about
Straightforward access to mono- and bis-cycloplatinated helicenes that display circularly polarized phosphorescence using crystallization resolution methods.Large-Scale Synthesis of Helicene-Like Molecules for the Design of Enantiopure Thin Films with Strong Chiroptical Activity.enantio-Enriched CPL-active helicene-bipyridine-rhenium complexes.Acid/base-triggered switching of circularly polarized luminescence and electronic circular dichroism in organic and organometallic helicenesConformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn(2+) binding.Calculating Natural Optical Activity of Molecules from First Principles.Delocalization error and "functional tuning" in Kohn-Sham calculations of molecular properties.Unravelling the structure of Magnus' pink salt.Tuned Range-Separated Time-Dependent Density Functional Theory Applied to Optical Rotation.Sterically less-hindered half-titanocene(IV) phenoxides: ancillary-ligand effect on mono-, bis-, and tris(2-alkyl-/arylphenoxy) titanium(IV) chloride complexes.Spin ground state and magnetic properties of cobalt(II): relativistic DFT calculations guided by EPR measurements of bis(2,4-acetylacetonate)cobalt(II)-based complexes.Helicene-grafted vinyl- and carbene-osmium complexes: an example of acid-base chiroptical switching.Assembly of helicene-capped N,P,N,P,N-helicands within Cu(I) helicates: impacting chiroptical properties by ligand-ligand charge transfer.Optical rotation calculated with time-dependent density functional theory: the OR45 benchmark.Chiroptical properties of carbo[6]helicene derivatives bearing extended π-conjugated cyano substituents.Theoretical analysis of bonding in N-heterocyclic carbene-rhodium complexes.Synthesis, Spectroelectrochemical Behavior, and Chiroptical Switching of Tris(β-diketonato) Complexes of Ruthenium(III), Chromium(III), and Cobalt(III).QTAIM and ETS-NOCV analyses of intramolecular CH···HC interactions in metal complexes.Iron Alkynyl Helicenes: Redox-Triggered Chiroptical Tuning in the IR and Near-IR Spectral Regions and Suitable for Telecommunications Applications.Ruthenium-Grafted Vinylhelicenes: Chiroptical Properties and Redox Switching.Enantioselective Recognition of Ammonium Carbamates in a Chiral Metal-Organic Framework.Ion pairing as a possible clue for discriminating between sodium and potassium in biological and other complex environments.Synthesis and Chiroptical Properties of Hexa-, Octa-, and Deca-azaborahelicenes: Influence of Helicene Size and of the Number of Boron Atoms.Does a Molecule-Specific Density Functional Give an Accurate Electron Density? The Challenging Case of the CuCl Electric Field Gradient.Anion-π recognition between [M(CN)6]3- complexes and HAT(CN)6: structural matching and electronic charge density modification.Enantiopure Cycloiridiated Complexes Bearing a Pentahelicenic N-Heterocyclic Carbene and Displaying Long-Lived Circularly Polarized Phosphorescence.Bimetallic Gold(I) Complexes with Ethynyl-Helicene and Bis-Phosphole Ligands: Understanding the Role of Aurophilic Interactions in their Chiroptical Properties.Applications of the ETS-NOCV method in descriptions of chemical reactions.Exploring a reaction mechanism for acetato ligand replacement in paddlewheel tetrakisacetatodirhodium (II,II) complex by ammonia: computational density functional theory study.Redox-triggered chiroptical switching activity of ruthenium(III)-bis-(β-diketonato) complexes bearing a bipyridine-helicene ligand.Exciton coupling in diketopyrrolopyrrole-helicene derivatives leads to red and near-infrared circularly polarized luminescence.Giant Faraday Rotation in Mesogenic Organic MoleculesElectronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligandsCrucial Influence of the Intramolecular Hydrogen Bond on the Coordination Mode of RC(S)NHP(S)(OiPr)2in Homoleptic Complexes with NiIIInfluence of CH2Cl2for the structure stabilization of the NiIIcomplex [Ni{6-MeO(O)CC6H4NHC(S)NP(S)(OiPr)2-1,5-S,S′}2]·CH2Cl2Solvent-induced 1,3-N,S- vs. 1,5-S,S′-coordination in the NiII complex [Ni{p-Me2NC6H4NHC(S)NP(S)(OiPr)2}2]On Conformational Flexibility of Half-Titanocene Catalysts with Aryloxy Ligands for High-Temperature Olefin Polymerization Processes: Static and Dynamic Theoretical Studies†On preference of insertion mechanism in the ethylene polymerization catalyzed by half-titanocene complexes with aryloxy ligands: Static and dynamic theoretical studiesComputational Modeling of Polymerization CatalystsHalf-Metallocene Titanium(IV) Phenyl Phenoxide for High Temperature Olefin Polymerization: Ortho-Substituent Effect at Ancillaryo-Phenoxy Ligand for Enhanced Catalytic Performance
P50
Q33632020-AC390F98-ABBE-4799-B37A-376191A006CAQ35900802-DBBC4EC9-5097-47BF-BA01-3B98FF312F20Q36692083-80F4BADF-9977-4ECE-997D-390D315E4A9FQ36710026-2842608A-0BB3-4C2C-86DC-E2CF39B7F849Q36823222-88CB1E47-3DCB-44E6-B4C9-F06B3E051DD5Q38809079-B8390309-ACFF-4293-8874-2D33A22DBB69Q39169397-1ED7D0F7-2900-4064-AA97-185F6E74F8CCQ39270094-34556214-A84A-4847-A1E3-31E968777788Q40290981-742A9FF4-AA61-40D2-9911-1E522D206726Q43099930-5C6896BA-8B69-48D7-9065-B6D71C0D4178Q43978005-1CB5D705-04B9-4AAF-A6B8-0DBDF3BF7BD2Q44124196-9F8CDC14-8CF5-4387-95BA-0208F0D0B3B9Q44681560-0C7E741B-A9BA-4C39-8FDB-6E99908289BDQ45166127-4C88A83C-0F40-489C-9BC3-93C458950A91Q45764182-2AD9BCDA-3835-4B01-999C-4D16F862F05CQ46033471-65374EDD-6B5E-47B5-BC03-DA6D6320097EQ46389878-4742A62E-D329-40D8-B0C4-50BDC5AACA3BQ46461495-3BEBCCC0-B9F7-4D7E-9AF5-8CBCFA726985Q46546469-155BC210-D0A1-4118-BF05-74E89B42BCE9Q46659642-36A863AE-03BE-46DC-9C1A-9BF0911793EEQ46757398-7C55B1D4-A709-467B-A198-69F593100350Q46871922-CED1D90F-D775-4105-B8BF-E04F5804F5EDQ47266762-F3A228E7-480C-4CA8-BBC6-D451A6C61C95Q48007155-2236EBC6-8FCD-437D-8C4B-5A8C0E5D9009Q48045995-69FDC3CC-CAB1-42BA-B97D-F22551298F2CQ48093349-583EB49E-193F-4118-A224-424F5915EFA9Q51424951-4EE0C6DF-9CBD-4BD2-A3F1-752B1A57266EQ51584662-0B7B8F31-843B-4024-A931-1A60304A4B97Q51615042-4D93F00F-8792-44F1-AC4D-CD50BC1D2FEDQ51745294-2514C7B6-8BA3-4565-92C3-3B56C2416327Q52599551-EFAA6FF3-3A90-4FC5-9D50-D86B734A755FQ56335127-E7E71481-2F27-425C-830A-AC02A6F9612AQ59093923-88AEE014-0DA5-489A-A92B-969DF856E089Q59094007-2BFAC558-1B01-4E33-87F7-E07B7746CD03Q59094012-D0EB9150-D2DD-4F78-B86A-87D28CB1145DQ59094050-EEFD2B15-CFC4-4564-859F-668BCD8C7B79Q59094058-DC8CF926-BB3C-4ED2-9CBA-A06573AC01E6Q59094065-C0AE8A93-9E52-4690-99C7-C51B75D1CE9EQ59094072-67530B83-DCFE-455D-9666-DBB950E10D9AQ59094084-35AEF688-CF43-4F00-856F-19AAB5D66508
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Monika Srebro
@ast
Monika Srebro
@en
Monika Srebro
@es
Monika Srebro
@nl
Monika Srebro
@sl
type
label
Monika Srebro
@ast
Monika Srebro
@en
Monika Srebro
@es
Monika Srebro
@nl
Monika Srebro
@sl
altLabel
Monika Srebro
@en
prefLabel
Monika Srebro
@ast
Monika Srebro
@en
Monika Srebro
@es
Monika Srebro
@nl
Monika Srebro
@sl
P1053
E-7114-2017
P106
P21
P31
P3829
P496
0000-0003-4211-325X