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81.
Coronado E Gómez-García CJ Nuez A Romero FM Rusanov E Stoeckli-Evans H 《Inorganic chemistry》2002,41(18):4615-4617
The combination of hexacyanoferrate(III) anions, [Fe(CN)(6)](3)(-), with nickel(II) complexes derived from the chiral ligand trans-cyclohexane-1,2-diamine (trans-chxn) affords the enantiopure layered compounds [Ni(trans-(1S,2S)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (1) and [Ni(trans-(1R,2R)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (2). These chiral systems behave as ferromagnets (T(c) = 13.8 K) with a relatively high coercive field (H(c) = 0.17 T) at 2 K. They also exhibit an unusual magnetic behavior at low temperatures that has been attributed to the dynamics of the magnetic domains in the ordered phase. 相似文献
82.
M. P. Sánchez Sánchez J. M. Salas Peregrin M. A. Romero Molina 《Monatshefte für Chemie / Chemical Monthly》1987,118(8-9):883-891
Some news thiopyrimidine derivatives and complexes [4-amino-5-nitroso-6-oxo-1,2,3,6-tetrahydro-2-thio-pyrimidine (TANH), its 2-methylthio derivative (MTH), the ammonium salt ofTANH (sTANH) and six new complexes of formulas: Rh(MT)2Cl · 2H2O, Pd(MTH)2Cl2, Pt(MTH)2Cl4, Au(MTH)Cl3 Pd(TANH)2Cl2 and Au(TAN
–)Cl] have been synthesized and characterized by elemental analysis, IR and1H-NMR spectroscopy techniques. The thermal behaviour of all compounds has also been studied.
Rh(III), Pd(II), Pt(IV) und Au(III) Komplexe von 2-Thiopyrimidin Derivaten
Zusammenfassung Es wurden einige neue Thiopyrimidinderivate und deren Komplexe synthetisiert und mittels Elementaranalyse, IR und1H-NMR charakterisiert: 4-Amino-5-nitroso-6-oxo-1,2,3,6-tetrahydro-2-thio-pyrimidin (TANH), dessen 2-Methylthio-Derivat (MTH), das Ammoniumsalz vonTANH (sTANH) und sechs neue Komplexe der Formeln Rh(MT)2Cl · 2H2O, Pd(MTH)2Cl2, Pt(MTH)2Cl4, Au(MTH)Cl3, Pd(TANH)2Cl2 und Au(TAN –)Cl. Das thermische Verhalten der Verbindungen wurde ebenfalls untersucht.相似文献
83.
L. M. Cabalín D. Romero J. M. Baena J. J. Laserna 《Analytical and bioanalytical chemistry》1999,365(5):404-408
A pulsed Nd?:?YAG laser was used to generate a plasma from stainless steel targets in air at atmospheric pressure. Laser focusing was found to be an important factor in the ablation process. The influence of focal conditions on spatial profiles of plasma, emission intensity and averaged ablation rate (AAR, μm pulse–1) of stainless steel samples as a function of laser energy are discussed. At high energies and depending on laser beam focusing, ablation efficiency tends to decrease compared to that at lower energies. This effect can be due to plasma shielding and air breakdown. The averaged ablation rate was found to be dependent on the thickness of the sample. This effect results in shielding of the incoming laser beam and redeposition of removed material in the crater. By focusing the beam inside the material free expansion of plasma is allowed, resulting in more efficient erosion of the sample at larger energies. For comparative purposes, data on ablated mass per pulse are presented. 相似文献
84.
Tanay Kesharwani Cory Kornman Amanda Tonnaer Amanda Hayes Seoyoung Kim Nikesh Dahal Ralf Romero Andrew Royappa 《Tetrahedron》2018,74(24):2973-2984
A convenient methodology for the synthesis of mono- and di-halogenated benzo[b]thiophenes is described herein, which utilizes copper(II) sulfate pentahydrate and various sodium halides in the presence of substituted 2-alkynylthioanisoles. The proposed method is facile, uses ethanol as a green solvent, and results in uniquely substituted benzo[b]thiophene structures with isolated yields up to 96%. The most useful component of this methodology is the selective introduction of bromine atoms at every available position (2–7) around the benzo[b]thiophene ring, while keeping position 3 occupied by a specific halogen atom such as Cl, Br or I. Aromatic halogens are useful reactive handles; therefore, the selective introduction of halogens at specific positions would be valuable in the targeted synthesis of bioactive molecules and complex organic materials via metal-catalyzed cross coupling reactions. This work is a novel approach towards the synthesis of dihalo substituted benzo[b]thiophene core structures, which provides a superior alternative to the current methods discussed herein. 相似文献
85.
[reaction: see text]. Depending upon the nature of the alkene and allylic substituents, acid-promoted rearrangements of acetals derived from anti allylic diols give 12 or stereoisomeric acyltetrahydrofurans 13. Stereoelectronic effects of the allylic substituents and the extent of bonding in the Prins cyclization transition state are central features of a proposed new model for predicting stereoselection in the Prins-pinacol synthesis of acyltetrahydrofurans. 相似文献
86.
José Gustavo Ávila-Zárraga Ignacio Pérez Erick Beristain Irma Gavilan Moises Romero 《合成通讯》2017,47(4):364-367
Several new 6-(alkylamine)-6H-dibenz[c,e][1,2]oxaphosphinine-6-oxides were prepared through a one-pot reaction, starting with 2-phenylphenol, phosphorus trichloride, and a Zn catalyst, to form 6-chloro-6H-dibenz[c,e][1,2]oxaphosphine. The alkylamine derivatives were subsequently prepared through a nucleophilic substitution reaction involving aliphatic amines and H2O2 oxidation under soft conditions. This method has the advantages that it is a one-pot synthesis, does not require an inert atmosphere, and involves in situ catalyst formation. 相似文献
87.
The environmental contamination of transuranics following the Palomares accident in 1966 (Southern Spain) has been continuous monitored on land and scientific programs are still running. The study of the land to sea transfer of the contamination started in 1986, focussed on the depositional history recorded in marine sediments. At the continental shelf, south of the mouth of the Almanzora river, enhanced levels of plutonium and americium were found which could be related to the accident. Additional analysis of marine sediments, collected far from the impact point, showed the presence of a hot particle. The study of the chronology of this sediment core and the isotopic ratios are given in this paper to assess the origin and pathway of the particle. The route of this particle was found to be the aerial transfer at the time of the accident. 相似文献
88.
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90.
René Guardiola Romero Angel Dago Morales Julio Duque Rodríguez José Fernández Bertrán 《Transition Metal Chemistry》1992,17(6):573-574
The structure of K3(Me4N)3[Co(CN)6]2·3H2O has been determined from three-dimensional X-ray diffraction data. The unit cell is formed by parallel layers of cobalt
octahedra [CoC6] and potassium octahedra, [K(1)N5O(1)], separated byc/2. In each layer both types of octahedra are located alternatively. The [MeN4]+ tetrahedra are located in the cavities between the two layers of octahedra. The crystal structure of this compound is the
first example of its type.
TMC 2483 相似文献