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Relevant bibliographies by topics / 4-diamine

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Academic literature on the topic '4-diamine'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "4-diamine"

1

Farag, Abeer Mohamed, Teoh Siang Guan, Hasnah Osman, Mohd Mustaqim Rosli, and Hoong-Kun Fun. "N2-(4-Chlorobenzylidene)-4-nitrobenzene-1,2-diamine." Acta Crystallographica Section E Structure Reports Online 66, no. 9 (2010): o2220. http://dx.doi.org/10.1107/s1600536810030461.

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Astles, Peter C., Neil V. Harris, and Andrew D. Morley. "Diamine containing VLA-4 antagonists." Bioorganic & Medicinal Chemistry 9, no. 8 (2001): 2195–202. http://dx.doi.org/10.1016/s0968-0896(01)00132-8.

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Hawthorne, D. G., J. H. Hodgkin, M. B. Jackson, J. W. Loder, and T. C. Morton. "Preparation and characterization of some new diaminobisimides." High Performance Polymers 6, no. 4 (1994): 287–301. http://dx.doi.org/10.1088/0954-0083/6/4/001.

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A series of stable diaminobisimides (DABIs) has been prepared as alternatives to simple aromatic diamines for use in the preparation of condensation polymers. These DABIs were prepared by reacting two moles of an aromatic diamine with one mole of a dianhydride under conditions that minimize side reactions and the formation of oligomers. In many cases, the pure DABI consisting of two moles of the diamine and one mole of the dianhydride (i.e. the 2:1 product) can be obtained free of oligomers (i.e. the 3:2, 4:3 etc products). The studies have shown that the major factor determining the yield and

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4

Trilleras, Jorge, Jairo Quiroga, Justo Cobo, et al. "Anhydrous versus hydrated N 4-substituted 1H-pyrazolo[3,4-d]pyrimidine-4,6-diamines: hydrogen bonding in two and three dimensions." Acta Crystallographica Section B Structural Science 64, no. 5 (2008): 610–22. http://dx.doi.org/10.1107/s0108768108019903.

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Ten new N 4-substituted 1H-pyrazolo[3,4-d]pyrimidine-4,6-diamines have been synthesized and the structures of nine of them are reported here, falling into two clear groups, those which are stoichiometric hydrates and those which crystallize in solvent-free forms. In each of N 4-methyl-N 4-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine, C12H12N6 (I), N 4-cyclohexyl-N 4-methyl-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine, C12H18N6 (II), and N 4-(3-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine, C11H9ClN6 (III), the molecules are linked into hydrogen-bonded sheets. The molecules of 2-{4-(6-a

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5

Palί, R., Lorίa-Bastarrachea M., M. Aguilar-Vega, J. L. Angulo, and H. Vazquez. "Synthesis and Characterization of Aromatic Polyamides Obtained from 4-4'-(9-Fluorenylidene)Diamine, 4-4'-(Hexafluoro-Isopropylidene)Dianiline and 4-4'-Diamine-Benzophenone." High Performance Polymers 14, no. 1 (2002): 77–91. http://dx.doi.org/10.1177/0954008302014001087.

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6

Silversides, Jon D., Amanda E. Sparke, and Stephen J. Archibald. "N-(4-Nitrobenzyl)benzene-1,2-diamine." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5944—o5946. http://dx.doi.org/10.1107/s1600536806050136.

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Beltz, Mark W., and Frank W. Harris. "Synthesis and properties of aromatic polyimides containing oxyalkylene linkages." High Performance Polymers 7, no. 1 (1995): 23–40. http://dx.doi.org/10.1088/0954-0083/7/1/003.

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A series of para-catenated aromatic diamines containing oxyalkylene linkages, i.e., i.2-bis(4-aminophenoxy)ethane, bis[2-(4-aminnophenoxy)ethyl]ether, 1,2-bis[24{4-aminio-phenoxy)ethoxyjethane and bis{2-[2A4-aminophenoxy)ethoxy]ethyllether were polymerized with 3,3',4.4'benzophenonetetracarboxylic dianhydride (BTDA) and pyromellitic dianhydride. The poly(amic acid)s obtained were imidized by both chemical and thermal methods. It was postulated that the incorporation of the flexible linkages in the polyimides' backbones would result in solubility in organic solvents and moderate glass transitio

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8

Gao, Jun Gang, Xiao Na Zhang, and Yong Gang Du. "Synthesis of Three Novel Aromatic Biazomethine Liquid- Crystalline Epoxy Resins and Curing Reaction with Aromatic Diamine." Advanced Materials Research 216 (March 2011): 34–38. http://dx.doi.org/10.4028/www.scientific.net/amr.216.34.

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Three class of novel liquid crystalline epoxy resins containing azomething groups: N,N’-Bis[4-(2,3-epoxypropoxy)benzylidene]-4,4-diamino-diphenyl ether (p-BEPBDDE), N,N’-Bis[4-(2,3-epoxypropoxy)benzylidene]-4,4-diamino-diphenyl methane (p-BEPBDDM) and N,N’-Bis[(4-(2,3-epoxypropoxy)-benzyliden)-1,4- phenylene diamine] (p-BEPBPD) were synthesized and characterized. The results show that p-BEBDDE and p-BEBDDM belong to smectic texture and melting point is 239.5 and 178 oC, respectively. The p-BEPBD is nematic texture between its melting temperature (Tm) of 192 oC and clearing temperature (Ti) of

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9

Hamidian, Kourosh, Mohsen Irandoust, Ezzat Rafiee, and Mohammad Joshaghani. "Synthesis, Characterization, and Tautomeric Properties of Some Azo-azomethine Compounds." Zeitschrift für Naturforschung B 67, no. 2 (2012): 159–64. http://dx.doi.org/10.1515/znb-2012-0208.

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The primary azo compound 1-(3-formyl-4-hydroxyphenylazo)-4-nitrobenzene reacts with some aliphatic and aromatic diamines and yields the corresponding azo-azomethine compounds. These compounds were characterized by elemental analysis, IR, UV/Vis, and NMR spectroscopy. The primary azo compound exists entirely in the azo form in solution as well as in the solid phase. The tautomeric structure of azo-azomethine compounds heavily depends on the solvent and the substituents. Aliphatic diamine-based compounds favor the enol-imine tautomer while aromatic diamine-based compounds have structures that li

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10

Ge, Ji-long, and Xiao-min Qian. "N6-(4-Fluorobenzyl)-3-nitropyridine-2,6-diamine." Acta Crystallographica Section E Structure Reports Online 67, no. 6 (2011): o1481. http://dx.doi.org/10.1107/s1600536811018642.

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Dissertations / Theses on the topic "4-diamine"

1

Dunham, Jason C. "Synthesis of 4-alkyl-3,5-diamino-1-phenylpyrazoles." Virtual Press, 2006. http://liblink.bsu.edu/uhtbin/catkey/1339144.

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The goal of this project is to synthesize and purify a library of novel 4-alkyl-3,5-diamino-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoles. These molecules are similar to other fiproles, which have been shown by Sammelson et al. to have pesticidal activities at the GABA receptor.' Fiproles are analogues of Fipronil, a very important pesticide. Replacing the cyano group normally located at the 3-position of the pyrazole ring with an amino group will change the binding potency of the phenylpyrazoles. Changes in binding produced by the changes introduced in molecular structure can create more

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2

Hreleva-Caparrotti, Hinka. "Ein Alumopolysiloxan mit Al 4(OH) 4-Kern und sein Verhalten gegenüber Diaminen und Metallorganylen." [S.l. : s.n.], 2006.

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3

ARON, PHILIPPE. "Evaluation comparee de la cytotoxicite de 4 chelatants utilises en endodontie." Nice, 1994. http://www.theses.fr/1994NICE7501.

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4

Bamberger, Stephanie N. "Characterization of the 2,6-Diamino-4-hydroxy-N 5-(methyl)-formamidopyrimidine DNA Lesion." Thesis, Vanderbilt University, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=13877281.

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5

Weder, Christoph. "Synthese und Charakterisierung neuer Polyamide mit stabilen nichtlinear optischen Eigenschaften, basierend auf 2',5'-Diamino-4-(dimethylamino)-4'-nitrostilben /." [S.l.] : [s.n.], 1994. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=10749.

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Banerjee, Sumela. "Supramolecular self-assembly within polymeric materials utilising triple hydrogen bonded heterocomplexes of 4-hydroxy-2,6-diamino pyridine derivatives." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-164706.

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In recent years supramolecular chemistry has established as one of the most active fields of science. The most significant feature of supramolecular chemistry is the use of building blocks which reversibly held together by intermolecular forces, electrostatic or H-bonding. Therefore, the synthesis of supramolecular systems using different non-covalent assemblies provides some unique architectures and features which are extremely difficult to be obtained via covalent synthesis. One main application of such influencing supramolecular systems is the preparation of self-healing materials. Among va

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7

Lavaud, Lucien. "Des diamino-benzoquinone-diimines aux azacalixphyrines : développement de colorants émergents du proche infrarouge." Thesis, Aix-Marseille, 2018. http://www.theses.fr/2018AIXM0404/document.

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Les colorants organiques du proche infrarouge présentent un intérêt majeur dans différent secteurs technologiques. Les travaux présentés dans cette thèse portent sur le développement de ce type de chromophores à partir d’unités quinones possédant une conjugaison électronique particulière : les 2,5-diamino-1,4-benzoquinone-diimines (DABQDI). De nouvelles DABQDI ont pu être synthétisées et leur utilisation comme ligand a notamment permis d’obtenir des complexes absorbant du domaine visible jusqu’à celui du proche infrarouge. Ces unités DABQDI ont également pu être incorporées au sein de macrocyc

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8

Le, Bihan Yann-Vaï. "Etude structurale et fonctionnelle de la reconnaissance et de la métabolisation de lésions puriques et pyrimidiques dans l'ADN par la Formamidopyrimidine-ADN glycosylase." Thesis, Orléans, 2009. http://www.theses.fr/2009ORLE2004/document.

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Les oxydations sur les bases nucléiques constituent l’une des sources principale d’apparition de lésions sur l’ADN, qui peuvent être mutagènes ou létales pour les cellules en l’absence de réparation de l’ADN. La Formamidopyrimidine-ADN glycosylase (Fpg), une enzyme procaryote du système de réparation de l’ADN par excision de base (BER), initie la réparation d’un large panel de lésions de ce type via ses activités ADN glycosylase (excision de la base oxydée) et AP lyase (clivage du site abasique par ß,d-élimination). Nous avons réalisé des études fonctionnelles par des techniques biochimiques e

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9

Mais, Silvio. "Synthese von N-Benzhydryl-anilinen und Untersuchungen zu Struktur-Eigenschafts-Zusammenhaengen hinsichtlich der Photoleitung in Polymermatrizen." [S.l. : s.n.], 1996. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB10324489.

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10

Banerjee, Sumela [Verfasser], Brigitte [Akademischer Betreuer] Voit, and Wolfgang H. [Akademischer Betreuer] Binder. "Supramolecular self-assembly within polymeric materials utilising triple hydrogen bonded heterocomplexes of 4-hydroxy-2,6-diamino pyridine derivatives / Sumela Banerjee. Gutachter: Brigitte Voit ; Wolfgang H. Binder. Betreuer: Brigitte Voit." Dresden : Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://d-nb.info/1071785605/34.

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Books on the topic "4-diamine"

1

Huang, Sung-ben. Synthesis and oligomerization of Delta, 4-diamino-2-oxo-1(2H)-pyrimidinehexanoic acid. 1990.

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2

Nelson, Jeffrey Stephen. Synthesis and oligomerization of y,4-Diamino-2-oxo-1(2H)-pyrimidinepentanoic acid. 1989.

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Book chapters on the topic "4-diamine"

1

Bährle-Rapp, Marina. "4-Methoxytoluene-2,5-Diamine HCl." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_6473.

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2

Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with macrocyclic Schiff-base ligand of 2, 6-diformyl-4-methylphenol and α-ω-diamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_338.

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3

Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear cobalt(II) complex with reduced Schiff-base ligand derived from 2, 6-diformyl-4-methylphenol and α-ω-diamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_430.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear nickel(II) complex with macrocyclic Schiff-base ligand derived from 2, 6-diformyl-4-methylphenol and α-ω-diamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_714.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with macrocyclic Schiff-base ligand derived from 2, 6-diformyl-4-methylphenol and α-ω-diamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_336.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with macrocyclic Schiff-base ligand derived from 2, 6-diformyl-4-methylphenol and α-ω-diamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_337.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with macrocyclic Schiff-base ligand derived from 2, 6-diformyl-4-methylphenol and α-ω-diamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_339.

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8

Bährle-Rapp, Marina. "4,5-Diamino-1-((4-Chlorophenyl)Methyl)-1H-Pyrazole-Sulfate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2833.

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9

Schomburg, Dietmar, and Ida Schomburg. "2,5-diamino-6-(ribosylamino)-4(3H)-pyrimidinone 5’-phosphate reductase 1.1.1.302." In Class 1 Oxidoreductases. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36265-1_8.

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Winkelmann, Jochen. "Diffusion coefficient of (S)-2,4-diamino-4-oxobutanoic acid in water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_286.

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Conference papers on the topic "4-diamine"

1

OuYang, 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. Atlantis Press, 2016. http://dx.doi.org/10.2991/mmeceb-15.2016.158.

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2

McClung, Amber J. W., Joseph A. Shumaker, and Jeffery W. Baur. "Novel Bismaleimide-Based Shape Memory Polymers: Comparison to Commercial Shape Memory Polymers." In ASME 2011 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2011. http://dx.doi.org/10.1115/smasis2011-5044.

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A series of novel shape memory polymers, synthesized from 4-4-bismaleimidodiphenyl-methane, an extended chain aliphatic diamine, and a bis-isocyanate, have been created and characterized with the aim of providing a family of robust high temperature shape memory polymers with tailorable transition temperatures for use in reconfigurable aerospace structures. In the present study, three of the polymers are chosen for more detailed study of their thermomechanical properties. These materials are compared to commercial resins Veriflex® and Veriflex-E® which are styrene- and epoxy-based proprietary f

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Lohou, Elodie, N. André Sasaki, Agnès Boullier, and Pascal Sonnet. "New multifunctional diamine AGE/ALE inhibitors to prevent oxidative and carbonyl stress exacerbation in Alzheimer's disease." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05622.

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4

Vasconcelos, Luciana Mabel Ferreira, Raphael de Oliveira Rodrigues, A. A. Albuquerque, et al. "Polimorfismos de IL-10, IL-4, molécula regulatória CTLA-4 e enzima diamino oxidase em reações de hipersensibilidade cruzada a AINES." In II Encontro do Programa de Pós-Graduação em Ciências Farmacêuticas da Universidade Federal do Ceará e I Simpósio Norte-Nordeste de Ciências Farmacêuticas. Galoa, 2017. http://dx.doi.org/10.17648/ppgcf-2017-66436.

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5

Dotsenko, Victor, Ivan Didenko, Gennady Krapivin, Nikolay Aksenov, Inna Aksenova, and Sergey Krivokolysko. "Synthesis of 2,8-diamino-5-hydroxy-4H,10H-pyrano[2,3-f]chromene-3,9-dicarbonitrile ." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a059.

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Reports on the topic "4-diamine"

1

Drake, Greg, Tommy Hawkings, Leslie Hall, Jerry Boatz, and Ashwani Vij. Experimental and Theoretical Study of 1.5-Diamino-4-H-Tetrazolium Perchlorate. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada423054.

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2

Stromer, Bobbi, Rebecca Crouch, Katrinka Wayne, Ashley Kimble, Jared Smith, and Anthony Bednar. Methods for simultaneous determination of 29 legacy and insensitive munition (IM) constituents in aqueous, soil-sediment, and tissue matrices by high-performance liquid chromatography (HPLC). Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/1168142105.

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Standard methods are in place for analysis of 17 legacy munitions compounds and one surrogate in water and soil matrices; however, several insensitive munition (IM) and degradation products are not part of these analytical procedures. This lack could lead to inaccurate determinations of munitions in environmental samples by either not measuring for IM compounds or using methods not designed for IM and other legacy compounds. This work seeks to continue expanding the list of target analytes currently included in the US Environmental Protection Agency (EPA) Method 8330B. This technical report pr

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