about
Preparation of Enantiomerically Pure C76 with a General Electrochemical Method for the Removal of Di(alkoxycarbonyl)methano Bridges from Methanofullerenes: The Retro-Bingel ReactionChlorofluoroiodomethane as a potential candidate for parity violation measurements.The chiral molecule CHClFI: first determination of its molecular parameters by Fourier transform microwave and millimeter-wave spectroscopies supplemented by ab initio calculations.Chiral oxorhenium(V) complexes as candidates for the experimental observation of molecular parity violation: a structural, synthetic and theoretical study.Straightforward access to mono- and bis-cycloplatinated helicenes that display circularly polarized phosphorescence using crystallization resolution methods.Progress toward the first observation of parity violation in chiral molecules by high-resolution laser spectroscopy.High resolution spectroscopy of methyltrioxorhenium: towards the observation of parity violation in chiral molecules.Search for resolution of chiral fluorohalogenomethanes and parity-violation effects at the molecular level.A chiral rhenium complex with predicted high parity violation effects: synthesis, stereochemical characterization by VCD spectroscopy and quantum chemical calculations.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.pi-Conjugated phosphole derivatives: synthesis, optoelectronic functions and coordination chemistry.Chiral transfer in coordination complexes: towards molecular materials.Transfer of chirality from ligands to metal centers: recent examples.Assembly of pi-conjugated phosphole azahelicene derivatives into chiral coordination complexes: an experimental and theoretical study.Helicene-grafted vinyl- and carbene-osmium complexes: an example of acid-base chiroptical switching.Chiroptical properties of carbo[6]helicene derivatives bearing extended π-conjugated cyano substituents.An oxorhenium complex bearing a chiral cyclohexane-1-olato-2-thiolato ligand: Synthesis, stereochemistry, and theoretical study of parity violation vibrational frequency shifts.Synthesis, Spectroelectrochemical Behavior, and Chiroptical Switching of Tris(β-diketonato) Complexes of Ruthenium(III), Chromium(III), and Cobalt(III).Synthesis and Chiroptical Properties of Hexa-, Octa-, and Deca-azaborahelicenes: Influence of Helicene Size and of the Number of Boron Atoms.Triplet state CPL active helicene-dithiolene platinum bipyridine complexes.Enantiopure Cycloiridiated Complexes Bearing a Pentahelicenic N-Heterocyclic Carbene and Displaying Long-Lived Circularly Polarized Phosphorescence.Enantiopure versus Racemic Naphthalimide End-Capped Helicenic Non-fullerene Electron Acceptors: Impact on Organic Photovoltaics Performance.Synthesis of Carbo[6]helicene Derivatives Grafted with Amino or Aminoester Substituents from Enantiopure [6]Helicenyl Boronates.Triggering Emission with the Helical Turn in Thiadiazole-Helicenes.Asymmetric Sequential Cu-Catalyzed 1,6/1,4-Conjugate Additions of Hard Nucleophiles to Cyclic Dienones: Determination of Absolute Configurations and Origins of Enantioselectivity.Synthesis of a Helical Bilayer Nanographene.Chiral Organic Cages with a Triple-Stranded Helical Structure Derived from Helicene.Multifunctional and reactive enantiopure organometallic helicenes: tuning chiroptical properties by structural variations of mono- and bis(platinahelicene)s.Bimetallic Gold(I) Complexes with Ethynyl-Helicene and Bis-Phosphole Ligands: Understanding the Role of Aurophilic Interactions in their Chiroptical Properties.Redox-triggered chiroptical switching activity of ruthenium(III)-bis-(β-diketonato) complexes bearing a bipyridine-helicene ligand.Ethylenedithio-tetrathiafulvalene-helicenes: electroactive helical precursors with switchable chiroptical properties.Synthesis and vibrational circular dichroism of enantiopure chiral oxorhenium(V) complexes containing the hydrotris(1-pyrazolyl)borate ligand.Exciton coupling in diketopyrrolopyrrole-helicene derivatives leads to red and near-infrared circularly polarized luminescence.A racemic and enantiopure unsymmetric diiron(III) complex with a chiral o-carborane-based pyridylalcohol ligand: combined chiroptical, magnetic, and nonlinear optical properties.Synthesis and Structural Properties of Aza[n]helicene Platinum Complexes: Control of Cis and Trans Stereochemistry.Chiral Transmission to Cationic Polycobaltocenes over Multiple Length Scales Using Anionic SurfactantsRedox-Active Chiroptical Switching in Mono- and Bis-Iron Ethynylcarbo[6]helicenes Studied by Electronic and Vibrational Circular Dichroism and Resonance Raman Optical Activity
P50
Q29013621-8A2CD7D8-416E-4BEC-BA8C-1F089E6F00C5Q33234086-54429049-F0C7-416F-8E42-E7E999338324Q33249731-30D1FBDC-4E0A-431B-91B6-ED78115CA058Q33598732-EC3FC1E0-3F11-438A-A5F7-B61C1D5DBA2DQ33632020-2D2D959B-AAA9-44BB-AD7D-79BC6B7FE49EQ33691867-645177CC-B8A2-4940-A807-C47D0E523760Q33759425-6EA2EAE8-83BB-4195-9CD6-B3715420F5B2Q34210306-F28808C4-A9FF-488A-A98B-AAA83ABDB5C4Q34741477-4E95641D-53E6-4DA0-B36C-8840CCDDDE42Q35900802-95B3C9F0-4155-44C6-B362-BF83743EE579Q36692083-04F666B6-DFF6-429D-8CB0-1B2132AD72F1Q36710026-482351BF-AC59-4BA5-925D-7111B25FF8C8Q36823222-44A37579-1FB3-47EF-A698-22B32B4975BEQ37339749-0288A516-D294-42B9-97F5-6362CB280B5CQ37423903-8158C988-1DB6-4807-9C3E-D209346CACC1Q38012327-FBB882FC-10CA-47D0-A2AE-C72CC2975989Q43096926-F40B8821-4D73-4FBC-B18F-7D5FD4F33B4FQ44124196-F7CC1C38-7653-4F8B-852C-C6027EF98FB1Q45764182-BC2451DC-59A3-4512-A4BF-220B6D52D821Q46261120-59F76931-29E2-4372-8AD4-22F8D0C52577Q46389878-2D94B723-315A-42CC-8AB5-51544619F0B3Q47266762-25B2BE0A-EB85-4757-8EDA-B264BD4BBFAEQ48056685-76DACA89-BF6A-451F-9EA9-AC733E7BBE28Q48093349-83EA94D4-7617-49DA-A514-227B4CB200B5Q48116514-07FA9E20-B48C-4045-93A8-750DFEA29327Q48147784-942D4108-42BE-4CFD-8CB1-5060C2338409Q48288058-6FBA3C71-1403-4D3A-A89A-1372CF7B6DBDQ48332604-610C5DE3-56F2-473B-8D35-E02DB8F61816Q49976989-D935DEE8-E857-4C9E-963E-1E0DF7C3AC54Q50109850-B9863774-D5EB-44D3-B69D-445896BF35D5Q50523275-F7EE0833-E952-408F-839C-79274C7B97E6Q51424951-2305BC8E-A92D-496F-935D-71835FF7A27AQ51745294-3F3D730E-574E-4E60-B2ED-EBE84CE4FDA0Q51791516-704E2359-BB83-4A98-B185-1BD564250F9BQ51927763-B863B1D6-7C87-48EB-875D-53AA32E17099Q52599551-6C22385F-D9F4-425B-9074-DBF9A24E82E3Q54439219-77AA2CCD-D025-475C-AEA0-86576FD8A174Q54451234-5CD0A5C7-3E35-4490-B367-2F001A93BE24Q57375353-E98FBB1F-C87E-4699-8D40-851A76A1DECFQ57905269-62A9FC21-D923-40C1-A452-25246DCDC591
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jeanne Crassous
@ast
Jeanne Crassous
@en
Jeanne Crassous
@es
Jeanne Crassous
@sl
type
label
Jeanne Crassous
@ast
Jeanne Crassous
@en
Jeanne Crassous
@es
Jeanne Crassous
@sl
prefLabel
Jeanne Crassous
@ast
Jeanne Crassous
@en
Jeanne Crassous
@es
Jeanne Crassous
@sl
P106
P21
P31
P496
0000-0002-4037-6067