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Bibliographies thématiques / Organoplatinum compounds

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Littérature scientifique sur le sujet « Organoplatinum compounds »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 1 août 2024

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Articles de revues sur le sujet "Organoplatinum compounds"

1

Massa, W., G. Baum, B. S. Seo et J. Lorberth. « Organoplatinum compounds ». Journal of Organometallic Chemistry 352, n^o 3 (septembre 1988) : 415–20. http://dx.doi.org/10.1016/0022-328x(88)83130-9.

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Donath, H., E. V. Avtomonov, I. Sarraje, K. H. von Dahlen, M. El-Essawi, J. Lorberth et B. S. Seo. « Organoplatinum compounds VII ». Journal of Organometallic Chemistry 559, n^o 1-2 (mai 1998) : 191–96. http://dx.doi.org/10.1016/s0022-328x(98)00481-1.

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Benn, Reinhard, Rolf-Dieter Reinhardt et Anna Rufińska. « 195Pt NMR of organoplatinum compounds ». Journal of Organometallic Chemistry 282, n^o 2 (mars 1985) : 291–95. http://dx.doi.org/10.1016/0022-328x(85)87180-1.

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4

Deolka, Shubham, Orestes Rivada-Wheelaghan, Sandra L. Aristizábal, Robert R. Fayzullin, Shrinwantu Pal, Kyoko Nozaki, Eugene Khaskin et Julia R. Khusnutdinova. « Metal–metal cooperative bond activation by heterobimetallic alkyl, aryl, and acetylide PtII/CuI complexes ». Chemical Science 11, n^o 21 (2020) : 5494–502. http://dx.doi.org/10.1039/d0sc00646g.

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The selective formation of heterobimetallic Pt^II/Cu^I complexes demonstrates how facile bond activation processes can be achieved by altering the reactivity of common organoplatinum compounds through their interaction with another metal center.

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Mahato, Dibyendu, Rahla Naghma, Mohammad Jane Alam, Shabbir Ahmad et Bobby Antony. « Electron impact ionisation cross section for organoplatinum compounds ». Molecular Physics 114, n^o 21 (24 août 2016) : 3104–11. http://dx.doi.org/10.1080/00268976.2016.1219408.

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Nagashima, Hideo, Yoshiyuki Kato, Hirofumi Yamaguchi, Eiji Kimura, Teruhiko Kawanishi, Masanao Kato, Yahachi Saito, Masaaki Haga et Kenji Itoh. « Synthesis and Reactions of Organoplatinum Compounds of C60, C60Ptn ». Chemistry Letters 23, n^o 7 (juillet 1994) : 1207–10. http://dx.doi.org/10.1246/cl.1994.1207.

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Melnik, Milan, Ondrej Sprusansky, Clive Eduard Holloway et Peter Mikus. « Platinum organometallic compounds : classification and analysis of crystallographic and structural data. Monomeric Pt compounds with PtC2AB, PtA2BC and PtABCD compositions ». Reviews in Inorganic Chemistry 32, n^o 2-4 (1 décembre 2012) : 111–80. http://dx.doi.org/10.1515/revic-2012-0008.

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AbstractThis review covers almost 350 four-coordinated monomeric organoplatinum complexes with PtC2AB, PtA2BC and PtABCD compositions, and there is wide variability of chromophores. The most common ligands in addition to the C donor are PPh3 and chlorine. Platinum(II) is found only in a square-planar environment involving cis- as well as trans-configurations with a different degree of distortion, especially when bi- or terdentate ligands are present. The trans-effect decreases in the order of the atoms in which the effect dominates, H>C>P>Si>S. There are at least two types of isomerism, cis-trans and distortion. The data strongly suggest that distortion isomerism is, for platinum chemistry, more common than cis- and trans-isomerism.

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Melník, Milan, Peter Mikuš et Clive Eduard Holloway. « Platinum organometallic compounds : classification and analysis of crystallographic and structural data of monomeric five and higher coordinated ». Reviews in Inorganic Chemistry 33, n^o 1 (1 mai 2013) : 13–103. http://dx.doi.org/10.1515/revic-2013-0001.

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AbstractFour hundred and twenty monomeric organoplatinum compounds, in which platinum atoms are five- and higher coordinated, are analyzed. The platinum atoms are found in the oxidation states +2, +3 and +4. The Pt(II) compounds by far prevail. There are wide varieties of the inner coordination spheres about the platinum centers. The Pt(II) compounds are five-coordinated (trigonal bipyramidal and square pyramidal), six-coordinated (different degrees of distortion), seven-coordinated (pentagonal bipyramidal, piano stool) and sandwiched (PtC10). The Pt(III) compound is square-planar. The Pt(IV) compounds are six- and eight-coordinated. There are several relationships between the Pt-L bond distances, covalent radii of the coordinated atom/ligand, and metallocycles, which are discussed. The trans-effect plays an important role in the inner coordination spheres about the Pt centers, especially on the Pt-L bond distances.

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Hubbert, Christoph, Marcus Breunig, Kristen J. Carroll, Frank Rominger et A. Stephen K. Hashmi. « Simple Synthesis of New Mixed Isocyanide-NHC-Platinum(II) Complexes and Their Catalytic Activity ». Australian Journal of Chemistry 67, n^o 3 (2014) : 469. http://dx.doi.org/10.1071/ch13546.

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Using the new modular and convergent approach to isocyanide-N-hetrocyclic carbene-platinum(ii) complexes, eight new compounds have been synthesised. For three of these, detailed structural data could be obtained by X-ray crystal structure analyses. This new family of organoplatinum complexes is catalytically active for hydrosilylation reactions; styrene and phenylacetylene could be used as substrates; triethylsilane and 1,1,1,3,5,5,5-heptamethyltrisiloxane could be used as reagents. With some of the new platinum pre-catalysts, excellent regioselectivities of up to 98 : 2 could be obtained, and turnover numbers up to 840 were achieved.

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Noguchi, Kishie, Takashi Tamura, Hidetaka Yuge et Takeshi Ken Miyamoto. « Linkage isomerism of organoplatinum(II) compounds coordinated by two 1,3-dimethylbarbiturate anions ». Acta Crystallographica Section C Crystal Structure Communications 56, n^o 2 (15 février 2000) : 171–73. http://dx.doi.org/10.1107/s0108270199014109.

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Thèses sur le sujet "Organoplatinum compounds"

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Yang, Jun. « Carbonylation in organopalladium and organoplatinum compounds ». Thesis, University of Sheffield, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286872.

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Griffiths, D. C. « Thermal rearrangements of organoplatinum (II) compounds ». Thesis, Imperial College London, 1985. http://hdl.handle.net/10044/1/37713.

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Phelps, Jennifer. « Synthesis of homoleptic PT(0) acceptor phosphine complexes ». Laramie, Wyo. : University of Wyoming, 2008. http://proquest.umi.com/pqdweb?did=1594481221&sid=1&Fmt=2&clientId=18949&RQT=309&VName=PQD.

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吳玉如 et Yuk-yu Ng. « Photophysical properties and photochemistry of organoplatinum (II) complexes ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1995. http://hub.hku.hk/bib/B31213534.

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Ng, Yuk-yu. « Photophysical properties and photochemistry of organoplatinum (II) complexes / ». Hong Kong : University of Hong Kong, 1995. http://sunzi.lib.hku.hk/hkuto/record.jsp?B17506578.

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Li, Kai, et 李凯. « Photoluminescent organoplatinum (II) complexes containing N-heterocyclic carbene (NHC) ligands ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hub.hku.hk/bib/B50533915.

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The syntheses, structures, photophysical properties and applications of three types of photoluminescent organoplatinum(II) complexes containing N-heterocyclic carbene (NHC) ligands are described. The tetradentate dianionic bis(phenolate-NHC) type ligands provide a superior scaffold for constructing thermally stable and efficient deep-blue phosphorescent Pt(II) complexes with λmax of ~440-460 nm and solid-state emission quantum yields of ~30%. Highly efficient blue OLEDs with CIEx, y of (0.19, 0.21) were fabricated based on these emitters with maximum brightness, peak current efficiency and power efficiency of ~9500 cd m^(-2), 24 cd A^(-1) and 17 lm W^(-1), respectively. Structural modification by extending the π-conjugation of the tetradentate bis(phenolate-NHC) ligand leads to strongly phosphorescent platinum(II) complexes with long-lived emissive electronic states that can be used as a luminescent sensor for oxygen. DFT/TDDFT calculations and time-resolved spectroscopic characterizations were performed to gain insight into the structure-photophysics correlation. The N-heterocyclic carbene (NHC) ligand was incorporated into Pt(II) complexes containing tridentate deprotonated 1,3-bis(2-pyridyl)benzene (N^C^N) type ligand. In addition to the [(N^C^N)Pt(NHC)]PF6 type complexes with (N^C^N) in η3-tridentate coordination mode, Pt(II) complexes with η2-bidentate (N^CN) ligands, namely [(N^CN)Pt(NHC)2]PF6, have been isolated and structurally characterized. The highly phosphorescent [(N^C^N)Pt(NHC)]PF6 complexes were used for solution-processed green OLEDs fabrication. The peak current efficiency of 12.5 cd A^(-1) and maximum brightness higher than 2000 cd m^(-2) were achieved. The presence of the pendent pyridyl motif causes quenching of emission of the [(N^CN)Pt(NHC)2]PF6 complexes in solution at room temperature. Turning on solid-state emission of [(N^CN)Pt(nBu2Im)2]PF6 in the presence of an acidic vapor revealed its potential as a luminescent chemosensor. A class of dicationic platinum(II) terpyridyl complexes containing NHC ligand, namely [Pt(tpy)(NHC)](PF6)2, has been synthesized and structurally characterized. Even in the presence of the strong σ-donating NHC ligand, these complexes are non- or weakly emissive in solution at room temperature. However, this class of complexes displays intense emissions in solid state (298 K and 77 K), in glassy solution (77 K butyronitrile) and in PMMA (2 wt.%, 298 K). The ligand (terpyridine) displacement reaction arising from CN attack onto the Pt(II) center has been observed for [Pt(tpy)(nBu2Im)](PF6)2 leading to its application as a chemodosimeter for selective cyanide sensing in aqueous solution.
published_or_final_version
Chemistry
Doctoral
Doctor of Philosophy

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Basu, Sayanti. « Synthesis and catalytic applications of new acceptor platinum alkyl cations ». Laramie, Wyo. : University of Wyoming, 2009. http://proquest.umi.com/pqdweb?did=1939365871&sid=1&Fmt=2&clientId=18949&RQT=309&VName=PQD.

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8

Lai, Siu-wai. « Luminescent organoplatinum chemistry : photophysical and supramolecular properties of metallacyclic and polypyridine platinum(II) complexes / ». Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20792943.

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9

Crisp, Michael G. « Organoplatinum(II) complexes with hydrogen-bonding functionality and their potential use as molecular receptors for adenine : a thesis submitted for the degree of Master of Science ». Title page, abstract and contents only, 2002. http://web4.library.adelaide.edu.au/theses/09SM/09smc932.pdf.

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Errata pasted onto front end-paper. Includes bibliographical references (leaves 82-86). Describes the preparation and characterisation of a novel series of organoplatinum(II) complexes with hydrogen-bonding functionality.

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Hung, Faan-fung, et 孔繁峰. « Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/206318.

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Livres sur le sujet "Organoplatinum compounds"

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International Symposium on Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy (6th 1991 San Diego, Calif.). Platinum and other metal coordination compounds in cancer chemotherapy. New York : Plenum Press, 1991.

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2

Kuduk-Jaworska, Janina. Poszukiwania cytostatystycznych związków koordynacyjnych platyny. Wrocław : Wydawn. Uniwersytetu Wrocławskiego, 1993.

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3

Lu, Zheng. Organoplatinum complexes of cyclic allenes, alkynes and carbenes : Synthesis, structure and properties. 1992.

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Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy 2. Springer, 1996.

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The discovery, use and impact of platinum salts as chemoterapy agents for cancer. London : Wellcome Trust, 2007.

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Chapitres de livres sur le sujet "Organoplatinum compounds"

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Howell, B. A., E. W. Walles, R. Rashidianfar, J. R. Glass, B. J. Hutchinson et D. A. Johnson. « Complexes of Water Soluble Polymers and Organoplatinum Compounds as Potential Time-Release Antitumor Formulations ». Dans Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy, 670–83. Boston, MA : Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1717-3_76.

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