A nonpolar bond to hydrogen vs. lone pair: Incorporation of HPO32- and SeEO32- into a lead perrhenate framework

被引:6
作者
Charkin, Dmitri O. [1 ]
Grishaev, Vasili Yu. [2 ]
Borisov, Artem S. [2 ]
Chachin, Pavel A. [1 ]
Nazarchuk, Evgeni V. [2 ]
Siidra, Oleg I. [2 ,3 ]
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Vorobievy Gory 1-3, Moscow 119991, Russia
[2] St Petersburg State Univ, Dept Crystallog, Inst Earth Sci, Univ Emb 7-9, St Petersburg 199034, Russia
[3] Russian Acad Sci, Kola Sci Ctr, Fersmana Str 14, Apatity 184209, Murmansk Region, Russia
关键词
Lead; Perrhenate; Selenite; Phosphite; Lone pair; CRYSTAL-STRUCTURE; HYDROTHERMAL SYNTHESIS; VIBRATIONAL-SPECTRA; SELENITE; THORIUM; CHLORIDE; ANIONS;
D O I
10.1016/j.jssc.2022.123706
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new lead perrhenate compounds, [Pb-2(ReO4)(2)(SeO3)H2O]H2O (1) and [Pb-2(ReO4)(2)(HPO3)H2O]H2O (2), were prepared by adding selenious or phosphorous acid to boiling concentrated solutions of lead perrhenate. Both compounds adopt the same crystal structure illustrating similar structural impact of lone pair and nonpolar hydrogen bond on one-sided coordination and formation of loose structural architectures. The crystal structure of 1 and 2, which corresponds to a novel structure type, consists of lead-perrhenate double layers interconnected by the selenite or phosphite anions into framework; the channels are filled by water molecules. We briefly discuss the chemistry of compounds containing both regular-shaped and 'lone-pair' or 'inert bond' anions.
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页数:7
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