Relevant bibliographies by topics / Organic green chemistry

Academic literature on the topic 'Organic green chemistry'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Organic green chemistry"

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Das, Ananya, Abir Sadhukhan, Soumallya Chakraborty, Somenath Bhattacharya, Dr Amitava Roy, and Dr Arin Bhattacharjee. "Role of Green Chemistry in Organic Synthesis and Protection of Environment." International Journal for Research in Applied Science and Engineering Technology 10, no. 12 (December 31, 2022): 1850–53. http://dx.doi.org/10.22214/ijraset.2022.48373.

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Abstract: Nowadays green chemistry plays a vital role in organic chemistry. It minimizes the effect and use of hazardous substances on the environment and human health. The main goal of green chemistry is to use of green solvents (PEG, water, acetone, alcohol) eliminate the toxicity, uses of small quantity of catalyst and minimize the potential for chemical accident during work. Green chemistry is one type of chemistry where main focus is to eliminate or minimize the hazards by applying suitable process and raw materials. So it is more effective to pharmacists or chemists for avoiding this bad impact on human health, environment. Green chemistry also known as sustainable chemistry. Green chemistry is always interesting matter to pharmacists as well as chemists for synthesis pharmaceutical products. Green chemistry brings a new path for synthesizing safer chemical products. For manufacturing pharmaceutical products by using green chemistry, there have many criteria or methods that should be followed for synthesis chemical products during manufacturing condition. Some of these are prevention waste, Atom economy, less hazardous chemical syntheses, designing safer chemicals, safer solvents, design for more energy efficient chemical, use of renewable feed stocks, reduce derivatives in any compounds, catalysis, design for degradation, real time analysis for pollution prevention, inherently safer for accident prevention, etc. These methods should be considerable before synthesized chemical products by applying green chemistry for eliminating or minimizing hazardous in chemical products during synthesis.
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Mishra, Dr Sudhir Kumar. "Green Chemistry in Organic Synthesis." International Journal For Multidisciplinary Research 04, no. 01 (2022): 14–35. http://dx.doi.org/10.36948/ijfmr.2022.v04i01.003.

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The development of the concepts for “Green Chemistry” and the main principles of this field are reviewed. Examples of the application of these principles in different areas of chemistry are included. The frequently used alternative solvents (green solvents – water, PEG, perfluorinated solvents, supercritical liquids) in preparative organic chemistry are described. The present and the future developments of green chemistry in education and organic chemical technology are considered.
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Rubab, Laila, Ayesha Anum, Sami A. Al-Hussain, Ali Irfan, Sajjad Ahmad, Sami Ullah, Aamal A. Al-Mutairi, and Magdi E. A. Zaki. "Green Chemistry in Organic Synthesis: Recent Update on Green Catalytic Approaches in Synthesis of 1,2,4-Thiadiazoles." Catalysts 12, no. 11 (October 29, 2022): 1329. http://dx.doi.org/10.3390/catal12111329.

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Green (sustainable) chemistry provides a framework for chemists, pharmacists, medicinal chemists and chemical engineers to design processes, protocols and synthetic methodologies to make their contribution to the broad spectrum of global sustainability. Green synthetic conditions, especially catalysis, are the pillar of green chemistry. Green chemistry principles help synthetic chemists overcome the problems of conventional synthesis, such as slow reaction rates, unhealthy solvents and catalysts and the long duration of reaction completion time, and envision solutions by developing environmentally benign catalysts, green solvents, use of microwave and ultrasonic radiations, solvent-free, grinding and chemo-mechanical approaches. 1,2,4-thiadiazole is a privileged structural motif that belongs to the class of nitrogen–sulfur-containing heterocycles with diverse medicinal and pharmaceutical applications. This comprehensive review systemizes types of green solvents, green catalysts, ideal green organic synthesis characteristics and the green synthetic approaches, such as microwave irradiation, ultrasound, ionic liquids, solvent-free, metal-free conditions, green solvents and heterogeneous catalysis to construct different 1,2,4-thiadiazoles scaffolds.
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Vaccaro, Luigi. "Green chemistry." Beilstein Journal of Organic Chemistry 12 (December 15, 2016): 2763–65. http://dx.doi.org/10.3762/bjoc.12.273.

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Kaur, Navjeet. "Photochemical Reactions for the Synthesis of Six-Membered O-Heterocycles." Current Organic Synthesis 15, no. 3 (April 27, 2018): 298–320. http://dx.doi.org/10.2174/1570179414666171011160355.

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Background: The chemists have been interested in light as an energy source to induce chemical reactions since the beginning of the scientific chemistry. This review summarizes the chemistry of photochemical reactions with emphasis of their synthetic applications. The organic photochemical reactions avoid the polluting or toxic reagents and therefore offer perspectives for sustainable processes and green chemistry. In summary, this review article describes the synthesis of a number of six-membered O-heterocycles. Objective: Photochemistry is indeed a great tool synthetic chemists have at their disposal. The formation of byproducts was diminished under photochemical substrate activation that usually occurred without additional reagents. Photochemical irradiation is becoming more interesting day by day because of easy purification of the products as well as green chemistry. Conclusion: This review article represents the high applicability of photochemical reactions for organic synthesis and research activities in organic photochemistry. The synthesis of heterocyclic molecules has been outlined in this review. Traditional approaches require expensive or highly specialized equipment or would be of limited use to the synthetic organic chemist due to their highly inconvenient approaches. Photochemistry can be used to prepare a number of heterocycles selectively, efficiently and in high yield.
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Johnson, Sasha, Megan Meyers, Samantha Hyme, and Alexey Leontyev. "Green Chemistry Coverage in Organic Chemistry Textbooks." Journal of Chemical Education 97, no. 2 (December 18, 2019): 383–89. http://dx.doi.org/10.1021/acs.jchemed.9b00397.

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Burke, Daniel J., and Darren J. Lipomi. "Green chemistry for organic solar cells." Energy & Environmental Science 6, no. 7 (2013): 2053. http://dx.doi.org/10.1039/c3ee41096j.

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Sahoo, Tejaswini, Jagannath Panda, Jnanaranjan Sahu, Dayananda Sarangi, Sunil K. Sahoo, Braja B. Nanda, and Rojalin Sahu. "Green Solvent: Green Shadow on Chemical Synthesis." Current Organic Synthesis 17, no. 6 (September 25, 2020): 426–39. http://dx.doi.org/10.2174/1570179417666200506102535.

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The natural beauty and purity of our planet has been contaminated deeply due to human selfish activities such as pollution, improper waste management, and various industrial and commercial discharges of untreated toxic by-products into the lap of nature. The collective impact of these hazardous suspensions into the natural habitat is very deadly. Challenges due to human activity on the environment have become ubiquitous. The chemical industry has a major role in human evolution and, predictably, opened gates of increased risk of pollution if the production is not done sustainably. In these circumstances, the notion of Green Chemistry has been identified as the efficient medium of synthesis of chemicals and procedures to eradicate the toxic production of harmful substances. Principles of Green Chemistry guide the scientist in their hunt towards chemical synthesis which requires the use of solvents. These solvents contaminate our air, water, land and surrounding due to its toxic properties. Even though sufficient precautions are taken for proper disposal of these solvents but it is difficult to be recycled. In order to preserve our future and coming generation from the adverse impacts associated with solvents it is very important to find alternative of this which will be easy to use, reusable and also eco-friendly. Solvents are used daily in various industrial processes as reaction medium, as diluters, and in separation procedures. As reaction medium, the role of solvent is to bring catalysts and reactants together and to release heat thus affecting activity and selectivity. The proper selection of the solvent considering its biological, physical and chemical properties is very necessary for product separation, environmental, safety handling and economic factors. Green solvents are the boon in this context. They are not only environmentally benign but also cost effective. The biggest challenge faced by the chemists is adaptation of methods and selection of solvents during chemical synthesis which will give negligible waste product and will remain human and nature friendly. During designing compounds for a particular reaction it is difficult to give assurance regarding the toxicity and biodegradability of the method. Chemists are still far away from predicting the various chemical and biological effects of the compounds on the back of the envelope. To achieve that point is formidable task but it will definitely act as inspiration for the coming generation of chemists. The green solvents are undoubtedly a far better approach to eliminate the negative impacts and aftermath of any chemical synthesis on the environment. Our study in this review covers an overview of green solvents, their role in safer chemical synthesis with reference to some of the important green solvents and their detail summarization.
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Lai, Han. "Exploration on Infiltrating the Sense of Green Chemistry in University Teaching of Organic Chemistry." Advanced Materials Research 488-489 (March 2012): 1062–65. http://dx.doi.org/10.4028/www.scientific.net/amr.488-489.1062.

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This paper introduces methods of solving problems of environmental contamination and health hazard caused by organic chemistry by using green chemistry though, discusses green chemistry concept implemented in colleges and universities’ education of organic chemistry through methods including updating education and teaching idea, reorganizing teaching contents and optimizing teaching design, and through combining teaching practices, analyzes how to penetrate green chemistry into each teaching link by combining teaching contents, so as to better accomplish teaching tasks, broaden the scope of knowledge for students and foster modern green chemistry awareness and scientific research awareness of students.
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Devi, Barla Karuna, Swathi Naraparaju, Chaganti Soujanya, and Sayan Dutta Gupta. "Green Chemistry and Green Solvents: An Overview." Current Green Chemistry 7, no. 3 (December 2, 2020): 314–25. http://dx.doi.org/10.2174/2213346107999200709132815.

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: Green chemistry emphasizes designing novel routes to overcome health and environmental problems that occur during a chemical reaction. Green solvents are used in place of conventional solvents that are hazardous to both human and the environment. Solvents like water, ionic liquids, supercritical CO2, biosolvents, organic carbonates, and deep eutectic mixtures can be used as green solvents. The review focuses on the properties, applications, and limitations of these solvents.
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Dissertations / Theses on the topic "Organic green chemistry"

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Goei, Elisabeth Rukmini. "Using Green Chemistry Experiments to Engage Sophomore Organic Chemistry." Miami University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=miami1280437800.

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Dahl, Jennifer Ann. "Synthesis of functional nanomaterials within a green chemistry context /." Connect to title online (Scholars' Bank) Connect to title online (ProQuest), 2007. http://hdl.handle.net/1794/6131.

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Thesis (Ph. D.)--University of Oregon, 2007.
Typescript. Includes vita and abstract. Includes bibliographical references (leaves 158-183). Also available online in Scholars' Bank; and in ProQuest, free to University of Oregon users.
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Granville, Stephanie L. "Studies of Iron Polyfluorometallacycle Complexes Enroute to the "Green" Catalytic Synthesis of Hydrofluorocarbons." Thesis, University of Ottawa (Canada), 2011. http://hdl.handle.net/10393/28894.

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Chlorofluorocarbons were once commonly used as propellants and refrigerants due to their stability, low toxicity and excellent physical properties. They were phased out, however, after being identified as ozone-depleters, and have been replaced by hydrofluorocarbons (HFCs) and other fluorocarbon derivatives (FCDs). The high temperature-resistant characteristic of these materials is beneficial for many applications; however, the robust nature of the C-F bonds leads to their persistence in the environment. Frequently, the synthesis of HFCs and FCDs involves energy-intensive processes and toxic precursors, such as chlorocarbons and heavy metals. In accordance with the shift to greener, more sustainable chemistry, more energy efficient methods employing less hazardous and non-toxic materials for the generation of HFCs and FCDs need to be developed. Organometallic catalysis offers potential new routes to the synthesis of fluorinated compounds. We sought to study the reactivity of tetrafluoroethylene and 1,1-difluoroethylene with a variety of iron complexes to increase our understanding of the bonding and chemistry of coordinated fluoro-olefins. Crystal structures were obtained for the parent and dppe substituted metallaycles: Fe(CF2) 4(CO)4 and Fe(CF2)4(K2-dppe)(CO) 2. Sterics were found to be responsible for the preferential formation of three- versus five-membered metallacycles through investigating the reactivity of TFE with iron phosphine- and phosphite-carbonyl complexes, as well as with the homoleptic complex pentakis(2,6-dimethylphenylisocyanide)iron and the anionic complex K[FeCp(CO)2]. The five-membered metallacycle was selectively formed with the mono-substituted phosphine and phosphite complexes, whereas, the di-substituted complexes yield the olefin (three-membered metallacycle) complexes. With the goal of developing methods for iron-mediated fluoride abstraction, the reactivity of these iron fluoro-metallacycles with a variety of Lewis acids was probed. Extremely electrophillic fluoro-carbenes were generated. A more electron rich metal centre, as in the thermally synthesized K[FeCp(CF 2)4(CO)2], is required to facilitate fluoride abstraction and stabilize the fluor-ocarbene. The results that were obtained in this investigation set the stage well for further development of iron-based organofluorometallic chemistry and our desire to functionalize the alpha-carbon of the metallacycle enroute to the generation of novel FCs.
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Kherde, Yogesh A. "Green Synthesis and Evaluation of Catalytic Activity of Sugar Capped Gold Nanoparticles." TopSCHOLAR®, 2014. http://digitalcommons.wku.edu/theses/1388.

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Owing to the importance of gold nanoparticles in catalysis, designing of them has become a major focus of the researchers. Most of the current methods available for the synthesis of gold nanoaprticles (GNPs) suffer from the challenges of polydispersity, stability and use of toxic and harmful chemicals. To overcome these limitations of conventional methods, in our present study, we made an attempt to design a method for the green synthesis of monodispersed and stable gold nanoparticles by sugars which act as reducing and stabilizing agent. Characterization of synthesized nanoparticles was done by using various analytical techniques such as transmission electron microscope (TEM), dynamic light scattering spectroscopy (DLS), UV-Vis spectroscopy, scanning electron microscopy and electron dispersion spectroscopy. The synthesized sugar GNPs (S-GNPs) were spherical in shape and in the size range of 10 ± 5 nm. p-Nitrophenol reduction assay was used as a model system to determine the catalytic reduction activity of various sugar capped GNPs, monosaccharides (fructose), disaccharide (sucrose) and trisaccharide (raffinose) GNPs. The effect of temperature and the size of ligand on catalytic activity was also evaluated at different temperature using UV-Vis spectrometer. Using the spectroscopic data, rate constant (k) for three sugar capped GNPs was determined followed by its activation energy (Ea) and exponential (A) factor.
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Cook, Teresa L. "Developing Green One-Step Organic Reactions in the High Speed Ball Mill." University of Cincinnati / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1397736534.

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Jain, Shashank. "Establishing Chemical Mechanisms And Estimating Phase State Of Secondary Organic Aerosol From Atmospherically Relevant Organic Precursors." ScholarWorks @ UVM, 2016. http://scholarworks.uvm.edu/graddis/622.

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Organic aerosol (OA) is a ubiquitous component of atmospheric particulate that influences both human health and global climate. A large fraction of OA is secondary in nature (SOA), being produced by oxidation of volatile organic compounds (VOCs) emitted by biogenic and anthropogenic sources. Despite the integral role of SOA in atmospheric processes, there remains a limited scientific understanding of the chemical and physical changes induced in SOA as it ages in the atmosphere. This thesis describes work done to increase the knowledge of processes and properties of atmospherically relevant SOA. In the work presented in this thesis, I have worked on improving an existing innovative, soft ionization aerosol mass spectrometer and utilized it to establish chemical mechanisms for oxidation of atmospherically relevant organic precursors (i.e., Green Leaf Volatiles). I discovered that SOA formation from cis-3-hexen-1-ol is dominated by oligomer and higher molecular weight products, whereas the acetate functionality in cis-3-hexenylacetate inhibited oligomer formation, resulting in SOA that is dominated by low molecular weight products. One of the most important factors contributing to uncertainties in our estimations of SOA mass in the atmosphere, remains our basic assumption that atmospheric SOA is liquid-like, which we have found to be untrue. Hence, I developed a methodology to estimate the phase state of SOA and identified new parameters that can have significant influence on the phase state of atmospheric aerosol. This simplified method eliminates the need for a Scanning Mobility Particle Sizer (SMPS) and directly measures Bounce Factor (BF) of polydisperse SOA using only one multi-stage cascade Electrostatic Low Pressure Impactor (ELPI). The novel method allows for the real time determination of SOA phase state, permitting studies of the relationship between SOA phase, oxidative formation and chemical aging in the atmosphere. I demonstrated that SOA mass loading (CSOA) influences the phase state significantly. Results show that under nominally identical conditions, the maximum BF decreases by approximately 30% at higher CSOA and suggests that extrapolation of experiments not conducted at atmospherically relevant SOA levels to simulate the chemical properties may not yield results that are relevant to our natural environment. My work has provided a better understanding of the mechanisms of aerosol formation at atmospheric concentrations, which is necessary to understand its physical properties. This improved understanding is fundamental to accurately model aerosol formation in the atmosphere, and subsequently evaluate their large-scale effect on human health and environment.
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Demirci, Sema. "Synthesis Of Heteroaryl Substituted Dihydrofuran And Dihydropyran Derivatives By Green Chemistry Approach." Master's thesis, METU, 2009. http://etd.lib.metu.edu.tr/upload/2/12610966/index.pdf.

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The thesis subject is mainly involved in Green Chemistry approach. Thiophene, furan and pyridine carboxaldehydes were chosen as starting compounds and vinylation and allylation with Grignard reaction afforded the corresponding racemic heteroaryl substituted allylic and homoallylic alcohols. Subsequent resolution with enzymes (PS-Amano II, Lipozym and Novazym 435) gave enantiomerically enriched alcohols with the e.e. values varied between 65 and 99%. The absolute configurations of all substrates are known. As a result of O-allylation with the common procedure formed the feasible carbon backbone for the ring closing metathesis reaction. All ring closing metathesis reactions were performed by Grubbs&rsquo
catalyst with just 5% catalyst loading. The absolute configurations of dihydrofuran and dihydropyran derivatives are known, since the chiral center configurations of all substrates are preserved throughout all the applied processes.
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Harvey, Rebecca. "The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol." ScholarWorks @ UVM, 2016. http://scholarworks.uvm.edu/graddis/556.

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Aerosols play important roles in atmospheric and environmental processes. Not only do they impact human health, they also affect visibility and climate. Despite recent advances made to under their sources and fate, there remains a limited understanding of the mechanisms that lead to the formation of aerosols and their ultimate fate in the atmosphere. These knowledge gaps provide the crux of the research reported herein, which has focused on identifying novel sources of atmospheric aerosol, characterizing its physical and optical properties, and rationalizing these properties using an in-depth knowledge of the molecular level mechanisms that led to its formation. Upon mowing, turfgrasses emit large amounts of green leaf volatiles which can then be oxidized by ozone to form SOA. Overall, the mowing of lawns has the potential to contribute nearly 50 µg SOA per square meter of lawn mowed. This SOA contribution is on the same order of magnitude as other predominant SOA sources (isoprene, monoterpenes, sesquiterpenes). Turfgrasses represent an interesting and potentially meaningful SOA source because they contribute to SOA and also because they cover large land areas in close proximity to oxidant sources. Another related SOA precursor is sugarcane, which is in the same family as turfgrass and is among the largest agricultural crops worldwide. Globally, the ozonolysis of sugarcane has the potential to contribute 16 Mg SOA to the atmosphere, compared to global estimates of SOA loading that range from 12-70 Tg SOA. In order to fully understand the role of atmospheric SOA on the radiative budget (and therefore climate), it is also important to understand its optical properties; its ability to absorb vs scatter light. Turfgrass and sugarcane produced SOA that was weakly absorbing while its scatter efficiency was wavelength and size-dependent. Interestingly, SOA formed under both dry (10% RH) and wet (70% RH) conditions had the same bulk chemical properties (O:C), yet significantly different optical properties, which was attributed to differences in molecular-level composition. The work presented herein represents a unique, inclusive study of SOA precursors. A complete understanding of the chemistry leading to SOA formation is used to understand its physical and optical properties and evaluate these large-scale effects of SOA from these precursors.
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Borghese, Sophie. "Toward green processes organic synthesis by catalysis with metal-doped solids." Phd thesis, Université de Strasbourg, 2013. http://tel.archives-ouvertes.fr/tel-01017796.

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Nowadays, the modern chemical industry has to deal with increasing environmental concerns, including the disposal of waste and its economic impact, or the diminution of important worldwide resources such as transition metals. In this Ph.D. thesis, we aimed to bring improvement in this area by the development of green processes, based on the use of recyclable heterogeneous catalysts. By combining the catalytic properties of several metal cations with the properties of solid catalysts such as polyoxometalates or zeolites, we were able to set up new tools for organic synthesis. Silver-doped polyoxometalates proved to be very efficient catalysts in the rearrangement of alkynyloxiranes to furans. Acetals and spiroketals were synthetized by dihydroalkoxylation of alkynediols under catalysis with silver-zeolites. As a perspective, we highlighted the potential applications of such green procedures in the total synthesis of more complex molecules. The first results suggested that these environmental friendly processes should gain increasing interest in the future.
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Shah, Monic. "Antimicrobial Nanoparticles: A Green and Novel Approach for Enhancing Bactericidal Efficacy of Commercial Antibiotics." TopSCHOLAR®, 2014. http://digitalcommons.wku.edu/theses/1389.

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On the verge of entering the post-antibiotic era, numerous efforts are in place to regain the waning charm of antibiotics which are proving ineffective against most “Superbugs”. Engineered nanomaterials, especially gold nanoparticles (GNPs) capped with antibacterial agents, are proving to be an effective and novel strategy against multidrug resistant (MDR) bacteria. In this study, we report a one-step synthesis of antibioticcapped GNPs (25 ± 5 nm) utilizing the combined reducing and capping ability of a cephalosporin antibiotic, ceftazidime. No signs of aggregation or leaching of ceftazidime from GNP surface was observed upon its storage. Antibacterial testing showed dosedependent broad spectrum activity of Cef-GNPs against both Gram-positive (S. bovis and E. durans) and Gram-negative (P. aeruginosa and E. aerogenes) bacteria. A significant reduction in the minimum inhibition concentration (MIC) of Cef-GNPs was observed as compared to the ceftazidime by itself against Gram-negative bacteria. The MIC of Cef- GNPs were 0.1 mg mL-1 (P. aeruginosa and E. aerogenes) and 1.2 mg mL-1 (E. durans and S. bovis). Cef-GNPs exerted bactericidal action on both P. aeruginosa and E. durans by disrupting the cellular membrane resulting in leakage of cytoplasmic content and death of bacterial cell. Our investigation and results provides an additional step in the development of antibiotic capped GNP as potent next generation antibacterial agents.
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Books on the topic "Organic green chemistry"

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Green organic chemistry in lecture and laboratory. Boca Raton: Taylor & Francis, 2012.

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Zhang, Wei, and Berkeley W. Cue. Green techniques for organic synthesis and medicinal chemistry. Chichester, West Sussex: John Wiley & Sons, 2012.

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E, Hutchison James, ed. Green organic chemistry: Strategies, tools, and laboratory experiments. Southbank, Vic., Australia: Thomson-Brooks/Cole, 2004.

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Zhang, Wei, and Berkeley W. Cue, eds. Green Techniques for Organic Synthesis and Medicinal Chemistry. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9780470711828.

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Zhang, Wei, and Berkeley W. Cue, eds. Green Techniques for Organic Synthesis and Medicinal Chemistry. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119288152.

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M, Kidwai, ed. New trends in green chemistry. Boston: Kluwer Academic, 2004.

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Innovations in green chemistry and green engineering: Selected entries from the Encyclopedia of sustainability science and technology. New York: Springer, 2013.

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The algebra of organic synthesis: Green metrics, design strategy, route selection, and optimization. Boca Raton: CRC Press, 2012.

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Dr, Inamuddin, and SpringerLink (Online service), eds. Green Solvents II: Properties and Applications of Ionic Liquids. Dordrecht: Springer Netherlands, 2012.

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Microwave-assisted organic synthesis: A green chemical approach. Oakville, ON: Apple Academic Press Inc., 2015.

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Book chapters on the topic "Organic green chemistry"

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Colberg, Juan C. "Green Chemistry." In Practical Synthetic Organic Chemistry, 683–702. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118093559.ch16.

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Tiwari, Vinod K., Abhijeet Kumar, Sanchayita Rajkhowa, Garima Tripathi, and Anil Kumar Singh. "Enzymes in Organic Synthesis." In Green Chemistry, 317–52. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-2734-8_8.

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Hassan, Amal I., and Hosam M. Saleh. "Principles of Green Chemistry." In Green Organic Reactions, 15–32. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_2.

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Koel, Mihkel. "Green in Analytical Chemistry." In Green Organic Reactions, 111–30. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_7.

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Radhika, Sankaran, Mohan Neetha, and Gopinathan Anilkumar. "Green in Pharmaceutical Chemistry." In Green Organic Reactions, 131–47. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_8.

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Saleh, Hosam M., and Amal I. Hassan. "Introduction to Green Chemistry." In Green Organic Reactions, 1–14. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_1.

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Tiwari, Vinod K., Abhijeet Kumar, Sanchayita Rajkhowa, Garima Tripathi, and Anil Kumar Singh. "Energy-Efficient Process in Organic Synthesis." In Green Chemistry, 37–77. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-2734-8_2.

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Tiwari, Vinod K., Abhijeet Kumar, Sanchayita Rajkhowa, Garima Tripathi, and Anil Kumar Singh. "Green Solvents: Application in Organic Synthesis." In Green Chemistry, 79–112. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-2734-8_3.

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Bhaskaran, Rasmi P., and Beneesh P. Babu. "Green Chemistry of Recoverable Catalysts." In Green Organic Reactions, 299–322. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_16.

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Tiwari, Vinod K., Abhijeet Kumar, Sanchayita Rajkhowa, Garima Tripathi, and Anil Kumar Singh. "Catalysis: Application and Scope in Organic Synthesis." In Green Chemistry, 207–60. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-2734-8_6.

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Conference papers on the topic "Organic green chemistry"

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Santi, Claudio, Simona Propersi, Caterina Tidei, Luca Sancineto, Luana Bagnoli, and Francesca Marini. "PhSZn-halides: new  green thiolates." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a004.

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Gorincioi, Elena, Anastasia Verdes, and Fliur Makaev. "Fine organic synthesis approaches for obtaining monastrol by green chemical metodologies." In Ecological chemistry ensures a healthy environment. Institute of Chemistry, Republic of Moldova, 2022. http://dx.doi.org/10.19261/enece.2022.ab24.

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Santi, Claudio, Caterina Tidei, Valeria Saccomandi, Luana Bagnoli, and Francesca Marini. "Green Oxidations of Aldehydes to Carboxylic Acids and Esters." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01014.

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Bednarz, Szczepan, Marcin Lukasiewicz, Anna Ptaszek, Dariusz Bogdal, and Bohdan Achremowicz. "Microwave assisted starch oxidation – a ‘green’ way for polysaccharide modification." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01254.

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Manteghi, Faranak, Navid Shahmiri, Beheshteh Sohrabi, and Sina Golafshan. "Green Synthesis of BaCrO4 Nanoparticles Using Glycyrrhiza Glabra Extract." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b026.

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Maleki, Ali, Jamal Rahimi, and Razieh Firouzi Haji. "Green synthesis of quinazolinone derivatives by using a recyclable heteropoly acid catalyst." In The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04722.

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Shumway, Martin, Ryan McGonagle, Anthony Nerris, Janaina I. S. Aguiar, Amir Mahmoudkhani, and D. Marc Jacobs. "Green Well Stimulation Fluids for Enhanced Oil Recovery from Tight Sand Formations: Field Wide 70+ Wells Study Over 4 Years." In SPE International Conference on Oilfield Chemistry. SPE, 2021. http://dx.doi.org/10.2118/204370-ms.

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Abstract Legacy oil production from Appalachian basin has been in a decline mode since 2013. With more than 80% of wells producing less than 15 bbl/day, there is a growing interest in economically and environmentally viable options for well stimulation treatments. Analysis of formation mineralogy and reservoir fluids along with history of well interventions indicated formation damage in many wells due precipitation of organics and a change in wettability being partially responsible for production decline rates in excess of forecasts. The development and properties of a novel cost-effective biosurfactant based well-stimulation fluid are described here along lessons learned from several field trials in wells completed in the Upper Devonian Bradford Group. This group of 74 wells, completed in siltstone and sandstone reservoirs were presenting more than 12 well failures annually across the field, which was attributed to the accumulation of organic deposits in the tubulars. Based on these cases, batch stimulation treatments using a novel fluid comprising biosurfactants were proposed and implemented field wide. The treatments effectively removed organic deposits, changed formation wettability from oil to water wet and resulted in a sustained oil production increase. Well failures were significantly reduced as a result of this program and the group of 74 wells did not have a paraffin-related well failure for 18 months. Results from this program demonstrates the efficiency of the green well stimulation fluids in mitigating formation damage, reducing organics deposition and in increasing oil production as a promising method to stimulate tight formations.
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Zetra, Yulfi, Januar Kholik, R. Y. Perry Burhan, Agus Wahyudi, Zjahra Vianita Nugraheni, and Endah Mutiara Marhaeni Putri. "Organic geochemistry characteristic of aliphatic hydrocarbon fraction of Sawahlunto coal, Ombilin Basin, West Sumatra." In THE 3RD INTERNATIONAL SEMINAR ON CHEMISTRY: Green Chemistry and its Role for Sustainability. Author(s), 2018. http://dx.doi.org/10.1063/1.5082423.

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Sitorus, Berlian, Charlotte Pughe, Arin Mizouri, Andrew M. Ellis, and Shengfu Yang. "Ion-molecule reactions of organic molecules with noble metal atoms in superfluid helium droplets." In THE 3RD INTERNATIONAL SEMINAR ON CHEMISTRY: Green Chemistry and its Role for Sustainability. Author(s), 2018. http://dx.doi.org/10.1063/1.5082471.

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Lukasiewicz, Marcin. "Solid Complex of Hydrogen Peroxide as a Safe and Green Oxidant for Polysaccharide Modification." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01077.

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