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101.
Raymundo Cea-Olivares Jesús Wingartz Elsa Ríos Jesús Valdés-Martinez 《Monatshefte für Chemie / Chemical Monthly》1990,121(5):377-383
Summary The heterocyclic compounds ClMS2 (CH2)2 (M = As, Sb) are tested by first time as source of starting materials in the synthesis of complexes. The preparation and characterization of heterocyclic dithiocarbamatesR
2NCS2
MS2 (CH2)2, (M = As, Sb;R =Me,Et,i-Pr) is reported. Spectroscopic and analytical data suggest a bidentate behavior of the dithiocarbamate entity and the presence of aMS4 core.
Die Koordinationsfähigkeit der Heterocyclen 1,3-Dithia-2-arsa- und-stiba-cyclopentan gegenüber Schwefel enthaltenden Liganden, I. Dialkyldithiocarbamat-Komplexe
Zusammenfassung Die heterocyclischen Verbindungen ClMS2 (CH2)2 (M = As, Sb) werden erstmals als Quelle für Ausgangsmaterial zur Synthese von Komplexen herangezogen. Es wird über die Herstellung und Charakterisierung der heterocyclischen DithiocarbamateR 2NCS2 MS2 (CH2)2 (M = As, Sb;R =Me,Et,i-Pr) berichtet. Spektroskopische und analytische Daten sprechen für ein bidentates Verhalten der Dithiocarbamat-Einheit und der Präsenz einerMS4-Anordnung im Komplex.相似文献
102.
[reactions: see text] Two complementary and efficient strategies have been developed for the regiospecific synthesis of unsymmetrical indolopyrrolocarbazoles (IPCs) mono-N-substituted with a pentacycle. A halogen in position 2 of the intermediate bisindolylmaleimides 3a-e allows a selective Mitsunobu coupling by exploiting the increased acidity of the 2-chloro-substituted indole nitrogen. It also promotes an easier cyclization of bisindolylmaleimides 4a-e and 7b-e to IPCs. Alkylation of the 2-unsubstituted indole-3-carboxamides 2a,b and further processing to the corresponding IPCs gives access to the opposite regioisomers. 相似文献
103.
Conerney B Jensen P Kruger PE MacGloinn C 《Chemical communications (Cambridge, England)》2003,(11):1274-1275
The synthesis and structural characterisation of a novel C3-symmetric tris-bidentate ligand, L, featuring a triphenylamine core appended by pyridylimine coordination sites is reported: 1H NMR compleximetric titration studies with Ag(I) and ESMS indicate the presence of [Ag3L2]3+ species in solution, consistent with the formation of a trinuclear double helicate complex: the Trinity helix. 相似文献
104.
The evidence for the stabilizing nature of the H–H bonding in planar biphenyl is succinctly reviewed. The stabilizing nature
of the H–H bonding is revealed through a comparison of the atomic energy of every atom in planar biphenyl with the same atom
in the twisted equilibrium structure. It is shown that the barrier to rotation via the planar transition state is the net
resultant of a stabilisation of the four ortho-hydrogen atoms (by 8 kcal/mol each), a stabilisation of the two para-carbon atoms (by 3 kcal/mol each) and by the dominant destabilisation of the two carbon atoms joining the two rings—the two
junction carbon atoms—(by 22 kcal/mol each). The energetic stabilisation of the four ortho-hydrogen atoms is further shown to be in large proportion due to the formation of the hydrogen–hydrogen interatomic surface.
Furthermore, neither the “bond order” between the two junction carbon atoms nor the total electron delocalisation between
the two rings exhibit a significant change in going from the planar to the twisted equilibrium geometry. These findings are
in contrast with the classical view of a balance between “steric non-bonded repulsion” and better electron delocalisation
as a function of the twist dihedral angle. Similar conclusions have been recently reached by Pacios and Gómez through a study
of the electrostatic potential at the position of the hydrogen nuclei.
We dedicate this article to Professor TM Krygowski on the occasion of his 70th birthday wishing him a long and productive
life. 相似文献
105.
Ferreira H Lúcio M Lima JL Matos C Reis S 《Analytical and bioanalytical chemistry》2005,382(5):1256-1264
In this work the interaction of a non-steroidal anti-inflammatory drug (NSAID), diclofenac, with egg yolk phosphatidylcoline (EPC) liposomes, used as cell-membrane models, was quantified by determination of the partition coefficient. The liposome/aqueous phase partition coefficient was determined by derivative spectrophotometry, fluorescence quenching, and measurement of zeta-potential. Theoretical models based on simple partition of the diclofenac between two different media, were used to fit the experimental data, enabling the determination of Kp. The three techniques used yielded similar results. The effects of the interaction on the membranes characteristics were further evaluated, either by studying membrane potential changes or by effects on membrane fluidity. The liposome membrane potential and the size and size-homogeneity of liposomes were measured by light scattering. The effects of diclofenac on the internal viscosity or fluidity of the membrane were determined by use of spectroscopic probes—a series of n-(9-anthroyloxy) fatty acids in which the carboxyl terminal group is located at the interfacial region of the membrane and the fluorescent anthracene group is attached at different positions along the fatty acid chain. The location of the diclofenac on the membrane was also evaluated, by fluorescence quenching using the same series of fluorescent probes. Because the fluorescent anthracene group is attached at different positions along the fatty acid chain, it is possible to label at a graded series of depths in the bilayer. The interactions between the drug and the probe are a means of predicting the location of the drug on the membrane. 相似文献
106.
Córdova A Ibrahem I Casas J Sundén H Engqvist M Reyes E 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(16):4772-4784
Hexose sugars play a fundamental role in vital biochemical processes and their biosynthesis is achieved through enzyme-catalyzed pathways. Herein we disclose the ability of amino acids to catalyze the asymmetric neogenesis of carbohydrates by sequential cross-aldol reactions. The amino acids mediate the asymmetric de novo synthesis of natural L- and D-hexoses and their analogues with excellent stereoselectivity in organic solvents. In some cases, the four new stereocenters are assembled with almost absolute stereocontrol. The unique feature of these results is that, when an amino acid is employed as the catalyst, a single reaction sequence can convert a protected glycol aldehyde into a hexose in one step. For example, proline and its derivatives catalyze the asymmetric neogenesis of allose with >99 % ee in one chemical manipulation. Furthermore, all amino acids tested catalyzed the asymmetric formation of natural sugars under prebiotic conditions, with alanine being the smallest catalyst. The inherent simplicity of this catalytic process suggests that a catalytic prebiotic "gluconeogenesis" may occur, in which amino acids transfer their stereochemical information to sugars. In addition, the amino acid catalyzed stereoselective sequential cross-aldol reactions were performed as a two-step procedure with different aldehydes as acceptors and nucleophiles. The employment of two different amino acids as catalysts for the iterative direct aldol reactions enabled the asymmetric synthesis of deoxysugars with >99 % ee. In addition, the direct amino acid catalyzed C(2)+C(2)+C(2) methodology is a new entry for the short, highly enantioselective de novo synthesis of carbohydrate derivatives, isotope-labeled sugars, and polyketide natural products. The one-pot asymmetric de novo syntheses of deoxy and polyketide carbohydrates involved a novel dynamic kinetic asymmetric transformation (DYKAT) mediated by an amino acid. 相似文献
107.
Lisardo Núñez F. Fraga A. Castro L. Fraga 《Journal of Thermal Analysis and Calorimetry》1998,52(3):1013-1022
The influence of the resin/diamine ratio on the properties of the system diglycidyl ether of bisphenol A (BADGE n=0/m-xylylenediamine)
(m-XDA) was studied. Variation of this ratio resulted in significant effects on the cure kinetics and final dynamic mechanical
properties of the product material.
The study was made in terms of storage modulus (E′), vss modulus (E″) and molecular mass between cross-links (Mc) at different ratios. Two geometries (cylindrical and rectangular) were considered. The influence of temperature was studied
through the activation energy (Ea>), which depends on the epoxy/amine ratio and the geometry of the samples. Glass transition temperatures (Tg>) and glass transition temperatures for thermosets with null degree of conversion (Tgo>) were determined by DSC. Tg> decreases when amounts of curing agent greatly in excess of the stoichiometric composition were used.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
108.
D. Zorrilla Cuenca J. Sánchez Márquez M. Fernández Núñez R. Rodríguez Huertas 《International journal of quantum chemistry》2007,107(4):879-893
This project consists of two parts. In the first part, a series of test calculations is performed to verify that the integrals involved in the determination of atomic and molecular properties by standard self‐consistent field (SCF) methods can be obtained through Halton, Korobov, or Hammersley quasi‐random integration procedures. Through these calculations, we confirm that all three methods lead to results that meet the levels of precision required for their use in the calculation of properties of small atoms or molecules at least at a Hartree–Fock level. Moreover, we have ensured that the efficiency of quasi‐random integration methods that we have tested is Halton=Korobov>Hammersley?pseudo‐random. We also find that these results are comparable to those yielded by ordinary Monte Carlo (pseudo‐random) integration, with a calculation effort of two orders of smaller magnitude. The second part, which would not have been possible without the integration method previously analyzed, contains a first study of atoms constrained in spherical boxes through SCF calculations with basis functions adapted to the features of the problem: Slater‐type orbitals (STOs) trimmed by multiplying them by a function that yields 1 for 0 < r < (R‐δ), polynomial values for (R‐δ) < r < R and null for r > R, R being the radius of the box and δ a variationally determined interval. As a result, we obtain a equation of state for electrons of small systems, valid just in the limit of low temperatures, but fairly simple. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 相似文献
109.
The abilities of both 2,2,6,6-tetramethylpiperidine (I) and its nitroxyl (II) to trap radicals involved in hydrocarbon photo-oxidations have been studied in cumene and 1,3,5-trimethylcyclohexane at 27° using AIBN, hydroperoxide and dialkylperoxide as initiators: the light was either the band 300–400 nm or 366 nm. Under conditions of photolysis of ROOH (degenerate branching), I is oxidized to II. II is capable of trapping R' radicals, the rate constant being ~50 times lower than that for RO.2 formation. RO.2 radicals react with neither I nor II. Under the condition of degenerate branching, II is capable of intercepting the radical fragments from decomposing hydroperoxide. The rate constant of this process is ~500 times higher than that for hydrogen abstraction by these fragments. A reaction mechanism is suggested: hydrogen bonded associates formed between an N-containing stabilizer and ROOH play a dominant role. The principal intermediates in this mechanism are represented by >NO., >NOH and >NOR species. 相似文献
110.
Cuadra P Herrera R Fajardo V 《Journal of photochemistry and photobiology. B, Biology》2004,76(1-3):61-68
Treatment of Jaborosa magellanica with artificial UV-B radiation caused changes in plant growth, plant chemistry and increase DNA polymorphisms. Spectrophotometric analysis showed that UV-B radiation decreases the chlorophylls content, and increases the amount of UV-B absorbing compounds (e.g., phenylpropanoids). Other UV-induced alterations include reduction in leaf area, alterations in plant architecture, and DNA damage. Using random primers and PCR amplification procedure, a high degree of polymorphism was detected when treated plants were compared to non-irradiated plants. These biochemical changes may be interpreted as plant response to UV-B radiation stress and as an indicator of DNA damage. 相似文献