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Fluoroalkyl sulfones, from

Scheme 2.52 Structure of sulfonated poly(arylene ether sulfone) ionomers with three different types of acidic groups (fluoroalkyl sulfonic, aryl sulfonic, and alkyl sulfonic acids). Taken from Ref. [185]. Scheme 2.52 Structure of sulfonated poly(arylene ether sulfone) ionomers with three different types of acidic groups (fluoroalkyl sulfonic, aryl sulfonic, and alkyl sulfonic acids). Taken from Ref. [185].
However, most asymmetric 1,3-dipolar cycloaddition reactions of nitrile oxides with alkenes are carried out without Lewis acids as catalysts using either chiral alkenes or chiral auxiliary compounds (with achiral alkenes). Diverse chiral alkenes are in use, such as camphor-derived chiral N-acryloylhydrazide (195), C2-symmetric l,3-diacryloyl-2,2-dimethyl-4,5-diphenylimidazolidine, chiral 3-acryloyl-2,2-dimethyl-4-phenyloxazolidine (196, 197), sugar-based ethenyl ethers (198), acrylic esters (199, 200), C-bonded vinyl-substituted sugar (201), chirally modified vinylboronic ester derived from D-( + )-mannitol (202), (l/ )-menthyl vinyl ether (203), chiral derivatives of vinylacetic acid (204), ( )-l-ethoxy-3-fluoroalkyl-3-hydroxy-4-(4-methylphenylsulfinyl)but-1 -enes (205), enantiopure Y-oxygenated-a,P-unsaturated phenyl sulfones (206), chiral (a-oxyallyl)silanes (207), and (S )-but-3-ene-1,2-diol derivatives (208). As a chiral auxiliary, diisopropyl (i ,i )-tartrate (209, 210) has been very popular. [Pg.25]

Scheme 2.49 Structure of poly(arylene ether sulfone)s with sulfonated fluoroalkyl side chains (-CF2CF2-OCF2CF2SO3H). Taken from Ref. [182]. Scheme 2.49 Structure of poly(arylene ether sulfone)s with sulfonated fluoroalkyl side chains (-CF2CF2-OCF2CF2SO3H). Taken from Ref. [182].
Polyaniline (PAn)/inorganic composites have been considered as new class of materials due to their improved properties compared with those of pure conducting polymers and inorganic materials [73-77]. For example, the combination of electrical conductivity of PAn and UV sensitivity of anatase Ti02 are expected to find applications in electrochromic devices, nonlinear optical system, and photochemical devises [73], From this point of view, it is in particular interest to prepare fluoroalkyl end-capped oligomers/PAn/titanium oxide nanocomposites. In fact, fluoroalkyl end-capped acrylic acid oligomer [Rp—(ACA) —Rp]/, 2-methacryloyloxyethane sulfonic acid oligomer [Rp—(MES) —Rp]/, 2-acrylamido-2-methylpropanesulfonic acid... [Pg.69]


See other pages where Fluoroalkyl sulfones, from is mentioned: [Pg.68]    [Pg.373]    [Pg.95]    [Pg.158]    [Pg.1736]    [Pg.7]    [Pg.767]    [Pg.75]    [Pg.7]    [Pg.8]    [Pg.86]    [Pg.71]    [Pg.74]    [Pg.242]   


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Fluoroalkylation

Fluoroalkyls

From sulfonates

From sulfones

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