Please use this identifier to cite or link to this item:
http://doi.org/10.25358/openscience-297
Authors: | Förster, Christoph Dorn, Matthias Reuter, Thomas Otto, Sven Davarci, Güllü Reich, Tobias Carrella, Luca Rentschler, Eva Heinze, Katja |
Title: | Ddpd as expanded terpyridine : dramatic effects of symmetry and electronic properties in first row transition metal complexes |
Online publication date: | 7-Nov-2018 |
Year of first publication: | 2018 |
Language: | english |
Abstract: | The 2,2′:6′:2″-terpyridine ligand has literally shaped the coordination chemistry of transition metal complexes in a plethora of fields. Expansion of the ligand bite by amine functionalities between the pyridine units in the tridentate N,N’-dimethyl-N,N’-dipyridine-2-yl-pyridine-2,6-diamine ligand (ddpd) modifies the properties of corresponding transition metal complexes, comprising redox chemistry, molecular dynamics, magnetism and luminescence. The origins of these differences between ddpd and tpy complexes will be elucidated and comprehensively summarized with respect to first row transition metal complexes with d2–d10 electron configurations. Emerging applications of these ddpd complexes complementary to those of the well-known terpyridine ligand will be highlighted. |
DDC: | 540 Chemie 540 Chemistry and allied sciences |
Institution: | Johannes Gutenberg-Universität Mainz |
Department: | FB 09 Chemie, Pharmazie u. Geowissensch. |
Place: | Mainz |
ROR: | https://ror.org/023b0x485 |
DOI: | http://doi.org/10.25358/openscience-297 |
Version: | Published version |
Publication type: | Zeitschriftenaufsatz |
License: | CC BY |
Information on rights of use: | https://creativecommons.org/licenses/by/4.0/ |
Journal: | Inorganics 6 3 |
Pages or article number: | Art. 86 |
Publisher: | MDPI |
Publisher place: | Basel |
Issue date: | 2018 |
ISSN: | 2304-6740 |
Publisher URL: | http://dx.doi.org/10.3390/inorganics6030086 |
Publisher DOI: | 10.3390/inorganics6030086 |
Appears in collections: | JGU-Publikationen |