Synthesis of polypyridazinophthalazinediones from dibenzoylphthalic acids and aromatic dihydrazines

A novel class of polypyridazinophthalazinediones has been synthesized by the solution cyclopolycondensation in m-cresol of dibenzoylphthalic acids with aromatic dihydrazines such as bis(4-hydrazinophenyl)methane and bis(4-hydrazinophenyl) sulfone. The polyheterocycles derived from 4,6-dibenzoylisophthalic acid, which had inherent viscosities of up to 0.5, were soluble in m-cresol and hot dichloroacetic acid, whereas the polymers from 2,5-dibenzoylterephthalic acid were practically insoluble in organic solvents. Thermogravimetric analyses showed that all the polymers underwent weight losses of 10% at 490–520°C in both air and nitrogen.     

Impact of the macrocyclic structure and dynamic solvent effect on the reactivity of a localised singlet diradicaloid with π-single bonding character

Localised singlet diradicals are key intermediates in bond homolysis processes. Generally, these highly reactive species undergo radical–radical coupling reaction immediately after their generation. Therefore, their short-lived character hampers experimental investigations of their nature. In this study, we implemented the new concept of “stretch effect” to access a kinetically stabilised singlet diradicaloid. To this end, a macrocyclic structure was computationally designed to enable the experimental examination of a singlet diradicaloid with π-single bonding character. The kinetically stabilised diradicaloid exhibited a low carbon–carbon coupling reaction rate of 6.4 × 10³ s⁻¹ (155.9 μs), approximately 11 and 1000 times slower than those of the first generation of macrocyclic system (7.0 × 10⁴ s⁻¹, 14.2 μs) and the parent system lacking the macrocycle (5 × 10⁶ s⁻¹, 200 ns) at 293 K in benzene, respectively. In addition, a significant dynamic solvent effect was observed for the first time in intramolecular radical–radical coupling reactions in viscous solvents such as glycerin triacetate. This theoretical and experimental study demonstrates that the stretch effect and solvent viscosity play important roles in retarding the σ-bond formation process, thus enabling a thorough examination of the nature of the singlet diradicaloid and paving the way toward a deeper understanding of reactive intermediates.

An extremely long-lived localised singlet diradical with π-single bonding character is found in a macrocyclic structure that retards the radical–radical coupling reaction by the “stretch and solvent-dynamic effects”.     

Aurophilic Interactions in Multi-Radical Species: Electronic-Spin and Redox Properties of Bis- and Tris-[(Nitronyl Nitroxide)-Gold(I)] Complexes with Phosphine-Ligand Scaffolds

Multinuclear Au^I complexes with two or three nitronyl nitroxide-2-ide radical anion and phosphine-ligand scaffolds, (NN-Au)₂-1 o , (NN-Au)₂-1 m , and (NN-Au)₂-1 p , have been synthesized to investigate the influence of Au^I−Au^I (aurophilic) interactions on the properties of multispin molecular systems. The desired complexes were successfully prepared in moderate yields in a one-pot synthesis from the corresponding phosphine ligand, Au^I source, parent NN, and sodium hydroxide. Among the prepared complexes, (NN-Au)₂-1 o , in which an aurophilic interaction was clearly observed by crystal structure analysis, showed characteristic spin−spin interactions, electrochemical properties, and solvatochromic behavior. The results from theoretical calculations also suggested that the differences in properties between complex (NN-Au)₂-1 o and the other complexes are due to intramolecular aurophilic interactions.     

Solution structures of 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid saturated with CO2: Experimental evidence of specific anion-CO2 interaction

X-ray diffraction measurements for 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid ([BMIM][PF6])-CO2 systems were carried out at high pressures with a newly developed polymer cell. The intermolecular distribution functions (g(inter)(r)) were obtained at 25 degrees C for neat [BMIM][PF6] and its solutions saturated with CO2 at 4 and 15 MPa, where the mole fractions (x) of CO2 correspond to 0.5 and 0.7, respectively. In g(inter)(r) for x = 0.5, two peaks appeared at around 2.8 and 3.2 A. These two peaks in g(inter)(r) appreciably increased for x = 0.7; moreover, there was another peak observed at approximately 3.8 A. Only assuming the correlations between CO2 and [PF6]-, it is reasonably determined that the nearest-neighbor P([PF6]-). . .C(CO2) distances are 3.57 and 3.59 A with the coordination numbers being 1.8 and 4.0 for x = 0.5 and 0.7, respectively. It is concluded that CO2 molecules are preferentially solvated to the [PF6]- anion.     

Amphiphilic guest sorption of K2[Cr3O(OOCC2H5)6(H2O)3]2[alpha-SiW12O40] ionic crystal

An ionic crystal K2[Cr3O(OOCC2H5)6(H2O)3]2[alpha-SiW12O40] x 3H2O (1a) is synthesized by the complexation of a Keggin-type polyoxometalate of [alpha-SiW12O40]4- with K+ and a macrocation of [Cr3O(OOCC2H5)6(H2O)3]+. Compound 1a possesses both hydrophilic and hydrophobic channels in the crystal lattice. The 3 mol mol(-1) of the water of crystallization in 1a resides in the hydrophilic channel. The water of crystallization is removed by the evacuation at 303 K to form the guest-free phase 1b with small changes in the lattice lengths (+/-0.2 A). The water sorption profile is reproduced by the single rate constant. Therefore, the water sorbed probably resides in the hydrophilic channel. Compound 1b sorbs various kinds of polar organic molecules, and the amounts of < or = C3 alcohols are comparable to or larger than that of water, while chlorocarbons with no hydrogen-bonding ability and nonpolar molecules are excluded. Thus, 1b showed the amphiphilic sorption property. The states of the polar organic molecules sorbed in 1b have been quantitatively investigated using ethanol as a probe molecule. The IR, NMR, and single-crystal X-ray diffraction studies combined with the sorption kinetics reveal that ethanol molecules are mainly sorbed into the hydrophilic channel at P/P0 < or = 0.5, while the sorption into the hydrophobic channel is dominant at P/P0 > or = 0.6. Thus, it is demonstrated that ethanol molecules enter both hydrophilic and hydrophobic channels of 1b.     

Nitrogen-14 NMR Study on Solvent Exchange of the Octahedral Cobalt(II) Ion in Neat 1,3-Propanediamine and n-Propylamine at Various Temperatures and Pressures. Tetrahedral-Octahedral Equilibrium of the Solvated Cobalt(II) Ion in n-Propylamine As Studied by EXAFS and Electronic Absorption Spectroscopy

Solvated cobalt(II) ions in neat 1,3-propanediamine (tn) and n-propylamine (pa) have been characterized by electronic absorption spectroscopy and extended X-ray absorption fine structure (EXAFS) spectroscopy. The equilibrium between tetrahedral and octahedral geometry for cobalt(II) ion has been observed in a neat pa solution, but not in neat diamine solutions such as tn and ethylenediamine (en). The thermodynamic parameters and equilibrium constant at 298 K for the geometrical equilibrium in pa were determined to be DeltaH degrees = -36.1 +/- 2.3 kJ mol(-1), DeltaS degrees = -163 +/- 8 J mol(-1) K(-1), and K(298) = 6.0 x 10(-3) M(-2), where K = [Co(pa)(6)(2+)]/{[Co(pa)(4)(2+)][pa](2)}. The equilibrium is caused by the large entropy gain in formation of the tetrahedral cobalt(II) species. The solvent exchange of cobalt(II) ion with octahedral geometry in tn and pa solutions has been studied by the (14)N NMR line-broadening method. The activation parameters and rate constants at 298 K for the solvent exchange reactions are as follows: DeltaH() = 49.3 +/- 0.9 kJ mol(-1), DeltaS() = 25 +/- 3 J mol(-1) K(-1), DeltaV() = 6.6 +/- 0.3 cm(3) mol(-1) at 302.1 K, and k(298) = 2.9 x 10(5) s(-1) for the tn exchange, and DeltaH() = 36.2 +/- 1.2 kJ mol(-1), DeltaS() = 35 +/- 6 J mol(-1) K(-1), and k(298) = 2.0 x 10(8) s(-1) for the pa exchange. By comparison of the activation parameters with those for the en exchange of cobalt(II) ion, it has been confirmed that the kinetic chelate strain effect is attributed to the large activation enthalpy for the bidentate chelate opening and that the enthalpic effect is smaller in the case of the six-membered tn chelate compared with the five-membered en chelate.     

Synthesis of [6]helicene-based sulfonic acid,sulfonamide, and disulfonimides

The synthesis of helically chiral [6]helicene-based sulfonic acid and sulfonamide from enantiomerically pure 1-acetylthio-5,6,9,10-tetrahydro[6]helicene is reported. The first helically chiral disulfonimides were developed as a synthetic application of [6]helicene-based sulfonamide. This new class of organocatalysts was tested in an asymmetric Mukaiyama aldol reaction to obtain up to quantitative yields and enantioselectivities up to 24%.     

Simultaneous chiral resolution of monosaccharides as 8-aminonaphthalene-1,3,6-trisulfonate derivatives by ligand-exchange CE using borate as a central ion of the chiral selector

Six reducing monosaccharides (mannose, galactose, fucose, glucose, xylose, and arabinose) were derivatized with 8-aminonaphthalene-1,3,6-trisulfonate (ANTS). Based on the chiral ligand-exchange principle using borate as a central ion of the chiral selector and (S)-3-amino-1,2-propanediol (SAP) as a chiral selector ligand, all of the six ANTS-monosaccharides were simultaneously enantioseparated using absorbance at 245 nm for detection. The optimum conditions for both high resolution and moderately short migration time consisted of 200 mM SAP-200 mM borate buffer (pH 9.2) containing 10% ACN as a BGE at 30 degrees C with an applied voltage of +30 kV. It was revealed that the proposed chiral ligand-exchange CE using the SAP-borate system was applicable to enantioseparation of not only diols but also polyols.     

Selective cleavage of allyl and propargyl ethers to alcohols catalyzed by Ti(O-i-Pr)4/MXn/Mg

[reaction: see text] Allyl and propargyl ethers were effectively deallylated or depropargylated to the parent alcohols via a C-O bond cleavage catalyzed by a low-valent titanium reagent (LVT), Ti(O-i-Pr)4/TMSCl/Mg or Ti(O-i-Pr)4/MgBr2/Mg, under mild reaction conditions. Differentiation between the allyl and propargyl ethers was achieved by the reaction in the presence of AcOEt as an additive. The reagent also catalyzed intra- and intermolecular cyclotrimerization reactions of alkynes to substituted benzenes.     

Reduction‐Induced Highly Selective Uptake of Cesium Ions by an Ionic Crystal Based on Silicododecamolybdate

Cation adsorption and exchange has been an important topic in both basic and applied chemistry relevant to materials synthesis and chemical conversion, as well as purification and separation. Selective Cs⁺ uptake from aqueous solutions is especially important because Cs⁺ is expensive and is contained in radioactive wastes. However, the reported adsorbents incorporate Rb⁺ as well as Cs⁺, and an adsorbent with high selectivity toward Cs⁺ has not yet been reported. Highly selective uptake of Cs⁺ by an ionic crystal (etpyH)₂[Cr₃O(OOCH)₆(etpy)₃]₂[α‐SiMo₁₂O₄₀]?3 H₂O (etpy =4‐ethylpyridine) is described. The compound incorporated up to 3.8 mol(Cs⁺) mol(s)^?1 (where s=solid) by cation‐exchange with etpyH⁺ and reduction of silicododecamolybdate with ascorbic acid. The amount of Cs⁺ uptake was comparable to that of Prussian blue, which is widely recognized as a good Cs⁺ adsorbent. Moreover, other alkali‐metal and alkaline‐earth‐metal cations were almost completely excluded (<0.2 mol mol(s)^?1).