Auswahl der wissenschaftlichen Literatur zum Thema „Azo compounds“
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Zeitschriftenartikel zum Thema "Azo compounds":
Beck, Karin, Harald Burghard, Gabriele Fischer, Siegfried Hünig und Petra Reinold. „Azo Cope Rearrangements of Nonstabilized Azo Compounds“. Angewandte Chemie International Edition in English 26, Nr. 7 (Juli 1987): 672–73. http://dx.doi.org/10.1002/anie.198706721.
Jamain, Zuhair, Melati Khairuddean und Tay Guan-Seng. „Synthesis of New Star-Shaped Liquid Crystalline Cyclotriphosphazene Derivatives with Fire Retardancy Bearing Amide-Azo and Azo-Azo Linking Units“. International Journal of Molecular Sciences 21, Nr. 12 (16.06.2020): 4267. http://dx.doi.org/10.3390/ijms21124267.
Matsui, Masaki, Shigeo Kawamura, Katusoyoshi Shibata, Hiroshige Muramatsu, Motohiro Mitani, Hideo Sawada und Masaharu Nakayama. „Perfluoroalkylation of azo compounds“. Journal of Fluorine Chemistry 57, Nr. 1-3 (April 1992): 209–17. http://dx.doi.org/10.1016/s0022-1139(00)82833-x.
Hamidian, Kourosh, Mohsen Irandoust, Ezzat Rafiee und Mohammad Joshaghani. „Synthesis, Characterization, and Tautomeric Properties of Some Azo-azomethine Compounds“. Zeitschrift für Naturforschung B 67, Nr. 2 (01.02.2012): 159–64. http://dx.doi.org/10.1515/znb-2012-0208.
Kempa, S., L. Wallach und K. Rueck-Braun. „ChemInform Abstract: Aliphatic Azo Compounds“. ChemInform 43, Nr. 36 (09.08.2012): no. http://dx.doi.org/10.1002/chin.201236234.
Yadav, Pramod Kumar. „Synthesis, Characterization and Antimicrobial Studies of Some Azo-Compounds“. Academic Voices: A Multidisciplinary Journal 6 (04.06.2018): 24–27. http://dx.doi.org/10.3126/av.v6i0.20104.
Luo, Chao, Oleg Borodin, Xiao Ji, Singyuk Hou, Karen J. Gaskell, Xiulin Fan, Ji Chen et al. „Azo compounds as a family of organic electrode materials for alkali-ion batteries“. Proceedings of the National Academy of Sciences 115, Nr. 9 (09.02.2018): 2004–9. http://dx.doi.org/10.1073/pnas.1717892115.
Al-Mudhafar, May M. Jawad, Rana A. Kamoon und Tagreed N.-A. Omar. „Synthesis, Characterization and Antimicrobial Evaluation of New Azo Compounds Derived from Sulfonamides and Isatin Schiff Base“. International Journal of Drug Delivery Technology 10, Nr. 01 (25.03.2020): 150–55. http://dx.doi.org/10.25258/ijddt.10.1.26.
Jabar, Maha A., und Nisreen H. Karam. „Synthesis and characterization of azo liquid crystal compounds based on 5H-Thiazolo [3,4-b][1,3,4]thiadiazole unit“. Bionatura 7, Nr. 2 (15.05.2022): 1–4. http://dx.doi.org/10.21931/rb/2022.07.02.17.
Ali, Yousaf, Shafida Abd Hamid und Umer Rashid. „Biomedical Applications of Aromatic Azo Compounds“. Mini-Reviews in Medicinal Chemistry 18, Nr. 18 (12.10.2018): 1548–58. http://dx.doi.org/10.2174/1389557518666180524113111.
Dissertationen zum Thema "Azo compounds":
Iannarelli, Paul M. „Routes to novel azo compounds“. Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/3492.
Newington, Ian M. „Azo-anions in organic synthesis“. Thesis, University of Oxford, 1985. http://ora.ox.ac.uk/objects/uuid:690ab891-be13-4582-a029-47974d20adac.
MacDonald, Ranald John. „Novel routes to heterocyclic Azo compounds“. Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/5787.
江鳳思 und Fung-sze Kong. „The chemistry of Osmium carbonyl clusters containing organomercurials and azo-compounds“. Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31238695.
Kong, Fung-sze. „The chemistry of Osmium carbonyl clusters containing organomercurials and azo-compounds /“. Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21021545.
Clarke, Ronald James. „Kinetic and equilibrium studies of cyclodextrin-azo dye inclusion complexes /“. Title page, contents and abstract only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09phc5992.pdf.
Offprints of two author's journal articles inserted at end of the v. Includes bibliographical references (leaves 10-12).
McNair, Craig. „Synthetic approaches to substituted Ca4B-type azo compounds“. Thesis, University of Strathclyde, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366902.
Shahkar, G. R. „Thermal decomposition of azo compounds in the gas phase“. Thesis, Swansea University, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.638804.
West, Lee Charles. „A study of bibracchial lariat ether complexes and linked cyclodextrin dimer complexes“. Title page, contents and abstract only, 2000. http://web4.library.adelaide.edu.au/theses/09PH/09phw5182.pdf.
Hywel, Meilir. „Laser control of the photoisomerisation of azo-compounds : a theoretical study“. Thesis, Bangor University, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.520068.
Bücher zum Thema "Azo compounds":
R, Cary, Dobson S, Ball Ellen M, World Health Organization, International Program on Chemical Safety. und Inter-Organization Programme for the Sound Management of Chemicals., Hrsg. Azodicarbonamide. Geneva: World Health Organization, 1999.
H, Liu Michael T., Hrsg. Chemistry of diazirines. Boca Raton, Fla: CRC Press, 1987.
Joseph Johannes Gerardus Steven van Es. 1, 3-cycloaddition reactions of diphenylphosphinoyl-activated azomethine ylides and 2-azaallyl anions: Synthetic applications and mechanistic aspects. 'S-Gravenhage: Pasmans Offsetdrukkerij BV, 1992.
Zhao, Yue. Smart light-responsive materials: Azobenzene-containing polymers and liquid crystals. Hoboken, N.J: Wiley, 2009.
Bradshaw, J. S. Aza-crown macrocycles. New York: Wiley, 1993.
Commission, Monopolies and Mergers. Valhi Inc and Akzo NV: A report on the proposed merger. London: HMSO, 1991.
1934-, Neu Harold C., Young Lowell S und Zinner Stephen H. 1939-, Hrsg. The New macrolides, azalides, and streptogramins: Pharmacology and clinical applications. New York: M. Dekker, 1993.
Patai, Saul. Chemistry of the Hydrazo, Azo and Azoxy Groups. Wiley & Sons, Incorporated, John, 2006.
Patai, Saul. Chemistry of the Hydrazo, Azo and Azoxy Groups. Wiley & Sons, Incorporated, John, 2008.
Rappoport, Zvi, und Saul Patai. Chemistry of the Hydrazo, Azo and Azoxy Groups, Volume 2. Wiley & Sons, Incorporated, John, 2000.
Buchteile zum Thema "Azo compounds":
Koeber, Karl, Helga Köttelwesch, Dietrich Schneider, Helga Demmer und Edith Schleitzer-Rust. „Complexes with Azo Compounds“. In Mn Manganese D 5, 278–317. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-08175-4_8.
Davies, A. G. „17.9.4 Radical cations of azo compounds“. In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 425–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_43.
Horowitz, A., und L. A. Rajbenbach. „Radiation chemistry of hydrazo and azo compounds“. In Chemistry of Functional Groups, 313–27. Chichester, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9780470686317.ch10.
Mackenzie, Kenneth. „Formation and fragmentation of cyclic azo compounds“. In Chemistry of Functional Groups, 329–442. Chichester, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9780470686317.ch11.
Bruce, M. I., und B. L. Goodall. „The transition metal chemistry of azo compounds“. In Chemistry of Functional Groups, 259–311. Chichester, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9780470686317.ch9.
Thomas, F. G., und K. G. Boto. „The electrochemistry of azoxy, azo and hydrazo compounds“. In Chemistry of Functional Groups, 443–93. Chichester, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9780470686317.ch12.
Tam, S. W. „Mass spectra of hydrazo, azo and azoxy compounds“. In Chemistry of Functional Groups, 109–27. Chichester, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9780470686317.ch5.
Pardasani, R. T., und P. Pardasani. „Magnetic properties of dinuclear cobalt(II) complex with ONNO donor azo dye“. In Magnetic Properties of Paramagnetic Compounds, 1233. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_727.
Pardasani, R. T., und P. Pardasani. „Magnetic properties of dinuclear cobalt(II) complex with chelating azo dye ligand“. In Magnetic Properties of Paramagnetic Compounds, 1234–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_728.
Pardasani, R. T., und P. Pardasani. „Magnetic properties of dinuclear cobalt(II) complex with chelating azo dye ligand“. In Magnetic Properties of Paramagnetic Compounds, 1236–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_729.
Konferenzberichte zum Thema "Azo compounds":
Simu, Georgeta M., Gianina Bals, Mihaiel ANDONI, Germaine Savoiu-Blaint, Maria Grad und Anca Dragomirescu. „AZO COMPOUNDS WITH ANTIMICROBIAL ACTIVITY“. In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00492.
Czaplicki, Robert, Sylvie Dabos Seignon, Francois Kajzar, Mina Bakasse, Jacek Niziol, Monika Bednarz und Bouchta Sahraoui. „Functionalized Azo-Carbazole Compounds for Nonlinear Optical Application“. In Proceedings of 2006 8th International Conference on Transparent Optical Networks. IEEE, 2006. http://dx.doi.org/10.1109/icton.2006.248336.
Petruskevicius, R., D. Urbonas, M. Gabalis, A. Balcytis, G. Seniutinas, R. Tomasiunas und V. Getautis. „Optical poling of azo-compounds for applications in nanophotonics“. In 2013 15th International Conference on Transparent Optical Networks (ICTON). IEEE, 2013. http://dx.doi.org/10.1109/icton.2013.6602722.
Haddad, Batool S., und Mariam Abdul-bary. „Synthesis of new Azo compounds combining with heterocyclic groups“. In International Conference of Chemistry and Petrochemical Techniques (ICCPT). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0093536.
Tadić, Julijana D., Jelena M. Lađarević, Maja D. Marković, Aleksandra M. Ivanovska, Mirjana M. Kostić und Dušan Ž. Mijin. „A NOVEL AZO-AZOMETHINE DYE: SYNTHESIS, DYEING AND ANTIOXIDANT PROPERTIES“. In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.379t.
Umeda, Minoru. „Electron transfer and geminate pair dissociation processes in layered photoreceptors containing azo compounds“. In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, herausgegeben von Stephen Ducharme und James W. Stasiak. SPIE, 1998. http://dx.doi.org/10.1117/12.328162.
Körtvélyesi, T., M. Görgényi und L. Seres. „Estimation and prediction of the retention indices using quantum-chemical calculations: alkanes and azo compounds“. In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47697.
Jamain, Zuhair, Samerah Habil, Mohamad Zul Hilmey Makmud und Melati Khairuddean. „Synthesis, Structural and Dielectric Characteristics of Liquid Crystalline Azo-Based Compounds with Different Terminal Length“. In 2021 IEEE International Conference on the Properties and Applications of Dielectric Materials (ICPADM). IEEE, 2021. http://dx.doi.org/10.1109/icpadm49635.2021.9493959.
Jing Xiaoping und Wu changcheng. „Synthesis and characterization of dimesogenic liquid crystalline compounds containing cholesteryl and azo-imine linking group“. In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5965822.
Zuben, Theodora Von, Airton Salles Junior und Gabriela de Souza. „A metal-catalyst-free oxidative coupling of anilines to aromatic azo compounds in water using bleach“. In Congresso de Iniciação Científica UNICAMP. Universidade Estadual de Campinas, 2019. http://dx.doi.org/10.20396/revpibic2720192327.
Berichte der Organisationen zum Thema "Azo compounds":
Marinov, Yordan G., und Georgi B. Hadjichristov. Electro-optical Characteristics of Thin Films of Aerosil-7CB Nematic Gel Nanocomposites Doped with Photoresponsive Liquid Crystalline Azo - compounds. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, Oktober 2020. http://dx.doi.org/10.7546/crabs.2020.10.05.
Phillips, Donald A., Yitzhak Spiegel und Howard Ferris. Optimizing nematode management by defining natural chemical bases of behavior. United States Department of Agriculture, November 2006. http://dx.doi.org/10.32747/2006.7587234.bard.
Galili, Gad, Harry J. Klee und Asaph Aharoni. Elucidating the impact of enhanced conversion of primary to secondary metabolism on phenylpropanoids secondary metabolites associated with flavor, aroma and health in tomato fruits. United States Department of Agriculture, Januar 2012. http://dx.doi.org/10.32747/2012.7597920.bard.