Unknown

Dataset Information

0

Design, synthesis and characterization of a modular bridging ligand platform for bio-inspired hydrogen production.


ABSTRACT: Synthesis and characterization of a novel type of ambident bridging ligands joining together the functional prerequisites for visible-light absorption, photoinduced electron transfer and catalytic proton reduction is presented. This class of compounds consists of a chromophoric 1,2-diimine-based ?-acceptor site and a rigid polyaromatic dithiolate chelator. Due to the presence of a common conjugated linker moiety with an intrinsic two-electron redox reactivity and a suitable orbital coupling of the subunits, a favourable situation for vectorial multielectron transfer from attached electron donors to a catalytic acceptor site is provided. As an example for the application of this kind of bifunctional ligand systems, a [FeFe]-hydrogenase enzyme model compound is prepared and structurally characterized. Electrocatalytic hydrogen formation with this complex is demonstrated.

SUBMITTER: Topf C 

PROVIDER: S-EPMC4022161 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Design, synthesis and characterization of a modular bridging ligand platform for bio-inspired hydrogen production.

Topf Christoph C   Monkowius Uwe U   Knör Günther G  

Inorganic chemistry communications 20120701 15


Synthesis and characterization of a novel type of ambident bridging ligands joining together the functional prerequisites for visible-light absorption, photoinduced electron transfer and catalytic proton reduction is presented. This class of compounds consists of a chromophoric 1,2-diimine-based π-acceptor site and a rigid polyaromatic dithiolate chelator. Due to the presence of a common conjugated linker moiety with an intrinsic two-electron redox reactivity and a suitable orbital coupling of t  ...[more]

Similar Datasets

| S-EPMC7698539 | biostudies-literature
| S-EPMC9581417 | biostudies-literature
| S-EPMC6335634 | biostudies-literature
| S-EPMC3089944 | biostudies-literature
| S-EPMC6345739 | biostudies-literature
| S-EPMC6915113 | biostudies-literature
| S-EPMC4857079 | biostudies-literature
| S-EPMC5097671 | biostudies-literature
| S-EPMC10161113 | biostudies-literature
| S-EPMC6163941 | biostudies-literature