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Immobilization of 1,2‐cyclohexylenebis(5‐chlorosalicylideneiminato)vanadium dichloride on the magnesium support obtained in the reaction of MgCl2·3.4EtOH with Et2AlCl gives a highly active precursor for ethylene homopolymerization and its copolymerization with 1‐octene. This catalyst exhibits the highest activity in conjunction with MAO, but it is also highly active with AlMe3 as a cocatalyst. On the other hand, when combined with chlorinated alkylaluminum compounds, Et2AlCl and EtAlCl2, it gives traces of polyethylene. Moreover, its catalytic activity is strongly affected by the reaction temperature: it increased with rising polymerization temperature from 20 °C to 60 °C. The kinetic curves obtained for the supported vanadium catalyst, in contrast to its titanium analogue, are of decay type, yet the reduction in the polymerization rate is rather moderate in the early stages of polymerization, and then it is relatively very slow. The vanadium catalyst gives copolymers at a lower yield than the titanium one does, but with the significantly higher 1‐octene content. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 471–478, 2010  相似文献   
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Summary Contact angles for water and diiodomethane drops were measured on the surface of thermally and chemically (by Carbowax 20M bonding) modified porous glasses and on the surface of naphthalene, diphenyl and anthracene. Using the obtained results to a modified Young equation, dispersion and nondispersion components of the surface free energy of these glasses and organic substances were calculated. The work of adhesion (WA) for benzene, naphthalene, diphenyl, anthracene, nitrobenzene was estimated and correlated with the capacity factors, (k′) of these substances. On the basis of experimental and calculated data it can be stated that the thermal treatment of porous glasses increases, their hydrophobicity but the Carbowax layer causes hydrophilicity. There is a linear relationship between k′ and WA which can be helpful for predicting retention data of chromatographed substances on the base of surface free energy which can be calculated from contact angle measurements.  相似文献   
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In a previous paper [1] the complexation behavior of 1,4,8,12-tetraazacyclopentadecane with various anions was studied. This analysis depended on various assumptions involving the accuracy and the interpretation of the experimental data. In this paper these assumptions are examined using pH potentiometry,13C NMR, and conductometric techniques. The validity of each of the assumptions was confirmed.  相似文献   
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The incorporation of a phenanthrene moiety into a porphyrin framework results in the formation of a hybrid macrocycle—phenanthriporphyrin—merging the structural features of polycyclic aromatic hydrocarbons and porphyrins. An antiaromatic aceneporphyrinoid, adopting the trianionic {CCNN} core, is suitable for the incorporation of a phosphorus(V) center to form a hypervalent organophosphorus(V) derivative.  相似文献   
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Sortin1 is a chemical genetic-hit molecule that causes specific mislocalization of plant and yeast-soluble and membrane vacuolar markers. To better understand its mode of action, we designed a Sortin1-hypersensitive screen and identified several Sortin1-hypersensitive and flavonoid-defective mutants. Mechanistically, Sortin1 mimics the effect of the glutathione inhibitor buthionine sulfoximine and alters the vacuolar accumulation of flavonoids, likely blocking their transport through vacuole-localized ABC transporters. Structure-activity relationship studies conducted in Arabidopsis revealed the structural requirements for Sortin1 bioactivity and demonstrated that overlapping Sortin1 substructures can be used to discriminate between vacuolar-flavonoid accumulations and vacuolar-biogenesis defects. We conclude that Sortin1 is a valuable probe for dissecting novel links among flavonoid transport, vacuolar integrity, and the trafficking of vacuolar targeted cargoes in Arabidopsis.  相似文献   
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The aim of the paper is to prove the Main Theorem which says that, in any complex normal variety with an action of a reductive groupG, there are only finitely many subsets which are maximal in the family of all openG-invariant subsets admitting a good quotient. The author is in part supported by Polish KBN Grant 2 PO3A 038 08.  相似文献   
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