Relevant bibliographies by topics / Palladium complexes

Academic literature on the topic 'Palladium complexes'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Contents

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Palladium complexes.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Palladium complexes"

1

Murahashi, Tetsuro, and Hideo Kurosawa. "Organopalladium complexes containing palladiumpalladium bonds." Coordination Chemistry Reviews 231, no. 1-2 (September 2002): 207–28. http://dx.doi.org/10.1016/s0010-8545(02)00121-2.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Stromnova, Tat'yana A., and Ilya I. Moiseev. "Palladium carbonyl complexes." Russian Chemical Reviews 67, no. 6 (June 30, 1998): 485–514. http://dx.doi.org/10.1070/rc1998v067n06abeh000414.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

AL-Jaffer, Thaaer K. Maki, Zeki O. Naser, and Ali Jameel Hameed. "Spectroscopic and Thermal Studies of Some Palladium(II) Complexes with 2-amino-4-(4-subsistuted phenyl)thiazole Derivatives." Biomedicine and Chemical Sciences 1, no. 2 (April 1, 2022): 78–82. http://dx.doi.org/10.48112/bcs.v1i2.104.

Full text
Abstract:
Six new complexes of palladium(II) with a general formula [Pd(L)2Cl2], where L = 2-amino-4-(4-subsistuted phenyl)thiazole. The palladium complexes were prepared by the reaction of 2-amino-4-(4-subsistuted phenyl)thiazole ligands with with Bis(benzonitrile)palladium(II) dichloride in chloroform solvent at molar ratio Pd:L=1:2. The resulting complexes were characterized by the magnetic susceptibility, conductivity measurements, infrared, 1H NMR and the thermo gravimetric analysis. Elemental analyses, spectroscopic and another physical studies of the prepared palladium (II) complexes allowed structures to be proposed. The thermal properties of the prepared complexes indicated the all-decomposition steps and gave an insight about the stability of palladium(II) complexes. The physical analysis indicated that prepared ligands behaved as mono dental, bounding Pd(II) through the nitrogen atoms from the thiazole ring.
APA, Harvard, Vancouver, ISO, and other styles
4

Muhammad Anwar Saeed, Muhammad Anwar Saeed, Hizbullah Khan Hizbullah Khan, Muhammad Sirajuddin Muhammad Sirajuddin, and Syed Muhammad Salman Syed Muhammad Salman. "DNA Interaction and Biological Activities of Heteroleptic Palladium (II) Complexes." Journal of the chemical society of pakistan 43, no. 2 (2021): 227. http://dx.doi.org/10.52568/000566/jcsp/43.02.2021.

Full text
Abstract:
The manuscript describes the binding of DNA as well as biological studies of some mixed ligand dithiocarbamate Palladium (II) complexes (1-5). The observed compounds are of general formulae [PdCl(DT)(PR3)]. The dithiocarbamate “DT” and “PR3” groups are varied among the studied complexes as DT = bis[(2-methoxyethyl) dithiocarbamate)] (1 and 2), dibutyl dithiocarbamate (4 and 5), bis[(2-ethyl) hexyl dithiocarbamate)] (3); PR3 = triphenyl phosphine (1), benzy diphenyl phosphine (2), diphenyl-tert-butyl phpsphine (3), diphenyl-p-tolyl phosphine (4) and diphenyl-2-methoxy phenyl phosphine (5). The synthesized complexes were screened for DNA binding study via (UV Visible spectrophotometry and Viscometery) and biological activities such as anti-bacterial and anti-fungal, Molinspiration calculations and antioxidant potencies stimulated by hydrogen peroxide in human blood lymphocytes. In case of drug DNA interaction, complexes showed some sort of interaction with DNA solution. Almost all the complexes exhibited moderate antifungal and antibacterial behavior (against Gram positive and negative bacterial strains). The Molinspiration calculation study revealed that the said Pd (II) mixed complexes are biologically significant drugs having adequate molecular properties regarding drug likeness, except the log P values of complexes 3-5 because some structural adjustments must be done for enhancement of their bioavailability and hydrophilic nature. Regarding the antioxidant potential of complexes 1, 2 and 4, the H2O2 treatment of complexes violently decreased the action of antioxidant enzymes, superoxide dismutase and catalase and enhanced the level of thiobarbituric acid-reacting substances. Under experimental conditions, we conclude that all complexes act as anti-mutagens as they significantly suppress H2O2-induced oxidative damage at non-genotoxic concentrations.
APA, Harvard, Vancouver, ISO, and other styles
5

Muhammad Anwar Saeed, Muhammad Anwar Saeed, Hizbullah Khan Hizbullah Khan, Muhammad Sirajuddin Muhammad Sirajuddin, and Syed Muhammad Salman Syed Muhammad Salman. "DNA Interaction and Biological Activities of Heteroleptic Palladium (II) Complexes." Journal of the chemical society of pakistan 43, no. 2 (2021): 227. http://dx.doi.org/10.52568/000566.

Full text
Abstract:
The manuscript describes the binding of DNA as well as biological studies of some mixed ligand dithiocarbamate Palladium (II) complexes (1-5). The observed compounds are of general formulae [PdCl(DT)(PR3)]. The dithiocarbamate “DT” and “PR3” groups are varied among the studied complexes as DT = bis[(2-methoxyethyl) dithiocarbamate)] (1 and 2), dibutyl dithiocarbamate (4 and 5), bis[(2-ethyl) hexyl dithiocarbamate)] (3); PR3 = triphenyl phosphine (1), benzy diphenyl phosphine (2), diphenyl-tert-butyl phpsphine (3), diphenyl-p-tolyl phosphine (4) and diphenyl-2-methoxy phenyl phosphine (5). The synthesized complexes were screened for DNA binding study via (UV Visible spectrophotometry and Viscometery) and biological activities such as anti-bacterial and anti-fungal, Molinspiration calculations and antioxidant potencies stimulated by hydrogen peroxide in human blood lymphocytes. In case of drug DNA interaction, complexes showed some sort of interaction with DNA solution. Almost all the complexes exhibited moderate antifungal and antibacterial behavior (against Gram positive and negative bacterial strains). The Molinspiration calculation study revealed that the said Pd (II) mixed complexes are biologically significant drugs having adequate molecular properties regarding drug likeness, except the log P values of complexes 3-5 because some structural adjustments must be done for enhancement of their bioavailability and hydrophilic nature. Regarding the antioxidant potential of complexes 1, 2 and 4, the H2O2 treatment of complexes violently decreased the action of antioxidant enzymes, superoxide dismutase and catalase and enhanced the level of thiobarbituric acid-reacting substances. Under experimental conditions, we conclude that all complexes act as anti-mutagens as they significantly suppress H2O2-induced oxidative damage at non-genotoxic concentrations.
APA, Harvard, Vancouver, ISO, and other styles
6

Lo, Pang-Chia, Chun-Wei Yang, Wen-Kai Wu, and Chi-Tien Chen. "Synthesis, Characterization, and Catalytic Application of Palladium Complexes Containing Indolyl-NNN-Type Ligands." Molecules 26, no. 15 (July 22, 2021): 4426. http://dx.doi.org/10.3390/molecules26154426.

Full text
Abstract:
In this study, a series of N-heterocyclic indolyl ligand precursors 2-Py-Py-IndH, 2-Py-Pz-IndH, 2-Py-7-Py-IndH, 2-Py-7-Pz-IndH, and 2-Ox-7-Py-IndH (L1H-L5H) were prepared. The treatment of ligand precursors with 1 equivalent of palladium acetate affords palladium complexes 1–5. All ligand precursors and palladium complexes were characterized by NMR spectroscopy and elemental analysis. The molecular structures of complexes 3 and 5 were determined by single crystal X-ray diffraction techniques. The application of those palladium complexes 1–5 to the Suzuki reaction with aryl halide substrates was examined.
APA, Harvard, Vancouver, ISO, and other styles
7

Kublanovsky, V. S., and V. N. Nikitenko. "Classical, barrierless, and activationless discharge of palladium(II) iminodiacetate complexes." Reports of the National Academy of Sciences of Ukraine, no. 10 (November 16, 2016): 67–72. http://dx.doi.org/10.15407/dopovidi2016.10.067.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Salishcheva, Olesya, and Alexander Prosekov. "Antimicrobial activity of mono- and polynuclear platinum and palladium complexes." Foods and Raw Materials 8, no. 2 (September 30, 2020): 298–311. http://dx.doi.org/10.21603/2308-4057-2020-2-298-311.

Full text
Abstract:
Introduction. Infectious diseases remain a serious threat to humanity worldwide as bacterial pathogens grow more diverse. Bacteria, fungi, and parasites develop resistance to clinically approved antimicrobials, which reduces the efficacy of available drugs and treatment measures. As a result, there is an ever growing demand for new highly effective pharmaceuticals. This review describes mono- and polynuclear platinum and palladium complexes with antimicrobial properties. We compared several groups of antibacterial agents: antibiotics, antioxidant biologically active substances, antimicrobial nanoparticles, nanocomposite materials, biopolymers, micellar systems, and plant extracts. Study objects and methods. The review covered relevant articles published in Web of Science, Scopus, and Russian Science Citation Index for the last decade. The list of descriptors included such terms as mononuclear and binuclear complexes of platinum, palladium, and antimicrobial activity. Results and discussion. Chelates of platinum, palladium, silver, iridium, rhodium, ruthenium, cobalt, and nickel are popular therapeutic agents. Their antimicrobial activity against pathogenic microorganisms can be enhanced by increasing their bioavailability. Metalbased drugs facilitate the transport of organic ligands towards the bacterial cell. The nature of the ligand and its coordination change the thermodynamic stability, kinetic lability, and lipophilic properties of the complex, as well as the reactivity of the central atom. Polynuclear platinum and palladium complexes contain two or more bound metal (coordinate) centers. Covalent bonding with bacterial DNA enables them to form a type of DNA adducts, which is completely different from that of mononuclear complexes. Conclusion. Metal-based drugs with functional monodentate ligands exhibit a greater antimicrobial effect compared to free ligands. Poly- and heteronuclear complexes can increase the number of active centers that block the action of bacterial cells. When combined with other antibacterial agents, they provide a synergistic effect, which makes them a promising subject of further research.
APA, Harvard, Vancouver, ISO, and other styles
9

Grirrane, Abdessamad, Hermenegildo Garcia, and Eleuterio Álvarez. "Isolation and X-ray characterization of palladium–N complexes in the guanylation of aromatic amines. Mechanistic implications." Beilstein Journal of Organic Chemistry 9 (July 22, 2013): 1455–62. http://dx.doi.org/10.3762/bjoc.9.165.

Full text
Abstract:
In the context of palladium-catalyzed guanylation of anilines herein, we have been able to characterize and isolate bis(anilino) and bis(guanidino)Pd(II) complexes using reaction conditions under which stoichiometric amounts of palladium salts are used. Characterization of these palladium complexes strongly supports a mechanistic proposal for the catalytic guanylation of anilines using PdCl2(NCCH3)2 as catalyst that involves the intermediacy of these Pd(II) complexes.
APA, Harvard, Vancouver, ISO, and other styles
10

Edwards, Gavin L., David St C. Black, Glen B. Deacon, and Laurence PG Wakelin. "In vitro and in vivo studies of neutral cyclometallated complexes against murine leukæmias." Canadian Journal of Chemistry 83, no. 6-7 (June 1, 2005): 980–89. http://dx.doi.org/10.1139/v05-109.

Full text
Abstract:
Cyclometallated µ-halogeno dimers derived from nitrogen donor ligands (1-phenylpyrazoles, 2-phenylpyridine, and 1-(2′-pyridyl)indole) were treated with unidentate nitrogen and phosphorus donor ligands to give a series of neutral monomeric palladium(II) and platinum(II) complexes. An initial prescreen of the complexes against the mouse lymphoid leukæmia cell line L1210 indicated that the complexes exhibited growth inhibitory activity over a relatively wide concentration range. Two factors that gave rise to increased activity were steric hindrance about the metal centre resulting from hindered ligands such as 2,6-dimethylpyridine, or the presence of a phosphorus donor ligand. Little correlation between palladium and platinum complexes was noted. Four complexes were selected for further in vivo study and, while none of the palladium complexes showed more than marginal activity against P388 leukæmia at doses below toxic levels, one platinum complex with a hindered metal centre did display significant antitumour activity against this model.Key words: cyclometallation, palladium, platinum, cytotoxicity, anticancer.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Palladium complexes"

1

Bangun, Nimpan. "NMR study of palladium methoxide and palladium carbomethoxide complexes." Thesis, This resource online, 1993. http://scholar.lib.vt.edu/theses/available/etd-12052009-020137/.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Clentsmith, Guy Kenneth Bruce. "Dinuclear palladium complexes with bridging hydrides." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/29800.

Full text
Abstract:
The palladium hydride dimer, [(dippp)Pd]₂(µ--H)₂, (2) (dippp = 1,3-bis(diisopropylphosphino)propane), was synthesized, and its interaction with lithium tetraethylborate examined. When the two compounds were mixed in stoichiometric amounts high yields of the adduct, [(dippp)Pd]₂(µ-H) ₂•LiBEt₄ (1) — previously isolated adventitiously by a co-worker — were obtained. Variable temperature ³¹P{¹H} NMR spectroscopy showed a condition of chemical equilibrium between 2 and 1, but the value of the equilibrium constant, Keq, could not be determined owing to its large magnitude. Extension of this chemistry to other sources of Li⁺ led to the isolation of the aluminate adduct, [(dippp)Pd]₂((µ-H)₂,•LiA1Et₄ (3). Likewise when NaBEt₄ was substituted an adduct formulated as [(dippp)Pd]₂(µ-H)₂•NaBEt₄ (4) was obtained. The interaction of tetraethylborate salts with other transition-metals was also examined, with evidence of adduct formation for both [(dippp)Rh]₂(µ-H)₂ and [(dippp)Ni]₂(µ-H)₂ (6) with LiBEt₄. It was not possible to isolate these compounds as analytically pure samples. This general interaction is discussed in terms of metal basicity. The reactivity of 2 towards organic donor species was also studied. Addition of excess donor results in the formation of tricoordinate Pd(0) species: (dippp)Pd(ɳ²-H₂C=CH₂) (5), (dippp)Pd(PPh₃) (7), and (dippp)Pd(DMAD) (8) (DMAD = dimethylacetylenedicarboxylate) were thus isolated. When a stoichiometric equivalent of donor was added to 2, no dimeric intermediates could be observed.
Science, Faculty of
Chemistry, Department of
Graduate
APA, Harvard, Vancouver, ISO, and other styles
3

Ford, S. "New palladium complexes containing organoselenium ligands." Thesis, Swansea University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.636990.

Full text
Abstract:
The aim of the work contained within this thesis was to investigate the reactions of bicyclic 1,2,3-selenadiazoles and their diselenin derivatives with Pd (0) phosphine complexes. Chapter one is a review of previous research on organoselenium ligands that have been shown to bond to palladium and platinum. It also summaries other relevant chemistry of the ligands under investigation. Chapter two describes the reactions between a variety of palladium trialkylphosphine complexes, and cycloalkeno-1,2,3-selenadiazoles. It includes the first analysis by x-ray crystallography of a simple uncoordinated bicyclic 1,2,3-selenadiazole, and full characterisation of all the products obtained. Chapter three describes the reactions between tetrakis(triphenylphosphine)palladium and both cycloalkeno-1,2,3-selenadiazoles and their diselenin derivatives. Also included in this section is a new method for the preparation of bis(cycloalkeno)-1,4-diselenins. Chapter four looks at the reaction between the palladium starting materials used in chapter two, and bis(cycloalkeno)-1, 4-diselenins. The products obtained are fully characterised, and further research into their chemistry is documented in chapter five. Here, they are shown to undergo bridge cleavage reactions with both monodentate and bidentate phosphine ligands. This chapter also includes the direct synthesis of palladium diselenolenes containing 1,2-bis(diphenylphosphino)ethane. Experimental details concerning the synthesis of all complexes, both products and starting materials, used in this study are contained in the final chapter six.
APA, Harvard, Vancouver, ISO, and other styles
4

Spankie, S. A. A. "Ylide complexes of palladium and platinum." Thesis, Heriot-Watt University, 1987. http://hdl.handle.net/10399/1018.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Cairns, Graham R. "Hydrogenation catalysts from supported palladium complexes." Thesis, University of Glasgow, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360177.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Kuma, Karl Earl Adjetey. "A study of palladium cyclopentadienyl complexes." Thesis, University of Salford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299126.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Dooley, Ruth Elizabeth. "Isomerisation of palladium π-allyl complexes." Thesis, University of Edinburgh, 2016. http://hdl.handle.net/1842/15976.

Full text
Abstract:
The palladium-catalysed asymmetric allylic alkylation is a mild and versatile bond forming reaction between a nucleophile and allylic electrophile. The wide scope of nucleophiles used, and the high regio- and stereoselectivity obtainable renders this transformation an important technique in enantioselective synthesis. The mechanism is known to go via a key palladium π-allyl intermediate, followed by nucleophilic addition occurring at the terminal allylic carbon. Both the formation of the palladium π-allyl, and the nucleophilic addition to generate the alkylated product and palladium(0) proceed with high levels of inversion of stereochemistry, and both provide an opportunity for the induction of stereochemistry. However in the case of ligand controlled nucleophilic addition memory effects have been observed. The epimerisation of the palladium π-allyl before nucleophilic attack is key to achieving high levels of selectivity when racemic starting materials and chiral ligands are employed. Previous work in the Lloyd-Jones group has determined that prolonging the lifetime of the palladium π-allyl species, either by the use of weakly coordinating counter ions or slow addition of the nucleophile reduces this memory effect, however increasing the rate of epimerisation would have a result in a similar effect. One of the mechanisms resulting in the epimerisation of the palladium π-allyl species is mediated by palladium(0), however the details of the mechanism are not well understood. We describe the synthesis of a diastereotopic palladium cyclohexenyl ester and labelled the complex with 108palladium and d3 at the cyclohexenyl ester. Using simultaneous 31P NMR and mass spectrometry, we have acquired strong evidence against mechanisms involving a single electron transfer, as proposed by Stille, of formation of a dinuclear palladium(I) species followed by an inversion event, and we have gained evidence supporting the direct nucleophilic addition of the palladium(0), resulting in inversion of stereochemistry. The differences in rates of nucleophilic attack involving monodentate and bidentate phosphine ligands on both the palladium I-cyclohexenyl ester have also been explored. Throughout the mechanistic investigation, it was noted that the 31P NMR spectroscopy experiment used gave non-quantitative results, and in fact the differences in quantification of the species varied with the spectrometer used. We also describe our investigations into where these differences arise from and an optimum set of parameters for quantitative 31P NMR spectroscopy. The conclusions are also applicable to other heternuclear NMR spectroscopic experiments.
APA, Harvard, Vancouver, ISO, and other styles
8

Alshgari, Razan. "Crystal engineering of palladium terpyridine complexes." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/47726/.

Full text
Abstract:
The ability of 2,2':6',2"-terpyridine (terpy) to chelate to a wide variety of metal ions has led to the synthesis of different metal-terpyridine complexes. In addition, there are different synthetic strategies have been improved, allowing 2,2':6',2"-terpyridine and its derivatives to find a wide range of applications assensors and catalysts. This thesis concerns the synthesis of a series of Pd(terpy) complexes with different para- and meta-substituted pyridine ligands and their properties are studied by X-ray crystallography. In order to extend the experimental observations and the range of applicability of the proposed interpretation, another system involving the tridentate aromatic nitrogen donor 4,4',4''-tri-tert-butyl-2,2':6',2''-terpyridine (tBu3-terpy) has been examined. A range of N,N-bidentate ligandsare introduced in next section. These can be potentially used to bridge two metal centres. The reactivity of [Pd(terpy)(NCCH3)](CF3SO3)2 was investigated with a wide range of N,N-bidentate ligands. Substitution of the acetonitrile ligand of [P(terpy)(NCCH3)](CF3SO3)2 with these ligands was found to be efficient and facile with reactions occurring at room temperature. Extension of this reaction to meso-tetra (4-pyridyl)porphyrin results in tetranuclear Pd(terpy) complex and affords [{Pd(terpy)}4(H2T(4-Py)P)](CF3SO3)8. In Chapter 6, similarly to terpyridine, 2-phenyl-4,6-bis(2-pyridyl)-1,3,5-triazine (pbptz) is coordinated to palladium as a tridentate ligand and no complex was seen to adopt any of the other potential binding modes for this molecule.
APA, Harvard, Vancouver, ISO, and other styles
9

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Haaren, Richard Johannes van. "Palladium and rhodium allyl complexes in catalysis." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2002. http://dare.uva.nl/document/64738.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Palladium complexes"

1

Rahuma, Sed Mohamed Ammar. Agostic interaction in palladium complexes. Salford: University of Salford, 1994.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Purser, Alexander Simon. Novel organo-palladium complexes containing 1,1[superior ,]- substituted ferrocenyl diphosphine ligands. Birmingham: University of Birmingham, 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Sutaria, Adil Dinyar. The effect of heterodentate chelatin P-N ligands on allyl and alkyl complexes of palladium and platinum. Salford: University of Salford, 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Prim/Campagne. Complexes de palladium en synthese organique. CNRS Editions, 2001.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Maitlis, Peter. Metal Complexes: The Organic Chemistry of Palladium. Elsevier Science & Technology Books, 2012.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Campbell, Michael Glenn. Synthesis, Structure, and Reactivity of New Palladium(III) Complexes. 2014.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Hsu, Noel Yu Wee. Catalytic hydrogenation of canola and soybean oils using transition metal complexes and supported/unsupported palladium. 1988.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Fire in the Genes- Poly-MVA the Cancer Answer? (A Personal research on Cancer and Palladium Lipoic Complexes). Foundation for the Advancement of Med, 2000.

Find full text
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Palladium complexes"

1

Tatsuno, Yoshitaka, Toshikatsu Yoshida, Seiotsuka, Najeeb Al-Salem, and Bernard L. Shaw. "(η3 -Allyl)Palladium(II) Complexes." In Inorganic Syntheses, 220–23. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132500.ch51.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Tatsuno, Yoshitaka, Toshikatsu Yoshida, Sei Otsuka, Najeeb Al-Salem, and Bernard L. Shaw. "(η3 -Allyl)Palladium(II) Complexes." In Inorganic Syntheses, 342–45. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch88.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Saito, T., H. Munakata, H. Imoto, A. Davison, K. Jonas, and B. Albiez. "Nickel and Palladium Chlorohydridobis-(Phosphine) Complexes." In Inorganic Syntheses, 83–88. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132487.ch25.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Hayashi, Tamio. "Asymmetric Reactions Catalyzed by Palladium-MOP Complexes." In Organic Synthesis via Organometallics OSM 5, 171–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-49348-5_14.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Williams, J. M. J. "Palladium allyl π-complexes in asymmetric synthesis." In Advanced Asymmetric Synthesis, 299–312. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-007-0797-9_15.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Hoyos, Mario, Daniel Guest, and Oscar Navarro. "(N-Heterocyclic Carbene)-Palladium Complexes in Catalysis." In N-Heterocyclic Carbenes, 85–110. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch04.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Drew, D., J. R. Doyle, and Alan G. Shaver. "Cyclic Diolefin Complexes of Platinum and Palladium." In Inorganic Syntheses, 47–55. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch11.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Lukas, J., B. E. Morris, and R. A. Clement. "π-Allyl Complexes of Palladium and Platinum." In Inorganic Syntheses, 75–81. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132463.ch17.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Visser, A., R. Van Der Linde, R. O. De Jongh, H. Selbeck, M. Molin, and G. Wilke. "Ethylenebis(Triphenylphosphine)Palladium(0) and Related Complexes." In Inorganic Syntheses, 127–30. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132470.ch35.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Munakata, H., T. Saito, K. Jonas, and B. Albiez. "Hydrido[Tetrahydroborato(1-)] Nickel and Palladium Complexes." In Inorganic Syntheses, 88–91. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132487.ch26.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Palladium complexes"

1

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

MOISEEV, ILYA I. "METAL COMPLEX CATALYSIS OF OXIDATION REACTIONS: CATALYSIS WITH PALLADIUM COMPLEXES." In Proceedings of the NIOK (Netherlands Institute for Catalysis Research) Course on Catalytic Oxidation. WORLD SCIENTIFIC, 1995. http://dx.doi.org/10.1142/9789814503884_0010.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

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. Basel, Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11448.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Sortland, Miriam, Ryan Del Re, James Passarelli, Jodi Hotalen, Michaela Vockenhuber, Yasin Ekinci, Mark Neisser, Daniel Freedman, and Robert L. Brainard. "Positive-tone EUV resists: complexes of platinum and palladium." In SPIE Advanced Lithography, edited by Obert R. Wood and Eric M. Panning. SPIE, 2015. http://dx.doi.org/10.1117/12.2086598.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Sharma, Krishna, Nighat Fahmi, and R. V. Singh. "Microwave synthesis, antimicrobial and antiamoebic activity of palladium and platinum complexes." In 2008 International Conference on Recent Advances in Microwave Theory and Applications (MICROWAVE). IEEE, 2008. http://dx.doi.org/10.1109/amta.2008.4763113.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
7

Sanmartin, Raul, Esther Domínguez, Garazi Urgoitia, and María Teresa Herrero. "Diyne formation from alkynes in the presence of palladium pincer complexes." In MOL2NET 2017, International Conference on Multidisciplinary Sciences, 3rd edition. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/mol2net-03-05090.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

LAULLOO, SABINA, SALMA Moosun, SHABNEEZ Bhewa, and MINU BHOWON. "Palladium Schiff Base Complexes: Potential catalysts for C-C bond reactions." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a022.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Boyarsky, V., A. Mikherdov, S. Baikov, P. Savko, R. Suezov, and R. Trifonov. "С,N-CHELATED CARBENE COMPLEXES OF PALLADIUM(II) AS POTENTIAL PHARMACOLOGICALLY ACTIVE COMPOUNDS." In 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.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Palladium complexes"

1

Ribeiro, Fabio H. Complete oxidation of methane on palladium catalysts. Final Report. Office of Scientific and Technical Information (OSTI), July 2003. http://dx.doi.org/10.2172/820416.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Palladium complexes' for particular source types:
Journal articles Dissertations / Theses
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography