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Molecular ‘syringe

Ikeda, A., Tsudera, T., Shinkai, S., Molecular design of a molecular syringe mimic for metal cations using a 1,3-alternate calix[4]arene cavity. J. Org. Chem. 1997, 62, 3568-3574. [Pg.255]

Neumann has adapted the pendant drop experiment (see Section II-7) to measure the surface pressure of insoluble monolayers [70]. By varying the droplet volume with a motor-driven syringe, they measure the surface pressure as a function of area in both expansion and compression. In tests with octadecanol monolayers, they found excellent agreement between axisymmetric drop shape analysis and a conventional film balance. Unlike the Wilhelmy plate and film balance, the pendant drop experiment can be readily adapted to studies in a pressure cell [70]. In studies of the rate dependence of the molecular area at collapse, Neumann and co-workers found more consistent and reproducible results with the actual area at collapse rather than that determined by conventional extrapolation to zero surface pressure [71]. The collapse pressure and shape of the pressure-area isotherm change with the compression rate [72]. [Pg.114]

Laccase (PCL) as well as peroxidases (HRP and SBP) induced a new type of oxidative polymerization of the 4-hydroxybenzoic acid derivatives, 3,5-dimethoxy-4-hydroxybenzoic acid (syringic acid) and 3,5-dimethyl-4-hydroxybenzoic acid. The polymerization involved elimination of carbon dioxide and hydrogen from the monomer to give PPO derivatives with molecular weight up to 1.8 x lO (Scheme 22). - ... [Pg.233]

In a 10 mL round-bottomed flask equipped with a magnetic stirrer bar were placed activated molecular sieves 4A (44.9 mg), (R)-BINOL (6.4 mg), triphenylphosphine oxide (18.7 mg), and anhydrous tetrahydrofuran (0.9 mL) and the mixture was stirred for 5 minutes under argon. To this suspension was added a suspension of La(0 z-Pr)3 (7.1 mg) in tetrahydrofuran (1.4 mL) by a syringe. After stirring for 1 hour at room temperature, cumene hydro-... [Pg.66]

Note Phthalates, especially di-2-ethylhexyl phthalate (also known as dioctyl phthalate, DOP), are commonly used plasticizers in synthetic polymers. Unfortunately, they are extracted from the polymer upon exposure to solvents such as dichloromethane, chloroform or toluene, e.g., from syringes, tubing, vials etc. Therefore, they are often detected as impurities. They are easily recognized from their peaks at m/z 149 (often base peak), m/z 167, and [M-(R-2H)] m/z 279 in case of DOP). The molecular ion is often absent in their El spectra. [Pg.275]

Fig. 10 Illustrations of the microchannel confined surface-initiated polymerization (p-SIP) route for producing gradient polymer brush libraries a route for making polymer molecular weight and block copolymer libraries b route for making statistical copolymer libraries. Red arrows show the flow of monomer solution from a syringe pump used to gradually fill the microchannel. See text for details... Fig. 10 Illustrations of the microchannel confined surface-initiated polymerization (p-SIP) route for producing gradient polymer brush libraries a route for making polymer molecular weight and block copolymer libraries b route for making statistical copolymer libraries. Red arrows show the flow of monomer solution from a syringe pump used to gradually fill the microchannel. See text for details...

See other pages where Molecular ‘syringe is mentioned: [Pg.363]    [Pg.363]    [Pg.162]    [Pg.846]    [Pg.363]    [Pg.363]    [Pg.162]    [Pg.846]    [Pg.61]    [Pg.873]    [Pg.142]    [Pg.90]    [Pg.599]    [Pg.230]    [Pg.30]    [Pg.323]    [Pg.421]    [Pg.338]    [Pg.374]    [Pg.493]    [Pg.278]    [Pg.467]    [Pg.27]    [Pg.228]    [Pg.196]    [Pg.373]    [Pg.68]    [Pg.85]    [Pg.144]    [Pg.100]    [Pg.83]    [Pg.254]    [Pg.259]    [Pg.241]    [Pg.623]    [Pg.7]    [Pg.454]    [Pg.8]    [Pg.250]    [Pg.100]    [Pg.267]    [Pg.1614]    [Pg.231]    [Pg.84]    [Pg.78]    [Pg.99]   
See also in sourсe #XX -- [ Pg.208 ]




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