1-D polymers with alternate Cu2 and Ln2 units (Ln = Gd, Er, Y) and carboxylate linkages

Three isostructural Cu2Ln2 1-D polymers [Cu 2Ln2L10(H2O)4· 3H2O]n where Ln = Gd (1), Er (2), and Y (3) and HL= trans-2-butenoic acid, were synthesized and characterized by X-ray crystallography, electron paramagnetic resonance, and magnetic measurements. Pairs of alternate Cu2 and Ln2 dinuclear unit...

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Autor principal: Calvo, R.
Otros Autores: Rapp, R.E, Chagas, E., Sartoris, R.P, Baggio, R., Garland, M.T, Perec, M.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2008
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a copper, 15158-11-9, 7440-50-8; Copper, 7440-50-8; Crotonic Acids; Lanthanoid Series Elements; Ligands; Organometallic Compounds; Polymers 
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100 1 |a Calvo, R. 
245 1 0 |a 1-D polymers with alternate Cu2 and Ln2 units (Ln = Gd, Er, Y) and carboxylate linkages 
260 |c 2008 
270 1 0 |m Calvo, R.; Facultad de Bioquímica Y Ciencias Biológicas, Universidad Nacional del Litoral, INTEC (CONICET-UNL), Güemes 3450, 3000 Santa Fe, Argentina; email: calvo@fbcb.unl.edu.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Three isostructural Cu2Ln2 1-D polymers [Cu 2Ln2L10(H2O)4· 3H2O]n where Ln = Gd (1), Er (2), and Y (3) and HL= trans-2-butenoic acid, were synthesized and characterized by X-ray crystallography, electron paramagnetic resonance, and magnetic measurements. Pairs of alternate Cu2 and Ln2 dinuclear units are combined into a linear array by a set of one covalent η2: η1:μ2 carboxylate oxygen and two H bonds, at Cu⋯Ln distances of ca. 4.5 Å. These units exhibit four η1:η1:μ2 two η2: η1:μ2 carboxylate bridges, respectively. Magnetic measurements between 2 and 300 K, fields B0 = μ0H between 0 and 9 T, and electron paramagnetic resonance (EPR) measurements at the X-band and room temperature are reported. The magnetic susceptibilities indicate bulk antiferromagnetic behavior of the three compounds at low temperatures. Magnetization and EPR data for 1 and 3 allowed evaluation of the exchange couplings between both Cu and Gd ions in their dinuclear units and between Cu and Gd neighbor ions in the spin chains. The data for the isolated Cu2 units in 3 yield gII = 2.350 and g⊥ = 2.054, JCu-Cu = -338 (3) cm-1 for the exchange coupling [Hex(1,2) = -J1-2 S1·S2], and D0 = -0.342 (0.003) cm-1 and E0 = 0.003 (0.001) cm-1 for the zero-field-splitting parameters of the triplet state arising from anisotropic spin-spin interactions. Considering tetranuclear blocks Gd-Cu-Cu-Gd in 1, with the parameters for the Cu2 unit obtained for 3, we evaluated ferromagnetic interactions between Cu and Gd neighbors, JCu-Gd = 13.0 (0.1) cm-1, and between Gd ions in the Gd2 units, JGd-Gd = 0.25 (0.02) cm-1, with gGd = 1.991. The bulk antiferromagnetic behavior of 1 is a consequence of the antiferromagnetic coupling between Cu ions and of the magnitude, |JCu-Gd|, of the Cu-Gd exchange coupling. Compound 2 displays a susceptibility peak at 15 K that may be interpreted as the combined result from antiferromagnetic couplings between ErIII ions in Er 2 units and their coupling with the Cu2 units. © 2008 American Chemical Society.  |l eng 
593 |a Facultad de Bioquímica Y Ciencias Biológicas, Universidad Nacional del Litoral, INTEC (CONICET-UNL), Güemes 3450, 3000 Santa Fe, Argentina 
593 |a Universidade Federal do Rio de Janeiro, CP 68528, Rio de Janeiro 21941-972, RJ, Brazil 
593 |a Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, 1650 San Martín, Buenos Aires, Argentina 
593 |a Facultad de Ciencias Físicas Y Matemáticas, Universidad de Chile, Av. Blanco Encalada 2008, Santiago, Chile 
593 |a INQUIMAE-DQIAQF, Facultad de Ciencias Exactas Y Naturales, Ciudad Universitaria, C1428EHA, Buenos Aires, Argentina 
690 1 0 |a COPPER 
690 1 0 |a CROTONIC ACID DERIVATIVE 
690 1 0 |a LANTHANIDE 
690 1 0 |a LIGAND 
690 1 0 |a ORGANOMETALLIC COMPOUND 
690 1 0 |a POLYMER 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMICAL MODEL 
690 1 0 |a CHEMICAL STRUCTURE 
690 1 0 |a CHEMISTRY 
690 1 0 |a ELECTRON SPIN RESONANCE 
690 1 0 |a HYDROGEN BOND 
690 1 0 |a MAGNETISM 
690 1 0 |a X RAY CRYSTALLOGRAPHY 
690 1 0 |a COPPER 
690 1 0 |a CROTONIC ACIDS 
690 1 0 |a CRYSTALLOGRAPHY, X-RAY 
690 1 0 |a ELECTRON SPIN RESONANCE SPECTROSCOPY 
690 1 0 |a HYDROGEN BONDING 
690 1 0 |a LANTHANOID SERIES ELEMENTS 
690 1 0 |a LIGANDS 
690 1 0 |a MAGNETICS 
690 1 0 |a MODELS, CHEMICAL 
690 1 0 |a MODELS, MOLECULAR 
690 1 0 |a ORGANOMETALLIC COMPOUNDS 
690 1 0 |a POLYMERS 
700 1 |a Rapp, R.E. 
700 1 |a Chagas, E. 
700 1 |a Sartoris, R.P. 
700 1 |a Baggio, R. 
700 1 |a Garland, M.T. 
700 1 |a Perec, M. 
773 0 |d 2008  |g v. 47  |h pp. 10389-10397  |k n. 22  |p Inorg. Chem.  |x 00201669  |w (AR-BaUEN)CENRE-60  |t Inorganic Chemistry 
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856 4 0 |u https://doi.org/10.1021/ic8014089  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00201669_v47_n22_p10389_Calvo  |y Handle 
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