about
Light-powered, artificial molecular pumps: a minimalistic approachPhotoinduced reversible switching of porosity in molecular crystals based on star-shaped azobenzene tetramers.Artificial nanomachines based on interlocked molecular species: recent advances.Using light to induce energy and electron transfer or molecular motions in multicomponent systems.Artificial molecular machines driven by light.An Artificial Molecular Transporter.Redox control of molecular motion in switchable artificial nanoscale devices.Electrochemical properties of CdSe and CdTe quantum dots.Luminescent sensors based on quantum dot-molecule conjugates.Light operated molecular machines.All-optical integrated logic operations based on chemical communication between molecular switches.Reversible mechanical switching of magnetic interactions in a molecular shuttle.Plugging a Bipyridinium Axle into Multichromophoric Calix[6]arene Wheels Bearing Naphthyl Units at Different Rims.Reversible mechanical switching of magnetic interactions in a molecular shuttle.Reversible photoswitching of rotaxane character and interplay of thermodynamic stability and kinetic lability in a self-assembling ring-axle molecular system.Liposome destabilization by a 2,7-diazapyrenium derivative through formation of transient pores in the lipid bilayer.Self-assembly of calix[6]arene-diazapyrenium pseudorotaxanes: interplay of molecular recognition and ion-pairing effects.Hierarchical self-assembly of amphiphilic calix[6]arene wheels and viologen axles in water.Effect of protons on CdSe and CdSe-ZnS nanocrystals in organic solution.A mechanically interlocked bundle.Viologen-calix[6]arene pseudorotaxanes. Ion-pair recognition and threading/dethreading molecular motions.Operating molecular elevators.Toward directionally controlled molecular motions and kinetic intra- and intermolecular self-sorting: threading processes of nonsymmetric wheel and axle components.Towards controlling the threading direction of a calix[6]arene wheel by using nonsymmetric axles.A redox-driven multicomponent molecular shuttle.Probing donor-acceptor interactions and co-conformational changes in redox active desymmetrized [2]catenanes.Efficient active-template synthesis of calix[6]arene-based oriented pseudorotaxanes and rotaxanes.Shuttling dynamics in an acid-base-switchable [2]rotaxane.Light control of stoichiometry and motion in pseudorotaxanes comprising a cucurbit[7]uril wheel and an azobenzene-bipyridinium axle.Light-operated machines based on threaded molecular structures.Wire-type ruthenium(II) complexes with terpyridine-containing [2]rotaxanes as ligands: Synthesis, characterization, and photophysical properties.Self-assembly of a double calix[6]arene pseudorotaxane in oriented channels.A simple molecular machine operated by photoinduced proton transfer.Structural and size effects on the spectroscopic and redox properties of CdSe nanocrystals in solution: the role of defect states.Correction: Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen.Making and Operating Molecular Machines: A Multidisciplinary Challenge.Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen.Photochemical switching of luminescence and singlet oxygen generation by chemical signal communication.Photoinduced memory effect in a redox controllable bistable mechanical molecular switch.Light-driven directed proton transport across the liposomal membrane.
P50
Q26776004-B95603AE-E8B3-46E7-A554-8114FEF648E5Q30982113-C614A9D5-293E-4FD3-BB95-EF43694CC2DDQ36631721-DC40C842-F58A-40D2-95A9-766F61C07B0AQ36778720-A4FA59B1-B01F-4B96-9F28-636D7390BD5FQ36992017-FEA798B0-FD18-47D1-9EE5-EF3A14377BBEQ37000765-2A6F6906-70F7-4719-95B3-517DFF7FA1A5Q37766870-B4CAC96A-5CCD-4180-A3F5-7AD94AF745C2Q38024026-F4895054-1516-43B6-BA14-00ED12673FDCQ38442272-88877D0F-FF13-428E-A3D8-2E96479E6DA0Q39808771-3463487E-3B30-4F40-9154-4F6A1BFECB1BQ39863100-387CEC3D-26F9-4F6C-BCFB-028F57A17408Q41990480-42F321E6-DD8C-4BFB-8464-8E76712C0F05Q42078056-EA2EFA16-3BD3-46C8-82EE-E291BA6FDAD8Q42659605-45DC9FF2-6536-4328-A741-A602130B9BAAQ42906969-97EEE43D-59A9-4934-8EEA-238711731D47Q43120241-8B98E89D-9A2C-49E2-8325-ED12C050E336Q43167652-E926F64C-3F73-4141-A4CB-C017A7689377Q43816038-523717A4-74F9-417F-99F9-B17C4C48906DQ44100515-C11C5048-1EBF-4C26-AE48-A3BCCEC49D9DQ44840428-BF9FF3B4-7E8E-4BE0-BF1E-96236626203EQ45063207-53F3513F-0488-4FB9-8A50-6AD403A2E675Q45143630-8DDB6E83-0ACC-490F-ACDB-3401B5A55D6AQ46023080-35BB0323-CAF1-45F8-ABBC-3B763D9F1A6DQ46126981-D181DD8C-DD17-4B8E-93A2-0D4CE4FCB3E6Q46189677-A7D83AC2-0236-4E16-BE7E-EA60BFFB8700Q46306642-E3E4F3C1-0582-4469-84EF-E628AB60DB4BQ46327361-38082DC4-86CF-4B03-94D8-B9D8FC923B70Q46738776-F81E64AE-3981-4809-A57E-C3052ACC5AF5Q46879324-41467103-7AA9-41EE-848D-2CF0B1AF1A55Q46931306-A811FF22-05A7-471A-A332-E45443F72B2DQ46938124-2C1D407B-4418-4DCF-B3F8-045AA66BF419Q46978701-49673706-D446-47A6-ACF8-29EF25C962F8Q47265907-1DE7CE15-E5D5-4D91-9BD0-720C8ADA98FDQ47370070-30399C69-5D35-48ED-B6DD-39C5A860E84DQ48741365-45741144-8D7B-44C3-9956-45B7B30867D1Q49882701-1DC6451A-5C16-4702-B442-BEC40E53EFFEQ50439413-52CEE394-6D18-42DF-9507-A8D52FA63287Q50616207-9C0D7955-A79C-4428-BF47-5000DE14F005Q50975242-447A8637-1D08-483D-9BFD-8EF4FD2E0CB3Q53405275-587C5A61-009F-41F4-B317-6EC0ABA773CA
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Serena Silvi
@ast
Serena Silvi
@en
Serena Silvi
@es
Serena Silvi
@nl
Serena Silvi
@sl
type
label
Serena Silvi
@ast
Serena Silvi
@en
Serena Silvi
@es
Serena Silvi
@nl
Serena Silvi
@sl
prefLabel
Serena Silvi
@ast
Serena Silvi
@en
Serena Silvi
@es
Serena Silvi
@nl
Serena Silvi
@sl
P106
P1153
6506132214
P21
P31
P496
0000-0001-9273-4148