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Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y) : Synthesis and Crystal Structure. / Cherkasova, E. V.; Pervukhina, N. V.; Kuratieva, N. V. и др.

в: Russian Journal of Inorganic Chemistry, Том 64, № 3, 01.03.2019, стр. 329-334.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Cherkasova, EV, Pervukhina, NV, Kuratieva, NV & Cherkasova, TG 2019, 'Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y): Synthesis and Crystal Structure', Russian Journal of Inorganic Chemistry, Том. 64, № 3, стр. 329-334. https://doi.org/10.1134/S0036023619030070

APA

Cherkasova, E. V., Pervukhina, N. V., Kuratieva, N. V., & Cherkasova, T. G. (2019). Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y): Synthesis and Crystal Structure. Russian Journal of Inorganic Chemistry, 64(3), 329-334. https://doi.org/10.1134/S0036023619030070

Vancouver

Cherkasova EV, Pervukhina NV, Kuratieva NV, Cherkasova TG. Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y): Synthesis and Crystal Structure. Russian Journal of Inorganic Chemistry. 2019 март 1;64(3):329-334. doi: 10.1134/S0036023619030070

Author

Cherkasova, E. V. ; Pervukhina, N. V. ; Kuratieva, N. V. и др. / Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y) : Synthesis and Crystal Structure. в: Russian Journal of Inorganic Chemistry. 2019 ; Том 64, № 3. стр. 329-334.

BibTeX

@article{8b0d68aedef14340a79ce2fa4d3acb59,
title = "Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y): Synthesis and Crystal Structure",
abstract = " Double complex salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O, Ln = Lu (I), Ce (II), Y (III), have been synthesized by the reaction between aqueous solutions of Ln(NO 3 ) 3 (Ln = Lu, Ce, Y), K 3 [Cr(NCS) 6 ], and nicotinic acid (C 5 H 5 NCOO). The salts representing light lilac crystalline powders have been studied by chemical analysis, IR spectroscopy, and single-crystal X-ray diffraction. The salts crystallize in monoclinic system, space group P2 1 /n, Z = 4: a = 9.4969(15) {\AA}, b = 25.606(4) {\AA}, c = 15.541(2) {\AA}, β = 107.126(4)°, V = 3624.34 {\AA} 3 , ρ calcd = 1.864 g/cm 3 for I; a = 9.6559(2) {\AA}, b = 25.8492(5) {\AA}, c = 15.5303(3) {\AA}, β = 106.586(1)°, V = 3715.0(1) {\AA} 3 , ρ calcd = 1.756 g/cm 3 for II; and a = 9.5662(7) {\AA}, b = 25.756(2) {\AA}, c = 15.541(1) {\AA}, β = 107.122(2)°, V = 3659.3(4) {\AA} 3 , ρ calcd = 1.690 g/cm 3 for III. The cations in the crystal structures of complexes I–III have a chain polymer structure, and the coordination polyhedron of chromium(III) represents a slightly distorted octahedron. The steric factor has no appreciable effect on the specific features of the crystal structures in the series of lanthanide hexa(isothiocyanato)chromate(III) complexes with nicotinic acid, and the content of crystallization water molecules is varied alone in their composition. ",
keywords = "cerium(III), chromium(III), double complex salt, IR spectroscopy, lutetium(III), nicotinic acid, X-ray structural analysis, yttrium, THERMOLYSIS, LANTHANIDE(III)",
author = "Cherkasova, {E. V.} and Pervukhina, {N. V.} and Kuratieva, {N. V.} and Cherkasova, {T. G.}",
year = "2019",
month = mar,
day = "1",
doi = "10.1134/S0036023619030070",
language = "English",
volume = "64",
pages = "329--334",
journal = "Russian Journal of Inorganic Chemistry",
issn = "0036-0236",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "3",

}

RIS

TY - JOUR

T1 - Double Complex Salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O (Ln = Lu, Ce, Y)

T2 - Synthesis and Crystal Structure

AU - Cherkasova, E. V.

AU - Pervukhina, N. V.

AU - Kuratieva, N. V.

AU - Cherkasova, T. G.

PY - 2019/3/1

Y1 - 2019/3/1

N2 - Double complex salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O, Ln = Lu (I), Ce (II), Y (III), have been synthesized by the reaction between aqueous solutions of Ln(NO 3 ) 3 (Ln = Lu, Ce, Y), K 3 [Cr(NCS) 6 ], and nicotinic acid (C 5 H 5 NCOO). The salts representing light lilac crystalline powders have been studied by chemical analysis, IR spectroscopy, and single-crystal X-ray diffraction. The salts crystallize in monoclinic system, space group P2 1 /n, Z = 4: a = 9.4969(15) Å, b = 25.606(4) Å, c = 15.541(2) Å, β = 107.126(4)°, V = 3624.34 Å 3 , ρ calcd = 1.864 g/cm 3 for I; a = 9.6559(2) Å, b = 25.8492(5) Å, c = 15.5303(3) Å, β = 106.586(1)°, V = 3715.0(1) Å 3 , ρ calcd = 1.756 g/cm 3 for II; and a = 9.5662(7) Å, b = 25.756(2) Å, c = 15.541(1) Å, β = 107.122(2)°, V = 3659.3(4) Å 3 , ρ calcd = 1.690 g/cm 3 for III. The cations in the crystal structures of complexes I–III have a chain polymer structure, and the coordination polyhedron of chromium(III) represents a slightly distorted octahedron. The steric factor has no appreciable effect on the specific features of the crystal structures in the series of lanthanide hexa(isothiocyanato)chromate(III) complexes with nicotinic acid, and the content of crystallization water molecules is varied alone in their composition.

AB - Double complex salts [Ln(C 6 H 5 NO 2 ) 3 (H 2 O) 2 ][Cr(NCS) 6 ] · 2H 2 O, Ln = Lu (I), Ce (II), Y (III), have been synthesized by the reaction between aqueous solutions of Ln(NO 3 ) 3 (Ln = Lu, Ce, Y), K 3 [Cr(NCS) 6 ], and nicotinic acid (C 5 H 5 NCOO). The salts representing light lilac crystalline powders have been studied by chemical analysis, IR spectroscopy, and single-crystal X-ray diffraction. The salts crystallize in monoclinic system, space group P2 1 /n, Z = 4: a = 9.4969(15) Å, b = 25.606(4) Å, c = 15.541(2) Å, β = 107.126(4)°, V = 3624.34 Å 3 , ρ calcd = 1.864 g/cm 3 for I; a = 9.6559(2) Å, b = 25.8492(5) Å, c = 15.5303(3) Å, β = 106.586(1)°, V = 3715.0(1) Å 3 , ρ calcd = 1.756 g/cm 3 for II; and a = 9.5662(7) Å, b = 25.756(2) Å, c = 15.541(1) Å, β = 107.122(2)°, V = 3659.3(4) Å 3 , ρ calcd = 1.690 g/cm 3 for III. The cations in the crystal structures of complexes I–III have a chain polymer structure, and the coordination polyhedron of chromium(III) represents a slightly distorted octahedron. The steric factor has no appreciable effect on the specific features of the crystal structures in the series of lanthanide hexa(isothiocyanato)chromate(III) complexes with nicotinic acid, and the content of crystallization water molecules is varied alone in their composition.

KW - cerium(III)

KW - chromium(III)

KW - double complex salt

KW - IR spectroscopy

KW - lutetium(III)

KW - nicotinic acid

KW - X-ray structural analysis

KW - yttrium

KW - THERMOLYSIS

KW - LANTHANIDE(III)

UR - http://www.scopus.com/inward/record.url?scp=85065257800&partnerID=8YFLogxK

U2 - 10.1134/S0036023619030070

DO - 10.1134/S0036023619030070

M3 - Article

AN - SCOPUS:85065257800

VL - 64

SP - 329

EP - 334

JO - Russian Journal of Inorganic Chemistry

JF - Russian Journal of Inorganic Chemistry

SN - 0036-0236

IS - 3

ER -

ID: 20163740