About: Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core

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About: Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core Goto Sponge NotDistinct Permalink

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scientific article published on 25 June 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2012 (uk) im Juni 2012 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 25 June 2012 (en) artículu científicu espublizáu en xunu de 2012 (ast)
publication date	wds:Q59093995-0B26253A-D6DC-4C15-BEAC-869FF37BC69E
publication date	2012-06-25 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59093995-3FD9A57E-5010-4A9C-B500-75B47C71BB6E
language of work or name	English
author name string	wds:Q59093995-04175D91-61C9-421A-A222-C179C93E0F43 wds:Q59093995-AA200F18-C416-458F-9EDE-3F11E1EF7D2C wds:Q59093995-BD34A8B9-3363-4257-87E4-BD09B3D004FE wds:Q59093995-EDDCE179-F253-4F06-B17E-142E2BA0C4B5
author name string	Régis Réau Loïc Toupet Stéphane Rigaut Emmanuel Anger
rdfs:label	Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core (en) Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core (nl)
skos:prefLabel	Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core (en) Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core (nl)
name	Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core (en) Ruthenium-Vinylhelicenes: Remote Metal-Based Enhancement and Redox Switching of the Chiroptical Properties of a Helicene Core (nl)
author	wds:Q59093995-4B038337-3BCE-40C7-BA3B-5F3D15FE1A43 wds:Q59093995-987A0984-CEF7-4073-B217-579856D2530B wds:Q59093995-B6B7D304-7FFC-4D06-A7B0-316A6055AC75 wds:Q59093995-EA2B0BBB-4F2C-433A-BE5C-7A9819D828D2 wds:Q59093995-F3260C7D-58E2-436C-9E01-E52BFB031C1E
author	Jeanne Crassous Christian Roussel Jochen Autschbach Monika Srebro Nicolas Vanthuyne
title	wds:Q59093995-69E1B6D2-5E7F-45CC-A9E4-A0A193815572
title	Ruthenium-vinylhelicenes: remote metal-based enhancement and redox switching of the chiroptical properties of a helicene core (en)
page(s)	wds:Q59093995-3027F39B-D092-483D-8B82-942F5D37F260
page(s)	15628-15631
instance of	wds:Q59093995-FED69FA4-E24C-4936-9C7B-A6AF5EC7D8ED
instance of	scholarly article
main subject	wds:Q59093995-FE1690BE-91DC-4D93-AA27-DA9262AAEB4C
main subject	ruthenium
PubMed ID	wds:Q59093995-00AC0526-644E-45DF-9D36-8E3F787F7A11
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22715962
PubMed ID	22715962
published in	wds:Q59093995-51A1EFC0-27C6-496A-94FD-B573FF12A30B
published in	Journal of the American Chemical Society
issue	wds:Q59093995-DA012CFC-0FBC-44E0-96EE-5C6AFEAD8EF2
volume	wds:Q59093995-990DB7FA-ABB1-4607-A822-47C3C33BD2C3
issue	38
volume	134
DOI	wds:Q59093995-A295A3AB-345C-4908-BEC7-FC716277D152
DOI	http://dx.doi.org/10.1021/JA304424T
DOI	10.1021/JA304424T
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59093995
is cites work of	Diastereo- and Enantioselective Synthesis of Organometallic Bis(helicene)s by a Combination of CH Activation and Dynamic Isomerization Straightforward access to mono- and bis-cycloplatinated helicenes that display circularly polarized phosphorescence using crystallization resolution methods Acid/base-triggered switching of circularly polarized luminescence and electronic circular dichroism in organic and organometallic helicenes Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn(2+) binding Helicene-grafted vinyl- and carbene-osmium complexes: an example of acid-base chiroptical switching Ruthenium-Grafted Vinylhelicenes: Chiroptical Properties and Redox Switching Modular synthesis, orthogonal post-functionalization, absorption, and chiroptical properties of cationic [6]helicenes Triggering Emission with the Helical Turn in Thiadiazole-Helicenes. Chiroptical properties of carbo[6]helicene derivatives bearing extended π-conjugated cyano substituents Ethylenedithio-tetrathiafulvalene-helicenes: electroactive helical precursors with switchable chiroptical properties. Synthesis and Chiroptical Properties of Hexa-, Octa-, and Deca-azaborahelicenes: Influence of Helicene Size and of the Number of Boron Atoms. Functionalized cationic [4]helicenes with unique tuning of absorption, fluorescence and chiroptical properties up to the far-red range. Single helicates of dipalladium(II) hexapyrroles: helicity induction and redox tuning of chiroptical properties Assembly of helicene-capped N,P,N,P,N-helicands within Cu(I) helicates: impacting chiroptical properties by ligand-ligand charge transfer Bimetallic Gold(I) Complexes with Ethynyl-Helicene and Bis-Phosphole Ligands: Understanding the Role of Aurophilic Interactions in their Chiroptical Properties. Optical rotation calculations on large molecules using the approximate coupled cluster model CC2 and the resolution-of-the-identity approximation. Exciton coupling in diketopyrrolopyrrole-helicene derivatives leads to red and near-infrared circularly polarized luminescence. Iron Alkynyl Helicenes: Redox-Triggered Chiroptical Tuning in the IR and Near-IR Spectral Regions and Suitable for Telecommunications Applications Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation. Dioxygen-triggered transannular dearomatization of benzo[5]helicene diols: highly efficient synthesis of chiral π-extended diones. Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands Enantiopure versus Racemic Naphthalimide End-Capped Helicenic Non-fullerene Electron Acceptors: Impact on Organic Photovoltaics Performance. Electronically Connected [n]Helicenes: Synthesis and Chiroptical Properties of Enantiomerically Pure (E)-1,2-Di([6]helicen-2-yl)ethenes Configurationally Stable Chiral Dithia-Bridged Hetero[4]helicene Radical Cation: Electronic Structure and Absolute Configuration. Intense redox-driven chiroptical switching with a 580 mV hysteresis actuated through reversible dimerization of an azoniahelicene. Outstanding chiroptical properties: a signature of enantiomerically pure alleno-acetylenic macrocycles and monodisperse acyclic oligomers. Enantioseparation on Riboflavin Derivatives Chemically Bonded to Silica Gel as Chiral Stationary Phases for HPLC Modulation of circularly polarized luminescence through excited-state symmetry breaking and interbranched exciton coupling in helical push-pull organic systems Combined reversible switching of ECD and quenching of CPL with chiral fluorescent macrocycles Large-Scale Synthesis of Helicene-Like Molecules for the Design of Enantiopure Thin Films with Strong Chiroptical Activity. Electronic Structures and Chiroptical Properties of Post-functionalized Helicene Quinones Microwave-assisted synthesis of novel hetero[5]helicene-like molecules and coumarin derivatives. Chiral Diketopyrrolopyrrole-Helicene Polymer With Efficient Red Circularly Polarized Luminescence Redox-triggered chiroptical switching activity of ruthenium(III)-bis-(β-diketonato) complexes bearing a bipyridine-helicene ligand. One-pot synthesis of highly emissive dipyridinium dihydrohelicenes Dutch Resolution of a configurationally stable [5]helquat. Helicene Radicals: Molecules Bearing a Combination of Helical Chirality and Unpaired Electron Spin
is cites work of	wds:Q36710026-1A3991FD-69F5-47D8-941A-B19021AB1A04 wds:Q36823222-BB0A1E54-1A56-4C36-AE59-59A85F1AC153 wds:Q44238353-F42ED327-ECCA-481F-97FB-0FBA0F2087F3 wds:Q44124196-E82AF0DF-ECE7-4509-9F88-FF147E35E496 wds:Q51424951-EE17A509-9391-4C90-B79F-CDCFBACF39A1 wds:Q48181895-DD9CF2DE-4FBE-4318-9A1D-D7DB80A6F64B wds:Q51744412-22A35ED4-7DB4-48E5-A2DE-3DDAEAFEDF63 wds:Q57729200-A42CE657-CCA3-403B-BF63-9B84F3B82107

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