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  • 1
    ISSN: 1573-1561
    Keywords: Carpophilus hemiplerus ; C. mutilatus ; C. davidsoni ; C. humeralis ; Coleoptera ; Nitidulidae ; aggregation pheromones ; stone fruit ; phenology ; dose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Synthetic aggregation pheromones ofCarpophilus hemipterus (L.) andCarpophilus mutilatus Erichson were field tested during a 10-month period in southern New South Wales stone fruit orchards to determineCarpophilus spp. phenology and the effect of two pheromone doses on attraction. Aggregation pheromones synergize the attraction of host volatiles toCarpophilus spp. Four major species,C. hemipterus, C. mutilatus, C. davidsoni Dobson andC. (Urophorus) humeralis (F.), were trapped, with greater numbers of each species inC. hemipterus pheromone/fermenting whole-wheat breaddough-baited traps, than in dough-only-traps. InC. mutilatus pheromone/ fermenting-dough-baited traps, onlyC. mutilatus andC. davidsoni responded in greater numbers than to dough-only traps. Beetles first appeared in traps in late September (early spring) when daily maximum temperatures averaged 17.5
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 20 (1994), S. 3207-3219 
    ISSN: 1573-1561
    Keywords: Aggregation pheromone ; triene ; tetraene ; hydrocarbon ; Coleoptera ; Nitidulidae ; Carpophilus davidsoni ; Australian sap beetle ; trapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract A male-produced aggregation pheromone was identified for the Australian sap beetle,Carpophilus davidsoni Dobson (Coleoptera: Nitidulidae), by bioassay-guided fractionation of volatiles collected from feeding beetles. The most abundant components were: (2E,4E,6E)-5-ethyl-3-methyl-2,4,6-nonatriene, (3E,5E,7E)-6-ethyl-4-methyl-3,5,7-decatriene, (2E,4E,6E,8E)-3,5,7-trimethyl-2,4,6,8-undecatetraene, and (2E,4E,6E,8E)-7-ethyl-3,5-dimethyl-2,4,6,8-undecatetraene. The relative abundance of these components in collections from individual males feeding on artificial diet was 100:7:9:31, respectively. Pheromone production began within several days after males were placed onto diet medium and continued for at least 20 weeks. Peak production was 〉3 µg total pheromone per male per day. Males in groups of 50–60 emitted less pheromone (the peak level was 0.09 µg per beetle per day), and the emissions from groups contained relatively little tetraene (proportions of the components listed above were 100:7:2:7, respectively). Three additional trienes and one additional tetraene were identified in minor amounts; the entire eight-component male-specific blend is qualitatively identical and quantitatively similar to that of the North American sibling species,C. freemani Dobson. A synthetic blend of the four major components on rubber septa, prepared to emit in the same proportions as from individual males, was highly attractive in the field when synergized with fermenting whole-wheat bread dough. Cross-attraction was observed in the field involving the pheromones ofC. davidsoni, C. hemipterus (L.), andC. mutilatus Erichson. Potential uses of the pheromones in pest management are discussed.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-1561
    Keywords: Attractant ; alcohol ; aldehyde ; geranic acid ; monitoring ; aggregation pheromone ; Anthonomus eugenii ; pepper weevil ; Coleoptera ; Curculionidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract This study describes the identification of an aggregation pheromone for the pepper weevil,Anthonomus eugenii and field trials of a synthetic pheromone blend. Volatile collections and gas chromatography revealed the presence of six male-specific compounds. These compounds were identified using chromatographic and spectral techniques as: (Z)-2-(3,3-dimethylcyclohexylidene)ethanol, (E)-2-(3,3-dimethylcyclohexylidene)ethanol, (Z)-(3,3-dimethylcyclohexylidene)acetaldehyde, (E)-(3,3-dimethylcyclohexylidene)acetaldehyde, (E)-3,7-dimethyl-2,6-octadienoic acid (geranic acid), and (E)-3,7-dimethyl-2,6-octadien-1-ol (geraniol). The emission rates of these compounds from feeding males were determined to be about: 7.2, 4.8, 0.45, 0.30, 2.0, and 0.30µg/male/day, respectively. Sticky traps baited with a synthetic blend of these compounds captured more pepper weevils (both sexes) than did unbaited control traps or pheromone-baited boll weevil traps. Commercial and laboratory formulations of the synthetic pheromone were both attractive. However, the commercial formulation did not release geranic acid properly, and geranic acid is necessary for full activity. The pheromones of the pepper weevil and the boll weevil are compared. Improvements for increasing trap efficiency and possible uses for the pepper weevil pheromone are discussed. A convenient method for purifying geranic acid is also described.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 993-995 
    ISSN: 0887-624X
    Keywords: metathesis ; regioselective polymerization ; 7-alkylnorbornenes ; ab initio MO Calculations ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 3031-3037 
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; butyl acrylate ; poly(n-butyl acrylate) ; Electron Paramagnetic Resonance ; spin trapping ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The propagating radical in the emulsion polymerization reaction of butyl acrylate was detected by Electron Paramagnetic Resonance (EPR) spectroscopy using two spin-trapping agents, 2-methyl-2-nitrosopropane (MNP) and α-(4-pyridyl 1-oxide)-N-tert-butylnitrone (PyOBN). Through analysis of hyperfine structure of the spectra obtainedfrom the trapped radicals, the propagating radical is inferred to be the well known acrylate radical, — [CH2—CH(COOC4H9)]n—CH2—CH(COOC4H9)—. © 1994 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 33 (1994), S. 335-339 
    ISSN: 0959-8103
    Keywords: poly(ether sulphones) ; PES ; NMR ; CPMAS ; polymerisation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The synthesis of poly(ether sulphone) using the ‘carbonate’ route based on the reaction of 4,4′-dihydroxydiphenylsulphone, 4,4-dichlorodiphenylsulphone and potassium carbonate dispersed in diphenylsulphone has been studied by 13C CPMAS NMR spectroscopy. In the initial reaction the half potassium salt of 4,4′-dihydroxydiphenylsulphone is formed. No evidence for a stable full salt was found at any time during the polymerisation cycle and no appreciable oligomer formation took place before the polymerisation itself took place.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 2 (1991), S. 241-242 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: It is common experience that carbon fiber braids, which are passed through osseous tunnels, are not incorporated by osteointergration. Rather, they are separated from the boy walls of the tunnels by a granulomatous-cicatrizing interface membrane. In the exceptional case, however, Bony ingrowth into the braid occurs without an intervening soft tissular layer. Bony ingrowth may be contingent on the stability of the carbon fiber braid within the osseous tunnel.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 24 (1990), S. 605-620 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Variable takeoff angle x-ray photoelectron spectroscopy was used to determine the surface composition of five polyurethane block copolymers. The high-resolution C1s spectra from all five polyurethane samples had peaks at binding energies of 285.0, 286.5, and 289.5 eV, which are consistent with the presence of hydrocarbon, ether, and urethane carbon species. Both the measured elemental compositions at the low takeoff angles (deepest sampling depths) and the calculated elemental compositions for depths 〉 15 Å generally showed good agreement with the expected bulk compositions. The outer 15 Å of the surface of all five samples was depleted in the nitrogen-containing hard segment. For the base polyurethane sample in this series, an enrichment of the poly(tetramethylene oxide) soft segment and the presence of an organic silicone impurity were detected. Doubling the chain length of both the hard and soft segments resulted in a further decrease of the hard segment concentration in the outer surface of the sample. The grafting of C2 and C18 alkyl groups onto 10 or 20% of the ure-thane linkages resulted in an increase in the percentage of aliphatic carbon species present on the surface. In the case of the C18-alkylated material, the presence of alkyl chains at the surface was inferred using contact angle measurements.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 2907-2922 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ring-opened metathesis polymers of 7-methylnorbornadiene (1) have been synthesized with cis main-chain double bond contents ranging from 20 to 97% using several initiators; their microstructures have been examined in detail using 13C NMR spectroscopy. The result show that polymerization from the anti-exo orientation is greatly favoured over the syn-exo mode. A nonbonded repulsion energy of 6-8 kJ · mol-1 between the syn-7-methyl group and the double bond is estimated. The microstructural features also resemble those for polymers of the anti- and syn-7-methylnorbornenes, in contrast to poly(norbornadiene) itself and to poly(norbornene), in that the splitting of a given resonance due to tacticity effects is of the same order as splittings due to neighbouring double bonds. Cis double bond contents and tacticities using different catalysts agree well with those expected from previous work with norbornadiene and several methyl-substituted norbornenes, respectively, as monomers. The previous surprising observation that there is significantly less or no discrimination between the syn- and anti-orientations in polymerizing 7-tert-butoxy- and 7-acetoxynorbornadiene is discussed and is attributed to a pseudo [3 + 2] transition state replacing the normal one for [2 + 2] metallacyclobutanation. In the [3 + 2] mode a lone pair of electrons on the oxygen acts in conjunction with the π pairs of the C=C and [Mt]=C moieties. The net effect is to lower the energy barriers for the [2 + 2] cycloaddition and the reverse step. The same explanation, rather than chelation, is also believed to be correct for the beneficial effect on the metathesis polymerization of the 7-oxa group in several substituted 7-oxanorbornenes and 7-oxanorbornadienes when compared to the corresponding 7-methylene monomers.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 2965-2979 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Well defined, narrow molecular weight distribution polydimethylsiloxane (PDMS) oligomers containing single, terminal, reactive end groups were synthesised by the anionic polymerisation of hexamethylcyclotrisiloxane (D3). A variety of functionalities were obtained by termination with an appropriate silyl chloride end blocker, e.g. styryl, allyl, silyl chloride, silane, hexenyl etc. Certain monomeric end blockers were also synthesised where necessary. The resulting oligomers were subjected to detailed characterisation using 1H NMR, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and IR spectroscopy.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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