Structure, dielectric relaxation and electrical conductivity of 2,3,7,8-Tetramethoxychalcogenanthrene-2,3-dichloro-5,6-dicyano-1,4-benzoquinone 1:1 charger-transfer complexes

[EN] 2,3,7,8-Tetramethoxychalcogenanthrenes (5,10-chalcogena-cyclo-diveratrylenes, 'Vn(2)E(2)', E = S, Se) form isotypical 1:1 charge-transfer (CT) complexes with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ). X-ray analysis of Vn(2)S(2) . DDQ shows the compound to have a columnar structure with segregated stacks of donors and acceptors. The donors are virtually planar in accordance with a formulation of [Vn(2)E(2)](+)[DDQ](-). Donor cations and acceptor anions are equidistant in their respective stacks, but in each case they inclined to the stacking axis, nevertheless guaranteeing an optimum overlap of the half-filled frontier orbitals which are of pi-type character according to MNDO calculations. Dielectric ac measurements of permittivity epsilon' and loss factor E '' clearly reveal two processes, a dielectric one at low temperatures and a conductive one at high temperatures. The dielectric process can be described by the Havriliak-Negami (HN) and the Kohlrausch-Williams-Watts (KWW) model, and the conductive process by a Debye-type plot. Using these methods, the relevant parameters are evaluated. The de conductivities of polycrystalline samples moulded at 10(8) Pa show a temperature dependence in the plots of ln sigma vs. T-1, which is typical of semiconductors. Two slopes are found; that in the low-temperature region (<285 K) is explained by an easy-path model (intragrain conductivity with low activation energies), whereas in the high-temperature region conduction across the grain boundaries (with higher activation energies) is becoming predominant. The activation energies for the intrinsic conductivities obtained by the ac and de measurements are similar. Despite the columnar structure with segregated stacks, due to stoichiometric oxidation states of the components, the absolute values of conductivity are low ten. 10(-6) S cm(-1) at 293 K), though higher (by a factor of ca. 10(3)) than those of compounds like Vn(2)E(2) . TCNQ with stacks in which donor and acceptor molecules alternate.Behrens, U.; Díaz Calleja, R.; Dötze, M.; Franke, U.; Gunsser, W.; Klar, G.; Kudnig, J.... (1996). Structure, dielectric relaxation and electrical conductivity of 2,3,7,8-Tetramethoxychalcogenanthrene-2,3-dichloro-5,6-dicyano-1,4-benzoquinone 1:1 charger-transfer complexes. Journal of Materials Chemistry. 6(4):547-553. https://doi.org/10.1039/JM9960600547S54755364Behrens, J., Hinrichs, W., Link, T., Schiffling, C., & Klar, G. (1995). SELFSTACKING SYSTEMS, PART 6.1HOST LATTICE FUNCTION OF 2,3,8,9-TETRAMETHOXYDIBENZO[c,e][1,2]-DICHALCOGENINS IN THEIR ELECTRICALLY CONDUCTING IODINE COMPLEXES. Phosphorus, Sulfur, and Silicon and the Related Elements, 101(1-4), 235-244. doi:10.1080/10426509508042522Berges, P., Kudnig, J., Klar, G., Martínez, E. S., & Calleja, R. D. (1989). Elementorganische Verbindungen mit o-Phenylenresten, XVI . 2:1-Komplexe von 2,3,7,8-Tetramethoxychalcogenanthrenen mit Tetracyanethen / Organometallic Compounds with o-Phenylene Substituents, Part XVI 2:1-Complexes of 2,3,7,8-Tetramethoxychalcogenanthrenes with Tetracyanoethene. Zeitschrift für Naturforschung B, 44(2), 211-219. doi:10.1515/znb-1989-0219Hinrichs, W., Berges, P., Klar, G., Sánchez-Martínez, E., & Gunsser, W. (1987). Structure and electrical conductivity of TCNQ-2,3,7,8-tetramethoxychalcogenanthrene complexes. Synthetic Metals, 20(3), 357-364. doi:10.1016/0379-6779(87)90832-0Sánchez Martínez, E., Díaz Calleja, R., Gunsser, W., Berges, P., & Klar, G. (1989). Structure and dielectric relaxation of 2,3,7,8-tetramethoxychalcogenanthrene-TCNQ complexes. Synthetic Metals, 30(1), 67-78. doi:10.1016/0379-6779(89)90642-5Gunßer, W., Henning, J. H., Klar, G., & Martínez, E. S. (1989). Spin Density and Magnetic Susceptibility of Charge-Transfer Complexes with Chalkogenanthrene Donors. Berichte der Bunsengesellschaft für physikalische Chemie, 93(11), 1370-1373. doi:10.1002/bbpc.19890931148G. M. Sheldrick , SHELXTL-PLUS, Release 4.21/0, Siemens Analytical X-Ray Instruments, 1990.Bock, H., Rauschenbach, A., Näther, C., Havlas, Z., Gavezzotti, A., & Filippini, G. (1995). Orthorhombisches und monoklines 2,3,7,8-Tetramethoxythianthren: kleiner Strukturunterschied – große Gitteränderung. Angewandte Chemie, 107(1), 120-122. doi:10.1002/ange.19951070132Bock, H., Rauschenbach, A., Näther, C., Havlas, Z., Gavezzotti, A., & Filippini, G. (1995). Orthorhombic and Monoclinic 2,3,7,8-Tetramethoxythianthrene: Small Structural Difference–Large Lattice Change. Angewandte Chemie International Edition in English, 34(1), 76-78. doi:10.1002/anie.199500761Hinrichs, W., Berges, P., & Klar, G. (1987). Selbststapelnde Systeme, IV 2,3,7,8-Tetramethoxythianthreniumsalze/Selfstacking Systems, Part IV 2.3.7.8-Tetramethoxythianthrenium Salts. Zeitschrift für Naturforschung B, 42(2), 169-176. doi:10.1515/znb-1987-0209Peover, M. E. (1962). 879. A polarographic investigation into the redox behaviour of quinones: the roles of electron affinity and solvent. Journal of the Chemical Society (Resumed), 4540. doi:10.1039/jr9620004540Wheland, R. C., & Gillson, J. L. (1976). Synthesis of electrically conductive organic solids. Journal of the American Chemical Society, 98(13), 3916-3925. doi:10.1021/ja00429a030Zanotti, G., Del Pra, A., & Bozio, R. (1982). Structure of tetraethylammonium–2,3-dichloro-5,6-dicyano-p-benzoquinone. Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 38(4), 1225-1229. doi:10.1107/s0567740882005330Zanotti, G., Bardi, R., & Del Pra, A. (1980). Structure of 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ). Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 36(1), 168-171. doi:10.1107/s0567740880002750Handbook of Chemistry and Physics, ed. R. C. Weast, CRC Press, Cleveland, OH, 1977–1978, 58th edn., p. D–178.Sánchez Martínez, E., Díaz Calleja, R., Berges, P., Kudnig, J., & Klar, G. (1989). Structure, electrical conductivity and dielectric relaxation of a 1,2-dimethoxybenzene-tetracyanoethene 1:1 complex. Synthetic Metals, 32(1), 79-89. doi:10.1016/0379-6779(89)90831-xÅsbrink, L., Fridh, C., & Lindholm, E. (1977). HAM/3, a semi-empirical MO theory. I. The SCF method. Chemical Physics Letters, 52(1), 63-68. doi:10.1016/0009-2614(77)85121-xÅsbrink, L., Fridh, C., & Lindholm, E. (1977). HAM/3, a semi-empirical MO theory. III. Unoccupied orbitals. Chemical Physics Letters, 52(1), 72-75. doi:10.1016/0009-2614(77)85123-3Dewar, M. J. S., & Thiel, W. (1977). Ground states of molecules. 38. The MNDO method. Approximations and parameters. Journal of the American Chemical Society, 99(15), 4899-4907. doi:10.1021/ja00457a004Dewar, M. J. S., & Thiel, W. (1977). Ground states of molecules. 39. MNDO results for molecules containing hydrogen, carbon, nitrogen, and oxygen. Journal of the American Chemical Society, 99(15), 4907-4917. doi:10.1021/ja00457a005Åsbrink, L., Fridh, C., & Lindholm, E. (1978). Valence excitation of linear molecules.I. Excitation and UV spectra of N2, Co, acetylene and HCN. Chemical Physics, 27(2), 159-168. doi:10.1016/0301-0104(78)88001-xFridh, C., Åsbrink, L., & Lindholm, E. (1978). Valence excitation of linear molecules. II. Excitation and UV spectra of C2N2, CO2 and N2O. Chemical Physics, 27(2), 169-181. doi:10.1016/0301-0104(78)88002-1Lindholm, E., Bieri, G., Åsbrink, L., & Fridh, C. (1978). Interpretation of electron spectra. III. Spectra of formamide, studied withHAM/3. International Journal of Quantum Chemistry, 14(6), 737-740. doi:10.1002/qua.560140605Starkweather, H. W. (1981). Simple and complex relaxations. Macromolecules, 14(5), 1277-1281. doi:10.1021/ma50006a025Starkweather, H. W. (1990). Distribution of activation enthalpies in viscoelastic relaxations. Macromolecules, 23(1), 328-332. doi:10.1021/ma00203a056Havriliak, S., & Negami, S. (1967). A complex plane representation of dielectric and mechanical relaxation processes in some polymers. Polymer, 8, 161-210. doi:10.1016/0032-3861(67)90021-3J. Ross McDonald , Complex Nonlinear Least Squares Immitance Fitting Program, LEVM6, 1993;Impedance Spectroscopy, Wiley-Interscience, New York, 1987.Williams, G. (1978). Time-correlation functions and molecular motion. Chemical Society Reviews, 7(1), 89. doi:10.1039/cs9780700089Williams, G., & Watts, D. C. (1970). Non-symmetrical dielectric relaxation behaviour arising from a simple empirical decay function. Transactions of the Faraday Society, 66, 80. doi:10.1039/tf9706600080A. R. West , Solid State Chemistry and its Applications, Wiley, Chichester, 1984, ch. 13.Sánchez Martínez, E., Díaz Calleja, R., & Klar, G. (1990). Self-stacking systems 5. Electrical and dielectric properties of 5,5-dibromo-2,3,7,8-tetramethoxyselenanthrene. Synthetic Metals, 38(1), 93-98. doi:10.1016/0379-6779(90)90071-

Crop Updates 2010 - Crop Specific

This session covers twenty four papers from different authors: PLENARY 1. Challenges facing western Canadian cropping over the next 10 years, Hugh J Beckie, Research Centre, Agriculture and Agri-Food Canada, Saskatoon, Saskatchewan CROP SPECIFIC Breeding 2. The challenge of breeding canola hybrids – new opportunities for WA growers, Wallace Cowling, Research Director, Canola Breeders Western Australia Pty Ltd 3. Chickpea 2009 crop variety testing of germplasm developed by DAFWA/CLIMA/ICRISAT/COGGO alliance. Khan, TN1,3, Adhikari, K1,3, Siddique, K2, Garlinge, J1, Smith, L1, Morgan, S1 and Boyd, C1 1Department of Agriculture and Food, Western Australia (DAFWA), 2Insititute of Agriculture, The University of Western Australia (UWA), 3Centre for Legumes in Mediterranean Agriculture (CLIMA), The University of Western Australia 4. PBA Pulse Breeding Australia – 2009 Field Pea Results, Ian Pritchard1, Chris Veitch1, Colin Boyd1, Stuart Morgan1, Alan Harris1 and Tony Leonforte2, 1Department of Agriculture and Food, Western Australia, 2Department of Primary Industries, Victoria 5. PBA Pulse Breeding Australia – 2009 Chickpea Results, Ian Pritchard1, Chris Veitch1, Colin Boyd1, Murray Blyth1, Shari Dougal1 and Kristy Hobson2 1Department of Agriculture and Food, Western Australia, 2Department of Primary Industries, Victoria Decision Support 6. A tool for identifying problems in wheat paddocks, Ben Curtis and Doug Sawkins, Department of Agriculture and Food 7. DAFWA Seasonal Forecast for 2010, Stephens, D, Department of Agriculture and Food, Western Australian, Climate and Modelling Group Disease 8. Enhancement of black spot resistance in field pea, Kedar Adhikari, T Khan, S Morgan and C Boyd, Department of Agriculture and Food, 9. fungicide management of yellow spot in wheat, Ciara Beard, Kith Jayasena, Kazue Tanaka and Anne Smith, Department of Agriculture and Food 10. Resistance to infection by Beet western yellows virus in four Australian canola varieties, Brenda Coutts and Roger Jones, Department of Agriculture and Food 11. Yellow spot carryover risk from stubble in wheat-on-wheat rotations, Jean Galloway, Pip Payne and Tess Humphreys, Department of Agriculture and Food 12. Fungicides for the future: Management of Barley Powdery Mildew and Leaf Rust, Kith Jayasena, Kazue Tanaka and William MacLeod, Department of Agriculture and Food 13. 2009 canola disease survey and management options for blackleg and Sclerotinia in 2010, Ravjit Khangura, WJ MacLeod, M Aberra and H Mian, Department of Agriculture and Food 14. Impact of variety and fungicide on carryover of stubble borne inoculum and yellow spot severity in continuous wheat cropping, Geoff Thomas, Pip Payne, Tess Humphreys and Anne Smith, Department of Agriculture and Food 15. Limitations to the spread of Wheat streak mosaic virus by the Wheat curl mite in WA during 2009, Dusty Severtson, Peter Mangano, Brenda Coutts, Monica Kehoe and Roger Jones, Department of Agriculture and Food 16. Viable solutions for barley powdery mildew, Madeline A. Tucker, Australian Centre for Necrotrophic Fungal Pathogens, Murdoch University Marketing 17. The importance of varietal accreditation in a post-deregulation barley marketing environment, Neil Barker, Barley Australia 18. Can Australia wheat meet requirements for a new middle east market? Robert Loughman, Larisa Cato, Department of Agriculture and Food, and Ken Quail, BRI Australia VARIETY PERFORMANCE 19. Sowing rate and time for hybrid vs open-pollinated canola, Mohammad Amjad and Mark Seymour, Department of Agriculture and Food 20. HYOLA® National Hybrid vs OP Canola Hybrid F1 vs Retained Seed Generation Trial Results and recommendations for growers, Justin Kudnig, Mark Thompson, Anton Mannes, Michael Uttley, Chris Fletcher, Andrew Etherton, Nick Joyce and Kate Light, Pacific Seeds Australia 21. HYOLA® National Hybrid vs OP Canola Sowing Rate Trial Results and plant population recommendations for Australian growers, Justin Kudnig, Mark Thompson, Anton Mannes, Michael Uttley, Andrew Etherton, Chris Fletcher, Nick Joyce and Kate Light, Pacific Seeds Australia; Peter Hamblin, Agritech Research Young, NSW, Michael Lamond, Agrisearch, York, Western Australia 22. Desi chickpea agronomy for 2010, Alan Meldrum, Pulse Australia and Wayne Parker, Department of Agriculture and Food 23. New wheat varieties – exploit the benefits and avoid the pitfalls, Steve Penny, Sarah Ellis, Brenda Shackley, Christine Zaicou, Shahajahan Miyan, Darshan Sharma and Ben Curtis, Department of Agriculture and Food 24. The influence of genetics and environment on the level of seed alkaloid in narrow-leafed lupins, Greg Shea1, Bevan Buirchell1, David Harris2 and Bob French1, 1Department of Agriculture and Food, 2ChemCentr

The role and function of the ASX and its listing rules

In a joint submission to the Australian Stock Exchange Limited ("ASX") dated December 1989 (the "Joint Submission") the Law Institute of Victoria and the Law Council of Australia expressed the view that: "The ASX should be contained to its role of ensuring that the market is informed, efficient and fair, and not be allowed to effectively legislate on substantive issues of law outside this role."1 It was suggested in the Joint Submission that the ASX, through its listing rules, had over-extended its role so as to encroach on substantive company law matters which were more properly within the province of Parliament. 2 These criticisms have resulted in a considerable degree of public debate on the proper role of the ASX and the scope of its listing rules.3 In response to the Joint Submission and the public debate, a discussion paper was released by the ASX in October 1990 (the "Discussion Paper")4 in which the ASX expressed its views on these issues and invited submissions from interested members of the public. In its Discussion Paper, the ASX largely defended its perception of its current role in the business community and argued that the listing rules did not exceed their proper scope (although this view has since been refined). It was conceded by the ASX, however, that some of the concerns expressed in the Joint Submission relating to the drafting and adoption of listing rules had some validity".5 It was also conceded that some listing rules would be better contained in legislation. Both the Joint Submission and the Discussion Paper of the ASX will be examined in detail in this paper. Central to the argument concerning the proper scope of the ASX listing rules are sections 777 and 1114 of the Corporations Law (formerly sections 42 and 14 respectively of the Securities Industry Act 1980) which grant "statutory recognition" to the listing rules. On the view put forward in the Joint Submission, the listing rules do not have the clarity expected of legislation, which gives rise to uncertainty of their application in practice.6 Such uncertainty is increased, so it is said,7 by the fact that in the foreword to the listing rules, the ASX states that it looks to listed companies to comply with the "spirit' as well as the letter" of the listing rules. According to the Joint Submission, this gives rise to the undesirable possibility of action under the Corporations Law (formerly under Securities Industry Act 1980) to enforce the spirit of the listing rules.

Skin and subcutaneous tumors.

In dogs, approximately 25–30% of all neoplasms are reported to arise in the skin. The World Health Organization has a detailed histologic classification scheme for mesenchymal and epithelial skin tumors of domestic animals. All skin and subcutaneous masses should have fine needle aspiration cytology performed as part of the diagnostic process before surgical intervention. Appropriate treatment options in an individual case are based on the tumor type and degree of local tumor disease, the results of staging tests, the presence or absence of metastases, and the overall condition of the patient. Surgery can be used as the sole treatment modality or incombination with chemotherapy, radiation therapy, or other adjunctive treatments. The chapter covers mast cell tumors (MCTs) and soft tissue sarcomas. MCTs are the most common malignant cutaneous tumor in dogs and the second most common cutaneous tumor in cats. The treatment of choice for local cutaneous melanoma in both the cat and dog is surgical excision

Skin and subcutaneous tumors.

In dogs, approximately 25–30% of all neoplasms are reported to arise in the skin. The World Health Organization has a detailed histologic classification scheme for mesenchymal and epithelial skin tumors of domestic animals. All skin and subcutaneous masses should have fine needle aspiration cytology performed as part of the diagnostic process before surgical intervention. Appropriate treatment options in an individual case are based on the tumor type and degree of local tumor disease, the results of staging tests, the presence or absence of metastases, and the overall condition of the patient. Surgery can be used as the sole treatment modality or incombination with chemotherapy, radiation therapy, or other adjunctive treatments. The chapter covers mast cell tumors (MCTs) and soft tissue sarcomas. MCTs are the most common malignant cutaneous tumor in dogs and the second most common cutaneous tumor in cats. The treatment of choice for local cutaneous melanoma in both the cat and dog is surgical excision