Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2023Red Light Absorption of [ReI(CO)3(α-diimine)Cl] Complexes through Extension of the 4,4′-Bipyrimidine Ligand’s π-System3citations
  • 2021Anatase-wrapped rutile nanorods as an effective electron collector in hybrid photoanodes for vsible light-driven oxygen evolutioncitations

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Chart of shared publication
Sorsche, Dieter
1 / 1 shared
Pannwitz, Andrea
1 / 1 shared
Meitinger, Nicolas
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Mandal, Subrata
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Krivtsov, Igor
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Mundszinger, Manuel
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Mitoraj, Dariusz
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Biskupek, Johannes
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Beránek, Radim
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Gong, Ruihao
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Mengele, Alexander K.
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Kaiser, Ute
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Leiter, Robert
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2023
2021

Co-Authors (by relevance)

  • Sorsche, Dieter
  • Pannwitz, Andrea
  • Meitinger, Nicolas
  • Mandal, Subrata
  • Krivtsov, Igor
  • Mundszinger, Manuel
  • Mitoraj, Dariusz
  • Biskupek, Johannes
  • Beránek, Radim
  • Gong, Ruihao
  • Mengele, Alexander K.
  • Kaiser, Ute
  • Leiter, Robert
OrganizationsLocationPeople

article

Red Light Absorption of [ReI(CO)3(α-diimine)Cl] Complexes through Extension of the 4,4′-Bipyrimidine Ligand’s π-System

  • Sorsche, Dieter
  • Rau, Sven
  • Pannwitz, Andrea
  • Meitinger, Nicolas
  • Mandal, Subrata
Abstract

<jats:p>Rhenium(I) complexes of type [Re(CO)3(NN)Cl] (NN = α-diimine) with MLCT absorption in the orange-red region of the visible spectrum have been synthesized and fully characterized, including single crystal X-ray diffraction on two complexes. The strong bathochromic shift of MLCT absorption was achieved through extension of the π-system of the electron-poor bidiazine ligand 4,4′-bipyrimidine by the addition of fused phenyl rings, resulting in 4,4′-biquinazoline. Furthermore, upon anionic cyclization of the twisted bidiazine, a new 4N-doped perylene ligand, namely, 1,3,10,12-tetraazaperylene, was obtained. Electrochemical characterization revealed a significant stabilization of the LUMO in this series, with the first reduction of the azaperylene found at E1/2(0/−) = −1.131 V vs. Fc+/Fc, which is the most anodic half-wave potential observed for N-doped perylene derivatives so far. The low LUMO energies were directly correlated to the photophysical properties of the respective complexes, resulting in a strongly red-shifted MLCT absorption band in chloroform with a λmax = 586 nm and high extinction coefficients (ε586nm &gt; 5000 M−1 cm−1) ranging above 700 nm in the case of the tetraazaperylene complex. Such low-energy MLCT absorption is highly unusual for Re(I) α-diimine complexes, for which these bands are typically found in the near UV. The reported 1,3,10,12-tetraazaperylene complex displayed the [Re(CO)3(α-diimine)Cl] complex with the strongest MLCT red shift ever reported. UV–Vis NIR spectroelectrochemical investigations gave further insights into the nature and stability of the reduced states. The electron-poor ligands explored herein open up a new path for designing metal complexes with strongly red-shifted absorption, thus enabling photocatalysis and photomedical applications with low-energy, tissue-penetrating red light in future.</jats:p>

Topics
  • impedance spectroscopy
  • single crystal X-ray diffraction
  • single crystal
  • rhenium