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Tuning the spin crossover behavior of the polyanion [(H2O)6Fe3(μ-L)6]6–: the case of the cesium salt
Dalton Trans. 2018, 47, 11895-11902, DOI: 10.1039/C8DT01339J. -
Electrochemically Driven Water-Oxidation Catalysis Beginning with Six Exemplary Cobalt Polyoxometalates: Is It Molecular, Homogeneous Catalysis or Electrode-Bound, Heterogeneous CoOx Catalysis?
J. Am. Chem. Soc. 2018, 140 (38), 12040-12055, DOI: 10.1021/jacs.8b06303. -
Conducting Anilate-Based Mixed-Valence Fe(II)Fe(III) Coordination Polymer: Small-Polaron Hopping Model for Oxalate-Type Fe(II)Fe(III) 2D Networks
J. Am. Chem. Soc. 2018, 140 (39), 12611-12621, DOI: 10.1021/jacs.8b08032. -
A Chiral Bipyrimidine-Bridged Dy2 SMM: A Comparative Experimental and Theoretical Study of the Correlation Between the Distortion of the DyO6N2 Coordination Sphere and the Anisotropy Barrier
GO TO OPEN ACCESS Front. Chem 2018, 6, 537, DOI: 10.3389/fchem.2018.00537. -
Redox tuning the Weakley-type polyoxometalate archetype for the oxygen evolution reaction
Nat. Catal. 2018, 1, 208-213, DOI: 10.1038/s41929-018-0037-1. -
Multiple Halogenation of Aliphatic C−H Bonds within the Hofmann–Löffler Manifold
CHEM-EUR J 2018, 24 (65), 17225-17229, DOI: 10.1002/chem.201804504. -
An Electrophilic Bromine Redox Catalysis for the Synthesis of Indole Alkaloid Building Blocks by Selective Aliphatic C−H Amination
COVER Angew. Chem. Int. Ed. 2018, 57 (48), 15891-15895, DOI: 10.1002/anie.201808939. -
Domino Synthesis of Unsaturated Lactams via Stereoselective Amination of Tertiary Allylic Alcohols
Angew. Chem. Int. Ed. 2018, 57 (51), 16727-16731, DOI: 10.1002/anie.201810160. -
Diversity‐Orientated Stereoselective Synthesis through Pd‐Catalyzed Switchable Decarboxylative C‒N/C‒S Bond Formation in Allylic Surrogates
Chem. Eur. J. 2018, 24, 19156-19161, DOI: 10.1002/chem.201805295.* Among the top 10% most downloaded papers in Chemistry—A European Journal in the 12 months following online publication.
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Switching from Negative-Cooperativity to No-Cooperativity in the Binding of Ion-Pair Dimers by a Bis(calix[4]pyrrole) Macrocycle
J. Org. Chem. 2018, 83 (21), 13507-13514, DOI: 10.1021/acs.joc.8b02449.