Thermally Initiated cationic

J.V. Crivello and J.L. Lee, The synthesis and characterization of polymer-hound diaryliodonium salts and their use in photo and thermally initiated cationic polymerization. Polym. Bull. 1986, 16(4), 243-248. 

More recently, iodonium salts have been widely used as photoinitiators in the polymerization studies of various monomeric precursors, such as copolymerization of butyl vinyl ether and methyl methacrylate by combination of radical and radical promoted cationic mechanisms [22], thermal and photopolymerization of divinyl ethers [23], photopolymerization of vinyl ether networks using an iodonium initiator [24,25], dual photo- and thermally-initiated cationic polymerization of epoxy monomers [26], preparation and properties of elastomers based on a cycloaliphatic diepoxide and poly(tetrahydrofuran) [27], photoinduced crosslinking of divinyl ethers [28], cationic photopolymerization of l,2-epoxy-6-(9-carbazolyl)-4-oxahexane [29], preparation of interpenetrating polymer network hydrogels based on 2-hydroxyethyl methacrylate and N-vinyl-2-pyrrolidone [30], photopolymerization of unsaturated cyclic ethers [31] and many other works. 

Different initiation techniques have been investigated in polymerizations induced by iodonium salts, such as visible laser irradiation [32], dual photo- and thermally initiated cationic polymerization [23, 26] and a two-photon photopolymerization initiation system [33,34]. For example, dual photo- and thermal-initiation systems based on selective inhibition of the photoinifiated cationic ring-opening polymerization of epoxides by dialkyl sulfides have been developed [26]. Such a dual system, iodonium salt/dialkyl sulfide, in the... 

In the presence of triarylsulfonium and diaryliodonium salts, polymerization continues even if UV irradiation is terminated. This phenomenon is called dark cure and is due to the living nature of the superacid generated cation. The cure regime can be thought of as UV-initiated but thermally cured. Thermally initiated cationic catalysts are also available (129). 

The features and detail of the IPN kinetics were also studied in other works [274-276]. The kinetics of thermally initiated cationic epoxy polymerization and free radical acrylate photopolymerization were investigated in [277]. It was found that the preexistence of one polymer has a significant effect on the polymerization of the second monomer. The reaction kinetics and phase separations were studied for sequential IPNs in [278]. The kinetics of IPN formation was studied for IPNs based on PDMS-cellulose acetate butyrate [279]. All these and other works [280-282] confirm the general regularities of the reaction kinetics and its connection with phase separation in forming systems. 

Crivello, J. V., Lockhart, T. P., and Lee, J. L., Diaryl-iodonium salts as thermal initiators of cationic polymerization,... 

Turning from the intramolecular process to the intermolecular ones, we now extend our comparison of the thermal and cation-radical cyclizations. It is also interesting to take sonication into account as a route to initiate cyclizations. The reaction between 2-butenal A,A-dimethylhydrazone (a diene) and 5-hydroxy-l,4-naphthoquinone (a dienophile) gives such an opportunity. In toluene, at 20°C, the reaction follows as depicted in Scheme 7.28 (Nebois et al. 1996). 

The radiolysis of olefinic monomers results in the formation of cations, anions, and free radicals as described above. It is then possible for these species to initiate chain polymerizations. Whether a polymerization is initiated by the radicals, cations, or anions depends on the monomer and reaction conditions. Most radiation polymerizations are radical polymerizations, especially at higher temperatures where ionic species are not stable and dissociate to yield radicals. Radiolytic initiation can also be achieved using initiators, like those used in thermally initiated and photoinitiated polymerizations, which undergo decomposition on irradiation. 

Intramolecular cyclization of o-diethynylbenzene gives us an opportunity to compare the results of the thermal and cation radical variants of the reaction. There are three possible modes of cyclization (Scheme 6-21). While 1,6 cyclization takes place in the thermal process, cation radical initiation leads to 1,5 cylization (Ramkumar et al. 1996). Chemical oxidation of o-diethynylbenzene bearing two terminal phenyl groups by tris(/>bro-mophenyl)aminiumyl hexachloroatimonate as the catalytic oxidizing agent in the presence of oxygen yields 3-benzoyl-2-phenylindenone in 70% yield (Scheme 6-22). 

Although cyclobutanes with varying substitution patterns are known, cyclopropanes present a much wider variety and much greater ease of synthesis. Ethyl 2-(p-methoxyphenyl)-l-cyanocyclopropanecarboxylate has been shown to thermally initiate the diradical polymerization of acrylonitrile [138]. In the presence of zinc chloride as activator, it also initiates the diradical polymerization of styrene [139]. On the other hand, this same initiator also initiates the thermal cationic polymerization of AT-vinylcarbazole [140]. This direction of tetra- and trimethylene chemistry is currently under active investigation. 

The usefulness for this purpose of triarylsulphonium hexafluoroantimonate comes from its considerable thermal stability, stability in the presence of highly reactive monomer, and highly efficient photolysis to yield reactive cations capable of initiating cationic polymerization. These properties arise from the unique chemical composition of the photo-initiator, the effectiveness of which can be shown to be a result of the presence of a very weak cation and a similarly weak anion. 

Cationic polymerizations induced by thermally and photochemically latent N-benzyl and IV-alkoxy pyridinium salts, respectively, are reviewed. IV-Benzyl pyridinium salts with a wide range of substituents of phenyl, benzylic carbon and pyridine moiety act as thermally latent catalysts to initiate the cationic polymerization of various monomers. Their initiation activities were evaluated with the emphasis on the structure-activity relationship. The mechanisms of photoinitiation by direct and indirect sensitization of IV-alkoxy pyridinium salts are presented. The indirect action can be based on electron transfer reactions between pyridinium salt and (a) photochemically generated free radicals, (b) photoexcited sensitizer, and (c) electron rich compounds in the photoexcited charge transfer complexes. IV-Alkoxy pyridinium salts also participate in ascorbate assisted redox reactions to generate reactive species capable of initiating cationic polymerization. The application of pyridinium salts to the synthesis of block copolymers of monomers polymerizable with different mechanisms are described. 

TGA analyses were performed for polymer samples having different degrees of cross-linking. The decomposition of the linear oligomer starts at about 200 °C. Once cured and baked, the formed siloxane network is more thermally stable, and the decomposition begins at temperatures higher by 100-150 °C. The results are similar to those reported for analogous Tsi-modified siloxanes cross-linked by means of photo-initiated cationic polymerization of epoxides [8]. 

Free Radical Initiators as Reducing Agents for Dlaryllodonlua Salts. A final method by which dlaryllodonlum salts can be used as thermal Initiators of cationic polymerization has recently been reported by Ledwlth and his coworkers(14,15) and Is shown In Equations 17-19. 

Cationic vesicles typically used for DNA delivery often self-aggregate or bind to plasma proteins in vivo. Wu et al. [104] attempted to improve vesicle stability using a cationic lipid with a cross-linkable acrylamide attached to the headgroup (Fig. 16). Vesicles were polymerized using thermal initiation with AAPD. Compared to monomeric vesicles, polymerized vesicles were less cytotoxic, more resistant to aggregation in serum, and comparable in transfection activity using a vector encoding firefly luciferase. 

K. Takuma, T. Takata, and T. Endo, Cationic polymerization of epoxide with benzyl phosphonium salts as the latent thermal initiator. Macromolecules 1993,26(4), 862-863. 

T. Wang, et al., Several ferrocenium salts as efficient photoinitiators and thermal initiators for cationic epoxy polymerization. J. Photochem. Photobiol. A Chem. 2007, 187(2-3), 389-394. 

The evolution of nitrogen on photolysis of the aryIdiazonium salts appears to have limited the use of these systems to thin film applications such as container coatings and photoresists (23). Other efficient photoinitiators that do not produce highly volatile products have been disclosed (24-27). These systems are based on the photolysis of diaryliodonium and triarylsulfonium salts. Structures I and II, respectively. These salts are highly thermally stable salts that upon irradiation liberate strong Bronsted acids of the HX type (Reactions 43 and 44) that subsequently initiate cationic polymerization of the oxirane rings ... 

Crivello and Lee have described the synthesis and characterization of a series of (4-alkoxyphenyl)phenyliodonium salts 7, which are excellent photo- and thermal-initiators for the cationic polymerization of vinyl and heterocyclic monomers [17]. Iodonium salts 7 are conveniently prepared by the reaction of alkoxyphenols 6 with [hydroxy(tosyloxy)iodo]benzene followed by anion exchange with sodium hexafluoroantimonate (Scheme 7.2). Products 7 have very good solubility and photoresponse characteristics, which make them especially attractive for use in UV curing applications. Compounds 7 with alkoxy chains of eight carbons and longer are essentially nontoxic, compared to diphenyliodonium hexafluoroantimonate, which has an oral LD50 of 40 mg kg (rats) [17]. 

Like THF, cyclic acetals (e.g., 1,3-dioxolane and 1,3,5-trioxane) are polymerizable only with cationic initiators. The ring-opening polymerization of 1,3,5-trioxane (cyclic trimer of formaldehyde) leads to polyoxymethylenes (see Example 3.24), which have the same chain structure as polyformaldehyde (see Example 3.22). They are thermally unstable unless the semiacetal hydroxy end groups have been protected in a suitable way (see Example 5.7). Like the cyclic ethers, the polymerization of 1,3,5-trioxane proceeds via the addition of an initiator cation to a ring oxygen atom, with the formation of an oxonium ion which is transformed to... 

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