Littérature scientifique sur le sujet « Bis-adducts »
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Articles de revues sur le sujet "Bis-adducts"
Tagliatesta, Pietro, Angelo Lembo, Valentina Orlandi et Marzia Nuccetelli. « Synthesis and characterization of new β-disubstituted porphyrin-[60]fullerene cyclic bis-adducts ». Journal of Porphyrins and Phthalocyanines 14, no 08 (août 2010) : 727–31. http://dx.doi.org/10.1142/s1088424610002537.
Texte intégralYusifli, F. Kh, N. A. Aliyeva et G. A. Ramazanov. « USE OF BIS-ADDUCTS OF ETHANEDITHIOL WITH ALKYL- AND CYCLOALKYL SUBSTITUTED METHYLENE DIOXOLANES IN THE COMPOSITION OF POLYVINYL CHLORIDE ». Chemical Problems 21, no 1 (2023) : 72–77. http://dx.doi.org/10.32737/2221-8688-2023-1-72-77.
Texte intégralSharma, Mousami, Anju Sharma et Renu Sachar. « Synthesis and Characterization of the Adducts of Morpholinedithioccarbamate Complexes of Oxovanadium (IV), Nickel(II), and Copper(II) with Piperidine and Morpholine ». E-Journal of Chemistry 9, no 4 (2012) : 1929–40. http://dx.doi.org/10.1155/2012/689501.
Texte intégralBaer-Dubowska, W. « Alternative pathways of polycyclic aromatic hydrocarbons activation : the formation of polar DNA adducts. » Acta Biochimica Polonica 46, no 2 (30 juin 1999) : 263–74. http://dx.doi.org/10.18388/abp.1999_4160.
Texte intégralHossain, MM, ME Halim, MM Islam, K. Akhter, SM Ahmed, UKR Romman et MG Ahmed. « Michael 1:1 adducts by acid catalyzed reaction during synthesis of spiro and spiroketal compounds ». Bangladesh Journal of Scientific and Industrial Research 55, no 4 (27 décembre 2020) : 283–88. http://dx.doi.org/10.3329/bjsir.v55i4.50967.
Texte intégralKour, Gurpreet, Inderjeet Kour et Renu Sachar. « Synthesis and Characterization of the Adducts of Bis(O-ethyldithiocarbonato)copper(II) with Substituted Pyridines ». International Journal of Inorganic Chemistry 2013 (22 décembre 2013) : 1–4. http://dx.doi.org/10.1155/2013/502856.
Texte intégralBispinghoff, Mark, Aaron M. Tondreau, Hansjörg Grützmacher, Charly A. Faradji et Paul G. Pringle. « Carbene insertion into a P–H bond : parent phosphinidene–carbene adducts from PH3 and bis(phosphinidene)mercury complexes ». Dalton Transactions 45, no 14 (2016) : 5999–6003. http://dx.doi.org/10.1039/c5dt01741f.
Texte intégralSedenkova, Kseniya N., Elena B. Averina, Yuri K. Grishin, Julia V. Kolodyazhnaya, Victor B. Rybakov, Tamara S. Kuznetsova, Audrey Hughes, Gabriel dos Passos Gomes, Igor V. Alabugin et Nikolay S. Zefirov. « Substituent effects on stereoselectivity of dihalocarbene reactions with cyclohexadiene and on the reactivity of bis-dihalocyclopropanes in electrophilic nitrations en route to pyrimidine N-oxides ». Organic & ; Biomolecular Chemistry 15, no 44 (2017) : 9433–41. http://dx.doi.org/10.1039/c7ob02463k.
Texte intégralWang, Guowei, Linghua Zhuang et Jintang Wang. « A Route to a Tetrabenzothiazole from Michael Bis-Addition Compounds ». Journal of Chemical Research 2009, no 4 (avril 2009) : 212–13. http://dx.doi.org/10.3184/030823409x435883.
Texte intégralTalbi, Arbia, Aïcha Arfaoui, Talia Bsaibess, Mohamed Lotfi Efrit, Anne Gaucher, Damien Prim et Hédi M′Rabet. « Selective synthesis of mono- and bis-butenolide α-aminomethyl adducts ». Organic & ; Biomolecular Chemistry 15, no 15 (2017) : 3298–303. http://dx.doi.org/10.1039/c7ob00206h.
Texte intégralThèses sur le sujet "Bis-adducts"
Kuhn, Helene. « Syntheses of diplatinum polyynediyl complexes with bis(phosphine)pentafluorophenylplatinum endgroups and dicobalt adducts of their sp carbon chains ». kostenfrei, 2009. http://d-nb.info/999425994/34.
Texte intégralCarini, Marco. « New approaches to the multiple functionalization of fullerene ». Doctoral thesis, Università degli studi di Trieste, 2014. http://hdl.handle.net/10077/10131.
Texte intégralFullerene C60 is a charming molecule, its beautiful symmetry and its unique properties are still intriguing scientific community after almost three decades from its discovery. Investigation of its properties and applications is still an active field. In our group we are interested especially in the biological aspect of fullerene sciences. In this field, polyfunctional derivatives are particularly attractive, for the increased solubility and for the possibility to attach different biologically active molecules on the same carbon cage. In the first project we studied different methods to control the site selectivity of the double 1,3-dipolar cycloaddition of azomethine ylides. To this purpose, we synthesized several bis-reactive templates with very different design, and we could obtain unusual fullerene-macrocyclic and fullerene-cyclophanes structures. A good degree of control of the site selectivity was achieved in some cases. A supramolecular approach to the control of the second cycloaddition was also developed. In the second part we focused our efforts in finding a feasible and scalable method to produce bis- or poly-functional fullerene derivatives from the easily accessible monoadduct. Triazine chemistry in combination with oxyethylenic chains allowed us to easily synthesize a library of polyfunctional, versatile and highly soluble derivatives. Some toxicological results indicate that this kind of compounds can be very useful carriers for drug delivery and some application in this sense are currently under investigation. Finally in a third part of the work we synthesized several fullerene-bipyridyl ligands and their ruthenium complexes. In this way we want to combine in the same molecule both the antiproliferative properties of ruthenium complexes and the photosensitizing effect of fullerene in order to obtain a synergistic effect against tumor cells.
XXVI Ciclo
1986
Vartanian, Maida. « Cu(I) catalyzed alkyne-azide cycloaddition as a synthetic tool for the preparation of complex C60 derivatives ». Thesis, Strasbourg, 2012. http://www.theses.fr/2012STRAF016.
Texte intégralThe present PhD thesis manuscript is focused on the use of fullerene building blocks for the preparation of photoactive molecular devices combining C60 and porphyrins. Cu(I) Catalyzed alkyne-azide cycloaddition was used as a synthetic tool for the preparation of complex C60 derivatives. Specifically, in the first part (Chapter II-B), a flexible fullerene-porphyrin triad has been developed and the photophysical studies were performed. The flexible linker between the fullerene core and the azide groups prevented any conformational control on the relative orientation and distance between the two photoactive subunits connected together. This prompted the development of an analogous building block in which the azide unit is directly connected to the bridging phenyl ring (Chapter II-C). In this way, the click reaction with porphyrin-alkyne derivatives give access to hybrid systems with a controlled relative orientation of the two moieties. This is of fundamental importance for a better understanding of the structural parameters affecting the electron and/or energy transfer kinetic in such dyads.In the second part (Chapter III), a fullerene hexaadduct scaffold is used to build up sophisticated multiporphyrin systems for various applications. The preparation of these multi-chromophoric ensembles relies on the click-click approach developed in our group
Paul, Ursula Sofia Désirée [Verfasser], et Udo [Gutachter] Radius. « Studies on the Reactivity of Iridium Bis(phosphinite) Pincer Complexes towards Phosphines, Boranes and their Lewis Adducts and on the Reactivity of Cyclic (Alkyl)(Amino) Carbenes and Nickel Complexes thereof / Ursula Sofia Désirée Paul ; Gutachter : Udo Radius ». Würzburg : Universität Würzburg, 2018. http://d-nb.info/1163536210/34.
Texte intégralFang, Chuan-Chieh, et 方春傑. « Computational Study on the Bis-Adducts of the Phosphinidene Complexes ». Thesis, 2012. http://ndltd.ncl.edu.tw/handle/14761345415462791590.
Texte intégral國立臺北教育大學
自然科學教育學系碩士班
100
The bonding of bis-adducts between electron donors (D), such as NH3 and PH3, with phosphinidenes RP: (R = H, CH3, NH2, PH2, PF2) was examined using density functional theory calculations. The structures were optimized at the B3LYP/6-311++G** level of theory. The main interest of this work is to find the trend in structural symmetry of the D—PR—D system. Accordingly, the magnitude of bond strength correlates well with the difference in ionization potential (IP) of the orbitals involved in the D—P interaction. In addition, we found the magnitude of the first bonding energy between D and PR is decisive for the symmetry of the D—PR—D system.
Chou, Zi-Wei, et 周子偉. « Synthesis and Characterization of Ethyl Alkylbenzyl 1,2-Methano[60]fullerene-61,61-Dicarboxylate Derivatives and Their Bis Adducts ». Thesis, 2011. http://ndltd.ncl.edu.tw/handle/bp6n2f.
Texte intégral國立臺北科技大學
有機高分子研究所
99
Fullerene derivatives have been widely used as electron acceptor for fabricating efficient polymer solar cells due to their high electron affinity and good electron mobility. It has been demonstrated that the molecular levels, chemical compatibility to conjugated polymer and solubility in processing solvent are key parameters in affecting the cell efficiency. In this study, a series of mono- and bis-adducts of C60 with similar structure, including ethyl (4-methylbenzyl)1,2-methano[60]fullerene- 61,61-dicarboxylate (MBEMDC), ethyl (4-ethylbenzyl)1,2-methano[60]fullerene- 61,61-dicarboxylate(EBEMDC), ethyl (4-isopropylbenzyl) 1,2-methano[60]fullerene- 61,61-dicarboxylate (iPBEMDC), ethyl (4-tert-butylbenzyl) 1,2-methano[60] fullerene-61,61-dicarboxylate (tBBEMDC), (4-n-butylbenzyl) 1,2-methano[60] fullerene-61,61-dicarboxylate(nBBEMDC), bis-ethyl (4-ethylbenzyl)1,2-methano[60] fullerene-61,61-dicarboxylate (bis-EBEMDC), bis-ethyl (4-isopropylbenzyl) 1,2-methano[60]fullerene-61,61-dicarboxylate (bis-iPBEMDC), bis-ethyl (4-tert- butyl-benzyl)1,2-methano[60] fullerene-61,61-dicarboxylate(bis-tBBEMDC), benzyl- n-hexyl 1,2-methano[60]fullerene-61,61-dicarboxylate benzyl fulleropyrrolidine (BHMDCmix) and ethyl (4-tert-butylbenzyl) 1,2-methano[60]fullerene-61,61- dicarboxylate benzyl fulleropyrrolidine (tBBEMDCmix), were designed and synthesized via Bingel-Hirsch reaction and/or Prato reaction. The obtained products were characterized using NMR, MALDI-TOF and EA. Moreover, cyclic voltammetry (CV) and UV-vis were employed to investigate the energy levels and optical properties of these new molecules.
Kuhn, Helene [Verfasser]. « Syntheses of diplatinum polyynediyl complexes with bis(phosphine)pentafluorophenylplatinum endgroups and dicobalt adducts of their sp carbon chains / vorgelegt von Helene Kuhn ». 2009. http://d-nb.info/999425994/34.
Texte intégralZeits, Paul. « Olefin Metatheses in Metal Coordination Spheres : Development of Gyroscope-like trans-Spanning Bis(pyridine) Complexes and Organometallic pi-Adducts of Conjugated Polymers ». Thesis, 2011. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10265.
Texte intégralPaul, Ursula Sofia Désirée. « Studies on the Reactivity of Iridium Bis(phosphinite) Pincer Complexes towards Phosphines, Boranes and their Lewis Adducts and on the Reactivity of Cyclic (Alkyl)(Amino) Carbenes and Nickel Complexes thereof ». Doctoral thesis, 2018. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-151963.
Texte intégralDer erste Abschnitt der vorliegenden Arbeit gibt einen vertieften Einblick in die Reaktivität von Iridiumkomplexen, die den bis(Phosphinit)-Pincer tBuPOCOP (k3-C6H3-1,3-(OPtBu2)2) als Liganden aufweisen, gegenüber primären Boranen und Phosphanen sowie gegenüber Phosphan-Boran-Lewis-Paaren. Desweiteren sind detailliertere Untersuchungen zu deren Anwendung als Katalysator zur dehydrogenativen Kupplung von Phosphanboranen enthalten. Die erhaltenen Ergebnisse lassen sich in drei Teilbereiche gliedern: I. Synthese und Charakterisierung von Iridium(III)-Komplexen, die Aryldihydroboratliganden tragen, II. Arylphosphan-koordinierte Iridium(I)- und Iridium(III)-Komplexe, III. sowie Studien zur Reaktivität der zugrundeliegenden Iridiumpincerkomplexe gegenüber BH3-Addukten von primären Phosphanen. Diese führten zu ersten Ergebnissen in der homogen-katalytischen Dehydrokupplung von Phosphanboranen unter Verwendung der Iridiumpincerkomplexe als Katalysator. Der zweite Abschnitt der vorliegenden Arbeit gibt einen Einblick in die Chemie von Nickelkomplexen, die durch zyklische (Alkyl)(Amino) Carbene (cAACs) stabilisiert werden. Desweiteren sind Untersuchungen zu den Eigenschaften und zur Reaktivität der freien Carbene selbst enthalten. Die erhaltenen Ergebnisse lassen sich in vier Teilbereiche gliedern: I. Synthese und Charakterisierung von Nickelkomplexen, die durch zyklische (Alkyl)(Amino) Carbene stabilisiert werden, II. welche die Bestimmung und Quantifizierung von deren sterischen und elektronischen Eigenschaften zulassen, III. erste Studien zur Reaktivität dieser neuartigen Nickelkomplexe, sowie IV. Untersuchungen zur C–F- und C–H-Bindungsaktivierung am Carbenkohlenstoffatom der entsprechenden zyklische (Alkyl)(Amino) Carbene
Chapitres de livres sur le sujet "Bis-adducts"
Vergara, Alessandro, Cinzia Verde, Guido di Prisco et Lelio Mazzarella. « Bis-histidyl Ferric Adducts in Tetrameric Haemoglobins ». Dans Dioxygen Binding and Sensing Proteins, 93–105. Milano : Springer Milan, 2008. http://dx.doi.org/10.1007/978-88-470-0807-6_10.
Texte intégralClark, David L., Alfred P. Sattelberger et Richard A. Andersen. « Lewis Base Adducts of Uranium Triiodide and Tris[Bis(Trimethylsilyl)Amido]Uranium ». Dans Inorganic Syntheses, 307–15. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132623.ch55.
Texte intégralSCHUMANN, HERBERT, ILSE ALBRECHT, HARALD LAUKE et FRIEDRICH WILHELM REIER. « BIS(CYCLOPENTADIENYL) AND MONO- AND BIS(PENTAMETHYLCYCLOPENTADIENYL) METHYL DERIVATIVES OF THE LANTHANIDES : THEIR METHYLLITHIUM ADDUCTS ». Dans Organometallic Syntheses, 1–5. Elsevier, 1988. http://dx.doi.org/10.1016/b978-0-444-42956-8.50008-6.
Texte intégralSCHUMANN, HERBERT, ILSE ALBRECHT et EKKEHARDT HAHN. « BASE STABILIZED ALKALI METAL HALIDE ADDUCTS OF BIS(PENTAMETHYLCYCLOPENTADIENYL)LANTHANIDE CHLORIDES ». Dans Organometallic Syntheses, 9–12. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-444-42607-9.50007-3.
Texte intégralVergara, Alessandro, Luigi Vitagliano, Cinzia Verde, Guido di Prisco et Lelio Mazzarella. « Spectroscopic and Crystallographic Characterization of bis‐Histidyl Adducts in Tetrameric Hemoglobins ». Dans Methods in Enzymology, 425–44. Elsevier, 2008. http://dx.doi.org/10.1016/s0076-6879(08)36024-8.
Texte intégralEagle, P. A. C. « Perfluoroalkyltriorganoplumbanes from Triaryl- or Trialkylplumbyl Derivatives by Reactions with Bis(perfluoroalkyl)cadmium Adducts ». Dans Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00751.
Texte intégralWedler, C., K. Haage, M. Herbst, H. Tischer et E. Knofe. « Preparation and Some Properties of Amine Oxides Derived from Defined Ethylene Oxide Adducts ». Dans VI. Internationale Tagung über Grenzflächenaktive Stoffe, Berlin, 22. bis 27. April 1985, 589–94. De Gruyter, 1986. http://dx.doi.org/10.1515/9783112484265-087.
Texte intégralActes de conférences sur le sujet "Bis-adducts"
Bai, Bao-Qing, Li-Jiao Zhao et Ru-Gang Zhong. « Structural Characterization of the DNA Adducts Induced by 1,3-Bis-(2-Chloroethyl)-1-Nitrosourea Using Electrospray Ionization Tandem Mass Spectrometry ». Dans 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5516358.
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