Publications by authors named "M Bracker"

Heptazine derivatives are promising dopants for electroluminescent devices. Recent studies raised the question whether heptazines exhibit a small regular or an inverted singlet-triplet (IST) gap. It was argued that the S ← T reverse intersystem crossing (RISC) is a downhill process in IST emitters and therefore does not require thermal activation, thus enabling efficient harvesting of triplet excitons.

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We present an efficient implementation of nonadiabatic coupling matrix elements (NACMEs) for density functional theory/multireference configuration interaction (DFT/MRCI) wave functions of singlet and triplet multiplicity and an extension of the Vibes program that allows us to determine rate constants for internal conversion (IC) in addition to intersystem crossing (ISC) nonradiative transitions. Following the suggestion of Plasser et al. [J.

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An acridone derivative (-methyl-difluoro-acridone, NMA-dF) is characterized with respect to its utility as an emitter in organic light emitting diodes (OLEDs). Using steady-state and time-resolved spectroscopy as well as quantum chemistry, its ability to convert singlet and triplet excitons into light was scrutinized. NMA-dF emits in the deep blue range of the visible spectrum.

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In an effort to explain the experimentally observed variation of the photocatalytic activity of t Bu 3 P, n Bu 3 P and (MeO) 3 P in the blue-light regime [Helmecke et al., Org. Lett.

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10-Methylisoalloxazine (MIA) and its mono-fluorinated derivatives (6-9F-MIA) were investigated by means of quantum chemistry, looking into the influence of fluorination on fluorescence, absorption and inter-system crossing (ISC). A maximized fluorescence quantum yield (ΦFl) of this chromophore is desirable for application as a potential fluorescence marker in biodiagnostics/photobiological studies. An enhanced triplet quantum yield ΦT on the other hand may open a perspective for photodynamic therapies (PDT) in cancer treatment.

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