Auswahl der wissenschaftlichen Literatur zum Thema „Organohalides“
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Zeitschriftenartikel zum Thema "Organohalides"
Maucourt, Bruno, Stéphane Vuilleumier und Françoise Bringel. „Transcriptional regulation of organohalide pollutant utilisation in bacteria“. FEMS Microbiology Reviews 44, Nr. 2 (03.02.2020): 189–207. http://dx.doi.org/10.1093/femsre/fuaa002.
Der volle Inhalt der QuelleLee, Matthew, Chris Marquis, Bat-Erdene Judger und Mike Manefield. „Anaerobic microorganisms and bioremediation of organohalide pollution“. Microbiology Australia 36, Nr. 3 (2015): 125. http://dx.doi.org/10.1071/ma15044.
Der volle Inhalt der QuelleBolandi, Ali, Setare Tahmasebi Nick und Sherine O. Obare. „Nanoscale materials for organohalide degradation via reduction pathways“. Nanotechnology Reviews 1, Nr. 2 (01.03.2012): 147–71. http://dx.doi.org/10.1515/ntrev-2012-0003.
Der volle Inhalt der QuelleBertolini, Martina, Sarah Zecchin, Giovanni Pietro Beretta, Patrizia De Nisi, Laura Ferrari und Lucia Cavalca. „Effectiveness of Permeable Reactive Bio-Barriers for Bioremediation of an Organohalide-Polluted Aquifer by Natural-Occurring Microbial Community“. Water 13, Nr. 17 (05.09.2021): 2442. http://dx.doi.org/10.3390/w13172442.
Der volle Inhalt der QuelleFutagami, Taiki, Yuki Morono, Takeshi Terada, Anna H. Kaksonen und Fumio Inagaki. „Distribution of dehalogenation activity in subseafloor sediments of the Nankai Trough subduction zone“. Philosophical Transactions of the Royal Society B: Biological Sciences 368, Nr. 1616 (19.04.2013): 20120249. http://dx.doi.org/10.1098/rstb.2012.0249.
Der volle Inhalt der QuelleIto, Hajime, Eiji Yamamoto, Satoshi Maeda und Tetsuya Taketsugu. „Transition-Metal-Free Boryl Substitution Using Silylboranes and Alkoxy Bases“. Synlett 28, Nr. 11 (26.04.2017): 1258–67. http://dx.doi.org/10.1055/s-0036-1588772.
Der volle Inhalt der QuelleSpurling, TH, und DA Winkler. „CNDO/2 Calculations for Organohalides“. Australian Journal of Chemistry 39, Nr. 2 (1986): 233. http://dx.doi.org/10.1071/ch9860233.
Der volle Inhalt der QuelleWigginton, Nicholas S. „How bacteria break down organohalides“. Science 346, Nr. 6208 (23.10.2014): 435.9–436. http://dx.doi.org/10.1126/science.346.6208.435-i.
Der volle Inhalt der QuelleRupakula, Aamani, Thomas Kruse, Sjef Boeren, Christof Holliger, Hauke Smidt und Julien Maillard. „The restricted metabolism of the obligate organohalide respiring bacterium Dehalobacter restrictus: lessons from tiered functional genomics“. Philosophical Transactions of the Royal Society B: Biological Sciences 368, Nr. 1616 (19.04.2013): 20120325. http://dx.doi.org/10.1098/rstb.2012.0325.
Der volle Inhalt der QuelleLi, Sheng-Jun, Lu Han und Shi-Kai Tian. „1,2-Aminohalogenation of arynes with amines and organohalides“. Chemical Communications 55, Nr. 75 (2019): 11255–58. http://dx.doi.org/10.1039/c9cc05505c.
Der volle Inhalt der QuelleDissertationen zum Thema "Organohalides"
Michaud, Jon-Pierre. „Precision-cut liver slice culture: An in vitro tool for assessing hepatotoxic interactions of organohalides“. Diss., The University of Arizona, 1994. http://hdl.handle.net/10150/186937.
Der volle Inhalt der QuelleWagner, Anthony Jon. „Degradation of fluorine-containing organic thin films and organohalides mediated by ionizing radiation nitrogen-based surface modification of polymers and metallization of nitrogen-containing polymers /“. Available to US Hopkins community, 2003. http://wwwlib.umi.com/dissertations/dlnow/3080788.
Der volle Inhalt der QuelleBertrand, Xavier. „Synthèse d'halogénures tertiaires aliphatiques“. Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0033.
Der volle Inhalt der QuelleHalides have very interesting properties in organic chemistry. Organic molecules that bear halides have modified properties which make them interesting in many fields of chemistry such as pharmaceuticals, agrochemicals, and material science. Moreover, they are useful intermediate for the synthesis of a vast array of highly functionalized molecules. This thesis will therefore report on the development of new reaction for the incorporation of halides starting from abundant molecules such as alkenes and alcohols. The first project focused on the development of an hydrofluorination reaction. This allowed for the easy incorporation of a fluorine atom on various molecules starting from easily available alkenes. The reaction uses a combination of a strong acid, methanesulfonic acid, and a fluoride source, triethylamine trihydrofluoride. These conditions were compatible with a wide range of functional groups. However, the reaction was limited to 1,1-disubstituted and trisubstituted alkenes. The yields are generally good and similar to those of other reported methods. For the second project, a modification of the reaction conditions from the first project was performed to allow for the hydrochlorination, hydrobromination and hydroiodination of alkenes. The corresponding halides are obtained in excellent yields, usually without purification. Mechanistic studies have shown that the solvent, acetic acid, plays a role in the stabilization of the carbocation. Finally, an example of deuteriochlorination has been reported using deuterated acetic acid. In the third project, we focused on the transformation of alcohols into fluorides. The main objective of this project was to complement the existing methods of deoxyfluorination which work generally well on primary and secondary alcohols, but not so much on tertiary alcohols. By modifying the conditions from the first project, we were able to develop a deoxyfluorination reaction that gives tertiary fluorides in excellent yields. The reaction is compatible with a vast array of functional groups and the products are usually obtained without purification. The reaction has been extended for the fluorination of other C–O bonds such as ethers and esters. Mechanistic studies have been performed and show that the reaction proceeds in two steps via an elimination/hydrofluorination pathway. Finally, a modification of these conditions has been done to allow for an adaptation of this reaction in radiofluorination of alcohols
Hambsch, Mike, Qianqian Lin, Ardalan Armin, Paul L. Burn und Paul Meredith. „Efficient, monolithic large area organohalide perovskite solar cells“. Royal Society of Chemistry, 2016. https://tud.qucosa.de/id/qucosa%3A36282.
Der volle Inhalt der QuelleTrueba, Santiso Alba María. „Enrichment and characterization of anaerobic bacteria degrading organohalide compounds“. Doctoral thesis, Universitat Autònoma de Barcelona, 2018. http://hdl.handle.net/10803/565830.
Der volle Inhalt der QuelleLa frecuente contaminación de las aguas subterráneas por compuestos organohalogenados es un grave problema ambiental debido a los riesgos ecológicos y para la salud humana de ella derivados. La bioremediación es una tecnología sostenible que evita algunos inconvenientes que presentan los tratamientos físico-químicos. En este estudio nos proponemos obtener y caracterizar cultivos que contengan bacterias anaerobias que degraden compuestos organohalogenados ambientalmente peligrosos con potencial para la bioremediación in situ de aguas subterráneas. En trabajos previos de nuestro grupo de investigación, se obtuvo un cultivo enriquecido en bacterias del género Dehalogenimonas procedente de sedimentos del estuario del río Besós (Barcelona) que degrada alcanos con halógenos situados en carbonos adyacentes. En esta tesis se ha identificado la dehalogenasa reductora (RDasa) de esta cepa de Dehalogenimonas implicada en la conversión del dibromuro de etileno (EDB) al compuesto inocuo eteno combinando técnicas de proteómica basadas en geles de electroforesis, ensayos enzimáticos y nano-cromatografía líquida de alta resolución (nLC-MS/MS). Esta RDasa es designada EdbA, y constituye la primera RDasa identificada en este género bacteriano que cataliza una reacción de debromación. Además, es también la primera RDasa en ser demostrada funcional sin una subunidad B de anclaje a la membrana codificada de forma adyacente en el genoma. Adicionalmente, se ha detectado una única RDasa en cultivos que transforman 1,2,3-tricloropropano a cloruro de alilo combinando técnicas de ultracentrifugación, geles de electroforesis y nLC-MS/MS. Esta enzima ortóloga a DcpA, la responsable de la degradación de 1,2-dicloropropano a propeno, ha sido detectada en la fracción proteica de membrana, lo cual concuerta con las predicciones realizadas mediante herramientas bioinformáticas. El mecanismo por el cual EdbA y esta DcpA se anclan a la membrana citoplasmática es desconocido, atribuyéndose a proteínas todavía no descritas. En este trabajo se ha obtenido un segundo consorcio bacteriano estable a partir de lodos de una planta de tratamiento de aguas residuales industriales aplicando técnicas de cultivo de enriquecimiento y dilución por extinción. Este cultivo fermenta diclorometano (DCM) y dibromometano (DBM) a acetato y formato. Se ha demostrado que la bacteria responsable de la fermentación pertenece al género Dehalobacterium, y se ha procedido a su aislamiento. Sin embargo, las interacciones sinérgicas existentes entre las especies del consorcio han impedido obtener un cultivo puro. Seleccionando colonias en medio de cultivo semisólido, aplicando antibióticos y cambios en la composición del medio, se ha obtenido una abundancia relativa de Dehalobacterium del 67%. Le acompañan bacterias de los géneros Acetobacterium y Desulfovibrio, tal y como se detectó mediante análisis de genotecas. El fraccionamiento isotópico del carbono durante la fermentación del DCM por este cultivo fue determinado mediante análisis de isótopos estables de compuestos específicos (CSIA). El valor obtenido, -27 ± 2‰, difiere del publicado previamente para una cepa de Dehalobacter que también fermenta el DCM (-15.5 ± 1.5‰). Estos valores son significativamente diferentes de los obtenidos con bacterias metilotróficas degradadoras de DCM (-45 a -61‰), y podrían permitir diferenciar vías de degradación de DCM en trabajos de bioremediación in situ. Finalmente, se ha demostrado que la presencia de co-contaminantes que se detectan frecuentemente con el DCM, como el tricloroetileno (TCE), 1,2-dicloroetano (1,2-DCA), cis-dicloroetileno (cis-DCE), 1,1,2-tricloroetano (1,1,2-TCA), ácido perfluorooctanoico (PFOA) y 3,4-dicloroanilina (3,4-DCA) no provocan una inhibición significativa en la degradación de DCM por parte del cultivo de Dehalobacterium, a las concentraciones estudiadas. Una concentración de cloroformo de 100 mg/L provoca una inhibición total. De manera similar, 200 mg/L de sulfonato de perfluoroctano (PFOS), y ≥ 25 mg/L de diuron provocan una inhibición severa, impidiendo la degradación completa del DCM. Sin embargo, la actividad degradadora de DCM se recupera cuando los cultivos inhibidos se transfieren a medio libre de co-contaminantes.
The widespread groundwater contamination by organohalide compounds is of a major concern due to the human and ecological risks derived from it. Bioremediation is a sustainable technology that overcomes some limitations of the physical-chemical remediation techniques on these water bodies. In this study, we aimed to obtain and characterize cultures containing anaerobic bacteria capable of degrading organohalide compounds of environmental concern with potential for in situ groundwater bioremediation. In previous work carried out in our laboratory a highly enriched culture containing organohalide-respiring bacteria from the genus Dehalogenimonas degrading vicinally halogenated alkanes was obtained from sediments of the river Besós estuary (Barcelona). In this thesis, the reductive dehalogenase (RDase) from this Dehalogenimonas strain responsible for the catalysis of ethylene dibromide (EDB) to the innocuous ethene was identified combining gel-based proteomic techniques, specific enzymatic tests and nano-scale liquid chromatography tandem mass spectrometry (nLC-MS/MS). This RDase is therefore designated as EdbA, for ethylene dibromide RDase subunit A. EdbA is the first RDase identified for debrominating catalytic activity among species of this genus. Moreover, it is the first RDase shown to be functional for respiration without an adjacent membrane-anchoring subunit B encoded on the genome. Additionally, combining ultracentrifugation, gel electrophoresis and nLC-MS/MS, an orthologous enzyme of the dichloropropane-to-propene RDase (DcpA) was the only RDase detected in 1,2,3-trichloropropane-to-allyl chloride dehalogenating cultures. This DcpA was detected in the membrane fraction of the crude protein extract, in accordance to its predicted subcellular localization by bioinformatics tools and it is also not co-localised with an rdhB gene. The membrane-anchoring mechanisms of these RDases remains not known and may rely in yet-unidentified proteins. A second stable bacterial consortium was obtained in the present work from slurry samples of an industrial wastewater treatment plant with a combination of enrichment culture strategies and the dilution-to-extinction technique. This culture was demonstrated to ferment dichloromethane (DCM) and dibromomethane (DBM) into acetate and formate. The Dehalobacterium sp. present in this culture was shown to be the responsible for the dihalomethanes fermentation, and the isolation of this strain was attempted. However, the synergic interactions existing among the different accompanying species present in the bacterial consortia impeded the isolation. Despite a pure culture was not achieved via picking up colonies from semisolid agar cultures, changes in the medium composition, and the application of selected antibiotics, a final relative abundance of Dehalobacterium sp. of 67 % was attained. As determined by clone library analysis, bacteria from the genera Acetobacterium and Desulfovibrio remained present in the culture. The carbon isotope fractionation during DCM fermentation by this culture was determined by compound-specific stable isotope analysis (CSIA). The value obtained was -27 ± 2‰ and differs from the previously published value of -15.5 ± 1.5‰ of a Dehalobacter sp. performing also DCM fermentation. These values are yet significantly different from those reported for facultative methylotrophic bacteria degrading DCM (ranging from -45 to -61‰), and this would allow for further differentiation of these degradation pathways during in situ bioremediation works. Finally, the potential inhibitory effect of selected frequent groundwater co-contaminants over DCM degradation by the Dehalobacterium-containing culture was assessed for further in situ bioremediation applications. Trichloroethylene (TCE), 1,2-dichloroethane (1,2-DCA), cis-dichloroethylene (cis-DCE), 1,1,2-trichloroethane (1,1,2-TCA), perfluorooctanoic acid (PFOA), and 3,4-dichloroaniline (3,4-DCA) did not show significant inhibitory effects at the concentrations tested. Differently, a total inhibition was caused with a chloroform concentration of 100 mg/L. Also, the presence of 200 mg/L of perfluorooctanesulfonic acid (PFOS), as well as concentrations higher than 25 mg/L of the pesticide diuron caused a severe inhibitory effect, preventing the full depletion of DCM. Nevertheless, DCM degrading activity was recovered when inhibited cultures were transferred to co-contaminant free medium.
Wagner, Darlene Darlington. „Comparative genomics reveal ecophysiological adaptations of organohalide-respiring bacteria“. Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/45916.
Der volle Inhalt der QuelleKemp, Laura. „Functional studies of CprK : a transcriptional regulator of organohalide respiration“. Thesis, University of Manchester, 2014. https://www.research.manchester.ac.uk/portal/en/theses/functional-studies-of-cprk-a-transcriptional-regulator-of-organohalide-respiration(d1f3ecd2-78b2-4a91-b4a0-98761c487a11).html.
Der volle Inhalt der QuelleSjuts, Hanno. „Molecular insights into cobalamin-dependent enzyme systems from organohalide-respiring bacteria“. Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/molecular-insights-intocobalamindependent-enzyme-systemsfrom-organohaliderespiring-bacteria(e41ac569-b4b5-40b7-8c17-1740e476021e).html.
Der volle Inhalt der QuelleHossain, Ridwan Fayaz. „Inkjet Printed Transition Metal Dichalcogenides and Organohalide Perovskites for Photodetectors and Solar Cells“. Thesis, University of North Texas, 2020. https://digital.library.unt.edu/ark:/67531/metadc1703403/.
Der volle Inhalt der QuelleRocca, Marco <1989>. „Enrichment and characterization of marine organohalide respiring bacteria and of their dehalogenating enzymes“. Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2019. http://amsdottorato.unibo.it/8999/1/Rocca_Marco_tesi.pdf.
Der volle Inhalt der QuelleBücher zum Thema "Organohalides"
Adrian, Lorenz, und Frank E. Löffler, Hrsg. Organohalide-Respiring Bacteria. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49875-0.
Der volle Inhalt der QuelleAdrian, Lorenz, und Frank E. Löffler. Organohalide-Respiring Bacteria. Springer London, Limited, 2016.
Den vollen Inhalt der Quelle findenAdrian, Lorenz, und Frank E. Löffler. Organohalide-Respiring Bacteria. Springer, 2016.
Den vollen Inhalt der Quelle findenOrganohalide-Respiring Bacteria. Springer, 2018.
Den vollen Inhalt der Quelle findenGiorgi, Giacomo, und Koichi Yamashita, Hrsg. Theoretical Modeling of Organohalide Perovskites for Photovoltaic Applications. Routledge, 2017. http://dx.doi.org/10.1201/9781315152424.
Der volle Inhalt der QuelleTheoretical Modeling of Organohalide Perovskites for Photovoltaic Applications. Taylor & Francis Group, 2017.
Den vollen Inhalt der Quelle findenGiorgi, Giacomo, und Koichi Yamashita. Theoretical Modeling of Organohalide Perovskites for Photovoltaic Applications. Taylor & Francis Group, 2019.
Den vollen Inhalt der Quelle findenGiorgi, Giacomo, und Koichi Yamashita. Theoretical Modeling of Organohalide Perovskites for Photovoltaic Applications. Taylor & Francis Group, 2017.
Den vollen Inhalt der Quelle findenGiorgi, Giacomo, und Koichi Yamashita. Theoretical Modeling of Organohalide Perovskites for Photovoltaic Applications. Taylor & Francis Group, 2017.
Den vollen Inhalt der Quelle findenGiorgi, Giacomo, und Koichi Yamashita. Theoretical Modeling of Organohalide Perovskites for Photovoltaic Applications. Taylor & Francis Group, 2017.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Organohalides"
Furka, Árpád. „Organohalides“. In SpringerBriefs in Molecular Science, 81–90. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-06004-6_6.
Der volle Inhalt der QuelleGlockling, F. „From Germyl-Alkali-Metal Reagents with Group-IIB Halides and Organohalides“. In Inorganic Reactions and Methods, 348. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145258.ch102.
Der volle Inhalt der QuelleGlockling, F. „From Silyl-Alkali-Metal Reagents with Group-IIB Halides and Organohalides“. In Inorganic Reactions and Methods, 342–43. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145258.ch96.
Der volle Inhalt der QuelleDemchuk, Oleg M., Radomir Jasiński und Adam Formela. „The Halogen-Less Catalytic Transition Metal-Mediated Cross-Coupling Reactions: A Sustainable Alternative for Utilisation of Organohalides“. In Chemistry Beyond Chlorine, 17–94. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30073-3_2.
Der volle Inhalt der QuelleSanford, Robert A., Janamejaya Chowdhary und Frank E. Löffler. „Organohalide-Respiring Deltaproteobacteria Deltaproteobacteria“. In Organohalide-Respiring Bacteria, 235–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49875-0_11.
Der volle Inhalt der QuellePicer, M., V. Hocenski und N. Picer. „Possibilities of Predicting the Production of Lipophilic Volatile Organohalides Chlorination of Sea Water and Fresh Water Samples in Laboratory Conditions“. In Organic Micropollutants in the Aquatic Environment, 336–41. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4660-6_36.
Der volle Inhalt der QuelleAdrian, Lorenz, und Frank E. Löffler. „Organohalide-Respiring Bacteria—An Introduction“. In Organohalide-Respiring Bacteria, 3–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49875-0_1.
Der volle Inhalt der QuelleGoris, Tobias, und Gabriele Diekert. „The Genus Sulfurospirillum“. In Organohalide-Respiring Bacteria, 209–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49875-0_10.
Der volle Inhalt der QuelleMayer-Blackwell, Koshlan, Holly Sewell, Maeva Fincker und Alfred M. Spormann. „Comparative Physiology of Organohalide-Respiring Bacteria“. In Organohalide-Respiring Bacteria, 259–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49875-0_12.
Der volle Inhalt der QuelleWei, Kai, Ariel Grostern, Winnie W. M. Chan, Ruth E. Richardson und Elizabeth A. Edwards. „Electron Acceptor Interactions Between Organohalide-Respiring Bacteria: Cross-Feeding, Competition, and Inhibition“. In Organohalide-Respiring Bacteria, 283–308. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49875-0_13.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Organohalides"
Meredith, Paul, Qianqian Lin, Paul Burn und Ardalan Armin. „Organohalide Perovskite Photodetectors“. In 3rd International Conference on Perovskite Thin Film Photovoltaics, Photonics and Optoelectronics. Valencia: Fundació Scito, 2017. http://dx.doi.org/10.29363/nanoge.abxpvperopto.2018.081.
Der volle Inhalt der QuelleMosconi, Edoardo, García Espejo García Espejo und Filippo De Angelis. „First Principles Modeling of Mixed 2D/3D Organohalide Perovskites“. In nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.nfm.2018.165.
Der volle Inhalt der QuelleMosconi, Edoardo. „Mobile Ions in Organohalide Perovskites: Interplay of Electronic Structure and Dynamics“. In nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.fallmeeting.2018.165.
Der volle Inhalt der QuelleCossi, Maurizio, Alberto Fraccarollo und Leonardo Marchese. „Ab Initio Design of 2D Hybrid Organohalide Perovskites with Tunable Band Gap“. In 3rd International Conference on Perovskite Thin Film Photovoltaics, Photonics and Optoelectronics. Valencia: Fundació Scito, 2017. http://dx.doi.org/10.29363/nanoge.abxpvperopto.2018.009.
Der volle Inhalt der QuelleGallop, Nathaniel P., Dmitry R. Maslennikov, Katelyn Goetz, Woongmo Sung, Satoshi Nihonyanagi, Tahei Tahara, Yana Vaynzof und Artem A. Bakulin. „'Just Vibing': Coupled Organic and Inorganic Sublattices in Organohalide Perovskite Solar Cells“. In Online School on Hybrid, Organic and Perovskite Photovoltaics. València: Fundació Scito, 2020. http://dx.doi.org/10.29363/nanoge.hope-pv.2020.011.
Der volle Inhalt der QuelleSharma, Aastha, Josh Vura-Weis und Max Verkamp. „UNDERSTANDING CARRIER AND ELEMENT SPECIFIC DYNAMICS IN ORGANOHALIDE PEROVSKITE BY FEMTOSECOND TABLETOP XUV SPECTROSCOPY“. In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.tk02.
Der volle Inhalt der QuelleKaul, Anupama B. „Light-matter interactions in transition metal dichalcogenides and organohalide perovskites for photoabsorbers and solar cells“. In Low-Dimensional Materials and Devices 2022, herausgegeben von Nobuhiko P. Kobayashi, A. Alec Talin, Albert V. Davydov und M. Saif Islam. SPIE, 2022. http://dx.doi.org/10.1117/12.2632647.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Organohalides"
Haggblom, Max M., Donna E. Fennell, Lisa A. Rodenburg, Lee J. Kerkhof und Kevin R. Sowers. Quantifying Enhanced Microbial Dehalogenation Impacting the Fate and Transport of Organohalide Mixtures in Contaminated Sediments. Fort Belvoir, VA: Defense Technical Information Center, Februar 2012. http://dx.doi.org/10.21236/ada581955.
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