Academic literature on the topic 'Complexes of Pyridine'

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Journal articles on the topic "Complexes of Pyridine"

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Webber, Christopher K., Erica K. Richardson, Diane A. Dickie, and T. Brent Gunnoe. "Electrochemically Active Copper Complexes with Pyridine-Alkoxide Ligands." Inorganics 12, no. 8 (2024): 200. http://dx.doi.org/10.3390/inorganics12080200.

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Pyridine-alkoxide (pyalk) ligands that support transition metals have been studied for their use in electrocatalytic applications. Herein, we used the pyalk proligands diphenyl(pyridin-2-yl)methanol ([H]PhPyalk, L1), 1-(pyren-1-yl)-1-(pyridin-2-yl)ethan-1-ol ([H]PyrPyalk, L2), 1-(pyridine-2-yl)-1-(thiophen-2-yl)ethan-1-ol ([H]ThioPyalk, L3), and 1-(ferrocenyl)-1-(pyridin-2-yl)ethan-1-ol ([H]FePyalk, L4) to synthesize CuII complexes that vary in nuclearity and secondary coordination sphere. Also, the proligand 1-(ferrocenyl)-1-(5-methoxy-pyridin-2-yl)ethan-1-ol ([H]FeOMePyalk, L5) was synthesiz
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Niu, Xiang-Long, Lin Wei, Jian-Cheng Liu, et al. "Syntheses and structures of three macrocyclic supramolecular complexes and one ZnII-containing coordination polymer generated from a semi-rigid multidentate N-containing ligand." Acta Crystallographica Section C Structural Chemistry 77, no. 1 (2021): 29–39. http://dx.doi.org/10.1107/s2053229620016083.

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Semirigid organic ligands can adopt different conformations to construct coordination polymers with more diverse structures when compared to those constructed from rigid ligands. A new asymmetric semirigid organic ligand, 4-{2-[(pyridin-3-yl)methyl]-2H-tetrazol-5-yl}pyridine (L), has been prepared and used to synthesize three bimetallic macrocyclic complexes and one coordination polymer, namely, bis(μ-4-{2-[(pyridin-3-yl)methyl]-2H-tetrazol-5-yl}pyridine)bis[dichloridozinc(II)] dichloromethane disolvate, [Zn2Cl4(C12H10N6)2]·2CH2Cl2, (I), the analogous chloroform monosolvate, [Zn2Cl4(C12H10N6)2
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Śliwa, Wanda, and Małgorzata Deska. "Platinum(II) Complexes of Pyridines. A Review." Collection of Czechoslovak Chemical Communications 64, no. 3 (1999): 435–58. http://dx.doi.org/10.1135/cccc19990435.

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The chemistry of platinum(II) complexes of pyridine and related compounds is reviewed. Also the oxidative addition reaction to platinum(II) complexes of pyridines, as a method of conversion of Pt(II) into Pt(IV) species is described. A review with 90 references.
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Nakanishi, Takumi, and Osamu Sato. "Crystal structures of two nickel compounds comprising neutral NiIIhydrazone complexes and dicarboxylic acids." Acta Crystallographica Section E Crystallographic Communications 73, no. 2 (2017): 103–6. http://dx.doi.org/10.1107/s2056989016020326.

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Two isostructural NiIIcompounds, bis{N-[1-(pyridin-2-yl-κN)ethylidene]pyridine-4-carbohydrazonato-κ2N′,O}nickel(II)–2,5-dichloroterephthalic acid (1/1), [Ni(C13H11N4O)2](C8H4Cl2O4), and bis{N-[1-(pyridin-2-yl-κN)ethylidene]pyridine-4-carbohydrazonato-κ2N′,O}nickel(II)–2,5-dibromoterephthalic acid (1/1), [Ni(C13H11N4O)2](C8H4Br2O4), were synthesized and their crystal structures determined. The pair ofN,N′,O-tridentateN-[1-(pyridin-2-yl-κN)ethyl]pyridine-4-carbohydrazonateLligands result in acis-NiO2N4octahedral coordination sphere for the metal ions. The asymmetric units consist of two half-mol
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Fatih, Mehmet EMEN, and Esra DEMİRDÖĞEN Ruken. "SYNTHESIS OF PYRIDINE DERIVATIVE POLYMERIC COPPER COMPLEX WITH METAL-AZID BONDS." Journal of Natural Science and Technologies 1, no. 1 (2022): 143–50. https://doi.org/10.5281/zenodo.7384181.

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In this study, pyridine-derived polymeric copper (II) complexes containing metal azide bonds were prepared. The characterization of the complexes given with the general formula, [Cu(L)<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>Cl<sub>2</sub>]n (L1: 3,5-dimethyl pyridine, L2: 3,4-dimethyl pyridine, L3: 2-amino-3-methyl pyridine, L4: 2,6-diamino pyridine) was performed by FT-IR, AAS and magnetic susceptibility analyzes. The intense peak observed at 2045-2167 cm-1 in the spectra corresponds to the asymmetric azide vibrations, &upsilon;as(N<sub>3</sub><sup>-</sup>), which indicates that polymeric copp
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Wang, Xu, Bradford R. Sohnlein, Shenggang Li, Jason F. Fuller, and Dong-Sheng Yang. "Pulsed-field ionization electron spectroscopy and molecular structures of copper-(pyridine)n (n = 1, 2) complexes." Canadian Journal of Chemistry 85, no. 10 (2007): 714–23. http://dx.doi.org/10.1139/v07-068.

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Cu-(pyridine)n (n = 1, 2) complexes are prepared in a pulsed laser ablation cluster source and identified using laser photoionization time-of-flight mass spectrometry. High-resolution electron spectra of these complexes are obtained using pulsed-field ionization zero electron kinetic energy (ZEKE) photoelectron spectroscopy. Metal-pyridine and pyridine-based vibrational modes are identified by comparing the ZEKE spectra with previous spectroscopic studies of isolated pyridine, pyridine adsorbed on metal surfaces, and other Cu complexes. Ground electronic states and molecular structures are det
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Nagaraju, N., J. Sreeramulu, V. Anjaneyulu, P. Malleswarareddy, and G. Ramamohan. "A study of in vitro antimicrobial activities and antioxidant of lanthanide complexes with a tri dentate Schiff base ligand." Research Journal of Chemistry and Environment 27, no. 5 (2023): 42–51. http://dx.doi.org/10.25303/2705rjce042051.

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The tridentate N3-type Schiff base 4-(anthracen-10-yl)-2,6-di(pyridin-2-yl)pyridine was synthesized from the condensation reaction of 2-acetyl pyridine and anthracene-10-carbaldehyde with ammonia using one pot methodology. This hybrid ligand was used for synthesis of lanthanide complexes (La, Sm and Eu) as novel potential biological agent. The lanthanide complexes were characterized on the basis of elemental, FT-IR, UV-Visible, mass spectrometry as well as molar conductivity. The complexes were screened for in vitro antibacterial and antifungal activities against the multidrug resistant pathog
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Liu, Ting, Yu-Peng Pan, Suna Wang, and Jian-Min Dou. "Two novel lead(II) complexes of 2-(hydroxymethyl)pyridine: a threefold diamondoid supramolecular network based on Pb4O4cores and a two-dimensional (4,4) network based on Pb2O2units." Acta Crystallographica Section C Crystal Structure Communications 69, no. 4 (2013): 394–99. http://dx.doi.org/10.1107/s0108270113006987.

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Reactions of 2-(hydroxymethyl)pyridine (Hhmp) with PbCl2and Pb(NO3)2at room temperature led to the formation of two novel compounds, namely tetrakis[μ3-(pyridin-2-yl)methanolato]-tetrahedro-tetrakis[chloridolead(II)], [Pb4(C6H6NO)4Cl4], (I), and poly[(μ2-nitrato)[μ2-(pyridin-2-yl)methanolato]lead(II)], [Pb(C6H6NO)(NO3)]n, (II). Compound (I) exhibits a tetranuclear Pb4O4cubane structure, which is connected through π–π stacking interactions between the pyridine groups of the (pyridin-2-yl)methanolate (hmp−) ligands and through C—H...Cl interactions to form an interesting threefold diamondoid net
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Kacsir, István, Adrienn Sipos, Evelin Major, et al. "Half-Sandwich Type Platinum-Group Metal Complexes of C-Glucosaminyl Azines: Synthesis and Antineoplastic and Antimicrobial Activities." Molecules 28, no. 7 (2023): 3058. http://dx.doi.org/10.3390/molecules28073058.

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While platinum-based compounds such as cisplatin form the backbone of chemotherapy, the use of these compounds is limited by resistance and toxicity, driving the development of novel complexes with cytostatic properties. In this study, we synthesized a set of half-sandwich complexes of platinum-group metal ions (Ru(II), Os(II), Ir(III) and Rh(III)) with an N,N-bidentate ligand comprising a C-glucosaminyl group and a heterocycle, such as pyridine, pyridazine, pyrimidine, pyrazine or quinoline. The sugar-containing ligands themselves are unknown compounds and were obtained by nucleophilic additi
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Hatua, Kaushik, and Prasanta K. Nandi. "Third-order NLO property of beryllium-pyridyne complexes." Journal of Theoretical and Computational Chemistry 13, no. 01 (2014): 1350075. http://dx.doi.org/10.1142/s0219633613500752.

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Six pyridyne isomers and their complexes with beryllium have been considered for the theoretical study of the third-order polarizability. The NLO properties are calculated by employing the DFT functionals BLYP, B3LYP, BHHLYP, B3PW91, BP86 and B2PLYP for the 6-311++G(d,p) basis set. The C - Be bond length in the complexes varies within 1.644 Å–1.771 Å indicating covalent interactions between the metal and pyridynes. The present investigation reveals that the magnitude of second-hyperpolarizability of pyridynes strongly enhances upon complex formation with beryllium. The maximum hyperpolarizabil
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Dissertations / Theses on the topic "Complexes of Pyridine"

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Shipton, Mark Ralph. "Pyridine chromium tricarbonyl complexes." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.276844.

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Couchman, Samantha M. "Syntheses and structural studies of complexes of mixed donor pyridine/phenol and pyridine/pyrazole ligands." Thesis, University of Bristol, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299312.

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Pater, Boke Chan de. "Terpyridine complexes of rhodium (I, III)." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2003. http://dare.uva.nl/document/70850.

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Jiang, Bing. "Nickel and cobalt bis (imino)pyridine complexes as catalysts for the hydrogen evolution reaction." Doctoral thesis, Universitat Autònoma de Barcelona, 2019. http://hdl.handle.net/10803/667777.

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El subministrament d'energia sostenible és un desafiament crític que enfronta la humanitat. La dependència dels combustibles fòssils ha despertat l'interès en el desenvolupament de fonts d'energia lliures de carboni, entre les quals el dihidrogen que té una alta densitat d'energia seria un dels més prometedors sempre que es generi a partir d'alternatives renovables. En aquest context, dissociar l'aigua per produir hidrogen com a combustible és de gran interès i, per tant, s'estan desenvolupant una gran quantitat de catalitzadors per accelerar la velocitat d'aquesta reacció, preferiblement obti
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Taylor, Kenneth John. "Electrochemical and spectroelectrochemical studies on mixed halo/pyridine osmium complexes." Thesis, University of Edinburgh, 1990. http://hdl.handle.net/1842/13079.

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The complexes [OsCl<SUB>6</SUB>-<SUB>n</SUB>PY<SUB>n</SUB>]<SUP>(n-y)</SUP>+ , where n = 0, 1, 2(<i>trans</i>), 2(<i>cis</i>), 3(<i>mer</i>), 4(<i>trans</i>), 5 and 6, and y varies between 2 and 4, have been synthesised <i>via</i> redox induced substitution reactions of [OsCl<SUB>6</SUB>]<SUP>2-</SUP>. The series has been fully characterised using electrochemical and spectroelectrochemical techniques. Several key members namely <i>trans</i>-[TPA] [OsCl<SUB>4</SUB>py<SUB>2</SUB>], <i>cis</i>-[OsCl<SUB>4</SUB>py<SUB>2</SUB>], <i>trans</i>-[OsCl<SUB>2</SUB>py<SUB>4</SUB>] and [Ospy<SUB>6</SUB>]9B
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Taktak, Sonia. "Biomimetic amino-pyridine iron complexes for catalysis and small molecule activation /." Thesis, Connect to Dissertations & Theses @ Tufts University, 2005.

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Thesis (Ph.D.)--Tufts University, 2005.<br>Adviser: Elena V. Rybak-Akimova. Submitted to the Dept. of Chemistry. Includes bibliographical references. Access restricted to members of the Tufts University community. Also available via the World Wide Web;
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Manuel, Antonio David. "Dioxygen activation with Bis(arylimino)pyridine radical anion complexes of nickel." Diss., University of Iowa, 2014. https://ir.uiowa.edu/etd/4686.

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Complexes of redox-active ligands have received increasing attention, in part, because they have been shown to facilitate a variety of bond-forming and bond-breaking reactions, including the activation of small molecules. Unique attributes of redox-active ligands include that they influence the electronic properties of transition metal complexes and may participate in their multielectron redox chemistry. In this work, the utility of Ni complexes of redox-active bis(arylimino)pyridine ligands for the activation of dioxygen was explored. A series of bis(arylimino)pyridine complexes [Ni{2,6-(ArN=
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Travers, Guy. "New bis(benzimidazol-2-ylidene)pyridine-nickel complexes as homogeneous catalysts." Thesis, Curtin University, 2015. http://hdl.handle.net/20.500.11937/450.

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New nickel-based catalysts for carbon-carbon bond formation reactions were synthesized and tested. The catalysts were found to be effective, but not strongly influenced by changes in the catalyst structure. During the course of this work, an organic precursor was found to catalyse the decomposition of dimethylsulfoxide. A product of the decomposition was isolated in good yield and identified. This product was found to be a useful reagent for epoxidation reactions.
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Wang, Ban. "Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions." TopSCHOLAR®, 2019. https://digitalcommons.wku.edu/theses/3159.

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Metal catalysis of symmetric and asymmetric carbene transfer reactions has been widely applied in natural product synthesis and material science over years. Metal carbene can be easily generated from the extrusion of nitrogen under the catalysis of metal complexes to further undergo various organic reactions, O/N/C-H insertions, cycloadditions, and ylide formations. Currently, the dominant effective catalysts for carbene reactions are built with expensive precious metal, for example, rhodium, ruthenium, palladium, gold. Notably, the effective reactivity and enantioselectivity of the dirhodium(
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鄭睦奇 and Luk-ki Cheng. "Photophysics and photochemistry of some platinum (II) complexes with polypyridine ligands." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1996. http://hub.hku.hk/bib/B31234689.

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Books on the topic "Complexes of Pyridine"

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Tomasik, Piotr. Pyridine-metal complexes. Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. Wiley, 1985.

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Zbigniew, Ratajewicz, Newkome George R, and Strękowski Lucjan, eds. Pyridine-metal complexes. Wiley, 1985.

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Brown, Desmond J. Pyridine Metal Complexes, Part 6A. Wiley & Sons, Incorporated, John, 2009.

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Brown, Desmond J. Pyridine Metal Complexes, Part 6A. Wiley & Sons, Incorporated, John, 2008.

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Podbielski, Lisa A. New [mu]-oxo complexes of technetium with pyridine and halogen ligands. 1987.

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Book chapters on the topic "Complexes of Pyridine"

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Theorell, H. "Fluorimetric Studies on Pyridine-Nucleotide Enzyme Complexes." In Ciba Foundation Symposium - Significant Trends in Medical Research. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719176.ch3.

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García, F. J. Arnáiz, G. D. Ellis, and E. P. Schram. "Complexes of Aluminum Iodide with Pyridine and Related Bases." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132517.ch23.

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Li, Lidong, and Pedro T. Gomes. "Oligomerization and Polymerization of Olefins with Iron and Cobalt Catalysts Containing 2,6-Bis(imino)pyridine and Related Ligands." In Catalysis by Metal Complexes. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-0696-5_3.

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Chirik, Paul J. "Electronic Structures of Reduced Manganese, Iron, and Cobalt Complexes Bearing Redox-Active Bis(imino)pyridine Pincer Ligands." In Pincer and Pincer-Type Complexes. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527681303.ch7.

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Liu, Zhiwei, Munzarin F. Qayyum, Chao Wu, et al. "A Codeposition Route to CuI–Pyridine Coordination Complexes for Organic Light-Emitting Diodes." In Electrophosphorescent Materials and Devices. Jenny Stanford Publishing, 2023. http://dx.doi.org/10.1201/9781003088721-42.

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Singh, N. K., M. Singh, P. Tripathi, A. K. Srivastava, and M. J. K. Thomas. "Synthesis and spectroscopic investigation of iron(III) complexes of N′-(thioaroyl)pyridine-2-carbohydrazides." In ICAME 2007. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-78697-9_111.

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Gibson, Vernon C., and Gregory A. Solan. "Olefin Oligomerizations and Polymerizations Catalyzed by Iron and Cobalt Complexes Bearing Bis(imino)pyridine Ligands." In Catalysis without Precious Metals. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631582.ch5.

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Hahn, Christine, and Rudolf Taube. "Structure and Reactivity of 2,6-Bis(diphenylphosphinomethyl)pyridine Complexes of Rhodium(I) and Palladium(II)." In Selective Reactions of Metal-Activated Molecules. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-00975-8_28.

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Mohan, M. "Antitumor Properties of Metal (II) Complexes of 2-Pyridine Carboxaldehyde 2′-Pyridylhydrazones and Related Compounds." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1717-3_81.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of co-crystallized binuclear coper(II) complexes with benzoic acid and pyridine-N-oxide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_476.

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Conference papers on the topic "Complexes of Pyridine"

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Mangalagiu, Violeta, Dorina Amariucai-Mantu, Dumitrela Diaconu, and Vasilichia Antoci. "BENZIMIDAZOLE � PYRIDINE: A NEW TYPE OF HGHLY SENSITIVE CHEMOSENSOR FOR ZN2+." In SGEM International Multidisciplinary Scientific GeoConference. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/6.2/s23.01.

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Discovery of new chemosensors for M2+ cations represent a continuously and challenging issue for researcher because of their potential applications in nano and micro technologies. Among the other metals, zinc is the second most abundant transition metal ion in human body and plays a crucial role in many biological and environmental processes. In this work we present the design, synthesis and characterization of a Zn2+ chemosensors and its coordination complexes based on podants with benzimidazole - pyridine skeleton. The new chemosensor have in the same molecule a ?�reach heterocycles (benzimi
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Kopecky, Sarah E. "Investigation of Substituent Effects on the Corrosion Inhibition of Pyridine Derivatives with Acetylenic Alcohols on Steel in Acid Media." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05569.

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Abstract The corrosion inhibition of substituted pyridine derivatives and quaternized pyridines in the presence and absence of acetylenic alcohol synergists is reported. Electrochemical Frequency Modulation (EFM) was used as a method of monitoring corrosion rates of steel in acidic environments. Early stage pitting was evaluated via scanning electron microscope (SEM) for comparison of measured corrosion rates to observed pit formation. EFM was found to be a reliable and accurate method of monitoring general corrosion rates over time, and causality factor data was found to depend heavily on the
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Tsui, Kenny, and Jennifer E. Wong. "Effect of Corrosion Inhibitor Active Components on Corrosion Inhibition in a Sweet Environment." In CORROSION 2010. NACE International, 2010. https://doi.org/10.5006/c2010-10326.

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Abstract In sweet corrosion, corrosion scales such as iron carbonate are formed on the internal surfaces of oil and gas production and transport systems. Depending on the type of corrosion inhibition program and the age of production system before chemical treatment is implemented, the presence of corrosion scale could affect the performance of the inhibitor. Previous work completed by the authors' company investigated the interaction of iron carbonate and three inhibitor actives - quaternary amine, imidazoline, and phosphate ester. This study is a continuation and examines two more generic co
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Zheng, Lianying, Ying Zhao, Ruifa Zong, et al. "Synthesis and FT-IR study of Ln-Glucose-Pyridine complexes." In The eleventh international conference on fourier transform spectroscopy. AIP, 1998. http://dx.doi.org/10.1063/1.55791.

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Gauru, Imanuel, and Fahimah Martak. "Synthesis and toxicity test of tin(IV) pyridine-2,6-dicarboxylate complexes." In 3RD INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0062237.

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Carvalho, André, Paula M. T. Ferreira, and José A. Martins. "New 2,6-Bis(5-phenyloxazolyl)pyridine Ligands for Luminescent LnIII Complexes." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13714.

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Jovanović Stević, Snežana, Snežana Radisavljević, Aleksandar Mijatović, Biljana Petrović, and Ana Kesić. "The influence of structural modification of Pd(II) pincer-type complexes on the kinetics of substitution reactions." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.411js.

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This mini-review summarizes the kinetic data obtained for the substitution reactions of some palladium(II) complexes containing bis-pyrazolylpyridine derivatives as pincer-type ligands with biologically significant nitrogen- and sulfur-donor biomolecules as nucleophiles. Three structurally different palladium(II) complexes were selected: [Pd(L1)Cl]+(Pd1), [Pd(L2)Cl]+(Pd2) and [Pd(L3)Cl]+(Pd3) (where L1 = bis(2-(1H-pyrazol-1-yl)ethyl)amine, L2 = 2,6-bis(5-(tert-butyl)-1H-pyrazol-3-yl)pyridine, and L3 = 2,6-bis(5-(tert-butyl)-1-methyl-1H-pyrazol-3-yl)pyridine, while for the entering nucleophiles
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Mahjoub, Omima Abdalla, and Yang Farina. "Spectral studies of copper(II) complexes of 6-(3-thienyl) pyridine-2-thiosemicarbazone." In THE 2014 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2014 Postgraduate Colloquium. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4895193.

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Matonic, John H. "Plutonium (IV) Complexes of Mixed Pyridine N-Oxide and Phosphinoxide f-Element Extractants." In PLUTONIUM FUTURES - THE SCIENCE: Third Topical Conference on Plutonium and Actinides. AIP, 2003. http://dx.doi.org/10.1063/1.1594623.

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Curry, Richard J., Michael R. George, and Martin C. Grossel. "The potential of pyridine-2,6-dicarboxylic acid based organolanthanide complexes for efficient near-infrared emission." In Optics & Photonics 2005, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2005. http://dx.doi.org/10.1117/12.617079.

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Reports on the topic "Complexes of Pyridine"

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Tse, Yu-Hong, Pamela R. Auburn, and A. B. Lever. The Trans-Cis Isomerisation of Bis(dioxolene)bis(pyridine)Ruthenium Complexes. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada247896.

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