Phenylated polyimides: Diels-Alder reaction of biscyclopentadienones with dimaleimides

A series of phenylated polydihydrophthalimides has been synthesized by the Diels-Alder reactions of 3,3′-(oxydi-p-phenylene)bis(2,4,5-triphenylcyclopentadienone) and 3,3′-(p-phenylene)bis(2,4,5-triphenylcyclopentadienone) with N,N′-o-, -m-, and -p-phenylenedimaleimide. The polydihydrophthalimides were soluble in dimethylformamide (DMF) and had intrinsic viscosities that ranged from 0.33 to 1.01, the polymers were dehydrogenated thermally and chemically to afford the corresponding phenylated polyphthalimides. The totally aromatic polyimides were also soluble in DMF but had intrinsic viscosities only as high as 0.41. The thermogravimetric analyses of the polyphthalimides showed breaks near 530°C in air and in nitrogen atmospheres.     

An ab initio molecular orbital study of intramolecular H-bonding: 1,3 propanediol

An ab initio molecular orbital calculation has been carried out for three different conformations of 1,3 propanediol, one of which permits intramolecular H-bond studied by ab initio quantum mechanical methods. The ΔE for H-bonding formation is compated to be 0.9 kcal/mole and the charge redistributions and molecular orbital energy changes are compared to those found in intermolecular H-bonds.     

The first structural and spectroscopic characterization of a neptunyl polyoxometalate complex

The reaction between PW9O349- and NpO2+ has yielded the first structurally characterized neptunyl(V) polyoxometalate complex, [Na2(NpO2)2(A-PW9O34)2]14-. This complex is isostructural with the uranyl(VI) analogue, and there is also spectroscopic evidence for its existence in solution. The complex is readily extracted into toluene, and this may have significance in the sequestering and/or separation of the neptunyl ion in terms of nuclear waste management.     

Energetics of proton transfer between carbon atoms (H3CH ? CH3)−

Ab initio calculations were carried out to study the potential energy surface of (H₃C? H? CH₃)^?. The 6–31G* basis set is supplemented by a set of diffuse p functions on both C and H (with a range of exponents for the latter). The binding energy of CH₄ and CH₃^? to form the (H₃CH? CH₃)^? complex is about 2 kcal/mol, much smaller than for comparable ionic H-bonded systems involving O or N atoms. Nearly half of this interaction energy is due to correlation effects, computed at second and third orders of Møller-Plesset perturbation theory. Correlation is also responsible for substantial reductions in the energy barrier to proton transfer within the complex. This barrier is computed to be 13?15 kcal/mol at the MP3 level, depending upon the exponent used for the H p functions.     

Counterexamples to some results on the existence of field copies

Several criteria are known for determining which connectionsA are determined uniquely by their curvatureF, or byF and its covariant derivatives. On a principal bundle with semi-simple gauge groupG over a 4-manifoldM, a sufficient condition forF to determineA uniquely is that the linear mapB [F B] from Lie algebra-valued 1-forms to 3-forms (pulled back toM via a local gauge) be invertible on an open dense set inM. Recently F. A. Doria has claimed that this condition is also necessary. We present counterexamples to this claim, and also to his assertion thatF determinesA uniquely if the restriction of the bundle to every open subset ofM has holonomy group equal toG andF is not degenerate as a 2-form over spacetime.This research was supported in part by N. S. F. grant MCS80-03419 (first author) and by an NSERCC operating grant (second author)     

Synthesis of phenylated phthalimides. The diels-alder reaction of tetraphenylcyclopentadienone with maleimides

A series of phenylated dihydrophthalimides has been synthesized by the Diels-Alder reaction of tetraphenylcyclopentadienone with maleimide, N-phenylmaleimide, and N,N'-o-, -m-, and -p-phenylenedimaleimide. Subsequent dehydrogenation of these compounds yielded the corresponding phenylated phthalimides. These phthalimides were also obtained in one step when the initial reactions were carried out in refluxing nitrobenzene.     

Achiral Calcium‐Oxalate Crystals with Chiral Morphology from the Leaves of Some Solanacea Plants

The leaves of some plants, particularly among the Solanacea, contain crystals of calcium oxalate with a peculiar chiral pseudo‐tetrahedral morphology, even though the calcium oxalate crystal structure is centrosymmetric, hence achiral. We studied the morphology of these crystals extracted from the leaves of three Solanacea plants: the potato, the hot pepper, and a species of wild Solanum. The crystal morphology was the same in all three species. Based on the examination of more than 100 crystals from each plant, we showed that the crystal morphology is chiral with invariant chirality. We suggest that morphological chirality is induced by macromolecules during nucleation from a specific, genetically encoded crystal plane, and is further established during subsequent controlled crystal growth. This is one of few examples where it is possible to deduce a molecular mechanism for biologically induced breaking of morphological symmetry in organisms. A very high level of recognition is required by the macromolecules to allow them to distinguish between symmetry‐related crystal planes. It is also surprising that this finely controlled mechanism of crystal formation, including the chiral morphology, has been conserved during evolution.     

Non-covalent reconfigurable microgel colloidosomes with a well-defined bilayer shell

Microgels are extremely interfacially active and are widely used to stabilize emulsions. However, they are commonly used to stabilize oil-in-water emulsions due to their intrinsic hydrophilicity and initially dispersed in water. In addition, there have been no attempts to control microgel structural layers that are formed at the interface and as a result it limits applications of microgel in advanced materials. Here, we show that by introducing octanol into poly(N-isopropylacrylamide-co-methacrylic acid) (PNIPAM-co-MAA) microgels, octanol-swollen microgels can rapidly diffuse from the initially dispersed oil phase onto the water droplet surface. This facilitates the formation of microgel-laden interfacial layers with strong elastic responses and also generates stable inverse water-in-oil Pickering emulsions. These emulsions can be used as templates to produce microgel colloidosomes, herein termed ‘microgelsomes’, with shells that can be fine-tuned from a particle monolayer to a well-defined bilayer. The microgelsomes can then be used to encapsulate and/or anchor nanoparticles, proteins, vitamin C, bio-based nanocrystals or enzymes. Moreover, the programmed release of these substances can be achieved by using ethanol as a trigger to mediate shell permeability. Thus, these reconfigurable microgelsomes with a microgel-bilayer shell can respond to external stimuli and demonstrate tailored properties, which offers novel insights into microgels and promise wider application of Pickering emulsions stabilized by soft colloids.

Inverse W/O Pickering emulsions and reconfigurable microgelsomes with a well-defined bilayer structure are prepared from octanol-swollen PNIPAM-co-MAA microgels and the combination of binary microgels, which promise wider application of soft colloids.     

A new method for the determination of the 34S/32S ratio of water-soluble sulphur in soil

A new method for the determination of the ³⁴S/³²S ratio of water-extractable sulphate in soil is described. Soils are extracted directly with deionized water, which is evaporated down. The remaining residue is then rehydrated and transferred to tin cups containing an adsorbent and mixed with an oxygen donor (V₂O₅). Samples are then analysed using a continuous flow isotope ratio mass spectrometer. The new method requires around 10?g soil per determination, compared to much larger amounts (up to kilograms) of soil required for the previous methods. Sample preparation and subsequent analysis is quick and efficient. The method is demonstrated using a number of soils collected from around the world to provide a range of determined δ³⁴S values. The δ³⁴S values of water-extractable sulphur were broadly similar to those of the soil total sulphur.