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Hendrik Hans Herrmann

Name	Hendrik Hans Herrmann
Place	Kirchheimbolanden (Geburtsort) Deutschland
Gender	männlich
Academic degree	Dr. (an der Naturwissenschaftlich-Mathematischen Gesamtfakultät der Universität Heidelberg) (2017)
Variant	Hendrik Herrmann
Related	Anorganische Chemie (Studienfach)
Record type	Person
GND-Identifier	1139716093
Record ID	1139716093
Involved in show all Redox‐Active Guanidines with One or Two Guanidino Groups and Their Integration in Low‐Dimensional Perovskite Structures Incorporation of a Redox‐Active Bis (guanidine) in Low‐Dimensional Tin and Lead Iodide Structures Incorporation of a Redox‐Active Bis (guanidine) in Low‐Dimensional Tin and Lead Iodide Structures Hydrogen‐Atom Transfer (HAT) Initiated by Intramolecular Ligand–Metal Electron Transfer Elektronentransfer-Prozesse in Koordinationsverbindungen und Donor-Akzeptor-Materialien mit redoxaktiven Guanidinen Urea Azines (Bisguanidines): Electronic Structure, Redox Properties, and Coordination Chemistry Tetracyanoquinodimethane Reduction by Complexed Guanidinyl‐Functionalized Aromatic Compounds Redox Reactions Between Guanidine Electron Donors and Silver Dicyanamide: Synthesis of C,N Material Precursors and Coordination Polymers Tuning the Properties of Redox‐Active Guanidino‐Functionalized Aromatic Ligands by Substitution: Experiment and Theory Wrapping an Organic Reducing Reagent in a Cationic Boron Complex and Its Use in the Synthesis of Polyhalide Monoanionic Networks

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Hendrik Hans Herrmann

Redox‐Active Guanidines with One or Two Guanidino Groups and Their Integration in Low‐Dimensional Perovskite Structures

Incorporation of a Redox‐Active Bis (guanidine) in Low‐Dimensional Tin and Lead Iodide Structures

Incorporation of a Redox‐Active Bis (guanidine) in Low‐Dimensional Tin and Lead Iodide Structures

Hydrogen‐Atom Transfer (HAT) Initiated by Intramolecular Ligand–Metal Electron Transfer

Elektronentransfer-Prozesse in Koordinationsverbindungen und Donor-Akzeptor-Materialien mit redoxaktiven Guanidinen

Urea Azines (Bisguanidines): Electronic Structure, Redox Properties, and Coordination Chemistry

Tetracyanoquinodimethane Reduction by Complexed Guanidinyl‐Functionalized Aromatic Compounds

Redox Reactions Between Guanidine Electron Donors and Silver Dicyanamide: Synthesis of C,N Material Precursors and Coordination Polymers

Tuning the Properties of Redox‐Active Guanidino‐Functionalized Aromatic Ligands by Substitution: Experiment and Theory

Wrapping an Organic Reducing Reagent in a Cationic Boron Complex and Its Use in the Synthesis of Polyhalide Monoanionic Networks