Expansion and adaptation of the M5B12O25(OH) structure type to incorporate di- and trivalent transition metal cations

被引:2
作者
Pasqualini, Leonard C. [1 ]
Tribus, Martina [2 ]
Huppertz, Hubert [1 ]
机构
[1] Univ Innsbruck, Dept Gen Inorgan & Theoret Chem, Innrain 80-82, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Dept Mineral & Petrog, Innrain 52, A-6020 Innsbruck, Austria
来源
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES | 2024年 / 79卷 / 01期
关键词
high-pressure synthesis; borate; transition metal; crystal structure; BOND-VALENCE PARAMETERS; HIGH-PRESSURE SYNTHESIS; CRYSTAL-STRUCTURE;
D O I
10.1515/znb-2023-0082
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Five transition metal borates were synthesized in a Walker-type module under high-pressure/high-temperature conditions of 8-9 GPa and 800-1200 degrees C. They all exhibit the same interpenetrating, anionic borate network B12O2616-, crystallizing in the space group I4(1)/acd, and therefore show high similarities to the borates Ti5B12O26 and Ga5B12O25(OH). Cr5B12O25(OH) and V5B12O25(OH) are isotypic to Ga5B12O25(OH), whereas Mn5Mn0.83B12O26 and Fe5Fe0.14B12O24.3(OH)(1.7) feature the partial occupation of an additional, cuboctahedral cavity in the structure. This is due to a partial reduction of the cations to the oxidation state +2, as presented with the novel compound Mn5MnB12O22(OH)(4), which only features Mn2+ for charge compensation. These structures feature a twelvefold coordination of manganese and iron.
引用
收藏
页码:39 / 49
页数:11
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