about
Pyromellitic acid-sarcosine (1/2)A new polymorph of 5-nitro-uracil monohydrate.N,N',N''-Triphenyl-guanidinium 5-nitro-2,4-dioxo-1,2,3,4-tetra-hydro-pyrimidin-1-ide.Elucidating the Structure of Chiral Molecules by using Amplified Vibrational Circular Dichroism: From Theory to Experimental Realization.Interplay of Exciton Coupling and Large-Amplitude Motions in the Vibrational Circular Dichroism Spectrum of Dehydroquinidine.Chiral Analysis Using Broadband Rotational Spectroscopy.Direct Time-Domain Observation of Conformational Relaxation in Gas-Phase Cold Collisions.Flexibility unleashed in acyclic monoterpenes: conformational space of citronellal revealed by broadband rotational spectroscopy.Characterization of Porphyrin-Co(III)-'Nitrene Radical' Species Relevant in Catalytic Nitrene Transfer Reactions.Cold Snapshot of a Molecular Rotary Motor Captured by High-Resolution Rotational Spectroscopy.An optically transparent thin-layer electrochemical cell for the study of vibrational circular dichroism of chiral redox-active molecules.Elucidating the backbone conformation of photoswitchable foldamers using vibrational circular dichroism.On the structural intricacies of a metabolic precursor: Direct spectroscopic detection of water-induced conformational reshaping of mevalonolactone.Coherent Enantiomer-Selective Population Enrichment Using Tailored Microwave Fields.On the Performance of Hybrid Functionals for Non-linear Optical Properties and Electronic Excitations in Chiral Molecular Crystals: The Case of Butterfly-Shaped Dicinnamalacetone.Sensing Chirality with Rotational Spectroscopy.The structure of salt bridges between Arg(+) and Glu(-) in peptides investigated with 2D-IR spectroscopy: Evidence for two distinct hydrogen-bond geometries.Switchable amplification of vibrational circular dichroism as a probe of local chiral structure.A salt-bridge structure in solution revealed by 2D-IR spectroscopy.Amplified Vibrational Circular Dichroism as a Probe of Local Biomolecular StructureAmplifying vibrational circular dichroism by manipulation of the electronic manifoldAmplification of the linear and nonlinear optical response of a chiral molecular crystalWet Sunscreens in the Gas Phase: Structures of Isolated and Microsolvated OxybenzoneTaming conformational heterogeneity in and with vibrational circular dichroism spectroscopyWater Docking Bias in [4]HeliceneOn the origin of the extremely different solubilities of polyethers in water
P50
Q34228806-CD01103D-B2D9-44E3-9F74-6A9CC1793017Q34228851-53D580C2-B86E-4B88-A72C-4642DCBE4304Q34229267-D5CCAFE4-31FA-4EA6-AD85-B781A15E4FC5Q35750757-F77FB7E7-19D7-49EE-A786-8F7742E7A3D4Q35854055-7F7E7B57-98AC-4AFF-B0BF-090C7CBE1974Q35888678-A19E1AF7-97DE-4392-85C9-1CDFB63FA0E0Q35963001-DF333B6F-2E52-4CDF-8471-81A0BEEFF8F4Q36051346-42BA9A4F-8195-425D-8184-D221B6BD2474Q36570787-775600F1-0289-488F-A579-80201922C769Q42359301-2E6679AD-2582-43FC-85AF-03495A9C1304Q44397167-0FE3B6EF-5EC1-471C-9BA4-17B17008F573Q46741568-CAFDE422-A2E7-4C92-BACD-15B14E63D655Q47862954-2F6C0006-711B-4332-95E9-A2B7C1C9BACEQ48184789-7052FDDC-9EF4-4F17-8C48-4453C3C531C4Q48306593-A3BD3736-A722-4ECB-8D77-13A439780F77Q51410524-BA2AE237-1DC2-4835-AB99-1084E2D9D664Q53213855-4B97451A-93A4-4D54-AC33-9ED66AFE5ADDQ53260627-2C3281C3-E798-44E5-A2CD-8C8C572A1D4EQ53289296-2B5B2E1A-702D-476B-9B58-8C9E37885419Q56742448-830C68E9-B9E0-4993-ADF5-06221D7BA786Q57834474-A6EA0638-0039-45E9-836B-8420487B31CAQ61138894-B85E3346-438D-46D2-A102-22A4867CDAC9Q90851935-4BAD1595-C1C8-4F60-9559-51EBD7E1BE62Q91709617-EEA18AAD-A2A4-4BEF-A9BE-C06E84ABA04AQ91967109-405AE480-5F66-4E87-BEC0-B85341D8100FQ93116266-D6055C0C-C179-41A3-A459-2E7F1DB9C79D
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sérgio R Domingos
@ast
Sérgio R Domingos
@en
Sérgio R Domingos
@es
Sérgio R Domingos
@nl
Sérgio R Domingos
@sl
type
label
Sérgio R Domingos
@ast
Sérgio R Domingos
@en
Sérgio R Domingos
@es
Sérgio R Domingos
@nl
Sérgio R Domingos
@sl
prefLabel
Sérgio R Domingos
@ast
Sérgio R Domingos
@en
Sérgio R Domingos
@es
Sérgio R Domingos
@nl
Sérgio R Domingos
@sl
P106
P108
P21
P31
P496
0000-0002-7908-9778