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Artykuły w czasopismach na temat "Complexes de Fe(III)"
Rai, Dhanpat, Mikazu Yui i Dean A. Moore. "Isosaccharinate Complexes of Fe(III)". Journal of Solution Chemistry 41, nr 11 (7.11.2012): 1906–21. http://dx.doi.org/10.1007/s10953-012-9911-7.
Pełny tekst źródłaChen, Shangjun, Lu An i Shiping Yang. "Low-Molecular-Weight Fe(III) Complexes for MRI Contrast Agents". Molecules 27, nr 14 (18.07.2022): 4573. http://dx.doi.org/10.3390/molecules27144573.
Pełny tekst źródłaXue, Xiao Fei, Yan Xiang Liu, Yan Qing Shao i 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 (styczeń 2011): 130–34. http://dx.doi.org/10.4028/www.scientific.net/amr.183-185.130.
Pełny tekst źródłaHassen, Jasim, i Jack Silver. "Stability of Fe(III) and Sn(IV) Metalloporphyrins Adsorbed on Cation-Exchanged Montmorillonite". Trends in Sciences 19, nr 8 (27.03.2022): 3426. http://dx.doi.org/10.48048/tis.2022.3426.
Pełny tekst źródłaAnsari, Khairul I., Sahba Kasiri, James D. Grant i Subhrangsu S. Mandal. "Fe(III)-Salen and Salphen Complexes Induce Caspase Activation and Apoptosis in Human Cells". Journal of Biomolecular Screening 16, nr 1 (2.11.2010): 26–35. http://dx.doi.org/10.1177/1087057110385227.
Pełny tekst źródłaManimaran, P., i 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, nr 4 (27.02.2019): 780–84. http://dx.doi.org/10.14233/ajchem.2019.21719.
Pełny tekst źródłaK. Dideriksen, J. A. Baker i S. L. S. Stipp. "Fe isotope fractionation between inorganic aqueous Fe(III) and a Fe siderophore complex". Mineralogical Magazine 72, nr 1 (luty 2008): 313–16. http://dx.doi.org/10.1180/minmag.2008.072.1.313.
Pełny tekst źródłaMelník, Milan, i Marian Koman. "Pyridine-2,6-dicarboxylates in monomeric iron complexes – structural aspects". Reviews in Inorganic Chemistry 40, nr 2 (25.06.2020): 75–89. http://dx.doi.org/10.1515/revic-2019-0017.
Pełny tekst źródłaMonreal-Corona, Roger, Jesse Biddlecombe, Angela Ippolito i Nelaine Mora-Diez. "Theoretical Study of the Iron Complexes with Lipoic and Dihydrolipoic Acids: Exploring Secondary Antioxidant Activity". Antioxidants 9, nr 8 (28.07.2020): 674. http://dx.doi.org/10.3390/antiox9080674.
Pełny tekst źródłaRastogi, Raj Kamal, Sonu Sharma, Gulshan Rastogi i 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, nr 4 (14.12.2016): 177. http://dx.doi.org/10.18510/gctl.2016.242.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaPaul, 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.
Pełny tekst źródłaJones, Morris Edward. "Soluble organic-Fe(III) complexes: rethinking iron solubility and bioavailability". Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/42940.
Pełny tekst źródłaINGLE, 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.
Pełny tekst źródłaGreene, 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.
Pełny tekst źródłaWang, 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.
Pełny tekst źródłaFloquet, Sébastien. "Conversion de spin thermo- et photo-induite de complexes ioniques de fe(iii)". Paris 11, 2001. http://www.theses.fr/2001PA112211.
Pełny tekst źródłaQuirrenbach, 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.
Pełny tekst źródłaThe 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.
Pełny tekst źródłaWang, 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.
Pełny tekst źródłaKsiążki na temat "Complexes de Fe(III)"
Khan, Tasneem A. Chemistry of organogold (I) & (III) complexes. Manchester: UMIST, 1997.
Znajdź pełny tekst źródłaW, Buchler J., red. Metal complexes with Tetrapyrrole Ligands III. Berlin: Springer, 1995.
Znajdź pełny tekst źródłaHarris, J. Robin, i Jon Marles-Wright, red. Macromolecular Protein Complexes III: Structure and Function. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-58971-4.
Pełny tekst źródłaCañadillas-Delgado, Laura. Magnetic interactions in oxo-carboxylate bridged gadolinium (III) complexes. Hauppauge, N.Y: Nova Science Publishers, 2010.
Znajdź pełny tekst źródłaWright, J. P. The synthesis of organogold(III) complexes with potential medicinal interest. Manchester: UMIST, 1995.
Znajdź pełny tekst źródłaZemnuhova, L., R. Davidovich, A. Udovenko, A. Panasenko, E. Kovaleva, N. Makarenko, G. Fedorischeva i 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.
Pełny tekst źródła1978-, O'Shea Brian W., Heger Alexander i Abel Tom G. 1970-, red. First stars III: Santa Fe, New Mexico, 15-20 July 2007. Melville, N.Y: American Institute of Physics, 2008.
Znajdź pełny tekst źródłaBarrow, Maureen. Chemistry of some organometallic complexes derived from Iron bis-Triphenylphosphite Tricarbonyl, Fe{P(OPh } (CO). Dublin: University College Dublin, 1998.
Znajdź pełny tekst źródłaKlüglein, 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.
Znajdź pełny tekst źródłaEl-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.
Znajdź pełny tekst źródłaCzęści książek na temat "Complexes de Fe(III)"
Plyusnin, Victor, Ivan Pozdnyakov, Eugeny Glebov, Vjacheslav Grivin i Nikolai Bazhin. "Intermediates in Photochemistry of Fe(III) Complexes in Water". W 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.
Pełny tekst źródłaYe, Zhonghui, Qing Lin, Yun He, Min Liu i Yanfang Xia. "Magnetic Studies in Complexes Derived from the Reaction of Fe(III) Salen Base Complexes and Hexacyanoferrate". W Lecture Notes in Electrical Engineering, 807–14. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4847-0_99.
Pełny tekst źródłaBratu, I., V. Chis, L. David, O. Cozar, GH Bora, P. Legrand i J. P. Huvenne. "IR and EPR Studies of Some Fe(III)-Complexes With Antiinflammatory Drugs". W Spectroscopy of Biological Molecules, 557–58. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_257.
Pełny tekst źródłaHockertz, Joachim M., Steen Steenken, Claudia Stockheim i Karl Wieghardt. "Radicals in Aqueous Solution from Fe(III) Complexes with Macrocyclic Ligands Containing Phenolates". W Free Radicals in Biology and Environment, 133–44. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-1607-9_10.
Pełny tekst źródłaBenkelberg, H. J., U. Deister i P. Warneck. "OH Quantum Yields for the Photodecomposition of FE(III) Hydroxo Complexes in Aqueous Solution and the Reaction of OH with Hydroxymethanesulfonate". W Physico-Chemical Behaviour of Atmospheric Pollutants, 263–69. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0567-2_41.
Pełny tekst źródłaKlein, M., i F. Renz. "Chemical tuning of high-spin complexes based on 3- and 4-hydroxy-pentadentate-Fe (III) complex-units investigated by Mössbauer spectroscopy". W ICAME 2005, 1001–7. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-49853-7_49.
Pełny tekst źródłaRenz, F., P. Kerep, D. Hill i M. Klein. "Complexes based on ethylene- and propylene-bridged-pentadentate-Fe(III)-units allow interplay between magnetic centers and multistability investigated by Mössbauer spectroscopy". W ICAME 2005, 981–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-49853-7_46.
Pełny tekst źródłaSorenson, John J. R., Lee S. F. Soderberg, Max L. Baker, John B. Barnett, Louis W. Chang, Hamid Salari i 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". W 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.
Pełny tekst źródłaNakazawa, Hiroshi, i Masumi Itazaki. "Fe–H Complexes in Catalysis". W Iron Catalysis, 27–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-14670-1_2.
Pełny tekst źródłaSchmidtke, Hans-Herbert, C. W. Bradford i M. J. Cleare. "Pentaammineiridium(III) Complexes". W Inorganic Syntheses, 243–47. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132432.ch42.
Pełny tekst źródłaStreszczenia konferencji na temat "Complexes de Fe(III)"
Shukla, Kritika, Ashutosh Mishra i Pradeep Sharma. "Synthesis, characterization, XRD and EXAFS studies of Fe(III) complexes". W 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.
Pełny tekst źródłaZhou, Danna, Jie Wang, Liwei Hou, Jing Xu i Yan Zhao. "Photochemistry of Fe(III)-Tetracycline Complexes in Aqueous Solution under UV Irradiation". W 2012 Third International Conference on Digital Manufacturing and Automation (ICDMA). IEEE, 2012. http://dx.doi.org/10.1109/icdma.2012.144.
Pełny tekst źródłaPrajapat, Garima, Uma Rathore, Rama Gupta i N. Bhojak. "Thermal and biological evolution of Fe(III)-Sulfanilamide complexes synthesized by green strategy". W 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5032831.
Pełny tekst źródłaVidya, G. V., S. S. Meena, Pramod Bhatt, V. Sadasivan i S. Mini. "Spectroscopic studies on Fe(II) and Fe(III) complexes of 5-aryl azo substituted lH-pyrimidine-2,4-dione". W 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.
Pełny tekst źródłaErmolaeva, A. A., O. M. Lavrova i E. V. Tovkaleva. "Study of the prediction of biological activity and toxicity of Fe (III) complexes with organic ligands". W 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.
Pełny tekst źródłaRidhorkar, B. D., A. A. Ramteke, Y. K. Vyawahare i 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". W NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM2020. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0061306.
Pełny tekst źródłaPrananto, Yuniar P., Ade H. Rafika, Sasti G. Fadhilah, Muhammad M. Khunur i Rachmat T. Tjahjanto. "Effect of type of Fe(III) salts and reaction temperature in the synthesis of Fe(III)-Mn(II)-Tartrate heteronuclear complex". W 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.
Pełny tekst źródłaSow, Ibrahima Sory, Michel Gelbcke, Franck Meyer, Dong Yang, Koen Robeyns, Véronique Fontaine i 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". W 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07384.
Pełny tekst źródła"Synthesis, characterization and biological properties of new Codeine Fe(III) complex". W International Conference on Medicine, Public Health and Biological Sciences. CASRP Publishing Company, Ltd. Uk, 2016. http://dx.doi.org/10.18869/mphbs.2016.65.
Pełny tekst źródłaLUCCA, B. A. D., C. A. L. GRAÇA i A. C. S. C. TEIXEIRA. "DEGRADAÇÃO DE ENROFLOXACINA PELO PROCESSO FOTO-FENTON-LIKE UTILIZANDO COMPLEXO DE Fe(III)-TARTARATO COMO FONTE DE Fe (II)". W XXII Congresso Brasileiro de Engenharia Química. São Paulo: Editora Blucher, 2018. http://dx.doi.org/10.5151/cobeq2018-pt.0075.
Pełny tekst źródłaRaporty organizacyjne na temat "Complexes de Fe(III)"
Shen, Wen-Tang. A polarographic study of Fe(II) and Fe(III) complexes with catechol. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.2795.
Pełny tekst źródłaNieland i Ying. L52105 Improvement in Performance in the Mark III Elastic Wave. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), grudzień 2003. http://dx.doi.org/10.55274/r0011087.
Pełny tekst źródłaKemner, K. M., S. D. Kelly, Bill Burgos i Eric Roden. Reaction-based reactive transport modeling of Fe(III). Office of Scientific and Technical Information (OSTI), czerwiec 2006. http://dx.doi.org/10.2172/896240.
Pełny tekst źródłaAlexandar, Irina, Nikolay Kaloyanov, Veneta Parvanova, Christian Girginov i Alexander Zahariev. Antimicrobial Activity of Bi(III) Complexes with Some Sulphonic Acids. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, sierpień 2021. http://dx.doi.org/10.7546/crabs.2021.08.06.
Pełny tekst źródłaNeal, Andrew. Molecular Mechanism of Bacterial Attachment to Fe(III)-Oxide Surfaces. Office of Scientific and Technical Information (OSTI), czerwiec 2006. http://dx.doi.org/10.2172/896798.
Pełny tekst źródłaMaurice, P. Dissolution of Fe(III)(hydr)oxides by an Aerobic Bacterium. Office of Scientific and Technical Information (OSTI), grudzień 2004. http://dx.doi.org/10.2172/837302.
Pełny tekst źródłaRoden, Eric E., i Matilde M. Urrutia. Advanced Experiment Analysis of controls on Microbial FE(III) Oxide Reduction. Office of Scientific and Technical Information (OSTI), czerwiec 1999. http://dx.doi.org/10.2172/828053.
Pełny tekst źródłaKelley, 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), październik 1990. http://dx.doi.org/10.2172/6454295.
Pełny tekst źródłaBurgos, William D., Eric E. Roden i Gour-Tsyh Yeh. Reaction-Based Reactive Transport Modeling of Fe(III) and U(V) Reduction. Office of Scientific and Technical Information (OSTI), czerwiec 2005. http://dx.doi.org/10.2172/893413.
Pełny tekst źródłaLovley, Derek R. Mechanisms for Electron Transfer Through Pili to Fe(III) Oxide in Geobacter. Office of Scientific and Technical Information (OSTI), marzec 2015. http://dx.doi.org/10.2172/1172030.
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