Relevant bibliographies by topics / Palladium(II) Chloride Complexes

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

Academic literature on the topic 'Palladium(II) Chloride Complexes'

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

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Journal articles on the topic "Palladium(II) Chloride Complexes"

1

N., ANJANEYULU, BALIAH V., and GANAPATHY K. "Palladium(II) Chloride Complexes of some Aryl Methyl Sulphides. Synthesis and their Electronic Spectral Studies." Journal Of Indian Chemical Society Vol. 67, Aug 1990 (1990): 673–75. https://doi.org/10.5281/zenodo.6236470.

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Department of Chemistry, Annamalai University,&nbsp;Annamalainagar-608 002 <em>Manuscript received 21 August 1989, accepted 11 May 1990</em> Palladium(II) Chloride Complexes of some Aryl Methyl Sulphides. Synthesis and their Electronic Spectral Studies &nbsp;
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2

Tian, Jianwen, Xiaohui He, Jingyin Liu, Xiaodan Deng та Defu Chen. "Palladium(ii) and copper(ii) chloride complexes bearing bulky α-diimine ligands as catalysts for norbornene vinyl-addition (co)polymerization". RSC Advances 6, № 27 (2016): 22908–16. http://dx.doi.org/10.1039/c5ra23970b.

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Palladium(ii) and copper(ii) chloride complexes bearing bulky 9,10-dihydro-9,10-ethanoanthracene-11,12-diimine ligands were synthesized and sufficiently characterized by elemental and spectroscopic analysis along with X-ray diffraction analysis.
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Chandrasekaran, A., Setharampattu S. Krishnamurthy, and Munirathinam Nethaji. "Palladium(II) chloride complexes of bis(pyrazolyl)cyclotriphosphazenes." Inorganic Chemistry 32, no. 26 (1993): 6102–6. http://dx.doi.org/10.1021/ic00078a031.

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Machnitzki, Peter, Othmar Stelzer, and Claudia Landgrafe. "Komplexbildung und Ligandeneigenschaften der Chlormethylchlorphosphane R(Cl)P-CH2-Cl - Molekülstruktur von trans-Cl2Pd[tBu(Cl)P-CH2-Cl]2 / Coordination Chemistry and Ligand Properties of Chloromethylchlorophosphines R(Cl)P-CH2 -Cl - Molecular Structure of trans-Cl2Pd[tBu(Cl)P-CH2 -Cl]2." Zeitschrift für Naturforschung B 52, no. 9 (1997): 1103–13. http://dx.doi.org/10.1515/znb-1997-0915.

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Reaction of the chloromethylchlorophosphines R(Cl)P-CH2-Cl (R = Cl, tBu, C6H11, NEt2, NPh2) (L) with C7H8Mo(CO)4 or (CO)5W(Py), (CO)6W and (CO5W(THF) yields the complexes cis-Mo(CO)4L2(2a - 2e) or (CO)5 WL (3a - 3c), respectively, in high yields. The palladium(II) complexes PdCl2L2 (4a - 4c) are obtained on treatment of 1a, 1b and 1e with 1,5-cyclooctadiene palladium(II) chloride or anhydrous palladium(II) chloride in a homogeneous or heterogeneous reaction, respectively. 4a - 4c are formed as a mixture of cis- and trans-isomers. The 13C {1H} NMR and 1H NMR spectra of 2a - 4c have been analyse
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Pokharel, Komal, Gregory M. Ferrence, and Timothy D. Lash. "Late transition metal complexes of oxypyriporphyrin and the platinum(II) complex of oxybenziporphyrin." Journal of Porphyrins and Phthalocyanines 21, no. 07n08 (2017): 493–501. http://dx.doi.org/10.1142/s1088424617500535.

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Even though oxypyriporphyrin, a pyridone-containing porphyrinoid system, has the equivalent coordination core to true porphyrins, its coordination chemistry has been little explored. In this study, the first examples of palladium(II), platinum(II) and silver(II) oxypyriporphyrins have been synthesized. Conventional conditions failed to result in the formation of a platinum(II) complex, but moderate yields were obtained when oxypyriporphyrin was reacted with platinum(II) chloride in refluxing mixtures of DMF and acetic acid containing potassium acetate. The palladium(II) and platinum(II) deriva
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Krause-Heuer, Anwen M., Peter Leverett, Albert Bolhuis, and Janice R. Aldrich-Wright. "Copper(II) and Palladium(II) Complexes with Cytotoxic and Antibacterial Activity." Australian Journal of Chemistry 65, no. 7 (2012): 860. http://dx.doi.org/10.1071/ch12058.

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The synthesis of eight square pyramidal copper complexes with general structure [Cu(IL)(AL)H2O]2+, where IL represents various methylated 1,10-phenanthrolines, and AL represents either 1S,2S- or 1R,2R-diaminocyclohexane, is reported, with the complexes synthesised as both the perchlorate and chloride salts. The crystal structures of [Cu(1,10-phenanthroline)(1S,2S-diaminocyclohexane](ClO4)2·H2O and [Cu(5,6-dimethyl-1,10-phenanthroline)(1S,2S-diaminocyclohexane](ClO4)2·1.5H2O are reported. Four square planar palladium complexes with general structure [Pd(IL)(AL)]Cl2 have also been synthesised. T
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V., BALIAH, GANAPATHY K., and ANJANEYULU N. "Palladium(II) Chloride Complexes of some Aryl Methyl Sulphides. Part-2. Substituent Effect on Pd-S and Pd-CI Stretching Frequencies." Journal of Indian Chemical Society Vol. 63, Nov 1986 (1986): 990–91. https://doi.org/10.5281/zenodo.6297139.

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Department of Chemistry, A nnamalai University,&nbsp;Annamalainagar-608 002 <em>Manuscript received 11 January 1985, revised 18 August 1986,&nbsp;accepted 5 September 1986</em> Palladium(II) Chloride Complexes of some Aryl Methyl Sulphides. Part-2. Substituent Effect on Pd-S and Pd-CI Stretching Frequencies.
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Virendra, Singh Shekhawat, Varshney Sarita, and K. Varshney A. "Synthesis of palladium(II) complexes with semicarbazones and thiosemicarbazones using green solvent." Journal of Indian Chemical Society Vol. 94, Jan-2017 (2017): 21–28. https://doi.org/10.5281/zenodo.5603264.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004, Rajasthan, India <em>E-mail</em> : anilakv123@rediffmail.com <em>Manuscript received online 28 August 2016, accepted 01 October 2016</em> A new series of palladium(II) complexes of the type, [Pd(LH)Cl<sub>2</sub> ] have been isolated by the reaction of palladium(II) chloride with semicarbazones and thiosemicarbazones in 1 : 1 molar ratio using green solvent (methyltetrahydrofuran) as a reaction medium. Ligands used in these studies have been prepared by the condensation of semicarbazide/thiosemicarbazide and suitable carbonyls i
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Hadi, Falah Haasan, and Hayder Obaid Jamel. "Preparation and characterization of a new ligand derived from the compounds 2-hydrazinobenzothiazole and 2-amino-6-methoxy benzothiazole and its complexes with some metal ions, evaluating its antibacterial activity, and studying its nanoscale properties." Journal of Kufa for Chemical Sciences 4, no. 1 (2024): 133–52. https://doi.org/10.36329/jkcm/2024/v4.i1.14177.

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New-type Schiff bases were prepared: [2-(benzoxazol-2-yl)-hydrazinyl diene][-2,1-diphenyl-N-(6-methoxybenzothiazol-2-yl)-2,1-diphenylethane]. -1-amine (L) of the mixture. 2-mercaptobenzoxazole was dissolved with hydrazine in absolute ethanol as a first stage to form compound A. while the ligand was obtained in its final from the reaction of compound A with both benzal and 2-amino-6-methoxybenzothiazole. The complex of Ni(II) and Pd(II) was prepared by reacting palladium chloride and nickel chloride with ligand L. The structure of the prepared ligand and its complexes was diagnosed using severa
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Kuzovlev, Andrey S., Daria A. Volkova, Irina V. Parfenova, et al. "Copper(i) halide and palladium(ii) chloride complexes of 4-thioxo[1,3,5]oxadiazocines: synthesis, structure and antibacterial activity." New Journal of Chemistry 44, no. 19 (2020): 7865–75. http://dx.doi.org/10.1039/c9nj05958j.

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The first copper(i) and palladium(ii) complexes containing monastrol analogs, 4-thioxo[1,3,5]oxadiazocine derivatives, have been synthesized. The complexes demonstrated significant antibacterial activity in contrast to free heterocyclic thiones.
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Dissertations / Theses on the topic "Palladium(II) Chloride Complexes"

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Vuoti, S. (Sauli). "Syntheses and catalytic properties of palladium (II) complexes of various new aryl and aryl alkyl phosphane ligands." Doctoral thesis, University of Oulu, 2007. http://urn.fi/urn:isbn:9789514286483.

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Abstract Thirty three aryl and aryl alkyl phosphane ligands were prepared and characterized for catalytic purposes. The aryl groups in both types of ligands were modified with alkyl substituents (methyl, ethyl, isopropyl, cyclohexyl, phenyl) or hetero substituents (methoxy, N,N-dimethylaniline, thiomethyl). The alkyl groups directly attached to the phosphorous atom were ethyl, isopropyl or cyclohexyl. Mono- and in some cases also dinuclear palladium (II) complexes of the ligands were prepared and characterized. The syntheses of the palladium complexes are solvent-dependent and afford either mo
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Morin-Phelippeau, Brigitte. "Réactions de double carbonylation de dérivés organiques halogènes catalysées par les complexes du palladium." Paris 6, 1987. http://www.theses.fr/1987PA066539.

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Clapham, Sarah. "Organometallic amino and amido complexes of palladium(II)." Thesis, University of Salford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.420460.

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Zuideveld, Martin Alexander. "Solvolysis of palladium-carbon bonds in palladium(II) complexes containing diphosphine ligands." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2001. http://dare.uva.nl/document/60731.

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Pascu, Sofia I. "Nickel (II), palladium (II), platinum (II) and rhodium (I) complexes of iminophosphine ligands." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270258.

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Kato, Kazuhiko. "Some Asymmetric Reactions Catalyzed by Chiral Palladium(II)Complexes." 京都大学 (Kyoto University), 1998. http://hdl.handle.net/2433/182447.

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Fazio, Daniela. "Synthesis and mesomorphism of polycatenar complexes of palladium (II) and platinum (II)." Thesis, University of Exeter, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366619.

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Heß, David. "Palladium(II) complexes and phenylboronic acid esters of deoxy sugars." Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-151675.

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Steinborn, Martin. "Coordination chemistry of sugar-phosphate complexes with palladium(II), rhenium(V) and zinc(II)." Diss., Ludwig-Maximilians-Universität München, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-161901.

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Hameury, Sophie. "Oxygen-functionalized NHC ligands and their nickel(II), silver(I) and palladium(II) complexes." Thesis, Strasbourg, 2014. http://www.theses.fr/2014STRAF010.

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L’objectif de cette thèse portait sur la synthèse de complexes portant un ligand NHC associé à une fonction oxygénée et à leur application en catalyse d’oligomérisation de l’éthylène. Dans le but de synthétiser des complexes avec des ligands NHCalcool, les complexes d’argent correspondants ont été synthétisés et utilisés en transmétallation. Aucun résultat concluant n’a pu être obtenu avec le nickel à cause de l’acidité du proton alcoolique. Mais un ligand NHC-alcoolate a pu être obtenu par déprotonation directe du pro-ligand avec une base forte. Il fut alors possible d’accéder à des complexes
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Books on the topic "Palladium(II) Chloride Complexes"

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King, Richard N. The preparation of some Palladium (II) complexes and their activities in sulfur dioxide removal. UMIST, 1995.

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El-Sherif, Ahmed A. Coordination Chemistry of Palladium(II) Ternary Complexes with Relevant Biomolecules. INTECH Open Access Publisher, 2012.

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Book chapters on the topic "Palladium(II) Chloride Complexes"

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Tatsuno, Yoshitaka, Toshikatsu Yoshida, Seiotsuka, Najeeb Al-Salem, and Bernard L. Shaw. "(η3 -Allyl)Palladium(II) Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132500.ch51.

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Tatsuno, Yoshitaka, Toshikatsu Yoshida, Sei Otsuka, Najeeb Al-Salem, and Bernard L. Shaw. "(η3 -Allyl)Palladium(II) Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch88.

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Aucken, I., and Russell S. Drago. "Mercury(II) Chloride Thiourea Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132371.ch9.

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Walker, F. S., S. N. Bhattacharya, C. V. Senoff, Kent Barefield, and Gary M. Freeman. "30. Alkylated Polyamine Complexes of Palladium(II)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132524.ch30.

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White, D. A., J. R. Doyle, and H. Lewis. "Cationic Diene Complexes of Palladium(II) and Platinum(II)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch12.

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Hsu, Chao-Yang, Brian T. Leshner, Milton Orchin, and Michel Laurent. "Trans Phosphine Complexes of Platinum(II) Chloride." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132500.ch25.

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Castilho, T. J., M. F. C. Guedes Da Silva, A. J. L. Pombeiro, R. Bertani, M. Mozzon, and R. A. Michelin. "Electrochemical Behaviour of Aminooxy-, Dioxy- and Diaminocarbene Complexes of Palladium(II) and Platinum(II)." In Molecular Electrochemistry of Inorganic, Bioinorganic and Organometallic Compounds. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1628-2_31.

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Bertani, R., M. Mozzon, L. Zanotto, and R. A. Michelin. "Synthesis of Cyclic and Acyclic Carbene Complexes Derived from Isocyanide Ligands in Complexes of Palladium(II) and Platinum(II)." In Advances in Metal Carbene Chemistry. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2317-1_7.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of palladium(II) chloride complex with 1, 1′-bis(oxodiphenylphosphoranyl)ferrocene." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_833.

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Moret, Marc-Etienne. "Organometallic Platinum(II) and Palladium(II) Complexes as Donor Ligands for Lewis-Acidic d10 and s2 Centers." In Higher Oxidation State Organopalladium and Platinum Chemistry. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-17429-2_7.

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Conference papers on the topic "Palladium(II) Chloride Complexes"

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Schock, Michael R., Darren A. Lytle, and Jonathan A. Clement. "Effects of pH, Carbonate, Orthophosphate, and Redox Potential on Cuprosolvency." In CORROSION 1995. NACE International, 1995. https://doi.org/10.5006/c1995-95610.

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Abstract A comprehensive solubility model for copper in drinking water has been developed, that is consistent with available data for copper dissolution and passivation in drinking water systems. Copper solubility (cuprosolvency) is greatly affected by the redox conditions of the systems. The concentration of Cu(I) is dominated by Cu2O(s) or CuOH(s) solid phases, plus soluble aqueous ammonia and chloride complexes. In new piping, the concentration of Cu(II) is mainly governed by Cu(OH)2(s) (cupric hydroxide), rather than CuO(s) (tenorite) or Cu2(OH)2CO3(s)(malachite). Complexation of Cu(II) by
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2

El-Maraghy, Salah B., K. A. Salib, and S. L. Stefen. "Palladium (II) Hydrazopyrazolone Complexes." In Intl Conf on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron. SPIE, 1989. http://dx.doi.org/10.1117/12.969594.

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Kesić, Ana, Jovana Bogojeski, Ivana Raković, and Ivana Radojević. "Biological studies of organoselenium trans-palladium(II) complexes." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11448.

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Petrović, Đorđe, Maja Đukić, Edina Avdović, et al. "DNA binding and molecular docking of four palladium(II) complexes with O,O’-dialkyl esters of (S,S)-propylenediamine-N,N’-di-2-(2-benzyl) acetic acid." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.539p.

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The antitumor activity of platinum-based complexes still captures the attention of scientists and new potential drugs are being synthesized and investigated. Although complexes of palladium(II) ion show less cytotoxicity compared to platinum(II) complexes due to the high reactivity of the palladium center, research in this field has continued and many authors have found that auxiliary chelating ligands can improve complex stability and their cytotoxicity. As a consequence of rapid ligand exchange, the probability of palladium(II) complexes reaching the biological target in organisms seems to b
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Kepeňová, Martina, Michaela Benediková, Mária Vilková, Miroslava Litecká, and Ivan Potočňák. "Ionic palladium(II) complexes with nitro and halogen derivatives of 8-hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.443k.

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Four commercially unavailable derivatives of 8-hydroxyquinoline with different functional groups (nitro and halogen) in positions 5 and 7 were prepared: 5-nitro-7-iodo-8-hydroxyquinoline (HNIQ), 5-nitro-7-bromo-8-hydroxyquinoline (HNBrQ), 5-iodo-7-bromo-8-hydroxyquinoline (HIBrQ) and 5-chloro-7-bromo-8-hydroxyquinoline (HClBrQ). Their characterization was performed by IR and NMR spectroscopy, elemental analysis and in the case of HIBrQ and HClBrQ by single crystal X-ray structure analysis. Prepared compounds were used for the synthesis of new palladium(II) complexes NH2(CH3)2[PdCl2(XQ)], where
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Bakaev, I. V., N. F. Romashev, and A. L. Gushchin. "PALLADIUM(II) AND RHODIUM(III) COMPLEXES WITH ACENAPHTHENEMONOARYLHYDRAZONES: SYNTHESIS, STRUCTURE AND PHYSICOCHEMICAL PROPERTIES." In XXIII МЕЖДУНАРОДНАЯ ЧЕРНЯЕВСКАЯ КОНФЕРЕНЦИЯ ПО ХИМИИ, АНАЛИТИКЕ И ТЕХНОЛОГИИ ПЛАТИНОВЫХ МЕТАЛЛОВ. NIIC SB RAS, 2022. http://dx.doi.org/10.26902/chern-2022-100.

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Boyarsky, V., A. Mikherdov, S. Baikov, P. Savko, R. Suezov та R. Trifonov. "С,N-CHELATED CARBENE COMPLEXES OF PALLADIUM(II) AS POTENTIAL PHARMACOLOGICALLY ACTIVE COMPOUNDS". У MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-50.

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Stanić, Petar, Darko Ašanin, Marijana Vasić, Tanja Soldatović, and Biljana Šmit. "KINETICS OF THE REACTION OF AN ARYLIDENE 2-THIOHYDANTOIN DERIVATIVE WITH SOME Pd(II) COMPLEXES." In 1st INTERNATIONAL SYMPOSIUM ON BIOTECHNOLOGY. University of Kragujevac, Faculty of Agronomy, 2023. http://dx.doi.org/10.46793/sbt28.497s.

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Reactions of 3-(benzylideneamino)-2-thioxoimidazolidin-4-one with some palladium complexes (PdCl2, Pd(DMSO)2Cl2 and K2PdCl4) were monitored with NMR spectroscopy, which is used as a convenient and practical tool for determining the kinetic parameters of the reactions. Rate constants of the reactions were determined and reactivity of the complexes towards the 2-thiohydantoin derivative was compared.
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M. AHMED, Riyadh, Sarah S. ABDUL RAHMAN, Dhefaf H. BADRI, Khawla M. SULTAN, Ismaeel Y. MAJEED, and Ghada M. KAMIL. "SYNTHESIS AND CHARACTERISATION OF NEW Co(II), Zn(II) AND Cd(II) COMPLEXES DERIVED FROM OXADIAZOLE LIGAND AND 1,10-PHENANTHROLINE AS Co-LIGAND." In V. International Scientific Congress of Pure, Applied and Technological Sciences. Rimar Academy, 2022. http://dx.doi.org/10.47832/minarcongress5-5.

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In this work, prepared new ligand namely 5-(2,4—dichloro-phenyl)-1,3,4- oxadiazole-2-(3H)-thion, which was obtained from the 2,4-dichlorobenzoyl chloride with hydrazine, after that reaction with CS2/KOH in methanol. This ligand was reaction with (Co, Zn and Cd) and 1,10-phenanthroline as co-ligand. The ligand and complexes were characterised by IR, UV-Vis, C-H-N, magnetic moment, A.A, Cl content, and m.p.. The data that collected indicate the octahedral geometry around metal ions in all complexes. In IR spectra of complexes, the small shift in ν(C=S), indicating the exocyclic sulfur is not bon
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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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