Preparation of a dual-functionalized fumed silica nanoparticle catalysis for synthesis of azaluorenone derivatives

Research on Chemical Intermediates - A dual-functional silica-based catalyst was prepared by treating fumed silica with amino-containing silane then 1,4-butane sultone. The presence of functional...     

Quantum chemical study of the nature of interactions between the boraphosphinine and alumaphosphinine with some of the mono- and divalent cations: cation–π or cation–lone pair?

Structural Chemistry - Quantum chemical study of the nature of interactions between the boraphosphinine (BP) and alumaphosphinine (AlP) with some of the alkali metal cations (Li+, Na+, K+) and...     

A simple,rapid and effective protocol for synthesis of bis(pyrazolyl)methanes using nickel–guanidine complex immobilized on MCM-41

Research on Chemical Intermediates - In this paper, a rapid, easy and very efficient method for the synthesis of bis(pyrazolyl)methanes has been reported in the presence of nickel–guanidine...     

Computational Analysis of Mesomerism in para-Substituted mer-NCN Pincer Platinum(II) Complexes,Including its Relationships with Hammett σp Substituent Parameters

Density Functional Theory studies of square-planar Pt^II pincer structures, (4-Z-NCN)PtCl ([4-Z-NCN]⁻=[4-Z-2,6-(Me₂NCH₂)₂C₆H₂-N,C,N]⁻, Z=H, NO₂, CF₃, CO₂H, CHO, Cl, Br, I, F, SMe, SiMe₃, tBu, OH, NH₂, NMe₂), enable characterisation of mesomerism for the pincer-Pt interaction. Relationships between Hammett σ_p substituent parameters of Z and DFT data obtained from NBO6 and AOMix computation are used to probe the interaction of the 5d_yz orbital of platinum with π-orbitals of the arene ring. Analogous computation for 2,6-(Me₂CH₂)₂C₆H₃Z (Z=H, CF₃, CHO, Cl, Br, I, F, SMe, SiMe₃, tBu, OH, NH₂) and (4-H-NCN)PtZ allows an estimation of the relative substituent effects of “(CH₂NMe₂)₂PtZ” on π-delocalisation in the pincer system.     

Efficient RuIII-catalyzed synthesis of 9-aryl-9H-xanthene-3,6-diols as precursors to fluorones

Efficient condensation of resorcinol and various aromatic aldehydes in the presence of RuCl₃nH₂O as a homogeneous catalyst under reflux conditions was investigated.It was found that a very simple method afforded good to excellent yields of the desired products.     

Molecular structure and character of bonding of mono and divalent metal cations (Li+, Na+, K+, Mg2+, Ca2+, Zn2+, and Cu+) with guanosine: AIM and NBO analysis

The B3LYP/6-311++G (d,p) density functional approach was used to study the gas-phase metal affinities of Guanosine (ribonucleoside) for the Li⁺, Na⁺, K⁺, Mg²⁺, Ca²⁺, Zn²⁺, and Cu⁺ cations. In this study we determine coordination geometries, binding strength, absolute metal ion affinities, and free energies for the most stable products. We have also compared the results for Guanosine, with our previously reported results for 2′-Deoxyguanosine. Based on the results, it is obvious that MIA is strongly dependent on the charge-to-size ratio of the cation. Guanosine interacts more strongly with Zn²⁺ than do with Mg²⁺, Ca²⁺, and Cu⁺ and therefore stronger interactions lead to higher MIA. In both free molecules and their complexes, the Syn orientation of the base is stabilized by an intramolecular O5′–H···N3 hydrogen bond and the anti orientation of the base is stabilized by an intramolecular C–H···O hydrogen bond formed between the (C8-H8) and the O5′ atom of the sugar moiety. It is also interesting to mention that linear correlation between calculated MIA values and the atomic numbers (Z) of the metal ions of Li⁺, Na⁺, and K⁺ were found. Furthermore, the influences of metal cationization on the strength of the N-glycosidic bond, torsion angles, angle of pseudorotation (P), and intramolecular C–H···O and O–H···O hydrogen bonds have been studied. Natural bond orbital (NBO) analysis was performed to calculate the charge transfer and natural population analysis of the complexes. Quantum theory of atoms in molecules (QTAIM) was also applied to determine the nature of interactions.     

Hydrogen bonded arrays: the power of multiple hydrogen bonds

Hydrogen bond interactions in small covalent model compounds (i.e., deprotonated polyhydroxy alcohols) were measured by negative ion photoelectron spectroscopy. The experimentally determined vertical and adiabatic electron detachment energies for (HOCH(2)CH(2))(2)CHO(-)(2a), (HOCH(2)CH(2))(3)CO(-) (3a), and (HOCH(2)CH(2)CH(OH)CH(2))(3)CO(-) (4a)reveal that hydrogen-bonded networks can provide enormous stabilizations and that a single charge center not only can be stabilized by up to three hydrogen bonds but also can increase the interaction energy between noncharged OH groups by 5.8 kcal mol(-1) or more per hydrogen bond. This can lead to pK(a) values that are very different from those in water and can provide some of the impetus for catalytic processes.     

Surface behavior, aggregation and phase separation of aqueous mixtures of dodecyl trimethylammonium bromide and sodium oligoarene sulfonates: the transition to polyelectrolyte/surfactant behavior

The properties and phase diagrams of aqueous mixtures of dodecyltrimethylammonium bromide (C(12)TAB) with the sodium oligoarene sulphonates (POSn), POS2, POS3, POS4, and POS6 have been studied using surface tension and neutron reflectometry to study the surface, and neutron small angle scattering and fluorescence to study the bulk solution. The behavior of POS2 and POS3 is reasonably consistent with mixed micelles of C(12)TAB and POSn-(C(12)TA)(n). These systems exhibit a single critical micelle concentration (CMC) at which the surface tension reaches the usual plateau. This is contrary to a recent report which suggests that the onset of the surface tension plateau does not coincide with the CMC. In the POS3 system, the micelles conform to the core-shell model, are slightly ellipsoidal, and have aggregation numbers in the range 70-100. In addition, the dissociation constant for ionization of the micelles is significantly lower than for free C(12)TAB micelles, indicating binding of the POS3 ion to the micelles. Estimation of the CMCs of the POSn-(C(12)TA)(n) from n = 1-3 assuming ideal mixing of the two component surfactants and the observed values of the mixed CMC gives values that are consistent with the nearest related gemini surfactant. The POS4 and POS6 systems are different. They both phase separate slowly to form a dilute and a concentrated (dense) phase. Fluorescence of POS4 has been used to show that the onset of aggregation of surfactant (critical aggregation concentration, CAC) occurs at the onset of the surface tension plateau and that, at the slightly higher concentration of the phase separation, the concentration of POS4 and C(12)TAB in the dilute phase is at or below its concentration at the CAC, that is, this is a clear case of complex coacervation. The surface layer of the C(12)TA ion in the surface tension plateau region, studied directly by neutron reflectometry, was found to be higher than a simple monolayer (observed for POS2 and POS3) for both the POS4 and POS6 systems. In POS6 this evolved after a few hours to a structure consisting of a monolayer with an attached subsurface bilayer, closely resembling that observed for one class of polyelectrolyte/surfactant mixtures. It is suggested that this structured layer, which must be present on the surface of the dilute phase of the coacervated system, is a thin wetting film of the dense phase. The close resemblance of the properties of the POS6 system to that of one large group of polyelectrolyte/surfactant mixtures shows that the surface behavior of oligoion/surfactant mixtures can quickly become representative of that of true polyelectrolyte/surfactant mixtures. In addition, the more precise characterization possible for the POS6 system identifies an unusual feature of the surface behavior of some polyelectrolyte/surfactant systems and that is that the surface tension can remain low and constant through a precipitation/coacervation region because of the characteristics of two phase wetting. The well-defined fixed charge distribution in POS6 also suggests that rigidity and charge separation are the factors that control whether a given system will exhibit a flat surface tension plateau or the alternative of a peak on the surface tension plateau.     

Next-generation quantum theory of atoms in molecules for the photochemical ring-opening reactions of oxirane

The conical intersections corresponding to the C─O and C─C ring opening were optimized and the reaction paths traversing these intersections were obtained. Investigation of the C─O ring opening revealed that when traversing the lowest energy conical intersection, the reaction path returns to the closed ring geometry. The C─O path traversing the intersection featuring torsion of terminal CH₂ group however, led to a ring-opened geometry, an H-shift and the formation of acetaldehyde that can undergo further dissociation. The observation of different reaction paths was explained by the 3-D paths from quantum theory of atoms in molecules (QTAIM) that defined the most preferred direction of electronic motion that precisely tracked the mechanisms of bond breaking and formation throughout the photo-reactions. The size, orientation, and location of these most preferred 3-D paths indicated the extent and direction of motion of atoms, bonds, and the degree of torsion or planarity of a bond indicating a predictive ability.     

Effect of hydrogen bonds on pKa values: importance of networking

The pK(a) of an acyclic aliphatic heptaol ((HOCH(2)CH(2)CH(OH)CH(2))(3)COH) was measured in DMSO, and its gas-phase acidity is reported as well. This tertiary alcohol was found to be 10(21) times more acidic than tert-butyl alcohol in DMSO and an order of magnitude more acidic than acetic acid (i.e., pK(a) = 11.4 vs 12.3). This can be attributed to a 21.9 kcal mol(-1) stabilization of the charged oxygen center in the conjugate base by three hydrogen bonds and another 6.3 kcal mol(-1) stabilization resulting from an additional three hydrogen bonds between the uncharged primary and secondary hydroxyl groups. Charge delocalization by both the first and second solvation shells may be used to facilitate enzymatic reactions. Acidity constants of a series of polyols were also computed, and the combination of hydrogen-bonding and electron-withdrawing substituents was found to afford acids that are predicted to be extremely acidic in DMSO (i.e., pK(a) < 0). These hydrogen bond enhanced acids represent an attractive class of Br?nsted acid catalysts.