Littérature scientifique sur le sujet « Complexes de Fe(III) »
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Articles de revues sur le sujet "Complexes de Fe(III)"
Rai, Dhanpat, Mikazu Yui et Dean A. Moore. « Isosaccharinate Complexes of Fe(III) ». Journal of Solution Chemistry 41, no 11 (7 novembre 2012) : 1906–21. http://dx.doi.org/10.1007/s10953-012-9911-7.
Texte intégralChen, Shangjun, Lu An et Shiping Yang. « Low-Molecular-Weight Fe(III) Complexes for MRI Contrast Agents ». Molecules 27, no 14 (18 juillet 2022) : 4573. http://dx.doi.org/10.3390/molecules27144573.
Texte intégralXue, Xiao Fei, Yan Xiang Liu, Yan Qing Shao et Nan Sheng Deng. « Rapid Decolorization of Rhodamine B by UV/Fe(III)-Penicillamine Process under Neutral pH : Compared with UV/Fe(III)-Oxalate ». Advanced Materials Research 183-185 (janvier 2011) : 130–34. http://dx.doi.org/10.4028/www.scientific.net/amr.183-185.130.
Texte intégralHassen, Jasim, et Jack Silver. « Stability of Fe(III) and Sn(IV) Metalloporphyrins Adsorbed on Cation-Exchanged Montmorillonite ». Trends in Sciences 19, no 8 (27 mars 2022) : 3426. http://dx.doi.org/10.48048/tis.2022.3426.
Texte intégralAnsari, Khairul I., Sahba Kasiri, James D. Grant et Subhrangsu S. Mandal. « Fe(III)-Salen and Salphen Complexes Induce Caspase Activation and Apoptosis in Human Cells ». Journal of Biomolecular Screening 16, no 1 (2 novembre 2010) : 26–35. http://dx.doi.org/10.1177/1087057110385227.
Texte intégralManimaran, P., et S. Balasubramaniyan. « Synthesis, Characterization and Biological Evaluation of Fe(III) and Cu(II) Complexes with 2,4-Dinitrophenyl hydrazine and Thiocyanate Ions ». Asian Journal of Chemistry 31, no 4 (27 février 2019) : 780–84. http://dx.doi.org/10.14233/ajchem.2019.21719.
Texte intégralK. Dideriksen, J. A. Baker et S. L. S. Stipp. « Fe isotope fractionation between inorganic aqueous Fe(III) and a Fe siderophore complex ». Mineralogical Magazine 72, no 1 (février 2008) : 313–16. http://dx.doi.org/10.1180/minmag.2008.072.1.313.
Texte intégralMelník, Milan, et Marian Koman. « Pyridine-2,6-dicarboxylates in monomeric iron complexes – structural aspects ». Reviews in Inorganic Chemistry 40, no 2 (25 juin 2020) : 75–89. http://dx.doi.org/10.1515/revic-2019-0017.
Texte intégralMonreal-Corona, Roger, Jesse Biddlecombe, Angela Ippolito et Nelaine Mora-Diez. « Theoretical Study of the Iron Complexes with Lipoic and Dihydrolipoic Acids : Exploring Secondary Antioxidant Activity ». Antioxidants 9, no 8 (28 juillet 2020) : 674. http://dx.doi.org/10.3390/antiox9080674.
Texte intégralRastogi, Raj Kamal, Sonu Sharma, Gulshan Rastogi et Alok K. Singh. « SYNTHESIS AND CHARACTERIZATION OF TI (III), V (III),VO (IV), MOO (V),FE (II) AND FE (III) COMPLEXES OF BENZIL- 2,4-DINITROPHENYL HYDRAZONE P-BROMO ANILINE ». Green Chemistry & ; Technology Letters 2, no 4 (14 décembre 2016) : 177. http://dx.doi.org/10.18510/gctl.2016.242.
Texte intégralThèses sur le sujet "Complexes de Fe(III)"
Ingle, Shaktisingh K. « Photoactive fe(III) complexes of -hydroxy acid containing ligands ». Cincinnati, Ohio : University of Cincinnati, 2006. http://www.ohiolink.edu/etd/view.cgi?acc%5Fnum=ucin1144708291.
Texte intégralPaul, S. « Structure, properties and application of conducting polymers containing organo Fe(II)/Fe(III) complexes ». Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2007. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2615.
Texte intégralJones, Morris Edward. « Soluble organic-Fe(III) complexes : rethinking iron solubility and bioavailability ». Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/42940.
Texte intégralINGLE, SHAKTISINGH K. « Photoactive Fe(III) complexes of α-hydroxy acid containing ligands ». University of Cincinnati / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1144708291.
Texte intégralGreene, Shannon Nicolle. « Computational studies of Fe-type nitrile hydratase and related mononuclear, non-heme Fe(III) complexes ». [Gainesville, Fla.] : University of Florida, 2005. http://purl.fcla.edu/fcla/etd/UFE0013070.
Texte intégralWang, Lei. « Photodegradation of organic pollutants induced by Fe(III)-caoxylate complexes in aqueous solution ». Clermont-Ferrand 2, 2008. https://tel.archives-ouvertes.fr/tel-00728829.
Texte intégralFloquet, Sébastien. « Conversion de spin thermo- et photo-induite de complexes ioniques de fe(iii) ». Paris 11, 2001. http://www.theses.fr/2001PA112211.
Texte intégralQuirrenbach, Hanna Raquel. « Determinação das constantes de estabilidade, síntese e caracterização dos complexos de ácido fítico com os íons Fe(II) e Fe(III) ». UNIVERSIDADE ESTADUAL DE PONTA GROSSA, 2007. http://tede2.uepg.br/jspui/handle/prefix/696.
Texte intégralThe phytic acid depending on the pH value presents high potential quelante, quelanting metallic ions, inhibiting the production of species reactivates of oxygen, responsible for the destruction oxidative in biological systems. That potential quelante has been basing several applied studies to the antioxidant action in foods products, in environmental controls and as antioxidant in the human organism. The objective of this work was to study the degree of interaction of the phytic acid with the metallic ions Fe(II) and Fe(III), of biological importance, in near conditions of the physiologic and the stability of these complexes. Potentiometric titration were driven to determine the constants of formation of the complexes phytic acid-Fe(II) and phytic acid-Fe(III) in solution, under conditions of inert atmosphere, it ionic strength 0,1 mol.L-1 (KCl) at 36±0,1 ºC. For the system phytic acid- Fe(II), were determined seven constant of formation, corresponding to seven species formed in the range p[H] from 2,0 to 12,0. The first constant of formation of the complex phytic acid- Fe(II), it presented log K = 16,06 for the specie [MHL]9-, indicating that a great affinity exists among the ligand monoprotonated with the metal. For the system phytic acid-Fe(III) were determined seven constant of formation, seven species were detected in the range p[H] from 2,5 to 12,0. The first constant of formation of the complex presented log K = 18,87, very high value for the species [ML]9-, this denoted a strong interaction among the ligand deprotonated and the metallic ion. Studies spectroscopy in the region of the UV-Vis, were performed to accompany the formation of the complexes of the phytic acid with the metallic ions Fe(II) and Fe(III). In the studies of UV-Vis of the phytic acid in absence of the metallic ions, not occurred any absorption in the area of wavelength from 200 to 800 nm. Already for the ligand in the presence of the metallic ions two absorption bands were detected in 216 and 279 nm for the phytic acid-Fe(II) and 218 and 274 nm for the phytic acid Fe(III). Those are bands of transfer of electrons of the ligand for the metallic ion with formation of the linking coordinative. The complexes phytic acid-Fe(II) and phytic acid-Fe(III) were synthesized from the data potentiometric and characterized by absorption spectroscopy in the area of the infrared. The spectra for the system phytic acid in presence of the ions Fe(II), synthesized in pH=7,4, and Fe(III), pH=7,1, showed displacements in the areas of frequency of the groups O=PO3H2 of the phytic acid free. Those displacements, evidence that the ligant is coordinated to the metallic ions. Through the termogravimetry it verified that in the interval from 30 to 780 ºC the loss of total mass of the complex phytic acid-Fe(II) it was of 24,43 %. Of the room temperature up to 185 ºC, occurred the liberation of molecules of hydration water. In superior temperatures of this value the mass losses were relative to the decomposition of the compound, with liberation of constitution water and decomposition of the organic matter, with formation of double pyrophosphate of potassium and Fe(II) and potassium metaphosphate. The phytic acid-Fe(III) complexes presented thermal behavior similar to the complex phytic acid-Fe(II), however for the complex phytic acid-Fe(III) synthesized in pH 7,1 the loss of total mass of it was of 25,64 % in the area from 30 to 800 ºC, while the compound synthesized in pH 9,9 presented a loss of total mass of 31,98 % in the interval of temperature from 30 to 845 ºC. The obtained data, for the three complexes, indicate that the ligand is coordinated with the metallic ions so much in values of low pH as to you value of higher pH.
O ácido fítico dependendo do valor de pH apresenta alto potencial quelante, complexando íons metálicos, inibindo assim a produção de espécies reativas de oxigênio, responsáveis pela destruição oxidativa em sistemas biológicos. Esse potencial quelante tem fundamentado diversos estudos aplicados à ação antioxidante em produtos alimentícios, em controles ambientais e como antioxidante no organismo humano. O objetivo deste trabalho foi estudar o grau de interação do ácido fítico com os íons metálicos Fe(II) e Fe(III), de importância biológica, em condições próximas às fisiológicas e a estabilidade destes complexos. Titulações potenciométricas foram conduzidas para determinar as constantes de formação dos complexos ácido fítico-Fe(II) e ácido fítico-Fe(III) em solução, sob condições de atmosfera inerte, força iônica 0,100 mol.L-1 (KCl) a 36±0,1 ºC. Para o sistema ácido fítico- Fe(II), determinaram sete constantes de formação, correspondente a sete espécies formadas na faixa de p[H] de 2,0 a 12,0. A primeira constante de formação do complexo ácido fítico- Fe(II), apresentou log K=16,06 para a espécie [MHL]9-, indicando que existe uma grande afinidade entre o ligante monoprotonado com o metal. Para o sistema ácido fítico-Fe(III) foram determinadas sete constantes de formação, sete espécies foram detectadas na faixa de p[H] de 2,5 a 12,0. A primeira constante de formação do complexo apresentou log K=18,87, valor muito elevado para a espécie [ML]9-, isto denotou uma forte interação entre o ligante totalmente deprotonado e o íon Fe(III). Estudos espectroscópicos na região do UV-Vis foram realizados para acompanhar a formação dos complexos do ligante com os íons metálicos Fe(II) e Fe(III). Nos estudos de UV-Vis do ácido fítico em ausência dos íons metálicos não ocorreu nenhuma absorção na faixa de comprimento de onda de 200 a 800 nm. Já para o ligante na presença dos íons metálicos foram detectadas duas bandas de absorção em 216 e 279 nm para o ácido fítico-Fe(II) e 218 e 274 nm para o ácido fítico Fe(III). Essas são bandas de transferência de elétrons do ligante para o íon metálico com formação da ligação coordenativa. Os complexos ácido fítico-Fe(II) e ácido fítico-Fe(III) foram sintetizados a partir dos dados potenciométricos e caracterizados por espectroscopia de absorção na região do infravermelho. Os espectros para o sistema ácido fítico em presença do íon Fe(II), sintetizado em pH=7,4, e Fe(III), pH=7,1, mostraram deslocamentos nas regiões de freqüência dos grupamentos O=PO3H2 do ácido fítico livre. Esses deslocamentos evidenciam que o ligante encontra-se coordenado aos íons metálicos. Através da termogravimetria constatou-se que no intervalo de 30 a 780 ºC, a perda de massa total do complexo ácido fítico-Fe(II) foi de 24,43 %. Da temperatura ambiente até 185 ºC, ocorreu a liberação de moléculas de água de hidratação. Em temperaturas superiores deste valor as perdas de massa foram relativas à decomposição do complexo, com liberação de água de constituição e decomposição da matéria orgânica, com formação de pirofosfato duplo de potássio e Fe(II) e metafosfato de potássio. Os complexos ácido fítico-Fe(III) apresentaram comportamento térmico semelhante ao complexo ácido fítico-Fe(II), porém, para o complexo ácido fítico-Fe(III) sintetizado em pH 7,1 a perda de massa total do foi de 25,64 % na faixa de 30 a 800 ºC, enquanto que o complexo sintetizado em pH 9,9 apresentou uma perda de massa total de 31,98 % no intervalo de temperatura de 30 a 845 ºC. Os dados obtidos, para os três complexos, indicam que o ligante encontra-se coordenado com os íons metálicos tanto em valores de pH baixo como em valores de pH mais elevados.
Nasri, Habib. « Synthese et caracterisation de porphyrines de fe(ii) et fe(iii) : modelisation du site actif du centre p460 present dans l'hydroxylamine oxydoreductase de la bacterie nitrosomonas europaea ». Université Louis Pasteur (Strasbourg) (1971-2008), 1987. http://www.theses.fr/1987STR13149.
Texte intégralWang, Lei. « Photodégradation de pollutants organiques induite par des complexes Fe(III)-carboxylate en solutions aqueuses ». Phd thesis, Université Blaise Pascal - Clermont-Ferrand II, 2008. http://tel.archives-ouvertes.fr/tel-00728829.
Texte intégralLivres sur le sujet "Complexes de Fe(III)"
Khan, Tasneem A. Chemistry of organogold (I) & (III) complexes. Manchester : UMIST, 1997.
Trouver le texte intégralW, Buchler J., dir. Metal complexes with Tetrapyrrole Ligands III. Berlin : Springer, 1995.
Trouver le texte intégralHarris, J. Robin, et Jon Marles-Wright, dir. Macromolecular Protein Complexes III : Structure and Function. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-58971-4.
Texte intégralCañadillas-Delgado, Laura. Magnetic interactions in oxo-carboxylate bridged gadolinium (III) complexes. Hauppauge, N.Y : Nova Science Publishers, 2010.
Trouver le texte intégralWright, J. P. The synthesis of organogold(III) complexes with potential medicinal interest. Manchester : UMIST, 1995.
Trouver le texte intégralZemnuhova, L., R. Davidovich, A. Udovenko, A. Panasenko, E. Kovaleva, N. Makarenko, G. Fedorischeva et V. Logvinova. FLUORIDE COMPLEXES OF ANTIMONY(III). SYNTHESIS, STRUCTURE, PROPERTIES, AND APPLICATION. ru : Publishing Center RIOR, 2023. http://dx.doi.org/10.29039/978-5-6050261-1-2.
Texte intégral1978-, O'Shea Brian W., Heger Alexander et Abel Tom G. 1970-, dir. First stars III : Santa Fe, New Mexico, 15-20 July 2007. Melville, N.Y : American Institute of Physics, 2008.
Trouver le texte intégralBarrow, Maureen. Chemistry of some organometallic complexes derived from Iron bis-Triphenylphosphite Tricarbonyl, Fe{P(OPh } (CO). Dublin : University College Dublin, 1998.
Trouver le texte intégralKlüglein, Nicole. Bacterial Fe(III) reduction and Fe(II) oxidation : Relevance for magnetite formation in the environment and the mechanism of nitrate-dependent Fe(II) oxidation. [S.l : s.n.], 2014.
Trouver le texte intégralEl-Naby, Sultan Ahmed Abd. A study of the reactions of nucleophiles with [(Indenyl)Fe(CO)2([eta]1-dppa)]BF4 a=m,e,p. Dublin : University College Dublin, 1997.
Trouver le texte intégralChapitres de livres sur le sujet "Complexes de Fe(III)"
Plyusnin, Victor, Ivan Pozdnyakov, Eugeny Glebov, Vjacheslav Grivin et Nikolai Bazhin. « Intermediates in Photochemistry of Fe(III) Complexes in Water ». Dans The Role of Ecological Chemistry in Pollution Research and Sustainable Development, 65–76. Dordrecht : Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2903-4_7.
Texte intégralYe, Zhonghui, Qing Lin, Yun He, Min Liu et Yanfang Xia. « Magnetic Studies in Complexes Derived from the Reaction of Fe(III) Salen Base Complexes and Hexacyanoferrate ». Dans Lecture Notes in Electrical Engineering, 807–14. London : Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4847-0_99.
Texte intégralBratu, I., V. Chis, L. David, O. Cozar, GH Bora, P. Legrand et J. P. Huvenne. « IR and EPR Studies of Some Fe(III)-Complexes With Antiinflammatory Drugs ». Dans Spectroscopy of Biological Molecules, 557–58. Dordrecht : Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_257.
Texte intégralHockertz, Joachim M., Steen Steenken, Claudia Stockheim et Karl Wieghardt. « Radicals in Aqueous Solution from Fe(III) Complexes with Macrocyclic Ligands Containing Phenolates ». Dans Free Radicals in Biology and Environment, 133–44. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-1607-9_10.
Texte intégralBenkelberg, H. J., U. Deister et P. Warneck. « OH Quantum Yields for the Photodecomposition of FE(III) Hydroxo Complexes in Aqueous Solution and the Reaction of OH with Hydroxymethanesulfonate ». Dans Physico-Chemical Behaviour of Atmospheric Pollutants, 263–69. Dordrecht : Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0567-2_41.
Texte intégralKlein, M., et F. Renz. « Chemical tuning of high-spin complexes based on 3- and 4-hydroxy-pentadentate-Fe (III) complex-units investigated by Mössbauer spectroscopy ». Dans ICAME 2005, 1001–7. Berlin, Heidelberg : Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-49853-7_49.
Texte intégralRenz, F., P. Kerep, D. Hill et M. Klein. « Complexes based on ethylene- and propylene-bridged-pentadentate-Fe(III)-units allow interplay between magnetic centers and multistability investigated by Mössbauer spectroscopy ». Dans ICAME 2005, 981–87. Berlin, Heidelberg : Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-49853-7_46.
Texte intégralSorenson, John J. R., Lee S. F. Soderberg, Max L. Baker, John B. Barnett, Louis W. Chang, Hamid Salari et William M. Willngham. « Radiation Recovery Agents : Cu(II), Mn(II), Zn(II), OR Fe(III) 3,5-Diisopropylsalicylate Complexes Facilitate Recovery from Ionizing Radiation Induced Radical Mediated Tissue Damage ». Dans Advances in Experimental Medicine and Biology, 69–77. Boston, MA : Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5730-8_10.
Texte intégralNakazawa, Hiroshi, et Masumi Itazaki. « Fe–H Complexes in Catalysis ». Dans Iron Catalysis, 27–81. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-14670-1_2.
Texte intégralSchmidtke, Hans-Herbert, C. W. Bradford et M. J. Cleare. « Pentaammineiridium(III) Complexes ». Dans Inorganic Syntheses, 243–47. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132432.ch42.
Texte intégralActes de conférences sur le sujet "Complexes de Fe(III)"
Shukla, Kritika, Ashutosh Mishra et Pradeep Sharma. « Synthesis, characterization, XRD and EXAFS studies of Fe(III) complexes ». Dans PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS : NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098717.
Texte intégralZhou, Danna, Jie Wang, Liwei Hou, Jing Xu et Yan Zhao. « Photochemistry of Fe(III)-Tetracycline Complexes in Aqueous Solution under UV Irradiation ». Dans 2012 Third International Conference on Digital Manufacturing and Automation (ICDMA). IEEE, 2012. http://dx.doi.org/10.1109/icdma.2012.144.
Texte intégralPrajapat, Garima, Uma Rathore, Rama Gupta et N. Bhojak. « Thermal and biological evolution of Fe(III)-Sulfanilamide complexes synthesized by green strategy ». Dans 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5032831.
Texte intégralVidya, G. V., S. S. Meena, Pramod Bhatt, V. Sadasivan et S. Mini. « Spectroscopic studies on Fe(II) and Fe(III) complexes of 5-aryl azo substituted lH-pyrimidine-2,4-dione ». Dans PROCEEDING OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN APPLIED PHYSICS AND MATERIAL SCIENCE : RAM 2013. AIP, 2013. http://dx.doi.org/10.1063/1.4810574.
Texte intégralErmolaeva, A. A., O. M. Lavrova et E. V. Tovkaleva. « Study of the prediction of biological activity and toxicity of Fe (III) complexes with organic ligands ». Dans ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020) : Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0070194.
Texte intégralRidhorkar, B. D., A. A. Ramteke, Y. K. Vyawahare et A. R. Yaul. « Synthesis, characterization and biological screening of Ti(III), Cr(III), Fe(III) and UO2(VI) mononuclear complexes of hydrazone Schiff base ligand containing NON moiety ». Dans NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS : NCPCM2020. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0061306.
Texte intégralPrananto, Yuniar P., Ade H. Rafika, Sasti G. Fadhilah, Muhammad M. Khunur et Rachmat T. Tjahjanto. « Effect of type of Fe(III) salts and reaction temperature in the synthesis of Fe(III)-Mn(II)-Tartrate heteronuclear complex ». Dans CHEMISTRY BEYOND BORDERS : INTERNATIONAL CONFERENCE ON PHYSICAL CHEMISTRY : The 1st Annual Meeting of the Physical Chemistry Division of the Indonesian Chemical Society. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0174980.
Texte intégralSow, Ibrahima Sory, Michel Gelbcke, Franck Meyer, Dong Yang, Koen Robeyns, Véronique Fontaine et François Dufrasne. « Synthesis and antibacterial, antimycobacterial and antifungal activities of the complexes of Fe(II), Fe(III), Cu(II), Zn(II) and Ni(II) of aliphatic hydroxamic acids ». Dans 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland : MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07384.
Texte intégral« Synthesis, characterization and biological properties of new Codeine Fe(III) complex ». Dans International Conference on Medicine, Public Health and Biological Sciences. CASRP Publishing Company, Ltd. Uk, 2016. http://dx.doi.org/10.18869/mphbs.2016.65.
Texte intégralLUCCA, B. A. D., C. A. L. GRAÇA et A. C. S. C. TEIXEIRA. « DEGRADAÇÃO DE ENROFLOXACINA PELO PROCESSO FOTO-FENTON-LIKE UTILIZANDO COMPLEXO DE Fe(III)-TARTARATO COMO FONTE DE Fe (II) ». Dans XXII Congresso Brasileiro de Engenharia Química. São Paulo : Editora Blucher, 2018. http://dx.doi.org/10.5151/cobeq2018-pt.0075.
Texte intégralRapports d'organisations sur le sujet "Complexes de Fe(III)"
Shen, Wen-Tang. A polarographic study of Fe(II) and Fe(III) complexes with catechol. Portland State University Library, janvier 2000. http://dx.doi.org/10.15760/etd.2795.
Texte intégralNieland et Ying. L52105 Improvement in Performance in the Mark III Elastic Wave. Chantilly, Virginia : Pipeline Research Council International, Inc. (PRCI), décembre 2003. http://dx.doi.org/10.55274/r0011087.
Texte intégralKemner, K. M., S. D. Kelly, Bill Burgos et Eric Roden. Reaction-based reactive transport modeling of Fe(III). Office of Scientific and Technical Information (OSTI), juin 2006. http://dx.doi.org/10.2172/896240.
Texte intégralAlexandar, Irina, Nikolay Kaloyanov, Veneta Parvanova, Christian Girginov et Alexander Zahariev. Antimicrobial Activity of Bi(III) Complexes with Some Sulphonic Acids. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, août 2021. http://dx.doi.org/10.7546/crabs.2021.08.06.
Texte intégralNeal, Andrew. Molecular Mechanism of Bacterial Attachment to Fe(III)-Oxide Surfaces. Office of Scientific and Technical Information (OSTI), juin 2006. http://dx.doi.org/10.2172/896798.
Texte intégralMaurice, P. Dissolution of Fe(III)(hydr)oxides by an Aerobic Bacterium. Office of Scientific and Technical Information (OSTI), décembre 2004. http://dx.doi.org/10.2172/837302.
Texte intégralRoden, Eric E., et Matilde M. Urrutia. Advanced Experiment Analysis of controls on Microbial FE(III) Oxide Reduction. Office of Scientific and Technical Information (OSTI), juin 1999. http://dx.doi.org/10.2172/828053.
Texte intégralKelley, D. Kinetics and mechanisms of the reactions of alkyl radicals with oxygen and with complexes of Co(III), Ru(III), and Ni(III). Office of Scientific and Technical Information (OSTI), octobre 1990. http://dx.doi.org/10.2172/6454295.
Texte intégralBurgos, William D., Eric E. Roden et Gour-Tsyh Yeh. Reaction-Based Reactive Transport Modeling of Fe(III) and U(V) Reduction. Office of Scientific and Technical Information (OSTI), juin 2005. http://dx.doi.org/10.2172/893413.
Texte intégralLovley, Derek R. Mechanisms for Electron Transfer Through Pili to Fe(III) Oxide in Geobacter. Office of Scientific and Technical Information (OSTI), mars 2015. http://dx.doi.org/10.2172/1172030.
Texte intégral