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Aromatization groups

At Argon. Sometimes used as an abbreviation for an aromatic group. [Pg.40]

Apart from these simple silanes, derivatives witli aromatic groups at different places in tire chain have also been investigated [136, 137], It was found tliat tire average tilt angle of tliese molecules depends on tire specific functional entities contained in tire chains. It is likely tliat apart from packing considerations—important for bulky groups, for example—otlier factors also influence tire resulting tilt. [Pg.2624]

Tiiiman N, Uiman A and Eiman J F 1990 A novei seif-assembied monoiayer fiim containing a suifone-substituted aromatic group Langmuir 6 1512-8... [Pg.2636]

For the selection of descriptors, GA simulated evolution of a population. Each individual of the population represents a subset of descriptors and is defined by a chromosome of binary values. The chromosome has as many genes as there are possible descriptors (92 for the aromatic group, 119 for non-rigid aliphatic,... [Pg.527]

B) Picrates. Very useful for ethers containing an aromatic group. [Pg.397]

Apparently, 4.54 is extremely reluctant to undergo a retro Mannicli reaction. Riviere demonstrated that this behaviour is not unusual for (3-amino ketones. From the study of a large number of Mannich adducts. Riviere concludes that the retro Mannich reaction requires an aromatic group next to the carbonyl functionality. Qearly, 4.54 lacks this arrangement. [Pg.118]

Research activities in the area of PODs containing aromatic groups have been centered around the production of highly processible, soluble, and thermally stable polymers. In this particular class of PODs, the imide-and phenylene-containing backbones have been widely explored. [Pg.534]

In order for dipole—dipole and dipole-iaduced dipole iateractioas to be effective, the molecule must coataia polar groups and/or be highly polarizable. Ease of electronic distortion is favored by the presence of aromatic groups and double or triple bonds. These groups frequently are found ia the molecular stmcture of Hquid crystal compouads. The most common nematogenic and smectogenic molecules are of the type shown ia Table 2. [Pg.198]

Cosurfactant requirements can be minimized usiag a surfactant having a short-branched hydrophobe or a branched-alkyl substituent on an aromatic group (232,234) and a long ethoxy group chain (234). Blends of surfactants optimized for seawater or reservoir brine salinity include linear alkyl xylene sulfonate—alcohol ether sulfate mixtures (235). [Pg.194]

Diarylamines are compounds that have two aromatic groups and one hydrogen atom attached to nitrogen. Diphenyl amine (DPA), or... [Pg.242]

A classification based first on ion specificity, then on stmctural features has been suggested for the polyethers (7). Another method uses the presence of unsaturation or of aromatic groups in the molecular skeleton (8). In this review the compounds are classified based on the number of carbons in the backbone according to the numbering system proposed in reference 9. The carbon backbone or skeleton refers to the longest chain of contiguous carbons between the carboxyl group and the terminal carbon. [Pg.166]

In the presence of excess acid, a sulfonyl chloride group (—SO2CI) can be attached to an aromatic group, ie, chlorosulfonation can occur,... [Pg.86]

For alkylbenzenes, nitrobenzenes, halogenated benzenes and for secondary or tertiary amines where at least one aromatic group is connected to an amino nitrogen, add the following corrections for each aromatic nuclei is. If N < 16, increase AN by 0.60 if N > 16, increase AN by 3.055 — 0.161N for each aromatic group. For any N, increase AB by (—140.04 + 13.869 ). [Pg.410]

With H2/Pd-C, the normal conditions for benzyl group removal, it is difficult to remove the benzyl group on histidine without also causing reduction of other aromatic groups that may be present. ... [Pg.390]

Residue 189 is at the bottom of the specificity pocket. In trypsin the Asp residue at this position interacts with the positively charged side chains Lys or Arg of a substrate. This accounts for the preference of trypsin to cleave adjacent to these residues. In chymotrypsin there is a Ser residue at position 189, which does not interfere with the binding of the substrate. Bulky aromatic groups are therefore preferred by chymotrypsin since such side chains fill up the mainly hydrophobic specificity pocket. It has now become clear, however, from site-directed mutagenesis experiments that this simple picture does not tell the whole story. [Pg.213]

One of the most common modes of characterization involves the determination of a material s surface chemistry. This is accomplished via interpretation of the fiag-mentation pattern in the static SIMS mass spectrum. This fingerprint yields a great deal of information about a sample s outer chemical nature, including the relative degree of unsaturation, the presence or absence of aromatic groups, and branching. In addition to the chemical information, the mass spectrum also provides data about any surface impurities or contaminants. [Pg.552]

The common feature of the p-phenylene group stiffens the polymer backbone so that the polymers have higher TgS than similar polymers which lack the aromatic group. As a consequence the aromatic polymers tend to have high heat deformation temperatures, are rigid at room temperature and frequently require high processing temperatures. [Pg.584]

Originally the chemical industry was inorganic in the 1960s organic chemicals (means they contain carbon) came into prominence with the compounds benzene, phenol, ethylene, and vinyl chloride. The organic chemicals benzene, phenol, toluene, and the xylenes compose the aromatic group. [Pg.269]

Hydrolytic cleavage of single carbon-fluorine bonds generally requires activation by a neighboring group such as a carbonyl, sulfonyloxy, or olefinic bond or a negatively substituted aromatic group. [Pg.422]


See other pages where Aromatization groups is mentioned: [Pg.91]    [Pg.96]    [Pg.91]    [Pg.99]    [Pg.146]    [Pg.63]    [Pg.67]    [Pg.67]    [Pg.182]    [Pg.184]    [Pg.141]    [Pg.62]    [Pg.69]    [Pg.448]    [Pg.193]    [Pg.267]    [Pg.480]    [Pg.333]    [Pg.529]    [Pg.227]    [Pg.227]    [Pg.474]    [Pg.124]    [Pg.15]    [Pg.134]    [Pg.409]    [Pg.98]    [Pg.29]    [Pg.95]    [Pg.293]    [Pg.948]   
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See also in sourсe #XX -- [ Pg.31 ]

See also in sourсe #XX -- [ Pg.17 ]

See also in sourсe #XX -- [ Pg.17 ]

See also in sourсe #XX -- [ Pg.28 ]

See also in sourсe #XX -- [ Pg.29 ]

See also in sourсe #XX -- [ Pg.31 ]




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Aromatic groups

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