Ammonothermal Synthesis and Crystal Structures of Diamminetriamidodizinc Chloride [Zn2(NH3)2(NH2)3]Cl and Diamminemonoamidozinc Bromide [Zn(NH3)2(NH2)]Br
Theresia M. M. Richter,
Sabine Strobel,
Nicolas S. A. Alt,
Eberhard Schlücker,
Rainer Niewa
Affiliations
Theresia M. M. Richter
Institute of Inorganic Chemistry, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany
Sabine Strobel
Institute of Inorganic Chemistry, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany
Nicolas S. A. Alt
Institute of Process Machinery and Systems Engineering, University of Erlangen-Nuremberg, Cauerstraße 4, 91058 Erlangen, Germany
Eberhard Schlücker
Institute of Process Machinery and Systems Engineering, University of Erlangen-Nuremberg, Cauerstraße 4, 91058 Erlangen, Germany
Rainer Niewa
Institute of Inorganic Chemistry, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany
The treatment of excess zinc in the presence of ammonium chloride under ammonothermal conditions of 873 K and 97 MPa leads to diamminetriamidodizinc chloride [Zn2(NH3)2(NH2)3]Cl with a two-dimensionally μ-amido-interconnected substructure. Similar reaction conditions using ammonium bromide instead of the chloride (773 K, 230 MPa) result in diamminemonoamidozinc bromide [Zn(NH3)2(NH2)]Br with one-dimensional infinite μ-amido-bridged chains. Both compounds were obtained as colorless, very moisture sensitive crystals. Crystal structures and hydrogen bond schemes are analyzed. Raman spectroscopic data of the chloride are reported.