Poly kinetic mechanism

Kosenko, R. Yu. lordanskii, A. L. Markin, V. S. Arthanarivaran, G. Bonartsev, A. R and Bonartseva, G. A. Controlled release of antiseptic drug from poly(3-hydroxybutyrate)-based membranes, combination of diffusion and kinetic mechanisms. Pharmaceutical Chem. J. 2007, 41(12), 652-655. 

Poly(ADP-ribose) polymerase is a chromatin-associated enzyme which, in the presence of fragmented DNA, assembles branched homopolymers from the ADP-ribose moiety of NAD (reviewed in [1]). Fragmented DNA is an essential activator of the polymerase and is not modified by the reaction. This report presents data related to the kinetic mechanism of DNA activation of the poly(ADP-ribose) polymerase. 

Fig. 6. Proposed kinetic mechanism for poly(ADP-ribose) polymerase...

Alteration of Poly(ADP-Ribose) Metabolism By Ethanol Kinetic Mechanism Of Action... 

Swarc,M. The Kinetics and Mechanism of N-carboxy-a-amino-acid Anhydride (NCA) Polymerization to Poly-amino Acids. Vol. 4, pp. 1—65. 

The polymerization kinetics have been intensively discussed for the living radical polymerization of St with the nitroxides,but some confusion on the interpretation and understanding of the reaction mechanism and the rate analysis were present [223,225-229]. Recently, Fukuda et al. [230-232] provided a clear answer to the questions of kinetic analysis during the polymerization of St with the poly(St)-TEMPO adduct (Mn=2.5X 103,MW/Mn=1.13) at 125 °C. They determined the TEMPO concentration during the polymerization and estimated the equilibrium constant of the dissociation of the dormant chain end to the radicals. The adduct P-N is in equilibrium to the propagating radical P and the nitroxyl radical N (Eqs. 60 and 61), and their concentrations are represented by Eqs. (62) and (63) in the derivative form. With the steady-state equations with regard to P and N , Eqs. (64) and (65) are introduced, respectively ... 

Crosslinked polymer networks formed from multifunctional acrylates are completely insoluble. Consequently, solid-state nuclear magnetic resonance (NMR) spectroscopy becomes an attractive method to determine the degree of crosslinking of such polymers (1-4). Solid-state NMR spectroscopy has been used to study the homopolymerization kinetics of various diacrylates and to distinguish between constrained and unconstrained, or unreacted double bonds in polymers (5,6). Solid-state NMR techniques can also be used to determine the domain sizes of different polymer phases and to determine the presence of microgels within a poly multiacrylate sample (7). The results of solid-state NMR experiments have also been correlated to dynamic mechanical analysis measurements of the glass transition (1,8,9) of various polydiacrylates. 

Most helicates have linear axes, though a few helicates with circular axes are known - indeed the chiral (D4) molecular squares formed from Zn2+ and 2,5 -bis(2,2 -bipyridin- 6 -yl)pyrazine, 22, may be regarded as circular helicates (450). The formation of circular or linear forms seems to depend on balances between kinetic and thermodynamic control iron(II)-poly-2,2/-diimine systems with their substitutionally-inert metal centers provide useful systems for disentangling thermodynamic and kinetic contributions. The mechanism of formation of circular helicates of this type is believed to entail a kinetically favored triple helicate intermediate (484). Self-assembly of chiral-twisted iron(III)-porphyrin dimers into extended polynuclear species takes place through the intermediacy... 

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