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@article{a03a1d5492164c279c439dd4f7f9e812,
title = "Synthesis and Crystal-Chemical Features of Two New Uranyl Chromates with the Structures Derivedfrom [(UO2)(T6+O4)(H2O)n]0 (T = Cr6+, S6+, Se6+, n = 0–2).",
abstract = "Two new chromates of hexavalent uranium, [C3H10N][(UO2)(CrO4)(NO3)] (1) and [C2H8N]2[(UO2)2· (CrO4)2(Cr2O7)](H2O)2 (2), were prepared by a combination of hydrothermal synthesis and isothermal evaporation. Compounds 1 and 2 crystallize in the triclinic system, space group Р1¯; a = 7.245(3), b = 7.329(3), c = 11.359(4) {\AA}; α = 85.549(6)°, β = 82.547(6)°, γ = 80.174(6)° for 1; a = 7.2063(4), b = 11.5107(7), c = 16.0980(11) {\AA}; α = 70.736(4)°, β = 80.246(4)°, γ = 71.759(4)° for 2. The structures were solved by the direct methods and refined to R1 = 0.064 [for 1495 reflections with Fo > 4σ(Fo)] and 0.047 [for 4529 reflections with Fo > 4σ(Fo)] for 1 and 2, respectively. The crystal structure of 1 is based on [(UO2)(CrO4)(NO3)]– chains between which the isopropylamine molecules are arranged. In the structure of 2, the amine and H2O molecules are localized between the [(UO2)2(CrO4)2(Cr2O7)]2– layers. The uranyl chromate complexes described are derived from [(UO2)(TO4)(H2O)n]0 chains (T = Cr6+, S6+, Se6+, n = 0–2). A b",
author = "Назарчук, {Е. В.} and Сийдра, {О. И.} and Каюков, {Р. А.}",
year = "2016",
doi = "10.1134/S1066362216060023",
language = "English",
volume = "58",
pages = "571--577",
journal = "Radiochemistry",
issn = "1066-3622",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "6",

}

RIS

TY - JOUR

T1 - Synthesis and Crystal-Chemical Features of Two New Uranyl Chromates with the Structures Derivedfrom [(UO2)(T6+O4)(H2O)n]0 (T = Cr6+, S6+, Se6+, n = 0–2).

AU - Назарчук, Е. В.

AU - Сийдра, О. И.

AU - Каюков, Р. А.

PY - 2016

Y1 - 2016

N2 - Two new chromates of hexavalent uranium, [C3H10N][(UO2)(CrO4)(NO3)] (1) and [C2H8N]2[(UO2)2· (CrO4)2(Cr2O7)](H2O)2 (2), were prepared by a combination of hydrothermal synthesis and isothermal evaporation. Compounds 1 and 2 crystallize in the triclinic system, space group Р1¯; a = 7.245(3), b = 7.329(3), c = 11.359(4) Å; α = 85.549(6)°, β = 82.547(6)°, γ = 80.174(6)° for 1; a = 7.2063(4), b = 11.5107(7), c = 16.0980(11) Å; α = 70.736(4)°, β = 80.246(4)°, γ = 71.759(4)° for 2. The structures were solved by the direct methods and refined to R1 = 0.064 [for 1495 reflections with Fo > 4σ(Fo)] and 0.047 [for 4529 reflections with Fo > 4σ(Fo)] for 1 and 2, respectively. The crystal structure of 1 is based on [(UO2)(CrO4)(NO3)]– chains between which the isopropylamine molecules are arranged. In the structure of 2, the amine and H2O molecules are localized between the [(UO2)2(CrO4)2(Cr2O7)]2– layers. The uranyl chromate complexes described are derived from [(UO2)(TO4)(H2O)n]0 chains (T = Cr6+, S6+, Se6+, n = 0–2). A b

AB - Two new chromates of hexavalent uranium, [C3H10N][(UO2)(CrO4)(NO3)] (1) and [C2H8N]2[(UO2)2· (CrO4)2(Cr2O7)](H2O)2 (2), were prepared by a combination of hydrothermal synthesis and isothermal evaporation. Compounds 1 and 2 crystallize in the triclinic system, space group Р1¯; a = 7.245(3), b = 7.329(3), c = 11.359(4) Å; α = 85.549(6)°, β = 82.547(6)°, γ = 80.174(6)° for 1; a = 7.2063(4), b = 11.5107(7), c = 16.0980(11) Å; α = 70.736(4)°, β = 80.246(4)°, γ = 71.759(4)° for 2. The structures were solved by the direct methods and refined to R1 = 0.064 [for 1495 reflections with Fo > 4σ(Fo)] and 0.047 [for 4529 reflections with Fo > 4σ(Fo)] for 1 and 2, respectively. The crystal structure of 1 is based on [(UO2)(CrO4)(NO3)]– chains between which the isopropylamine molecules are arranged. In the structure of 2, the amine and H2O molecules are localized between the [(UO2)2(CrO4)2(Cr2O7)]2– layers. The uranyl chromate complexes described are derived from [(UO2)(TO4)(H2O)n]0 chains (T = Cr6+, S6+, Se6+, n = 0–2). A b

U2 - 10.1134/S1066362216060023

DO - 10.1134/S1066362216060023

M3 - Article

VL - 58

SP - 571

EP - 577

JO - Radiochemistry

JF - Radiochemistry

SN - 1066-3622

IS - 6

ER -

ID: 7607363