том 42 издание 18 страницы 5693-5698

Do Secondary and Tertiary Ammonium Cations Act as Structure-Directing Agents in the Formation of Layered Uranyl Selenites?

Тип публикацииJournal Article
Дата публикации2003-08-12
scimago Q1
wos Q1
БС1
SJR0.928
CiteScore7.6
Impact factor4.7
ISSN00201669, 1520510X
Inorganic Chemistry
Physical and Theoretical Chemistry
Краткое описание
Two new layered uranyl selenites, [C(4)H(12)N(2)](0.5)[UO(2)(HSeO(3))(SeO(3))] (1) and [C(6)H(14)N(2)](0.5)[UO(2)(HSeO(3))(SeO(3))].0.5H(2)O.0.5CH(3)CO(2)H (2), have been isolated from mild hydrothermal reactions. The preparation of 1 was achieved by reacting UO(2)(C(2)H(3)O(2))(2).2H(2)O with H(2)SeO(4) in the presence of piperazine at 130 degrees C for 2 d. Crystals of 2 were synthesized by reacting UO(2)(C(2)H(3)O(2))(2).2H(2)O, H(2)SeO(4), and 1,4-diazabicyclo[2.2.2]octane at 150 degrees C for 2 d. The structure of 1 consists of UO(2)(2+) cations that are bound by bridging HSeO(3)(-) anions and chelating/bridging SeO(3)(2)(-) anions to yield UO(7) pentagonal bipyramids. The joining of the uranyl moieties by the hydrogen selenite and selenite anions creates two-dimensional 2(infinity) [UO(2)(HSeO(3))(SeO(3))](-) layers that extend in the bc-plane. The stereochemically active lone pair of electrons on the HSeO(3)(-) and SeO(3)(2)(-) anions align along the a-axis making each layer polar. The 2(infinity)[UO(2)(HSeO(3))(SeO(3))](-) layers and piperazinium cations stack in a AA'BAA'B sequence where two layers stack on one another without intervening piperazinium cations. While each 2(infinity)[UO(2)(HSeO(3))(SeO(3))](-) layer is polar, in the AA' stacking, the polarity of the second sheet is reversed with respect to the first, yielding an overall structure that is centrosymmetric. The structure of 2 is constructed from uranyl cations that are bound by three bridging SeO(3)(2)(-) and two bridging HSeO(3)(-) anions to create UO(7) pentagonal bipyramids. The linking of the uranyl cations by the HSeO(3)(-) and SeO(3)(2-) anions creates 2(infinity)[UO(2)(HSeO(3))(SeO(3))](-) layers that extend in the ac-plane. In 1 and 2, the organic ammonium cations form hydrogen bonds with the anionic uranyl selenite layers. Crystallographic data: 1, monoclinic, space group P2(1)/c, a = 10.9378(5) A, b = 8.6903(4) A, c = 9.9913(5) A, beta = 90.3040(8) degrees, Z = 4; 2, orthorhombic, space group Pnma, a = 13.0858(8) A, b = 17.555(1) A, c = 10.5984(7) A, Z = 8.
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ГОСТ |
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Almond P. M., Albrecht-Schmitt T. E. Do Secondary and Tertiary Ammonium Cations Act as Structure-Directing Agents in the Formation of Layered Uranyl Selenites? // Inorganic Chemistry. 2003. Vol. 42. No. 18. pp. 5693-5698.
ГОСТ со всеми авторами (до 50) Скопировать
Almond P. M., Albrecht-Schmitt T. E. Do Secondary and Tertiary Ammonium Cations Act as Structure-Directing Agents in the Formation of Layered Uranyl Selenites? // Inorganic Chemistry. 2003. Vol. 42. No. 18. pp. 5693-5698.
RIS |
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TY - JOUR
DO - 10.1021/ic034308d
UR - https://doi.org/10.1021/ic034308d
TI - Do Secondary and Tertiary Ammonium Cations Act as Structure-Directing Agents in the Formation of Layered Uranyl Selenites?
T2 - Inorganic Chemistry
AU - Almond, Philip M.
AU - Albrecht-Schmitt, Thomas E.
PY - 2003
DA - 2003/08/12
PB - American Chemical Society (ACS)
SP - 5693-5698
IS - 18
VL - 42
PMID - 12950219
SN - 0020-1669
SN - 1520-510X
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2003_Almond,
author = {Philip M. Almond and Thomas E. Albrecht-Schmitt},
title = {Do Secondary and Tertiary Ammonium Cations Act as Structure-Directing Agents in the Formation of Layered Uranyl Selenites?},
journal = {Inorganic Chemistry},
year = {2003},
volume = {42},
publisher = {American Chemical Society (ACS)},
month = {aug},
url = {https://doi.org/10.1021/ic034308d},
number = {18},
pages = {5693--5698},
doi = {10.1021/ic034308d}
}
MLA
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Almond, Philip M., and Thomas E. Albrecht-Schmitt. “Do Secondary and Tertiary Ammonium Cations Act as Structure-Directing Agents in the Formation of Layered Uranyl Selenites?.” Inorganic Chemistry, vol. 42, no. 18, Aug. 2003, pp. 5693-5698. https://doi.org/10.1021/ic034308d.