Zobrazeno 1 - 10
of 400
pro vyhledávání: '"Hartmut Bögge"'
Autor:
Stephan Walleck, Thomas Philipp Zimmermann, Henning Hachmeister, Christian Pilger, Thomas Huser, Sagie Katz, Peter Hildebrandt, Anja Stammler, Hartmut Bögge, Eckhard Bill, Thorsten Glaser
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
Iron coordination complexes can be used to gain insight on biologically relevant iron-oxygen compounds generated in iron metalloenzymes. Here, the authors characterise a μ-1,2-hydroperoxo FeIIIFeIII and a μ-1,2-peroxo FeIVFeIII, and study their rea
Externí odkaz:
https://doaj.org/article/e119fe5876634e77868e5b9a13ed59e0
Autor:
Jürgen Schnack, Mihail Atanasov, Hartmut Bögge, Anja Stammler, Stephan Walleck, Eckhard Bill, Thorsten Glaser
Publikováno v:
Chemistry – A European Journal. 27:15240-15251
The first confacial pentaoctahedron comprised of transition metal ions namely ZnII FeIIIA FeIIIB FeIIIA ZnII has been synthesized by using a dinucleating nonadentate ligand. The face-sharing bridging mode enforces short ZnII ⋅⋅⋅FeIIIA and FeIII
Autor:
Ioannis Liratzis, Stephan Walleck, Jan Oldengott, Anja Stammler, Hartmut Bögge, Eckhard Bill, Thorsten Glaser
Publikováno v:
European Journal of Inorganic Chemistry. 26
Autor:
Fridolin L. B. Röhs, Susanne Dammers, Anja Stammler, Jan Oldengott, Hartmut Bögge, Eckhard Bill, Thorsten Glaser
The ligand susan(6-Me) (susan(6-Me) 4,7-dimethyl-1,1,10,10-tetra(6 methyl-2-pyridylmethyl)-1,4,7,10-tetraazadecane) allows the synthesis of a peroxo complex that is only a transient species under catalytic conditions with the closely related ligand s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c3228b5470f50ebfb3ecaa53817dce0
https://doi.org/10.1002/ejic.202200177
https://doi.org/10.1002/ejic.202200177
Autor:
Jasmin Simon, Claudia Horstmann née Gruschka, Andreas Mix, Anja Stammler, Jan Oldengott, Hartmut Bögge, Thorsten Glaser
A family of dinuclear complexes based on 2,7-disubstituted 1,8-naphthalenediol-ligands has been designed to bind covalently to two neighboring phosphate diester groups in the backbone of DNA. The dinuclear Cu-II and Ni-II complexes bind to DNA result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ee5b115b7e7d94afbeff18a45b7a54b
https://pub.uni-bielefeld.de/record/2961103
https://pub.uni-bielefeld.de/record/2961103
Autor:
Felix Depenbrock, Thomas Limpke, Anja Stammler, Jan Oldengott, Hartmut Bögge, Thorsten Glaser
Four dinuclear Co-II complexes have been synthesized and structurally characterized with the dinucleating ligand susan (susan - 4,7-di methyl-1,1,10,10-tetra(2-pyridyl methyl)-1,4,7,1 0tetraazadecane) varying in the exogeneous ligands: [(susan)- {Co-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c901b97f819ba21f9df011a475dc186
https://doi.org/10.1002/ejic.202100992
https://doi.org/10.1002/ejic.202100992
Autor:
Thomas Philipp, Zimmermann, Nicole, Orth, Sebastian, Finke, Thomas, Limpke, Anja, Stammler, Hartmut, Bögge, Stephan, Walleck, Ivana, Ivanović-Burmazović, Thorsten, Glaser
Publikováno v:
Inorganic chemistry. 59(21)
In nature, C-H bond oxidation of CH
Autor:
Antonina Lavrentieva, Claudia Horstmann née Gruschka, Thorsten Glaser, Hartmut Bögge, Sabrina Schwarzbich, Jasmin Simon, Anja Stammler, Gabriele Fischer von Mollard, Alexander Moreth, Thomas Scheper, Christiane Wiegand, Lena Siebe
Publikováno v:
Inorganic chemistry. 59(19)
Cytostatic metallo-drugs mostly bind to the nucleobases of DNA. A new family of dinuclear transition metal complexes was rationally designed to selectively target the phosphate diesters of the DNA backbone by covalent bonding. The synthesis and chara
We have rationally designed a family of dinuclear transition-metal complexes to bind two neighboring phosphate diester groups of DNA. The two metal ions are positioned at the distance of two neighboring phosphate diesters in DNA of 6-7 A by a 1,8-nap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf2a8cc698f2337e4cb9ad345c67d35
https://pub.uni-bielefeld.de/record/2946322
https://pub.uni-bielefeld.de/record/2946322
Autor:
Hartmut Bögge, Thomas Limpke, Sebastian Finke, Thomas Philipp Zimmermann, Nicole Orth, Thorsten Glaser, Ivana Ivanović-Burmazović, Anja Stammler, Stephan Walleck
In nature, C-H bond oxidation of CH4 involves a peroxo intermediate that decays to the high-valent active species of either a "closed" {FeIV(mu-O)2FeIV} core or an "open" {FeIV(O)(mu-O)FeIV(O)} core. To mimic and to obtain more mechanistic insight in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1921f40172c80a8fc1570d680ec049e7
https://doi.org/10.1021/acs.inorgchem.0c02698
https://doi.org/10.1021/acs.inorgchem.0c02698