PubMed Health⌕ Search

Biomedical subjects

Henning A Höppe

Publications and source records attributed to Henning A Höppe.

4 recordsLinked to original sources

Crystal structure, physical properties and HRTEM investigation of the new oxonitridosilicate EuSi2O2N2.

The new layered oxonitridosilicate EuSi(2)O(2)N(2) has been synthesized in a radio-frequency furnace at temperatures of about 1400 degrees C starting from europium(III) oxide (Eu(2)O(3)) and silicon diimide (Si(NH)(2)). The structure of the yellow material has been determined by single-crystal X-ray diffraction analysis (space group P1 (no. 1), a=709.5(1), b=724.6(1), c=725.6(1) pm, alpha=88.69(2), beta=84.77(2), gamma=75.84(2) degrees ,V=360.19(9)x10(6) pm(3), Z=4, R1=0.0631, 4551 independent reflections, 175 parameters). Its anionic Si(2)O(2)N(2) (2-) layers consist of corner-sharing SiON(3) tetrahedra with threefold connecting nitrogen and terminal oxygen atoms. High-resolution transmission electron micrographs indicate both ordered and disordered crystallites as well as twinning. Magnetic susceptibility measurements of EuSi(2)O(2)N(2) exhibit Curie-Weiss behavior above 20 K with an effective magnetic moment of 7.80(5) mu(B) Eu(-1), indicating divalent europium. Antiferromagnetic ordering is detected at 4.5(2) K. EuSi(2)O(2)N(2) shows a field-induced transition with a critical field of 0.50(5) T. The four crystallographically different europium sites cannot be distinguished by (151)Eu Mössbauer spectroscopy. The room-temperature spectrum is fitted by one signal at an isomer shift of delta=-12.3(1) mm s(-1) subject to quadrupole splitting of DeltaE(Q)=-2.3(1) mm s(-1) and an asymmetry parameter of 0.46(3). Luminescence measurements show a narrow emission band with regard to the four crystallographic europium sites with an emission maximum at lambda=575 nm.

Journal Article↗

Transformation of ammonium dicyanamide into dicyandiamide in the solid.

Ammonium dicyanamide NH(4)[N(CN)(2)] was synthesized through aqueous ion exchange. The crystal structure was investigated by single-crystal X-ray diffraction (P2(1)/c, a = 378.67(6) pm, b = 1240.9(3) pm, c = 911.84(14) pm, beta = 91.488(18) degrees, Z = 4). It derives from the CsCl structure type. Medium strong hydrogen bonds between NH(4)(+) and [N(CN)(2)](-) ions are indicative of the observed formation of dicyandiamide H(4)C(2)N(4) during heating. According to DSC and temperature-dependent X-ray powder diffractometry, this isomerization is exothermic and occurs between 102 and 106 degrees C in the solid. The reaction represents the isolobal analogue to the classical synthesis of urea by heating NH(4)OCN. While other alkali and alkaline earth dicyanamides undergo trimerization or polymerization of their anions during heating, ammonium dicyanamide thus shows a different reactivity.

Journal Article↗