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P-cydodextrins

In order to minimize the fast electron-hole recombination, Calzolari et al. [50] attached a donor-acceptor boronic acid spacer between the anthocyanins and a gold electrode, and the same molecule between the dye and a P-cydodextrin which is able to bind I3 dissolved in the electrolyte near the chromophore. In that configuration, the device shows an increase in the quantum yield of the photocurrent from a negligible value to 1.75%. Such studies were not repeated on Ti02 layers. [Pg.254]

Fig. 1. Structural diagram of (a) p-cydodextrin and (b) two of the glucopyranose units illustrating details of the a-(l,4) glycosidic linkage, C-l (d) chair... Fig. 1. Structural diagram of (a) p-cydodextrin and (b) two of the glucopyranose units illustrating details of the a-(l,4) glycosidic linkage, C-l (d) chair...
Fig. 2. Chromatogram showing (a) the lc separation of A, (+) (T)-(l-ferrocenyl-ethyl)thioethanol B, (+) 1-ferrocenyl-l-methoxyethane and C, ( ) 1-ruthenocenylethanol, on a 25-cm p-cyclodextrin column (see Table 2), and (b) the potential use of a p-cydodextrin column to determine optical purity... Fig. 2. Chromatogram showing (a) the lc separation of A, (+) (T)-(l-ferrocenyl-ethyl)thioethanol B, (+) 1-ferrocenyl-l-methoxyethane and C, ( ) 1-ruthenocenylethanol, on a 25-cm p-cyclodextrin column (see Table 2), and (b) the potential use of a p-cydodextrin column to determine optical purity...
The third input selected was molecular oxygen its paramagnetism allows it to be a powerful quencher of room temperature phosphorescence in fluid solution. 451 AND logic behavior was arranged in a phosphorescent system, by using p-cydodextrin as one input and Ca2+ as the second input. Room temperature phosphorescent systems such as 29 suffer triplet-triplet annihilations, hence quenching their phosphorescence unless the phosphors are sterically prevented from encountering one another. [Pg.356]

Fig. 7. A tethered cyclodextrin and the structure of p-cydodextrin, the most common cyclodextrin used as a bonded ligand in liquid chromatography. Fig. 7. A tethered cyclodextrin and the structure of p-cydodextrin, the most common cyclodextrin used as a bonded ligand in liquid chromatography.
Cholesterol P-Cyclodextrin hexamethylene diisocyanate or toluene 2,4-diisocyanate DMSO Using P-cydodextrin [93]... [Pg.86]

Woi sel et al reported reaction of bipyridinium ylides with an electron deficient propynamido-P-cydodextrin forming the pyridinoindolizine- 3-cyclodextrin conjugates <04TL1557>. Moreover, Wu has reported the reaction of pyridinium halides with 2,2-difluorovinyl tosylate in the presence of base to yield monofluorinated indolizines <04T5487> as shown in Scheme 24. When unsymmetrical pyridinium halides were used, a mixture of isomers represented by 52 and 53 was obtained. [Pg.272]

Properties Wh. ciyst. powd. sol. 23.2 g/100 ml in water m.w. 1297 Toxicology LD50 (acute IV, rat) > 3750 mg/kg nonirritating to eye Cavasol W7 HP [Wacker-Chemie GmbH/Biotei. Wacker Biochemj Chem. Descrip. Hydroxypropyi-p-cydodextrin CAS 12844 35-5... [Pg.173]

Mulrimiktoarm stars of A17B7 type, where A is PCL and B is poly(acrylic add) (PAA), wae prepared with a multifunctional initiator. A combination of CROP and ATRP techniques and a multistep reaction sequence wae used. In the first step. 14-arm stars of PCL homopolymas (CDSi-SPCL) wae synthesized via CROP of CL using pa-6-(tert-butyl-dimethylsilyl)-p-CD, where 3-CD is p-cydodextrine hydrate, as the multifimctional... [Pg.74]

Supramolecular polymeric complexes yielding graft copolymers based on the inclusion interactions of P-cydodextrin groups in poly(N-vinyl-2-pyrrolidone-co-6-deoxy-6-methacrylate ethylamino-p-cyclodextrin) with the adamantane group on the end of PGL were also reported by Ren et... [Pg.522]

The cydodextrins are produced from starch by enzymatic conversions and are composed of 5-32 units, but the typical cydodextrins for chromatographic use consists of 6 units (a-cyclodextrin), 7 units (P-cydodextrin), or 8 units (y-cydodextrin). [Pg.78]

Scheme 9.25 Tetradifferentiation using a selective delivery on the primary rim of P-cydodextrin. Scheme 9.25 Tetradifferentiation using a selective delivery on the primary rim of P-cydodextrin.

See other pages where P-cydodextrins is mentioned: [Pg.254]    [Pg.176]    [Pg.176]    [Pg.176]    [Pg.96]    [Pg.64]    [Pg.65]    [Pg.65]    [Pg.3]    [Pg.359]    [Pg.61]    [Pg.127]    [Pg.128]    [Pg.156]    [Pg.156]    [Pg.156]    [Pg.156]    [Pg.156]    [Pg.370]    [Pg.114]    [Pg.87]    [Pg.87]    [Pg.231]    [Pg.549]    [Pg.786]    [Pg.633]    [Pg.62]    [Pg.62]    [Pg.63]    [Pg.64]    [Pg.326]    [Pg.250]    [Pg.263]    [Pg.268]    [Pg.53]    [Pg.428]   
See also in sourсe #XX -- [ Pg.178 ]




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