Добірка наукової літератури з теми "N-phenyl"
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Статті в журналах з теми "N-phenyl"
Ajibade, Peter A., Benjamin C. Ejelonu, and Bernard Omondi. "N-Ethyl-N-phenyl{[ethyl(phenyl)carbamothioyl]disulfanyl}carbothioamide." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (June 23, 2012): o2182. http://dx.doi.org/10.1107/s1600536812027808.
Повний текст джерелаShen, Heng-Shui, Nan Liu, Zi-Cheng Li, and Wen-Cai Huang. "N-Ethyl-N-phenyl-N′-tosylformamidine." Acta Crystallographica Section E Structure Reports Online 65, no. 7 (June 17, 2009): o1582. http://dx.doi.org/10.1107/s1600536809021953.
Повний текст джерелаFu, T. Y., J. R. Scheffer, and J. Trotter. "N-Phenyl-N-(phenylthioxomethyl)benzamide." Acta Crystallographica Section C Crystal Structure Communications 54, no. 1 (January 15, 1998): 101–2. http://dx.doi.org/10.1107/s0108270197011244.
Повний текст джерелаDou, Shi-qi, B. Thimme Gowda, Helmut Paulus, and Alarich Weiss. "The Bond N-Cl. Crystal Structures and 35Cl NQR of N-Chloro-N-Phenyl-2-chloroacetamide, N-Chloro-N-phenyl-2,2-dichloroacetamide, N-Chloro-N-phenyl-2,2,2-trichloroacetamide, and N-Phenyl-2,2,2-trichloroacetamide." Zeitschrift für Naturforschung A 49, no. 12 (December 1, 1994): 1136–44. http://dx.doi.org/10.1515/zna-1994-1206.
Повний текст джерелаHan, Li-Ping, Bin Li, Jie Liu, and Qing-Chun Liu. "N-Phenyl-N-{4-[5-(2-phenyl-3-pyridyl)-1,3,4-oxadiazol-2-yl]phenyl}aniline." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (November 21, 2007): o4780. http://dx.doi.org/10.1107/s1600536807058382.
Повний текст джерелаYoung Chang, Ji, Tae Ja Kim, Man Jung Han, and Kyu Ho Chae. "Polymerization of N-[4-(azidocarbonyl)phenyl]maleimide and N-[4-(N′-phenoxycarbonylamino)phenyl]maleimide." Polymer 40, no. 14 (June 1999): 4049–54. http://dx.doi.org/10.1016/s0032-3861(98)00600-4.
Повний текст джерелаÖzçelik, Suzan, Muharrem Dinçer, Memet Şekerci, Ayla Balaban, and Ümmühan Özdemir. "N-Phenyl-N′-(2-thienylmethylene)hydrazine." Acta Crystallographica Section E Structure Reports Online 60, no. 9 (August 21, 2004): o1552—o1553. http://dx.doi.org/10.1107/s1600536804019932.
Повний текст джерелаFu, T. Y., J. R. Scheffer, and J. Trotter. "N-Phenyl-N-(phenylthioxomethyl)benzamide. Erratum." Acta Crystallographica Section C Crystal Structure Communications 54, no. 4 (April 15, 1998): 562. http://dx.doi.org/10.1107/s0108270198003357.
Повний текст джерелаMo, Shanyan. "N-Cyano-N-phenyl-p-toluenesulfonamide." Synlett 25, no. 09 (April 11, 2014): 1337–38. http://dx.doi.org/10.1055/s-0033-1341246.
Повний текст джерелаKhan, Islam Ullah, Mehmet Akkurt, Faiza Anwar, and Shahzad Sharif. "N-[4-(N-Cyclohexylsulfamoyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (March 20, 2010): o868—o869. http://dx.doi.org/10.1107/s160053681000961x.
Повний текст джерелаДисертації з теми "N-phenyl"
Zink, Landon. "Synthesis of N-(substituted phenyl) acetamides." Digital Commons @ East Tennessee State University, 2011. https://dc.etsu.edu/honors/131.
Повний текст джерелаChhetri, Manjit Singh. "N-cyclohenyl, N-phenyl nitrones and their potentiality in isoxazolidine and isoxazoline syntheses." Thesis, University of North Bengal, 2010. http://hdl.handle.net/123456789/1364.
Повний текст джерелаKafley, Saurav. "Synthesis and 1, 3 -dipolar cycloaddition reaction of N-phenyl £ chlora nitrone." Thesis, University of North Bengal, 2010. http://hdl.handle.net/123456789/1419.
Повний текст джерелаSharma, Prawin Kumar. "Greener approach to the synthesis of some novel class of isoxazolidine and isoxazoline derivatives using N-methyl and N-phenyl-a-chloro nitrones." Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/1884.
Повний текст джерелаDias, Marylene. "Cytokinines de la famille des n-phenyl-n-pyridylurees : synthèse d'analogues et étude photolytique d'un dérivé azido." Angers, 1994. http://www.theses.fr/1994ANGE0005.
Повний текст джерелаTomlinson, Ian David. "Studies of the mode of action of 2-phenoxy-N-phenyl nicotinamides as herbicides." Thesis, University of Essex, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328368.
Повний текст джерелаRoleder, Carly. "Synthesis and Characterization of a Novel Platinum Ligand Complex ((κ-N,C,N- 2,6-bis(diethylaminomethyl)phenyl)(4- tert-butylphenyl) platinum(II))". Scholarship @ Claremont, 2018. http://scholarship.claremont.edu/cmc_theses/1732.
Повний текст джерелаLAGE, NADIA. "Formation regioselective de liaisons carbone-carbone et synthese de cetenimines a partir de n-phenyl imidothioesters." Caen, 1992. http://www.theses.fr/1992CAEN2049.
Повний текст джерелаLi, Yi. "Studies Related to the Alternating Copolymerization of Substituted Stilbenes." Thesis, Virginia Tech, 2009. http://hdl.handle.net/10919/33235.
Повний текст джерелаA novel series of methyl substituted stilbenes were synthesized and copolymerized with maleic anhydride. A conversion-time study was undertaken to understand the methyl substituent effect on copolymerization rates. Methyl substituted stilbene-maleic anhydride copolymer compositions were determined by quantitative 13C 1D NMR. SEC measurements showed the weight average molecular weights of these copolymers vary from 3 000 to over 1 000 000 g/mol. No glass transition temperature or crystalline melting temperature was observed between 0 oC and 250 oC by DSC. TGA showed that these polymers have 5% weight loss around 290 oC.
Precursors to a polycation and a polyanion based on functionalized stilbenes and maleimides have been prepared: poly(di-t-butyl-(E)-4,4â -stilbenedicarboxylate-co- N-(4-(t-butoxycarbonyl)phenyl)maleimide) and poly(N,N,Nâ ,Nâ -tetraalkyl-4,4â -di- aminostilbenes-co-N-4-(Nâ ,Nâ -dimethylaminophenyl)-maleimide). These copolymer precursors were characterized by 1H NMR, SEC, TGA, and DSC. The 1H NMR spectrum indicated the rigidity of copolymer backbones. SEC measurements showed the weight average molecular weights of these copolymers vary from 5 000 to 11 700 g/mol. No glass transition temperature or crystalline melting temperature was observed between 0 oC and 175 oC by DSC for poly(di-t-butyl-(E)-4,4â -stilbenedicarboxylate-co-N-(4-(t-butoxy- carbonyl)phenyl)maleimide). TGA showed that this polymer has 5% weight loss around 210 oC and 26% weight loss on the first stage of decomposition which corresponds to elimination of t-butyl functional group in the copolymer.
The homopolymerization of EMS-III via free radical polymerization, anionic polymerization and cationic polymerization was attempted. However, no polymer was obtained from any of these polymerization methods. In anionic polymerization, the solution changed to red upon the addition of the initiator sec-bu-Li, indicating the successful addition of the sec-bu-Li to EMS-III. However, the initiated monomer did not propagate to form homopolymer.
Master of Science
FROMONT, CHRISTOPHE. "Etude de la reactivite de n-phenyl cetenimines silylees vis-a-vis de reactifs nucleophiles et electrophiles." Caen, 1997. http://www.theses.fr/1997CAEN2075.
Повний текст джерелаКниги з теми "N-phenyl"
Bhatti, Akmal Riaz. Synthesis and investigation of analogues of N-methyl-4- phenyl-1, 2, 3, 6-tetrahydropyridine, (MPTP), a specific dopaminergic neurotoxin. Birmingham: University of Birmingham, 1988.
Знайти повний текст джерелаN-phenyl-1-naphthylamine. Stuttgart: S. Hirzel, 1994.
Знайти повний текст джерелаN-phenyl-1-napthylamine (Concise International Chemical Assessment Documents). World Health Organization, 1998.
Знайти повний текст джерелаAl-Easa, Hala. The synthesis and characterization of N-(2-mercapto-phenyl) salicylaldimine and its complexes: A thesis in chemistry. 1985.
Знайти повний текст джерелаЧастини книг з теми "N-phenyl"
Bährle-Rapp, Marina. "N-Phenyl-p-Phenylenediamine." In Springer Lexikon Kosmetik und Körperpflege, 380. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_7021.
Повний текст джерелаBährle-Rapp, Marina. "N-Phenyl-p-Phenylenediamine HCl." In Springer Lexikon Kosmetik und Körperpflege, 380. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_7022.
Повний текст джерелаBährle-Rapp, Marina. "N-Phenyl-p-Phenylenediamine Sulfate." In Springer Lexikon Kosmetik und Körperpflege, 380. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_7023.
Повний текст джерелаJeschke, Peter. "N-Benzoyl-N′-Phenyl Ureas as Insecticides, Acaricides, and Termiticides." In Bioactive Carboxylic Compound Classes: Pharmaceuticals and Agrochemicals, 439–52. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527693931.ch33.
Повний текст джерелаWinkelmann, Jochen. "Diffusion coefficient of N-phenyl-acetamide in water." In Diffusion in Gases, Liquids and Electrolytes, 841. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_618.
Повний текст джерелаWohlfarth, Ch. "Partial specific volume of cellulose N-phenyl carbamate." In Polymer Solutions, 330. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_153.
Повний текст джерелаHolze, Rudolf. "Ionic conductivities of N,n,n,-trioctyl-n-methylammonium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate." In Electrochemistry, 1045. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_947.
Повний текст джерелаWohlfarth, Ch. "Second virial coefficient of amylose tris(N-phenyl carbamate)." In Polymer Solutions, 548. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_319.
Повний текст джерелаWohlfarth, Ch. "Second virial coefficient of cellulose tris(N-phenyl carbamate)." In Polymer Solutions, 555. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_326.
Повний текст джерелаWohlfarth, Ch. "pVT data of cellulose tris(N-phenyl carbamate) in cyclohexanol." In Polymer Solutions, 23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_22.
Повний текст джерелаТези доповідей конференцій з теми "N-phenyl"
Sen, Ibrahim, and Akın Azizoglu. "Computational Study on the Structure of N-(2-Amino-benzoyl)-N'-phenyl hydrazine." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e003.
Повний текст джерелаLi, Mei, Yi Gou, and Hong Liang. "Cytotoxicity of a bis (N-phenyl-salicydenaminato) copper(II) complex." In International Conference on Medical Engineering and Bioinformatics. Southampton, UK: WIT Press, 2014. http://dx.doi.org/10.2495/meb140511.
Повний текст джерелаSugiyama, T., T. Shigemoto, H. Komatsu, and T. Ukachi. "Crystal growth and characterization of N-(2,4-dinitrophenyl)-1-chloro-3-phenyl-2-propanamine: a new organic material for nonlinear optics." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/oam.1991.fq6.
Повний текст джерелаStojković, Danijela, Maja Đukić, Marija Ristić, Marina Ćendić Serafinović, Svetlana Belošević, Emina Mrkalić, and Ivan Jakovljević. "Synthesis, characterization and HSA interactions of a new piano-stool ruthenium(II) complex containing a thioamide-type ligand." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.507s.
Повний текст джерелаMou, Y. L., W. Xia, Z. Wang, and D. Zheng. "Synthesis and Characterization of Styrene, Maleic Anhydride and N-phenyl Maleimide Tripolymer." In 2nd Annual International Conference on Advanced Material Engineering (AME 2016). Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/ame-16.2016.180.
Повний текст джерелаXu, F., X. D. Zhang, X. R. Dong, and G. Liu. "Synthesis and Photochromic Properties of Unsymmetry Diarylethene1-[2-methyl-5- (4-n-amyl-phenyl)-3-thienyl]-2-[2-methyl-1-phenyl] Perfluorocyclopentene." In International Conference on Materials Chemistry and Environmental Protection 2015. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/meep-15.2016.20.
Повний текст джерелаChu, Cilong, Zixuan Rao, Pengwu Zheng, and Shan Xu. "Synthesis of 4-methyl-2-phenyl-N-(pyridin-2-yl) thiazole-5-carboxamide." In 3RD INTERNATIONAL CONFERENCE ON FRONTIERS OF BIOLOGICAL SCIENCES AND ENGINEERING (FBSE 2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0048959.
Повний текст джерелаLobankova, Anastasia A., Vyacheslav S. Grinev, and Alevtina Yu Yegorova. "Conformational Study of n,n’-(Alkane-1,n-diyl)bis(2-phenyl-3,5-dihydro-4H-imidazol-4-one)s with Different Spacer Length †." In ECSOC 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16053.
Повний текст джерелаOuYang, Yiqiang, Chen Chen, Ping Wang, Chao Sun, WuFu Zhu, and Shan Xu. "Synthesis of N-4-(4-chloro-3-trifluoromethyl-phenyl)-7-methoxy-quinazoline-4,6-diamine." In 2015 2nd International Conference on Machinery, Materials Engineering, Chemical Engineering and Biotechnology. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/mmeceb-15.2016.158.
Повний текст джерелаYanagisawa, M., M. Kunimoto, and T. Homma. "Chemical Analysis of Ultra-Thin DLC Films and Lubricant/DLC Interface Using Plasmonic Sensors." In ASME 2014 Conference on Information Storage and Processing Systems. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/isps2014-6908.
Повний текст джерелаЗвіти організацій з теми "N-phenyl"
Chen, Kitmin, Joel Kress, Dali Yang, Alexander Edgar, Oana Marina, Zhenghua Li та Jack Brett. Role of n-phenyl-β-naphthylamine in the Acid-Nitroplasticizer Thermal Aging (ANTA) Experiment. Office of Scientific and Technical Information (OSTI), листопад 2023. http://dx.doi.org/10.2172/2205031.
Повний текст джерелаNaim, Michael, Gary R. Takeoka, Haim D. Rabinowitch, and Ron G. Buttery. Identification of Impact Aroma Compounds in Tomato: Implications to New Hybrids with Improved Acceptance through Sensory, Chemical, Breeding and Agrotechnical Techniques. United States Department of Agriculture, October 2002. http://dx.doi.org/10.32747/2002.7585204.bard.
Повний текст джерела