Mixed Stability and Antimicrobial Properties of Gluconamide-Type Cationic Surfactants

The stability of anionic-cationic surfactant solutions and the antimicrobial properties of novel N,N-dimethyl-N-[3-(gluconamide/lactobionamide)]propyl-N-alkylammonium bromides (CnDGPB and CnDLPB), N-methyl-N-hydroxyethyl group-N-[3-(gluconamide)-propyl]-N-alkylammonium bromide (CnMHGPB) and star-shaped gluconamide-type cationic surfactants N-dodecyl-N,N-bis[(3-d-gluconylamido)propyl]-N-alkylammonium bromide (CnDBGB) were investigated. Mixed stability in combination with sodium n-alkylbenzenesulfonate (LAS) was determined via transmittance; stability is achieved when percent transmittance was greater than 90 %. Transmittance results suggest that these cationic surfactants can form stable solutions with anionic surfactants over a broad concentration range. The inhibition activity of C _n DBGB is the best among the three kinds of glucocationic surfactants. Antimicrobial activity of C₁₂ surfactants was the best, C₁₄ was the second and C₁₀ was the worst. Moreover, antibacterial activity of glucose-based cationic surfactants was greater than lactose-based cationic surfactants.     

Synthesis and crystal structure of the low-temperature modification of Li<Subscript>12</Subscript>Zn<Subscript>4</Subscript>(P<Subscript>2</Subscript>O<Subscript>7</Subscript>)<Subscript>5</Subscript>

The crystal structure of a low-temperature modification of the Li₁₂Zn₄(P₂O₇)₅ compound has been determined by full-profile analysis from the X-ray powder diffraction data. The compound crystallizes in the monoclinic crystal system (a = 5.130(1) Å, b = 13.454(1) Å, c = 8.205(1) Å, β = 90.36(1)°, space group P2₁/n, Z = 4) and has a framework structure in which the zinc and lithium atoms statistically occupy equivalent positions.     

Effect of the Molecular Structure on the Adsorption Properties of Cationic Surfactants at the Air–Water Interface

The surface activity and thermodynamic properties of adsorption at the air–water interface of two series of cationic surfactants based on isourea: the O-dodecyl-N,N′-diisopropylisourea hydrochloride, hydrobromide, and hydroiodide and the O-tridecafluorooctyl-N,N′-diisopropylisourea hydrochloride and hydrobromide were studied. The effect of structural parameters as the nature of the halide counter ion and the nature of the non-polar chain on the surface activity and thermodynamic properties of adsorption were investigated. The surface parameters, the maximum surface excess concentration (Γ _max), the minimum area per molecule (A _min) at the aqueous solution-air interface, effectiveness of surface tension reduction (π_CMC), and efficiency of surface tension reduction (pC ₂₀) were estimated. The standard Gibbs free energy of adsorption, (ΔG°_ads) change has been calculated at different temperatures.     

Synthesis,Characterization and Surface Properties of Amidosulfobetaine Surfactants Bearing Odd-Number Hydrophobic Tail

Three amidosulfobetaine surfactants were synthesized namely: 3-(N-pentadecanamidopropyl-N,N-dimethyl ammonium) propanesulfonate (2a); 3-(N-heptadecanamidopropyl-N,N-dimethyl ammonium) propanesulfonate (2b), and 3-(N-nonadecanamidopropyl-N,N-dimethyl ammonium) propanesulfonate (2c). These surfactants were prepared by direct amidation of commercially available fatty acids with 3-(dimethylamino)-1-propylamine and subsequent reaction with 1,3-propanesultone to obtain quaternary ammonium salts. The synthesized surfactants were characterized by IR, NMR and mass spectrometry. Thermogravimetric analysis (TGA) results showed that the synthesized surfactants have excellent thermal stability with no major thermal degradation below 300 °C. The critical micelle concentration (CMC) values of the surfactants 2a and 2b were found to be 2.2 × 10^?4 and 1.04 × 10^?4 mol/L, and the corresponding surface tension (γ_CMC) values were 33.14 and 34.89 mN m^?1, respectively. The surfactants exhibit excellent surface properties, which are comparable with conventional surfactants. The intrinsic viscosity of surfactant (2b) was studied at various temperatures and concentrations of multi-component brine solution. The plot of natural logarithm of relative viscosity versus surfactant concentration obtained from Higiro et al. model best fit the surfactant behavior. Due to good salt resistance, excellent surface properties and thermal stability, the synthesized surfactant has potential to be used in various oil field applications such as enhanced oil recovery, fracturing, acid diversion, and well stimulation.     

Crystal structure and thermal expansion of ammonium pentaborate NH<Subscript>4</Subscript>B<Subscript>5</Subscript>O<Subscript>8</Subscript>

Anhydrous ammonium pentaborate NH₄B₅O₈ has been synthesized by thermal dehydration of larderellite NH₄[B₅O₇(OH)₂] · H₂O at a temperature of 290°C for 7 h. The crystal structure has been determined from the X-ray powder diffraction data: a = 7.58667(5) Å, b = 12.00354(8) Å, c = 14.71199(8) Å, R _p = 6.23, R _wp = 7.98, R _B = 12.7, R _F = 8.95, and β-KB₅O₈ structure type. The double interpenetrating framework is formed by pentaborate groups, each consisting of a boron-oxygen tetrahedron and four triangles, in which all oxygen atoms are bridging. The thermal behavior of the NH₄B₅O₈ compound has been investigated using thermal X-ray diffraction. As for other pentaborates of this type, the thermal expansion of the NH₄B₅O₈ compound is anisotropic and reaches a maximum along the a axis. The thermal expansion coefficients are as follows: α _a = 39 × 10^?6, α _b = 6 × 10^?6, α _c = 20 × 10^?6, and α _V = 65 × 10^?6 °C^?1.     

A Comprehensive Study on the Synthesis and Micellization of Disymmetric Gemini Imidazolium Surfactants

Two groups of disymmetric Gemini imidazolium surfactants, [C₁₄C₄C _m im]Br₂ (m = 10, 12, 14) and [C _m C₄C _n im]Br₂ (m + n = 24, m = 12, 14, 16, 18) surfactants, were synthesized and their structures were confirmed by ¹H NMR and ESI–MS spectroscopy. Their adsorption at the air/water interface, thermodynamic parameters and aggregation behavior were explored by means of surface tension, electrical conductivity and steady-state fluorescence. A series of surface activity parameters, including cmc, γ _cmc, π _cmc, pC ₂₀, cmc/C ₂₀, Γ _max and A _min, were obtained from surface tension measurements. The results revealed that the overall hydrophobic chain length (N _c) for [C₁₄C₄C _m im]Br₂ and the disymmetry (m/n) for [C _m C₄C _n im]Br₂ had a significant effect on the surface activity. The cmc values decreased with an increase of N _c or m/n. The thermodynamic parameters of micellization (ΔG _m ^θ , ΔH _m ^θ , ΔS _m ^θ ) derived from the electrical conductivity indicated that the micellization process of [C₁₄C₄C _m im]Br₂ and [C _m C₄C _n im]Br₂ was entropy-driven at different temperatures, but the contribution of ΔH _m ^θ to ΔG _m ^θ was enhanced by increasing N _c or m/n. The micropolarity and micellar aggregation number (N _agg) were estimated by steady-state fluorescence measurements. The results showed that the surfactant with higher N _c or m/n can form larger micelles, due to a tighter micellar structure.     

Attractiveness of Host Plant Volatile Extracts to the Asian Citrus Psyllid, <Emphasis Type="Italic">Diaphorina citri,</Emphasis> is Reduced by Terpenoids from the Non-Host Cashew

Diaphorina citri is a vector of the bacterial causative agent of Huanglongbing (HLB?=?Citrus greening), a severe disease affecting citrus crops. As there is no known control for HLB, manipulating insect behaviour through deployment of semiochemicals offers a promising opportunity for protecting citrus crops. The behavioural responses of D. citri to plant volatiles, and the identity of these plant volatiles were investigated. Volatiles were collected from host plants Murraya paniculata, Citrus sinensis, C. reshni, C. limettioides, Poncirus trifoliata, and from non-host plants Psidium guajava, Mangifera indica, Anacardium occidentale. In behavioural assays, female D. citri spent more time in the arms containing volatiles from either M. paniculata or C. sinensis compared to the control arms. When D. citri was exposed to volatiles collected from A. occidentale, they preferred the control arm. Volatiles emitted from the other studied plants did not influence the foraging behaviour of D. citri. Chemical analyses of volatile extracts from C. sinensis, M. paniculata, and A. occidentale revealed the presence of the terpenoids (E)-4,8-dimethylnona-1,3,7–triene (DMNT) and (E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene (TMTT) in higher amounts in A. occidentale. In further behavioural bioassays, female D. citri spent less time in arms containing a synthetic blend of DMNT and TMTT compared to the control arms. Female D. citri also spent less time in arms containing the synthetic blend in combination with volatile extracts from either M. paniculata or C. sinensis compared to the control arms. Results suggest that higher release of the two terpenoids by A. occidentale make this species unattractive to D. citri, and that the terpenoids could be used in reducing colonisation of citrus plants and therefore HLB infection.     

(1<Emphasis Type="Italic">S</Emphasis>,3<Emphasis Type="Italic">R</Emphasis>)-<Emphasis Type="Italic">cis</Emphasis>-Chrysanthemyl Tiglate: Sex Pheromone of the Striped Mealybug, <Emphasis Type="Italic">Ferrisia virgata</Emphasis>

Derivatives of 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylic acid (chrysanthemic acid) are classic natural pyrethroids discovered in pyrethrum plants and show insecticidal activity. Chrysanthemic acid, with two asymmetric carbons, has four possible stereoisomers, and most natural pyrethroids have the (1R,3R)-trans configuration. Interestingly, chrysanthemic acid–related structures are also found in insect sex pheromones; carboxylic esters of (1R,3R)-trans-(2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl)methanol (chrysanthemyl alcohol) have been reported from two mealybug species. In the present study, another ester of chrysanthemyl alcohol was discovered from the striped mealybug, Ferrisia virgata (Cockerell), as its pheromone. By means of gas chromatography–mass spectrometry, nuclear magnetic resonance spectrometry, and high-performance liquid chromatography analyses using a chiral stationary phase column and authentic standards, the pheromone was identified as (1S,3R)-(?)-cis-chrysanthemyl tiglate. The (1S,3R)-enantiomer strongly attracted adult males in a greenhouse trapping bioassay, whereas the other enantiomers showed only weak activity. The cis configuration of the chrysanthemic acid–related structure appears to be relatively scarce in nature, and this is the first example reported from arthropods.     

Inducible <Emphasis Type="Italic">De Novo</Emphasis> Biosynthesis of Isoflavonoids in Soybean Leaves by <Emphasis Type="Italic">Spodoptera litura</Emphasis> Derived Elicitors: Tracer Techniques Aided by High Resolution LCMS

Isoflavonoids are a characteristic family of natural products in legumes known to mediate a range of plant-biotic interactions. For example, in soybean (Glycine max: Fabaceae) multiple isoflavones are induced and accumulate in leaves following attack by Spodoptera litura (Lepidoptera: Noctuidae) larvae. To quantitatively examine patterns of activated de novo biosynthesis, soybean (Var. Enrei) leaves were treated with a combination of plant defense elicitors present in S. litura gut content extracts and L-α-[¹³C₉, ¹⁵N]phenylalanine as a traceable isoflavonoid precursor. Combined treatments promoted significant increases in ¹³C-labeled isoflavone aglycones (daidzein, formononetin, and genistein), ¹³C-labeled isoflavone 7-O-glucosides (daidzin, ononin, and genistin), and ¹³C-labeled isoflavone 7-O-(6″-O-malonyl-β-glucosides) (malonyldaidzin, malonylononin, and malonylgenistin). In contrast levels of ¹³C-labeled flavones and flavonol (4′,7-dihydroxyflavone, kaempferol, and apigenin) were not significantly altered. Curiously, application of fatty acid-amino acid conjugate (FAC) elicitors present in S. litura gut contents, namely N-linolenoyl-L-glutamine and N-linoleoyl-L-glutamine, both promoted the induced accumulation of isoflavone 7-O-glucosides and isoflavone 7-O-(6″-O-malonyl-β-glucosides), but not isoflavone aglycones in the leaves. These results demonstrate that at least two separate reactions are involved in elicitor-induced soybean leaf responses to the S. litura gut contents: one is the de novo biosynthesis of isoflavone conjugates induced by FACs, and the other is the hydrolysis of the isoflavone conjugates to yield isoflavone aglycones. Gut content extracts alone displayed no hydrolytic activity. The quantitative analysis of isoflavone de novo biosynthesis, with respect to both aglycones and conjugates, affords a useful bioassay system for the discovery of additional plant defense elicitor(s) in S. litura gut contents that specifically promote hydrolysis of isoflavone conjugates.     

Conspecific and Heterogeneric Lacewings Respond to (<Emphasis Type="Italic">Z</Emphasis>)-4-Tridecene Identified from <Emphasis Type="Italic">Chrysopa formosa</Emphasis> (Neuroptera: Chrysopidae)

Green lacewings (Chrysopidae) are predators of soft-bodied pest insects and are among the most important biological control agents in crop protection. Chrysopa spp. are of special importance since, unlike most green lacewing species, adults are also predatory. The current study was undertaken in search of Chrysopa formosa compounds with semiochemical activity. Using coupled gas chromatography-electroantennography (GC-EAG), head and thorax extracts of C. formosa elicited EAG responses to a compound subsequently identified by coupled GC/mass spectrometry, microchemistry, chemical synthesis and GC peak enhancement as (Z)-4-tridecene. In field experiments, this compound decreased attraction of adult C. formosa to (1R,4aS,7S,7aR)-nepetalactol and that of Chrysoperla carnea species-complex to a ternary floral lure, with the inhibitory effect found to be dose-dependent. Our results suggest that (Z)-4-tridecene may serve as a general warning signal among multiple green lacewing species. Perspectives for potential practical applications are discussed.     

Aqueous radical polymerization of <Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>-dimethylacrylamide redox-initiated by aerobically catalytic oxidation of water-soluble tertiary amines

Catalytic oxidation of water-soluble tertiary amines by complexes of Cu^II, Fe^III and Co^II was utilized to initiate radical polymerization of N,N-dimethylacrylamide (DMAAm) in aqueous solution at 70–80 °C. The oxidation of tertiary amines by Cu^II was studied by proton nuclear magnetic resonance spectroscopy and online ultraviolet–visible spectrophotometry. The polymerization kinetics was monitored by gas chromatography, and molecular weight of the PDMAAm was measured by gel-permeation chromatography coupled with multi-angle laser light scattering. Oxidation of tertiary amines occurs predominantly via formation of C_alpha·radicals to initiate polymerization of electron-deficient monomers and N-dealkylation, and redox equilibrium between Cu^I/L and Cu^II/L is established at a faster rate in aqueous media. Fe^III and Cu^II complexes are efficient catalysts as each catalyst molecule could generate above 10 propagating radicals in 5 h, while Co^II complex might involve in oxidation of tertiary amines in non-radical pathway, leading to a low catalytic efficiency. Water-soluble tertiary amines such as N,N-dialkylethanolamine (alkyl = methyl, ethyl etc.) are reducing agents of a higher activity in aqueous media than those primary or secondary analogues. Our strategy renders it possible to prepare polymer of alpha-amino functionality via one-pot process from commercially available commodity reagents under practical conditions with negligible catalyst residue.     

Dolichodial: A New Aphid Sex Pheromone Component?

The sex pheromones of many aphid species from the subfamily Aphididae comprise a mixture of the iridoids (cyclopentanoids) (1R,4aS,7S,7aR)-nepetalactol and (4aS,7S,7aR)-nepetalactone. In this paper, we investigate whether other chemicals, in addition to nepetalactol and nepetalactone, are released from Dysaphis plantaginea (rosy apple aphid) oviparae as part of their sex pheromone. Four compounds present in an air entrainment sample collected from D. plantaginea oviparae feeding on apple (Malus silvestris c.v. Braburn) elicited electrophysiological responses from male D. plantaginea. Active peaks were tentatively identified by gas chromatography (GC) coupled with mass spectrometry, with identification confirmed by peak enhancement with authentic compounds on GC columns of different polarities. The electroantennography-active chemicals were (1R,4aS,7S,7aR)-nepetalactol, (4aS,7S,7aR)-nepetalactone, (1S,2R,3S)-dolichodial, and phenylacetonitrile. (1S,2R,3S)-Dolichodial elicited a behavioral response from male D. plantaginea and naïve-mated female parasitoids, Aphidius ervi. This is the first report of electrophysiological and behavioral responses from any aphid morph to (1S,2R,3S)-dolichodial. Whether or not (1S,2R,3S)-dolichodial is a third component of the aphid sex pheromone is discussed.     

Structure of a biologically active binuclear palladium complex in the compound bis(bis[(μ<Subscript>2</Subscript>-2-chloroethylammonium) (1,10-phenanthroline)-palladium(I)]) · octanitrates · dihydrates

The structure of a biologically active binuclear palladium complex, namely, [(1,10-phenanthroline) Pd(μ₂-2-chloroethylammonium) ₂ ⁴⁺ · 4NO ₃ ^? · H₂O, has been determined using X-ray diffraction analysis. The compound crystallizes in the monoclinic system, space group of symmetry Cc, with the unit cell parameters a = 24.527(3) Å, b = 13.097(1) Å, c = 22.651(3) Å, β = 104.23(1)°, V = 7052(2) ų, Z = 8, and ρ = 1.88 g/cm³. The final discrepancy factor is R1 = 0.0316 for 15581 symmetrically nonequivalent reflections with I ≥ 2σ(I), wR2 = 0.0513, and GooF = 1.047. The palladium atoms reside in the oxidation state of 1+, which is rarely encountered in organometallic compounds. The asymmetric part of the unit cell contains two chemically equivalent but crystallographically independent positively charged binuclear palladium complexes, eight NO ₃ ^? anions, and two water molecules. The π-π stacking interaction between the nearest 1,10-phenanthroline rings of the neighboring layers takes place. Moreover, the interlayer and intralayer interactions occur through electrostatic interaction forces and a complex three-dimensional system of hydrogen bonds, which are formed by water molecules and N ₃ ⁺ groups.     

IR Spectroscopy in Rank and Group Assignment of Coal

The possibility of express determination of the characteristics V _IR ^daf , R_{o, IR}, y_IR, ΣLC_IR, and A _IR ^d used in the ranking of coal on the basis of IR spectroscopy is assessed for a specific example: Kuznetsk coals of different maceral composition and metamorphic development. The IR characteristics are compared with values obtained by standard methods (V^daf, R_{o, r, y}, ΣLC, and A^d).     

Effect of nitrogen to niobium atomic ratio on superconducting transition temperature of δ-NbN<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript> powders

Powders of cubic niobium nitride δ-NbN _x with a particle size of below 20 μm were prepared by reactive diffusion at T = 1455?1475°C under nitrogen pressures of P ₁(N₂) = 0.1?3 MPa and P ₂(N₂) = 25 MPa. For these powders, the values of the stoichiometric coefficient x, lattice parameter a, and the superconducting transition temperature Tc were measured and the a(x), T _c(x) and T _c(a) functions were analyzed. The T _c values were found to linearly grow with increasing a (decreasing structure imperfection). A maximum value of T _c (15.8 K) corresponded to a maximum value of a (4.3934 Å). Maximain the a(x) and T _c(x) curves were found to correspond to a slightly substoichiometric nitride with x = 0.98. Having synthesized cubic niobium nitrides with 0.892 < x < 1.062, we managed to measure the dependences of a and T _c on x all over the almost entire homogeneity range for δ-NbN _x . Our a(x) and T _c(a) functions were found to reasonably agree with those previously reported for SHS-produced δ-NbN _x powders.     

Maxima of the Specific Heat at Constant Pressure of the <Emphasis Type="Italic">n</Emphasis>-Alkanes C<Subscript>7</Subscript>-C<Subscript>9</Subscript> in the Supercritical Region

Precision measurements of the specific heat at constant pressure, C _p , of high-purity samples of the normal alkanes C₇-C₉ in the supercritical region of state parameters are carried out using an adiabatic flow calorimeter equipped with a calorimetric flowmeter. Currently, this is the most accurate method. The coordinates of maxima of C _p on isobars are determined. A generalized equation for the line of the maxima of C _p in reduced coordinates π-τ and an equation for C _p along this line in corresponding states for the homologous series are obtained in terms of thermodynamic similarity theory using the most reliable published data. Existing experimental methods for determining the critical parameters of individual substances are analyzed.     

Interspecific Cross-Attraction between the South American Cerambycid Beetles <Emphasis Type="Italic">Cotyclytus curvatus</Emphasis> and <Emphasis Type="Italic">Megacyllene acuta</Emphasis> is Averted by Minor Pheromone Components

During field screening trials conducted in Brazil in 2015, adults of both sexes of the cerambycid beetles Cotyclytus curvatus (Germar) and Megacyllene acuta (Germar) (subfamily Cerambycinae, tribe Clytini) were significantly attracted to racemic 3-hydroxyhexan-2-one and racemic 2-methylbutan-1-ol, chemicals which previously have been identified as male-produced aggregation-sex pheromones of a number of cerambycid species endemic to other continents. Subsequent analyses of samples of beetle-produced volatiles revealed that males of C. curvatus sex-specifically produce only (R)-3-hydroxyhexan-2-one, whereas males of M. acuta produce the same compound along with lesser amounts of (2S,3S)-2,3-hexanediol and (S)-2-methylbutan-1-ol. Follow-up field trials showed that both sexes of both species were attracted to synthetic reconstructions of their respective pheromones, confirming that males produce aggregation-sex pheromones. The minor pheromone components of M. acuta, (S)-2-methylbutan-1-ol and (2S,3S)-2,3-hexanediol, synergized attraction of that species, but antagonized attraction of C. curvatus to (R)-3-hydroxyhexan-2-one. Beetles of other cerambycine species also were attracted in significant numbers, including Chrysoprasis linearis Bates, Cotyclytus dorsalis (Laporte & Gory), and Megacyllene falsa (Chevrolat). Our results provide further evidence that 3-hydroxyhexan-2-one is a major component of attractant pheromones of numerous cerambycine species world-wide. Our results also highlight our increasing understanding of the crucial role of minor pheromone components in imparting species specificity to cerambycid pheromone blends, as is known to occur in numerous species in other insect families.     

CO and CO<Subscript>2</Subscript> methanation over Ni catalysts supported on alumina with different crystalline phases

The effect of alumina crystalline phases on CO and CO₂ methanation was investigated using alumina-supported Ni catalysts. Various crystalline phases, such as α-Al₂O₃, θ-Al₂O₃, δ-Al₂O₃, η-Al₂O₃, γ-Al₂O₃, and κ-Al₂O₃, were utilized to prepare alumina-supported Ni catalysts via wet impregnation. N₂ physisorption, H₂ chemisorption, temperature-programmed reduction with H₂, CO₂ chemisorption, temperature-programmed desorption of CO₂, and X-ray diffraction were employed to characterize the catalysts. The Ni/θ-Al₂O₃ catalyst showed the highest activity during both CO and CO₂ methanation at low temperatures. CO methanation catalytic activity appeared to be related to the number of Ni surface-active sites, as determined by H₂-chemisorption. During CO₂ methanation, Ni dispersion and the CO₂ adsorption site were found to influence catalytic activity. Selective CO methanation in the presence of excess CO₂ was performed over Ni/γ-Al₂O₃ and Ni/δ-Al₂O₃; these substrates proved more active for CO methanation than for CO₂ methanation.     

Identification,Synthesis, and Field Tests of the Sex Pheromone of <Emphasis Type="Italic">Margarodes prieskaensis</Emphasis> (Jakubski)

Here, we report the identification and synthesis of the sex pheromone of female Margarodes prieskaensis (Jakubski), and the attractiveness of the synthetic pheromone to males in field trapping tests. Volatile organic compounds were collected from virgin females using a sample enrichment probe (SEP). Analyses by gas chromatography coupled to mass spectrometry revealed the presence of only two constituents. By scaling up the SEP, sufficient of the major constituent was collected for ¹H and ¹³C nuclear magnetic resonance (NMR) analyses and ancillary NMR techniques. The sex attractant was identified as (2R,4R,6R,8R)-2,4,6,8-tetramethylundecan-1-ol. The enantiomerically pure compound was synthesized from octadecyl (2R,4R,6R,8R)-2,4,6,8-tetramethylundecanoate, a minor component of the uropygial (preen) gland secretion of the domestic goose, Anser domesticus. Field trapping experiments, carried out in vineyards in the Northern Cape Province of South Africa, showed that the synthetic compound was as attractive to winged males of M. prieskaensis as virgin females. The second compound detected was identified as the corresponding acetate, but addition of this did not affect the attractiveness of the major component. We believe this to be the first identification of a sex attractant of the Margarodidae.     

Solid-phase synthesis and characterization of rare-earth chromates

Simple chromates(V) MCrO₄ (M = Sc, Y, Gd, Er, or Yb) and chromate(V) vanadates Gd(CrO₄) _x (VO₄)_{1 ? x} have been synthesized by a solid-phase method. All compounds crystallize in the xenotime-type structure, space group I4₁/amd, Z = 4. The unit cell parameters have been calculated as follows: for GdCrO₄, a = 7.209(5) Å, c = 6.318(4) Å; for ErCrO₄, a = 7.088(2) Å, c = 6.231(1) Å; for YbCrO₄, a = 7.034(1) Å, c = 6.205(2) Å; for YCrO₄, a = 7.108(3) Å, c = 6.254(3) Å; and for ScCrO₄, a = 7.012(2) Å, c = 6.188(2) Å. Symmetry D _2d , established for the CrO₄ tetrahedron during the Rietveld structure refinement, is verified by IR spectroscopy. The MCrO₄ simple chromates are paramagnets; their magnetic moments range from 1.7 to 8.1 μ _B .