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Статті в журналах з теми "Palladium compounds"
Mammadova, S. R. "EXTRACTION OF PALLADIUM." Azerbaijan Chemical Journal, no. 3 (September 28, 2021): 67–71. http://dx.doi.org/10.32737/0005-2531-2021-3-67-71.
Повний текст джерелаPerić, Tanja S., and Slobodan M. Janković. "Cardiotoxicity of Palladium Compounds / Kardiotoksičnost Jedinjenja Paladijuma." Journal of Medical Biochemistry 32, no. 1 (January 1, 2013): 20–25. http://dx.doi.org/10.2478/v10011-012-0010-5.
Повний текст джерелаBurrows, Andrew D., D. Michael, and P. Mingos. "Palladium cluster compounds." Transition Metal Chemistry 18, no. 2 (April 1993): 129–48. http://dx.doi.org/10.1007/bf00139944.
Повний текст джерелаSoejima, Takashi, and Kei-ji Iwatsuki. "Innovative Use of Palladium Compounds To Selectively Detect Live Enterobacteriaceae in Milk by PCR." Applied and Environmental Microbiology 82, no. 23 (September 23, 2016): 6930–41. http://dx.doi.org/10.1128/aem.01613-16.
Повний текст джерелаBURROWS, A. D., and D. M. P. MINGOS. "ChemInform Abstract: Palladium Cluster Compounds." ChemInform 24, no. 33 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199333281.
Повний текст джерелаNiu, Ben, Yin Wei та Min Shi. "Recent advances in annulation reactions based on zwitterionic π-allyl palladium and propargyl palladium complexes". Organic Chemistry Frontiers 8, № 13 (2021): 3475–501. http://dx.doi.org/10.1039/d1qo00273b.
Повний текст джерелаBoriskin, O. I., S. N. Larin, G. A. Nuzhdin, and I. V. Murav’eva. "THE PALLADIUM COMPLEXES DURING THERMAL DECOMPOSITION PHASE COMPOSITION INVESTIGATION." Kontrol'. Diagnostika, no. 290 (August 2022): 44–48. http://dx.doi.org/10.14489/td.2022.08.pp.044-048.
Повний текст джерелаJain, Vimal K. "Internally functionalized multifaceted organochalcogen compounds." Dalton Transactions 49, no. 26 (2020): 8817–35. http://dx.doi.org/10.1039/d0dt01160f.
Повний текст джерелаYoshimura, Akihiro, Shunta Tochigi, and Yasunari Matsuno. "Fundamental Study of Palladium Recycling Using “Dry Aqua Regia” Considering the Recovery from Spent Auto-catalyst." Journal of Sustainable Metallurgy 7, no. 1 (February 16, 2021): 266–76. http://dx.doi.org/10.1007/s40831-020-00335-x.
Повний текст джерелаAullón, Gabriel, and Santiago Alvarez. "On the Existence of Molecular Palladium(VI) Compounds: Palladium Hexafluoride." Inorganic Chemistry 46, no. 7 (April 2007): 2700–2703. http://dx.doi.org/10.1021/ic0623819.
Повний текст джерелаДисертації з теми "Palladium compounds"
Farhad, Mohammad. "Studies on new trinuclear palladium compounds." Connect to full text, 2007. http://hdl.handle.net/2123/2477.
Повний текст джерелаThe present study deals with the synthesis and characterization of six tri-palladium complexes code named MH3, MH4, MH5, MH6, MH7 and MH8 that contained two planaramine ligands bound to the central or each of the terminal metal ions. The activity of the compounds against human cancer cell lines: A2780, A2780cisR and A2780ZD0473R, cell uptake, levels of DNA-binding and nature of interaction with salmon sperm and pBR322 plasmid DNA have also been determined. Whereas cisplatin binds with DNA forming mainly intrastrand GG adduct that causes local bending of a DNA strand, the tri-palladium complexes are expected to bind with DNA forming a number of long-range interstrand GG adducts that would cause a global change in DNA conformation. Among the designed complexes, MH6 that has two 2-hydroxypyridine ligands bound to each of the two terminal palladium ions is found to be most active. The compound also has the highest cell uptake and Pd-DNA binding levels. In contrast, MH8 which has two 4-hydroxypyridine ligands bound to each of the two terminal palladium ions is found to be least active. The results indicate that, as applied to the terminal metal centres, 2-hydroxypyridine would be more activating than 4-hydroxypyridine perhaps because of greater protection provided to the terminal centres from coming in contact with the solvent molecules. In contrast, when bound to the central metal centre, 4-hydroxypyridine appears to play a slightly greater activating role than 2-hydroxypyridine or 3-hydroxypyridine, suggesting that non-covalent interactions such as hydrogen bonding associated with the ligand rather than its steric effect may be a more important determinant of antitumour property. The results illustrate structure-activity relationships and suggest that the tri-palladium complex containing two 2-hydroxypyridine ligands bound to each of the three metal centres or the compound that contains two 2-hydroxypyridine ligands bound to each of the two terminal metal centres and two 4-hydroxypyridine ligands bound to the central metal centre, may be much more active than any of the designed complexes.
Burrows, Andrew David. "Cluster compounds of palladium and platinum." Thesis, University of Oxford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302903.
Повний текст джерелаHoogervorst, Wilhelmus Johannes. "Isophthalaldimine compounds of palladium, platinum and rhodium." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2003. http://dare.uva.nl/document/69284.
Повний текст джерелаEzomo, O. J. "Studies on palladium and platinum cluster compounds." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234990.
Повний текст джерелаChiffey, Andrew Francis. "Bimetallic compounds of palladium, platinum and gold." Thesis, University of Southampton, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294602.
Повний текст джерелаKelly, P. F. "Sulphur-nitrogen compounds of platinum and palladium." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/46826.
Повний текст джерелаPhillips, David J. "Palladium-catalysed synthesis of highly functionalised compounds." Thesis, University of Glasgow, 2018. http://theses.gla.ac.uk/9011/.
Повний текст джерелаCloete, Jezreel. "Synthesis and applications of functionalized pyridinyl imine complexes of palladium." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&.
Повний текст джерела-diimine Pd(II) complexes having a functionalized hydrocarbon attached to the imino nitrogen was performed. The catalytic activity of these complexes were then evaluated in the polymerization of ethylene and in the Heck coupling reaction of methyl acrylate with iodobenzene.
Unconjugated &beta
-diimine complexes of palladium were also synthesized and their activities towards ethylene polymerization and the Heck coupling of methyl acrylate and iodobenzene also evaluated and compared to that of the &alpha
-diimine complexes. Three of the &alpha
-diimine complexes synthesized showed activity towards ethylene polymerization, these being the complexes bearing the allyl, styrene and phenol functionalities. &omega
-Carboxylato complexes which were also synthesized showed no activity towards ethylene polymerization.
The polymer produced was found to be high density linear polyethylene with an average PDI of 2.54 with Mn values ranging between 3.42 and 6.90 x 10-5 and Mw values ranging between 6.05 and 17.6 x 10-5.
The complexes bearing the allyl, styrene and phenol functionalities, as well as the &omega
-carboxylato complexes active in the Heck coupling reactions of methyl acrylate with iodobenzene. None of the unconjugated &beta
-diimine complexes prepared showed any activity towards ethylene polymerization even at high Al/Pd ratios. The activity of these complexes towards the Heck arylation reaction was comparable to that of the &alpha
-diimine complexes showing similar activities.
Wallner, Olov. "Palladium-Catalyzed Synthesis and Transformations of Organometallic Compounds." Doctoral thesis, Stockholm : Dept. of Organic Chemistry, Stockholm University, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-804.
Повний текст джерелаTarlton, Stephen Vijay. "Low oxidation state compounds of palladium and platinum." Thesis, Imperial College London, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300855.
Повний текст джерелаКниги з теми "Palladium compounds"
Scott, Peter J. H. Solid-phase palladium chemistry. Hoboken, NJ: Wiley, 2012.
Знайти повний текст джерелаPalladium reagents in organic syntheses. London: Academic Press, 1985.
Знайти повний текст джерелаTsuji, Jiro. Palladium reagents and catalysts: Innovations inorganic synthesis. Chichester: Wiley, 1995.
Знайти повний текст джерелаShirran, Colette. Novel sulfur ligands for palladium catalysis. Dublin: University College Dublin, 1998.
Знайти повний текст джерелаTsuji, Jiro. Palladium reagents and catalysts: Innovations in organic synthesis. Chichester: Wiley, 1995.
Знайти повний текст джерелаThe Mizoroki-Heck reaction. Hoboken, N.J: Wiley, 2008.
Знайти повний текст джерелаLi, Jie Jack. Palladium in heterocyclic chemistry: A guide for the synthetic chemist. Amsterdam: Pergamon, 2000.
Знайти повний текст джерела1935-, Negishi Ei-ichi, and Meijere A. de, eds. Handbook of organopalladium chemistry for organic synthesis. New York: Wiley-Interscience, 2002.
Знайти повний текст джерелаTsuji, Jiro. Palladium reagents and catalysts: Innovations in organic synthesis. Chichester: Wiley & Sons, 1995.
Знайти повний текст джерелаTsuji, Jiro. Palladium reagents and catalysts: New perspectives for the 21st century. Hoboken, NJ: Wiley, 2004.
Знайти повний текст джерелаЧастини книг з теми "Palladium compounds"
Macintyre, J. E. "Pd Palladium." In Dictionary of Organometallic Compounds, 262–71. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4615-6847-6_38.
Повний текст джерелаMacIntyre, Jane E. "Pd Palladium." In Dictionary of Organometallic Compounds, 178–84. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-6848-7_41.
Повний текст джерелаMacintyre, J. E., F. M. Daniel, D. J. Cardin, S. A. Cotton, R. J. Cross, A. G. Davies, R. S. Edmundson, et al. "Pd Palladium." In Dictionary of Organometallic Compounds, 144–50. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-4966-3_42.
Повний текст джерелаNagy, Zoltán. "Pd—Palladium." In Electrochemical Synthesis of Inorganic Compounds, 383. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-0545-1_50.
Повний текст джерелаDavison, Suzanne F., and Peter M. Maitlis. "Oxidations using Palladium Compounds." In Organic Syntheses by Oxidation with Metal Compounds, 469–502. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2109-5_9.
Повний текст джерелаTsuji, Jiro, and Tadakatsu Mandai. "Palladium-Catalyzed Coupling Reactions of Propargylic Compounds." In Metal-Catalyzed Cross-Coupling Reactions, 455–89. Weinheim, Germany: Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527612222.ch11.
Повний текст джерелаMiller, J. S. "Compounds Containing Nickel, Palladium, and Platinum Chains." In Inorganic Reactions and Methods, 101. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch85.
Повний текст джерелаGebel, T. "Toxicology of platinum, palladium, rhodium, and their compounds." In Anthropogenic Platinum-Group Element Emissions, 245–55. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-59678-0_25.
Повний текст джерелаBuckley, Robert G. "Rhodium, iridium and palladium compounds as experimental anticancer drugs." In Metal Compounds in Cancer Therapy, 92–108. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1252-9_5.
Повний текст джерелаBreyer, David, and Thomas Braun. "Palladium-Mediated Synthesis of 4-Vinyltetrafluoropyridine and 2,3,5,6-Tetrafluoropyridine." In Efficient Preparations of Fluorine Compounds, 237–39. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch35.
Повний текст джерелаТези доповідей конференцій з теми "Palladium compounds"
Kostić, Marina, Vera Divac, and Sven Mangelinckx. "SYNTHESIS AND CHARACTERIZATION OF PALLADIUM (II)–2- (AZIDOMETHYL)CYCLOPROPANE-1,1-DICARBOXYLIC ACID COMPLEX." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.297k.
Повний текст джерелаRúa-Sueiro, Marcos, Paula Munin-Cruz, Francisco Reigosa, José M. Vila, M. Teresa Pereira, and Juan M. Ortigueira. "Synthesis of mono- and dinuclear cyclometallated compounds with palladium and platinum." In The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08299.
Повний текст джерелаRúa-Sueiro, Marcos, Paula Munín-Cruz, Sara Bermúdez-Fernández, and José M. Vila. "Palladium Cyclometallated Compounds: Evaluation of Their Catalytic Activity in Cross-Coupling Reactions." In ECCS 2021. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eccs2021-11034.
Повний текст джерелаBoyarsky, 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.
Повний текст джерелаLim, Adeline B. Y., Xin Long, Lu Shen, Xi Chen, Raju Ramanujan, Chee Lip Gan, and Zhong Chen. "Effect of palladium on the mechanical properties of Cu and Cu-Al intermetallic compounds." In 2013 IEEE 15th Electronics Packaging Technology Conference (EPTC 2013). IEEE, 2013. http://dx.doi.org/10.1109/eptc.2013.6745727.
Повний текст джерелаLucio Martinez, Fatima, Adofo Fernández-Figueiras, Francisco Reigosa, Jose M. Vila, Mª Teresa Pereira, Paula Munín, and Paula Polo. "Synthesis and catalytic study in the Suzuki-Miyaura reaction of a family of palladium compounds." In The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04754.
Повний текст джерелаAvdović, Edina, Žiko B. Milanović, Milanka Radulović, and Dušan S. Dimić. "ANTIMICROBIAL ACTIVITY OF 3- (1- (3- HYDROXYPHENYL) AMINO) ETHYLIDENE) CHROMAN-2,4-DIONE AND ITS CORRESPONDING PALLADIUM(II) COMPLEX." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.387a.
Повний текст джерелаSulman, Esther. "THE ROLE OF ALKALI METAL COMPOUNDS IN SYNTHESIS OF EFFECTIVE POLYMER-BASED PALLADIUM CATALYSTS OF SELECTIVE HYDROGENATION." In 18th International Multidisciplinary Scientific GeoConference SGEM2018. Stef92 Technology, 2018. http://dx.doi.org/10.5593/sgem2018/4.1/s17.094.
Повний текст джерелаGoenawan, Isna Y., Linjie (Robin) Hu, and Shazam Williams. "Exhaust Conditioning Technology to Prevent Sulfur Poisoning on Methane Oxidation Catalyst." In ASME 2015 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/icef2015-1118.
Повний текст джерелаNichols, R., G. Ramos, R. Taylor, P. Schreier, and S. Heinemann. "The influence of intermetallic compounds on high speed shear testing with a specific interest in Electroless Palladium and Autocatalytic Gold." In 2017 IEEE CPMT Symposium Japan (ICSJ). IEEE, 2017. http://dx.doi.org/10.1109/icsj.2017.8240056.
Повний текст джерела