Zeitschriftenartikel zum Thema „Azo compounds“
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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.
Klismeta, K., J. Teteris und J. Aleksejeva. „Photoinduced mass transport in azo compounds“. IOP Conference Series: Materials Science and Engineering 49 (13.12.2013): 012036. http://dx.doi.org/10.1088/1757-899x/49/1/012036.
Ungureanu, Eleonora-Mihaela, Alexandru C. Razus, Liviu Birzan, Mariana-Stefania Cretu und George-Octavian Buica. „Electrochemical study of azo–azulene compounds“. Electrochimica Acta 53, Nr. 24 (Oktober 2008): 7089–99. http://dx.doi.org/10.1016/j.electacta.2008.04.087.
MATSUI, M., S. KAWAMURA, K. SHIBATA, H. MURAMATSU, M. MITANI, H. SAWADA und M. NAKAYAMA. „ChemInform Abstract: Perfluoroalkylation of Azo Compounds.“ ChemInform 24, Nr. 28 (20.08.2010): no. http://dx.doi.org/10.1002/chin.199328132.
Cheon, Kap-Soo, Peter M. Kazmaier, Sam-Rok Keum, Kuk-Tae Park und Erwin Buncel. „Azo-functionalized dendrimers“. Canadian Journal of Chemistry 82, Nr. 4 (01.04.2004): 551–66. http://dx.doi.org/10.1139/v04-009.
Sarah Mohammed Abed und Hasan Thamer Ghanem. „Synthesis and characterization Some of heterocyclic compounds from Nitrogen derivative“. International Journal of Research in Pharmaceutical Sciences 10, Nr. 4 (16.10.2019): 3186–96. http://dx.doi.org/10.26452/ijrps.v10i4.1621.
Azeez, Hadi, Ahmed Al-kadhimi und Nashwan Tapabashi. „Synthesis, Characterization and Biological Evaluation of Some Azo and Azo-Schiff Compounds“. Kirkuk University Journal-Scientific Studies 14, Nr. 1 (28.03.2019): 97–119. http://dx.doi.org/10.32894/kujss.2019.14.1.8.
Purwono, Bambang, und Catur Mahardiani. „SYNTHESIS OF AZO COMPOUNDS DERIVATIVE FROM EUGENOL AND ITS APPLICATION AS A TITRATION INDICATOR“. Indonesian Journal of Chemistry 9, Nr. 1 (20.06.2010): 95–98. http://dx.doi.org/10.22146/ijc.21568.
Mirkovic, Jelena, Gordana Uscumlic, Aleksandar Marinkovic und Dusan Mijin. „Azo-hydrazone tautomerism of aryl azo pyridone dyes“. Chemical Industry 67, Nr. 1 (2013): 1–15. http://dx.doi.org/10.2298/hemind120309053m.
Sridhara, M. B., G. R. Srinivasa und D. Channe Gowda. „Ammonium chloride mediated reduction of azo compounds to hydrazo compounds“. Journal of Chemical Research 2004, Nr. 1 (01.01.2004): 74–75. http://dx.doi.org/10.3184/030823404323000873.
Ali, Wisam Hassan, Buthyna Abd el-hassan Naser und Intisar Obaid Alfatlawi. „Coupling Compounds Behavior on Types of Fungi“. American International Journal of Sciences and Engineering Research 2, Nr. 1 (25.01.2019): 22–36. http://dx.doi.org/10.46545/aijser.v2i1.51.
Lan, Li Hong, Jian Hua Chen, Ping Lan, Mei Lian Liang und Ye Chen. „Depression Performance of Azo Dyes to Sulfide Minerals“. Advanced Materials Research 287-290 (Juli 2011): 3074–80. http://dx.doi.org/10.4028/www.scientific.net/amr.287-290.3074.
KITAMURA, Akihide, Nobukazu MIYAGAWA und Takashi KARATSU. „Photoinduced Electron-transfer Reaction of Azo Compounds.“ Journal of Synthetic Organic Chemistry, Japan 55, Nr. 8 (1997): 678–85. http://dx.doi.org/10.5059/yukigoseikyokaishi.55.678.
Büyükgüngör, O., Ç. Albayrak und M. Odabasoglu. „Spectroscopic investigation of some azo-azomethine compounds“. Acta Crystallographica Section A Foundations of Crystallography 61, a1 (23.08.2005): c315. http://dx.doi.org/10.1107/s0108767305086605.
Du, Ke-Si, und Jing-Mei Huang. „Electrochemical dehydrogenation of hydrazines to azo compounds“. Green Chemistry 21, Nr. 7 (2019): 1680–85. http://dx.doi.org/10.1039/c9gc00515c.
Matsui, Masaki, Yoshiyuki Iwata, Toshio Kato und Katsuyoshi Shibata. „Reaction of aromatic azo compounds with ozone“. Dyes and Pigments 9, Nr. 2 (Januar 1988): 109–17. http://dx.doi.org/10.1016/0143-7208(88)80010-x.
Wagner-Wysiecka, Ewa, Natalia Łukasik, Jan F. Biernat und Elżbieta Luboch. „Azo group(s) in selected macrocyclic compounds“. Journal of Inclusion Phenomena and Macrocyclic Chemistry 90, Nr. 3-4 (08.01.2018): 189–257. http://dx.doi.org/10.1007/s10847-017-0779-4.
Orshulyak, O. O., und G. D. Levitskaya. „Voltammetric determination of zirconium using azo compounds“. Journal of Analytical Chemistry 63, Nr. 3 (März 2008): 271–74. http://dx.doi.org/10.1134/s1061934808030143.
Roldo, Marta, Eugen Barbu, James F. Brown, David W. Laight, John D. Smart und John Tsibouklis. „Azo compounds in colon-specific drug delivery“. Expert Opinion on Drug Delivery 4, Nr. 5 (September 2007): 547–60. http://dx.doi.org/10.1517/17425247.4.5.547.
Rowe, F. M., und W. G. Dangerfield. „Decomposition of Azo Compounds by Mineral Acida“. Journal of the Society of Dyers and Colourists 52, Nr. 2 (22.10.2008): 48–57. http://dx.doi.org/10.1111/j.1478-4408.1936.tb01908.x.
McGowan, J. C., und T. Powell. „Rates of decompositions of certain AZO compounds“. Recueil des Travaux Chimiques des Pays-Bas 81, Nr. 12 (02.09.2010): 1061–67. http://dx.doi.org/10.1002/recl.19620811208.
Bickel, A. F., und W. A. Waters. „The decomposition of aliphatic azo-compounds. I“. Recueil des Travaux Chimiques des Pays-Bas 69, Nr. 3 (02.09.2010): 312–20. http://dx.doi.org/10.1002/recl.19500690310.
Bickel, A. F., und W. A. Waters. „The decomposition of aliphatic azo-compounds: II“. Recueil des Travaux Chimiques des Pays-Bas 69, Nr. 12 (02.09.2010): 1490–94. http://dx.doi.org/10.1002/recl.19500691204.
Pricelius, S., C. Held, M. Murkovic, M. Bozic, V. Kokol, A. Cavaco-Paulo und G. M. Guebitz. „Enzymatic reduction of azo and indigoid compounds“. Applied Microbiology and Biotechnology 77, Nr. 2 (22.09.2007): 321–27. http://dx.doi.org/10.1007/s00253-007-1165-8.
Velasco, Manuel I., Claudio O. Kinen, Rita Hoyos de Rossi und Laura I. Rossi. „A green alternative to synthetize azo compounds“. Dyes and Pigments 90, Nr. 3 (September 2011): 259–64. http://dx.doi.org/10.1016/j.dyepig.2010.12.009.
Bevington, John C. „Initiation of polymerization: Azo compounds and peroxides“. Makromolekulare Chemie. Macromolecular Symposia 10-11, Nr. 1 (Oktober 1987): 89–107. http://dx.doi.org/10.1002/masy.19870100106.
Yousif Al-labban, Hutham mahmood, Adil ibadi Al-luhaiby, Nuha salman salih, Widad ibrahem Yahya und Ahmed Abdul jabbar Jaloob Aljanaby. „STUDY OF AZO COMPOUNDS DERIVED FROM P-CRESOL LIGAND: SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL ACTIVITY“. Journal of Experimental Biology and Agricultural Sciences 9, Nr. 3 (25.06.2021): 401–6. http://dx.doi.org/10.18006/2021.9(3).401.406.
Pakeeraiah, K., Sujit Kumar Mohanty, K. Eswar und K. Raju. „Azo benzimidazole - A biologically active scaffold“. International Journal of PharmTech Research 13, Nr. 3 (2020): 159–71. http://dx.doi.org/10.20902/ijptr.2019.130305.
Akwi, Faith M., und Paul Watts. „The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors“. Beilstein Journal of Organic Chemistry 12 (06.09.2016): 1987–2004. http://dx.doi.org/10.3762/bjoc.12.186.
H�nig, Siegfried, und Michael Schmitt. „Azo bridges from azines. XV. Oxygenation of Unsaturated Cyclic Azo Compounds with peracids“. Journal f�r Praktische Chemie/Chemiker-Zeitung 338, Nr. 1 (1996): 74–82. http://dx.doi.org/10.1002/prac.19963380113.
Liakou, S., M. Kornaros und G. Lyberatos. „Pretreatment of azo dyes using ozone“. Water Science and Technology 36, Nr. 2-3 (01.07.1997): 155–63. http://dx.doi.org/10.2166/wst.1997.0508.
Navirra Ayu Khudzaifah und Maria Monica Sianita Basukiwardojo. „Determination of the optimum concentration of the coupling agent in chloramphenicol analysis“. World Journal of Advanced Research and Reviews 15, Nr. 1 (30.07.2022): 525–33. http://dx.doi.org/10.30574/wjarr.2022.15.1.0719.
Et al., Khammas. „Synthesis, Cytotoxicity, Xanthine Oxidase Inhibition, Antioxidant of New Pyrazolo{3,4 d}Pyrimidine Derivatives“. Baghdad Science Journal 16, Nr. 4(Suppl.) (18.12.2019): 1003. http://dx.doi.org/10.21123/bsj.2019.16.4(suppl.).1003.
Karim, M. R., M. R. K. Sheikh, M. S. Islam, N. M. Salleh und R. Yahya. „Synthesis, Crystal Structure, Mesophase Behaviour and Optical Property of Azo-ester Bridged Compounds“. Journal of Scientific Research 11, Nr. 3 (01.09.2019): 383–95. http://dx.doi.org/10.3329/jsr.v11i3.41578.
Burcă, Ion, Valentin Badea, Calin Deleanu und Vasile-Nicolae Bercean. „5-((8-Hydroxyquinolin-5-yl)diazenyl)-3-methyl-1H-pyrazole-4-carboxylic Acid“. Molbank 2021, Nr. 2 (16.06.2021): M1238. http://dx.doi.org/10.3390/m1238.
Koshti, Shivaji. „SYNTHESIS, CHARACTERIZATION AND IN-VITRO RELEASE STUDY OF MUTUAL PRODRUGS OF MESALAMINE AND SULPHONAMIDES AS AZO COMPOUNDS“. Journal of Advanced Scientific Research 13, Nr. 01 (10.02.2022): 355–64. http://dx.doi.org/10.55218/jasr.202213142.
Akram, Dana, Ismail A. Elhaty und Shaikha S. AlNeyadi. „Synthesis and Antibacterial Activity of Rhodanine-Based Azo Dyes and Their Use as Spectrophotometric Chemosensor for Fe3+ Ions“. Chemosensors 8, Nr. 1 (25.02.2020): 16. http://dx.doi.org/10.3390/chemosensors8010016.
Srinivasa, G. R., K. Abiraj und D. Channe Gowda. „Facile Synthesis of Azo Compounds from Aromatic Nitro Compounds using Magnesium and Triethylammonium Formate“. Australian Journal of Chemistry 57, Nr. 6 (2004): 609. http://dx.doi.org/10.1071/ch03143.
Almashal, Faeza, Abeer Mohamed Jabar und Adil Muala Dhumad. „Synthesis, characterization and DFT computational studies of new heterocyclic azo compounds“. European Journal of Chemistry 9, Nr. 2 (30.06.2018): 84–88. http://dx.doi.org/10.5155/eurjchem.9.2.84-88.1683.
Jawad, Shatha Abd Alameer, und Ibtihal Kadhim Kareem. „Synthesis, Characterization of New Azo-Schiff Ligand Type N2O2 and Metal Complexes with Di Valance Nickel, Palladium and Tetra Valance Platinum“. NeuroQuantology 20, Nr. 1 (04.02.2022): 62–70. http://dx.doi.org/10.14704/nq.2022.20.1.nq22009.
Hiba Ibrahim Abdulla AL-Joubory und Khalid Mohamad Motny Al-janaby. „Synthesis, Characterization and Biological Activity Study of New Compounds Tetrazole Derivatives Azo-Schiff Base“. journal of the college of basic education 25, Nr. 103 (23.06.2019): 68–89. http://dx.doi.org/10.35950/cbej.v25i103.4547.