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A test statistic is developed that checks the validity of the extreme value conditions without specifiying the shape parameter of the limiting extreme value distribution. 相似文献
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Beverina L Abbotto A Landenna M Cerminara M Tubino R Meinardi F Bradamante S Pagani GA 《Organic letters》2005,7(19):4257-4260
[graph: see text] Condensation of squaric acid with a number of differently substituted 2-pyrrolyl derivatives afforded three new classes of squaraines. Their sharp and intense absorption bands in the biological window (700-900 nm), inherent singlet oxygen generation capabilities, together with proper functionalization allowing good water solubility make them suitable candidates as new non-porphyrinic singlet oxygen photosensitizers for photodynamic therapy (PDT). 相似文献
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Giampiero Bettinetti Milena Sorrenti Laura Catenacci Franca Ferrari Silvia Rossi Ilaria Salvadeo Paolo Carraro 《Journal of inclusion phenomena and macrocyclic chemistry》2007,57(1-4):329-332
Triacetyl α-cyclodextrin, triacetyl β-cyclodextrin and triacetyl γ-cyclodextrin were tested as possible hydrophobic carriers
to prolong the release of hydrophilic teicoplanin (TCP). Physical–chemical characterization of individual components, drug-carrier
physical mixtures at 0.5, 0.67 and 0.75 mass fraction of carrier, and the respective interaction products by kneading or evaporative
crystallization under microwave irradiation was carried out using differential scanning calorimetry (DSC) and thermogravimetric
analysis (TGA). In vitro drug release in pH 7.4 phosphate buffer at 37 °C was determined by intrinsic dissolution rate (IDR)
measurements on non disintegrating compressed discs. Solid-state interactions of TCP with triacetyl α-cyclodextrin by evaporative
crystallization and kneading and with triacetyl β-cyclodextrin by evaporative crystallization (probably resulting in carrier
amorphization) were demonstrated. The role of carrier hydrophobicity, carrier mass fraction and preparation method of solid
drug-carrier combinations on solid-state drug-carrier interactions and slowing down of TCP release was assessed. Modulation
of drug release can be achieved using TCP-triacetyl γ-cyclodextrin combinations at 0.5 mass fraction of carrier. 相似文献
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Hans-Detlev Gilsing Jürgen Angerer Dietrich Prescher 《Monatshefte für Chemie / Chemical Monthly》2005,1(10):795-801
The synthesis of an oxidative major metabolite of bis(2-ethylhexyl) phthalate is described. The target molecule and its ring-deuterated isomer were obtained via acylation of the appropriate -hydroxy benzyl ester or the corresponding carboxylate with phthalic anhydride or phthalic anhydride-d4. All transformation steps proceed with high yields. 相似文献
30.
Grell D. Grell E. Bugnon P. Dietrich B. Lehn J.-M. 《Journal of Thermal Analysis and Calorimetry》2004,77(2):483-495
The coordination of divalent and monovalent inorganic anions to synthetic polyammonium receptors is investigated in aqueous
solution around neutral pH by titration calorimetry and NMR spectroscopy. High-affinity 1:1 complexes are formed by a pyrrole
type cryptand (1) with sulfate and phosphate, characterized by association constants of almost 107 M-1. Affinities close to 105 M-1 are found for polyazacryptands (3 and 4) exhibiting F-/Cl- selectivity. The binding affinities and the anion selectivities are mainly caused by the charges of ligands and anions, which
is discussed on the basis of simple calculations of the electrostatic contribution to the anion/receptor interactions. The
binding of all investigated anions is exothermic at 298.2 K. The contribution of the large negative ΔH values to the free
energy of anion binding of the pyrrole type ligand is partially compensated by marked negative ΔS values. These unfavorable
entropic contributions are attributed to the additional inclusion of water molecules in the anion/receptor complexes.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献