Jasper Nickelsen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jasper Nickelsen has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- David van Gerven
Universität zu Köln Institut für Anorganische Chemie Greinstrasse 6 50939 Köln Germany
2 shared publications - Mathias Siegfried Wickleder
Institut für Anorganische und Materialchemie Universität zu Köln Köln Germany
2 shared publications - Arthur Edelmann
Institut für Anorganische und Materialchemie Universität zu Köln Greinstraße 6 50939 Cologne Germany
1 shared publication - Jörn Bruns
Institut für Chemie Technische Universität Berlin Berlin Germany
1 shared publication - Marios Symeonidis
Institut für Chemie Technische Universität Berlin Berlin Germany
1 shared publication
Latest Publications
- Open Access
- 11 October 2025
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 651 (18)
Synthesis and Crystal Structure of Rb[B(SO 4 ) 2 ]: A Borosulfate Obtained from a Reaction with Chlorosulfuric Acid
The solvothermal reaction of RbCl, boric acid, and chlorosulfuric acid yielded Rb[B(SO 4 ) 2 ]. The crystal structure of Rb[B(SO 4 ) 2 ] (tetragonal, P 4/ ncc, Z = 4, a = 9.1823(3) Å, c = 7.4559(5) Å, V = 628.64(6) Å) is isotypical to the previously published borosulfates A [B(SO 4 ) 2 ] ( A = K , Ag) and exhibits 1D anionic chains of vertex‐connected (SO 4 )‐ and (BO 4 )‐tetrahedra. The product has been obtained phase pure according to powder X‐ray diffraction and subsequent Rietveld refinement.
- 11 October 2025
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 651 (18)
Open AccessSynthesis and Crystal Structure of Rb[B(SO 4 ) 2 ]: A Borosulfate Obtained from a Reaction with Chlorosulfuric Acid
The solvothermal reaction of RbCl, boric acid, and chlorosulfuric acid yielded Rb[B(SO 4 ) 2 ]. The crystal structure of Rb[B(SO 4 ) 2 ] (tetragonal, P 4/ ncc, Z = 4, a = 9.1823(3) Å, c = 7.4559(5) Å, V = 628.64(6) Å) is isotypical to the previously published borosulfates A [B(SO 4 ) 2 ] ( A = K , Ag) and exhibits 1D anionic chains of vertex‐connected (SO 4 )‐ and (BO 4 )‐tetrahedra. The product has been obtained phase pure according to powder X‐ray diffraction and subsequent Rietveld refinement.
- 14 September 2022
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 648 (18)
Front Cover: In situ single crystal growth of tris(trimethylsilyl)phosphate, (Me3SiO)3PO (Z. Anorg. Allg. Chem. 18/2022)
- 14 September 2022
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 648 (18)
Front Cover: In situ single crystal growth of tris(trimethylsilyl)phosphate, (Me3SiO)3PO (Z. Anorg. Allg. Chem. 18/2022)
- Open Access
- 26 July 2022
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 648 (18)
In situ single crystal growth of tris(trimethylsilyl)phosphate, (Me3SiO)3PO
(Me3SiO)3PO has been prepared by the reaction of Na[H2PO4] and (Me3Si)Cl. Crystallization of the liquid was successful using an Optical Heating and Crystallization Device (OHCD) and allow the determination of the crystal structure of the compound (monoclinic, P21, Z=4), a=1016.67(6) pm, b=1053.70(6) pm, c=1759.2(1) pm, β=91.916(2)°, wR2=0.0979). The molecular structure shows the phosphorous atom tetrahedrally coordinated by three (Me3SiO) groups and one oxygen atom. The compound can be seen as a missing link between the related cation and anion [(Me3SiO)4P]+ and [(Me3SiO)2PO2]−, respectively.
- 26 July 2022
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 648 (18)
Open AccessIn situ single crystal growth of tris(trimethylsilyl)phosphate, (Me3SiO)3PO
(Me3SiO)3PO has been prepared by the reaction of Na[H2PO4] and (Me3Si)Cl. Crystallization of the liquid was successful using an Optical Heating and Crystallization Device (OHCD) and allow the determination of the crystal structure of the compound (monoclinic, P21, Z=4), a=1016.67(6) pm, b=1053.70(6) pm, c=1759.2(1) pm, β=91.916(2)°, wR2=0.0979). The molecular structure shows the phosphorous atom tetrahedrally coordinated by three (Me3SiO) groups and one oxygen atom. The compound can be seen as a missing link between the related cation and anion [(Me3SiO)4P]+ and [(Me3SiO)2PO2]−, respectively.