Academic literature on the topic 'Imina'

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Journal articles on the topic "Imina"

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Al Hakimi, Nurush Shofi, Ahmand Hanapi, and Ahmad Ghanaim Fasya. "Green Synthesis Senyawa Imina dari Vanillin and Anilina dengan Katalis Alami Air Jeruk Nipis (Citrus aurantifolia)." ALCHEMY 5, no. 4 (2018): 120. http://dx.doi.org/10.18860/al.v5i4.4706.

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<p class="BodyAbstract">Sintesis imina dari vanilin dan anilina dapat dilakukan tanpa pelarut dengan bantuan katalis asam alami dari jeruk nipis (Citrus aurantifolia). Penelitian ini bertujuan untuk mengkarakterisasi produk imina dengan variasi volume katalis jeruk nipis. Volume katalis jeruk nipis yang digunakan adalah 0,5; 1,0; 1,5; 2,0; dan 2,5 mL. Produk imina dikarakterisasi berdasarkan bentuk, warna, titik lebur dan rendemen. Produk juga identifikasi menggunakan FTIR dan KG-SM. Sintesis imina menghasilkan P1 sebagai produk terbaik dengan rendemen sebesar 64,12% dan tingkat kemurnia
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Garcia, Tania, Sylvain Bernés, Guadalupe Hernández, René Gutiérrez, and Jaime Vázquez. "Conformación molecular y estructura cristalina de una diimina quiral: 1,4-BTS[(+)-(1-Feniletilimino)Metil)]Benceno." Quimica Hoy 1, no. 1 (2010): 4. http://dx.doi.org/10.29105/qh1.1-49.

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La síntesis de una nueva bis-imina quiralmente pura, de fórmula C24H24N2, se llevó a cabo por síntesis directa, en ausencia de disolvente, y la caracterización estructural se realizó por difracción de Rayos X en monocristal. Los grupos imino tienen la configuración E, común en aldiminas secundarias con un grupo estorboso sustituyendo el átomo de nitrógeno. Las moléculas se empacan en el estado sólido sin formar contactos intermoleculares significativos, a diferencia de sistemas imínicos y bis-imínicos cercanos, donde grupos aromáticos extendidos generan interacciones estabilizantes en el estad
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Solihati, Ditya Putri, Enny Fachriyah, and Ismiyarto Ismiyarto. "Waktu Optimum pada Reaksi Veratraldehid dan Anilin." Jurnal Kimia Sains dan Aplikasi 14, no. 3 (2011): 69–71. http://dx.doi.org/10.14710/jksa.14.3.69-71.

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Imina merupakan senyawa dengan gugus fungsi C=N yang mempunyai potensi sebagai antibakteri, antikanker, antijamur, antitumor dan antimalaria. Sintesis imina dapat dilakukan menggunakan bahan dasar aldehida dan amina primer. Pada penelitian ini, digunakan veratraldehid dan anilin. Tujuan penelitian ini adalah mensintesis 3,4 dimetoksibenzilimina dan menentukan waktu reaksi optimum dari proses sintesis tersebut. Kemurnian produk sintesis berdasarkan pengujian titik leleh. Penentuan hasil sintesis maksimum dilakukan dengan variasi waktu pelarutan. Hasil penelitian menunjukkan bahwa produk sintesi
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Syamsudin, Dimas, Ismiyarto Ismiyarto, and Ngadiwiyana Ngadiwiyana. "Synthesis and Antibacterial Testing of Imina Derivative Compounds from Piperonal and Anilin." Jurnal Kimia Sains dan Aplikasi 21, no. 1 (2018): 44–48. http://dx.doi.org/10.14710/jksa.21.1.44-48.

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Synthesis of Imine derivates used as antibacterial activity has been done. Synthesis was conducted by condensation reaction between piperonal and aniline. The product synthesis was characterized by melting point, LC-MS, FTIR and 1H-NMR, then application of the product as antibacterial towards bacteria Staphylococcus aureus and Escherichia coli. The product of synthesis was pale-brown solid, and had melting point at 56-61 0C. Identification by LC-MS showed the compound molecular weight was 225.30 gram/mol, identification by FTIR showed a compound contained imine C=N at 1620.21 cm-1, C-H aromati
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Ceballos, Mauricio, Héctor Holguín, César González, and Pedro Amariles. "Interacción warfarina y acetaminofén: Evaluación para establecer su relevancia clínica." Acta Médica Colombiana 38, no. 1 (2013): 22–27. http://dx.doi.org/10.36104/amc.2013.228.

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Objetivo: realizar una revisión estructurada de la interacción warfarina y acetaminofén, buscando establecer su relevancia clínica y profundizar en el mecanismo de dicha interacción. 
 Método: revisión estructurada en PubMed/Medline, de artículos en inglés y español, buscando los términos warfarin AND (acetaminophen OR paracetamol) en el título o resumen. La búsqueda se complementó con las referencias de artículos valorados como importantes. Los trabajos se agruparon en: relacionados con el aumento de sangrado por la interacción warfarina-acetaminofén, o relacionados con el mecanismo de l
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Jiang, Ren-Wang, Shuang-Cheng Ma, Paul P. H. But, and Thomas C. W. Mak. "ChemInform Abstract: Isolation and Characterization of Spirocaesalmin, a Novel Rearranged Vouacapane Diterpenoid from Caesalpinia imina Hance." ChemInform 33, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.200212220.

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Su, Biyun, Yaning Li, Dandan Pan, Paison Faida, Tingyu Yan, and Zhan Qu. "Microwave Irradiation Syntheses and Crystal Structures of Two Series of Novel Fivemembered Heterocyclic Mono-Imine Compounds." Current Organic Synthesis 16, no. 3 (2019): 444–48. http://dx.doi.org/10.2174/1570179416666181207125604.

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Aim and Objective: The late transition metal complexes with five-membered heterocyclic mono-imine ligands have attracted much attention because of their potential application in olefin polymerization catalysis. In order to increase the coordination ability of heteroatom N and S to center metals, CH3 group was introduced into the side arm of pyrrole imine and thiophene imine respectively, to get two series of novel five-membered heterocyclic imine compounds, mono(imino)pyrroles and mono(imino)thiophenes Materials and Methods: Two series of novel five-membered heterocyclic compounds with the mon
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Lecourt, Constance, Warren Madanamoothoo, Vivian Ferreol, et al. "Mononuclear manganese(iii) complexes with reduced imino nitroxide radicals by single-electron transfer and intermolecular hydrogen bonds as an intramolecular structural driving force." Dalton Transactions 48, no. 35 (2019): 13378–87. http://dx.doi.org/10.1039/c9dt02158b.

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One-electron transfer from Mn(ii) ions to an imino nitroxide radical gives mononuclear Mn(iii) complexes of the reduced amino imine-oxide form for which crystal structures evidence hydrogen bonds networks acting as a stabilizing driving-force.
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Fletcher, James T., Matthew D. Hanson, Joseph A. Christensen, and Eric M. Villa. "Revisiting ring-degenerate rearrangements of 1-substituted-4-imino-1,2,3-triazoles." Beilstein Journal of Organic Chemistry 14 (August 10, 2018): 2098–105. http://dx.doi.org/10.3762/bjoc.14.184.

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The 1-substituted-4-imino-1,2,3-triazole motif is an established component of coordination compounds and bioactive molecules, but depending on the substituent identity, it can be inherently unstable due to Dimroth rearrangements. This study examined parameters governing the ring-degenerate rearrangement reactions of 1-substituted-4-imino-1,2,3-triazoles, expanding on trends first observed by L’abbé et al. The efficiency of condensation between 4-formyltriazole and amine reactants as well as the propensity of imine products towards rearrangement was each strongly influenced by the substituent i
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Mason, Helen E., Judith A. K. Howard, and Hazel A. Sparkes. "Synthesis and structures of three isoxazole-containing Schiff bases." Acta Crystallographica Section C Structural Chemistry 76, no. 9 (2020): 927–31. http://dx.doi.org/10.1107/s2053229620010530.

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The synthesis and structures of three isoxazole-containing Schiff bases are reported, namely, (E)-2-{[(isoxazol-3-yl)imino]methyl}phenol, C10H8N2O2, (E)-2-{[(5-methylisoxazol-3-yl)imino]methyl}phenol, C11H10N2O2, and (E)-2,4-di-tert-butyl-6-{[(isoxazol-3-yl)imino]methyl}phenol, C18H24N2O2. All three structures contain an intramolecular O—H...N hydrogen bond, alongside weaker intermolecular C—H...N and C—H...O contacts. The C—O(H) and imine C=N bond lengths were consistent with structures existing in the enol rather than the keto form. Despite having dihedral angles <25°, none of the compoun
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Dissertations / Theses on the topic "Imina"

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Caovilla, Alessandra. "Catalisadores de zinco(II) e alumínio(III) contendo ligantes imina-pirrol e imina-fenolato aplicados na polimerização de lactídeos." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2018. http://hdl.handle.net/10183/181332.

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Novos catalisadores de ZnII e AlIII contendo ligantes imina-pirrol e imina-fenolato foram preparados, estruturalmente caracterizados em solução e no estado sólido e usados na polimerização por abertura de anel do rac- e L-lactídeo em solução ou condições industrialmente preferidas (livre de solvente a 130 °C), na presença de um álcool como coiniciador/agente de transferência de cadeia (BnOH e iPrOH). Os catalisadores de ZnII bis-imina-pirrol Zn1-Zn4 demonstraram que a flexibilidade da estrutura do ligante, bem como o átomo doador (oxigênio versus enxofre), exercem influência na atividade da po
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Profirio, Daniel de Moraes 1989. "Atividades antibacteriana e citotóxica de um complexo de Au(III) contendo ligante pirrolil-imina." [s.n.], 2014. http://repositorio.unicamp.br/jspui/handle/REPOSIP/248530.

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Orientador: André Luiz Barboza Formiga<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-25T06:44:24Z (GMT). No. of bitstreams: 1 Profirio_DanieldeMoraes_M.pdf: 7198649 bytes, checksum: 018efc71d59b6427976118e0cc5f772a (MD5) Previous issue date: 2014<br>Resumo: Neste trabalho realizou-se a síntese de três ligantes contendo a unidade pirrolil-imina e de um complexo de Au(III). Os ligantes foram sintetizados partindo-se do pirrol-2-carboxaldeído e etilenodiamina ou orto-fenilenodiamina, obtendo-se assim o N,N'-bis(pirrol-
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Milani, Jorge Luiz Sônego. "Catalisadores de níquel (II) contendo ligantes imina-furano aplicados a dimerização seletiva do etileno." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2012. http://hdl.handle.net/10183/55481.

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Neste trabalho, uma nova classe de catalisadores de NiII contendo ligantes imina-furano tais como NiCl2{N-((5-metilfurano-2-il)metileno)-2-fenoxietanimina} (1), NiCl2{N-((5- metilfurano-2-il)metileno)-2-fenoxibenzimina} (2), NiCl2 {2-metoxifenil-N-((5-metilfurano-2- il)metileno) metanimina} (3), NiCl2{N-((furano-2-il)metileno)-2-fenoxibenzimina} (4) foram sintetizados e caracterizados por espectrometria de massas de alta resolução e espectroscopia na região do infra-vermelho. Estes catalisadores de níquel, quando ativados com metilaluminoxano (MAO), apresentaram freqüências de rotação (FRs) en
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Gomes, Fernando da Silva. "Catalisadores do grupo 4 contendo ligantes tridentados imina-fenolato aplicados a homo e copolimerização do etileno." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2012. http://hdl.handle.net/10183/102026.

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Uma série de complexos de tricloreto do grupo 4, coordenados com ligantes tridentados, foram estudados na homopolimerização de etileno e copolimerização etileno/hexeno. Os complexos (Ln)TiCl3, n = 1 – 4 (L1 = 3,5-tBu-2-(OH)C6H2CH-N-8- C9H6N, L2 = 3,5-tBu-2-(OH)C6H2CH-N-C2H4-O-C6H5, L3 = 3,5-tBu-2-(OH)C6H2CHN- CH2-C6H4OMe e L4 = 3,5-tBu-2-(OH)C6H2CH-N-C6H4-O-C6H5), foram sintetizados pela reação do respectivo pré-ligante, com 1 eq de TiCl4 a -94 ºC, formando os complexos Ti1 – Ti4. Os complexos (L1)ZrCl3 (Zr1) e (L1)HfCl3 (Hf1) foram sintetizados pela reação do sal de lítio do ligante Li(L1) a
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Junior, Jorge Ferreira. "Catalisadores de cromo contendo ligantes do tipo imina-tiofeno aplicados à produção de alfa olefinas lineares." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2014. http://hdl.handle.net/10183/116450.

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Uma nova classe de complexos (PC1-PC7) de cromo (III) e cromo (0) contendo ligantes imina-tiofeno foi sintetizada e seu potencial catalítico avaliado para reações de oligomerização de etileno. Utilizando MAO como cocatalisador, os sistemas catalíticos apresentaram atividades que variaram de acordo com a estrutura do ligante num um intervalo de 0,5 e 7,6x104h-1 [(mol de etileno oligomerizado) x (mol de cromo)-1 x h-1]. A influência de alguns parâmetros de reação no desempenho catalítico (atividade e seletividade) foi avaliada. Variando a temperatura de reação observou-se a tendência de aumento
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Richards, Polly. "Imina sangha : (masque aÃ?? la mode) : a study of Dogon masquerade at the turn of the millenium." Thesis, SOAS, University of London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407129.

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Martins, Nayara Teodoro do Prado. "Catalisadores de vanádio (III) contendo ligantes do tipo tio-imina-fenol aplicados a homo e copolimerização do etileno." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2014. http://hdl.handle.net/10183/102020.

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Uma nova classe de complexos de vanádio(III) contendo ligantes do tipo tio-imina-fenol foi sintetizada e seu desempenho catalítico foi avaliado na reação de polimerização do etileno. Sob ativação com metilaluminoxano (MAO), os catalisadores apresentaram atividades que variaram de acordo com a estrutura do ligante (213,6 – 887,2 kg de PE/mol(V)h). A influência de alguns fatores sobre o desempenho catalítico dos complexos foi avaliada. O aumento da temperatura de polimerização provocou a diminuição da atividade catalítica, comportamento que é usualmente observado para os catalisadores de vanádi
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Toledano, Navarro Estefanía. "Síntesis Asimétrica de Heterociclos Nitrogenados vía Adición de Triorganozincatos con Cadenas Insaturadas a N-(terc-Butilsulfinil)iminas." Doctoral thesis, Universidad de Alicante, 2015. http://hdl.handle.net/10045/83547.

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En esta memoria se describe la síntesis de N-(terc-butilsulfinil)iminas promovida por microondas, así como su aplicación a la preparación de diferentes heterociclos nitrogenados ópticamente enriquecidos por adición diastereoselectiva de reactivos organozíncicos. Esta memoria ha sido dividida en los siguientes capítulos: Capítulo I: Síntesis de N-(terc-Butilsulfinil)iminas promovida por microondas. En este capítulo se describe la síntesis de diferentes aldiminas y cetiminas por condensación del correspondiente aldehído o cetona con 2-metilpropano-2-sulfinamida en ausencia de disolvente y promo
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Bergamo, Adão Lauro. "Complexos de cr (III) e ni (II) contendo ligantes tridentados pirazol-imina-fenolato/pirrolato : síntese, caracterização e aplicação na oligo/polimerização do etileno." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2018. http://hdl.handle.net/10183/181414.

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Foi sintetizada e caracterizada uma nova classe de ligantes tridentados do tipo pirazol-imina-fenolato/pirrolato e com estes ligantes foram sintetizados 12 complexos de Cr(III) e 8 complexos de Ni(II) e foi avaliado o desempenho destes complexos em sistemas de reações de oligomerização e polimarização do etileno. Os complexos de Cr(III) foram sintetizados e caracterizados por meio de espectroscopia de infravermelho e espectrometria de massas de alta resolução. Monocristais de Cr1 foram obtidos e analisados por meio de difração de Raios-X comprovando a estrutura monomérica de coordenação do lig
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Milani, Jorge Luiz Sônego. "Catalisadores de cromo (III) e níquel (II) contendo ligantes do tipo pirazol/éter e imina/tioéter seletivos para a produção de alfa-olefinas lineares." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2016. http://hdl.handle.net/10183/147182.

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Neste trabalho, duas novas classes de complexos de CrIII contendo ligantes pirazol-éter (N^O) CrCl3[(3-fenoxipropil)pirazol] (Cr1), CrCl3[1-(3-fenoxipropil)- (3,5-dimetil-pirazol)] (Cr2), CrCl3[1-(3-fenoxipropil)-(3-fenil-pirazol)] (Cr3), CrCl3[1-(3-fenoxipropil)-3,5-bis(trifluormetil)pirazol] (Cr4) e ligantes imina-tioéter (N^S) CrCl3[(E)-2-metil-N-(2-(feniltio)benzilideno)propan-2-amina] (Cr5), CrCl3[(E)-4-metoxi-N-(2-(feniltio)benzilideno)anilina] (Cr6), CrCl3[(E)-N-(2-(feniltio)benzilideno)anilina] (Cr7), CrCl3[(E)-N-(2-(terc-butiltio)benzilideno)-2-metilpropan-2-amina (Cr8), CrCl3[(E)-N-(
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Books on the topic "Imina"

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Eti︠u︡di po bŭlgarska antroponimii︠a︡: Lichni imena = Studia z antroponimii bułgarskiej : imiona chrzestne. UI "Sv. sv. Kiril i Metodiĭ", 2006.

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Nenarokomov, Maksim. Imena. Kruglyĭ god, 1996.

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A, Florenskiĭ P. Imena. EKSMO-Press, 1998.

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Nātha, Prabodha. Imana. Bidyā Mandira, 1994.

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Arsenʹeva, Elena. Imena--. Aĭris press, Rolʹf, 1998.

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A, Florenskiĭ P. Imena. Izd-vo "Kupina", 1993.

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Vozvrashchennye imena. [s.n.], 2009.

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Imiona wojny. Zysk i S-ka, 2009.

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Muck, Kristijan. Imena igre. Mondena, 1999.

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Kupis, Bogdan. Nasze imiona. Wydawn. Naukowo-Techniczne, 1991.

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Book chapters on the topic "Imina"

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Wagner, Michele D. "Imana." In Encyclopedia of African Religions and Philosophy. Springer Netherlands, 2021. http://dx.doi.org/10.1007/978-94-024-2068-5_180.

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Balzer, Edeltraud. "Imiza von Xanten." In Das St. Viktor-Stift Xanten. Böhlau Verlag, 2012. http://dx.doi.org/10.7788/boehlau.9783412214838.17.

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Kimenyi, Alexandre. "Rwanda, Imana in." In Encyclopedia of African Religions and Philosophy. Springer Netherlands, 2021. http://dx.doi.org/10.1007/978-94-024-2068-5_341.

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Wills, Martin. "Imino Transfer Hydrogenation Reductions." In Topics in Current Chemistry Collections. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43051-5_2.

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Lane, J. D., C. J. Pickett, and D. R. Stanley. "Synthesis of Imine Complexes." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch53.

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Davies, A. G. "16.2.1.8 Imino-1,2-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_11.

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Rueping, Magnus, Erli Sugiono, Cengiz Azap, et al. "Imine Reduction and Reductive Amination." In Regio- and Stereo- Controlled Oxidations and Reductions. John Wiley & Sons, Ltd, 2007. http://dx.doi.org/10.1002/9780470090244.ch4.

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Jamieson, Craig, and Keith Livingstone. "Applications of Nitrile Imine Derivatives." In The Nitrile Imine 1,3-Dipole. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-43481-6_4.

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"Migrant as cr iminal : the jud ic ia ltreatment of migrant cr imina l i ty FABIO QUASSOLI." In Controlling a New Migration World. Routledge, 2003. http://dx.doi.org/10.4324/9780203164938-14.

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"Imine Reductases." In Biocatalysis in Organic Synthesis, edited by Faber, Fessner, and Turner. Georg Thieme Verlag, 2015. http://dx.doi.org/10.1055/sos-sd-215-00205.

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Conference papers on the topic "Imina"

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Pedersen, Isabel, Pejman Mirza-Babaei, and Nathan Gale. "iMind." In the 2015 ACM International Joint Conference. ACM Press, 2015. http://dx.doi.org/10.1145/2800835.2801664.

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"Kazalo imena." In Desničini susreti 2011. Filozofski fakultet u Zagrebu, FF Press, 2014. http://dx.doi.org/10.17234/desnicini_susreti2011.19.

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"Kazalo imena." In Desničini susreti 2014. Filozofski fakultet u Zagrebu, FF Press, 2015. http://dx.doi.org/10.17234/desnicini_susreti2014.23.

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Gilmore, John F., and Larry E. Williams. "Semiautomated IMINT processing baseline system." In AeroSense '97, edited by Robert Trebits and James L. Kurtz. SPIE, 1997. http://dx.doi.org/10.1117/12.276112.

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Hakimzadehy, Kamal, Patrick K. Nicholsonz, Diego Lugonesz, and Amir H. Payberahy. "IMITA: Imitation Learning for Generalizing Cloud Orchestration." In 2021 IEEE/ACM 21st International Symposium on Cluster, Cloud and Internet Computing (CCGrid). IEEE, 2021. http://dx.doi.org/10.1109/ccgrid51090.2021.00033.

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Shaoxiang, Zhou, Wang Wendon, and Hu Yuxi. "KD-9 IMANA Film Analyzer And Its Applications." In 18th Intl Congress on High Speed Photography and Photonics, edited by DaHeng Wang. SPIE, 1989. http://dx.doi.org/10.1117/12.969209.

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Pedersen, Isabel, Pejman Mirza-Babaei, and Nathan Gale. "iMind: An alternative dialogue between viewers and artists." In 2014 IEEE Games, Media, Entertainment (GEM) Conference. IEEE, 2014. http://dx.doi.org/10.1109/gem.2014.7048085.

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García-Deibe, Ana, Matilde Fondo, Jesús Sanmartín, and Cristina Portela. "Imine-tetrahydroquinazoline tautomerism in a tosilated Schiff base." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00426.

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Brandi, Alberto, Stefano Cicchi, Franca Cordero, and Andrea Goti. "Imino-sugars by Stereoselective Processes Employing Pyrroline N-oxides." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01843.

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Larroque, Serge. "Recce NG: from Recce sensor to image intelligence (IMINT)." In International Symposium on Optical Science and Technology, edited by Wallace G. Fishell and Arthur A. Andraitis. SPIE, 2001. http://dx.doi.org/10.1117/12.451119.

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Reports on the topic "Imina"

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DuBois, D. A., and R. H. Neilson. Addition Reactions of a Silylated Imino(Methylene)Phosphorane. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada203987.

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Arapoglou, Stergios. Dispute in the Aegean Sea the Imia/Kardak Crisis. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada420639.

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Hall, H. K., and Jr. Synthesis and Polymerization of New Imine Monomers: Azaethylenes, Azabutadienes, and Azaallenes. Defense Technical Information Center, 1996. http://dx.doi.org/10.21236/ada314001.

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Loveland, Jo L., Rick Barbour, Al Krum, and August C. Neitzel. Rollout and Installation of Risk Management at the IMINT Directorate, National Reconnaissance Office. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada375848.

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