-9973-D21AA538A44CQ51656928-49BD64CB-0034-4577-9692-17A17B346661Q54095008-E844C1CA-B670-4C23-B47C-5096B630E7A8Q55175733-02822B77-769B-4BD0-984D-4BE060AF816AQ55210306-A9E4ED45-46E8-44E7-95CE-A1BC113B4DA1Q57587312-8A2A1F43-F19C-45F5-AA2D-9CD49D784677Q57727744-46183F18-0F04-46C3-8EA2-E45853DCC79AQ59191890-73D83BAB-9B32-4A54-95B7-1DFA969D0550Q60547560-B132EA75-3FDB-40A0-BDE3-B94BC0FEFAE6Q60547569-B9892C28-D40B-4817-A760-962E6A0EF5ABQ60547570-DF3CBE30-5955-4526-B8FE-653EA9C7CB69Q60547572-4470072F-35B2-48B2-A2BF-A253EDCF6313Q60547603-57EB9048-F3A8-4ED1-94DE-D7A11F8BD3F3
P50
description
polski chemik
@pl
researcher
@en
ricercatore
@it
scheikundige
@nl
հետազոտող
@hy
name
Grzegorz Schroeder
@ast
Grzegorz Schroeder
@en
Grzegorz Schroeder
@es
Grzegorz Schroeder
@nl
Grzegorz Schroeder
@pl
Grzegorz Schroeder
@sl
type
label
Grzegorz Schroeder
@ast
Grzegorz Schroeder
@en
Grzegorz Schroeder
@es
Grzegorz Schroeder
@nl
Grzegorz Schroeder
@pl
Grzegorz Schroeder
@sl
altLabel
Grzegorz Marek Schroeder
@pl
prefLabel
Grzegorz Schroeder
@ast
Grzegorz Schroeder
@en
Grzegorz Schroeder
@es
Grzegorz Schroeder
@nl
Grzegorz Schroeder
@pl
Grzegorz Schroeder
@sl
P214
P244
P106
P1153
7102298304
P1207
P21
P213
0000 0000 7145 318X
P214
P244
P27
P31
P3124
P496
0000-0002-6626-9542
P569
1950-01-01T00:00:00Z
P691
mzk2003200013
P734
P7859
lccn-n88221428