PubMed Health⌕ Search

Biomedical subjects

H Keul

Publications and source records attributed to H Keul.

2 recordsLinked to original sources

Domain sizes in heterogeneous polymers by spin diffusion using single-quantum and double-quantum dipolar filters.

1H spin-diffusion experiments employing a double-quantum (DQ) dipolar filter were performed for the characterization of the microdomain structure of heterogeneous samples. For this purpose the NMR spin-diffusion process was analysed based on a model morphology of three different domains with arbitrary sizes, diffusivities, and filter efficiency. General analytical solutions for z magnetization source and sink were obtained valid for a one-dimensional lamellar morphology in the full range of spin-diffusion times. These solutions of the spin-diffusion equations were used for determining the crystalline, interface, and amorphous domain sizes in polystyrene-poly(ethylene oxide) (PS-PEO) and poly(hydroxyethylmethacrylate)-poly(ethylene oxide) (PHEMA-PEO). The DQ dipolar filter has a good efficiency for PS-PEO but is only partially efficient in filtering the signal of the mobile domains in the PHEMA-PEO diblock copolymer. The domain sizes measured by the DQ filter method are compared to those obtained using the traditional dipolar filter creating z magnetization in the mobile domains.

Journal Article↗

Postulation of the mechanism of the selective synthesis of isotactic poly(methyl methacrylate) catalysed by [Zr[(Cp)(Ind)CMe2](Me)(thf)](BPh4): a Hartree-Fock, MP2 and density functional study.

The bridged. C1-symmetric, single-component zirconocene [Zr((Cp)(Ind)CMe2](Me)(thf)](BPh4) (Ind = indenyl, Cp = cyclopentadienyl) polymerises methyl methacrylate (MMA) selectively to isotactic poly(methyl methacrylate) (PMMA) without further cocatalysts or activators. To elucidate the stereoselective steps of the polymerisation of MMA by using this catalyst we studied the propagation steps occurring with the derivative [Zr[(Cp)(Ind)CH2][-O-C(OMe)=C(Me)(Et)](MMA)]+ by ab initio calculations at the Hartree-Fock(HF) level of theory. After the initiation step, which consumes the first two MMA molecules, each new catalytic cycle begins with the stereoselective addition of a new MMA molecule at the indenyl side of the zirconocene fragment. At the same time the enolate ring undergoes a stereoselective in-plane ring shift to the side opposite to the indenyl ring. These findings are used to postulate a mechanism for the polymerisation that explains the stereoselective synthesis of isotactic PMMA.

Journal Article↗