Radical promoted Wagner-Meerwein-type rearrangement of epoxides in camphoric systems using a Ti(III) radical source

[Chemical reaction: see text] A radical based Wagner-Meerwein-type rearrangement has been observed in camphoric systems. The radical was generated from the epoxide using Cp2TiCl as the radical source. The radical initiator Cp2TiCl was prepared in situ from commercially available Cp2TiCl2 and Zn dust in THF under argon.     

Host-guest interactions template: the synthesis of a [3]catenane

Formation of a [3]catenane containing dibenzo-24-crown ether wheels and a large dipyridiniumethane ring is templated by formation of a host-guest adduct between the [3]catenane and the external crown ether.     

Determination of tungsten in rocks and minerals by chelate extraction and atomic-absorption spectrometry

An atomic-absorption method for determination of tungsten in rocks and minerals is proposed. The method involves sample decomposition by acid digestion or by pyrosulphate fusion, followed by chelate extraction of tungsten by N-benzoylphenylhydroxylamine in toluene. Atomic-absorption measurements are made on the organic phase aspirated into a nitrous oxide-acetylene flame. Quantitative extraction with efficient separation from other elements is achieved in a single extraction from strong acid media. The method is rapid and reliable in terms of precision and accuracy and is applicable to rocks and minerals containing tungsten in the range from 100 ppm to 15%.     

Rotational spectrum, potential energy surface, and bound states of the weakly bound complex He-N2O

Pure rotational transitions of the weakly bound complex He-N(2)O and three minor isotopomers (He-(14)N(15)NO, He-(15)N(14)NO, and He-(15)N(15)NO) were measured in the frequency region from 6 to 20 GHz. Predictions for the microwave transition frequencies were based on the infrared work by Tang and McKellar [J. Chem. Phys. 117, 2586 (2002)]. In the case of (14)N containing isotopomers, nuclear quadrupole hyperfine structure of the rotational transitions was observed and analyzed. The resulting spectroscopic parameters were used to determine geometrical and dynamical information about the complex. An ab initio potential energy surface was calculated at the coupled cluster level of theory with single and double excitations and perturbative inclusion of triple excitations. This surface was constructed using the augmented correlation consistent polarized valence triple zeta basis set for all atoms with the inclusion of bond functions for the van der Waals bond. Bound state calculations were done to determine the energies of low-lying rovibrational levels that are supported by the potential energy surface. The resulting transition energies agree with the experimental values to 1% or better.     

Building mass spectrometers and a philosophy of research

Development of the techniques of ion kinetic energy spectrometry and mass-analyzed ion kinetic energy spectrometry is described. The extension of these concepts to the method of tandem mass spectrometry for direct mixture analysis is traced, and a rationale for the construction of hybrid mass spectrometers is presented. Collisions of polyatomic ions with surfaces are discussed as an outgrowth of gaseous collisions. An attempt is made to describe a philosophy of research that guided the construction of a dozen mass spectrometers and the exploration of organic ion chemistry in as many contexts.     

Synthesis of a tetraazacyclotetradecadiene and a pentaazacyclotetradecatriene

Useful procedures for preparing a novel tetraazacyclotetradecadiene and a pentaazacyclotetradecatriene are reported. J. Heterocyclic Chem., 14, 1097 (1977)     

o-hydroxylmethylphenylchalcogens: synthesis, intramolecular nonbonded chalcogen...OH interactions, and glutathione peroxidase-like activity

[Structure: see text]. The synthesis and characterization of a series of organochalcogen (Se, Te) compounds derived from benzyl alcohol 13 are described. The synthesis of the key precursor dichalcogenides 15, 22, and 29 was achieved by the ortho-lithiation route. Selenide 18 was obtained by the reaction of the dilithiated derivative 14 with Se(dtc)2. Oxidation of 15 and 22 with H2O2 afforded the corresponding cyclic ester derivatives 17 and 24, respectively. Oxidation of selenide 18 with H2O2 affords the spirocyclic compound 19. The presence of intramolecular interactions in dichalcogenides 15 and 22 has been proven by single-crystal X-ray studies. The cyclic compounds 17 and 19 have also been characterized by single-crystal X-ray studies. GP(X)-like antioxidant activity of selenium compounds has been evaluated by the coupled bioassay method. Density functional theory calculations at the mPW1PW91 level on ditelluride 22 have identified a fairly strong nonbonding interaction between the hydroxy oxygen and tellurium atom. The second-order perturbation energy obtained through NBO analysis conveys the involvement of n(O) --> sigma(Te-Te) orbital overlap in nonbonding interaction. Post wave function analysis with the Atoms in Molecules (AIM) method identified distinct bond critical point in 15 and 22 and also indicated that the nonbonding interaction is predominantly covalent. Comparison between diselenide 15 and ditelluride 22 using the extent of orbital interaction as well as the value of electron density at the bond critical points unequivocally established that a ditelluride could be a better acceptor in nonbonding interaction, when the hydroxy group acts as the donor.     

Grafting of monosaccharide derivatives to cellulose acetate

Grafting of 1,2-O-isopropylidene-α-D -xylofuranose to commercial cellulose diacetate has been accomplished by using a boron trifluoride catalyst. The reaction proceeds quickly at 25 and 40°C, resulting in degrees of molar substitution (MS) of 0.37 and 0.34, respectively. If monomer and catalyst are added over an extended period of time to maintain low concentrations, MS values as high as 0.89 and 0.85 are obtained at 25 and 40°C, respectively. Major side reactions are depolymerization of the cellulose acetate backbone and grafted D -xylose and the homopolymerization of the monomer. These side reactions may be minimized by conducting the reaction at 40°C for a short time or by adding monomer and catalyst over an extended period of time. Grafting has also been accomplished by using D -xylose derivatives with various reactive groups at the anomeric carbon atom. The grafted material of MS greater than 0.7 is insoluble in acetone and after deacetylation is soluble in water under alkaline, neutral and acidic conditions. Oxalic acid hydrolysis of the deacetylated material indicates that most of the grafted D -xylose units are in the furanose form. Methylation and hydrolysis of the methylated material shows that 75% of the D -xylose residues are terminal units and indicates the presence of many singly grafted D -xylose residues and a few di-and trisaccharide grafts.     

Spectrophotometric determination of platinum with substituted pyrimidine-2-thiol

The yellow complex of Pt(IV) with 1-pyridyl-4,4,6-trimethyl-1H,4H-pyrimidine-2-thiol (PyTPT) which has maximum absorbance at 430 nm, is studied for the spectrophotometric determination of the metal. Molar absorptivity is 5000 liters mol^?1 cm^?1 and Sandell's sensitivity is 0.039 μg/cm². The determination of Pt(IV) (2.8–8.4 ppm) in the presence of diverse ions is described.     

Nonperturbative modeling of two-photon absorption in a three-state system

The physics of the two-photon absorption process is investigated for a three-state system. The density-matrix equations for the two-photon interaction are solved in the steady-state limit assuming that the pump laser radiation is monochromatic. Collisional broadening, saturation, and Stark shifting of the two-photon resonance are investigated in detail by numerical solution of the steady-state density-matrix equations. Analytical expressions for the saturation intensity and the Stark shift are derived for the case where the single-photon transitions between the intermediate state and the initial and final states are far from resonance with the pump laser. For this case, it is found that the direction of the Stark shift is dependent on the relative magnitudes of the dipole-moment matrix elements for the single-photon transitions that couple the intermediate state with the initial and final states. Saturation and Stark shifting are also investigated for the case where the single-photon transitions between the intermediate state and the initial and final states are close to resonance with the pump laser.