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Cross-link, biphenyl

At the same time that reduction of the nitro group occurs in NBT SAMs, cross-linking also occurs between adjacent biphenyl groups. This may be exploited to yield micro- and nanostructures. Eck et al. showed that freestanding sheets of cross-linked biphenyls may be formed by electron-induced cross-hnking and released by exposure of the samples to iodine vapor (which oxidizes the S-Au bond). Alternately, NBT SAMs may be cross-linked and the unexposed adsorbates removed by thermal desorption (thiols readily desorb from gold surfaces because the activation barrier for conversion of two thiolates to a disulfide is small). ... [Pg.3599]

Cross-linking of EPR can be promoted by the addition of a variety of additives, particularly by those that were found effective in polypropylene. Tetravinyl silane, chlorobenzene, nitrous oxide, allyl acrylate and neopentyl chloride,191192 and biphenyl maleimide177 were reported to promote the process. [Pg.107]

The experimental apparatus and technique has been described in detail elsewhere.(20>21) The retention factors of naphthalene and biphenyl under isothermal conditions at various pressures were obtained using capillary columns coated with a cross-linked phenyl polymethylphenyl-slloxane stationary phase with carbon dioxide as the fluid mobile phase. A Varian 8500 syringe pump was operated under computer control providing accurate, pulsefree control of the fluid pressure. [Pg.178]

Fig. 7.7. Some of the covalent links which occur in structural proteins. ABCD represents one protein, EFB C G another. The N-terminal amino acid A is linked to an o-quinone which is also linked to a lysyl residue F(=quinone tanning) BB represents two tyrosyl residues coupled by a biphenyl linkage CC represents two cysteinyl residues coupled by a cystine linkage (as in keratin) D, E and G are not cross-linked. (After Brunet, 1967.)... Fig. 7.7. Some of the covalent links which occur in structural proteins. ABCD represents one protein, EFB C G another. The N-terminal amino acid A is linked to an o-quinone which is also linked to a lysyl residue F(=quinone tanning) BB represents two tyrosyl residues coupled by a biphenyl linkage CC represents two cysteinyl residues coupled by a cystine linkage (as in keratin) D, E and G are not cross-linked. (After Brunet, 1967.)...
The analysis of the extracts was made in a Perkin Elmer Gas Chromatograph model 8700 with an detector NPD. The analysis conditions were 423 K for 1 minute followed by ramp of 15.0 K/min until 523 K and another ramp with 30.0 K/min until 553 K. Injector and detector were setted at 533 K and 543 K, respectively. It was used a capillar column BP5 (cross-linked 5 % biphenyl, 95 % dimethylssiloxane) with 50 m long and 0.25 pm of diameter from SGE. Carrier gas used was He at 2 ml 7 min. [Pg.477]

Two characteristics of macroporous supports are worth mentioning. First, the transfer of specific reaction conditions from solution to the macroporous support should be easier because the influence of swelling in different solvents and diffusion rates, typical for low-cross-linked PS resins, is not relevant. Second, this support can be washed more easily than the classical PS resins. A study of the retention of biphenyl in hydrophobic PS and AP-PS resins treated with solutions of biphenyl in methylene chloride (26) shows how after two identical wash cycles AP-PS retains 0.01% of biphenyl while hydrophobic PS retains 2.63% of the same impurity. This is due to the... [Pg.5]

The insoluble fraction is composed primarily of a poorly characterized, structurally heterogeneous, macromolecular material, which has been variously named, but commonly referred to as either a meteorite polymer or kerogenlike material Hayatsu et al. [45,46] concluded that the material is comprised of condensed aromatic, heteroaromatic, and hydroaromatic ring systems in up to four-ring clusters, cross linked by short methyl chains, ethers, sulfides and biphenyl groups. [Pg.79]

Stationary phases in capillary SFC [30] are usually based on a polysiloxane backbone, cross-linked by means of a free-radical initiator, and methyl, phenyl, octyl, biphenyl, and cyanopropyl substituents are incorporated into them. These polysiloxane phases exhibit wide ranges between their glass transition and decomposition temperatures, and this feature sets them apart from most high molecular-mass polymers, as they allow useful operating conditions for chromatography. Polysiloxanes can be tailor-made for specific... [Pg.226]

Although both of the previously mentioned methods yield high-quality polyparaphenylene films, polyparaphenylene can also be formed electrochemically from biphenyl (Fig. 21c) dissolved in acetonitrile under similar mild anodic conditions [367]. The electropolymerization of biphenyl may be advantageous in that the toxicity of biphenyl is lower than that of benzene. Furthermore, the resulting films are reported to have longer chain lengths and less cross-linking than the films synthesized directly from benzene [368]. [Pg.803]

Early resin materials used in mold compound formulations were sihcones, phenolic resins, and bisphenol-A or bisphenol-F epoxies. Because of shortcomings in performance, these materials have been displaced by epoxy phenol or cresol novalac resins (ECN resins) and by the biphenyl- and tris(triphenylmethane)-type epoxies (70) (Fig. 20). The high cross-link density of ECN-based materials results in low moisture absorption rate and higher thermal stabihty than... [Pg.2511]

The concept of induced-fit recognition of DNA by organometallic Ru(II) arene complexes containing dynamic stereogenic centers via dynamic epimerization, intercalation and cross-linking may be useful in the design of anticancer drugs [72]. The and diastereomers of [(ri -biphenyl)RuCl(Et-en)] ... [Pg.54]


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See also in sourсe #XX -- [ Pg.181 , Pg.192 ]




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