Relevant bibliographies by topics / Amidah

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Amidah'

Author: Grafiati
Published: 4 June 2021
Last updated: 29 January 2023

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Journal articles on the topic "Amidah"

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Marcus, Joel. "A Jewish-Christian 'Amidah?" Early Christianity 3, no. 2 (2012): 215. http://dx.doi.org/10.1628/186870312800778220.

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Schonfield, Jeremy. "Including the Matriarch in the Amidah?" European Judaism 52, no. 1 (March 1, 2019): 135–49. http://dx.doi.org/10.3167/ej.2019.520115.

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Progressive liturgists seek to introduce gender parity into the first paragraph of the Amidah by adding the names of the Matriarchs immediately after those of the Patriarchs. I argue that this misrepresents their marriages and the role played by the concubines. A more balanced understanding is made possible by distancing the names of the Matriarchs from those of their husbands, and inserting them in the form of a brief piyyut, composed of biblical citations, just before the concluding blessing formula. The proposed insertion reflects the agency displayed by the Matriarchs and alludes obliquely to the concubines. Account is taken of the appropriateness of the piyyut for use in traditional settings.
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Smith, Sara. "The Imahot in the Amidah: A History." Contemporary Jewry 32, no. 3 (October 2012): 309–27. http://dx.doi.org/10.1007/s12397-012-9092-0.

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Kimelman, Reuven. "The Daily 'Amidah and the Rhetoric of Redemption." Jewish Quarterly Review 79, no. 2/3 (October 1988): 165. http://dx.doi.org/10.2307/1454251.

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Kimelman, Reuven. "The Messiah of the Amidah: A Study in Comparative Messianism." Journal of Biblical Literature 116, no. 2 (1997): 313. http://dx.doi.org/10.2307/3266226.

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Fleischer, E. (Ezra). "On the Origins of the 'Amidah: Response to Ruth Langer." Prooftexts 20, no. 3 (2000): 380–84. http://dx.doi.org/10.1353/ptx.2000.0017.

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Kaunfer, Elie. "Reception of the Bible in Rabbinic Liturgy: Expression and Interpretation." Journal of the Bible and its Reception 9, no. 2 (November 1, 2022): 247–68. http://dx.doi.org/10.1515/jbr-2021-0031.

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Abstract This essay explores two questions: How is the Bible received and expressed in classical rabbinic Jewish liturgy? What is the implication for the understanding and interpretation of Jewish prayer, given the role of the Bible in the liturgy? We will review the prevailing theories of the Bible’s reception in the liturgy and classify the different forms of this reception. We will then explore the implications for interpretation of liturgy by analyzing a piece of the daily Jewish liturgy—the first blessing of the amidah.
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Lieber, Laura S. "“On This Day, We Are Perfect”: Embodiment in Yannai’s Yom Kippur Qerova." Journal of Jewish Thought and Philosophy 30, no. 1 (March 31, 2022): 37–69. http://dx.doi.org/10.1163/1477285x-12341326.

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Abstract This article analyzes two poetic units within a much longer composition (translated in full here) composed by Yannai (6th c. CE, Galilee) for recitation on Yom Kippur. Specifically, it offers readings of Unit 8, which prefaces the third blessing of the Amidah (the Qedushah), and Unit 15, which concludes the work. Both units dwell on the physical experience of Yom Kippur and the ways in which ritual affects the body, permitting us to consider the role of “kinesthetic theology” (borrowing Kathryn Reklis’ coinage) – i.e., how physical expression and embodied experiences not only reflect but shape belief – in the composition.
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Janse, S. "De joodse achtergrond van het gebed in Aphrahats Demonstrationes 23.53-59." NTT Journal for Theology and the Study of Religion 59, no. 1 (January 18, 2005): 41–59. http://dx.doi.org/10.5117/ntt2005.59.041.jans.

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The prayer of the Syrian theologian Aphrahat in Demonstratio 23.53-59 displays at least seven analogies with the Jewish prayer Amidah. Textual analysis suggests that there are more instances of Jewish influence in this prayer. In this study it is considered plausible that Jewish prayers from the period after 70 AD or 135 AD, have found a way into the Christian liturgy of Syriac-speaking Persia through Jewish proselytes. It is probable that the borrowing took place in the short period between the outbreak of the persecutions in 340 under the Persian king Shapur II and the writing of Demonstratio 23 in 345.
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Jacobs, Irving. "Kingship and Holiness in the Third Benediction of the Amidah and in the Yoẓer." Journal of Jewish Studies 41, no. 1 (April 1, 1990): 62–74. http://dx.doi.org/10.18647/1510/jjs-1990.

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Dissertations / Theses on the topic "Amidah"

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Katz, Tyler. "Amidah - תפילת העמידה." Thesis, University of Iowa, 2019. https://ir.uiowa.edu/etd/6777.

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Amidah - תפילת העמידה – for soprano voice, clarinet, cello, and piano – is a liturgical work in three movements that uses common Jewish prayers as its text. These three movements focus on specific prayers that can be found in the Amidah, the central portion of a Jewish prayer service. This work uses prayers that can be performed on a Friday evening Shabbat service. The first movement focuses on accompanimental music to the Silent Amidah, a silent prayer. The prelude uses the traditional Jewish melody of the opening prayer of the Amidah, Adonai S’fatai Tiftach (אדני שפתי תפתח), leading directly into the first movement. This movement, while harkening to some Jewish melodies, takes ideas from classical Western harmony. While conveying both a sense of calmness and unease, the movement allows for the listener to silently reflect and meditate while absorbing the music. The second movement, Oseh Shalom (עושה שלום), takes its root in Freylach music, a traditional, fast-paced, upbeat style of Klezmer music. While keeping traditional elements, it also uses contemporary harmony and extensive ornamentation in a joyous, energetic fashion. The third movement, Mi Shebeirach (מי שברך), combines flowing lines, ornamental ancient Hebrew trope cantillation, liturgical elements, Middle-Eastern aspects, and spectral harmonies to create a slow, lamenting prayer for healing, a prayer that cries out in pain and suffering, begging for a restoration of mind, body, and soul. The movement closes in mournful sadness comforted by the presence of the Divine.
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Silva, Alexandre Vieira. "Síntese de organo-seleno aminas e sua resolução cinética via reação de acetilação enantiosseletiva mediada por lipases." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-02072008-125408/.

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Nesse trabalho foi desenvolvido um método de síntese quimioenzimática de organo-seleno aminas (1-((2, 3 ou 4 selenocianato)fenil)etanonas) e amidas (N-(1-(2, 3 ou 4-(etilseleno)fenil)etil)acetamida) enantiomericamente enriquecidas. Inicialmente, as organo-seleno aminas, na forma racêmica, foram sintetizadas a partir das orto-, meta- e para- aminoacetofenonas. A incorporação do átomo de selênio nas cetonas aromáticas foi realizada através da reação de selenocianato de potássio com sais de diazônio, preparados a partir das aminoacetofenonas, para levar as o, m ou p-selenocianato acetofenonas (28-65 %). Reações desses compostos com NaBH4, formaram os intermediários organo-selenoboro, que foram posteriormente alquilados com haletos de alquila de modo a formar as organo-seleno acetofenonas (1-(2, 3 ou 4-(etilseleno)fenil)etanona) (63-78 %). As Organo-seleno aminas racêmicas foram preparadas por aminação redutiva das cetonas correspondentes (39-73 %). Após desenvolvido o protocolo de síntese das organo-seleno aminas, nós estudamos a resolução cinética desses compostos através de reação de acetilação mediada por lipases. Um estudo inicial foi conduzido com a amina para substituído, como substrato modelo, de modo a buscar a lipase, solvente, temperatura, razão lipase/substrato e acilante apropriados para a resolução cinética. De acordo com os resultados obtidos, as condições ideais para se conduzir a resolução cinética foi CAL-B como biocatalisador, hexano como solvente e acetato de etila ou metóxi-acetato de etila como acilante a 30°C. Utilizando esse protocolo, as organo-seleno amidas foram preparadas com excelentes excessos enantioméricos (99 %).
In this work, we have developed a chemoenzymatic method to enantiomerically synthesize enriched organoselenium amines (1-(2, 3 or 4 -(ethylselanyl)phenyl)ethanamine) and amides (N-(1-(2, 3 or 4-(ethylselanyl)phenyl)ethyl)acetamide). Initially, the organoselenium amines, in the racemic form, were synthesized from ortho-, meta- and para- aminoacetophenones. The incorporation of the selenium atom into the aromatic ketones was achieved by the use of reaction of potassium selenocyanate and diazonium salts, prepared from aminoacetophenones, to afford selenocyanate acetophenones (28-65 %). These compounds were alkylated with alkyl halide to yield the organoselenium acetophenones (1-(2, 3 or 4-(ethylselanyl)phenyl)ethanone) (63-78 %) which were converted into their corresponding racemic organoselenium amines by reductive amination (39-73 %). After developing the protocol for the synthesis of racemic organoselenium amines, we studied the kinetic resolution of these compounds by their acetylation mediated by lipases. An initial study was carried out with the organoselenium amine para substituted, as a model substrate, in order to screen for appropriate lipase, solvent, temperature, lipase/substrate ratio and acylant. This study showed that the ideal condition to conduct the kinetic resolution was CAL-B as biocatalyst, hexane as solvent and ethyl acetate or ethyl methoxyacetate as acylant at 30°C. By using this protocol, the organoselenium amides were prepared in excellent enantiomeric excess (99 %).
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Almeida, Angelina Maria de. "Preparação e avaliações biológica e físico-química de novas aminas e amidas aromáticas anfifílicas." Universidade Federal de Juiz de Fora (UFJF), 2013. https://repositorio.ufjf.br/jspui/handle/ufjf/4326.

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CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Neste trabalho foram realizadas as sínteses de aminas e amidas aromáticas anfifílicas inéditas derivadas do Tris. A primeira série foi obtida através da reação de aminação redutiva de p- alquiloxibenzadeídos com o TRIS. A série das amidas foi obtida a partir do ácido p- alquiloxibenzóicos: esses foram convertidos a cloretos de acila e tratados com TRIS. As metodologias usadas foram simples e todos os compostos foram obtidos em rendimentos satisfatórios. Após purificação e caracterização através das técnicas espectroscópicas usuais (IV, RMN de ¹H e ¹³C e espectroscopia de massas). Os compostos sintetizados foram avaliados quanto as suas propriedades biológicas in vitro. A atividade antimicrobiana foi avaliada frente a bactérias Gram-positivas (ATCC e MRSA), bactérias Gram-negativas (ATCC) e fungos Candida. O potencial anti-inflamatório foi avaliado através da capacidade dos compostos de inibirem a produção de óxido nítrico por macrófagos ativados. A citotoxicidade foi investigada através do método do MTT. Os resultados obtidos mostraram que apenas as aminas foram ativas nos testes, com concentrações inibitórias mínimas comparáveis ou superiores as dos padrões usados como controle (cloranfenicol e itraconazol), e não apresentaram toxicidade nessas concentrações. Foi possível estabelecer uma boa correlação positiva entre a lipofilicidade dos compostos testados e a atividade antimicrobiana. Os estudos físico-químicos ainda estão em andamento com o intuito de estabelecer uma relação entre atividade biológica e propriedades surfactantes das novas aminas anfifílicas.
In this work were carried out the synthesis of novel amphiphilic aromatic amines and amides derived from Tris. The first set was obtained by reductive amination reaction of p- alkyloxybenzadehydes with TRIS. The series of amides was obtained starting from p- akyloxylbenzoic acid: these were converted to the acyl chlorides and treated with TRIS. The methodologies used were simple and all compounds were obtained in satisfactory yields. After purification and characterization through the usual spectroscopic techniques (IR, 1 H NMR, ¹³C NMR and mass spectroscopy), the synthesized compounds were evaluated for their biological properties in vitro. The antimicrobial activity was evaluated against Gram-positive bacteria (ATCC and MRSA), Gram-negative bacteria (ATCC) and fungi of Candida. The anti inflammatory potential was assessed by the ability of the compounds to inhibit nitric oxide production by activated macrophages. Cytotoxicity was assessed by the MTT method. The results showed that only the amines were active in the tests, with minimum inhibitory concentrations comparable or superior to the standards used as control (chloramphenicol and itraconazole), and showed no toxicity in these concentrations. It was possible to establish a good correlation between the lipophilicity of the tested compounds and the antimicrobial activity. The physico-chemical studies are still under going aiming to establish a relationship between the biological activity and the surfactant properties of the new amphiphilic amines.
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Thomson, Jaclyn Alexa. "Yttrium amidate complexes for the catalytic synthesis of biodegradable polymers and amides." Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/44266.

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Castagnaro, Denise. "Avaliação da interação entre aflatoxina M1 e B1 com a fração proteica do leite." Universidade Tecnológica Federal do Paraná, 2015. http://repositorio.utfpr.edu.br/jspui/handle/1/1538.

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Dissertação composta por 02 artigos.
CNPq; Capes
O leite é uma das principais fontes de nutrientes da dieta humana e é um alimento que acompanha o ser humano durante toda a vida, tanto como leite de consumo como através de seus derivados. Entretanto, são inúmeras as formas e os tipos de contaminação que acometem o leite, destacando-se, dentre os contaminantes de ordem química, as aflatoxinas. Dentre os métodos de análise de aflatoxinas em leite e derivados, destaca-se a Cromatografia Líquida de Alta Eficiência (CLAE), principalmente devido a sua versatilidade, rapidez e acuracidade das medidas quantitativas. Entretanto, trata-se de um sistema complexo em que as propriedades dos constituintes da fase móvel são afetadas por mudanças nas condições de processo nas quais são realizados os experimentos. Normalmente as condições de análise por CLAE são determinadas empiricamente, pelo método “tentativa e erro” em que inúmeras tentativas são realizadas sem um estudo mais detalhado do sistema. Diante disso, a primeira etapa deste estudo objetivou a otimização de multirrespostas em CLAE, por meio da seleção das condições ótimas como a composição da fase móvel, sua vazão no sistema cromatográfico e a temperatura da coluna, a fim de identificar, separar e quantificar simultaneamente a aflatoxina M1 (AFM1) e a aflatoxina B1 (AFB1). Para tanto, realizou-se planejamento experimental de misturas para três componentes com restrições combinado com um planejamento fatorial 22 para as variáveis de processo (temperatura da coluna e vazão). Após a definição dos modelos para as variáveis dependentes, foi realizada busca das condições ótimas usando o método simplex sequencial e as funções de desejabilidade de Derringer e Suich. As variáveis avaliadas foram: composição da fase móvel (acetonitrila, metanol e solução aquosa de ácido acético 1%), vazão da fase móvel e temperatura da coluna. Os parâmetros cromatográficos obtidos como respostas foram: tempo e fator de retenção para ambas as aflatoxinas, fator de separação, resolução da coluna e altura dos picos. Após a validação do planejamento, foi realizada a validação analítica do método otimizado através das figuras analíticas de mérito: linearidade, precisão, exatidão e limites de detecção e quantificação. O planejamento realizado foi capaz de produzir modelos confiáveis que possibilitaram a estimativa das melhores condições atendendo aos múltiplos objetivos. Na validação analítica do método cromatográfico, os parâmetros analíticos avaliados ficaram dentro dos intervalos de confiança, podendo o método ser considerado exato e preciso, apresentando limites de quantificação de 0,3 e 0,5 μg L-1 para AFM1 e AFB1, respectivamente e linearidade com R2 > 0,99 para ambas as aflatoxinas. A segunda etapa do estudo objetivou a avaliação da interação entre as AFM1 e AFB1 com proteínas lácteas, tendo em vista que estudos demonstram que aquelas, especialmente a AFM1, localizam-se predominantemente nas frações proteicas. Entretanto, esses estudos não avaliaram a interação entre aflatoxinas e as proteínas do leite, mas apenas baseiam-se na sua quantificação nas frações proteicas do leite. Portanto, buscou-se por meio deste estudo avaliar a possível interação entre as AFM1 e AFB1 com as frações proteicas do leite. Análises por Espectroscopia na região de infravermelho com transformada de Fourier (FTIR) foram realizadas para avaliação de possíveis modificações na estrutura secundária das proteínas lácteas quando fortificadas com as aflatoxinas e Calorimetria Exploratória Diferencial (DSC). Para tanto, preliminarmente foram avaliados os espectros obtidos com padrões de caseína e β-lactoglobulina em solução tampão fosfato-salino (PBS) e em solução modelo, assim como no leite propriamente dito, integral e desnatado. Na segunda etapa, regiões espectrais específicas foram avaliadas por meio de técnicas de deconvolução e curve-fitting. Os resultados indicam que a solução PBS foi mais adequada para o estudo da interação entre as AFB1 e AFM1 e proteínas lácteas avaliadas, β-lactoglobulina e caseína. Foram observadas alterações nas estruturas secundárias e essas sugerem que, embora possivelmente ocorram interações de caráter hidrofílico entre β-lactoglobulina e as aflatoxinas (especialmente com AFM1), ocorram também interações de caráter hidrofóbico (especialmente de AFB1) com os pacotes hidrofóbicos da β-lactoglobulina. Já com a caseína, as alterações promovidas nas estruturas secundárias proteicas foram mais discretas, porém deslocamentos de picos foram observados indicando alterações estruturais da proteína, especialmente na presença de AFB1, o que sugere que ocorram interações químicas entre os componentes avaliados. As alterações espectrais, mais evidentes com a fração β-lactoglobulina, do que com a fração caseína sugerem que, embora a quantificação de aflatoxinas seja comumente superior na fração caseína, não se pode afirmar que por esse motivo ocorram interações mais tangíveis entre aflatoxinas e caseína do que entre aflatoxinas e β-lactoglobulina. Possivelmente a quantificação em maior percentual de aflatoxinas na fração caseína é atribuída ao fato dessa proteína encontrar-se, no leite, em percentual superior às proteínas do soro. Outra hipótese levantada pelo estudo é a possibilidade das aflatoxinas avaliadas encontrarem-se “mascaradas” por estarem conjugadas com a β-lactoglobulina e não sendo, portanto, detectadas pelos métodos analíticos convencionais ocasionando sua subestimação nessa fração.
Milk is one of the main sources of nutrients in the human diet and is a food that accompanies the human being throughout life, both as drinking milk as through its derivatives. However, there are countless forms and types of contamination that affect milk, especially among the contaminants of chemical order, aflatoxins. Among the methods of analysis of aflatoxins in milk and dairy products, the High Performance Liquid Chromatography (HPLC) stands out mainly due to its versatility, speed and accuracy of quantitative measurements. However, it is a complex system in which the properties of the constituents of the mobile phase are affected by changes in process conditions under which the experiments are performed. Typically the HPLC analysis conditions are determined empirically, using the "trial and error" in which numerous attempts are made without a more detailed study of the system. Therefore, the first step of this aimed to optimize multiresponses in HPLC, by selecting the optimal conditions as the mobile phase composition, its flow into the chromatographic system and the column temperature in order to identify, separate and quantify aflatoxin M1 (AFM1) and aflatoxin B1 (AFB1) simultaneously. Therefore, it was carried out experimental a mixture design for three components with restrictions combined with a 22 factorial design to the process variables (flow and column temperature). After defining the models for the dependent variables, a search of the optimum conditions was made using the sequential simplex method and the Derringer and Suich desirability functions. The variables evaluated were: mobile phase composition (acetonitrile, methanol and aqueous solution of acetic acid 1%), the mobile phase flow rate and column temperature. The chromatographic parameters obtained as responses were time and factor of retention for both aflatoxins, separation factor, column resolution and height of the peaks. After the design validation, analytical validation was performed through the analytical figures of merit: linearity, precision, accuracy and limits of detection and quantification. The experimental design carried out was able to produce reliable models that allowed better conditions estimation regarding multiple objectives. In the analytical validation of the chromatographic method, the analytical parameters evaluated were within the confidence interval, the method can be considered accurate and precise showing quantitation limits of 0.3 and 0.5 μg L-1 for AFB1 and AFM1, respectively, and linearity with R2> 0.99 for both aflatoxins. The second stage of the study aimed to evaluate the interaction between the AFB1 and AFM1 with dairy proteins, considering that studies show that those, especially AFM1, are located predominantly in the protein fractions. However, these studies did not evaluate the possibility of interaction between aflatoxins and dairy proteins, but only based on its quantification in the dairy protein fractions. Therefore, we sought through this study to evaluate a possible interaction between AFM1 and AFB1 with dairy protein fractions. Analyzes were performed by Fourier transformation infrared spectroscopy (FTIR) to assess possible changes in the secondary structure of dairy proteins when spiked with aflatoxins and Differential Scanning Calorimetry (DSC). For this purpose, preliminarily the spectra obtained were evaluated with standard casein and β-lactoglobulin in phosphate buffer saline solution (PBS) and a bovine milk model solution as well as in actual milk, whole and skim. In the second step, specific spectra bands were assessed through deconvolution and curve-fitting techniques. The results show that PBS was more suitable for the interaction study between aflatoxins B1 and M1 and the dairy proteins evaluated, β-lactoglobulin and casein. Changes in secondary structures suggest that although possibly occurring interactions with hydrophilic characters between β-lactoglobulin and aflatoxins were observed (especially with AFM1) also occur interactions with hydrophobic character (especially AFB1) with the hydrophobic β-lactoglobulin packages. Already with the casein, the changes introduced in protein secondary structure were more discreet but peak shifts were observed indicating structural changes of the protein, especially in the presence of AFB1, which suggests that chemical interactions occur between the components evaluated. The spectral changes, more evident with the β-lactoglobulin fraction than the casein fraction, suggests that although the quantification of aflatoxins is commonly higher in the casein fraction, it’s not possible to ensure that for this reason occur more tangible interactions between aflatoxins and casein than between aflatoxins and whey proteins (β-lactoglobulin). The greater quantify percentage of aflatoxins in the casein fraction, apparently, is attributed to the fact that this protein is found, in milk, in superior percentage to the whey proteins. Another hypothesis is the possibility of the aflatoxins evaluated are "masked" by being combined with β-lactoglobulin and not, therefore, being detected by conventional analytical methods leading to their underestimation in this fraction.
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Navas, Escrig Javier. "NANOPARTÍCULAS Y CLÚSTERES METÁLICOS SOPORTADOS PARA LA FORMACIÓN DE ENLACES C-O, C-N, C-S Y S-S." Doctoral thesis, Universitat Politècnica de València, 2016. http://hdl.handle.net/10251/64077.

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[EN] During the work done in this thesis, new catalysts based on metallic nanoparticles and clusters supported on materials with different properties have been designed and developed trying to improve their stability and potentiate their catalytic activity. For this reason, different physical and chemical properties (oxidation state, particle size, etc.) have been studied for each catalyst and, besides, mechanistic studies needed to optimize the performance of these materials in a specific reaction under the best possible experimental reaction conditions have been carried out. In particular, chapters 3, 4 and 5 have been focused on the development of catalysts based on Au, Pd and CuO supported nanoparticles for the synthesis of organic compounds of interest in different fields. Specifically, it's been possible to synthesize secondary amines, propargilamines, thioethers and amides with good yields, through sustainable methodologies like the hydrogen autotransfer or the oxidative amidation with molecular oxygen as the oxidant agent. Besides, re-use of the different nanocatalysts has been evaluated systematically (aspect of great relevance from the industrial point of view), and also the scope of the reaction by using as starting materials reactants with different substituent groups in each reaction. Finally, chapter 6 has been focused on the study of the catalytic activity presented by Au clusters supported on multi-walled carbon nanotubes (MWCNTs) in the formation of diphenyldisulfide starting from benzenethiol. It's been demonstrated that the number of atoms that formed the cluster has a strong influence on its activity. Specifically, the catalyst shows high activities when the metallic cluster contains a number of atoms in the range between 5 and 10 atoms, while lower or higher cluster atomicities are associated to induction periods or inactive catalysts. The explanation resides in the activation capacity of the reactants presented by the metallic clusters with atomicities inside the aforementioned range or interval, needed for reaction to take place.
[ES] Durante el trabajo realizado en la presente tesis doctoral, se han diseñado y desarrollado catalizadores basados en nanopartículas y clústeres metálicos soportados sobre materiales de diferente naturaleza con objeto de mejorar su estabilidad y potenciar su actividad catalítica. Para ello, se han estudiado las características físico-químicas (estado de oxidación, tamaño de partícula, etc.) de cada catalizador, además de llevar a cabo estudios mecanísticos necesarios para optimizar el desempeño de estos materiales en una determinada reacción en las mejores condiciones experimentales posibles. En particular, los capítulos 3, 4 y 5 se han centrado en el desarrollo de catalizadores basados en nanopartículas soportadas de Au, Pd y CuO para la síntesis de compuestos orgánicos de interés. En concreto, ha sido posible obtener con buenos rendimientos aminas secundarias, propargilaminas, tioéteres y amidas, a través de metodologías sostenibles como la autotransferencia de hidrógeno o la amidación oxidativa empleando oxígeno como agente oxidante. Además, se ha evaluado la reutilización de los catalizadores basados en nanopartículas de forma sistemática (aspecto de gran relevancia desde el punto de vista industrial), así como la generalidad de su uso introduciendo diferentes grupos sustituyentes en los sustratos de partida en cada reacción en particular. Por último, el capítulo 6 se ha centrado en el estudio de la actividad catalítica presentada por clústeres de Au soportados sobre nanotubos de carbono de pared múltiple (MWCNTs) en la formación de difenildisulfuro partiendo de bencenotiol. Se ha podido comprobar como el número de átomos que componen el clúster influye drásticamente en su actividad. En concreto, el catalizador presenta elevadas actividades cuando el clúster contiene un conjunto de átomos dentro de un rango comprendido entre 5-10 átomos, mientras que atomicidades de clúster inferiores o superiores dan lugar a la aparición de periodos de inducción o a catalizadores inactivos. La explicación radica en la capacidad de activación de los reactivos presentada por los clústeres con atomicidades dentro del citado rango o intervalo, necesaria para que la reacción pueda tener lugar.
[CAT] Durant el treball realitzat en la present tesi doctoral, s'han dissenyat i desenvolupat catalitzadors basats en nanopartícules i clústers metàl·lics suportats sobre materials de diferent naturalesa, amb l'objectiu de millorar la seua estabilitat i potenciar l'activitat catalítica. Per aquest motiu, s'han estudiat les característiques físico-químiques (estats d'oxidació, grandària de partícula, etc.) de cada catalitzador, a més de dur a terme estudis mecanístics necessaris per optimitzar la utilització d'aquests materials en una determinada reacció en les millors condicions possibles. En particular, els capítols 3, 4, i 5 s'han centrat en el desenvolupament de nanopartícules suportades de Au, Pd i CuO per a la síntesis de compostos orgànics d'interès. Mes concretament, ha sigut possible obtenir bons rendiments a amines secundaries, propargilamines, tioeters i amides, mitjançant metodologies sostenibles como la autotransferència d'hidrogen o la amidació oxidativa amb l'ús d'oxigen com agent oxidant. A més, s'han avaluat la re-utilització dels catalitzadors basats en nanopartícules de manera sistemàtica (aspecte de gran rellevància des del punt de vista industrial), així com la generalitat del seu us mitjançant la introducció de diferents grups substituents en els substrats de partida de cada reacció en particular. Per últim, el capítol 6 s'ha centrat en l'estudi de l'activitat catalítica presentada per clústers d'Au suportats sobre nanotubs de carboni de paret múltiple (MWCNTs) en la formació de disulfurs amb l'ús de bencenotiol de partida. S'ha pogut comprovar com el nombre d'àtoms que constitueixen el clúster influeix de manera dràstica en la seu activitat. Particularment, el catalitzador presenta elevades activitats quan el clústers esta constituït per un conjunt d'àtoms dins el rang comprés entre 5 i 10 àtoms, mentre que atomicitats de clúster inferiors i superiors donen lloc a l'aparició de períodes d'inducció o catalitzadors inactius. L'explicació radica en la capacitat d'activació dels reactius presentada pels clústers amb una atomicitat dins l'esmentat rang o interval, necessària per a que la reacció puga tindre lloc.
Navas Escrig, J. (2016). NANOPARTÍCULAS Y CLÚSTERES METÁLICOS SOPORTADOS PARA LA FORMACIÓN DE ENLACES C-O, C-N, C-S Y S-S [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/64077
TESIS
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7

Silva, Luana. "Síntese de glicosil amidas e glicoconjugação via utilização de selenocarboxilatos como reagentes traceless." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2016. http://hdl.handle.net/10183/143838.

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A química de carboidratos têm sido um importante link entre a síntese orgânica, a biologia e a química medicinal devido ao papel fundamental que açúcares apresentam na glicobiologia. Neste contexto, a ligação amida glicosídica é uma importante conexão encontrada na natureza, sendo uma das formas de ligar um núcleo de carboidrato a outras biomoléculas e produtos naturais, como glicopeptídeos e N-glicosil amidas. Dessa forma, o desenvolvimento de métodos sintéticos para a introdução de núcleos de carboidratos em diferentes estruturas é fundamental. Tendo em vista o interesse do nosso grupo de pesquisa em desenvolver novas estratégias utilizando a química de selênio na funcionalização de derivados de carboidratos, o presente projeto descreve uma metodologia de síntese de N-glicosil amidas e de glicoconjugação via formação de ligação amida, envolvendo a reação entre selenocarboxilatos, gerados in situ, com azidas glicosídicas. Foi possível sintetizar com sucesso uma série de derivados de carboidratos, para uma variedade de substratos que incluíram: N-glicosil amidas furanosídicas (20 exemplos), piranosídicas (13 exemplos) e também N-glicoconjugados graxos (10 exemplos). A metodologia foi baseada na geração in situ de selenocarboxilatos de lítio, a partir de Se0/ LiEt3BH e derivados de ácidos carboxílicos, e suas reações com azidas derivadas de açúcares. Um aspecto importante deste protocolo é que a reação se inicia com selênio elementar e apresenta como subprodutos N2 e Se0. O isolamento e manipulação de espécies intermediárias reativas de selênio são evitadas durante o curso reacional, conferindo ao selenocarboxilato o status de reagente traceless.
Carbohydrate chemistry has been an important link between organic synthesis, biology and medicinal chemistry due to the fundamental roles that sugars play in glycobiology. In this context, the glycosyl amide linkage is an important connection found in nature, since it is one of the ways in which a sugar unit can be found attached to other biomolecules and natural products, such as N-glycosyl amides and glycopeptides that are known for possessing a wide range of bioactivities. Therefore, the development of synthetic methods for the introduction of sugar moieties into various different scaffolds is of paramount importance. In connection with our interest on the development of new strategies using selenium chemistry for the functionalization of carbohydrate derivatives, we describe herein an efficient synthesis of glycosyl amides and glycoconjugation methodology via amide bond-formation, enabled by the reaction of in situ generated selenocarboxylates with glycosyl azides. Carbohydrate-derived amides were successfully prepared in good yields for a broad range of substrates, including: furanosyl (20 examples), pyranosyl (13 examples) N-glycosil amides derivatives and also fatty acids glycoconjugates (10 examples). The methodology relied in the in situ generation of lithium selenocarboxylates, from Se/LiEt3BH and acyl chlorides or carboxylic acids and their reaction with sugar azides. A key aspect of the present protocol is that we start from elemental selenium and as by-products we have harmless gaseous nitrogen and elemental selenium. Isolation and handling of all reactive and sensitive seleniumcontaining intermediates is avoided, therefore assigning to the selenocarboxylate the status of a traceless reagent.
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Silva, Aline Hara da. "Nanocompósitos de amido termoplástico contendo hidróxidos duplos lamelares." reponame:Repositório Institucional da UFPR, 2013. http://hdl.handle.net/1884/31749.

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Resumo: Neste trabalho investigou-se o efeito da adição de nanopartículas inorgânicas, no caso os hidróxidos duplos lamelares contendo ânions orgânicos intercalados, com a matriz polimérica do amido de mandioca plastificada com glicerol. O objetivo consiste em produzir um polímero totalmente biodegradável e de baixo custo para potencialmente substituir os polímeros convencionais. Os hidróxidos duplos lamelares estudados foram sintetizados em razões molares Zn: Al de 2:1, 3:1 e 4:1 utilizando dois métodos, a co-precipitação direta e a troca iônica. Os ânions intercalados foram o salicilato, o citrato, o gluconato e o mucicato, sendo que os nanocompósitos de amido termoplástico foram preparados somente com o ânion salicilato. Os nanocompósitos foram obtidos pela mistura do amido com o glicerol (plastificante) e as cargas e os corpos de prova foram obtidos por e extrusão e injeção e acondicionados em uma umidade controlada de 30%. Os materiais foram investigados por difração de raios X (XRD), espectroscopia vibracional na região do infravermelho (FTIR), espectroscopia fotoeletrônica de raios X (XPS), análise térmica (TGA/DTA) e ensaios mecânicos. Em geral as análises mostraram que os HDLs sintetizados apresentam dimensões nanométricas, em geral o biopolímero não apresentou melhoras significativas com relação a suas propriedades mecânicas, quando comparado ao do amido termoplástico puro. Isso se deve provavelmente à baixa interação entre carga e a matriz polimérica.
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Cardoso, Valéria Maria de Oliveira Cardoso [UNESP]. "Síntese e caracterização de hidrogéis de amido retrogradado e goma gelana utilizados como matriz em sistemas de liberação cólon específica de fármacos." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/122044.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
O amido resistente é um polissacarídeo que apresenta elevada estabilidade térmica e baixa solubilidade. A gelana é um polissacarídeo natural com importantes propriedades bioadesivas. Ambos os polímeros podem formar hidrogéis capazes de controlar a liberação de fármacos. A associação desses polissacarídeos naturais pode permitir o aperfeiçoamento das características físico-químicas desses materiais que muitas vezes são inexistentes nos polímeros isolados. A mistura de gelana/amido retrogradado, bem como a reticulação desses polímeros bioadesivos permite a modificação de importantes propriedades como resistência mecânica, intumescimento e mucoadesividade e desta forma, representam uma estratégia importante para aperfeiçoar o desempenho de sistemas de liberação sítio-específica de fármacos. No presente trabalho, hidrogéis de gelana/amido retrogradado foram utilizadas para obtenção de micropartículas pelo método de geleificação ionotrópica ou reticulação iônica (interações entre íons de cargas opostas) e dupla reticulação (introdução de ligações covalentes). A caracterização físico-química dos hidrogéis foi realizada através das análises de textura (dureza, adesividade e coesividade), propriedades reológicas, morfologia e difração de raiosx. Na análise do comportamento de textura foi verificado que as maiores concentrações de polímeros melhoraram as propriedades mecânicas dos hidrogéis e que a reticulação iônica contribuiu para o aumento da dureza e coesividade, enquanto a dupla reticulação aumentou a adesividade. A análise reológica demonstrou que as técnicas de reticulação contribuíram para obtenção de sistemas de caráter predominantemente elástico, sendo que a dupla reticulação originou estruturas com maior grau de elasticidade. As análises da estrutura interna dos hidrogéis evidenciaram a formação de estruturas mais densas e compactas na presença do ...
Resistant starch exhibits high thermal stability and low solubility. Gellan gum is a natural polysaccharide with important bioadhesive properties. Both polymers can build hydrogels able to control drug release rates. The blending of these natural polysaccharides can improve the physicochemical characteristics of these materials that are often absent in the isolated polymers. Gellan gum/retrograded starch association and crosslinking reaction should promote important modification of properties of these materials such as mechanical strength, swelling and mucoadhesiveness and thus, these strategies can improve the performance of site-specific drug delivery systems. In this study, hydrogels of gellan gum/retrograded starch were used to obtain microparticles by ionotropic gelation or ionic crosslinking (interactions between oppositely charged ions) and dual crosslinking (introducing covalent bonds) methods. The physicochemical characterization of the hydrogels was performed by analysis of profile (hardness, adhesiveness and cohesiveness), rheological properties, morphology and X-ray diffraction. Texture analysis of the behavior was found that higher concentrations of polymer improved the mechanical properties of hydrogels and that the ionic crosslinking improved the hardness and cohesiveness of hydrogels, while the dual crosslinking increased adhesiveness. The set of rheological properties showed that the crosslinking techniques contributed to the elastic character of the systems, and the dual crosslinking originated structures with the most elasticity degree. SEM analysis showed that denser and more packed structures were built in the presence of the ketoprofen. According to the XRD data, the microparticles showed semicrystalline structures and the DR increased the crystallinity. Physicochemical characterization of microparticles was performed by analyzes as moisture content, yield, encapsulation efficiency, size and shape. Ionotropic ...
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10

Cardoso, Valéria Maria de Oliveira Cardoso. "Síntese e caracterização de hidrogéis de amido retrogradado e goma gelana utilizados como matriz em sistemas de liberação cólon específica de fármacos /." Araraquara, 2014. http://hdl.handle.net/11449/122044.

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Orientador: Beatriz Stringhetti Ferreira Cury
Banca: Ana Dóris de Castro
Banca: Ruth Meri Lucinda Silva
Resumo: O amido resistente é um polissacarídeo que apresenta elevada estabilidade térmica e baixa solubilidade. A gelana é um polissacarídeo natural com importantes propriedades bioadesivas. Ambos os polímeros podem formar hidrogéis capazes de controlar a liberação de fármacos. A associação desses polissacarídeos naturais pode permitir o aperfeiçoamento das características físico-químicas desses materiais que muitas vezes são inexistentes nos polímeros isolados. A mistura de gelana/amido retrogradado, bem como a reticulação desses polímeros bioadesivos permite a modificação de importantes propriedades como resistência mecânica, intumescimento e mucoadesividade e desta forma, representam uma estratégia importante para aperfeiçoar o desempenho de sistemas de liberação sítio-específica de fármacos. No presente trabalho, hidrogéis de gelana/amido retrogradado foram utilizadas para obtenção de micropartículas pelo método de geleificação ionotrópica ou reticulação iônica (interações entre íons de cargas opostas) e dupla reticulação (introdução de ligações covalentes). A caracterização físico-química dos hidrogéis foi realizada através das análises de textura (dureza, adesividade e coesividade), propriedades reológicas, morfologia e difração de raiosx. Na análise do comportamento de textura foi verificado que as maiores concentrações de polímeros melhoraram as propriedades mecânicas dos hidrogéis e que a reticulação iônica contribuiu para o aumento da dureza e coesividade, enquanto a dupla reticulação aumentou a adesividade. A análise reológica demonstrou que as técnicas de reticulação contribuíram para obtenção de sistemas de caráter predominantemente elástico, sendo que a dupla reticulação originou estruturas com maior grau de elasticidade. As análises da estrutura interna dos hidrogéis evidenciaram a formação de estruturas mais densas e compactas na presença do ...
Abstract: Resistant starch exhibits high thermal stability and low solubility. Gellan gum is a natural polysaccharide with important bioadhesive properties. Both polymers can build hydrogels able to control drug release rates. The blending of these natural polysaccharides can improve the physicochemical characteristics of these materials that are often absent in the isolated polymers. Gellan gum/retrograded starch association and crosslinking reaction should promote important modification of properties of these materials such as mechanical strength, swelling and mucoadhesiveness and thus, these strategies can improve the performance of site-specific drug delivery systems. In this study, hydrogels of gellan gum/retrograded starch were used to obtain microparticles by ionotropic gelation or ionic crosslinking (interactions between oppositely charged ions) and dual crosslinking (introducing covalent bonds) methods. The physicochemical characterization of the hydrogels was performed by analysis of profile (hardness, adhesiveness and cohesiveness), rheological properties, morphology and X-ray diffraction. Texture analysis of the behavior was found that higher concentrations of polymer improved the mechanical properties of hydrogels and that the ionic crosslinking improved the hardness and cohesiveness of hydrogels, while the dual crosslinking increased adhesiveness. The set of rheological properties showed that the crosslinking techniques contributed to the elastic character of the systems, and the dual crosslinking originated structures with the most elasticity degree. SEM analysis showed that denser and more packed structures were built in the presence of the ketoprofen. According to the XRD data, the microparticles showed semicrystalline structures and the DR increased the crystallinity. Physicochemical characterization of microparticles was performed by analyzes as moisture content, yield, encapsulation efficiency, size and shape. Ionotropic ...
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Books on the topic "Amidah"

1

Belson, Mark. Silent Amidah: A remembrance. Henley Beach, SA, Australia: Seaview Press, 1999.

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Fridlander, Ḥayim ben Mosheh. Sefer Śifte Ḥayim: Rinat Ḥayim : beʼure tefilat Shemoneh ʻeśreh. Bene Beraḳ: ha-Rabanit Frindlander, 2007.

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Plisḳin, Mosheh Mordekhai. Sefer Lev Betsalʼel: Perushim, beʼurim, ḥidushim ṿe-heʼarot be-seder tefilat Shemoneh ʻeśreh li-yemot ha-ḥol. Ashdod: Mekhon Binyan śimḥah, 1998.

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Leff, Zev. Shemoneh esrei: The depth and beauty of our daily tefillah. Southfield, MI: Targum Press, 2008.

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Ḥayim ben Shalom Eliʻezer Herbsṭ. Sefer Nafshi ḥolat ahavatekha: Leḳeṭ diburim ḳedoshim me-Ḥazal ha-ḳedoshim ... Yerushalayim: Mishpaḥat Herbsṭ, 2000.

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Birnbaum, Mayer. Kụntṛes ʻAvodat ha-tefilah: Shalosh regalim : kolel perush ʻal derekh ha-peshat ̣ʻal ... ha-ʻamidah shel ha-Shalosh regalim : vẹ-gam Maʾamre ha-moʻadim. Passaic, N.Y. (81 Ascension St., Passaic 07055): M. ha-Levị Birnboim, 1998.

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Herbsṭ, Ḥayim ben Shalom Eliʻezer. Sefer Nafshi ḥolat ahavatekha: Leḳeṭ diburim ḳedoshim me-Ḥazal ha-ḳedoshim ... ʻarukh u-mesudar ʻal Pesuḳe de-zimrah ... Yerushalayim: Ḥayim ben Shalom Eliʻezer Herbsṭ, 2002.

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Fridlander, Ḥayim ben Mosheh. Sefer Śifte Ḥayim: Midot ṿa-ʻavodat H. : pirḳe hadrakhah be-midot uva-ʻavodat Eloḳim ḥayim ... Bene Beraḳ: ha-Rabanit Fridlander, 2003.

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Birnbaum, Mayer. Kụntṛes ʻAvodat ha-tefilah: Shalosh regalim : kolel perush ʻal derekh ha-peshat ̣ʻal ... ha-ʻamidah shel ha-Shalosh regalim : vẹ-gam Maʾamre ha-moʻadim. Passaic, N.Y. (81 Ascension St., Passaic 07055): M. ha-Levị Birnboim, 1998.

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Fridlander, Ḥayim ben Mosheh. Sefer Śifte Ḥayim: Rinat ḥayim - beʼure tefilah : Birkhot ha-shaḥar, Pesuḳe de-zimrah, Keriʼat shemaʻ, Ḳ. sh., Ashre, ʻAlenu le-shabeaḥ. Bene Beraḳ: [ha-Rabanit Fridlander], 2012.

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Book chapters on the topic "Amidah"

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Tabory, Joseph. "The Rabbinic Traditions about the Establishment of the Amidah: Some Observations." In On Wings of Prayer, edited by Nuria Calduch-Benages, Michael W. Duggan, and Dalia Marx, 337–54. Berlin, Boston: De Gruyter, 2019. http://dx.doi.org/10.1515/9783110630282-021.

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Schomburg, Dietmar, and Margit Salzmann. "Amidase." In Enzyme Handbook 4, 667–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84437-9_122.

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Paulus, Wilfried. "Amides." In Microbicides for the Protection of Materials, 241–64. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2118-7_10.

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Gooch, Jan W. "Amides." In Encyclopedic Dictionary of Polymers, 33. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_546.

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Paulus, Wilfried. "Amides." In Directory of Microbicides for the Protection of Materials, 608–18. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/1-4020-2818-0_33.

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Smith, Robert M., and Arthur E. Martell. "Amides." In Critical Stability Constants, 423–25. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4615-6764-6_23.

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"IV. Short 'Amidah." In Studies in Jewish Liturgy, edited by Abraham I. Schechter, 91–92. Piscataway, NJ, USA: Gorgias Press, 2010. http://dx.doi.org/10.31826/9781463226350-022.

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"The Weekday Amidah." In Literature of the Synagogue, 29–36. Piscataway, NJ, USA: Gorgias Press, 2006. http://dx.doi.org/10.31826/9781463211110-009.

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"Interpretation of the Amidah Prayer." In Rabbi Joseph Dov Soloveitchik on the Experience of Prayer, 349–98. Academic Studies Press, 2019. http://dx.doi.org/10.2307/j.ctv1zjg21k.14.

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"XVII. 'Amidah for the Sabbath Minḥah." In Studies in Jewish Liturgy, edited by Abraham I. Schechter, 114. Piscataway, NJ, USA: Gorgias Press, 2010. http://dx.doi.org/10.31826/9781463226350-031.

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Conference papers on the topic "Amidah"

1

Maxman, Tobaron. "Amidah." In ACM SIGGRAPH ASIA 2009 Art Gallery & Emerging Technologies: Adaptation. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1665137.1665162.

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Ishio, Takashi, Yui Watanabe, and Katsuro Inoue. "AMIDA." In Companion of the 13th international conference. New York, New York, USA: ACM Press, 2008. http://dx.doi.org/10.1145/1370175.1370212.

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Nettleton, Donna, and Richard Groenwald. "AMIDARS Flight Performance." In 32nd Annual Technical Symposium, edited by Paul A. Henkel, Francis R. LaGesse, and Wayne W. Schurter. SPIE, 1989. http://dx.doi.org/10.1117/12.948609.

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Kikuchi, Hiroaki, Kota Sasa, and Yuta Shimizu. "Interactive History Sniffing Attack with Amida Lottery." In 2016 10th International Conference on Innovative Mobile and Internet Services in Ubiquitous Computing (IMIS). IEEE, 2016. http://dx.doi.org/10.1109/imis.2016.109.

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Döbrich, Stefan, and Christian Hochber. "Effects of Simplistic Online Synthesis for AMIDAR Processors." In 2009 International Conference on Reconfigurable Computing and FPGAs (ReConFig). IEEE, 2009. http://dx.doi.org/10.1109/reconfig.2009.21.

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Hochberger, Christian, Lukas Johannes Jung, Andreas Engel, and Andreas Koch. "Synthilation: JIT-compilation of microinstruction sequences in AMIDAR processors." In 2014 Conference on Design and Architectures for Signal and Image Processing (DASIP). IEEE, 2014. http://dx.doi.org/10.1109/dasip.2014.7115634.

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Albu, Felix. "Fast recursive AMIPAP algorithm." In 2015 7th International Conference on Electronics, Computers and Artificial Intelligence (ECAI). IEEE, 2015. http://dx.doi.org/10.1109/ecai.2015.7301213.

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Renals, Steve, Thomas Hain, and Herve Bourlard. "Interpretation of Multiparty Meetings the AMI and Amida Projects." In 2008 Hands-Free Speech Communication and Microphone Arrays (HSCMA 2008). IEEE, 2008. http://dx.doi.org/10.1109/hscma.2008.4538700.

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Venkitasubramaniam, Parv, and Lang Tong. "Anonymous networking amidst active adversaries." In MILCOM 2009 - 2009 IEEE Military Communications Conference. IEEE, 2009. http://dx.doi.org/10.1109/milcom.2009.5379947.

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Gopalakrishnan, Ganesh, Ignacio Laguna, Ang Li, Pavel Panchekha, Cindy Rubio-Gonzalez, and Zachary Tatlock. "Guarding Numerics Amidst Rising Heterogeneity." In 2021 IEEE/ACM 5th International Workshop on Software Correctness for HPC Applications (Correctness). IEEE, 2021. http://dx.doi.org/10.1109/correctness54621.2021.00007.

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Reports on the topic "Amidah"

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Niles, Keron. Resilience Amidst Rising Tides. Geneva, Switzerland: International Centre for Trade and Sustainable Development, 2010. http://dx.doi.org/10.7215/co_ip_20100224.

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Roy, Denny. China-Japan Relations: Cooperation Amidst Antagonism. Fort Belvoir, VA: Defense Technical Information Center, October 2004. http://dx.doi.org/10.21236/ada627502.

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Dutra, Achilles, Iranildes Santos, Caroline Brigido, and Flavio Lemos. Projeto desenvolvimento de processo eletroquímico para tratamento de efluente do armazém de fertilizantes do porto de Tubarão/ES e de rejeito de minério de ferro (eletro-amido-amina). ITV, 2021. http://dx.doi.org/10.29223/prod.tec.itv.mi.2021.14.dutra.

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Lin, Terri C. Poly(amido amine) Dendrimers in Supercapacitors. Office of Scientific and Technical Information (OSTI), August 2013. http://dx.doi.org/10.2172/1091321.

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Whitaker, Craig, Jay R. Heckert, and Ian C. Uber. Synthesis of Amide Functionalized Carbon Nanotubes. Fort Belvoir, VA: Defense Technical Information Center, January 2007. http://dx.doi.org/10.21236/ada519137.

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Glardon, Thomas L. Balancing U.S. Interests Amidst the India and Pakistan Conflict. Fort Belvoir, VA: Defense Technical Information Center, April 2005. http://dx.doi.org/10.21236/ada432021.

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Brown, Sylvester H. The Army Reserve Meeting Homeland Security Obligations Amidst Transformation. Fort Belvoir, VA: Defense Technical Information Center, February 2008. http://dx.doi.org/10.21236/ada478342.

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McCall, Jamie, Khaliid Scott, and Urmi Bhatt. Small Business Stories: Surviving and Thriving Amidst the Pandemic. Carolina Small Business Development Fund, August 2021. http://dx.doi.org/10.46712/covid.stories.

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Abstract:
The COVID-19 pandemic will leave an enduring mark on North Carolina’s small business community. Using a phenomenological framework, we conducted a series of in-depth semi-structured interviews with small business owners about how they addressed the pandemic’s challenges. Four central themes emerged that illustrate the complexity and nuance of small business resiliency. Our data suggest that to survive and thrive, entrepreneurs had to: (1) be adaptable and willing to pivot, (2) have an entrepreneurial spirit, (3) leverage their social capital, and (4) have the knowledge and ability to apply for aid programs.
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Velarde, O., F. Bernete, and B. Casas-Mas. Las interacciones virtuales con personas conocidas que no son amigas. Revista Latina de Comunicación Social, March 2019. http://dx.doi.org/10.4185/rlcs-2019-1351.

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Bleakley, Hoyt, Louis Cain, and Joseph Ferrie. Amidst Poverty and Prejudice: Black and Irish Civil War Veterans. Cambridge, MA: National Bureau of Economic Research, October 2013. http://dx.doi.org/10.3386/w19605.

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