Diazadiboraacenes: Synthesis, Spectroscopy and Computations

dc.contributor.authorRuhl, Julia
dc.contributor.authorOberhof, Nils
dc.contributor.authorDreuw, Andreas
dc.contributor.authorWegner, Hermann A.
dc.date.accessioned2023-12-07T08:10:23Z
dc.date.available2023-12-07T08:10:23Z
dc.date.issued2023
dc.description.abstractThe incorporation of heteroatoms into hydrocarbon compounds greatly expands the chemical space of molecular materials. In this context, B−N doping takes a center stage due to its isosterism with a C=C-bond. Herein, we present a new and modular synthetic concept to access novel diazadiborabenzo[b]triphenylenes 7 a–h using the B−N doped biradical 16 as intermediate. Characterization of the photophysical properties revealed the emission spectra of the diazadibora benzo[b]triphenylenes 7 a–h can conveniently be tuned by small changes of the substitution on the boron-atom. All of the diazadibora compounds show a short life-time phosphorescence. Additionally, we were able to rationalize the excited-state relaxation of the diazadiboraacene 7 a via intersystem crossing by quantum chemical calculations. The new synthetic strategy provides an elegant route to various novel B−N doped acenes with great potential for applications in molecular materials.
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (DFG); ROR-ID:018mejw64
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/18760
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-18124
dc.language.isoen
dc.rightsNamensnennung - Nicht kommerziell 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subject.ddcddc:540
dc.titleDiazadiboraacenes: Synthesis, Spectroscopy and Computations
dc.typearticle
local.affiliationFB 08 - Biologie und Chemie
local.source.articlenumbere202300785
local.source.journaltitleAngewandte Chemie. International edition
local.source.urihttps://doi.org/10.1002/anie.202300785
local.source.volume62

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