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  • Magnetism  (7,282)
  • Matter waves and collective properties of cold atoms and molecules  (3,696)
  • 2015-2019  (5,492)
  • 2010-2014  (5,478)
  • 1995-1999  (8)
  • 1
    Publication Date: 2017-04-04
    Description: The complex magnetic and gravity anomaly fields of the Southern Tyrrhenian Sea provide a record of the complicated properties and evolution of the underlying crust. Geologic interpretation of these anomalies is hindered by the effects of anomaly superposition and source ambiguity inherent to potential field analysis. A common approach to minimizing interpretational ambiguities is to consider analyses of anomaly correlations. Spectral correlation filters are used to separate positively and negatively correlated anomaly features based on the correlation coefficient given by the cosine of the phase difference between common wavenumber components. This procedure is applied to reduced-to-pole magnetic and first vertical derivative gravity anomalies for mapping correlative crustal magnetization and density contrasts. Adding and subtracting the standardized outputs of the filters yield summed (SLFI) and differenced (DLFI) local favorability indices that, respectively highlight positive and negative feature correlations in the anomaly data sets. Correlative maxima mainly reflect volcanic structures, and secondarily intrusive bodies and pre- Tortonian carbonates of the Maghrebian chain and the basement rocks of the Sardinia eastern margin. Correlative minima mostly mark sediment-filled peri-Tyrrhenian structural basins related to the Pliocene extensional tectonics, and intra-slope marine depressions related to post-Pliocene and still-active compressional tectonics off Northern Sicily. Prominent inverse anomaly correlations mainly reflect crustal features around the southern margin of the Tyrrhenian Sea that include higher density, lower magnetization pelagic-to-terrigenous and flysch-type nappes of the Sicilian-Maghrebian chain, as well as lower density, higher magnetization sediments filling depressions of the chain, and syn-rift sediments of Southeastern Sardinia.
    Description: Published
    Description: 27-41
    Description: 3.2. Tettonica attiva
    Description: 3.4. Geomagnetismo
    Description: 5.7. Consulenze in favore di istituzioni nazionali e attività nell'ambito di trattati internazionali
    Description: JCR Journal
    Description: restricted
    Keywords: Magnetism ; Gravity ; Modelling ; Back-arc basin ; Volcanism ; Tectonics ; Tyrrhenian Sea ; 04. Solid Earth::04.02. Exploration geophysics::04.02.99. General or miscellaneous ; 04. Solid Earth::04.05. Geomagnetism::04.05.04. Magnetic anomalies ; 04. Solid Earth::04.07. Tectonophysics::04.07.08. Volcanic arcs ; 04. Solid Earth::04.08. Volcanology::04.08.07. Instruments and techniques
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 2
    ISSN: 0009-2940
    Keywords: Tripod ligands ; Dinuclear cobalt complexes ; Dihydroxynaphthoquinones ; Dihydroxyanthraquinones ; Magnetism ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dinuclear Tripod Cobalt Complexes with Bridging 1,4,5,8-Tetraoxonaphthalene and 1,4,9,10-Tetraoxoanthracene Ligands: Structures, Spectroscopic, Magnetic, and Electrochemical PropertiesThe syntheses, structures, optical, magnetic, and redox properties of dinuclear tripodcobalt(II) complexes [tripod = CH3C(CH2PPh2)3] with briding 1,4,5,8-tetraoxonaphthalene 12- and 1,4,9,10-tetraoxoanthracene 22- are described. UV/Vis/NIR spectroscopy indicates interaction between the ligand and the metal orbitals. The magnetic interactions involving the two cobalt(II) centers and the bridging ligand are characterized by EPR spectroscopy and magnetic measurements and are analyzed in terms of qualitative Molecular Orbital calculations. The redox chemistry of these complexes is investigated by cyclic voltammetry and interpreted as metal-based oxidations and ligand-based reductions.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 547-549 
    ISSN: 1434-1948
    Keywords: Copper ; Trinuclear ; Formamidines ; Magnetism ; Crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In situ reaction of CuII triflate with aminopyridine or aminopyrimidine and triethylorthoformate in ethanol results in unique linear trinuclear CuII complexes with the general formula [Cu3(L-)4](CF3SO3)2(EtOH)x (L = dehydronated ligand N,N′-bis(pyridine-2-yl)formamidine or the new ligand N,N′-bis(pyrimidine-2-yl)formamidine). The structure [Cu-Cu-Cu angle 175.19(2)°] consists of four nearly flat molecules of the ligand which contribute to the propeller-type structure around the Cu-Cu-Cu axis. A strong antiferromagnetic interaction between the CuII ions is observed, resulting in an S = 1/2 ground state below 100 K.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2201-2207 
    ISSN: 1434-1948
    Keywords: Carboxylate syn-anti ; N-centered tripodal ligand ; Manganese ; Imidazole ; Helicoïdal inorganic chiral chain ; Magnetism ; π-π interaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of an infinite inorganic chain consisting of MnII and an N-centered tripodal ligand N,N-(2-pyridylmethyl)[(1-methylimidazol-2-yl)-methyl]glycinate is presented. It exhibits a chiral helical structure with a pitch of two monomeric units (each monomeric unit containing one Mn atom). Each manganese is connected to its neighbor through a carboxylate bridge in a syn-anti geometry. Around each manganese center, two carboxylates bind in a cis geometry. This peculiar bridging geometry (syn-anticis) provides a broken-line chain, running in a zig-zag manner along the b axis of the P21 space group. The magnetic properties have been investigated. They show a pseudo-2D magnetic structure, with one major pathway along the chain and an inter-chain minor one. The intrachain coupling is a weak antiferromagnetic interaction (J/k = -0.25). This low value is entirely consistent with the geometry of the bridge. The interchain coupling is a weaker antiferromagnetic coupling (J′/k = -0.11) and could be mediated through π-π interactions between pyridine and imidazole from two adjacent helixes.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1369-1375 
    ISSN: 1434-1948
    Keywords: Cluster ; Metal-rich antimonides ; Magnetism ; Sb-Sb bonds ; Structure and bonding ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The metal-rich antimonide Zr2V6Sb9 has been prepared by arc-melting of stoichiometric mixtures of Zr, V, and VSb2. Zr2V6Sb9 is the first example of a ternary ordered (filled) variant of the unusual V15Sb18 structure type. In addition to strong metal-antimony bonding, the crystal structure is significantly stabilized by bonding V-V and Sb-Sb interactions, whereas the Zr atoms do not form short metal-metal bonds. Band structure calculations using the Extended Hückel approximation reveal Zr2V6Sb9 being metallic, in agreement with the Pauli paramagnetism experimentally observed.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1434-1948
    Keywords: Copper ; Trinuclear complexes ; Formamidines ; Magnetism ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three new copper(II) linear trinuclear compounds are reported, all of which were synthesized in-situ, with the general formula [Cu3(L)4](CF3SO3)2(Y)x, where L is the dehydronated ligand: N,N′-bis(pyridine-2-yl)formamidine (abbreviated as Hpdf), N,N′-bis(pyrimidine-2-yl)formamidine (abbreviated as Hpmf) and N,N′-bis(5-methylpyridine-2-yl)formamidine (abbreviated as Hmpdf), Y = EtOH or H2O and x = 0.5-1.5. The compounds were characterized by X-ray diffraction, IR, LF, and EPR spectroscopy and by magnetic susceptibility down to 4 K. The structure of the compound [Cu3(pmf)4](CF3SO3)2(H2O)1/2 was determined by X-ray crystallography; it was found to crystallise in the triclinic space group P-1 with a = 8.529(5), b = 15.760(5), c = 19.639(5) Å, α = 101.793(5), β = 101.263(5), γ = 102.389(5)°, Z = 2. The structure [Cu-Cu-Cu angle 174.96(11)°] consists of four nearly flat molecules of the ligand, which contribute to the propeller-type structure around the Cu-Cu-Cu axis. A strong antiferromagnetic interaction between the CuII ions is observed with calculated J values, based on the Hamiltonian H = -2J(S1·S2 + S2·S3) - 2J′·S1·S3, of -174(1) cm-1, -120(1) cm-1, and -167(1) cm-1 for the compounds studied with L = pdf, pmf, and mpdf, respectively. These values are in agreement with an S = 1/2 ground state below temperatures of 120-160 K.
    Additional Material: 5 Ill.
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  • 7
    ISSN: 1434-1948
    Keywords: Crystal structures ; Nickel complexes ; Dinuclear complexes ; Magnetism ; Far-infrared ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ligand bis(2-benzimidazolyl)propane coordinates to NiII with chloride as an anion, thereby forming a dinuclear compound with the formula: [NiCl2(tbz)2]2(C2H6O)2. This compound crystallizes in the space group P21/c. Each five-coordinated NiII ion has a distorted trigonal bipyramidal environment which consist of two asymmetrically bridging Cl anions with distances of 2.3556(17) and 2.4275(16) Å, a terminal Cl anion with a distance of 2.3496(17) Å and two nitrogen atoms of the ligand with distances of 2.022(4) and 2.000(4) Å. The Ni-Ni distance is 3.5891(12) Å, while the Ni-Cl-Ni angle is 97.23(6)°. The magnetic properties of the compound, as studied in the range 5-280 K, have been fitted with a zero-field splitting parameter D (-14.3 cm-1) and a ferromagnetic exchange between the Ni ions in the dinuclear unit (J = +2.5 cm-1). The title compound appears to be the second example for a five-coordinated ferromagnetic dinuclear NiII compound of this type, and its magnetic properties appear to correlate with the ligand structure. With the availability of an increasing number of examples of such species it appears that antiferromagnetic exchange is found for all cases with the chromophore N2ClNiCl2NiClN2 where the MN2 ring is 5-membered. In the case, where this ring is six-membered, the exchange is ferromagnetic.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 432-436 
    ISSN: 0044-2313
    Keywords: Europium ; Bismuth ; Crystal Structure ; Magnetism ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Eu4Bi3: Kristallstruktur, magnetische und elektronische EigenschaftenDas System Eu—Bi enthält die Phasen Eu5Bi3, Eu4Bi3 und Eu11Bi10. Die Strukturen dieser Phasen wurden durch Pulver-Röntgenbeugungsuntersuchungen bestimmt. Kristalle von Eu4Bi3 (kubisch, Raumgruppe I43d; a = 9,920 Å, Z = 4, T = 130 K, R1/wR2 = 4,86/10,84%) wurden in geringer Ausbeute durch Reaktion von Eu, Mn und Bi im molaren Verhältnis 14:1:11 in einer verschlossenen Niobampulle erhalten (Aufheizrate: 30°C/h; Reaktion bei 1050°C, 300 h; Abkühlrate: 100°C/h). Die Kristallstruktur besteht aus [EuBi6]-Oktaedern, wobei Eu zu drei weiteren Eu-Atomen koordiniert ist und ein dreidimensionales Netzwerk aus miteinander verknüpften Ringen bildet. Die Bi-Atome haben 8 Eu-Atome als nächste Nachbarn. Eu4Bi3 kann in hoher Ausbeute durch Umsetzung von stöchiometrischen Mengen der Elemente in einer verschlossenen Tantalampulle bei 1100°C (24 h) erhalten werden. Messungen der magnetischen Suszeptibilität in Abhängigkeit von der Temperatur zeigen antiferromagnetisches Verhalten mit einer Ordnungstemperatur von 18 K. Die Werte gehorchen dem Curie-Weiss-Gesetz mit einem magnetischen Moment von 7,38 μB/Eu, was für zweiwertiges Europium spricht. Widerstandsmessungen in Abhängigkeit von der Temperatur zeigen, daß Eu4Bi3 metallisch ist mit einem Widerstand von 1,3 Ωcm bei Raumtemperatur.
    Notes: The Eu—Bi system contains the phases Eu5Bi3, Eu4Bi3 and Eu11Bi10. The structure types of these phases have been determined by powder X-ray diffraction. Crystals of Eu4Bi3 (cubic, space group I43d; a = 9.920 Å, Z = 4, T = 130 K, R1/wR2 = 4.86/10.84%) were obtained in low yield by reaction of Eu, Mn, and Bi in the ratio 14:1:11 in a closed niobium tube (heating rate 30°C/h; reaction at 1050°C for 300 h, cooling rate 100°C/h). The crystal structure consists of distorted octahedra made up of six Bi coordinated to a central Eu atom. Eu is also coordinated to a three other Eu atoms and forms a three-dimensional network composed of interconnected rings. The Bi atoms are coordinated to eight Eu atoms. High yields of Eu4Bi3 can be prepared by reacting stoichiometric amount of the elements in a sealed tantalum tube at 1100°C for 24 h. Temperature dependent magnetic susceptibility is consistent with antiferromagnetic behavior with an ordering temperature of 18 K. The data could be fit with the Curie-Weiss law and a moment of 7.38 μB/Eu is obtained, consistent with all Eu atoms being Eu11. Temperature dependent resistivity indicates that Eu4Bi3 is a metal with a room temperature resistance of 1.3 Ωcm.
    Additional Material: 4 Ill.
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  • 9
    ISSN: 0044-2313
    Keywords: Octaisopropylchromocene ; Magnetism ; Spin Transition ; Metallocene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Octaisopropylchromocene: The First Chromocene with Gradual low spin/high spin-TransitionOctaisopropylchromocene (1) exists in a low spin state at very low temperatures and undergoes a gradual spin transition on warming up. At 300 K a high spin state with four unpaired electrons has been found for solid 1 by investigation of its magnetic properties.
    Additional Material: 1 Ill.
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  • 10
    Publication Date: 2015-08-11
    Description: Author(s): Simon C. Davenport and Nigel R. Cooper We study a model of a two-dimensional ultracold atomic gas subjected to an “optical flux lattice”: a laser configuration where Raman-dressed atoms experience a strong artificial magnetic field. This leads to a band structure of narrow energy bands with nonzero Chern numbers. We consider the case of … [Phys. Rev. A 92, 023608] Published Mon Aug 10, 2015
    Keywords: Matter waves and collective properties of cold atoms and molecules
    Print ISSN: 1050-2947
    Electronic ISSN: 1094-1622
    Topics: Physics
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