Cover Picture: Heterogeneously Hybridized Porous Coordination Polymer Crystals: Fabrication of Heterometallic Core–Shell Single Crystals with an In‐Plane Rotational Epitaxial Relationship (Angew. Chem. Int. Ed. 10/2009)

A porous copper coordination framework grew epitaxially as a single crystal on the surface of a single crystal of a porous zinc coordination framework, as described by S. Kitagawa and co‐workers in their Communication on page 1766 ff. The picture shows the structural relationship between the copper and zinc frameworks, which has been unveiled by synchrotron surface X‐ray diffraction measurements; in‐plane rotational epitaxial growth compensates for the different lattice constants of the two crystals.

     

Density functional study on geometrical features and electronic structures of di-mu-oxo-bridged [Mn2O2(H2O)8]q+ with Mn(II), Mn(III), and Mn(IV)

We report the geometrical features and electronic structures of di-mu-oxo-bridged Mn-Mn binuclear complexes with H2O ligands [Mn2O2(H2O)8]q+ in the iso- and mixed-valence oxidation states. All of the combinations among Mn(II), Mn(III), and Mn(IV) ions are considered the oxidation states of the Mn-Mn center, and the changes in molecular structure induced by the different electron configurations of Mn-based orbitals are investigated in relation to the oxygen-evolving complex (OEC) of photosystem II. The stable geometries of complexes are determined by using the hybrid-type density functional theory for both of the highest- and lowest-spin couplings between Mn sites, and the lowest-spin-coupled states are energetically more favorable than the highest-spin-coupled states except in the case of the complexes with the Mn(II) ion. The coordination positions of H2O ligands at the Mn(II) site tend to shift from the octahedral positions in contrast to those at the Mn(III) and Mn(IV) sites. The shape of the Mn2O2 core and the distances between the Mn ions and the H2O ligands vary depending on the electron occupations of the octahedral eg orbitals on the Mn site with an antibonding nature for the Mn-ligand interactions, indicating the trend as Mn(II)-O > Mn(III)-O and Mn(IV)-O, O-Mn(II)-O > O-Mn(III)-O > O-Mn(IV)-O among the iso-valence Mn2O2 cores, and O-Mn(lower)-O < O-Mn(higher)-O within the mixed-valence Mn2O2 core, and as Mn(II)-OH2 and Mn(III)-OH2 > Mn(IV)-OH2 for the axial H2O ligand. The optimized geometries of model complexes are compared with the X-ray structure of the OEC, and it is suggested that the cubane-like Mn cluster of the active site may not contain a Mn(II) ion. The effective exchange integrals are estimated by applying the approximate spin projection to clarify the magnetic coupling between Mn sites, and the superexchange pathways through the di-mu-oxo bridge are examined on the basis of the singly occupied magnetic orbitals derived from the singlet-coupled natural orbitals in the broken-symmetry state. The comparisons of the calculated results between [Mn2O2(H2O)8]q+ in this study and [Mn2O2(NH3)8]q+ reported by McGrady et al. suggest that the symmetric pathways are dominant to the exchange coupling constant, and the crossed pathway would be less important for the former than it would for the latter in the Mn(III)-Mn(III), Mn(IV)-Mn(IV), and Mn(III)-Mn(IV) oxidation states.     

Multi-frequency ESR study of the polycrystalline phenoxyl radical of alpha-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-tert-butylnitrone in the diamagnetic matrix

Multifrequency (X-, Q-, and W-band) electron spin resonance (ESR) spectroscopy has been used to characterize the phenoxyl radical produced from alpha-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-tert-butylnitrone, which is a new spin-trapping reagent. The X-band measurement did not resolve the powder-pattern ESR spectrum. Because of its higher resolution with g value, the Q-band ESR study revealed that the g factor has an axial-like symmetry and that the observed hyperfine structure in the Z-direction is caused by the nitrogen nucleus at the para-position. Furthermore, the results of the W-band ESR experiment more clearly distinguished the perpendicular components from the parallel component, resolving the perpendicular components into x and y components. The X-band powder spectrum was similar to the X-band ESR spectrum of the radical in a frozen solution of toluene. The computer simulation spectra performed using the obtained parameters fitted the experimental spectra well. A comparison of the amplitude of g( perpendicular)(gx, gy) with that of gz showed that the unpaired electron is delocalized over the pi-conjugated framework. Considering the hyperfine coupling constant, it was concluded that about 16% of the unpaired electron distributed over the nitrogen nucleus at the para-position. This study thus showed the significant potential of a multifrequency ESR approach to a powder sample radical in terms of its high resolution with g value.     

Synthetic study for two 2H‐chromenic acids, 8‐chlorocannabiorcichromenic acid and mycochromenic acid

Two 2H‐chromenes having a fully substituted benzene ring, 8‐chlorocannabiorcichromene ( 1 ) and mycochromenic acid ( 2 ), were synthesized by a condensation of salicylaldehydes with isopropylidenemalonate or the thermal cyclization of corresponding propargyl ethers.     

Olefin metathesis of the aligned assemblies of conjugated polymers constructed through supramolecular bundling

The ordered structures constructed from an aligner molecule 1o and conjugated polymers (CPs) were efficiently converted into the poly-pseudo-rotaxane structures by the template-assisted ring-closing olefin metathesis (RCM) of olefinic groups at the peripheral positions of 1o. Moreover, the poly-pseudo-rotaxane structures permitted the separation of the crystalline ordered assemblies of CP by size exclusion chromatography and the preservation of the sheet morphologies after the treatment with trifluoroacetic acid. The morphologies and the periodicities of assemblies were also maintained after the retrieving treatments.     

Synthesis of urea-tethered neoglycoconjugates and pseudooligosaccharides in water

A novel approach to the synthesis of urea glycosides in aqueous media has been explored. Steyermark's glucopyranosyl oxazolidinone was found to be a good synthon for anchoring glucosyl moieties onto amines and thiols. The present method was successfully applied to establish a new route for the synthesis of urea-tethered neoglycoconjugates and pseudooligosaccharides in water.     

Blow-up set for a semilinear heat equation with small diffusion

We consider the blow-up problem for a semilinear heat equation,

     

Synthesis of bitetrathiafulvalenes with FeCl3-mediated homo-coupling of tetrathiafulvalenylmagnesium bromide and formation of nanostructures from bitetrathiafulvalenes having long alkylthio chains

The FeCl₃-mediated homo-coupling of 4,5-bis(alkylthio)-4′-tetrathiafulvalenylmagnesium bromide 5 produced the corresponding bitetrathiafulvalene derivatives 2a-d in moderate yields (25-51%). Bitetrathiafulvalenes 2c and 2d having long alkylthio chains formed nanostructures and showed bulk electric conductivities (σ_rt = 2.6 − 8.0 × 10⁻⁵ S cm⁻¹) in the neutral state owing to the fastener effect. Interestingly, the nanofiber of tetrakis(dodecylthio)bitetrathiafulvalene 2d exhibited a p-type semiconductivity as detected by AFM.     

Use of Side‐Chain Incompatibility for Tailoring Long‐Range p/n Heterojunctions: Photoconductive Nanofibers Formed by Self‐Assembly of an Amphiphilic Donor–Acceptor Dyad Consisting of Oligothiophene and Perylenediimide

To tailor organic p/n heterojunctions with molecular‐level precision, a rational design strategy using side‐chain incompatibility of a covalently connected donor–acceptor (D–A) dyad has been successfully carried out. An oligothiophene–perylenediimide dyad, when modified with triethylene glycol side chains at one terminus and dodecyl side chains at the other ( 2 Amphi ), self‐assembles into nanofibers with a long‐range D/A heterojunction. In contrast, when the dyad is modified with dodecyl side chains at both termini ( 2 Lipo ), ill‐defined microfibers result. In steady‐state measurements using microgap electrodes, a cast film of the nanofiber of 2 Amphi displays far better photoconducting properties than that of the microfiber of 2 Lipo . Flash‐photolysis time‐resolved microwave conductivity measurements, in conjunction with transient absorption spectroscopy, clearly indicate that the nanofiber of 2 Amphi intrinsically allows for better carrier generation and transport properties than the microfibrous assembly of 2 Lipo .