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Stabilizing reagents

For transition and precious metals, thiols have been successfully employed as the stabilizing reagent (capping reagent) of metal nanoparticles [6]. In such cases, various functionalities can be added to the particles and the obtained nanoparticles may be very unique. It is well known that thiols provide good self-assembled monolayers (SAM) on various metal surfaces. When this SAM technique is applied to the nanoparticle preparation, nanoparticles can be covered constantly by functionalized moieties, which are connected to the terminal of thiol compounds. [Pg.453]

In this study, three a,thiol compounds) were used as the stabilizing reagent of gold nanoparticles (Figure 3). [Pg.454]

NMR measurements are very useful to understand the properties of the stabilizing reagents of metal nanoparticles. Author s group reported the structure of stabilization of non-ionic and cationic surfactants on platinum nanoparticles [22] and that of ternary amines on rhodium nanoparticles [23]. Such information is considerably important for applications of nanoparticles such as... [Pg.455]

Entries 5 to 9 illustrate some of the modified reagents and catalytic procedures. Entry 5 uses a phosphine-stabilized reagent, whereas Entry 6 includes BF3. Entry 7 involves use of TMS-C1. Entries 8 and 9 involve cyanocuprates. In Entry 9, the furan ring is closed by a Mukaiyama-aldol reaction subsequent to the conjugate addition (Section 2.1.4). [Pg.689]

Solidification of the upper layers can be accomplished by blending pozzolanic additives, modified clay, or stabilization reagents into moist soil and compacting the mass. Pozzolanic additives include such fixatives as portland cement, quick lime,... [Pg.292]

Uses Manufacture of vanillin, Michler s ketone, methyl violet, and other dyes solvent reagent for methyl alcohol, hydrogen peroxide, methyl furfural, nitrate, and formaldehyde chemical intermediate stabilizer reagent. [Pg.469]

The equations in Ref. 137 are more complex since the substitution of the free endgroups by stabilizing reagents have been taken into account see Ref. 140... [Pg.122]

In contrast, the corresponding reactions of RCu/BFa reagents (R = phenyl or alkenyl) with allylic acetals obviously proceed in an anti 5n2 fashion, as shown in (67b). The unsaturated acetals (68), prepared from (R )-butane-1,2-diol, are opened by the PBu3-stabilized reagents to give, after hydrolysis, the (3-substituted aldehydes (69) with high ee (Scheme 27).68,69 The method has been applied to the preparation of a key intermediate (85% ee) for the synthesis of the California red scale pheromone.69... [Pg.209]

Stabilized reagents give thermodynamically more stable -isomers preferentially. For example, amino aldehyde 4.26 was alkenated with the phosphorane 4.27 to afford mainly the -enoate 4.28 in 95% yield. ... [Pg.159]

The resulting Mn(III) is the final product if it is stabilized by the formation of a fluoride or metaphosphate complex. In the absence of such stabilizing reagents the Mn(III) disproportionates to give Mn(IV), which then precipitates as MnOj ... [Pg.302]

Use Manufacture of antihistamines, resin and rubber stabilizer, reagent for aldehydes. [Pg.388]

Availability and choice of instrumentation and how use of different equipment could affect assay performance need to be discussed. Definitions of experimental and storage conditions, reagent sources and quality, and lab personnel experiences should be discussed early on. This also applies to the process of assigning expiry dates, assessment of reagent stability, reagent handling, and shipping processes. [Pg.274]

TMS). These silylated reagents, which also react with nonresonance-stabilized reagents, provide access... [Pg.1003]

Most of the reported reactions of gem-amino ethers have been confined to the use of crotyl or propar-gyl/allenic reagents. A few examples involving allyl reagents are shown in Table 25 and involve mainly N-(trimethylsilyl)- and/V,N-bis(trimethylsilyl)-gem-amino ethers (133 R2 = TMS, R3 = alkyl R2 = R3 = TMS). These silylated reagents, which also react with nonresonance-stabilized reagents, provide access... [Pg.1003]

The phase that is similar to the stabilizing reagent tends to become a dispersion medium, as clearly seen in the example of emulsions stabilized by finely dispersed powders. Such stabilization is possible under the condition of a finite selective wetting of powder, i.e. at finite values of contact angle, 0° < 0<180°. The powders are able to stabilize the phase that poorer wets the particles, while the liquid that is more similar to the powder becomes the dispersion medium. The reasons of such behavior are apparent from Fig. VIII-12. If water droplets covered by hydrophobic powder, such as e.g. carbon black, are placed into hydrocarbon phase (oil), the layer of carbon black due... [Pg.615]

The final steps of the synthesis are summarized in Scheme 34. After a sequence of protection-reduction-oxydation, 171 was transformed to aldehyde 172 which was directly submitted to a Horner-Wadsworth-Emmons homologation with the requisite stabilized reagent K under Ando conditions [115] to give the corresponding a,(3-unsaturated ester 173 (Z/E > 95/5) in 84% yield. Treatment of ester 173 with 1% HC1, EtOH led to (-)-pironetin after purification (89% yield). [Pg.46]

In model systems, the hydrophilic polymer PVP is frequently used as a stabilizing reagent for Au clusters. Here, to reduce computational costs, the PVP molecule shown in Fig. 19.5 was used as a model molecule to investigate the interactions between Au atoms and PVP. The optimized structure of Au-PVP is displayed in Fig. 19.5. The adsorption energy of this model was estimated to be 3.93 kcal/mol, and the Mulliken charge on the Au atom was —0.214. [Pg.370]

To produce a stabilized base or subbase aggregate, RAP must also be crushed and screened, then blended with one or more stabilization reagents so that the blended material, when compacted, will gain strength... [Pg.129]

Immediately after sampling add 1 ml of the stabilizing reagent per 100 mi of sample volume to the water samples in order to prevent losses by absorption of mercury at the vessel walls. [Pg.386]


See other pages where Stabilizing reagents is mentioned: [Pg.454]    [Pg.455]    [Pg.168]    [Pg.164]    [Pg.168]    [Pg.23]    [Pg.302]    [Pg.159]    [Pg.228]    [Pg.183]    [Pg.201]    [Pg.173]    [Pg.204]    [Pg.168]    [Pg.362]    [Pg.512]    [Pg.95]    [Pg.499]    [Pg.1075]    [Pg.635]    [Pg.1532]    [Pg.62]    [Pg.139]    [Pg.113]    [Pg.343]    [Pg.386]    [Pg.1557]    [Pg.3919]    [Pg.71]   
See also in sourсe #XX -- [ Pg.201 ]




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