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Journal articles on the topic 'Iron, structural'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 August 2024

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1

van der Lee, A., and R. Astier. "Structural evolution in iron tellurates." Journal of Solid State Chemistry 180, no. 4 (April 2007): 1243–49. http://dx.doi.org/10.1016/j.jssc.2007.01.022.

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2

de Wit, H. J., F. W. A. Dirne, and C. H. M. Witmer. "Magnetic and structural properties of iron/amorphous iron alloy multilayers." Journal of Applied Physics 67, no. 9 (May 1990): 5131–33. http://dx.doi.org/10.1063/1.344664.

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3

Mann, S., V. J. Wade, D. P. E. Dickson, N. M. K. Reid, R. J. Ward, M. O'Connell, and T. J. Peters. "Structural specificity of haemosiderin iron cores in iron-overload diseases." FEBS Letters 234, no. 1 (July 4, 1988): 69–72. http://dx.doi.org/10.1016/0014-5793(88)81305-x.

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4

Jormakka, Mika. "Structural insights into ferroportin mediated iron transport." Biochemical Society Transactions 51, no. 6 (December 20, 2023): 2143–52. http://dx.doi.org/10.1042/bst20230594.

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Iron is a vital trace element for almost all organisms, and maintaining iron homeostasis is critical for human health. In mammals, the only known gatekeeper between intestinally absorbed iron and circulatory blood plasma is the membrane transporter ferroportin (Fpn). As such, dysfunction of Fpn or its regulation is a key driver of iron-related pathophysiology. This review focuses on discussing recent insights from high-resolution structural studies of the Fpn protein family. While these studies have unveiled crucial details of Fpn regulation and structural architecture, the associated functional studies have also at times provided conflicting data provoking more questions than answers. Here, we summarize key findings and illuminate important remaining questions and contradictions.
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5

Fuentealba, Mauricio, Deborah Gonzalez, and Vania Artigas. "Structural Characterization of Iron(iii) Dinuclear Complexes." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1695. http://dx.doi.org/10.1107/s2053273314083041.

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Dinuclear complexes have been studied for different purposes: magnetic materials[1], Non-linear optics materials[2], molecular switches [3], mixed-valence systems, etc. With these antecedents in mind, we present in this work a new series of dinuclear Iron(III) complexes formed by different Schiff bases ligands. The reaction starting from the iron chloride salts with the 5-chloro or 5-bromo-salycilaldehyde and ethylendiamine yields two different kinds of dinuclear iron complexes in different reaction conditions. The first one (Fig N°1), are methoxo-bridged dinuclear iron(III) complexes in which each metal centre is coordinated with one mono-condensated Schiff base ligand, one 4-chloro or 4-bromo-2-(dimethoxymethyl)phenoxo ligand and two bridging methoxo ligands. The iron(III) centres are hexacoordinated (FeN2O4), the coordination sphere is formed by 2 nitrogen atoms of the ethylendiamine fragment, 2 oxygen atoms from the hydroxyl of the Schiff base and two O atoms from the methoxo ligands. Both iron(III) centres are related by a inversion centre. The second one (Fig N°2), the dinuclear complex is formed for the double condensation of ethylendiamine with 5-chloro or 5-bromo-salycilaldehyde and one oxygen from the dianionic ligand act as bridge with another unit. The iron (III) centres are also hexaccordinated (FeN2O3Cl) formed by 2 nitrogen atoms from ethylendiamine fragment and 3 oxygen atoms from hydroxyl from Schiff base ligands and one chloro ligand. Finally, the electronic and redox properties have been studied by UV-Visible and cyclic voltammetry. ACKNOWLEDGMENT FONDECYT N01130640, FONDEQUIP EQM120095 and Beca CONICYT folio 21130944
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6

Rutz, Frederick R., Joel Watters, Preeda Chromshrimake, and Zachary Rogers. "Welding of Historic Structural Wrought Iron." Journal of Materials in Civil Engineering 30, no. 6 (June 2018): 04018097. http://dx.doi.org/10.1061/(asce)mt.1943-5533.0002222.

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7

Sikka, Vinod K., and Chain T. Liu. "Iron-Aluminide Alloys for Structural Use." Materials Technology 9, no. 7-8 (July 1994): 159–62. http://dx.doi.org/10.1080/10667857.1994.11785056.

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8

Lindley, Peter F. "Iron in biology: a structural viewpoint." Reports on Progress in Physics 59, no. 7 (July 1, 1996): 867–933. http://dx.doi.org/10.1088/0034-4885/59/7/002.

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9

Marasinghe, G. "Structural features of iron phosphate glasses." Journal of Non-Crystalline Solids 222, no. 1-2 (December 11, 1997): 144–52. http://dx.doi.org/10.1016/s0022-3093(97)00393-1.

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10

Marasinghe, G. K., M. Karabulut, C. S. Ray, D. E. Day, M. G. Shumsky, W. B. Yelon, C. H. Booth, P. G. Allen, and D. K. Shuh. "Structural features of iron phosphate glasses." Journal of Non-Crystalline Solids 222 (December 1997): 144–52. http://dx.doi.org/10.1016/s0022-3093(97)90107-1.

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11

Krewulak, Karla D., and Hans J. Vogel. "Structural biology of bacterial iron uptake." Biochimica et Biophysica Acta (BBA) - Biomembranes 1778, no. 9 (September 2008): 1781–804. http://dx.doi.org/10.1016/j.bbamem.2007.07.026.

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12

Reis, Signo T., Walter M. Pontuschka, Andrea Moguš-Milanković, and Carmen S. M. Partiti. "Structural features of iron-phosphate glass." Journal of the American Ceramic Society 100, no. 5 (March 7, 2017): 1976–81. http://dx.doi.org/10.1111/jace.14731.

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13

Болдырев, Денис, Denis Boldyrev, Сергей Давыдов, Sergey Davydov, Виталий Сканцев, Vitaliy Skantsev, Лариса Попова, and Larisa Popova. "Structural iron with compact forms of graphite." Bulletin of Bryansk state technical university 2015, no. 3 (September 30, 2015): 24–29. http://dx.doi.org/10.12737/22979.

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The identity of the mechanical properties of ductile iron (QP) and cast iron with compact forms of graphite, in particular, with nodular and vermicular graphite (CSWG). Given the fundamental differences in techniques of obtaining QP and CSUG in terms of their labor, material and energy intensity at virtually the identical strength properties shown to be technically and economically preferable for the manufacture of castings of CSWG and other cast iron with a compact form of graphite.
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14

Marita, Yusrini, and Iskandar Idris Yaacob. "Structural Characterization of Electrodeposited Nickel-Iron Alloy Films." Materials Science Forum 654-656 (June 2010): 2430–33. http://dx.doi.org/10.4028/www.scientific.net/msf.654-656.2430.

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Nickel-iron nanocrystalline alloy films were prepared on copper substrates by electrochemical deposition at various current densities of 6, 9.7, 11.5 and 15.2 A dm-2. X-ray diffraction measurements confirmed that all nickel-iron alloy films formed have face-centered cubic structure. The structural parameters such as the lattice constant, crystallite size, microstrain and dislocation density were determined for the nickel-iron alloy films. The crystallite size of the films reduced from 17 to 12.9 nm when the current densities were decreased. The reduction in crystallite size increased the dislocation density. Magnetic property measurements using alternating gradient magnetometer indicated that these alloys were ferromagnetic. The saturation magnetization Ms of nickel-iron alloy films increased with decreasing deposition current density, which was attributed to the increase of iron content. Nickel-iron alloy film prepared at deposition current density of 6 A dm-2 showed the maximum value of Ms. The coercivity of nickel-iron alloy films increased with decreasing current density, which was likely caused by reduction in crystallite size.
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15

Collette, Quentin, Ine Wouters, Michael De Bouw, Leen Lauriks, and Abdelrahman Younes. "Victor Horta’s Iron Architecture: A Structural Analysis." Advanced Materials Research 133-134 (October 2010): 373–78. http://dx.doi.org/10.4028/www.scientific.net/amr.133-134.373.

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The internationally acknowledged Art Nouveau architect Victor Horta built remarkable artifacts of public iron architecture in Brussels. His projects display an innovative philosophy based on apparent iron frameworks used in a very efficient manner. As a supplement to the ample historical and architectural studies on Belgium’s most famous Art Nouveau architect, this paper puts Horta’s innovative structural practice of iron into the picture. To reach this goal, a structural analysis of four of Horta’s most interesting projects is carried out, going into the following topics: conceptual philosophy (structural typology), building techniques (shapes, connection details) and the coherence of the structural logic (structural usefulness).
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16

Kuhn, L. Theil, A. Bojesen, L. Timmermann, M. Meedom Nielsen, and S. M rup. "Structural and magnetic properties of core shell iron iron oxide nanoparticles." Journal of Physics: Condensed Matter 14, no. 49 (November 27, 2002): 13551–67. http://dx.doi.org/10.1088/0953-8984/14/49/311.

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17

Sah, Stuti, and Rajni Singh. "Siderophore: Structural And Functional Characterisation – A Comprehensive Review." Agriculture (Polnohospodárstvo) 61, no. 3 (September 1, 2015): 97–114. http://dx.doi.org/10.1515/agri-2015-0015.

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Abstract Plants and microbes have enormous importance in our daily life. Iron is said to be the fourth most abundant element in the earth's crust from soil, still many plants face problem in uptaking iron because it is found in insoluble form, which severely restricts the bioavailability of this metal. In response to this, microorganisms present in soil such as Pseudomonas sp., Enterobacter genera, Bacillus and Rhodococcus produce special iron carriers or iron-binding compounds called as ‘siderphores’ or ‘siderochromes’. This paper is an attempt to review the importance of siderphores in enhancing plants’ iron utilisation strategies, the mode of transport of siderophores along with iron across the memberane and depending on the difference in their chemical structure, functional moiety and their source of isolation of four different types of siderophore (hydroxamates, catecholates, carboxylates and siderophore with mixed ligand). Siderophore and their derivative have large application in agriculture as to increase soil fertility and as biocontrol for fungal pathogen. This review unlike other reviews includes (1) types of siderophore, (2) the structural difference amongst them, (3) siderophore biosynthesis, (4) transport mechanism, (5) the genetics of siderophore and (6) their efficacy in human life.
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18

Astashchenko, V. I., G. F. Mukhametzyanova, and I. R. Mukhametzyanov. "Structural Heredity of Cast Iron in Bimetallic Products." Solid State Phenomena 316 (April 2021): 221–26. http://dx.doi.org/10.4028/www.scientific.net/ssp.316.221.

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Properties of cast iron on the bimetallic part depend on the initial structural state of the cladded cast iron and technological parameters of its induction cladding process. Methodology of predicting the properties of the cast iron in the bimetallic valve tappets ICE largest hardness billets was used for cladding, the silicon content in the alloy cladding and the technological parameters of the process, as well. A hereditary relationship between the initial state of the cast iron of the semi-finished product, used for induction cladding, and the structural state of the layer of weld on the steel base of the part, has been established.
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19

Preza, Gloria, Augustine Fernandes, Richard J. Clark, David J. Craik, Tomas Ganz, and Elizabeta Nemeth. "Structural Aspects of Hepcidin-Ferroportin Binding." Blood 112, no. 11 (November 16, 2008): 119. http://dx.doi.org/10.1182/blood.v112.11.119.119.

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Abstract Hepcidin, a 25-amino acid peptide hormone, is the principal regulator of plasma iron concentrations in a wide range of organisms, from humans to fish. The hepcidin receptor is the iron channel ferroportin (Fpn), which exports iron from duodenal enterocytes, macrophages and hepatocytes into plasma. Hepcidin binding to Fpn results in internalization and degradation of the ligand-receptor complex and reduced iron efflux from cells into plasma. Abnormal production of hepcidin or abnormal interaction with Fpn causes a spectrum of iron disorders. We analyzed the nature of the interaction and critical structural features of hepcidin and Fpn. The binding of hepcidin to Fpn showed an unusual temperature dependence, with loss of binding/internalization at temperatures lower that 15C. To establish whether initiation of internalization stabilized binding, we used Fpn mutated at Tyr302 and Tyr303, which does not internalize and showed that the mutant was still able to bind 125I-hepcidin, with a similar EC50 and temperature dependence as wt Fpn. We next addressed Fpn structural features required for interaction with hepcidin. Several Fpn mutations in humans cause a phenotype consistent with resistance to hepcidin. We thus generated Fpn plasmids carrying the specific human mutations, transiently transfected cells with the mutants, and measured 125I-hepcidin binding to cells. The results showed that thiol form of Cys326 is essential for hepcidin binding since substitution of this Cys with Ser or Thr preserved the iron exporting function of Fpn but resulted in a complete loss of hepcidin binding, as did the treatment of cells with non-permeable sulfhydryl alkylating agents. The essential role of the C326 residue in hepcidin binding accounts for the early and severe iron overload in patients with C326S or Y substitution. We also showed that the N-terminus of hepcidin is essential for its binding to Fpn. The sequential truncation of five N-terminal residues resulted in a gradual reduction in activity. Ala scanning of the N-terminus showed that Phe4 and Ile6 substitutions resulted in >80% and 50% decrease in binding respectively. To understand the requirements for biological activity at position 4, we tested a series of Phe4 analogues. Substitution with a similar hydrophobic residue, cyclohexylalanine, had no effect on activity; substitution with polar Tyr caused a 50% reduction in activity; substitution with charged residues Lys or Asp resulted in a complete loss of activity, as did substitution with D-Phe. The results indicated that position 4 requires a bulky hydrophobic residue and that the interaction with Fpn is stereospecific. Similarly, substitution of Ile at position 6 with charged residues caused a complete loss of activity. Understanding the molecular framework responsible for hepcidin-Fpn interaction will facilitate the development of drug leads for a range of iron disorders.
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20

Yu, S., and G. M. Chow. "Synthesis, structural, magnetic, and cytotoxic properties of iron oxide coated iron/iron-carbide nanocomposite particles." Journal of Applied Physics 98, no. 11 (December 2005): 114306. http://dx.doi.org/10.1063/1.2138375.

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21

Baker, Edward N., Heather M. Baker, and Richard D. Kidd. "Lactoferrin and transferrin: Functional variations on a common structural framework." Biochemistry and Cell Biology 80, no. 1 (February 1, 2002): 27–34. http://dx.doi.org/10.1139/o01-153.

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Lactoferrin shares many structural and functional features with serum transferrin, including an ability to bind iron very tightly, but reversibly, a highly-conserved three-dimensional structure, and essentially identical iron-binding sites. Nevertheless, lactoferrin has some unique properties that differentiate it: an ability to retain iron to much lower pH, a positively charged surface, and other surface features that give it additional functions. Here, we review the structural basis for these similarities and differences, including the importance of dynamics and conformational change, and specific interactions that regulate iron binding and release.Key words: transferrin, protein structure, dynamics, iron binding.
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22

Mnati, Ali A., Kadhim K. Resan, and Ehsan Omaraa. "Structural Characterization and Mechanical Properties of Ductile Iron - Enhanced Alloyed Ductile Iron." Key Engineering Materials 924 (June 30, 2022): 37–46. http://dx.doi.org/10.4028/p-oko587.

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In this study, an attempt has been made to produce ductile iron or spheroidal graphite iron and to study its important properties with a view to reduce the import of machinery parts made of ductile iron. Locally available compressor scrap (i.e. the compressor cylinder) which is made from grey cast iron was used to produce ductile iron using a crucible furnace that is fired by oil. Also, recycling of the grey cast iron to ductile iron was investigated and its effect on the microstructure, chemical composition, mechanical properties and chip shape. The mechanical and structural characteristics of the ductile irons that alloyed by the supplement of Ni, Mo, Mg, and Cr were studied In this study, four kilograms of the scrap were charged into an oil-fired crucible furnace. The scrap was heated to 1400°C with using a temperature controller to monitor the temperature with an inserted thermocouple. For desulphurization, the mixture of 3 wt.% burnt lime with 1 wt.% fluorspar of scrap weight was added to the molten at 1400°C by direct tapping into the molten. Then, 2.75 wt.% nickel element, 0.75 wt.% ferromolybdenum and 0.5wt.% ferromanganese of the scrap weight were added. Also, 1.25 wt.% spheroidizing alloy (FeSiMg9) and 1wt.% inoculant alloy of scrap weight were used to treat the iron melt at 1450°C. The analysis of scrap sample and product sample was done to determine their chemical composition, tensile strength, impact strength, hardness, and microstructure. The scrap and the as-cast product analysis determine its chemical composition, tensile, impact, hardness and microstructure. The microstructures revealed that the scrap contains flake graphite and the as-cast product contains spheroid graphite. An increase of the ultimate tensile stress (537.17 MPa), elongation (10%), hardness value (480.4 HB) and impact value (11.21 J) was observed for the alloyed ductile iron as compared with the mechanical properties of grey cast iron scrap, including (247.75 MPa), (6%), (400.3 HB) and (5.66 J), respectively. One of the important conclusions is the plunge container manufactured, and that was used according to the plunging technique followed in this investigation proved successful
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23

Marchewka, Damian, Irena Roterman, Magdalena Strus, Klaudyna Śpiewak, and Grzegorz Majka. "Structural Analysis of the Lactoferrin Iron Binding Pockets." bams 8, no. 4 (December 2012): 351–59. http://dx.doi.org/10.1515/bams-2012-0024.

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ABSTRACT Lactoferrin (Lf) - member of the transferrin family of proteins responsible for many different functions in the body of mammals participates in regulation of free iron level in the body fluids making the protein bacteriostatic. The main goal of studies was to test the suitability of molecular dynamic simulation to study structural changes in the tertiary structure of lactoferrin. According to ConSurf Server analysis one of the most conservative amino acids was found not only in iron- but also in carbohydrates- binding pockets which may suggest a significant impact of carbohydrates on the functions performed by lactoferrin. Pocket-Finder program applied to find iron-binding pockets revealed the potential Fe binding area. The stability of the ligand deprived protein was verified performing the 50 ns dynamic simulation using the Gromacs program. The tertiary structure changes during the simulation were observed in N-lob solely. No structural changes were observed in C-lob iron-binding pocket.
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24

Tabassam, Misbah, Muhammad Imran, Amna Farooq, Syeda Robina Gillani, Zaid Mehmood, Asad Gulzar, and Liviu Mitu. "Synthesis and Structural Studies of (h3-allyl)carbonylnitrosyl Triphenylphosphine Iron Complexes." Revista de Chimie 70, no. 11 (December 15, 2019): 3893–98. http://dx.doi.org/10.37358/rc.19.11.7666.

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In this paper we report the preparation of two (h3-allyl)carbonylnitrosyltriphenylphosphine iron complexes i.e.(p-allyl)carbonylnitrosyltriphenylphosphine iron (1) and (2-methyl-p-allyl) carbonylnit rosyltriphenylphosphine iron (2). These complexes (1) and (2) were prepared by reacting (p-allyl)dicarbonylnitrosyl iron and (2-methyl-p-allyl)dicarbonylnitrosyl iron with triphenylphosphine under inert atmospheric conditions. Both the resulting complexes were sufficiently and well characterized by IR, 1H NMR, 13C NMR, ESI/MS, HRMS and single crystal XRD. Triphenylphosphine ligand was found to be strong sigma donor and replaced carbonyl ligand readily. XRD revealed that the geometry of iron in both complexes is distorted octahedral.
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25

Tabassam, Misbah, Muhammad Imran, Amna Farooq, Syeda Robina Gillani, Zaid Mehmood, Asad Gulzar, and Liviu Mitu. "Synthesis and Structural Studies of (h3-allyl)carbonylnitrosyl Triphenylphosphine Iron Complexes." Revista de Chimie 70, no. 11 (December 15, 2019): 3893–98. http://dx.doi.org/10.37358/rc.70.19.11.7666.

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In this paper we report the preparation of two (h3-allyl)carbonylnitrosyltriphenylphosphine iron complexes i.e.(p-allyl)carbonylnitrosyltriphenylphosphine iron (1) and (2-methyl-p-allyl) carbonylnit rosyltriphenylphosphine iron (2). These complexes (1) and (2) were prepared by reacting (p-allyl)dicarbonylnitrosyl iron and (2-methyl-p-allyl)dicarbonylnitrosyl iron with triphenylphosphine under inert atmospheric conditions. Both the resulting complexes were sufficiently and well characterized by IR, 1H NMR, 13C NMR, ESI/MS, HRMS and single crystal XRD. Triphenylphosphine ligand was found to be strong sigma donor and replaced carbonyl ligand readily. XRD revealed that the geometry of iron in both complexes is distorted octahedral.
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26

Clarke, Teresa, Leslie Tari, and Hans Vogel. "Structural Biology of Bacterial Iron Uptake Systems." Current Topics in Medicinal Chemistry 1, no. 1 (May 1, 2001): 7–30. http://dx.doi.org/10.2174/1568026013395623.

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27

Thew, Iain, Alastair Sutherland, and Dimitris Theodossopoulos. "Structural response of drystone Iron Age brochs." Proceedings of the Institution of Civil Engineers - Structures and Buildings 166, no. 6 (June 2013): 316–24. http://dx.doi.org/10.1680/stbu.11.00056.

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28

Melník, M., and P. Mikuš. "Structural Characterization of Heterometallic Gold – Iron Clusters." International Research Journal of Pure and Applied Chemistry 5, no. 4 (January 10, 2015): 273–317. http://dx.doi.org/10.9734/irjpac/2015/11690.

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29

Mangani, S., I. Bertini, D. Lalli, C. Pozzi, C. Rosa, and P. Turano. "Structural insight into iron pathways in ferritin." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (August 22, 2011): C772. http://dx.doi.org/10.1107/s0108767311080482.

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30

Greneche, J. M., A. Le Bail, M. Leblanc, A. Mosset, F. Varret, J. Galy, and G. Ferey. "Structural aspects of amorphous iron(III) fluorides." Journal of Physics C: Solid State Physics 21, no. 8 (March 20, 1988): 1351–61. http://dx.doi.org/10.1088/0022-3719/21/8/011.

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31

Udovsky, A. L. "On the structural stratification of iron nanoparticles." Journal of Physics: Conference Series 1658 (October 2020): 012065. http://dx.doi.org/10.1088/1742-6596/1658/1/012065.

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32

Baird, Thomas, Kenneth C. Campbell, Peter J. Holliman, Robert Hoyle, Diane Stirling, and B. Peter Williams. "Structural and morphological studies of iron sulfide." Journal of the Chemical Society, Faraday Transactions 92, no. 3 (1996): 445. http://dx.doi.org/10.1039/ft9969200445.

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33

Fox, S., and H. J. F. Jansen. "Structural and magnetic properties of trigonal iron." Physical Review B 53, no. 9 (March 1, 1996): 5119–22. http://dx.doi.org/10.1103/physrevb.53.5119.

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34

Tan, Lay Ling, R. H. Holm, and Sonny C. Lee. "Structural analysis of cubane-type iron clusters." Polyhedron 58 (July 2013): 206–17. http://dx.doi.org/10.1016/j.poly.2013.02.031.

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35

Chen, W. M., J. Chen, N. L. Chen, X. Zhang, X. S. Wu, X. Jin, and S. S. Jiang. "Structural transition of La.Ba.Cu.O doped with iron." Physica C: Superconductivity 282-287 (August 1997): 753–54. http://dx.doi.org/10.1016/s0921-4534(97)00391-2.

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36

Orolínová, Zuzana, and Annamária Mockovčiaková. "Structural study of bentonite/iron oxide composites." Materials Chemistry and Physics 114, no. 2-3 (April 2009): 956–61. http://dx.doi.org/10.1016/j.matchemphys.2008.11.014.

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37

Reis, S. T., D. L. A. Faria, J. R. Martinelli, W. M. Pontuschka, D. E. Day, and C. S. M. Partiti. "Structural features of lead iron phosphate glasses." Journal of Non-Crystalline Solids 304, no. 1-3 (June 2002): 188–94. http://dx.doi.org/10.1016/s0022-3093(02)01021-9.

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38

Antoni, Emilie, Lionel Montagne, Sylvie Daviero, Gérard Palavit, Jean-Luc Bernard, Alain Wattiaux, and Hervé Vezin. "Structural characterization of iron–alumino–silicate glasses." Journal of Non-Crystalline Solids 345-346 (October 2004): 66–69. http://dx.doi.org/10.1016/j.jnoncrysol.2004.07.045.

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39

Eremyashev, V. E., L. A. Shabunina, and A. B. Mironov. "Structural Particulars of Iron-Containing Borosilicate Glasses." Glass and Ceramics 70, no. 11-12 (March 2014): 391–94. http://dx.doi.org/10.1007/s10717-014-9587-0.

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40

Taft, K. L., G. C. Papaefthymiou, R. Sessoli, C. D. Delfs, D. Gatteschi, and S. J. Lippard. "Polynuclear iron complexes: Three new structural types." Journal of Inorganic Biochemistry 51, no. 1-2 (July 1993): 484. http://dx.doi.org/10.1016/0162-0134(93)85512-7.

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41

Nishchev, K. N., M. A. Golub’ev, Yu V. Maksimov, V. I. Beglov, V. M. Kyashkin, and A. A. Panov. "Structural changes in iron-cobalt oxide nanosystems." Technical Physics 60, no. 5 (May 2015): 695–99. http://dx.doi.org/10.1134/s1063784215050187.

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Ennis, Marie, and Donald Friedman. "Cast-Iron Façades as Structural Shear Walls." Journal of Architectural Conservation 17, no. 3 (January 2011): 43–58. http://dx.doi.org/10.1080/13556207.2011.10785096.

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Vasilevsky, I., N. J. Rose, and R. E. Stenkamp. "Structural studies of oxygen-bridged iron compounds." Acta Crystallographica Section B Structural Science 48, no. 4 (August 1, 1992): 444–49. http://dx.doi.org/10.1107/s0108768192000107.

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Crow, Allister, Tamara L. Lawson, Allison Lewin, Geoffrey R. Moore, and Nick E. Le Brun. "Structural Basis for Iron Mineralization by Bacterioferritin." Journal of the American Chemical Society 131, no. 19 (May 20, 2009): 6808–13. http://dx.doi.org/10.1021/ja8093444.

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Sales, B. C., M. M. Abraham, J. B. Bates, and L. A. Boatner. "Structural properties of lead-iron phosphate glasses." Journal of Non-Crystalline Solids 71, no. 1-3 (May 1985): 103–12. http://dx.doi.org/10.1016/0022-3093(85)90279-0.

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46

Karabulut, M., M. Yuksek, G. K. Marasinghe, and D. E. Day. "Structural features of hafnium iron phosphate glasses." Journal of Non-Crystalline Solids 355, no. 31-33 (September 2009): 1571–73. http://dx.doi.org/10.1016/j.jnoncrysol.2009.06.005.

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Mandal, S., S. Hazra, D. Das, and A. Ghosh. "Structural studies of binary iron vanadate glass." Journal of Non-Crystalline Solids 183, no. 3 (April 1995): 315–19. http://dx.doi.org/10.1016/0022-3093(94)00571-0.

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Matsuda, C. K., R. Barco, P. Sharma, V. Biondo, A. Paesano, J. B. M. da Cunha, and B. Hallouche. "Iron-containing pyrochlores: structural and magnetic characterization." Hyperfine Interactions 175, no. 1-3 (February 2007): 55–61. http://dx.doi.org/10.1007/s10751-008-9588-x.

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Tiwari, M. K., Arjun Singh, Ajay Khooha, and U. K. Goutam. "Structural investigation of Ayurveda Lauha (Iron) Bhasma." Journal of Ayurveda and Integrative Medicine 14, no. 2 (March 2023): 100690. http://dx.doi.org/10.1016/j.jaim.2023.100690.

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Yunfei, Lin, Zhang Yan, Huang Weiwei, Lu Kunquan, and Zhao Yaqin. "Structural study of iron in phosphate glasses." Journal of Non-Crystalline Solids 112, no. 1-3 (October 1989): 136–41. http://dx.doi.org/10.1016/0022-3093(89)90508-5.

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