Gotowe bibliografie tematyczne / Organoplatinum compounds

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  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek

Gotowa bibliografia na temat „Organoplatinum compounds”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 1 sierpnia 2024

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Artykuły w czasopismach na temat "Organoplatinum compounds"

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Massa, W., G. Baum, B. S. Seo i J. Lorberth. "Organoplatinum compounds". Journal of Organometallic Chemistry 352, nr 3 (wrzesień 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 i B. S. Seo. "Organoplatinum compounds VII". Journal of Organometallic Chemistry 559, nr 1-2 (maj 1998): 191–96. http://dx.doi.org/10.1016/s0022-328x(98)00481-1.

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Benn, Reinhard, Rolf-Dieter Reinhardt i Anna Rufińska. "195Pt NMR of organoplatinum compounds". Journal of Organometallic Chemistry 282, nr 2 (marzec 1985): 291–95. http://dx.doi.org/10.1016/0022-328x(85)87180-1.

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

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The selective formation of heterobimetallic PtII/CuI 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 i Bobby Antony. "Electron impact ionisation cross section for organoplatinum compounds". Molecular Physics 114, nr 21 (24.08.2016): 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 i Kenji Itoh. "Synthesis and Reactions of Organoplatinum Compounds of C60, C60Ptn". Chemistry Letters 23, nr 7 (lipiec 1994): 1207–10. http://dx.doi.org/10.1246/cl.1994.1207.

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Melnik, Milan, Ondrej Sprusansky, Clive Eduard Holloway i 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, nr 2-4 (1.12.2012): 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 i 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, nr 1 (1.05.2013): 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 i A. Stephen K. Hashmi. "Simple Synthesis of New Mixed Isocyanide-NHC-Platinum(II) Complexes and Their Catalytic Activity". Australian Journal of Chemistry 67, nr 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 i Takeshi Ken Miyamoto. "Linkage isomerism of organoplatinum(II) compounds coordinated by two 1,3-dimethylbarbiturate anions". Acta Crystallographica Section C Crystal Structure Communications 56, nr 2 (15.02.2000): 171–73. http://dx.doi.org/10.1107/s0108270199014109.

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Rozprawy doktorskie na temat "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 i 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, i 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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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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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, i 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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Książki na temat "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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Kuduk-Jaworska, Janina. Poszukiwania cytostatystycznych związków koordynacyjnych platyny. Wrocław: Wydawn. Uniwersytetu Wrocławskiego, 1993.

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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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Części książek na temat "Organoplatinum compounds"

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Howell, B. A., E. W. Walles, R. Rashidianfar, J. R. Glass, B. J. Hutchinson i D. A. Johnson. "Complexes of Water Soluble Polymers and Organoplatinum Compounds as Potential Time-Release Antitumor Formulations". W 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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