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41.
James D. Korp Ivan Bernal Steven F. Watkins F. R. Fronczek 《Journal of heterocyclic chemistry》1982,19(3):459-462
The molecular structure of 10-(1,3-Dithiolan-2-ylidene)-10H-indeno[1,2-f] -1,2,3,4,5-pentathiepin S7C12H89 has been determined by single crystal X-ray diffraction. The crystals are triclinic, space group PI, with two molecules in a unit cell of dimensions α = 8.931(2), b = 9.387(2), c = 10.175(2) Å, α = 75.73(2), β = 73.35(1), γ = 64.37(2)°. The structure was solved by direct methods, and refined to a final R value of 3.3% for 1925 independent reflections. The molecule consists of an indene core with a nearly co-planar dithiolane and a fused pentasulfide chain. The S5C2 ring is in the chair configuration, with an average S? S distance of 2.052 Å. There is no variation of bond lengths as is frequently seen in multi-sulfur chains. The indenone ring shows no evidence of any delocalization, while the dithiolane ring is disordered at the two methylene positions. No attempt was made to resolve the disorder, since it is frequently seen and has been thoroughly investigated previously. 相似文献
42.
Iliya Bl. Rashkov Ivan Gitsov 《Journal of polymer science. Part A, Polymer chemistry》1984,22(4):905-910
The anionic polymerization of δ-valerolactone initiated by KC24 in xylene or tetrahydrofuran was investigated. The influence of the polymerization conditions on the amount and composition of the oligomers fraction and high polymers formed was tested. Experiments were done with a potassium mirror and benzophenone-potassium as initiators of the polymerization to check the influence of the layered structure of the initiator. It was found that the amount of the oligomers formed under comparable conditions increases in the order KC24 (9%), potassium mirror (22%), benzophenone-potassium (56%). The highest yields of poly(δ-valerolactone) (over 90%) and highest intrinsic viscosities (1.0 dL/g and more) were achieved by the KC24-initiated polymerizations in xylene. 相似文献
43.
Krivovichev SV Kahlenberg V Tananaev IG Kaindl R Mersdorf E Myasoedov BF 《Journal of the American Chemical Society》2005,127(4):1072-1073
A first amine-templated uranyl selenate based upon highly porous uranyl selenate nanotubules, (C4H12N)14[(UO2)10(SeO4)17(H2O)], has been prepared in the room-temperature reaction of uranyl nitrate, butylamine, and H2SeO4 in aqueous solution. The structure consists of nanometer-scale tubular [(UO2)10(SeO4)17(H2O)]14- units packed in a hexagonal-type fashion. The tubules have elliptical cross section with outer dimensions of 25 x 23 A = 2.5 x 2.3 nm. The internal free crystallographic diameter of the tubules is 12.6 A = 1.26 nm, which is comparable to the effective pore size in large-pore zeolites. This finding demonstrates the possibility of nanostructures for actinides in higher oxidation states and opens up a new area of research and exploration. 相似文献
44.
Frederick L. Hedberg Patricia M. Lindley Charles Y-C. Lee Ivan J. Goldfarb 《Journal of polymer science. Part A, Polymer chemistry》1982,20(11):3069-3078
The Synthesis of 3,3′-bis(4-[3-ethynylphenoxy]phenyl)-7,7′-bis(phenylethynyl)-2,2′-diphenyl-6,6′-biquinoxaline (I) was accomplished by the reaction of 2,2′-bis(phenylethynyl)-5,5′-diaminobenzidine (II) and 4-(3-ethynylphenoxy)benzil. Thermal analysis of I indicated a softening temperature of 107°C, followed by an exotherm above 150°C that corresponded to a independent crosslinking reaction of the terminal acetylene groups and an intramolecular cycloaddition (IMC) reaction of the 2,2′-bis(phenylethynyl)biphenyl moieties. In the synthetic work substantial improvements were made in the synthesis of II. The sample of I was cured at 200°C and the maximum partially cured transition temperature attained was 280°C. A sample of 3,3′-bis(4,[3-ethynylphenoxy]phenyl)-2,2′-diphenyl-6,6′-biquinoxaline (IV) was similarly tested as a model without IMC capability and its corresponding value was 250°C. The difference between these two values is discussed briefly. 相似文献
45.
Infrared laser ablation study of pressed soil pellets with inductively coupled plasma atomic emission spectrometry 总被引:1,自引:0,他引:1
Mikolás J Musil P Stuchliková V Novotný K Otruba V Kanický V 《Analytical and bioanalytical chemistry》2002,374(2):244-250
Potential of infrared laser ablation (LA) coupled with ICP-AES as a technique suitable for the determination of trace elements (Zn, Cu, Ni, Cr, and V) in agricultural soils was studied. Operating parameters such as laser beam energy, laser beam focusing with respect to the sample surface, and velocity of the sample translation in the plane perpendicular to the laser beam were optimized. Soil samples were mixed with powdered Ag as a binder, and an internal standard (GeO(2)), and pressed into pellets. Calibration samples were prepared by adding known amounts of oxides of elements of interest into soils of known elemental composition and then processed in the same way as the analyzed samples. Calibration curves were found to be linear at least up to several hundreds of mg kg(-1) for the elements of interest. The elemental contents obtained by using LA-ICP-AES were compared with those obtained by analysis using wet chemistry followed by ICP-AES with pneumatic nebulization (PN). The results were in good agreement. Accuracy was also tested using certified reference soils with a bias not exceeding 10% relative. 相似文献
46.
Darbost U Rager MN Petit S Jabin I Reinaud O 《Journal of the American Chemical Society》2005,127(23):8517-8525
The host-guest properties of calix[6]tren 1 have been evaluated. The receptor is based on a calix[6]arene that is covalently capped at the narrow rim by a tren unit. As a result, the system presents a concave hydrophobic cavity with, at its bottom, a grid-like nitrogenous core. Despite its well-defined cavity and opening to the outside at the large rim, 1 did not behave as a good receptor for neutral molecules in chloroform. However, it exhibited efficient endo-complexation of ammonium guests. By contrast, the per-protonated host, 1.4H(+), behaved as a remarkable receptor for small organic molecules. The complexation is driven by a strong charge-dipole interaction and hydrogen bonds between the polar guest and the tetracationic cap of the calixarene. Finally, coordination of Zn(2+) to the tren core led to the asymmetrization of calixarene cavity and to the strong but selective endo-binding of neutral ligands. This study emphasizes the efficiency of a receptor presenting a concave hydrophobic cavity that is polarized at its bottom. The resulting combination of charge-dipole, hydrogen bonding, CH-pi, and van der Waals interactions highly stabilizes the supramolecular architectures. Also, importantly, the tren cap allows the tuning of the polarization, offering either a basic (1), a highly charged and acidic (1.4H(+)), or a coordination (1.Zn(2+)) site. As a result, the system proved to be highly versatile, tunable, and interconvertible in solution by simple addition of protons, bases, or metal ions. 相似文献
47.
Jaroslav Koutecký 《Theoretical chemistry accounts》1967,8(3):244-248
Approximate pairing properties are proved for the Hartree-Fock solutions for highly symmetric heteroatomic molecules. These molecules have an alternant topology and are built from two kinds of atoms in such a way that by an operation the atoms of one kind go over into the atoms of the second kind and vice versa.
Supported in part by a grant to The Johns Hopkins University from the Petroleum Research Fund of the American Chemical Society. 相似文献
Zusammenfassung Es werden genäherte alternierende Eigenschaften für Hartree-Fock-Lösungen hochsymmetrischer heterocyclischer Moleküle abgeleitet. Diese Moleküle haben eine alternierende Topologie, sie sind aus zwei Sorten von Atomen in solcher Weise aufgebaut, daß die Atome der ersten Sorte in die Atome der zweiten Sorte — und umgekehrt — transformiert werden können.
Résumé Des propriétés d'accouplement orbital approché sont prouvées pour les solutions de type Hartree-Fock des molécules hétéroatomiques hautement symétriques. Ces molécules ont une topologie alternante et sont formées de deux classes d'atomes de telle sorte qu'il existe une opération interchangeant les atomes des deux classes.
Supported in part by a grant to The Johns Hopkins University from the Petroleum Research Fund of the American Chemical Society. 相似文献
48.
The solubility products for some rare earth hydroxides and their temperature dependence have been shown. Greater solubility is shown for larger atomic radii and for lower temperature. 相似文献
49.
Ivan Gutman Sabina Gojak Boris Furtula Slavko Radenkovi? Andrej Vodopivec 《Monatshefte für Chemie / Chemical Monthly》2006,46(2):1127-1138
Within classes of isomeric benzenoid hydrocarbons various Kekulé- and Clar-structure-based parameters (Kekulé structure count, Clar cover count, Herndon number, Zhang–Zhang polynomial) are all mutually correlated. This explains why both the total π-electron energy (E), the Dewar resonance energy (DRE), and the topological resonance energy (TRE) are well correlated with all these parameters. Nevertheless, there exists an optimal value of the variable of the Zhang–Zhang polynomial for which it yields the best results. This optimal value is negative-valued for E, around zero for TRE, and positive-valued for DRE. A somewhat surprising result is that TRE and DRE considerably differ in their dependence on Kekulé- and Clar-structure-based parameters. 相似文献
50.
A protocol has been established for the transformation of chiral ortho 1-hydroxyethyl propenyl benzenes under both anaerobic and oxidative mercury(II) mediated conditions to produce chiral isochromanes. Further transformations of the former products yielded chiral isochromanquinones, while the latter afforded the corresponding chiral 4-hydroxyisochromanquinones. 相似文献