Structural, Magnetic, and Redox Diversity of First-Row Transition Metal Complexes of a Pyridine-Based Macrocycle: Well-Marked Trends Supported by Theoretical DFT Calculations-Reference-Cited by-同舟云学术

Structural, Magnetic, and Redox Diversity of First-Row Transition Metal Complexes of a Pyridine-Based Macrocycle: Well-Marked Trends Supported by Theoretical DFT Calculations

Published:2015-03-11 Issue:7 Volume:54 Page:3352-3369
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Drahoš Bohuslav¹,Herchel Radovan¹,Trávníček Zdeněk¹

Affiliation:

1. Department of Inorganic Chemistry, Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacký University, 17. listopadu 12, CZ-771 46 Olomouc, Czech Republic

Funder

Ministry of Education, Youth and Sports

Czech Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic503054m

Reference96 articles.

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2. Seven-co-ordination in metal complexes of quinquedentate macrocyclic ligands. Part 7. Synthesis and properties of some manganese(II), iron(III), iron(II), zinc(II), and cadmium(II) complexes of an N3O2 macrocycle and the crystal and molecular structure of {2,13-dimethyl-6,9-dioxa-3,12,18-triazabicyclo[12.3.1]octadeca-1(18),2,12,14,16-pentaene}di-isothiocyanatomanganese(II)