Macromonomer molecule

Largest constitutional unit contributed by a single macromonomer molecule to the structure of a macromolecule. 

Note The homopolymerization or copolymerization of macromonomer molecules, each of... 

A polymer composed of macromonomer molecules, macromonomer molecule... 

The number of styrene group in a macromonomer molecule could be accurately determined by measuring the intensities of the signals due to group at the left-... 

Another example of the flexibility of ADMET is the demonstration of successful polymerization of o /v-telechelic diene carbosilane macromonomers.45 The synthesis of macromonomer 30 is achieved using catalyst 23 and copolymerized with a rigid small-molecule diene, 4,4/-di-trans-l-propenylbiphenyl (Fig. 8.17). 

Brushes with long side chains can be synthesized by polymerization of macromonomers [117-119] or by grafting of the side chains to [16-20] or from [21] a main chain. In contrast to globular dendrimers, these molecules have an anisotropic primary structure and experience bending or coiling of the molecular contour. Depending on the relative stiffness of the main and side chains, one may distinguish four types of molecular cylinders (Fig. 20). 

A concept has been presented for preparing a large macromonomer - the molecular weight can be 10,000 or 20-30,000 grams/ mole - with a single unsaturated group at the end of the polymer chain. How can it be proved that a molecule this big, if indeed it has functionality, will react and how will it react with typical commercially available low molecular weight monomeric species ... 

The use of alkyllithium initiators which contain functional groups provides a versatile method for the preparation of end functionalized polymers and macromonomers. For a living anionic polymerization, each functionalized initiator molecule produces one macromolecule with the functional group from the initiator residue at one chain end and the active carbanionic propagating species at the other chain end. 

In this review we summarize and discuss the amphiphilic properties of polyoxyethylene (PEO) macromonomers and PEO graft copolymer molecules, the aggregation of amphiphilic PEO macromonomers into micelles, the effect of organized aggregation of macromonomers on the polymerization process, and the kinetics of radical polymerization and copolymerization of PEO macromonomer in disperse (dispersion, emulsion, miniemulsion, microemulsion, etc.) systems [1-5]. 

Gramain and Frere [82] observed that the free radical polymerization of co-meth-acryloyl terminated PEO macromonomers in the aqueous phase deviates from the solution polymerization. Polymerizations initiated by KPS in water were much faster than those that proceeded in the solution. Low molecular weight polymers were formed in the aqueous systems (ca. up to 20 macromonomer units were incorporated into polymer molecules). 

Well-defined macromonomers of poly(BVE), poly(IBVE), and poly(EVE) with co-methacrylate end group [91] were prepared by living cationic polymerization of the corresponding monomers initiated by trifluoromethanesulfonic add in CH2C12 at -30 °C in the presence of thiolane as a Lewis base. After complete conversion, the polymers were quenched with 37 in the presence of 2,6-lu-tidine or with 41 to produce macromonomers with Mn up to 10,000 g mol-1, with narrow MWD, bearing one polymerizable methacrylate function per molecule. The same polymers were also quenched with 38 in the presence of 2,6-lutidine to give poly(vinyl ether)s with an allylic terminal group. 

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