Artigos de revistas sobre o tema "Azo compounds"
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Beck, Karin, Harald Burghard, Gabriele Fischer, Siegfried Hünig e Petra Reinold. "Azo Cope Rearrangements of Nonstabilized Azo Compounds". Angewandte Chemie International Edition in English 26, n.º 7 (julho de 1987): 672–73. http://dx.doi.org/10.1002/anie.198706721.
Jamain, Zuhair, Melati Khairuddean e 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, n.º 12 (16 de junho de 2020): 4267. http://dx.doi.org/10.3390/ijms21124267.
Matsui, Masaki, Shigeo Kawamura, Katusoyoshi Shibata, Hiroshige Muramatsu, Motohiro Mitani, Hideo Sawada e Masaharu Nakayama. "Perfluoroalkylation of azo compounds". Journal of Fluorine Chemistry 57, n.º 1-3 (abril de 1992): 209–17. http://dx.doi.org/10.1016/s0022-1139(00)82833-x.
Hamidian, Kourosh, Mohsen Irandoust, Ezzat Rafiee e Mohammad Joshaghani. "Synthesis, Characterization, and Tautomeric Properties of Some Azo-azomethine Compounds". Zeitschrift für Naturforschung B 67, n.º 2 (1 de fevereiro de 2012): 159–64. http://dx.doi.org/10.1515/znb-2012-0208.
Kempa, S., L. Wallach e K. Rueck-Braun. "ChemInform Abstract: Aliphatic Azo Compounds". ChemInform 43, n.º 36 (9 de agosto de 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 (4 de junho de 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, n.º 9 (9 de fevereiro de 2018): 2004–9. http://dx.doi.org/10.1073/pnas.1717892115.
Al-Mudhafar, May M. Jawad, Rana A. Kamoon e 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, n.º 01 (25 de março de 2020): 150–55. http://dx.doi.org/10.25258/ijddt.10.1.26.
Jabar, Maha A., e 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, n.º 2 (15 de maio de 2022): 1–4. http://dx.doi.org/10.21931/rb/2022.07.02.17.
Ali, Yousaf, Shafida Abd Hamid e Umer Rashid. "Biomedical Applications of Aromatic Azo Compounds". Mini-Reviews in Medicinal Chemistry 18, n.º 18 (12 de outubro de 2018): 1548–58. http://dx.doi.org/10.2174/1389557518666180524113111.
Klismeta, K., J. Teteris e J. Aleksejeva. "Photoinduced mass transport in azo compounds". IOP Conference Series: Materials Science and Engineering 49 (13 de dezembro de 2013): 012036. http://dx.doi.org/10.1088/1757-899x/49/1/012036.
Ungureanu, Eleonora-Mihaela, Alexandru C. Razus, Liviu Birzan, Mariana-Stefania Cretu e George-Octavian Buica. "Electrochemical study of azo–azulene compounds". Electrochimica Acta 53, n.º 24 (outubro de 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 e M. NAKAYAMA. "ChemInform Abstract: Perfluoroalkylation of Azo Compounds." ChemInform 24, n.º 28 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199328132.
Cheon, Kap-Soo, Peter M. Kazmaier, Sam-Rok Keum, Kuk-Tae Park e Erwin Buncel. "Azo-functionalized dendrimers". Canadian Journal of Chemistry 82, n.º 4 (1 de abril de 2004): 551–66. http://dx.doi.org/10.1139/v04-009.
Sarah Mohammed Abed e Hasan Thamer Ghanem. "Synthesis and characterization Some of heterocyclic compounds from Nitrogen derivative". International Journal of Research in Pharmaceutical Sciences 10, n.º 4 (16 de outubro de 2019): 3186–96. http://dx.doi.org/10.26452/ijrps.v10i4.1621.
Azeez, Hadi, Ahmed Al-kadhimi e Nashwan Tapabashi. "Synthesis, Characterization and Biological Evaluation of Some Azo and Azo-Schiff Compounds". Kirkuk University Journal-Scientific Studies 14, n.º 1 (28 de março de 2019): 97–119. http://dx.doi.org/10.32894/kujss.2019.14.1.8.
Purwono, Bambang, e Catur Mahardiani. "SYNTHESIS OF AZO COMPOUNDS DERIVATIVE FROM EUGENOL AND ITS APPLICATION AS A TITRATION INDICATOR". Indonesian Journal of Chemistry 9, n.º 1 (20 de junho de 2010): 95–98. http://dx.doi.org/10.22146/ijc.21568.
Mirkovic, Jelena, Gordana Uscumlic, Aleksandar Marinkovic e Dusan Mijin. "Azo-hydrazone tautomerism of aryl azo pyridone dyes". Chemical Industry 67, n.º 1 (2013): 1–15. http://dx.doi.org/10.2298/hemind120309053m.
Sridhara, M. B., G. R. Srinivasa e D. Channe Gowda. "Ammonium chloride mediated reduction of azo compounds to hydrazo compounds". Journal of Chemical Research 2004, n.º 1 (1 de janeiro de 2004): 74–75. http://dx.doi.org/10.3184/030823404323000873.
Ali, Wisam Hassan, Buthyna Abd el-hassan Naser e Intisar Obaid Alfatlawi. "Coupling Compounds Behavior on Types of Fungi". American International Journal of Sciences and Engineering Research 2, n.º 1 (25 de janeiro de 2019): 22–36. http://dx.doi.org/10.46545/aijser.v2i1.51.
Lan, Li Hong, Jian Hua Chen, Ping Lan, Mei Lian Liang e Ye Chen. "Depression Performance of Azo Dyes to Sulfide Minerals". Advanced Materials Research 287-290 (julho de 2011): 3074–80. http://dx.doi.org/10.4028/www.scientific.net/amr.287-290.3074.
KITAMURA, Akihide, Nobukazu MIYAGAWA e Takashi KARATSU. "Photoinduced Electron-transfer Reaction of Azo Compounds." Journal of Synthetic Organic Chemistry, Japan 55, n.º 8 (1997): 678–85. http://dx.doi.org/10.5059/yukigoseikyokaishi.55.678.
Büyükgüngör, O., Ç. Albayrak e M. Odabasoglu. "Spectroscopic investigation of some azo-azomethine compounds". Acta Crystallographica Section A Foundations of Crystallography 61, a1 (23 de agosto de 2005): c315. http://dx.doi.org/10.1107/s0108767305086605.
Du, Ke-Si, e Jing-Mei Huang. "Electrochemical dehydrogenation of hydrazines to azo compounds". Green Chemistry 21, n.º 7 (2019): 1680–85. http://dx.doi.org/10.1039/c9gc00515c.
Matsui, Masaki, Yoshiyuki Iwata, Toshio Kato e Katsuyoshi Shibata. "Reaction of aromatic azo compounds with ozone". Dyes and Pigments 9, n.º 2 (janeiro de 1988): 109–17. http://dx.doi.org/10.1016/0143-7208(88)80010-x.
Wagner-Wysiecka, Ewa, Natalia Łukasik, Jan F. Biernat e Elżbieta Luboch. "Azo group(s) in selected macrocyclic compounds". Journal of Inclusion Phenomena and Macrocyclic Chemistry 90, n.º 3-4 (8 de janeiro de 2018): 189–257. http://dx.doi.org/10.1007/s10847-017-0779-4.
Orshulyak, O. O., e G. D. Levitskaya. "Voltammetric determination of zirconium using azo compounds". Journal of Analytical Chemistry 63, n.º 3 (março de 2008): 271–74. http://dx.doi.org/10.1134/s1061934808030143.
Roldo, Marta, Eugen Barbu, James F. Brown, David W. Laight, John D. Smart e John Tsibouklis. "Azo compounds in colon-specific drug delivery". Expert Opinion on Drug Delivery 4, n.º 5 (setembro de 2007): 547–60. http://dx.doi.org/10.1517/17425247.4.5.547.
Rowe, F. M., e W. G. Dangerfield. "Decomposition of Azo Compounds by Mineral Acida". Journal of the Society of Dyers and Colourists 52, n.º 2 (22 de outubro de 2008): 48–57. http://dx.doi.org/10.1111/j.1478-4408.1936.tb01908.x.
McGowan, J. C., e T. Powell. "Rates of decompositions of certain AZO compounds". Recueil des Travaux Chimiques des Pays-Bas 81, n.º 12 (2 de setembro de 2010): 1061–67. http://dx.doi.org/10.1002/recl.19620811208.
Bickel, A. F., e W. A. Waters. "The decomposition of aliphatic azo-compounds. I". Recueil des Travaux Chimiques des Pays-Bas 69, n.º 3 (2 de setembro de 2010): 312–20. http://dx.doi.org/10.1002/recl.19500690310.
Bickel, A. F., e W. A. Waters. "The decomposition of aliphatic azo-compounds: II". Recueil des Travaux Chimiques des Pays-Bas 69, n.º 12 (2 de setembro de 2010): 1490–94. http://dx.doi.org/10.1002/recl.19500691204.
Pricelius, S., C. Held, M. Murkovic, M. Bozic, V. Kokol, A. Cavaco-Paulo e G. M. Guebitz. "Enzymatic reduction of azo and indigoid compounds". Applied Microbiology and Biotechnology 77, n.º 2 (22 de setembro de 2007): 321–27. http://dx.doi.org/10.1007/s00253-007-1165-8.
Velasco, Manuel I., Claudio O. Kinen, Rita Hoyos de Rossi e Laura I. Rossi. "A green alternative to synthetize azo compounds". Dyes and Pigments 90, n.º 3 (setembro de 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, n.º 1 (outubro de 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 e 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, n.º 3 (25 de junho de 2021): 401–6. http://dx.doi.org/10.18006/2021.9(3).401.406.
Pakeeraiah, K., Sujit Kumar Mohanty, K. Eswar e K. Raju. "Azo benzimidazole - A biologically active scaffold". International Journal of PharmTech Research 13, n.º 3 (2020): 159–71. http://dx.doi.org/10.20902/ijptr.2019.130305.
Akwi, Faith M., e 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 (6 de setembro de 2016): 1987–2004. http://dx.doi.org/10.3762/bjoc.12.186.
H�nig, Siegfried, e Michael Schmitt. "Azo bridges from azines. XV. Oxygenation of Unsaturated Cyclic Azo Compounds with peracids". Journal f�r Praktische Chemie/Chemiker-Zeitung 338, n.º 1 (1996): 74–82. http://dx.doi.org/10.1002/prac.19963380113.
Liakou, S., M. Kornaros e G. Lyberatos. "Pretreatment of azo dyes using ozone". Water Science and Technology 36, n.º 2-3 (1 de julho de 1997): 155–63. http://dx.doi.org/10.2166/wst.1997.0508.
Navirra Ayu Khudzaifah e Maria Monica Sianita Basukiwardojo. "Determination of the optimum concentration of the coupling agent in chloramphenicol analysis". World Journal of Advanced Research and Reviews 15, n.º 1 (30 de julho de 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, n.º 4(Suppl.) (18 de dezembro de 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 e R. Yahya. "Synthesis, Crystal Structure, Mesophase Behaviour and Optical Property of Azo-ester Bridged Compounds". Journal of Scientific Research 11, n.º 3 (1 de setembro de 2019): 383–95. http://dx.doi.org/10.3329/jsr.v11i3.41578.
Burcă, Ion, Valentin Badea, Calin Deleanu e Vasile-Nicolae Bercean. "5-((8-Hydroxyquinolin-5-yl)diazenyl)-3-methyl-1H-pyrazole-4-carboxylic Acid". Molbank 2021, n.º 2 (16 de junho de 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, n.º 01 (10 de fevereiro de 2022): 355–64. http://dx.doi.org/10.55218/jasr.202213142.
Akram, Dana, Ismail A. Elhaty e Shaikha S. AlNeyadi. "Synthesis and Antibacterial Activity of Rhodanine-Based Azo Dyes and Their Use as Spectrophotometric Chemosensor for Fe3+ Ions". Chemosensors 8, n.º 1 (25 de fevereiro de 2020): 16. http://dx.doi.org/10.3390/chemosensors8010016.
Srinivasa, G. R., K. Abiraj e D. Channe Gowda. "Facile Synthesis of Azo Compounds from Aromatic Nitro Compounds using Magnesium and Triethylammonium Formate". Australian Journal of Chemistry 57, n.º 6 (2004): 609. http://dx.doi.org/10.1071/ch03143.
Almashal, Faeza, Abeer Mohamed Jabar e Adil Muala Dhumad. "Synthesis, characterization and DFT computational studies of new heterocyclic azo compounds". European Journal of Chemistry 9, n.º 2 (30 de junho de 2018): 84–88. http://dx.doi.org/10.5155/eurjchem.9.2.84-88.1683.
Jawad, Shatha Abd Alameer, e 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, n.º 1 (4 de fevereiro de 2022): 62–70. http://dx.doi.org/10.14704/nq.2022.20.1.nq22009.
Hiba Ibrahim Abdulla AL-Joubory e 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, n.º 103 (23 de junho de 2019): 68–89. http://dx.doi.org/10.35950/cbej.v25i103.4547.