Research output: Contribution to journal › Article › peer-review
Metal-organic frameworks based on polynuclear lanthanide complexes and octahedral rhenium clusters. / Litvinova, Yulia M.; Gayfulin, Yakov M.; Van Leusen, Jan et al.
In: Inorganic Chemistry Frontiers, Vol. 6, No. 6, 01.06.2019, p. 1518-1526.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Metal-organic frameworks based on polynuclear lanthanide complexes and octahedral rhenium clusters
AU - Litvinova, Yulia M.
AU - Gayfulin, Yakov M.
AU - Van Leusen, Jan
AU - Samsonenko, Denis G.
AU - Lazarenko, Vladimir A.
AU - Zubavichus, Yan V.
AU - Kögerler, Paul
AU - Mironov, Yuri V.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - The octahedral chalcocyanide cluster anion [Re6S8(CN)6]4- can serve as a metallolinker for the self-assembly of metal-organic frameworks (MOFs) comprising polynuclear lanthanide complexes, which have been illustrated for a series of nine compounds isolated as [{Ln4(μ3-OH)4(ina)4(H2O)n}{Re6S8(CN)6}]·mH2O (Ln = Pr-Er, ina = isonicotinate). Their solid-state framework structures are based on {Ln4(μ3-OH)4}8+ cubane fragments interlinked by isonicotinate and rhenium cyanide clusters. The coordination environment of the lanthanide ions, the coordination numbers and even the number of bridging isonicotinate moieties changes systematically within the lanthanide row, however, the framework topology remains unchanged, confirming the structure-directing role of the rhenium cluster. Structures, magnetochemical properties, luminescence and thermal stability of the new MOFs have been thoroughly analyzed.
AB - The octahedral chalcocyanide cluster anion [Re6S8(CN)6]4- can serve as a metallolinker for the self-assembly of metal-organic frameworks (MOFs) comprising polynuclear lanthanide complexes, which have been illustrated for a series of nine compounds isolated as [{Ln4(μ3-OH)4(ina)4(H2O)n}{Re6S8(CN)6}]·mH2O (Ln = Pr-Er, ina = isonicotinate). Their solid-state framework structures are based on {Ln4(μ3-OH)4}8+ cubane fragments interlinked by isonicotinate and rhenium cyanide clusters. The coordination environment of the lanthanide ions, the coordination numbers and even the number of bridging isonicotinate moieties changes systematically within the lanthanide row, however, the framework topology remains unchanged, confirming the structure-directing role of the rhenium cluster. Structures, magnetochemical properties, luminescence and thermal stability of the new MOFs have been thoroughly analyzed.
KW - COORDINATION POLYMERS
KW - GD
KW - LN
UR - http://www.scopus.com/inward/record.url?scp=85067249651&partnerID=8YFLogxK
U2 - 10.1039/c9qi00339h
DO - 10.1039/c9qi00339h
M3 - Article
AN - SCOPUS:85067249651
VL - 6
SP - 1518
EP - 1526
JO - Inorganic Chemistry Frontiers
JF - Inorganic Chemistry Frontiers
SN - 2052-1545
IS - 6
ER -
ID: 20583813