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Metal‐Chelating N , N ′‐Bis(4‐dimethylaminophenyl)acetamidinyl Radical: A New Chromophore for the Near‐Infrared Region
Author(s) -
Ehret Fabian,
Bubrin Martina,
Záliš Stanislav,
Kaim Wolfgang
Publication year - 2015
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201501875
Subject(s) - chromophore , ruthenium , ligand (biochemistry) , chemistry , infrared , metal , chelation , photochemistry , radical ion , redox , stereochemistry , inorganic chemistry , organic chemistry , catalysis , ion , biochemistry , physics , receptor , optics
A new non‐innocent ligand redox system, N , N ′‐bis(4‐dimethylaminophenyl) substituted acetamidinato/acetamidinyl, has been designed and described by example of structurally and spectroscopically characterized ruthenium complexes. The hitherto unreported ligand is responsible for rather intense and narrow absorptions in the near‐infrared region of the one‐ and two‐electron oxidized forms. The spectroscopic, computational, and first structural characterization of an amidinyl radical complex adds to the list of established N‐based radical ligands.

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