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New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations. / Atamas, L.; Klimchuk, O.; Rudzevich, V.; Pirozhenko, V.; Kalchenko, Vik; Smirnov, Igor; Babain, V.; Efremova, T.; Varnek, A.; Wipff, G.; Arnaud-Neu, F.; Roch, M.; Saadioui, M.; Böhmer, V.

в: Journal of Supramolecular Chemistry, Том 2, № 4-5, 01.08.2002, стр. 421-427.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Atamas, L, Klimchuk, O, Rudzevich, V, Pirozhenko, V, Kalchenko, V, Smirnov, I, Babain, V, Efremova, T, Varnek, A, Wipff, G, Arnaud-Neu, F, Roch, M, Saadioui, M & Böhmer, V 2002, 'New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations', Journal of Supramolecular Chemistry, Том. 2, № 4-5, стр. 421-427. https://doi.org/10.1016/S1472-7862(03)00052-2

APA

Atamas, L., Klimchuk, O., Rudzevich, V., Pirozhenko, V., Kalchenko, V., Smirnov, I., Babain, V., Efremova, T., Varnek, A., Wipff, G., Arnaud-Neu, F., Roch, M., Saadioui, M., & Böhmer, V. (2002). New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations. Journal of Supramolecular Chemistry, 2(4-5), 421-427. https://doi.org/10.1016/S1472-7862(03)00052-2

Vancouver

Atamas L, Klimchuk O, Rudzevich V, Pirozhenko V, Kalchenko V, Smirnov I и пр. New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations. Journal of Supramolecular Chemistry. 2002 Авг. 1;2(4-5):421-427. https://doi.org/10.1016/S1472-7862(03)00052-2

Author

Atamas, L. ; Klimchuk, O. ; Rudzevich, V. ; Pirozhenko, V. ; Kalchenko, Vik ; Smirnov, Igor ; Babain, V. ; Efremova, T. ; Varnek, A. ; Wipff, G. ; Arnaud-Neu, F. ; Roch, M. ; Saadioui, M. ; Böhmer, V. / New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations. в: Journal of Supramolecular Chemistry. 2002 ; Том 2, № 4-5. стр. 421-427.

BibTeX

@article{afcd3c3de6dc466cab09bf587f0889c0,
title = "New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations",
abstract = "New calix[4]arene phosphoryl derivatives have been synthesized, starting from a calix[4]arene (cone conformer) bearing four P(O)-H functional groups at the wide rim as synthon. Their binding properties towards trivalent lanthanide and actinide cations are investigated by complexation studies in methanol, and liquid-liquid extraction studies. The carbamoylmethylphosphine oxide and diphosphine dioxide derivatives display the 'calixarene effect', i.e., they are more efficient than their constitutive binding sites. The studies also reveal the importance of the attachment mode of CMPO-functions to the calixarene platform for the cation binding properties.",
keywords = "Actinide, Calixarene, Extraction, Lanthanide, Phosphoryl",
author = "L. Atamas and O. Klimchuk and V. Rudzevich and V. Pirozhenko and Vik Kalchenko and Igor Smirnov and V. Babain and T. Efremova and A. Varnek and G. Wipff and F. Arnaud-Neu and M. Roch and M. Saadioui and V. B{\"o}hmer",
year = "2002",
month = aug,
day = "1",
doi = "10.1016/S1472-7862(03)00052-2",
language = "English",
volume = "2",
pages = "421--427",
journal = "Journal of Supramolecular Chemistry",
issn = "1472-7862",
publisher = "Elsevier",
number = "4-5",

}

RIS

TY - JOUR

T1 - New organophosphorus calix[4]arene ionophores for trivalent lanthanide and actinide cations

AU - Atamas, L.

AU - Klimchuk, O.

AU - Rudzevich, V.

AU - Pirozhenko, V.

AU - Kalchenko, Vik

AU - Smirnov, Igor

AU - Babain, V.

AU - Efremova, T.

AU - Varnek, A.

AU - Wipff, G.

AU - Arnaud-Neu, F.

AU - Roch, M.

AU - Saadioui, M.

AU - Böhmer, V.

PY - 2002/8/1

Y1 - 2002/8/1

N2 - New calix[4]arene phosphoryl derivatives have been synthesized, starting from a calix[4]arene (cone conformer) bearing four P(O)-H functional groups at the wide rim as synthon. Their binding properties towards trivalent lanthanide and actinide cations are investigated by complexation studies in methanol, and liquid-liquid extraction studies. The carbamoylmethylphosphine oxide and diphosphine dioxide derivatives display the 'calixarene effect', i.e., they are more efficient than their constitutive binding sites. The studies also reveal the importance of the attachment mode of CMPO-functions to the calixarene platform for the cation binding properties.

AB - New calix[4]arene phosphoryl derivatives have been synthesized, starting from a calix[4]arene (cone conformer) bearing four P(O)-H functional groups at the wide rim as synthon. Their binding properties towards trivalent lanthanide and actinide cations are investigated by complexation studies in methanol, and liquid-liquid extraction studies. The carbamoylmethylphosphine oxide and diphosphine dioxide derivatives display the 'calixarene effect', i.e., they are more efficient than their constitutive binding sites. The studies also reveal the importance of the attachment mode of CMPO-functions to the calixarene platform for the cation binding properties.

KW - Actinide

KW - Calixarene

KW - Extraction

KW - Lanthanide

KW - Phosphoryl

UR - http://www.scopus.com/inward/record.url?scp=0042442285&partnerID=8YFLogxK

U2 - 10.1016/S1472-7862(03)00052-2

DO - 10.1016/S1472-7862(03)00052-2

M3 - Article

AN - SCOPUS:0042442285

VL - 2

SP - 421

EP - 427

JO - Journal of Supramolecular Chemistry

JF - Journal of Supramolecular Chemistry

SN - 1472-7862

IS - 4-5

ER -

ID: 53581391