Reversible addition -fragmentation molecular weight distribution

The development of controlled radical polymerization (CRP) methods,(1,2) including atom transfer radical polymerization (ATRP),(3-6) nitroxide-mediated radical polymerization,(7) and reversible addition fragmentation chain transfer polymerization,(8,9) has led to the synthesis of an unprecedented number of novel, previously inaccessible polymeric materials. Well-defined polymers, i.e., polymers with predetermined molecular weight, narrow molecular weight distribution, and high degree of chain end functionalization, prepared by... 

CRP provides a versatile route for the preparation of (co) polymers with controlled molecular weight, narrow molecular weight distribution (i.e., Mw/Mn, or PDI < 1.5), designed architectures, and useful end-functionalities. Various methods for CRP have been developed however, the most successful techniques include ATRP, stable free radical polymerization, " and reversible addition fragmentation chain transfer (RAFT) polymerization. " " CRP techniques have been explored for the synthesis of gels " " and cross-linked nanoparticles of well-controlled polymers in the presence of cross-linkers. 

In most reports, the peptide-polymer-conjugates are prepared by using a polymeric macroinitiator for the polymerization of the polypeptide however, the sequence can also be reversed. Polypeptides can be prepared and used as macroinitiators for a polymerization. Particularly suited for this approach are controlled polymerization techniques because they usually allow good end-group control and adjustment of the molecular weight and the molecular weight distribution of the polymer block. There are different mechanisms for a controlled radical polymerization that can be used for this purpose stable free-radical polymerization (SFRP), ATRP, and reversible addition fragmentation chain transfer (RAFT) polymerization. 

Reversible addition-fragmentation chain transfer polymerization is a reversible deactivation radical polymerization and it represents one of the most versatile methods for providing living characteristics to radical polymerization and polymers of predictable chain length and narrow molecular weight distribution. 

Living free radical polymerizations were also carried out in miniemulsion systems via the reversible addition-fragmentation chain transfer mechanism [66]. The colloidal stability of miniemulsions is the key issue, and nonionic surfactants result in the best results. The polydispersity index of molecular weight distribution for the resultant miniemulsion polymer is generally smaller than 1.2. 

---