Relevant bibliographies by topics / Ligand imine

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

Academic literature on the topic 'Ligand imine'

Author: Grafiati
Published: 13 July 2024
Last updated: 31 July 2025

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Journal articles on the topic "Ligand imine"

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Hou, Lulu, Hongyu Ren, and Baoli Guo. "Research progress of pre-transition metal olefin polymerization catalyst for salicylaldehyde imine." Journal of Polymer Science and Engineering 5, no. 1 (2018): 281. http://dx.doi.org/10.24294/jpse.v5i1.281.

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Salicylaldehyde imine transition metal catalyst is a kind of olefin polymerization catalyst that is widely used in the coordination of salicylaldehyde imine ligand and pre-transition metal. Salicylaldehyde imine ligands have the characteristic of easily inserting different substituents via organic synthesis. Therefore, the regulation of the polymerization activity, polymerization product, and product distribution can be achieved by changing the steric hindrance effect, the electronic effect, and the number of metal active sites near the catalytic active center. The development status of the trans
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Khatua, Manas, Bappaditya Goswami, and Subhas Samanta. "Dehydrogenation of amines in aryl-amine functionalized pincer-like nitrogen-donor redox non-innocent ligands via ligand reduction on a Ni(ii) template." Dalton Transactions 49, no. 20 (2020): 6816–31. http://dx.doi.org/10.1039/d0dt00466a.

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Ferraz de Paiva, Raphael Enoque, Douglas Hideki Nakahata, Marcos Alberto de Carvalho, Fernando Rodrigues Goulart Bergamini, and Pedro Paulo Corbi. "N,N′,N′′versus N,N′,Oimine-containing coordination motifs: ligand-directed synthesis of mononuclear and binuclear CuIIcompounds." Acta Crystallographica Section E Crystallographic Communications 73, no. 10 (2017): 1563–67. http://dx.doi.org/10.1107/s2056989017013652.

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It is demonstrated here that tridentate imine ligands can control the nuclearity of copper(II) complexes based on the donor atoms present in the ligand. TheN,N′,N′′-donating imine ligand led to a mononuclear compound, namely dichlorido[N,N-dimethyl-N′-(pyridin-2-ylmethylidene)ethane-1,2-diamine]copper(II) monohydrate, [CuCl2(C10H15N3)]·H2O,1, while theN,N′,O-donating imine ligand produced a binuclear metal complex, namely μ2-chlorido-dichlorido(μ2-2-{[2-(dimethylamino)ethyl]iminomethyl}phenolato)(N,N-dimethylethylenediamine)dicopper(II) 0.11-hydrate, [Cu2(C11H15N2O)Cl3(C4H12N2)]·0.11H2O,2. The
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Bernhard, P., DJ Bull, WT Robinson, and AM Sargeson. "The Synthesis and Properties of an Encapsulated Ruthenium(II) Ion by an N3S3 Macrobicyclic Ligand." Australian Journal of Chemistry 45, no. 8 (1992): 1241. http://dx.doi.org/10.1071/ch9921241.

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The complex [ Ru(capten)]2+ ( capten = 1-methyl-3,13,16-trithia-6,10,19-triazabicyclo[6.6.6]- icosane ) has been synthesized from [ Ru ( dmf )6]2+ ( dmf = N,N- dimethylformamide ) and the free ligand . An X-ray crystallographic analysis of [ Ru ( capten )] (CF3SO3)2 at 138 K reveals a lel3 conformation of the ligand with an average II-N bond length of 2.136(5) � and an average RuII-S bond length of 2.284(8) � . Visible spectra and the redox potential (1.26 V v. n.h.e .) show that the RuII state is stabilized by c. 0.9 V relative to the complex with six nitrogen donor atoms. Oxidation of Ru11 t
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Eliseev, Ivan I., Nadezhda A. Bokach, Matti Haukka та Irina A. Golenya. "cis-Dichlorido(dimethyl sulfoxide-κS)(N,N,N′,N′-tetramethylguanidine-κN′′)platinum(II)". Acta Crystallographica Section E Structure Reports Online 69, № 2 (2013): m117—m118. http://dx.doi.org/10.1107/s160053681300130x.

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In the title compound,cis-[PtCl2(C5H13N3)(C2H6OS)], the four-coordinate PtIIatom is bonded to one N atom of theN,N,N′,N′-tetramethylguanidine ligand, one dimethyl sulfoxide S atom and two chloride ligands, forming acis-square-planar geometry. The bond lengths and angles of the N—Pt—Cl functionality are typical for imine dichloridoplatinum(II) complexes. The H atom of the imino group is oriented towards the O atom of the sulfoxide group of a neighboring molecule and forms an N—H...O hydrogen bond.
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Khalaf, Mai M., Hany M. Abd El-Lateef, Abdulrahman Alhadhrami, et al. "Synthesis, Spectroscopic, Structural and Molecular Docking Studies of Some New Nano-Sized Ferrocene-Based Imine Chelates as Antimicrobial and Anticancer Agents." Materials 15, no. 10 (2022): 3678. http://dx.doi.org/10.3390/ma15103678.

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The newly synthesized organometallic acetyl ferrocene imine ligand (HL) was obtained by the direct combination of 2-acetyl ferrocene with 2-aminothiophenol. The electronic and molecular structure of acetyl ferrocene imine ligand (HL) was refined theoretically and the chemical quantum factors were computed. Complexes of the acetyl ferrocene imine ligand with metal(II)/(III) ions (Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II)) were fabricated. They were inspected by thermal (DTG /TG), spectroscopic techniques (FT-IR, 1H NMR, mass, UV–Vis), molar conductivity, and CHNClM to
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Adeleke, Adesola A., Sizwe J. Zamisa, and Bernard Omondi. "Ag(I) Complexes of Imine Derivatives of Unexpected 2-Thiophenemethylamine Homo-Coupling and Bis-(E)-N-(furan-2-ylmethyl)-1-(quinolin-2-yl)methanimine." Molbank 2021, no. 2 (2021): M1235. http://dx.doi.org/10.3390/m1235.

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Imines are fundamental organic compounds used as synthetic intermediates and as ligands in coordination chemistry. They are also found to be important pharmacophores in various bioactive compounds. In this report, two Schiff bases were prepared using the traditional condensation of 4-pyridinecarboxaldehyde with 2-thiophenemethylamine and 2-quinolinecarboxaldehyde with furfurylamine to form (E)-1-(pyridin-4-yl)-N-(thiophen-2-ylmethyl)methanimine (L1) and (E)-N-(furan-2-ylmethyl)-1-(quinolin-2-yl)methanimine (L2) respectively. L1 and L2 were complexed with silver perchlorate in 2:1 [M:L] stoichi
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Rafid, Mahmood, and Abdul Salam Abdul Kareem Abdul Rahman. "Synthesis, Characterization and Biological Activity of a new Schiff base oxime-imine ligand and its Zn (II) and Ni (II) complexes." Iraqi Journal for Applied Sciences 1, no. 3 (2024): 1–10. https://doi.org/10.69923/ijas.2024.010301.

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In this study, a new ligand derived from Schiff base oxime-imine, namely (3Z)-3-((2-aminophenyl) imino) butan-2-one oxime (L) was prepared by the reaction of o-phenylenediamine with diacetyl monooxime at refluxing methanol. The structure of the ligand was confirmed by elemental analysis, and spectroscopic instruments (IR, UV-Vis, 1H, 13CNMR and Maas spectrometry). Complexes of Zn (II) and Ni (II) metal ions with the specified ligand have been synthesized by reacting their chloride salts with the ligand in refluxing methanol, using a 1:1 mole ratio of (ligand: metal). Elemental analysis, spectr
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Zabłocka, Maria, Alain Igau, Victorio Cadierno, Marek Koprowski та Jean-Pierre Majoral. "α-Phosphino-Imine Ligand Design". Phosphorus, Sulfur, and Silicon and the Related Elements 177, № 8-9 (2002): 1965. http://dx.doi.org/10.1080/10426500213421.

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Li, Mingyuan, Hu Zhang, Zhengguo Cai, and Moris S. Eisen. "Norbornene polymerization and copolymerization with 1-alkenes by neutral palladium complexes bearing aryloxide imidazolin-2-imine ligand." Polymer Chemistry 10, no. 21 (2019): 2741–48. http://dx.doi.org/10.1039/c9py00176j.

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Dissertations / Theses on the topic "Ligand imine"

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Holub, Jan. "Generation of coordination architectures from dynamic covalent ligand libraries." Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF060/document.

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La Chimie Dynamique Combinatoire basée sur les liaisions imines (-C=N-), avec l’aide de la chimie de coordination, donne accès à différentes types d’architectures metallosupramoléculaires et de réseaux dynamiques fonctionnels. Le travail effectué au cours de cette thèse traite de ces deux aspects. Dans un premier temps des structures de types grilles moléculaire et de type hélicate ont été synthétisés, à l’aide de métaux donnant une coordination octahédrale ou tétraédrale, et leurs propriétés dans un environnement dynamique ont été étudiées. Dans un deuxième temps des réseaux dynamiques, prése
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Prema, Dipesh. "Different coordination modes of bis(imine-ridine) and bis(quinaldine) ligands." Diss., Manhattan, Kan. : Kansas State University, 2007. http://hdl.handle.net/2097/267.

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Barner, Claudia Jane. "Part I. Coordination chemistry of high-valent osmium polyanionic chelating ligand complexes with imine, imido and nitrido ligands. : Part II. Asymmetric hydrogenation using a resolved chiral scandium hydride complex /." Diss., Pasadena, Calif. : California Institute of Technology, 1990. http://resolver.caltech.edu/CaltechETD:etd-06112007-095040.

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Magee, Chad Leroy Keller S. W. "The synthesis and characterization of 1,1'-disubstituted ferrocene imine Schiff base ligand systems for use as potential environmental heavy metal cationic sensors." Diss., Columbia, Mo. : University of Missouri--Columbia, 2008. http://hdl.handle.net/10355/7117.

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Title from PDF of title page (University of Missouri--Columbia, viewed on Feb. 23, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Dr. Steven W. Keller, Dissertation Supervisor. Vita. Includes bibliographical references.
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Gunler, Zeynep Inci. "Synthesis Of N-(2-propylphenyl) Substituted Chiral Amino Alcohols And Their Usage In Enantioselective Diethylzinc Addition Reactions." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613001/index.pdf.

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Chiral 1,2-amino alcohols were synthesized via newly developed &ldquo<br>intramolecular unsaturation transfer&rdquo<br>using cyclohexanone, propargyl bromide, and various chiral amino alcohols as starting components. These amino alcohols can be potential chiral ligands for many asymmetric transformation reactions. Therefore, their effectiveness as chiral ligands in diethylzinc addition to benzaldehyde and N-diphenylphosphinoyl imines were tested. Various parameters including temperature, solvent, ligand amount etc. were screened for the synthesized chiral ligands. In diethylzinc addition to be
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Pierre, Fabrice. "Synthese et reduction electrochimique de complexes (#5-cyclopentadienyl) (#6-arene) fer(ii)pf#6 porteurs d'une fonction imine ou nitrone en position benzylique du ligand arene." Rennes 1, 1997. https://tel.archives-ouvertes.fr/tel-00343810.

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Ce memoire rapporte une etude de fonctionnalisation de complexes (cp fe arene)#+, dans un cadre fondamental d'activation de liaison c-h benzylique par les metaux de transition. La condensation entre le (cp fe diphenylmethane)#+ et le nitrosobenzene ou les nitrosotoluenes, initiee par 5% de t-buok, conduit a des melanges de complexes (cp fe benzophenone-n-arylnitrones)#+ et (cp fe benzophenone-anils)#+ (env. 80:20) avec de bons rendements (80-92%. Les complexes nitrones sont obtenus purs par recristallisation fractionnee (rdt. 22-35%). La condensation de nitrosoarenes varies r-ph-no (r = h, 2-m
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Zakis, Janis Mikelis. "Catalyseurs d'iridium cyclométallés pour la borylation ortho-dirigée de C–H." Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAF006.

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Au cours des deux dernières décennies, la borylation C–H a continué d'évoluer, passant des premiers exemples de réactions stœchiométriques à la synthèse de blocs de construction à l'échelle du kilogramme.1 Plus récemment, l'accent a été mis sur la borylation dirigée permettant un meilleur contrôle de la régiosélectivité dans des molécules plus complexes (Figure 1B).2,3 Généralement, cela est réalisé par une conception astucieuse du ligand introduisant des groupements chélateurs sur le ligand permettant l'interaction ligand-groupe directeur du matériau de départ (Figure 1A, II). La deuxième app
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Tanh, Jeazet Harold Brice. "Metallo-supramolecular Architectures based on Multifunctional N-Donor Ligands." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-39665.

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Self-assembly processes were used to construct supramolecular architectures based on metal-ligand interactions. The structures formed strongly depend on the used metal ion, the ligand type, the chosen counter ion and solvent as well as on the experimental conditions. The focus of the studies was the design of multifunctional N-donor ligands and the characterization of their complexing and structural properties. This work was divided into three distinct main parts: The bis(2-pyridylimine), the bis(2-hydroxyaryl) imine and the tripodal imine / amine ligand approach. In the first part a series o
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Mukherjee, Soumen. "Transition metal complexes with imine-phenolate and imino-benzosemiquinone ligands synthesis, characterization, and their catalytic reactivity /." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=971568197.

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Wietzke, Raphaël. "Complexation des éléments par des ligands tripodes azotés : application à l'extraction sélective des actinides(III)." Université Joseph Fourier (Grenoble), 1999. http://www.theses.fr/1999GRE10223.

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Ce travail s'inscrit dans le cadre des recherches sur la separation actinides(iii)/lanthanides(iii) par extraction liquide-liquide. Nous nous sommes interesses a l'etude de la chimie de coordination des lanthanides(iii) et de l'uranium(iii) (modele des actinides(iii)), dans le but de mettre en evidence des differences entre les deux familles et de mieux comprendre les processus moleculaires impliques dans l'extraction. Nous avons ainsi etudie la complexation des lanthanides(iii) et de l'uranium(iii) par des ligands tripodes contenant des azotes aromatiques. Plusieurs ligands tripodes azotes on
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Books on the topic "Ligand imine"

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Development of metal-alkynylide additions to imines, iminiums and epoxides: Synthesis of novel, chiral diene ligands for iradium(I) and their application in allylic displacement reactions. 2004.

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Book chapters on the topic "Ligand imine"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of bis(heterodinuclear) [CuIINiII]2 complex with unsymmetrical discompartmental imine-oxime ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_384.

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Horozić, Emir, and Jasmin Suljagić. "Characterization and Investigation of Bioactivity of Copper(II) and Cobalt(II) Complexes with Imine Ligand." In New Technologies, Development and Application II. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-18072-0_73.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with half unit of vicinal oxime-imine and chloride." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_347.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of linear heterotrinuclear FeIIICuIINiII complex with 1,4,7-trimethyl-1,4,7-triazacyclononane and asymmetric dicompartmented imine–oxime ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_221.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of linear heterotrinuclear FeIIINiIICuII complex with 1,4,7-trimethyl-1,4,7-triazacyclononane and asymmetric dicompartmented imine-oxime ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_222.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of linear heterotrinuclear FeIIIMnIICuII complex with 1,4,7-trimethyl-1,4,7-triazacyclononane and asymmetric dicompartmented imine-oxime ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_223.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of linear heterotrinuclear CoIIICuIINiII complex with 1,4,7-trimethyl-1,4,7-triazacyclononane and asymmetric dicompartmented imine-oxime ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_678.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with half unit of vicinal oxime-imine and acetic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_341.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with half unit of vicimal oxime-imine and monochloroethanoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_342.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with half unit of vicimal oxime-imine and dichloroethanoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_343.

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Conference papers on the topic "Ligand imine"

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Romero, María J., Luis M. González-Barcia, Manuel R. Bermejo, M. Isabel Fernández, and Esther Gómez-Fórneas. "Supramolecular self-assembly of a symmetric imine ligand functionalized with a dansyl fluorophore moiety." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-d002.

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Baral, Minati, Amit Gupta, and B. K. Kanungo. "Development of a dipodal Schiff base ligand with N-imine and O-naphtholate donors: A potential chelator towards Cu(II) metal ion established through potentiometric and spectrophotometric studies." In ADVANCED MATERIALS AND RADIATION PHYSICS (AMRP-2015): 4th National Conference on Advanced Materials and Radiation Physics. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4929176.

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Al Janabi, Basma, Juan M. Ortigueira, and Jose Manuel Vila. "Synthesis and X-ray Diffraction of Cyclopalladated Compounds Derived from Imine Ligands." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13699.

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Harmošová, Michaela, Martin Kello, Mária Vilková, Erika Samoľová, and Ivan Potočňák. "Synthesis, structure and anticancer activity of Zr(IV) complexes with Schiff bases derived from 8-hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.439h.

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The Schiff base 2-{[(2-hydroxyphenyl)imino]methyl}quinolin-8-ol (HLH) and its 5,7-dibromo- (HBrLH) and 5,7-diiodo-derivatives (HILH), which were prepared by multi-step organic synthesis, were used to synthesize [Zr(L)2]·2DMF (1), [Zr(BrL)2]·DMF (2), and [Zr(IL)2]·2DMF (3) complexes. The prepared products were characterized by elemental analysis, IR and NMR spectroscopy, which also monitored the stability of the prepared substances in DMSO, and in the case of HBrLH, HILH and 3, also by single crystal X-ray structural analysis. In the complex 3, two IL ligands are tetradentately bound to the cen
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Ibrahim, Noor Shakir, and Rasim Farraj Muslim. "Preparation and identification of nickel complexes from Di-imine organic ligands and anti-fungal activity." In THE NATIONAL UNIVERSITY OF SCIENCE AND TECHNOLOGY INTERNATIONAL CONFERENCE FOR ENGINEERING SCIENCES. AIP Publishing, 2025. https://doi.org/10.1063/5.0264001.

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Maneiro, Marcelino, Gustavo González-Riopedre, M. Isabel Fernández-García, Ana González-Noya, Rosa Pedrido, and Laura Rodríguez. "Synthetic Route to Novel Asymmetric Tetradentate Ligands Containing Both Amino and Imino Groups." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a018.

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Romero, María J., Sandra Fernández-Fariña, Luis M. González-Barcia, Rosa Pedrido, Ana M. González-Noya, and Marcelino Maneiro. "Synthesis of two asymmetric half-salen imine-type ligands as precursors of polynuclear metal complexes." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04752.

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González-Díaz, Humberto, Eugenio Uriarte, Esther Lete, Nuria Sotomayor, and Sonia Arrasate. "QSRR prediction of Enantioselectivity Complex Networks related to the addition of organolithium reagents to imines in presence of chiral ligands." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00239.

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Silva, Laila Taniellen Rodrigues Da, Lucas Lopes Barbosa, Milane Da Silva Viana, Jorge Luis De Oliveira Borges, and Athauany Nogueira Dos Santos. "RELAÇÃO DA RESPOSTA IMUNE INATA E ADAPTATIVA À INFECÇÃO DE PARASITOS HELMÍNTICOS." In I Congresso Brasileiro de Parasitologia Humana On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1960.

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Introdução: A resposta imunológica envolve mecanismos especializados, como órgãos, células e componentes humorais que constituem o sistema inato e o adaptativo, afim de garantir a sobrevivência do hospedeiro. A resposta imune inata é uma resposta primária, rápida e inespecífica, pronta para atacar a qualquer momento. A resposta imune adaptativa tem os linfócitos T e B como principais células de defesa, desenvolvida após contato com vários antígenos imunogênicos. Objetivo: O presente trabalho busca discutir sobre a relação da resposta imune inata e adaptativa contra helmintos. Material e método
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Oliveira, Nicolly Rayanne Flor, CAMILA SOUSA FARIAS ARAÚJO, and MORGANNA POLLYNNE NÓBREGA. "VÍRUS DA IMUNODEFICIÊNCIA HUMANA (HIV): DA ETIOLOGIA AO TRATAMENTO EM DIAS ATUAIS." In II Congresso Brasileiro de Imunologia On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/ii-conbrai/6205.

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Introdução: O vírus da imunodeficiência humana (HIV), é um retrovírus que apresenta tropismo por células do sistema imune, especialmente linfócitos TCD4. Objetivo: Estabelecer correlações entre a etiologia ao tratamento de pacientes soro positivo em dias atuais. Métodos: Trata-se de uma revisão bibliográfica descritiva literária de análises de 12 artigos em português e inglês publicados em periódicos nos bancos de dados PubMed, Scentific Eletronic library (Scielo) entre 2018 e 2021. Resultados: Na infecção por HIV os Linfócitos T são afetados primariamente, neste processo os Receptores CD4 e q
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