Standard

Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters. / Litvinova, Yulia M.; Gayfulin, Yakov M.; Kovalenko, Konstantin A. и др.

в: Inorganic Chemistry, Том 57, № 4, 19.02.2018, стр. 2072-2084.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Litvinova, YM, Gayfulin, YM, Kovalenko, KA, Samsonenko, DG, Van Leusen, J, Korolkov, IV, Fedin, VP & Mironov, YV 2018, 'Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters', Inorganic Chemistry, Том. 57, № 4, стр. 2072-2084. https://doi.org/10.1021/acs.inorgchem.7b02974

APA

Litvinova, Y. M., Gayfulin, Y. M., Kovalenko, K. A., Samsonenko, D. G., Van Leusen, J., Korolkov, I. V., Fedin, V. P., & Mironov, Y. V. (2018). Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters. Inorganic Chemistry, 57(4), 2072-2084. https://doi.org/10.1021/acs.inorgchem.7b02974

Vancouver

Litvinova YM, Gayfulin YM, Kovalenko KA, Samsonenko DG, Van Leusen J, Korolkov IV и др. Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters. Inorganic Chemistry. 2018 февр. 19;57(4):2072-2084. doi: 10.1021/acs.inorgchem.7b02974

Author

Litvinova, Yulia M. ; Gayfulin, Yakov M. ; Kovalenko, Konstantin A. и др. / Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters. в: Inorganic Chemistry. 2018 ; Том 57, № 4. стр. 2072-2084.

BibTeX

@article{52bbc7f45c7f494abd9bf56afafcc9c2,
title = "Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters",
abstract = "The redox-active rhenium octahedral cluster unit [Re6Se8(CN)6]4- was combined with Gd3+ ions and dicarboxylate linkers in novel types of metal-organic frameworks (MOFs) that display a set of functional properties. The hydrolytically stable complexes [{Gd(H2O)3}2(L)Re6Se8(CN)6]·nH2O (1, L = furan-2,5-dicarboxylate, fdc; 2, L = thiophene-2,5-dicarboxylate, tdc) exhibit a 3D framework of trigonal symmetry where 1D chains of [{Gd(H2O)3}2(L)]4+ are connected by [Re6Se8(CN)6]4- clusters. Frameworks contain spacious channels filled with H2O. Solvent molecules can be easily removed under vacuum to produce permanently porous solids with high volumetric CO2 uptake and remarkable CO2/N2 selectivity at room temperature. The frameworks demonstrate an ability for reversible redox transformations of the cluster fragment. The orange powders of compounds 1 and 2 react with Br2, yielding dark-green powders of [{Gd(H2O)3}2(L)Re6Se8(CN)6]Br·nH2O (3, L = fdc; 4, L = tdc). Compounds 3 and 4 are isostructural with 1 and 2 and also have permanently porous frameworks but display different optical, magnetic, and sorption properties. In particular, oxidation of the cluster fragment {"}switches off{"} its luminescence in the red region, and the incorporation of Br- leads to a decrease of the solvent-accessible volume in the channels of 3 and 4. Finally, the green powders of 3 and 4 can be reduced back to the orange powders of 1 and 2 by reaction with hydrazine, thus displaying a rare ability for fully reversible chemical redox transitions. Compounds 1-4 are mentioned as a new class of redox-active cluster-based MOFs with potential usage as multifunctional materials for gas separation and chemical contamination sensors.",
keywords = "BRIDGED RE(6)Q(8) Q, COORDINATION POLYMERS, CARBON-DIOXIDE, CRYSTAL, HYDRAZINE, COMPLEXES, SE, LUMINESCENCE, ADSORPTION, OXIDATION",
author = "Litvinova, {Yulia M.} and Gayfulin, {Yakov M.} and Kovalenko, {Konstantin A.} and Samsonenko, {Denis G.} and {Van Leusen}, Jan and Korolkov, {Ilya V.} and Fedin, {Vladimir P.} and Mironov, {Yuri V.}",
year = "2018",
month = feb,
day = "19",
doi = "10.1021/acs.inorgchem.7b02974",
language = "English",
volume = "57",
pages = "2072--2084",
journal = "Inorganic Chemistry",
issn = "0020-1669",
publisher = "American Chemical Society",
number = "4",

}

RIS

TY - JOUR

T1 - Multifunctional Metal-Organic Frameworks Based on Redox-Active Rhenium Octahedral Clusters

AU - Litvinova, Yulia M.

AU - Gayfulin, Yakov M.

AU - Kovalenko, Konstantin A.

AU - Samsonenko, Denis G.

AU - Van Leusen, Jan

AU - Korolkov, Ilya V.

AU - Fedin, Vladimir P.

AU - Mironov, Yuri V.

PY - 2018/2/19

Y1 - 2018/2/19

N2 - The redox-active rhenium octahedral cluster unit [Re6Se8(CN)6]4- was combined with Gd3+ ions and dicarboxylate linkers in novel types of metal-organic frameworks (MOFs) that display a set of functional properties. The hydrolytically stable complexes [{Gd(H2O)3}2(L)Re6Se8(CN)6]·nH2O (1, L = furan-2,5-dicarboxylate, fdc; 2, L = thiophene-2,5-dicarboxylate, tdc) exhibit a 3D framework of trigonal symmetry where 1D chains of [{Gd(H2O)3}2(L)]4+ are connected by [Re6Se8(CN)6]4- clusters. Frameworks contain spacious channels filled with H2O. Solvent molecules can be easily removed under vacuum to produce permanently porous solids with high volumetric CO2 uptake and remarkable CO2/N2 selectivity at room temperature. The frameworks demonstrate an ability for reversible redox transformations of the cluster fragment. The orange powders of compounds 1 and 2 react with Br2, yielding dark-green powders of [{Gd(H2O)3}2(L)Re6Se8(CN)6]Br·nH2O (3, L = fdc; 4, L = tdc). Compounds 3 and 4 are isostructural with 1 and 2 and also have permanently porous frameworks but display different optical, magnetic, and sorption properties. In particular, oxidation of the cluster fragment "switches off" its luminescence in the red region, and the incorporation of Br- leads to a decrease of the solvent-accessible volume in the channels of 3 and 4. Finally, the green powders of 3 and 4 can be reduced back to the orange powders of 1 and 2 by reaction with hydrazine, thus displaying a rare ability for fully reversible chemical redox transitions. Compounds 1-4 are mentioned as a new class of redox-active cluster-based MOFs with potential usage as multifunctional materials for gas separation and chemical contamination sensors.

AB - The redox-active rhenium octahedral cluster unit [Re6Se8(CN)6]4- was combined with Gd3+ ions and dicarboxylate linkers in novel types of metal-organic frameworks (MOFs) that display a set of functional properties. The hydrolytically stable complexes [{Gd(H2O)3}2(L)Re6Se8(CN)6]·nH2O (1, L = furan-2,5-dicarboxylate, fdc; 2, L = thiophene-2,5-dicarboxylate, tdc) exhibit a 3D framework of trigonal symmetry where 1D chains of [{Gd(H2O)3}2(L)]4+ are connected by [Re6Se8(CN)6]4- clusters. Frameworks contain spacious channels filled with H2O. Solvent molecules can be easily removed under vacuum to produce permanently porous solids with high volumetric CO2 uptake and remarkable CO2/N2 selectivity at room temperature. The frameworks demonstrate an ability for reversible redox transformations of the cluster fragment. The orange powders of compounds 1 and 2 react with Br2, yielding dark-green powders of [{Gd(H2O)3}2(L)Re6Se8(CN)6]Br·nH2O (3, L = fdc; 4, L = tdc). Compounds 3 and 4 are isostructural with 1 and 2 and also have permanently porous frameworks but display different optical, magnetic, and sorption properties. In particular, oxidation of the cluster fragment "switches off" its luminescence in the red region, and the incorporation of Br- leads to a decrease of the solvent-accessible volume in the channels of 3 and 4. Finally, the green powders of 3 and 4 can be reduced back to the orange powders of 1 and 2 by reaction with hydrazine, thus displaying a rare ability for fully reversible chemical redox transitions. Compounds 1-4 are mentioned as a new class of redox-active cluster-based MOFs with potential usage as multifunctional materials for gas separation and chemical contamination sensors.

KW - BRIDGED RE(6)Q(8) Q

KW - COORDINATION POLYMERS

KW - CARBON-DIOXIDE

KW - CRYSTAL

KW - HYDRAZINE

KW - COMPLEXES

KW - SE

KW - LUMINESCENCE

KW - ADSORPTION

KW - OXIDATION

UR - http://www.scopus.com/inward/record.url?scp=85042217303&partnerID=8YFLogxK

U2 - 10.1021/acs.inorgchem.7b02974

DO - 10.1021/acs.inorgchem.7b02974

M3 - Article

C2 - 29400450

AN - SCOPUS:85042217303

VL - 57

SP - 2072

EP - 2084

JO - Inorganic Chemistry

JF - Inorganic Chemistry

SN - 0020-1669

IS - 4

ER -

ID: 10422224