Analysis of the terphenyls by a compressed pellet infrared method involving micro-distillation

A quantitative compressed pellet infrared method used together with a micro-distillation to effect separation of the isomer has been developed and reported here for the analysis of ortho-, meta-, and para-terphonyl. The terphenyl content is determined on fractions isolated by distillation from radiation damaged samples. The compressed pellet infrared method is preferred instead of the more conventional solution technique since smaller quantities of isolated terphcnyl are required. The pellet method is applicable also to polyphenyls higher than the terphenyls. The solution technique is not due to the insolubility of the polyphenyls. It is expected that the compressed pellet spectral method developed here might well find application in the analysis of compounds other than polyphenyls. Results presented here appear to be the, first quantitative infrared data reported in the literaturu on polyphenyl compounds.     

Organomineral sorbents based on clinoptilolite-containing tuffs

The anion-exchange properties of a new organomineral sorbent obtained by modification of clinoptilolite-containing tuffs by polyhexamethyleneguanidine have been studied after different periods of storage (time after synthesis) and numbers of sorption-regeneration cycles. The sorbent can be used as a cation- and an anion-exchanger simultaneously. Selectivity coefficients (exchange constants) for F^–, SO₄ ^2–, and HPO₄ ^2– ionsvs. Cl^– ions on modified clinoptilolite-containing tuffs have been determined. The modification improves the mechanical properties of clinoptilolite tuffs.For part 1, see Ref. 1.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1554–1556, September, 1994.     

Chlorido­bis[(2‐oxoazocan‐1‐yl)methyl]­germanium(IV) trifluoro­methane­sulfonate

In the title compound, [Ge(C₈H₁₄NO)₂Cl]CF₃SO₃, which is the first complex containing an eight‐membered lactam (enantho­lactam) as ligand, the coordination polyhedron of the Ge^IV atom is inter­mediate between trigonal–bipyramidal and square‐pyramidal. Quantum chemical calculations of the crystal structure indicate the absence of additional coordination bonding between the Ge^IV atom and the trifluoro­methane­sulfonate anion.     

Studies Related to Biological Detoxification of Kraft Pulp Mill Effluent. IV.The Biodegradation of 14-Chlorodehydroabietic Acid with Mortierella isabellina

One of the fish-toxic chlorinated resin acids, 14-chlorodehydroabietic acid ( 5 ), found in kraft mill effluent is examined. When exposed to the fungus Mortierella isabellina, 5 is converted into a number of hydroxylated derivatives which show low levels of toxicity to fish. These biotransformation products were isolated and characterized.     

A molecular approach to rationally constructing specific fluorogenic substrates for the detection of acetylcholinesterase activity in live cells,mice brains and tissues

Acetylcholinesterase (AChE) is an extremely critical hydrolase tightly associated with neurological diseases. Currently, developing specific substrates for imaging AChE activity still remains a great challenge due to the interference from butyrylcholinesterase (BChE) and carboxylesterase (CE). Herein, we propose an approach to designing specific substrates for AChE detection by combining dimethylcarbamate choline with a self-immolative scaffold. The representative P10 can effectively eliminate the interference from CE and BChE. The high specificity of P10 has been proved via imaging AChE activity in cells. Moreover, P10 can also be used to successfully map AChE activity in different regions of a normal mouse brain, which may provide important data for AChE evaluation in clinical studies. Such a rational and effective approach can also provide a solid basis for designing probes with different properties to study AChE in biosystems and another way to design specific substrates for other enzymes.

In this work, a new approach was developed for designing the representative P10 with high selectivity and sensitivity for imaging AChE activity in the cells and normal mouse brain.     

A dimeric constrained‐geometry titanium complex linked by double Ti–CH2–Al–CH2 heterocycles

In the structure of bis({N‐[di­methyl(1η⁵‐2,3,4,6‐tetra­methyl­in­den­yl)­silyl]­cyclo­hexyl­amido‐1κN}(methyl‐3κC)‐di‐μ₃‐methyl­ene‐1:2:3κ³C;1:3:3′κ³C‐tris(pentafluorophenyl‐2κC)titanium) benzene disolvate, [Me₂Si(η⁵‐2,3,4,6‐Me₄C₉H₂)(C₆H₁₁N)]Ti[(μ₃‐CH₂)Al(C₆F₅)₃][AlMe(μ₃‐CH₂)]₂ or [Ti₂(C₂₁H₇AlF₁₅)₂(C₂₁H₃₁NSi)₂]·2C₆D₆, the dimer is located on an inversion center, and the two Ti centers are linked by double Ti(μ₃‐CH₂)Al(C₆F₅)₃AlMe(μ₃‐CH₂) heterocycles. The electron‐deficient Ti centers are further stabilized by two α‐agostic interactions between Ti and one H atom of each bridging methyl­ene group.     

Polymerization of MMA by oscillating zirconocene catalysts, diastereomeric zirconocene mixtures, and diastereospecific metallocene pairs

Characteristics of methyl methacrylate (MMA) polymerization using oscillating zirconocene catalysts, (2-Ph-Ind)₂ZrX₂ (X = Cl, 1; X = Me, 2), mixtures of rac- and meso-zirconocene diastereomers, (SBI)ZrMe₂ [3, SBI = Me₂Si(Ind)₂] and (EBI)ZrMe₂ [4, EBI = C₂H₄(Ind)₂], as well as diastereospecific metallocene pairs, rac-4/Cp₂ZrMe₂ (5) and rac-4/CGCTiMe₂ [6, CGC = Me₂Si(Me₄C₅)(t-BuN)], are reported. MMA polymerization using the chloride catalyst precursor 1 activated with a large excess of the modified methyl aluminoxane is sluggish, uncontrolled, and produces atactic PMMA. On the other hand, the polymerization by a 2/1 ratio of 2/B(C₆F₅)₃ or 2/Ph₃CB(C₆F₅)₄ is controlled and produces syndiotactic PMMA. Mixtures of diastereomeric ansa-zirconocenes 3 or 4 containing various rac/meso ratios, when activated with B(C₆F₅)₃, yield bimodal PMMA; this behavior is attributed to the meso-diastereomer that, in its pure form, affords bimodal, syndio-rich atactic PMMA. For MMA polymerization using diastereospecific metallocene pairs, rac-4/5 and rac-4/6, the isospecific catalyst site dominates the polymerization events under the conditions employed in this study, and the aspecific and syndiospecific sites are largely nonproductive, thereby forming only highly isotactic PMMA.     

Calculation of the viscosity of binary liquids at various temperatures using Jouyban-Acree model

Applicability of the Jouyban-Acree model for calculating absolute viscosity of binary liquid mixtures with respect to temperature and mixture composition is proposed. The correlation ability of the model is evaluated by employing viscosity data of 143 various aqueous and non-aqueous liquid mixtures at various temperatures collected from the literature. The results show that the model is able to correlate the data with an overall percentage deviation (PD) of 1.9+/-2.5%. In order to test the prediction capability of the model, three experimental viscosities from the highest and lowest temperatures along with the viscosities of neat liquids at all temperatures have been employed to train the model, then the viscosity values at other mixture compositions and temperatures were predicted and the overall PD obtained is 2.6+/-4.0%.     

The structures of 5-methyl-5-phenyl-5H-dibenzo[b,f] silepin and its saturated analog

The structures of 5-methyl-5-phenyl-5H-dibenzo[b,f] silepin (I) and 5-methyl- 5-phenyl-1O,11-dihydro-5H-dibenzo [b,f] silepin (II) have been determined from three-dimensional X-ray data collected by counter methods. I crystallizes in the orthorhombic space group Pnam with a 7.596(3), b 18.102(5) and c 12.190(2) Å; observed and calculated densities (Z = 4) are 1.17 and 1.18 g cm^?3, respectively. II crystallizes in the monoclinic space group $\text{P}\text{2}{}_1\text{c}$ with a 11.115(3), b 7.920(3), c 20.765(5) Å and β 111.71(2)°; observed and calculated densities (Z = 4) are 1.17 g cm^?3. Anisotropic refinement of nonhydrogen atoms, with hydrogen atoms included at fixed ideal locations, gave conventional R-factors of 4.5% (I) and 5.0% (II). Compound I exhibits the boat conformation for the tricyclic framework and is located on a crystallographically required mirror plane. Com- pound II has the expected folded boat conformation. The torsion angle about the 10,11-bond is 0.0° for I, a crystallographic symmetry requirement, and 89.9° for II. Mean SiC bond distances are 1.863 Å(I) and 1.875 Å(II). The dihedral angles between the planar benzo groups are 129.7° (I) and 137.2° (II); introduc- tion of unsaturation at the 10,11-position decreases the dihedral angle in the tri- cyclic system, i.e., the tricyclic system is more bent.