0000000001309324
AUTHOR
Gereon Niedner-schatteburg
Transient FTIR spectroscopy after one- and two-colour excitation on a highly luminescent chromium(III) complex.
The development of photoactive transition metal complexes with Earth-abundant metals is a rapidly growing research field, where a deeper understanding of the underlying photophysical processes is of great importance. A multitude of potential applications in the fields of photosensitizing, optical sensing, photoluminescence and photoredox catalysis motivates demanding spectroscopic studies. We applied a series of high-level spectroscopic methods on the previously reported highly luminescent chromium(iii) complex [Cr(ddpd)2](BF4)3 (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine) possessing two near-IR emissive doublet states with microsecond lifetimes. Luminescence measurements…
Strongly Red-Emissive Molecular Ruby [Cr(bpmp)2]3+ Surpasses [Ru(bpy)3]2+
Gaining chemical control over the thermodynamics and kinetics of photoexcited states is paramount to an efficient and sustainable utilization of photoactive transition metal complexes in a plethora of technologies. In contrast to energies of charge transfer states described by spatially separated orbitals, the energies of spin-flip states cannot straightforwardly be predicted as Pauli repulsion and the nephelauxetic effect play key roles. Guided by multireference quantum chemical calculations, we report a novel highly luminescent spin-flip emitter with a quantum chemically predicted blue-shifted luminescence. The spin-flip emission band of the chromium complex [Cr(bpmp)2]3+ (bpmp = 2,6-bis(…
Ultrafast and long-time excited state kinetics of an NIR-emissive vanadium(iii) complex I: synthesis, spectroscopy and static quantum chemistry.
In spite of intense, recent research efforts, luminescent transition metal complexes with Earth-abundant metals are still very rare owing to the small ligand field splitting of 3d transition metal complexes and the resulting non-emissive low-energy metal-centered states. Low-energy excited states decay efficiently non-radiatively, so that near-infrared emissive transition metal complexes with 3d transition metals are even more challenging. We report that the heteroleptic pseudo-octahedral d2-vanadium(iii) complex VCl3(ddpd) (ddpd = N,N′-dimethyl-N,N′-dipyridine-2-yl-pyridine-2,6-diamine) shows near-infrared singlet → triplet spin–flip phosphorescence maxima at 1102, 1219 and 1256 nm with a …
CCDC 1989536: Experimental Crystal Structure Determination
Related Article: Florian Reichenauer, Cui Wang, Christoph Förster, Pit Boden, Naz Ugur, Ricardo Báez-Cruz, Jens Kalmbach, Luca M. Carrella, Eva Rentschler, Charusheela Ramanan, Gereon Niedner-Schatteburg, Markus Gerhards, Michael Seitz, Ute Resch-Genger, Katja Heinze|2021|J.Am.Chem.Soc.|143|11843|doi:10.1021/jacs.1c05971
CCDC 2083757: Experimental Crystal Structure Determination
Related Article: Florian Reichenauer, Cui Wang, Christoph Förster, Pit Boden, Naz Ugur, Ricardo Báez-Cruz, Jens Kalmbach, Luca M. Carrella, Eva Rentschler, Charusheela Ramanan, Gereon Niedner-Schatteburg, Markus Gerhards, Michael Seitz, Ute Resch-Genger, Katja Heinze|2021|J.Am.Chem.Soc.|143|11843|doi:10.1021/jacs.1c05971
CCDC 1989537: Experimental Crystal Structure Determination
Related Article: Florian Reichenauer, Cui Wang, Christoph Förster, Pit Boden, Naz Ugur, Ricardo Báez-Cruz, Jens Kalmbach, Luca M. Carrella, Eva Rentschler, Charusheela Ramanan, Gereon Niedner-Schatteburg, Markus Gerhards, Michael Seitz, Ute Resch-Genger, Katja Heinze|2021|J.Am.Chem.Soc.|143|11843|doi:10.1021/jacs.1c05971