Hybrid graft copolymers using

Several approaches used to prepare hybrid polymers in which polyacetylene is an electroactive component are presented. Specifically, these involve the preparation of (1) composites by in-situ polymerization, (2) graft copolymers utilizing carbanions in n-type (CH)X as polymerization initiators, and (3) A-B diblock copolymers exploiting anionic-to-Ziegler-Natta transformation reactions. 

In the area of novel materials CMU protected (co)polymers prepared by ATRP except with CCI4 initiator and telechelic polymers prepared by CRP with MW > 20,000 (49) copolymers with a tme gradient segment (30) polar ABA block copolymers, (30) and well defined graft copolymers and segmented copolymers with one or more CRP blocks where the macroinitiator had been prepared by another polymerization process. (36) In addition, the use of tethered initiators allowed synthesis of hybrid core/shell copolymers. Pending applications disclose other novel polymeric materials. 

Numerous polymers and copolymers have been synthesized using NMP techniques. See, for example, the reviews by Hawker [58, 59]. Graft copolymers and hybrid materials synthesized by NMP are reviewed in Chapter 10. 

Figure 35.7 Enzymatic extension of DNA-synthetic polymer hybrids and preparation of DNA-synthetic polymer graft architectures. (a) Schematic representation of enzymatic extension of ss DNA diblock copolymer using TDT and dNTP. P denotes the phosphate group(s) of the nucleotide ...

From a topological point of view, the IPN s are closely related to polymer blends, block and graft copolymers, AB-crosslinked copolymers " and ionomeric blends. Some interesting hybrids exist between the IPN s and other polymer materials. The thermoplastic IPN s contain physical crosslinks rather than chemical (covalent) crosslinks. Physical crosslinks can be formed from block copolymers, ionomers or semi-crystalline polymers. When the temperature is raised above the softening point of the respective components, the material flows like a thermoplastic. At service temperatures, it behaves like an IPN, with thermoset behavior. Table 1 summarizes some of the terminology used to describe IPN structure and morphology. 

The concept of PO macroinitiators centers on the introduction of an initiation moiety into an olefinic polymer chain for polymerization. The most effective route for preparing PO macroinitiators is by employing functional polyolefins containing hydroxyl groups or other reactive groups. These functional POs are prepared by copolymerization of olefins with functional monomers and post-polymerization reaction, as mentioned above. In the case where an initiation moiety was at the chain-end of the polyolefins, a block type copolymer is produced. It has been reported that thiol-terminated PP was used as polymeric chain transfer agent in styrene and styrene/acrylonitrile polymerization to form polypropylene-b/odc-polystyrene (PP-b-PS) and polypropylene-btock-poly(styrene-co-acrylonitrile) (PP-b-SAN) block copolymer [19]. On the other hand, polymer hybrids with block and graft structures can be produced if initiation moieties are in the polymer chain. 

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