Magnetic Observation of Anion Binding in Iron Coordination Complexes: Toward Spin-Switching Chemosensors

2009 ◽  
Vol 131 (1) ◽  
pp. 32-33 ◽  
Author(s):  
Zhaoping Ni ◽  
Matthew P. Shores
Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3083
Author(s):  
Wisam A. Al Isawi ◽  
Gellert Mezei

Anion binding and extraction from solutions is currently a dynamic research topic in the field of supramolecular chemistry. A particularly challenging task is the extraction of anions with large hydration energies, such as the carbonate ion. Carbonate-binding complexes are also receiving increased interest due to their relevance to atmospheric CO2 fixation. Nanojars are a class of self-assembled, supramolecular coordination complexes that have been shown to bind highly hydrophilic anions and to extract even the most hydrophilic ones, including carbonate, from water into aliphatic solvents. Here we present an expanded nanojar that is able to bind two carbonate ions, thus doubling the previously reported carbonate-binding capacity of nanojars. The new nanojar is characterized by detailed single-crystal X-ray crystallographic studies in the solid state and electrospray ionization mass spectrometric (including tandem MS/MS) studies in solution.


2017 ◽  
Vol 8 (5) ◽  
pp. 3660-3667 ◽  
Author(s):  
Olaf Cussó ◽  
Michael W. Giuliano ◽  
Xavi Ribas ◽  
Scott J. Miller ◽  
Miquel Costas

The combination of peptides and a chiral iron coordination complex catalyzes high yield highly asymmetric epoxidation with aqueous hydrogen peroxide.


Nature ◽  
2014 ◽  
Vol 509 (7500) ◽  
pp. 345-348 ◽  
Author(s):  
Wenkai Zhang ◽  
Roberto Alonso-Mori ◽  
Uwe Bergmann ◽  
Christian Bressler ◽  
Matthieu Chollet ◽  
...  

2018 ◽  
Vol 141 (1) ◽  
pp. 323-333 ◽  
Author(s):  
Zoel Codolà ◽  
Ilaria Gamba ◽  
Ferran Acuña-Parés ◽  
Carla Casadevall ◽  
Martin Clémancey ◽  
...  

2017 ◽  
Vol 53 (6) ◽  
pp. 1029-1032 ◽  
Author(s):  
Basil M. Ahmed ◽  
Gellert Mezei

The use of tethers between ligands allows for the preparation of novel multimetallic complexes, not obtainable without tethers, and leads to unexpected properties, such as selective binding of the carbonate vs. sulfate anion by nanojars.


2013 ◽  
Vol 47 (17) ◽  
pp. 9918-9927 ◽  
Author(s):  
Maite Canals ◽  
Rafael Gonzalez-Olmos ◽  
Miquel Costas ◽  
Anna Company

2010 ◽  
Vol 8 (5) ◽  
pp. 965-991 ◽  
Author(s):  
Milan Melnik ◽  
Mária Kohútová

AbstractThe coordination chemistry of iron covers a wide field, as shown by a survey covering the crystallographic and structural data of almost one thousand and three hundred coordination complexes. About 6.7% of these complexes exist as isomers and are summarized in this review. Included are distortion (96.6%) and cis — trans (3.4%) isomers. These are discussed in terms of the coordination about the iron atom, bond length and interbond angles. Distortion isomers, differing only by degree of distortion in Fe-L, Fe-L-Fe and L-Fe-L parameters, are the most common. Iron is found in the oxidation states zero, +2 and +3 of which +3 is most common. The stereochemistry around iron centers are tetrahedral, five — coordinated (mostly trigonal — bipyramid) and six — coordinated. The most common ligands have O and N donor sites.


2017 ◽  
Vol 8 (1) ◽  
pp. 515-523 ◽  
Author(s):  
Wenkai Zhang ◽  
Kasper S. Kjær ◽  
Roberto Alonso-Mori ◽  
Uwe Bergmann ◽  
Matthieu Chollet ◽  
...  

Optical and X-ray free-electron laser measurements reveal ligand substitution in an Fe(ii)-centered complex extends its MLCT lifetime.


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