Polymer-induced alignment of DL-alanine nanocrystals to crystalline mesostructures

Crystallization of DL-alanine by cooling of a supersaturated solution in the presence of a chiral double-hydrophilic block copolymer poly(ethylene glycol)-block-poly(ethylene imine)-S-isobutyric acid (PEG4700-PEI1200-S-iBAc) yields crystal superstructures with an astonishing morphology. Although analysis by light microscopy reveals these crystals to be apparently well facetted, electron microscopy shows that they consist of three-dimensionally, well-aligned nanocrystals that are scaffolded to a so-called mesocrystal. This mesocrystal is formed by polymer-mediated structuration, and provides evidence for the importance of mesoscopic events in a typical crystallization process.     

Extremely base-resistant organic phosphazenium cations

A series of peralkylated polyaminophosphazenium cations exhibiting extraordinary base resistance under phase-transfer conditions were efficiently synthesized from readily available starting materials. Their half lives under these conditions exceed those of the most stable conventional organic cations by factors of up to 3000.     

Electrospray ionization mass spectrometric study of purine base-cisplatin complexes

By mixing cisplatin (cis-diamminedichloroplatinum(II)) with purine base the following ions have been obtained under electrospray ionization conditions: [A+Pt(NH3)2 Cl]+, [A+PtNH3Cl]+, [G+Pt(NH3)2 Cl]+ and [G+PtNH3)Cl]+. Their collision-induced dissociation led to the loss of NH3 and HCl and formation of the protonated base. The last process is strongly favoured for adenine over guanine. It confirms that, analogously as for DNA, formation of the guanine-cisplatin complex is favoured over that of the adenine complex and, as a consequence, it suggests that the mass spectrometric study of nucleic base complexes with platinum may provide some information on the interactions of DNA with other platinum drugs. The loss of NH3 accompanied by that of CO from the guanine ring has experimentally confirmed the presence of a strong hydrogen bond between the NH3 molecule and the O=C6 moiety of guanine found by theoretical calculations.     

Manipulating 2D metal-organic networks via ligand control

High-resolution scanning tunneling microscopy has revealed how ligand control can be successfully employed to eliminate isomeric phases and defects in 2D coordination networks that are self-assembled at a surface support by replacing symmetric dicarboxylato linker ligands to dissymmetric carboxylpyridyl linker ligands.     

Three dimensional k-space trajectory design using genetic algorithms

Image quality and total scan time in MRI are determined in large part by the trajectory employed to sample the Fourier space. Each trajectory has different properties like coverage of k-space, scan time, sensitivity to off-resonance conditions, etc. These properties are often contradictory, therefore a universal optimal trajectory does not exist and ultimately, it will depend on the image characteristics sought. Most trajectories used today are designed based on intuition and k-space analysis more than with optimization methods. This work presents a 3D k-space trajectory design method based on Genetic Algorithm optimization. Genetic Algorithms have been chosen because they are particularly good for searching large solution spaces. They emulate the natural evolutionary process allowing better offsprings to survive. The objective function searches the maximum of the trajectory's k-space coverage subject to hardware constraints for a fixed scanning time using the trajectory's torsion as its optimization variable.The method proved to be effective for generating k-space trajectories. They are compared with well-established trajectories. The results of simulated experiments show that they can be appropriate for image acquisition under certain special conditions, like off-resonance and undersampling. This design method can be extended to include other objective functions for different behaviors.     

A novel bis(imino)amine ligand as a result of acetonitrile coupling with the diiodides of Dy(II) and Tm(II)

Complexes of Dy(III) and Tm(III) with novel 1,1'-bis(iminoethyl)ethylamine ligands, [{(HN=CMe)2MeCNH2}Ln(MeCN)6]I3, were obtained by the reactions of LnI2 (Ln = Dy(II), Tm(II)) with acetonitrile.     

Template-directed olefin cross metathesis

[reaction: see text] A template containing two secondary dialkylammonium ion recognition sites for encirclement by olefin-bearing dibenzo[24]crown-8 derivatives has been used to promote olefin cross metatheses with ruthenium-alkylidene catalysts. For monoolefin monomers, the rates of metatheses and yields of the dimers are both amplified in the presence of the template. Likewise, for a diolefin monomer, the yield of the dimer is enhanced in the presence of the template under conditions where higher oligomers are not formed.