Porphyrin J-aggregates as a probe for chiral impurities as demonstrated by their symmetry breaking by confinement in montmorillonite clay.

In this paper, we demonstrate that chiral J-aggregates of porphyrins are able to detect minute chiral impurities, in this case, the presence of right-handed quartz in acid-activated K10 montmorillonite clay. Aggregation and symmetry breaking of 5,10,15,20-(tetra-4-carboxyphenyl) porphyrin (TCPP) and 5,10,15,20-(tetra-4-sulfonatophenyl) porphyrin (TPPS) were observed upon interaction with acid-activated montmorillonite clay (MMT-K10). A panel of characterization techniques, including UV-visible, electronic circular dichroism, IR, and vibrational circular dichroism spectroscopies, as well as X-ray scattering, were employed to investigate the aggregation of the confined TPPS and TCPP.

Size-tunable silicon nanoparticles synthesized in solution a redox reaction.

A current challenge in silicon chemistry is to perform liquid-phase synthesis of silicon nanoparticles, which would permit the use of colloidal synthesis techniques to control size and shape. Herein we show how silicon nanoparticles were synthesized at ambient temperature and pressure in organic solvents through a redox reaction. Specifically, a hexacoordinated silicon complex, bis(,'-diisopropylbutylamidinato)dichlorosilane, was reduced by a silicon Zintl phase, sodium silicide (NaSi).

Induced circular dichroism from helicoidal nano substrates to porphyrins: the role of chiral self-assembly.

Because the combination of chiral and magnetic properties is becoming more and more attractive for magneto-chiral phenomena, we here aim at exploring the induction of chirality to achiral magnetic molecules as a strategy for the preparation of magneto-chiral objects. To this end, we have associated free base- and metallo-porphyrins with silica nano helices, using a variety of elaboration methods, and have studied them mainly by electronic natural circular dichroism (NCD) and magnetic circular dichroism (MCD) spectroscopies. While electrostatic or covalent surface grafting uniformly yielded very low induced CD (ICD) for the four assayed porphyrins, a moderate response was observed when the porphyrins were incorporated into the interior of the double-walled helices, likely due to the association of the molecules with the chirally-organized gemini surfactant.

Design of Binary NbO-SiO Self-Standing Monoliths Bearing Hierarchical Porosity and Their Efficient Friedel-Crafts Alkylation/Acylation Catalytic Properties.

Alkylation of aromatic hydrocarbons is among the most industrially important reactions, employing acid catalysts such as AlCl, HSO, HF, or HPO. However, these catalysts present severe drawbacks, such as low selectivity and high corrosiveness. Taking advantage of the intrinsic high acid strength and Lewis and Brønsted acidity of niobium oxide, we have designed the first series of NbO-SiO(HIPE) monolithic catalysts bearing multiscale porosity through the integration of a sol-gel process and the physical chemistry of complex fluids.

A linear metal-metal bonded tri-iron single-molecule magnet.

The linear trinuclear complex cation [Fe(DpyF)] was prepared as [Fe(DpyF)](BF)·2CHCN. With large Fe-Fe distances of 2.78 Å, this complex demonstrates intramolecular ferromagnetic coupling between the anisotropic Fe centers (/ = +20.

Chirality determination in crystals.

This tutorial review article discusses chirality determination in the solid state, both in single crystals and in crystal assemblies, with an emphasis on X-ray diffraction. The main principles of using X-ray diffraction to reliably determine absolute structure are summarized, and the complexity which can be encountered in chiral structures-kryptoracemates, scalemates, and inversion twinning-is illustrated with examples from our laboratories and the literature. We then address the problem of the bulk crystallization and discuss different techniques to determine chirality in a large assembly of crystal structures, with a special prominence given to an X-ray natural circular dichroism mapping technique that we recently reported.

Magneto-chiral anisotropy: From fundamentals to perspectives.

The interplay between chirality and magnetic fields gives rise to a cross effect referred to as magneto-chiral anisotropy (MChA), which can manifest itself in different physical properties of chiral magnetized materials. The first experimental demonstration of MChA was by optical means with visible light. Further optical manifestations of MChA have been evidenced across most of the electromagnetic spectrum, from terahertz to X-rays.

Rapid Discrimination of Crystal Handedness by X-ray Natural Circular Dichroism (XNCD) Mapping.

An original method for determining the handedness of individual non-centrosymmetric crystals in a mixture using a tightly-focused, circularly polarized X-ray beam is presented. The X-ray natural circular dichroism (XNCD) spectra recorded at the metal K-edge on selected crystals of [Δ-M(en) ](NO ) and [Λ-M(en) ](NO ) (M=Co , Ni ) show extrema at the metal pre-edge (7712 eV for Co, 8335 eV for Ni). A mapping of a collection of some 220 crystals was performed at the respective energies by using left and right circular polarizations.

Resolution, structures, and vibrational circular dichroism of helicoidal trinickel and tricobalt paddlewheel complexes.

It has been recently shown that enantiomers of the helicoidal paddlewheel complex [Co (dpa) (CH CN) ] (dpa = the anion of 2,2'-dipyridylamine) can be resolved using the chiral [As (tartrate) ] anion (AsT) and that these complexes demonstrate a strong chiroptical response in the ultraviolet-visible and X-ray energy regions. Here we report that the nickel congener, [Ni (dpa) (CH CN) ] , can likewise be resolved using AsT. Depending on the stereochemistry of the enantiopure AsT anion, one or the other of the trinickel enantiomers crystallize from CH CN and diethyl ether in space group P42 2 as the (NBu ) [Ni (dpa) (CH CN) ](AsT) ·[solvent] salt.

The Origin of Magnetic Anisotropy and Single-Molecule Magnet Behavior in Chromium(II)-Based Extended Metal Atom Chains.

Chromium(II)-based extended metal atom chains have been the focus of considerable discussion regarding their symmetric versus unsymmetric structure and magnetism. We have now investigated four complexes of this class, namely, [Cr(dpa)X] and [Cr(tpda)X] with X = Cl and SCN [Hdpa = dipyridin-2-yl-amine; Htpda = ,-di(pyridin-2-yl)pyridine-2,6-diamine]. By dc/ac magnetic techniques and EPR spectroscopy, we found that all these complexes have easy-axis anisotropies of comparable magnitude in their = 2 ground state (|| = 1.

Enantiopure Chiral Coordination Polymers Based on Polynuclear Paddlewheel Helices and Arsenyl Tartrate.

Herein, we report the preparation of chiral, one-dimensional coordination polymers based on trinuclear paddlewheel helices [M₃(dpa)₄] (M = Co(II) and Ni(II); dpa = the anion of 2,2'-dipyridylamine). Enantiomeric resolution of a racemic mixture of [M₃(dpa)₄] complexes was achieved by chiral recognition of the respective enantiomer by [Δ-As₂(tartrate)₂] or [Λ-As₂(tartrate)₂] in ,-dimethylformamide (DMF), affording crystalline coordination polymers formed from [(Δ-Co₃(dpa)₄)(Λ-As₂(tartrate)₂)]·3DMF (Δ-), [(Λ-Co₃(dpa)₄)(Δ-As₂(tartrate)₂)]·3DMF (Λ-), [(Δ-Ni₃(dpa)₄)(Λ-As₂(tartrate)₂)]·(4 - )DMF∙Et₂O (Δ-) or [(Λ-Ni₃(dpa)₄)(Δ-As₂(tartrate)₂)]·(4 - )DMF∙Et₂O (Λ-) repeating units. UV-visible circular dichroism spectra of the complexes in DMF solutions demonstrate the efficient isolation of optically active species.

Temperature dependence of the spin state and geometry in tricobalt paddlewheel complexes with halide axial ligands.

Trinuclear cobalt paddlewheel complexes, [Co3(dpa)4X2] (dpa = the anion of 2,2'-dipyridylamine, X = Cl-, Br-, -NCS-, -CN-, (NC)2N-), are known to demonstrate a thermally-induced spin-crossover (SCO). Despite a wealth of structural and magnetic information about such complexes, the role of the axial ligand on the characteristic SCO temperature (T1/2) remains ambiguous. The situation is complicated by the observation that the solid state geometry of the complexes, symmetric or unsymmetric, with respect to the central cobalt ion, also appears to influence the SCO behavior.

Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain.

A simple procedure based on anion exchange was employed for the enantiomeric resolution of the extended metal atom chain (EMAC) [Co(dpa)(MeCN)]. Use of the chiral salt (NBu)[As(tartrate)], (Λ- or Δ-), resulted in the selective crystallization of the EMAC enantiomers as [Δ-Co(dpa)(MeCN)](NBu)[Λ-As(tartarte)], (Δ-) and [Λ-Co(dpa)(MeCN)](NBu)[Δ-As(tartrate)] (Λ-), respectively, in the 422 space group, whereas a racemic mixture of yielded [Co(dpa)(MeCN)][As(tartrate)]·2MeCN (-), which crystallized in the 2/ space group. The local electronic and magnetic structure of the EMAC enantiomers was studied, exploiting a variety of dichroisms in single crystals.

Isomeric Column-Forming Esters and Imides with Varying Curvatures of the Aromatic Plane.

Dibenzo[a,j]coronene-tetracarboxylic alkyl esters and imides with either a centrosymmetric bis-peri substitution pattern or a polar bis-ortho substitution pattern form hexagonal columnar mesophases, which in the case of the imides persist at room temperature. The bis-peri isomers are obtained via a two-fold oxidative photocyclization; the bis-ortho isomers are accessed via a glyoxylic Perkin reaction of triphenylene and naphthalene building blocks. Steric congestion between the substituents and the adjacent benzo protrusion in the bis-ortho esters and imides leads to bending of the aromatic plane, which thus avoids twisting.

From 1,4-Phenylenebis(phenylmaleate) to a Room-Temperature Liquid-Crystalline Benzo[ghi]perylene Diimide.

The photocyclization of tetraethyl 1,4-phenylenebis(phenylmaleate) in the presence of iodine and oxygen predominantly yields tetraethyl [5]helicene-5,6,9,10-tetracarboxylate, together with small amounts of tetraethyl dibenz[a,h]anthracene-5,6,12,13-tetracarboxylate and tetraethyl benzo[ghi]perylene-3,4,11,12-tetracarboxylate. The helicene tetraester is planarized to the benzoperylene tetraester by Scholl reaction with AlCl followed by reesterification of the partially hydrolyzed crude product. Subsequent treatment with a branched alkylamine yields a columnar liquid-crystalline benzoperylene diimide whose mesophase is stable at room temperature despite its limited and non-centrosymmetric alkyl periphery.

Columnar Liquid-Crystalline Dibenzopentacenodithiophenes by Photocyclization.

The twofold glyoxylic Perkin reaction of perylene-3,9-diglyoxylic acid with thiophene-diacetic acid followed by oxidative photocylization and reaction with α-branched primary alkylamines yields columnar liquid-crystalline diimides with two sulfur atoms in the condensed arene system. A broad temperature range of the hexagonal columnar mesophase is induced by racemic doubly branched alkyl chains. The HOMO and LUMO energy levels of these thiophene-derived diimides qualify them as electron donors with respect to perylene diimides.

High rectification in organic diodes based on liquid crystalline phthalocyanines.

The optical and electrical properties of mesogenic metal-free and metalated phthalocyanines (PCs) with a moderately sized and regioregular alkyl periphery were investigated. In solution, the individualized molecules show fluorescence lifetimes of 4-6 ns in THF. When deposited as solid thin films the materials exhibit significantly shorter fluorescence lifetimes with bi-exponential decay (1.

One-dimensional coordination polymers of [Co3(dpa)4](2+) and [MF6](2-) (M = Re(IV), Zr(IV) and Sn(IV)).

One-dimensional coordination polymers of alternating metal-metal bonded trinuclear [Co3(dpa)4](2+) (dpa = the anion of 2,2'-dipyridylamine) building blocks and [ReF6](2-) (1), [ZrF6](2-) (2) or [SnF6](2-) (3) linkers have been self-assembled and crystallographically characterized. Magnetic measurements reveal a significant ferromagnetic coupling (J/k(B) = +9.9 K) between S = 1/2 {Co3(6+)} and S = 3/2 Re(IV) magnetic sites through a single, unsupported fluoride bridge in 1.

Electronic Structure of Ru2(II,II) Oxypyridinates: Synthetic, Structural, and Theoretical Insights into Axial Ligand Binding.

Reduction of (4,0)-Ru2(chp)4Cl (1) (chp = 6-chloro-2-oxypyridinate) with Zn or FeCl2 yields a series of axial ligand adducts of the Ru2(II,II) species Ru2(chp)4(L), with L = tetrahydrofuran (2), dimethyl sulfoxide (DMSO; 3), PPh3 (4), pyridine (5), or MeCN (6). Zn reduction in noncoordinating solvents such as toluene or CH2Cl2 leads to the dimeric species [Ru2(chp)4]2 (7) or [Ru2(chp)4]2(ZnCl2) (8), whereas addition of strongly σ-donating ligands such as CO causes cleavage of the Ru-Ru bond. Density functional theory (DFT) models of these complexes, the axially free species, and the axial adducts of several other potential ligands (H2O, NH3, CH2Cl2, S-bound DMSO, N2, and CO) indicate that these compounds can be divided into three distinct categories, based on their Ru-Ru bond length and electronic structure.

Plank-shaped column-forming mesogens with substituents on one side only.

Prolonged glyoxylation of pyrenyl-1-glyoxylic acid ethyl ester leads to a mixture of isomers with polar pyrenylene-1,8-diglyoxylic acid as the main product, whereas the centrosymmetric 1,6-isomer is obtained in good yield from the corresponding dibromopyrene. Perkin condensations followed by Pd-catalyzed cyclizations lead to isomeric dinaphthopyrene-tetracarboxdiimides that self-assemble into columnar liquid crystals of hexagonal and rectangular symmetry, of which the rectangular mesophases have unusually elongated unit cells. The cisoid diimides with both alkylimide substituents on the same side of the oblong arene system show a much greater tendency to self-assemble into fluid stacks of disks than their centrosymmetric isomers.

Columnar liquid-crystalline dinaphthoperylenetetracarboxdiimides.

Although the double Friedel-Crafts acylation of arenes with ethyl chloroglyoxylate is hindered by the strongly deactivating effect of the first-entering glyoxylic substituent, the double reaction is successful with the reactive arene perylene under long reaction times and with concomitant ester hydrolysis. The reaction is regiospecific, giving the 3,9-regioisomer exclusively. This perylenylenediglyoxylic acid is condensed first with o-bromophenylacetic acid and then with α-branched alkylamines to yield the title compounds.

An "intermediate spin" nickel hydride complex stemming from delocalized Ni2(μ-H)2 bonding.

The nickel hydride complex [Cp'Ni(μ-H)]2 (1, Cp' = 1,2,3,4-tetraisopropylcyclopentadienyl) is found to have a strikingly short Ni-Ni distance of 2.28638(3) Å. Variable temperature and field magnetic measurements indicate an unexpected triplet ground state for 1 with a large zero-field splitting of +90 K (63 cm(-1)).

Molecular mechanism of action of 2-ferrocenyl-1,1-diphenylbut-1-ene on HL-60 leukemia cells.

The aim of this work was to investigate the mechanism of action of 2-ferrocenyl-1,1-diphenylbut-1-ene (1) on HL-60 human leukemia cells. While inactive against noncancerous cells, 1 provoked a concentration-dependent decrease in viable tumor cells, primarily via apoptosis, as evidenced by analysis of cell morphology, activation of caspases 3 and 7, increased DNA fragmentation, and externalization of phosphatidylserine. Necrosis was observed only at the highest tested concentration (4 μM).

Oxidative stretching of metal-metal bonds to their limits.

Oxidation of quadruply bonded Cr2(dpa)4, Mo2(dpa)4, MoW(dpa)4, and W2(dpa)4 (dpa = 2,2'-dipyridylamido) with 2 equiv of silver(I) triflate or ferrocenium triflate results in the formation of the two-electron-oxidized products [Cr2(dpa)4](2+) (1), [Mo2(dpa)4](2+) (2), [MoW(dpa)4](2+) (3), and [W2(dpa)4](2+) (4). Additional two-electron oxidation and oxygen atom transfer by m-chloroperoxybenzoic acid results in the formation of the corresponding metal-oxo compounds [Mo2O(dpa)4](2+) (5), [WMoO(dpa)4](2+) (6), and [W2O(dpa)4](2+) (7), which feature an unusual linear M···M≡O structure. Crystallographic studies of the two-electron-oxidized products 2, 3, and 4, which have the appropriate number of orbitals and electrons to form metal-metal triple bonds, show bond distances much longer (by >0.

Helicenes from diarylmaleimides.

Perkin condensations of arylglyoxylic acids with arylacetic acids, followed by the addition of alkylamine, yield diarylmaleimides in a one-pot procedure. The arylglyoxylic acids are obtained by arene acylation with ClCOCO2Et and reduced with NaI and hypophosphorous acid to the arylacetic acids. With 2,7-di-tert-butyl-pyren-4-yl or chrysen-6-yl as the aryl, photocyclodehydrogenation of the diarylmaleimides yields substituted helicenes which can be reduced to stable anions.