Photo luminescent Lanthanide-Organic Bilayer Networks with 2,3-Pyrazinedicarboxylate and Oxalate
authors Soares-Santos, PCR; Cunha-Silva, L; Paz, FAA; Ferreira, RAS; Rocha, J; Carlos, LD; Nogueira, HIS
nationality International
journal INORGANIC CHEMISTRY
keywords COORDINATION POLYMERS; CRYSTAL-STRUCTURE; MAGNETIC-PROPERTIES; MICROPOROUS METAL; CARBON-DIOXIDE; 2-PYRAZINECARBOXYLIC ACID; MULTIFUNCTIONAL MATERIALS; SILICA NANOPARTICLES; ENERGY-TRANSFER; UP-CONVERSION
abstract The hydrothermal reaction between lanthanide nitrates and 2,3-pyrazinedicarboxylic acid led to a new series of two-dimensional (2D) lanthanide-organic frameworks: [Ln(2)(2,3-pzdc)(2)(ox)(H(2)O(2)](n)[where 2,3-pzdc2 = 2,3-pyrazinedicarboxylate, ox(2-) = oxalate, and Ln(III) = Ce, Nd, Sm, Eu, Gd, Tb, or Er]. The structural details of these materials were determined by single-crystal X-ray diffraction (for Ce(3+) and Nd(3+)) that revealed the formation of a layered structure. Cationic monolayers of if {(2)(infinity)n(2,3-pzdc)(H(2)O](+)} are interconnected via the ox 2 ligand leading to the formation of neutral Ln2(2,3-pzdc)(2)(ox)(H(2)O(2)] bilayer networks; structural cohesion of the crystalline packing is reinforced by the presence of highly directional 0 H " " 0 hydrogen bonds between adjacent bilayers. Under the employed hydrothermal conditions 2,3-pyrazinedicarboxylic acid can be decomposed into ox(2) and 2-pyrazinecarboxylate (2-pzc), as unequivocally proved by the isolation of the discrete complex ITb(2)(2pzO(4)(ox)(H(2)O)(6) ]" (10)H(2)O Single-crystal X-ray diffraction of this latter complex revealed its co-crystallization with an unprecedented (H(2)O)(16) water cluster. Photoluminescence measurements were performed for the Nd3(+), Sm(3+), Eu(3+), and Tb(3+) compounds which show, under UV excitation at room temperature, the Ln(3+) characteristic intra-4f(N) emission peaks. The energy level of the triplet states of 2,3-pyrazinedicarboxylic acid (18939 cm(-1)) and oxalic acid (24570 cm(-1)) was determined from the 12K emission spectrum of the Gd(3+) compound. The (5)D(0) and (3)D(4) lifetime values (0.333 +/- 0.006 and 0.577 +/- 0.017 ms) and the absolute emission guantum yields (0.13 +/- 0.01 and 0.05 +/- 0.01) were determined for the Eu(3+) and Tb(3+) compounds, respectively. For the Eu3+ compound the energy transfer efficiency arising from the ligands' excited states was estimated (0.93 +/- 0.01).
publisher AMER CHEMICAL SOC
issn 0020-1669
year published 2010
volume 49
issue 7
beginning page 3428
ending page 3440
digital object identifier (doi) 10.1021/ic902522j
web of science category Chemistry, Inorganic & Nuclear
subject category Chemistry
unique article identifier WOS:000276073000047
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