Relevant bibliographies by topics / Oxalate complexes

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Oxalate complexes'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Oxalate complexes"

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Aplin, R., A. J. Feitz, and T. D. Waite. "Effect of Fe(III)-ligand properties on effectiveness of modified photo-Fenton processes." Water Science and Technology 44, no. 5 (2001): 23–30. http://dx.doi.org/10.2166/wst.2001.0243.

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This paper examines a modified photo-Fenton (UV/Fe oxalate/H2O2 process. The degradation of oxalate in this system in the absence of Reactive Red 235 was studied using both experimentation and kinetic modelling. The degradation of Reactive Red 235 in this system was also studied. Light intensity and solution pH had large effects on the degradation of both oxalate and Reactive Red 235, with the effect of pH not due simply to speciation changes. The most important properties of the oxalate ligand in the UV/Fe oxalate/H2O2 process are that it forms Fe(III)-oxalato complexes that are easily photol
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A., K. BANERJEE, SATYA PRAKASH SHEO, and K. ROY S. "Metal Complexes as Ligands. Polynuclear Alkali Metal Complexes with Diaquomonooxalato-nickel(ll) and -cobalt(ll)." Journal of Indian Chemical Society Vol. 62, Nov 1985 (1985): 818–20. https://doi.org/10.5281/zenodo.6324806.

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Chemistry Department, Patna University, Patna-800 005 Polymeric octahedral, diaquomonooxalato-nickel(II) and -cobalt(II) (Ni/Co(ox). 2H<sub>2</sub>O]&nbsp;have been used as &#39;metal complex ligands&#39; in the synthesis of oxygen-bridged binuclear alkali metal complexes of the general formula [(M<sub>b</sub>L).M<sub>a</sub>ox.2H<sub>2</sub>O], <em>where </em>M<sub>b</sub> =Li, Na and K ; L=deprotonated organic acids ; M<sub>a</sub>= Ni or Co ; and ox=oxalate. In these binuclear alkali metal transition metal oxalates, the C=O frequencies have been observed only below 1 650 cm<sup>-1</sup> sug
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Farrell, RP, and PA Lay. "13C N.M.R. Spectroscopic Studies on the Reactions of Vanadium(V) With 13C2-Labeled Oxalate in Aqueous and 50% v/v Aqueous Acetic Acid Solutions." Australian Journal of Chemistry 48, no. 4 (1995): 763. http://dx.doi.org/10.1071/ch9950763.

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13 C n.m.r, spectroscopy has been used to study the reactions of vanadate , H2VO4-, with 13C2-labelled oxalate in aqueous and 50% v/v aqueous acetic acid media. The results of the aqueous system corroborate the natural abundance oxalate 13C n.m.r. studies of Ehde and coworkers ( Ehde, P.M., Petterson , L., and Glaser, J., Acta Chem. Scand., 1991, 45, 998) who report the formation of both mono( oxalato )-, [VO2(ox)(OH2)] - , and bis(oxalato)-vanadium(V), cis-[VO2(ox)2]3-, complexes in solution. At 270 K, pH 3.3, and an n.m.r. operating frequency of 100.16 MHz, the former complex appears as a si
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Furukawa, T., and Y. Takahashi. "Oxalate metal complexes in aerosol particles: implications for the hygroscopicity of oxalate-containing particles." Atmospheric Chemistry and Physics 11, no. 9 (2011): 4289–301. http://dx.doi.org/10.5194/acp-11-4289-2011.

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Abstract. Atmospheric aerosols have both a direct and an indirect cooling effect that influences the radiative balance at the Earth's surface. It has been estimated that the degree of cooling is large enough to weaken the warming effect of carbon dioxide. Among the cooling factors, secondary organic aerosols (SOA) play an important role in the solar radiation balance in the troposphere as SOA can act as cloud condensation nuclei (CCN) and extend the lifespan of clouds because of their high hygroscopic and water soluble nature. Oxalic acid is an important component of SOA, and is produced via s
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Xiong, Yongliang, and Yifeng Wang. "Uranyl oxalate species in high ionic strength environments: stability constants for aqueous and solid uranyl oxalate complexes." Radiochimica Acta 109, no. 3 (2021): 177–85. http://dx.doi.org/10.1515/ract-2020-0083.

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Abstract Uranyl ion, UO2 2+, and its aqueous complexes with organic and inorganic ligands can be the dominant species for uranium transport on the Earth surface or in a nuclear waste disposal system if an oxidizing condition is present. As an important biodegradation product, oxalate, C2O4 2−, is ubiquitous in natural environments and is known for its ability to complex with the uranyl ion. Oxalate can also form solid phases with uranyl ion in certain environments thus limiting uranium migration. Therefore, the determination of stability constants for aqueous and solid uranyl oxalate complexes
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Ferri, Diego, Mauro Iuliano, Carla Manfredi, et al. "Dioxouranium(VI) oxalate complexes †." Journal of the Chemical Society, Dalton Transactions, no. 19 (2000): 3460–66. http://dx.doi.org/10.1039/b006544g.

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Furukawa, T., and Y. Takahashi. "Metal complexation inhibits the effect of oxalic acid in aerosols as cloud condensation nuclei (CCN)." Atmospheric Chemistry and Physics Discussions 10, no. 11 (2010): 27099–134. http://dx.doi.org/10.5194/acpd-10-27099-2010.

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Abstract. Atmospheric aerosols have both a direct and an indirect cooling effect that influences the radiative balance at the Earth's surface. It has been estimated that the degree of cooling is large enough to cancel the warming effect of carbon dioxide. Among the cooling factors, secondary organic aerosols (SOA) play a key role in the solar radiation balance in the troposphere as SOA can act as cloud condensation nuclei (CCN) and extend the lifespan of clouds because of their high hygroscopic and water soluble nature. Oxalic acid is one of the major components of SOA, and is produced via sev
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Chandra, N. R., M. M. Prabu, J. Venkatraman, S. Suresh, and M. Vijayan. "X-ray Studies on Crystalline Complexes Involving Amino Acids and Peptides. XXXIII. Crystal Structures of L- and DL-Arginine Complexed with Oxalic Acid and a Comparative Study of Amino Acid–Oxalic Acid Complexes." Acta Crystallographica Section B Structural Science 54, no. 3 (1998): 257–63. http://dx.doi.org/10.1107/s0108768197011543.

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The DL- and L-arginine complexes of oxalic acid are made up of zwitterionic positively charged amino acid molecules and semi-oxalate ions. The dissimilar molecules aggregate into separate alternating layers in the former. The basic unit in the arginine layer is a centrosymmetric dimer, while the semi-oxalate ions form hydrogen-bonded strings in their layer. In the L-arginine complex each semi-oxalate ion is surrounded by arginine molecules and the complex can be described as an inclusion compound. The oxalic acid complexes of basic amino acids exhibit a variety of ionization states and stoichi
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A., K. BANERJEE, SATYA PRAKASH SHEO, and K. ROY S. "Metal Complexes as Ligand. Binuclear Alkali Metal Complexes with Nickel Ethylenediamine Oxalate and Cobalt Ethylenediamine Oxalate." Journal of Chemical Indian Society Vol. 65, May 1988 (1988): 378–79. https://doi.org/10.5281/zenodo.6280110.

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Chemistry Department, Patna University, Patna.-800 005 <em>Manuscript received 24 November 1986, revised 1 March 1988, accepted 17 March 1988</em> Metal Complexes as Ligand. Binuclear Alkali Metal Complexes with Nickel Ethylenediamine Oxalate and Cobalt Ethylenediamine Oxalate.
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Xue, Xiao Fei, Yan Xiang Liu, Yan Qing Shao, and 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 (January 2011): 130–34. http://dx.doi.org/10.4028/www.scientific.net/amr.183-185.130.

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This study investigated the decolorization of Rhodamine B by the UV/Fe(III)-Oxalate and UV/Fe(III)-Penicillamine process under neutral pH. Fe(III)-Penicillamine complexes showed much higher photoactivity than that of Fe(III)-Oxalate complexes. The efficiency for decolorization of Rhodamine B at pH 5.0 was 59% and 88% in Fe(III)-Oxalate and Fe(III)-Penicillamine complexes aqueous solution after 60 min irradiation, respectively, whereas, 35% and 57% was achieved at pH 7.0. Compared to the Fe(III)/Oxalate system, the kinetic constants kapp (min-1) for Rhodamine B decolorization in Fe(III)/Penicil
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Dissertations / Theses on the topic "Oxalate complexes"

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Lescouëzec, Rodrigue. "Synthèse, structure et propriètés magnétiques de complexes à pont cyanure et oxalate de dimension variable." Paris 6, 2002. http://www.theses.fr/2002PA066535.

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Bouayad, Abdelouahed. "Complexes hétérobimétalliques à ligand assembleur oxo ou thiooxo d'éléments s, d et f : influence des ligands oxalate et squarate sur la structure ; étude de tels complexes comme précurseurs de céramiques." Toulouse 3, 1990. http://www.theses.fr/1990TOU30061.

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Les composes heterobimetalliques suivants ont ete prepares et structuralement caracterises par diffraction x sur monocristal: ba(h#2o)#5cu(c#2o#4)#2(h#2o) 1, ba(h#2o)#2#2cu(h#2o)#2(c#4o#4)#3 2, gd(h#2o)#4#2cu(h#2o)#4(c#4o#4)#4, 2h#2o 3 et cu#0#. #9mn#0#. #1(h#2o)#4(c#4o#4) 4. 1 contient des colonnes d'anions cu(h#2o)(c#2o#4)#2#2#. 2 est fait de couches cationiques ba(h#2o)#2(c#4o#4)#2#+#2# dans lequelles le ligand squarate est a la fois bischelatant et tetramonodentate; ces couches sont liees par des anions cu(h#2o)#2(c#4o#4)#2#. 3 est constitue de feuillets neutres heterobimetalliques (mu#3c#
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Bacsa, John. "Structures and thermal behaviour of some monooxalato and dioxalato metal complexes." Thesis, Rhodes University, 1996. http://hdl.handle.net/10962/d1005016.

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The crystal structure of Ba [Cu(C₂0₄)₂(H₂O)].5H₂O has been determined using single crystal X-ray diffractometry. It crystallises in the triclinic system, space group Pī , with a = 6.539(2) Å, b = 9.211(3) Å, c = 10.928(3) Å, a = 85.42(3)°, β = 79.22(3)° , γ = 80.30(3)°, V = 636.08(8)ų and Z = 2. The structure consists of [Cu(C₂0₄)₂(H₂O)]²⁻ ions weakly bridged by barium ions and water molecules. The copper(II) ions are in a tetragonally elongated square-pyramidal environment with some trigonal distortion. The two oxalate groups occupy the equatorial positions and a water molecule occupies the
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Ezahri, Mohamed. "Etude de la solubilité dans l'eau et de la décomposition thermique des oxalates complexes : (NH4)3Al(C2O4)3, (NH4)3Fe(C2O4)3, (NH4)3Cr(C2O4)3, (NH4)2TiO(C2O4)2 et (NH4)2VO(C2O4)2." Lyon 1, 1994. http://www.theses.fr/1994LYO10164.

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L'objectif de ce travail est la mise au point de techniques douces en vue de l'elaboration de materiaux d'oxydes a matrice alumine. Dans ce but, ont ete etablis les diagrammes de solubilite dans l'eau d'oxalates complexes et sont presentes: les systemes binaires h#2o(nh#4)#3al(c#2o#4)#3 et h#2o-(nh#4)#3ad(c#2o#4)#2 (m=ti, v) les isothermes 25c des ternaires h#2o-(nh#4)#3al(c#2o#4)#3-(nh#4)#3n(c#2o#4)#3 (n=fe, cr) et h#2o-(nh#4)#3al(c#2o#4)#3-(nh#4)#2mo(c#2o#4)#2 la coupe 25c du quaternaire h#2o-(nh#4)#3al(c#2o#4)#3-1/2(nh#4)#3fe(c#2o#4)#3-1/2(nh#4)#ocr(c#2o#4)#3. Toutes les phases solides renc
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Jeanneau, Erwann. "Nouveaux oxalates complexes nanoporeux élaborés à partir d'éléments en coordinence huit : structures, propriétés et prévisions cristallochimiques." Rennes 1, 2003. http://www.theses.fr/2003REN10061.

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Ce travail concerne l'étude de la structure cristalline de nouveaux oxalates élaborés à partir d'éléments en coordinence huit. L'étude des oxalates mixtes de cadmium et de zirconium associés à des cations bivalents ou monovalents a révélé l'existence de deux types structuraux. Le premier type structural est constitué d'une charpente anionique construite à partir de dodécaèdres. Les composés de la seconde famille possèdent une charpente de formulation chimique identique, mais cette fois construite à partir d'antiprismes à base carrée et topologiquement distincte de celle de la famille précédent
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LEQUART, CHRISTELLE. "Destructuration des parois vegetales lignifiees par une endoxylanase et un complexe abiotique mno2/oxalate-application a la paille de ble." Reims, 1999. http://www.theses.fr/1999REIMS010.

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Les co-produits agricoles constituent une matiere premiere renouvelable et disponible en grande quantite. La valorisation des lignocelluloses par voie enzymatique represente une alternative aux procedes chimiques polluants employes pour leur fractionnement. Le son et la paille de ble ont ete hydrolyses par une endoxylanase purifiee pour la production d'oligosaccharides. Le taux de lignines, les interactions entre les lignines et les hemicelluloses par le biais des acides hydroycinnamiques ainsi que la nature des xylanes semblent influencer l'hydrolyse enzymatique. L'etude d'une fraction des pr
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Haidon, Blaise. "Synthèse de complexes d’actinides à propriétés physico-chimiques contrôlées pour la fabrication de combustibles oxyde." Thesis, Lille 1, 2017. http://www.theses.fr/2017LIL10086.

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Dans le cadre des recherches sur le traitement-recyclage des combustibles nucléaires du futur, la conversion oxalique, éprouvée industriellement pour le plutonium (IV), est le procédé de référence envisagé pour la production finale d’oxydes d’actinides. L’optimisation de ce procédé, basé sur une étape de précipitation oxalique suivie de la calcination en oxyde de l’oxalate précipité, nécessite de maîtriser les propriétés des solides formés dès l’étape initiale de précipitation. La morphologie de l’oxalate, conservée après calcination en oxyde, impacte toutes les étapes du procédé. Dans ce cont
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Duvieubourg, Laurence. "Synthèse et structure de nouveaux oxalates ou squarates d'uranium (VI), d'uranium (IV) et de lanthanide (III)." Lille 1, 2007. https://pepite-depot.univ-lille.fr/LIBRE/Th_Num/2007/50376-2007-153.pdf.

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L'uranium à ses différents degrés d'oxydation présente une cristallochimie très variée et passionnante. Les combinaisons de l'uranium avec les acides dicarboxyliques, notamment l'acide oxalique, conduisent à un grand nombre de composés de structures originales. Dans le cas de l'uranium (VI), l'utilisation des synthèses en conditions hydrothermales a conduit à la formation de composés hybrides organiques-inorganiques·. La partie inorganique résulte de l'association d'entité UO7 pour former des blocs de dimension variable (dimère, tétramère, chaîne. . . ). Ces blocs sont ensuite reliés par des i
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Nishino, Katsutoshi. "Chemical ecology of the (oxalato)aluminate complex as an antimicrobial substance from the “shiro” of Tricholoma matsutake." Kyoto University, 2017. http://hdl.handle.net/2433/226789.

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Kolli, Ramya. "Effect of Leaving Ligands of Platinum(II) Diamine Complexes on DNA and Protein Residues." TopSCHOLAR®, 2013. http://digitalcommons.wku.edu/theses/1268.

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Platinum compounds are widely used drugs in cancer treatments. Although DNA is the biological target, reaction of platinum compounds with proteins is also potentially significant. Our objective is to study the effects of leaving ligands on the relative reactivity between 5'-GMP (guanosine 5' phosphate), a key DNA target, and N-Acetyl - L-Methionine (N-AcMet), a key protein target. We have used NMR spectroscopy to monitor reactions with N-AcMet and 5'-GMP added to a platinum complex to see which products are formed preferentially. Previous research showed that both a non-bulky complex such as [
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Books on the topic "Oxalate complexes"

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Vaughan, David. 5. Minerals and the living world. Oxford University Press, 2014. http://dx.doi.org/10.1093/actrade/9780199682843.003.0005.

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‘Minerals and the living world’ considers various mineral–microbe interactions, biomineralization, and how minerals interact with the human body and human health. Biomineralization is the process where living organisms produce minerals such as calcite, apatite, and silica. An example is the unicellular, ocean-living radiolaria that have complex silica skeletons. After death their skeletal remains sink to the ocean floor and can be seen preserved in cherts and flints. Human biominerals can be divided into those which are an essential part of the bodies’ systems, such as hydroxylapatite found in
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Book chapters on the topic "Oxalate complexes"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of a compound having two different (oxalato)(bipyridine)copper(II) complexes in one single crystal." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_563.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of a compound having two different (oxalato)(bipyridine)copper(II) complexes in one single crystal." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_564.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of a compound having two different (oxalato)(bipyridine)copper(II) complexes in one single crystal." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_565.

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Sposito, Garrison. "Soil Humus." In The Chemistry of Soils. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780190630881.003.0007.

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Biomoleculesare compounds synthesized to sustain the life cycles of organisms. In soil humus, they are usually products of litter degradation, root excretion, and microbial metabolism, ranging in molecular structure from simple organic acids to complex biopolymers. Organic acids are among the best-characterized biomolecules. Table 3.1 lists five aliphatic (meaning the C atoms are arranged in open-chain structures) organic acids associated commonly with the soil microbiome. These acids contain the unit R—COOH, where COOH is the carboxyl groupand R represents either H or an organic moiety. The c
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Nikalje, Ganesh Chandrakant, Apurva Chonde, Sudhakar Srivastava, and Penna Suprasanna. "Wild Vegetables of the Family Amaranthaceae." In Wild Vegetables: Morphology, Phytochemistry and Utility Part 1. BENTHAM SCIENCE PUBLISHERS, 2025. https://doi.org/10.2174/9789815313116125010008.

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The Amaranthaceae family comprises nearly 175 genera and more than 2,500 species. The plants are found nearly worldwide, with some species thriving in tropical regions and others adapted to cool temperate climates. Several species of this family are important food crops, including Amaranth, Quinoa, Beet, etc. and some species are ornamental including cocks comb, globe amaranth, etc. Amaranthaceae members are rich in nutrients, essential amino acids, dietary fibers, vitamins A, B complex (particularly B6), C, E, and minerals like calcium, iron, magnesium, phosphorus, and potassium. In addition,
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Nikalje, Ganesh Chandrakant, Apurva Chonde, Sudhakar Srivastava, and Penna Suprasanna. "Wild Vegetables of the Family Anacardiaceae." In Wild Vegetables: Morphology, Phytochemistry and Utility Part 1. BENTHAM SCIENCE PUBLISHERS, 2025. https://doi.org/10.2174/9789815313116125010009.

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The Amaranthaceae family comprises nearly 175 genera and more than 2,500 species. The plants are found nearly worldwide, with some species thriving in tropical regions and others adapted to cool temperate climates. Several species of this family are important food crops, including Amaranth, Quinoa, Beet, etc. and some species are ornamental including cocks comb, globe amaranth, etc. Amaranthaceae members are rich in nutrients, essential amino acids, dietary fibers, vitamins A, B complex (particularly B6), C, E, and minerals like calcium, iron, magnesium, phosphorus, and potassium. In addition,
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Verma, Dr Ashi, Dr Krishna Kant Singh, and Dr Jitendra Kushwaha. "MANAGEMENT OF URETERIC STONE DISEASE." In Futuristic Trends in Medical Sciences Volume 3 Book 13. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bdms13p1ch21.

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Ureteric stone disease is a common problem with rising incidence in the past few decades due to present lifestyle as well as better technology leading to early detection. However, it is also associated with complete cure and can even be prevented with proper measures. Calcium oxalate stones are the most common ones followed by uric acid stones, infection stones (struvite and apatite), calcium phosphate stones and cysteine stones. Patients can be initially asymptomatic or may present in the emergency department with ureteric colic. Detection is done mainly by radiological imaging (X- Ray KUB, I
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Agrawal, Pratibha S., M. K. N. Yenkie, M. G. Bhotmange, B. D. Deshpande, and S. J. Dhoble. "Degradation of Substituted Benzoic Acids Related to Structural Reactivity." In Water Pollution Sources and Purification: Challenges and Scope. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815050684122010006.

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The existence of organic acids in aqueous waste continues to be an important environmental concern because of the odor and toxicity they impart to water. The photochemical degradation of benzoic acids (BA) and some of the substituted benzoic acids (SBA), which act as environmental pollutants, are studied in the present investigation using the Advanced Oxidation Processes (AOPs) and combinations of different oxidants and UV irradiation (UV/H2O2 , UV/TiO2 , UV/ZnO, and Fe(III)- oxalate complex). The photo-oxidative degradation of these pollutants was followed by studying their concentration deca
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Silvestri, Giuseppe, Salvatore Gambino, and Giuseppe Filardo. "Electrochemical Syntheses Involving Carbon Dioxide." In Carbon Dioxide Fixation and Reduction in Biological and Model Systems. Oxford University PressOxford, 1994. http://dx.doi.org/10.1093/oso/9780198547822.003.0013.

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Abstract The early speculations on the possibility of carbon dioxide being the starting material for chemical synthesis of organic compounds are due to one of the founders of modem organic chemistry, Justus Liebig. In 1847 he suggested that in the future a laboratory mimesis of the natural pathway to complex molecules such as carboxylic acids, alcohols or sugars would be possible. In 1861 two other illustrious German chemists, Kolbe and Schmitt, described the occurrence of formates by addition of carbon dioxide and water vapour to metallic sodium or potassium, thus confirming the hypothesis Li
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Lambert, Tristan H. "Reactions Involving Carbon–Carbon Bond Cleavage." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0028.

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Although they have historically played a relatively lesser role in organic synthesis, the appearance of a number of interesting methods that utilize C–C bond cleavage has prompted coverage in this chapter. Christopher W. Bielawski at the University of Texas at Austin found (Chem. Sci. 2012, 3, 2986) that the diamidocarbene 1 inserted into the C(O)–C(O) bond of dione 2 to produce 3 at room temperature. The use of oxalate monoester 5 for the decarboxylative cross-coupling with pyridine 4 to produce 6 was reported (Tetrahedron Lett. 2012, 53, 5796) by Yi-Si Feng at Hefei University of Technology.
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Conference papers on the topic "Oxalate complexes"

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Zhang, Jingxuan, Guo Yu, Cuimei Bo, and Jun Li. "Data-Driven Dynamic Modeling and Fault Diagnosis of Dimethyl Oxalate Industrial Production Process." In 2024 6th International Conference on Data-driven Optimization of Complex Systems (DOCS). IEEE, 2024. http://dx.doi.org/10.1109/docs63458.2024.10704444.

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Sastri, V. S., R. H. Packwood, and J. R. Brown. "Role of Modern Surface Analytical Techniques in Corrosion Inhibition Mechanisms." In CORROSION 1988. NACE International, 1988. https://doi.org/10.5006/c1988-88155.

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Abstract Corrosion inhibition is a complex phenomenon and depends on the formation of protective layers on the metal surface. Of the many factors that affect the protective nature of the surface layers, the incorporation of the inhibitor in the surface layer is the most important. The manner in which the inhibitor is incorporated in the surface layer leads to three types of inhibition namely - interface inhibition, interphase inhibition and precipitation coating. Determining the composition of the surface layers of metals is facilitated by modern surface analytical techniques, such as X-ray ph
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Rilak Simović, Ana, Milica Međedović, Dejan Lazić, Milan Vraneš, Ghodrat Mahmoudi, and Biljana Petrović. "Biological activity of thienyl-terpyridine Ru(II) complex in the presence of biocompatible ionic liquids." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.519rs.

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New mononuclear Ru(II)-thienyl-terpyridine complex [Ru(thienyl-tpy)(bpy)Cl]Cl (where thienyl-tpy = 4’-(2-thienyl)-2,2’:6’,2’’-terpyridine, bpy = 2,2’-bipyridine) has been synthesized and then characterized through elemental analysis, followed by various spectroscopic (IR, UV−vis, 1H and 13C NMR) and mass spectrometric technique (ESI Q-TOF MS). Furthermore, the interactions with CT DNA were performed both in the absence and presence of biocompatible ionic liquids 1-amino-2-propanol-lactate (IL1), 1-amino-2-propanol-oxalate (IL2) and 1-amino-2-propanol-citrate (IL3).
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Chaoyan, Zhang, and Yang Jingya. "The Inhibitory Effect on the Crystallization of Calcium Oxalate of Taurine and Complex Magnesium Taurate." In 2011 International Conference on Measuring Technology and Mechatronics Automation (ICMTMA). IEEE, 2011. http://dx.doi.org/10.1109/icmtma.2011.783.

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Direm, Amani, zina Boutobba, Koray Sayın, Brahim El Bali, Mohammed Lachkar, and Nourredine Benali-Cherif. "A combined experimental and theoretical study of an oxalato-bridged copper(II) complex: Crystal structure and <em>Hirshfeld</em> surface analysis of the non-covalent interactions." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07402.

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Lucas Fernandes, Samuel, and Gabriela Leal Peres Fernandes. "PROTOCOLOS DE DESENSIBILIZAÇÃO DENTINÁRIA EM QUADROS DE LESÕES CERVICAIS NÃO CARIOSAS." In ANAIS V CONTEC BRASIL 2024. Universidade Brasil, 2024. https://doi.org/10.63021/vcontec.978-6589249313.2024.art166.

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Introdução: O protocolo de dessensibilização dentinária em quadros de lesões cervicais não cariosas é um tratamento utilizado para pacientes com hipersensibilidade dentinária, que é uma sensação dolorosa de etiologia multifatorial suscetível a estímulos térmicos, químicos, táteis, osmóticos e de pressão, em regiões de dentes com túbulos dentinários expostos subgengivais, supragengivais, em trincas de esmalte e abaixo de defeitos estruturais, os quais desencadeiam uma dor curta e aguda de rápida duração. Objetivos: O objetivo deste estudo é revisar a literatura a fim de estabelecer protocolos d
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