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Formation intermolecular

Complex coacervation in aqueous solution may be considered as a special case of network formation. Intermolecular forces such as Coulomb, van der Waals, hydrophobic, hydrogen bond, and dipol-charge transfer between polymers themselves, or polymers and low... [Pg.607]

After the radical formation, intermolecular chain transfer reactions take place. A special case of chain transfer is the propagation reaction (see Section 2.1) of the type ... [Pg.48]

Griesbeck, A. G., Bondock, S. Oxetane formation intermolecular additions. CRC Handbook of Organic Photochemistry and Photobiology... [Pg.646]

By definition, cross-linking involves the formation intermolecular connections through chemical bonds. This process necessarily results in reduction in chain mobility. Consequently, Tg increases. For lightly cross-linked systems like vulcanized rubber, Tg shows a moderate increase over the uncross-linked polymer. In this case, Tg and the degree of cross-linking have a linear dependence, as shown by the following approximate empirical equation. [Pg.119]

Chelate-assisted C-H bond aminations often require the presence of an oxidant in analogy to the previously discussed C-H oxygenations. Therefore, many protocols use a mixture of amine source and oxidant as reagents in order to achieve C-N bond formation. Intermolecular directed C-H aminations have been realized with this approach by Che and coworkers (Scheme 23.36). Remarkably, this methodology is capable of employing a variety of different directing groups as well as primary amides as amine sources [129]. [Pg.662]

Many other agents promoting oxidative coupling catalyze the gelation process. It has therefore been proposed that an oxidative coupling process could be involved (45). The gel formation process is in all circumstances a three-stage one complex formation—> intermolecular bridge formation—>gel formation. [Pg.200]

SCHEME 7.20 Carbonyl ylide formation/intermolecular cycloaddition sequence by Hodgson et al. [Pg.194]

SCHEME 7.22 Carbonyl ylide formation/intermolecular cycloadditions of ester-derived carbonyl ylides with DMAD. [Pg.195]


See other pages where Formation intermolecular is mentioned: [Pg.279]    [Pg.235]    [Pg.76]    [Pg.514]    [Pg.277]    [Pg.257]    [Pg.257]    [Pg.123]    [Pg.1236]    [Pg.1242]    [Pg.1244]    [Pg.1256]   
See also in sourсe #XX -- [ Pg.425 ]




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Bond formation intermolecular

Carbon-nitrogen bond formation intermolecular reactions

Cyclodextrin Inclusion Complexes Mechanism of Adduct Formation and Intermolecular Interactions

Formate derivatives intermolecular trapping

Formation by intermolecular

Formation of 3-, 4- and 5-Membered Cycles by Intermolecular Reactions

Gel Formation by Intermolecular Physical Bonding

Intermolecular Addition Formation of Unsaturated Ethers and Furans

Intermolecular Addition with Rearrangement Formation of Unsaturated Ketones

Intermolecular Coupling with Cycle Formation

Intermolecular complex formation

Intermolecular ester formation

Intermolecular interactions, formation

Intermolecular junction formation

Intermolecular reaction formation

Intermolecular reactions bond formation

Intermolecular reactions ether formation

Intermolecular reactions formate anions

Polymer Formation by Intermolecular Interactions

Solid with intermolecular compound formation

Solution formation intermolecular forces

The Effect of Intermolecular Forces on Solution Formation

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