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首页> 外文期刊>Inorganica Chimica Acta >Stabilization of [BiCl_6]~(3-) and [Bi_2Cl _(10)]~(4-) with various organic precursors as cations leading to inorganic-organic supramolecular adducts: Syntheses, crystal structures and properties of [C_5H_7N_2]_3[BiCl _6], [C_5H_7N_2][C_5H _8N_2]
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Stabilization of [BiCl_6]~(3-) and [Bi_2Cl _(10)]~(4-) with various organic precursors as cations leading to inorganic-organic supramolecular adducts: Syntheses, crystal structures and properties of [C_5H_7N_2]_3[BiCl _6], [C_5H_7N_2][C_5H _8N_2]

机译:用各种有机前体作为阳离子稳定[BiCl_6]〜(3-)和[Bi_2Cl _(10)]〜(4-),导致无机有机超分子加合物的合成:[C_5H_7N_2] _3 [BiCl]的合成,晶体结构和性质_6],[C_5H_7N_2] [C_5H _8N_2]

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摘要

Syntheses, crystal structures and properties of three ion pair compounds [C_5H_7N_2]_3[BiCl_6] (1), [C_5H_7N_2][C_5H_8N _2][BiCl_6] (2) and [C_(10)H_(10)N _2]_2[Bi_2Cl_(10)] (3) have been described. Compounds 1 and 2 crystallize in triclinic system (space group, P-1), whereas compound 3 crystallizes in monoclinic sysyem (space group, P2 1/c). In their crystal structures, supramolecular hydrogen bonding interactions between bismuth-chloro anion and organic cation play an important role in the stabilization of [BiCl_6]~(3-) and [Bi _2Cl_(10)]~(4-) anions in the title ion pair compounds. Compounds 1, 2 and 3 are characterized by routine spectral analyses and elemental analyses, besides crystal structure determinations. Compounds 1, 2 and 3 are additionally characterized by thermogravimetric analyses. Compound [C_5H_7N_2][C_5H_8N _2][BiCl_6] (2) exhibits emission spectrum at room temperature in the visible region.
机译:三种离子对化合物[C_5H_7N_2] _3 [BiCl_6](1),[C_5H_7N_2] [C_5H_8N _2] [BiCl_6](2)和[C_(10)H_(10)N _2] _2 []的合成,晶体结构和性质已经描述了Bi_2Cl_(10)](3)。化合物1和2在三斜晶系中结晶(空间组,P-1),而化合物3在单斜系统中结晶(空间组,P2 1 / c)。在其晶体结构中,铋-氯阴离子与有机阳离子之间的超分子氢键相互作用在标题中的[BiCl_6]〜(3-)和[Bi _2Cl_(10)]〜(4-)阴离子的稳定化中起重要作用。离子对化合物。除了确定晶体结构外,还通过常规光谱分析和元素分析来表征化合物1、2和3。化合物1、2和3还通过热重分析来表征。化合物[C_5H_7N_2] [C_5H_8N_2] [BiCl_6](2)在室温下在可见光区显示发射光谱。

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