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Group chain

Step-growth polymerizations can be schematically represented by one of the individual reaction steps VA + B V —> Vab V with the realization that the species so connected can be any molecules containing A and B groups. Chain-growth polymerization, by contrast, requires at least three distinctly different kinds of reactions to describe the mechanism. These three types of reactions will be discussed in the following sections in considerable detail. For now our purpose is to introduce some vocabulary rather than develop any of these beyond mere definitions. The principal steps in the chain growth mechanism are the following ... [Pg.347]

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]

Group chains suitable for the nonrigid limit have been discussed by van Roosmalen et al. (1983a). [Pg.189]

Gilmore, R., and Draayer, J. P. (1985), Dynamical Group Chains and Integrity Bases,./. [Pg.226]

It is therefore quite easy to see why such a very large number of silicates is possible. In fact, the chemistry of these substances is now so developed that it can be classed next in importance to the chemistry of carbon compounds. It must not be assumed, however, that there is any direct relationship between the chemistry of silicates and that of carbon compounds. It is true that in both groups chains, rings and layers of atoms occur, but the structural features of the two groups are totally different. The silicon ions in silicates are always coupled to each other by oxygen ions, while in the carbon compounds the carbon atoms are joined directly to each other. Again, the bonds between carbon atoms are purely homo-polar, while the silicates must be regarded as partly ionic compounds. [Pg.144]

Polyacetylene consists of CH-group chains which form a quasi one-dimensional (ID) lattice [104-107], There are cis and trans forms of polyacetylene. [Pg.28]

There are several reports wherein head-head dimers were not formed preferentially in micellar solutions. For example, the syn head-tail simers, 61, the same ones obtained in solution formed when a number of 7-al-koxycoumarins (60) (alkoxy group chain length was varied between methoxy to octadecyloxy) were irradiated in SDS and HDTC1 micelles [194,195], The same head-tail dimers, obtained in solution, were formed when 9-methyl-anthracene and 9-anthracenecarboxylic acid were irradiated in CTAB and... [Pg.142]

In the special case of /-electrons we have additionally the group chain... [Pg.128]

Although the synthetic transformations that can be accomplished by radical reactions are virtually limitless, precious few general methods exist by which radical reactions can be conducted. These methods can be classified in two main groups chain and nonchain. [Pg.724]

In the case of styrene the polymer contains at both ends a carboxyl group (chain termination by coupling), while polymers characterized by a termination reaction by disproportionation (polyvinyl acetate, polymethyl methacrylate) contain only one carboxyl end group. The carboxyl groups in these polymers were transformed to acid chlorides and coupled with a diol, e.g. 1,6-hexanediol. The comparison of the molecular weight of the polymers before and after condensation permits to elucidate the... [Pg.207]

In the recent work [BAL85] we give a detailed study of various level schemes for odd-odd nuclei obtained by analytical solutions of Hamiltonians associated with either (2) or (3). The isomorphisms between the two group chains are elaborated for the case where the unpaired nucleons occupy same or all of levels with j = 1/2,3/2,5/2 and the analytical expressions for the corresponding energy eigenvalues are given. [Pg.24]

Table 2.6. Types of ZDDPs (primary, secondaiy) with R-group chain structure (long, medium, short) and examples of alcohols... Table 2.6. Types of ZDDPs (primary, secondaiy) with R-group chain structure (long, medium, short) and examples of alcohols...
ZDDP type R-group chain structure example Chemical name Abbreviation... [Pg.47]

The case study 2. Evaluation of ZDDP (primary, secondary) with R-group chain structure (long, medium, short) in oil formulation was done during the field tests. The various aspects of valve train wear performance of lubricating oils through field testing in a passenger car vehicle were compared with laboratory data (Smolenski and Kabel, 1983). [Pg.259]


See other pages where Group chain is mentioned: [Pg.193]    [Pg.474]    [Pg.11]    [Pg.642]    [Pg.296]    [Pg.127]    [Pg.329]    [Pg.722]    [Pg.85]    [Pg.45]    [Pg.39]    [Pg.42]    [Pg.283]    [Pg.21]    [Pg.98]    [Pg.74]    [Pg.83]    [Pg.244]    [Pg.554]    [Pg.265]    [Pg.150]    [Pg.205]    [Pg.32]    [Pg.120]    [Pg.350]    [Pg.127]    [Pg.12]    [Pg.150]    [Pg.34]    [Pg.291]    [Pg.14]    [Pg.15]    [Pg.38]    [Pg.272]    [Pg.2]   
See also in sourсe #XX -- [ Pg.152 ]




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Acylation amino groups with acidic chains

Aliphatic terminal chains/mesogenic groups

Alkyl chain end groups

Alkyl groups branched-chain

Amino acids group 1- nonpolar side chains

Amino acids group 2- electrically neutral polar side chains

Amino acids group 4- basic side chains

Bacterial polysaccharide chains groups

Blocking of Side Chain Amino Groups

Borane chain transfer agents group

Branched-chain alkanes alkyl groups, 752 naming

Carbohydrate chains structural reporter groups

Carbonyl group in chain formation and cleavage

Carboxyl groups Chain length, dependence

Chain Polymetallocenes with Short Spacer Groups

Chain end group

Chain ending groups

Chain initiation group transfer polymerization

Chain modification pendant functional groups

Chain structure terminal groups

Chain-end methyl groups

Copolymers side-chain groups

Defect groups unsaturated chain ends

Dicarbonyls, Group chains

Flexible Chain Polymers with Mesogenic Groups

Fluorescamine assay for the availability of side-chain amino groups

Functional groups, at chain

Glass Transition with the Chain Length and Nature of Terminal Group

Group 13 systems polymers/chains

Group 16 systems chains

Group transfer polymerization chain modification

Groups in Chain Formation and Cleavage

Head groups, tethered chains

Heme groups chains

Hydroxyl groups acylation with acidic chains

Long-chain alkyl groups, vinyl

Lysozyme catalytic side chain groups

Macromolecules with Main-chain Mesogenic Groups

Macromolecules with Side-chain Mesogenic Groups

Networks from Aromatic Linear Chains Created by Reacting Backbone Diacetylene or Pendant Acetylene Groups

Networks with Flexible Chains and Stiff Mesogenic Groups

Polymer chains repetition symmetry groups

Polymers with side chain carbonyl groups

Polymetallocenes main-chain with short spacer group

Polyolefins side chain functional groups

Polyurethanes side-chain groups

Preparation of branched oligomethyl(phenyl)siloxanes with metacrylethoxyl groups in the lateral chain

Preparation of branched oligoorganosiloxanes with alkoxyoxyalkylene groups in the lateral chain

Protein side chain groups, reactions

Quantitative Determinations and Modification Reactions of Side Chain Groups

Rigid-chain polymers mesogenic groups

Semiflexible-chain polymers mesogenic groups

Side chain/group

Side chain/group influence

Side chains residue group frequencies

Side-chain carboxyl groups

Side-chain carboxyl groups, acidity

Side-chain functional groups, bile acid

Side-chain functional groups, glass

Side-chain hydroxyl group

Side-chain protecting groups

Side-chain protecting groups common

Side-chain protecting groups deprotection

Siloxane group chains, adsorption

Solid-phase peptide synthesis amino acid side chain protecting groups

Spectra of chain silicates Amphibole group

Spectra of chain silicates Pyroxene group

Steric effect, long-chain alkyl group

Sulfur Chains Terminated by Cyano Groups

Sulfur Chains Terminated by Sulfonate Groups The Polythionates

Sulfur Chains Terminated by Sulfonyl Groups

Synthesis of Phenols and Naphthols with Side-chains containing Oxy or Alkoxycarbonyl Groups

Use of group chains to utilize molecular symmetry

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