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A. V. Ivanova E. L. Gerasimova E. R. Gazizullina K. G. Popova A. I. Matern 《Journal of Analytical Chemistry》2017,72(4):415-420
Infusions of medicinal plants are investigated by potentiometry using a system of K3[Fe(CN)6]/K4[Fe(CN)6]. Models of some flavonoids, phenol carbonic acids, ascorbic acid, and their mixtures are studied. The total polyphenol concentration in these samples is determined by the Folin–Ciocalteu method. Dependences of antioxidant activity on extraction time are obtained. 相似文献
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Dr. Sunewang R. Wang Dr. Merle Arrowsmith Julian Böhnke Prof. Dr. Holger Braunschweig Dr. Theresa Dellermann Dr. Rian D. Dewhurst Hauke Kelch Dr. Ivo Krummenacher James D. Mattock Jonas H. Müssig Torsten Thiess Dr. Alfredo Vargas Dr. Jiji Zhang 《Angewandte Chemie (International ed. in English)》2017,56(27):8009-8013
The diborene 1 was synthesized by reduction of a mixture of 1,2-di-9-anthryl-1,2-dibromodiborane(4) ( 6 ) and trimethylphosphine with potassium graphite. The X-ray structure of 1 shows the two anthryl rings to be parallel and their π(C14) systems perpendicular to the diborene π(B=B) system. This twisted conformation allows for intercalation of the relatively high-lying π(B=B) orbital and the low-lying π* orbital of the anthryl moiety with no significant conjugation, resulting in a small HOMO–LUMO gap (HLG) and ultimately a C−H borylation of the anthryl unit. The HLG of 1 was estimated to be 1.57 eV from the onset of the long wavelength band in its UV/Vis absorption spectrum (THF, λonset=788 nm). The oxidation of 1 with elemental selenium afforded diboraselenirane 8 in quantitative yield. By oxidative abstraction of one phosphine ligand by another equivalent of elemental selenium, the B−B and C1−H bonds of 8 were cleaved to give the cyclic 1,9-diborylanthracene 9 . 相似文献
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Mina Mazzeo Marina Lamberti Ilaria D'Auria Stefano Milione Jonas C. Peters Claudio Pellecchia 《Journal of polymer science. Part A, Polymer chemistry》2010,48(6):1374-1382
New Group 3 metal complexes of the type [LM(CH2SiMe3)2(THF)n] supported by tridentate phosphido‐diphosphine ligands [(o‐C6H4PR2) 2 PH; L1‐H : R = iPr; L2‐H : R = Ph] have been synthesized by reaction of L1‐H and L2‐H with [M(CH2SiMe3)3(THF)2)] (M = Y and Sc). All the new complexes [(o‐C6H4PR2) 2 PM(CH2SiMe3)2(THF)n] [M = Y, R = iPr (1), R = Ph (2); M = Sc, R = iPr (3), R = Ph (4)] were studied as initiators for the ring opening polymerization of lactide. The yttrium complexes ( 1 and 2 ) exhibited high activity and good polymerization control, shown by the linear fits in the plot of number‐averaged molecular weight (Mn) versus the percentage conversion and versus the monomer/initiator ratio and by the low polydispersity index values. Interestingly, very good molar‐mass control was observed even when L ‐Lactide was polymerized in the absence of solvent at 130 °C. A good molar‐mass control but lower activities were observed in the polymerization reaction of lactide promoted by the analogous scandium complexes 3 and 4 . © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1374–1382, 2010 相似文献
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Jonas Sjöstrand 《Journal of Combinatorial Theory, Series A》2007,114(7):1182-1198
We characterise the permutations π such that the elements in the closed lower Bruhat interval [id,π] of the symmetric group correspond to non-taking rook configurations on a skew Ferrers board. It turns out that these are exactly the permutations π such that [id,π] corresponds to a flag manifold defined by inclusions, studied by Gasharov and Reiner.Our characterisation connects the Poincaré polynomials (rank-generating function) of Bruhat intervals with q-rook polynomials, and we are able to compute the Poincaré polynomial of some particularly interesting intervals in the finite Weyl groups An and Bn. The expressions involve q-Stirling numbers of the second kind, and for the group An putting q=1 yields the poly-Bernoulli numbers defined by Kaneko. 相似文献
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