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941.
942.
A series of six chemically treated and untreated fumed silicas with increasing particle size (ranging from the nano- to the micrometer size) was prepared. Surface areas (and morphologies) and surface energies were determined by nitrogen adsorption and inverse gas chromatography, respectively. The adsorption of a series of PDMS with different and well-defined molecular weights was studied at different polymer concentrations. Amounts of adsorbed polymer were determined by gravimetry and the energies of adsorption were assessed by flow-microcalorimetry. Results are discussed in terms of particle surface energy and morphology effects on the conformation and the inter-connectivity of adsorbed polymer molecules.  相似文献   
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A facile nonaqueous synthetic route to methylaluminoxane (MAO) by heating a mixture of benzophenone and trimethylaluminium (TMA) is described. The MAO prepared such reveals to be an efficient activator of metallocenes and late transition metal complexes for ethylene polymerization. The [TMA]/[benzophenone] ratio used for the preparation of MAO is shown to have a dramatic effect on the catalytic activity as well as the molecular weight distribution of the resulting polyethylenes.  相似文献   
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948.
A new strategy for the synthesis of vinyl type macrocyclic polymers of controlled molecular weight and molecular weight distribution has been investigated. It involves the direct coupling of an α-ω-heterodifunctional linear polymer precursor previously prepared by living polymerization. The cyclization is achieved under high dilution, by an appropriate activation of one of the polymer-ends in order to allow its reaction with the other end function. Its application to the preparation of polystyrenes and poly(vinyl ether)s with a macrocyclic structure, as well as ring closure mechanisms in the presence of different cyclization agents are reported.  相似文献   
949.
The endocannabinoidome (expanded endocannabinoid system, eCBome)-gut microbiome (mBIome) axis plays a fundamental role in the control of energy intake and processing. The liver-expressed antimicrobial peptide 2 (LEAP2) is a recently identified molecule acting as an antagonist of the ghrelin receptor and hence a potential effector of energy metabolism, also at the level of the gastrointestinal system. Here we investigated the role of the eCBome-gut mBIome axis in the control of the expression of LEAP2 in the liver and, particularly, the intestine. We confirm that the small intestine is a strong contributor to the circulating levels of LEAP2 in mice, and show that: (1) intestinal Leap2 expression is profoundly altered in the liver and small intestine of 13 week-old germ-free (GF) male mice, which also exhibit strong alterations in eCBome signaling; fecal microbiota transfer (FMT) from conventionally raised to GF mice completely restored normal Leap2 expression after 7 days from this procedure; in 13 week-old female GF mice no significant change was observed; (2) Leap2 expression in organoids prepared from the mouse duodenum is elevated by the endocannabinoid noladin ether, whereas in human Caco-2/15 epithelial intestinal cells it is elevated by PPARγ activation by rosiglitazone; (3) Leap2 expression is elevated in the ileum of mice with either high-fat diet—or genetic leptin signaling deficiency—(i.e., ob/ob and db/db mice) induced obesity. Based on these results, we propose that LEAP2 originating from the small intestine may represent a player in eCBome- and/or gut mBIome-mediated effects on food intake and energy metabolism.  相似文献   
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