Abstract

Abstract The novel potassium nickel borate nitrate K7Ni[B18O24(OH)9](NO3)6 ·(H3BO3) was obtained from a simple hydrothermal synthesis in a stainless-steel autoclave at T = 513 K starting with nickel dichloride hexahydrate, and boric and nitric acid with the pH adjusted to 8 by KOH. Single-crystal X-ray diffraction data provided the basis for the structure analysis and refinement. The compound crystallizes in the trigonal space group R3̅ (no. 148) with the lattice parameters a = 1222.29(8) and c = 5478.4(4) pm. Generally, K7Ni[B18O24(OH)9](NO3)6 ·(H3BO3) is comprised of nitrate layers and complex nickel borate layers surrounded by boric acid, nitrate anions, and potassium cations.

Highlights

  • Borates incorporating cations from the transition metal group have long been of interest in our working group

  • The novel potassium nickel borate nitrate K7Ni[B18O24(OH)9](NO3)6 · (H3BO3) was obtained from a simple hydrothermal synthesis in a stainless-steel autoclave at T = 513 K starting with nickel dichloride hexahydrate, and boric and nitric acid with the pH adjusted to 8 by KOH

  • K7Ni[B18O24(OH)9] (NO3)6 · (H3BO3) is comprised of nitrate layers and ­complex nickel borate layers surrounded by boric acid, nitrate anions, and potassium cations

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Summary

Introduction

Borates incorporating cations from the transition metal group have long been of interest in our working group This is especially true for high-pressure/high-temperature conditions as shown by several publications in the last decade. The synthesis conditions could thereby be shifted from high-pressure/high-temperature conditions to ambient pressure in simple stainless-steel autoclaves and glass ampoules. Similar to these syntheses, our group has prepared several new compounds containing borate and nitrate groups like K3Na[B6O9(OH)3]NO3 [12], Na3−xKx[B6O10]NO3 [13], Lu2B2O5(NO3)2 · 2H2O [14], and RE[B5O8(OH)(H2O)x] NO3 · 2H2O [RE = Pr (x = 0.87), Nd (x = 0.85), Sm (x = 0)] [15, 16]. As the title compound could only be synthesized as a side phase, the characterization in this work is only focused on a X-ray single-crystal structure determination

Synthesis
X -ray structure determination
Crystal structure
Conclusion
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