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A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes

dc.contributor.authorBraunschweig, Holger
dc.contributor.authorClaes, Christina
dc.contributor.authorDamme, Alexander
dc.contributor.authorDeisenberger, Andrea
dc.contributor.authorDewhurst, Rian D.
dc.contributor.authorHorl, Christian
dc.contributor.authorKramer, Thomas
dc.date.accessioned2022-08-10T05:36:53Z
dc.date.issued2015
dc.date.updated2021-08-01T08:29:42Z
dc.description.abstractWe analytically show that an incident light can be almost completely diffracted into the −1st order in wide-angle and broadband by suitably designed thin metallic nano-gratings with simple rectangular cross sections. Such extraordinary optical diffraction results from the excitation of localized cavity modes and exists even when the grating period is modulated in a broad range. By modulating the period with binary holography techniques, we can shape an incident wave into arbitrary wavefronts with near-unity conversion efficiencies. To show the efficacy of this approach, we demonstrate three reflection-type metasurfaces for achieving near-complete conversions from a Gaussian beam into a focused beam, Bessel beam, and vortex beam, respectively, with the complete suppression of the undesired specular reflection. Our findings provide a facile approach to build arbitrary wavefront-shaping metasurfaces with wide-angle, broadband, and high efficiency performance.en_AU
dc.description.sponsorshipWeare grateful to the DFG (Deutsche Forschungsgemeinschaft) for financial support.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1359-7345en_AU
dc.identifier.urihttp://hdl.handle.net/1885/270360
dc.language.isoen_AUen_AU
dc.publisherRoyal Society of Chemistryen_AU
dc.rights© 2015 The Royal Society of Chemistryen_AU
dc.sourceChemical Communicationsen_AU
dc.subjectborane derivativeen_AU
dc.subjectboronen_AU
dc.subjectcarbonen_AU
dc.subjecthydrogenen_AU
dc.subjectplatinumen_AU
dc.subjectsodium chlorideen_AU
dc.subjectstilbene derivativeen_AU
dc.subjectchemical structureen_AU
dc.subjectcovalent bonden_AU
dc.subjectcyclizationen_AU
dc.subjectcycloadditionen_AU
dc.subjectdehalogenationen_AU
dc.subjectdiastereoisomeren_AU
dc.subjectenantiomeren_AU
dc.subjecthydroborationen_AU
dc.subjectmolecular stabilityen_AU
dc.subjectproton nucen_AU
dc.titleA facile and selective route to remarkably inert monocyclic NHC-stabilized boriranesen_AU
dc.typeJournal articleen_AU
dcterms.dateAccepted2014-12-02
local.bibliographicCitation.issue9en_AU
local.bibliographicCitation.lastpage1630en_AU
local.bibliographicCitation.startpage1627en_AU
local.contributor.affiliationBraunschweig, Holger, Julius-Maximilians-Universit t Wìrzburgen_AU
local.contributor.affiliationClaes, Christina, Julius-Maximilians-Universitaten_AU
local.contributor.affiliationDamme, Alexander, Julius-Maximilians-Universitaten_AU
local.contributor.affiliationDeisenberger, Andrea, Julius-Maximilians-Universitaten_AU
local.contributor.affiliationDewhurst, Rian, Julius-Maximilians-Universitaten_AU
local.contributor.affiliationHorl, Christian, Julius-Maximilians-Universitaten_AU
local.contributor.affiliationKramer, Thomas, Julius-Maximilians-Universitaten_AU
local.contributor.authoruidDewhurst, Rian, u4040731en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor349999 - Other chemical sciences not elsewhere classifieden_AU
local.identifier.ariespublicationU3488905xPUB23509en_AU
local.identifier.citationvolume51en_AU
local.identifier.doi10.1039/c4cc09036een_AU
local.identifier.scopusID2-s2.0-84921310352
local.identifier.thomsonID000348200100017
local.publisher.urlhttps://pubs.rsc.org/en_AU
local.type.statusPublished Versionen_AU

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