Efficient Fluorophores Based on Pyridyl-Enolato and Enamido Difluoroboron Complexes: Simple Alternatives to Boron-Dipyrromethene (BODIPY) Dyes

Markus Graser; Holger Kopacka; Klaus Wurst; Markus Rütz; Christoph Kreutz; Thomas Müller; Christa Hirtenlehner; Uwe Monkowius; Günther Knör; Benno Bildstein

doi:10.1016/j.ica.2013.05.034

Efficient Fluorophores Based on Pyridyl-Enolato and Enamido Difluoroboron Complexes: Simple Alternatives to Boron-Dipyrromethene (BODIPY) Dyes

Markus Graser, Holger Kopacka, Klaus Wurst, Markus Rütz, Christoph Kreutz, Thomas Müller, Christa Hirtenlehner, Uwe Monkowius, Günther Knör, Benno Bildstein

Institute of Inorganic Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Simple [N,O] and [N,N]beta-pyridyl or quinolyl enolato/enamido difluoroboron complexes are easily accessible and highly luminescent with good photophysical properties, comparable to BODIPY benchmark dyes. Complete characterization by multinuclear NMR and by single crystal structure analysis as well as pertinent photophysical data are reported.

Original language	English
Pages (from-to)	116-120
Number of pages	5
Journal	Inorganica Chimica Acta
Volume	405
DOIs	https://doi.org/10.1016/j.ica.2013.05.034
Publication status	Published - 2013

Fields of science

103 Physics, Astronomy
104003 Inorganic chemistry
204 Chemical Process Engineering
104016 Photochemistry
104021 Structural chemistry
107 Other Natural Sciences

JKU Focus areas

Nano-, Bio- and Polymer-Systems: From Structure to Function
Engineering and Natural Sciences (in general)

Access to Document

10.1016/j.ica.2013.05.034

Cite this

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title = "Efficient Fluorophores Based on Pyridyl-Enolato and Enamido Difluoroboron Complexes: Simple Alternatives to Boron-Dipyrromethene (BODIPY) Dyes",

abstract = "Simple [N,O] and [N,N]beta-pyridyl or quinolyl enolato/enamido difluoroboron complexes are easily accessible and highly luminescent with good photophysical properties, comparable to BODIPY benchmark dyes. Complete characterization by multinuclear NMR and by single crystal structure analysis as well as pertinent photophysical data are reported.",

author = "Markus Graser and Holger Kopacka and Klaus Wurst and Markus R{\"u}tz and Christoph Kreutz and Thomas M{\"u}ller and Christa Hirtenlehner and Uwe Monkowius and G{\"u}nther Kn{\"o}r and Benno Bildstein",

year = "2013",

doi = "10.1016/j.ica.2013.05.034",

language = "English",

volume = "405",

pages = "116--120",

journal = "Inorganica Chimica Acta",

issn = "1873-3255",

publisher = "Elsevier",

}

TY - JOUR

T1 - Efficient Fluorophores Based on Pyridyl-Enolato and Enamido Difluoroboron Complexes: Simple Alternatives to Boron-Dipyrromethene (BODIPY) Dyes

AU - Graser, Markus

AU - Kopacka, Holger

AU - Wurst, Klaus

AU - Rütz, Markus

AU - Kreutz, Christoph

AU - Müller, Thomas

AU - Hirtenlehner, Christa

AU - Monkowius, Uwe

AU - Knör, Günther

AU - Bildstein, Benno

PY - 2013

Y1 - 2013

N2 - Simple [N,O] and [N,N]beta-pyridyl or quinolyl enolato/enamido difluoroboron complexes are easily accessible and highly luminescent with good photophysical properties, comparable to BODIPY benchmark dyes. Complete characterization by multinuclear NMR and by single crystal structure analysis as well as pertinent photophysical data are reported.

AB - Simple [N,O] and [N,N]beta-pyridyl or quinolyl enolato/enamido difluoroboron complexes are easily accessible and highly luminescent with good photophysical properties, comparable to BODIPY benchmark dyes. Complete characterization by multinuclear NMR and by single crystal structure analysis as well as pertinent photophysical data are reported.

U2 - 10.1016/j.ica.2013.05.034

DO - 10.1016/j.ica.2013.05.034

M3 - Article

SN - 1873-3255

VL - 405

SP - 116

EP - 120

JO - Inorganica Chimica Acta

JF - Inorganica Chimica Acta

ER -