Chiral transfer in coordination complexes: towards molecular materials.
about
Dynamic chiral-at-metal stability of tetrakis(d/l-hfc)Ln(III) complexes capped with an alkali metal cation in solution.Allenes in molecular materials.Speciation, luminescence, and alkaline fluorescence quenching of 4-(2-methylbutyl)aminodipicolinic acid (H2MEBADPA).Chirality transfer from gold nanocluster to adsorbate evidenced by vibrational circular dichroism.Spin crossover properties of enantiomers, co-enantiomers, racemates, and co-racemates.Metal-controlled diastereoselective self-assembly and circularly polarized luminescence of a chiral heptanuclear europium wheel.Acid/base-triggered switching of circularly polarized luminescence and electronic circular dichroism in organic and organometallic helicenesLuminescent chiral lanthanide(III) complexes as potential molecular probesVCD spectroscopy as a novel probe for chirality transfer in molecular interactions.Layered hydroxide hybrid nanostructures: a route to multifunctionality.Transfer of chirality from ligands to metal centers: recent examples.Asymmetric catalysis mediated by the ligand sphere of octahedral chiral-at-metal complexes.Chiral chemistry of metal-camphorate frameworks.Chiral metallosupramolecular architectures.Stereochemical Communication within a Chiral Ion Pair Catalyst.Diaqua-bis-(hydrogen tartrato)cobalt(II) dihydrate.Multiple-stimulus-responsive supramolecular gels and regulation of chiral twists: the effect of spacer length.Assembly of pi-conjugated phosphole azahelicene derivatives into chiral coordination complexes: an experimental and theoretical study.Chirality transfer in propeller-shaped cyclen-calcium(II) complexes: metal-coordinating and ion-pairing anion procedures.Enantioselective self-assembly of antiferromagnetic hexacopper(II) wheels with chiral amino acid oxamates.Programmed multiple complexation for the creation of helical structures from acyclic phenol-bipyridine oligomer ligands.Vibrational and electronic circular dichroism monitoring of copper(II) coordination with a chiral ligand.A chiroptical switch based on supramolecular chirality transfer through alkyl chain entanglement and dynamic covalent bonding.Stereodynamics of metal-ligand assembly: what lies beneath the "simple" spectral signatures of C2-symmetric chiral chelates.Chirality transfer based on reversible C-C bond formation/breaking in nickel(II) complexes.Coordinative Alignment of Chiral Molecules to Control over the Chirality Transfer in Spontaneous Resolution and Asymmetric Catalysis.First one-dimensional homochiral stairway-like Cu(II) chains: crystal structures, circular dichroism (CD) spectra, ferroelectricity and antiferromagnetic properties.Synthesis of helically twisted [1 + 1]macrocycles assisted by amidinium-carboxylate salt bridges and control of their chiroptical properties.Creation of Optically Pure Crystals from a Meso-Type Gold(I) Metalloligand with d- and l-Amino Acids: A Coordination Trick.Induced Circular Dichroism in Phosphine Gold(I) Aryl Acetylide Urea Complexes through Hydrogen-Bonded Chiral Co-Assemblies.Response speed control of helicity inversion based on a "regulatory enzyme"-like strategy.Alanine-Based Chiral Metallogels via Supramolecular Coordination Complex Platforms: Metallogelation Induced Chirality Transfer.Chirality of 20-membered unclosed cryptand: Macroring distortion via lariat arm modification.Easy separation of Δ and Λ isomers of highly luminescent [Ir(III)]-cyclometalated complexes based on chiral phenol-oxazoline ancillary ligands.Two mono- and dinuclear Eu(III) enantiomeric pairs based on chiral bis-bidentate bridging ligands: synthesis, structures, luminescent and ferroelectric properties.Multifunctional and reactive enantiopure organometallic helicenes: tuning chiroptical properties by structural variations of mono- and bis(platinahelicene)s.The Construction of Homochiral Lanthanide Quadruple-Stranded Helicates with Multiresponsive Sensing Properties toward Fluoride Anions.Creation of chiral thixotropic gels through a crown-ammonium interaction and their application to a memory-erasing recycle system.Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation.Bimetallic Gold(I) Complexes with Ethynyl-Helicene and Bis-Phosphole Ligands: Understanding the Role of Aurophilic Interactions in their Chiroptical Properties.
P2860
Q34248827-B64490E7-2030-4609-919C-F08A7B484B30Q34252320-CB614737-D845-4D26-86F6-822CF3E307ADQ35164140-B6EDF020-DF5B-469D-85D9-D145E2EA4075Q35608950-A79A3E93-1CF9-4E41-807D-395967CD065EQ35972125-ABB50BDE-320F-4E3D-B683-3C3B61E40577Q36340742-FD5053F0-6758-43B6-B792-E7500C654A40Q36710026-22A10DC9-7E28-4185-9759-46512F9EBBC6Q37445128-FE394802-9543-4D3D-9503-BDDDA8B8E789Q37737082-2E6CA2A0-75D6-46E7-9D9B-FEF42EF6401DQ37827358-C36AAA12-1EA9-4752-8377-B9053CF01102Q38012327-1C244576-134E-4DAE-8D2A-406BA81592C1Q38243303-DFDA2207-E5C9-4001-A9DB-402651E7E028Q38791605-4D9059A3-4CD8-4050-9E49-3B8535D1A14EQ39269215-B3BC297D-784A-4964-8075-CF03C5773EABQ40809719-E9850279-F0E6-42B6-95B5-434BCDE7D45AQ40931607-D1720C0B-3116-4ED7-B004-D45161072263Q41125618-FB6E0511-CD4B-4B29-B320-A5644EF6BC89Q43096926-2A53C61B-1A9A-451B-91F9-9AAEC6477614Q43697972-F9E8375E-F1D1-4043-9556-719FD430D7A3Q44020172-2E9D135E-3E5D-4BE6-8168-1BF0C661BBA9Q44543880-C9AE207B-874E-4312-A82C-8F0854B164FAQ44707438-C6F5288D-FCBD-48BD-A95E-19AC413E561DQ44731777-7DAFBBCB-D665-4C19-9DF1-FA0CE48514B2Q45373018-4E59EC9F-1BF9-464C-94F9-B1098E62B1B6Q45801657-D797CC87-9F20-4B87-9B47-517DA6EF12ABQ46106653-BF7870A6-D5FF-44FF-8C36-48C87CA85A98Q46527711-218B0B55-1A77-41FA-B7A6-8AEFFED4B15BQ46545496-7D831288-08F9-41A2-9548-4C0A18A05028Q47815194-1C3F5783-C07B-4238-99F7-4E9DD1335A6AQ48260058-ABA6B1FE-A9DC-44C0-B298-1AB95DF6C7E6Q48276590-825AADEE-4289-4847-866D-AD9BC4517FD9Q48327311-05D9FCF3-06A1-4355-873F-45AE0C3437C4Q48351915-C45CE05D-D565-44BD-8140-53761A742A97Q50245646-5D816566-9D80-40E5-858D-910F2DC7ACE4Q50504904-4FAFAC43-39B0-4434-9EAE-14C899E9AA89Q50523275-FD67FD22-793A-4842-8089-ABDD60ED1E4BQ50903233-683254C2-EF30-40C9-80EF-E88FB479958FQ50970481-59F0CC11-A3E6-477A-8F92-EADCE5960FC6Q51306149-3C251311-52AE-4EFA-9688-A0B5B2C9460AQ51424951-18544031-20DF-4C6B-9C51-B8D603CB6904
P2860
Chiral transfer in coordination complexes: towards molecular materials.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 14 January 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Chiral transfer in coordination complexes: towards molecular materials.
@en
Chiral transfer in coordination complexes: towards molecular materials.
@nl
type
label
Chiral transfer in coordination complexes: towards molecular materials.
@en
Chiral transfer in coordination complexes: towards molecular materials.
@nl
prefLabel
Chiral transfer in coordination complexes: towards molecular materials.
@en
Chiral transfer in coordination complexes: towards molecular materials.
@nl
P356
P1476
Chiral transfer in coordination complexes: towards molecular materials.
@en
P304
P356
10.1039/B806203J
P577
2009-01-14T00:00:00Z