A solid dioxygen derivative of phthalocyaninatoiron(II)
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Reference9 articles.
1. Reversible addition of O2, NO, and CO to phthalocyanineiron(II) in concentrated sulphuric acid
2. C. Ercolani, G. Rossi and F. Monacelli, Inorg. Chem., in press.
3. Concentrations ranges and temperature required for reversibility are described in the kinetic study (C. Ercolani, F. Monacelli and G. Rossi, private communication).
4. Binding of dioxygen to iron(II). Reversible behavior in solution
5. Reversible oxygen adduct formation in ferrous complexes derived from a picket fence porphyrin. Model for oxymyoglobin
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2. Iron‐Catalyzed Oxidative C−C Cross‐Coupling Reaction of Tertiary Anilines with Hydroxyarenes by Using Air as Sole Oxidant;Chemistry – A European Journal;2020-02-04
3. Conversion of Olefins into Ketones by an Iron-Catalyzed Wacker-type Oxidation Using Oxygen as the Sole Oxidant;Angewandte Chemie International Edition;2017-12-28
4. Conversion of Olefins into Ketones by an Iron-Catalyzed Wacker-type Oxidation Using Oxygen as the Sole Oxidant;Angewandte Chemie;2017-12-28
5. Single-Atom Bridged Dinuclear Metal Complexes with Emphasis on Phthalocyanine Systems;The Porphyrin Handbook;2003
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