Artykuły w czasopismach na temat „Organometallic compounds”

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1

Polosan, Silviu, Iulia Corina Ciobotaru i Claudiu Constantin Ciobotaru. "Organometallic Coatings for Electroluminescence Applications". Coatings 10, nr 3 (17.03.2020): 277. http://dx.doi.org/10.3390/coatings10030277.

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Organometallic compounds embedded in thin films are widely used for Organic Light-Emitting Diodes (OLED), but their functionalities are strongly correlated with the intrinsic properties of those films. Controlling the concentration of the organometallics in the active layers influences the OLED performances through the aggregation processes. These aggregations could lead to crystallization processes that significantly modify the efficiency of light emission in the case of electroluminescent devices. For functional devices with organometallic-based thin films, some improvements, such as the optimization of the charge injection, are needed to increase the light output. One dual emitter IrQ(ppy)2 organometallic compound was chosen for the aggregation correlations from a multitude of macromolecular organometallics that exist on the market for OLED applications. The choice of additional layers like conductive polymers or small molecules as host for the active layer may significantly influence the performances of the OLED based on the IrQ(ppy)2 organometallic compound. The use of the CBP small molecule layer may lead to an increase in the electroluminescence versus the applied voltage.
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2

Dong, Zhi-Bing, i Jin-Quan Chen. "Recent Progress in Utilization of Functionalized Organometallic Reagents in Cross Coupling Reactions and Nucleophilic Additions". Synthesis 52, nr 24 (4.11.2020): 3714–34. http://dx.doi.org/10.1055/s-0040-1706550.

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AbstractOrganometallic compounds have become increasingly important in organic synthesis because of their high chemoselectivity and excellent reactivity. Recently, a variety of organometallic reagents were found to facilitate transition-metal-catalyzed cross-coupling reactions and nucleophilic addition reactions. Here, we have summarized the latest progress in cross-coupling reactions and in nucleophilic addition reactions with functionalized organometallic reagents present to illustrate their application value. Due to the tremendous contribution made by the Knochel group towards the development of novel organometallic reagents, this review draws extensively from their work in this area in recent years.Introduction1 Transition-Metal-Catalyzed Cross Couplings Involving Organo­zinc Reagents2 Transition-Metal-Catalyzed Cross Couplings Involving Organomagnesium Reagents3 Transition-Metal-Free Cross Couplings Involving Zn and Mg ­Organometallic Reagents4 Nucleophilic Additions Involving Zn and Mg Organometallic Reagents5 Cross-Coupling Reactions or Nucleophilic Additions Involving Mn, Al-, La-, Li-, Sm- and In-Organometallics6 Conclusion
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3

Sutton, Derek. "Organometallic diazo compounds". Chemical Reviews 93, nr 3 (maj 1993): 995–1022. http://dx.doi.org/10.1021/cr00019a008.

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4

Gasser, Gilles, Ingo Ott i Nils Metzler-Nolte. "Organometallic Anticancer Compounds". Journal of Medicinal Chemistry 54, nr 1 (13.01.2011): 3–25. http://dx.doi.org/10.1021/jm100020w.

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5

Carr, G. E., R. D. Chambers, T. F. Holmes i D. G. Parker. "Polyfluoroaryl organometallic compounds". Journal of Organometallic Chemistry 325, nr 1-2 (maj 1987): 13–23. http://dx.doi.org/10.1016/0022-328x(87)80383-2.

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6

Asaad, Noora, Ahmed Z. M. AL-Bassam i Sahar S. M. Alabdullah. "Uses of organometallic compounds in chemical processes". International Journal of Research in Engineering and Innovation 06, nr 02 (2022): 98–103. http://dx.doi.org/10.36037/ijrei.2022.6203.

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This review is proposed to address knowledge of organometallic compounds (OMC) in chemical applications and show these compounds' depth scope in different scientific studies. This review is based on outlining the gap between the traditional preparations and green chemistry synthesis of organometallic materials purposes in the experimental section of a researcher's papers. The most comparative research considers the drawbacks of organometallic compounds, including their applications in industrial, clinical, drug forms, and chemical reactions. However, many organometallic compounds are inherently poisonous. The most general challenge is producing alternative substances to creative green organometallic compounds, specifically in drug formulations systems. A wide range of chemical reactions have been investigated and formulated new organometallic properties this may be associated with an increased level of enhancement health systems. This study aims to determine the importance of organometallic compound in many path ways in various articles and confirmed how papers trying to characterize new organometallic substances in various chemical processes. Particular interest is given to knowledge synthesis OMC in medicine and industrially.
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7

Gadd, G. M. "Microbial formation and transformation of organometallic and organometalloid compounds". FEMS Microbiology Reviews 11, nr 4 (sierpień 1993): 297–316. http://dx.doi.org/10.1111/j.1574-6976.1993.tb00003.x.

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8

Kwofie, Samuel K., Emmanuel Broni, Bismark Dankwa, Kweku S. Enninful, Joshua Teye, Cedar R. Davidson, Josephine B. Nimely i in. "Review of Atypical Organometallic Compounds as Antimalarial Drugs". Journal of Chemistry 2020 (20.05.2020): 1–9. http://dx.doi.org/10.1155/2020/9414093.

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Organometallic compounds are molecules that contain at least one metal-carbon bond. Due to resistance of the Plasmodium parasite to traditional organic antimalarials, the use of organometallic compounds has become widely adopted in antimalarial drug discovery. Ferroquine, which was developed due to the emergence of chloroquine resistance, is currently the most advanced organometallic antimalarial drug and has paved the way for the development of new organometallic antimalarials. In this review, a general overview of organometallic antimalarial compounds and their antimalarial activity in comparison to purely organic antimalarials are presented. Furthermore, recent developments in the field are discussed, and future applications of this emerging class of therapeutics in antimalarial drug discovery are suggested.
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9

Lappert, Michael F. "Organometallic intramolecular-coordination compounds". Journal of Organometallic Chemistry 319, nr 3 (styczeń 1987): C60. http://dx.doi.org/10.1016/s0022-328x(00)99620-7.

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10

Eaborn, Colin. "Dictionary of organometallic compounds". Journal of Organometallic Chemistry 286, nr 3 (maj 1985): c51—c52. http://dx.doi.org/10.1016/0022-328x(85)80060-7.

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11

Dewar, M. J. S., E. F. Healy i J. Ruiz. "Cruciaromaticity in organometallic compounds". Pure and Applied Chemistry 58, nr 1 (1.01.1986): 67–74. http://dx.doi.org/10.1351/pac198658010067.

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12

Schrock, Richard. "Dictionary of Organometallic Compounds". Organometallics 5, nr 3 (marzec 1986): 607. http://dx.doi.org/10.1021/om00134a905.

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13

S.J.S. "Dictionary of Organometallic Compounds". Journal of Molecular Structure 144, nr 1-2 (kwiecień 1986): 194–95. http://dx.doi.org/10.1016/0022-2860(86)80182-x.

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14

Halpern, Jack. "Oxidation of Organometallic Compounds". Angewandte Chemie International Edition in English 24, nr 4 (kwiecień 1985): 274–82. http://dx.doi.org/10.1002/anie.198502741.

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15

Eaborn, Colin. "Dictionary of organometallic compounds". Journal of Organometallic Chemistry 503, nr 1 (listopad 1995): C36. http://dx.doi.org/10.1016/0022-328x(95)90002-v.

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16

Novikov, Alexander S. "Non-Covalent Interactions in Coordination and Organometallic Chemistry". Crystals 10, nr 6 (23.06.2020): 537. http://dx.doi.org/10.3390/cryst10060537.

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The problem of non-covalent interactions in coordination and organometallic compounds is a hot topic in modern chemistry, material science, crystal engineering and related fields of knowledge. Researchers in various fields of chemistry and other disciplines (physics, crystallography, computer science, etc.) are welcome to submit their works on this topic for our Special Issue “Non-Covalent Interactions in Coordination and Organometallic Chemistry”. The aim of this Special Issue is to highlight and overview modern trends and draw the attention of the scientific community to various types of non-covalent interactions in coordination and organometallic compounds. In this editorial, I would like to briefly highlight the main successes of our research group in the field of the fundamental study of non-covalent interactions in coordination and organometallic compounds over the past 5 years.
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17

TOKUDA, Masao. "Organometallic compounds in electroorganic synthesis." Journal of Synthetic Organic Chemistry, Japan 43, nr 6 (1985): 522–32. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.522.

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18

Smith, J. J., W. L. Carrick i A. K. Ingberman. "ORGANOMETALLIC COMPOUNDS IN OLEFIN POLYMERIZATION". Annals of the New York Academy of Sciences 125, nr 1 (16.12.2006): 183–88. http://dx.doi.org/10.1111/j.1749-6632.1965.tb45389.x.

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19

Yale, Harry L. "THERAPEUTIC APPLICATIONS OF ORGANOMETALLIC COMPOUNDS". Annals of the New York Academy of Sciences 125, nr 1 (16.12.2006): 189–97. http://dx.doi.org/10.1111/j.1749-6632.1965.tb45390.x.

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20

Tolstikov, Genrikh A., Ramil G. Bulgakov i Valeri P. Kazakov. "The Chemiluminescence of Organometallic Compounds". Russian Chemical Reviews 54, nr 11 (30.11.1985): 1058–73. http://dx.doi.org/10.1070/rc1985v054n11abeh003157.

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21

Forgacs, E., i T. Cserhati. "LIQUID CHROMATOGRAPHY OF ORGANOMETALLIC COMPOUNDS". Journal of Liquid Chromatography & Related Technologies 25, nr 13-15 (18.09.2002): 2023–38. http://dx.doi.org/10.1081/jlc-120013993.

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22

Kadmiri, A., J. Amaudrut, M. Camelot, C. Roques-Carmes, F. Louis i T. Mathia. "Tribochemistry of Cyclopentadienyl Organometallic Compounds". A S L E Transactions 30, nr 1 (styczeń 1987): 111–20. http://dx.doi.org/10.1080/05698198708981738.

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23

SUHR, H., J. BALD, L. DEUTSCHMANN, A. ETSPÜLER, E. FEURER, H. GRÜNWALD, C. HAAG i in. "PLASMA CVD USING ORGANOMETALLIC COMPOUNDS". Le Journal de Physique Colloques 50, nr C5 (maj 1989): C5–739—C5–746. http://dx.doi.org/10.1051/jphyscol:1989589.

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24

Taraban, Marc B., Alexander I. Kruppa, Vladimir I. Rakhlin, Stanislav I. Grigor'ev, Olga S. Volkova, Rudolph G. Mirskov i Tatyana V. Leshina. "Spin chemistry of organometallic compounds". Journal of Organometallic Chemistry 636, nr 1-2 (listopad 2001): 12–16. http://dx.doi.org/10.1016/s0022-328x(01)00812-9.

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25

Taraban, Marc B., Alexander I. Kruppa, Nikolai E. Polyakov, Mikhail G. Voronkov, Vladimir I. Rakhlin, Stanislav V. Grigor'ev, Olga S. Volkova, Rudolph G. Mirskov i Tatyana V. Leshina. "Spin chemistry of organometallic compounds". Journal of Organometallic Chemistry 658, nr 1-2 (wrzesień 2002): 228–34. http://dx.doi.org/10.1016/s0022-328x(02)01662-5.

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26

Florjańczyk, Z., E. Zygadło-Monikowska i W. Bzducha. "Polymer electrolytes comprising organometallic compounds". Electrochimica Acta 45, nr 8-9 (styczeń 2000): 1203–9. http://dx.doi.org/10.1016/s0013-4686(99)00382-5.

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27

Schumann, Herbert, Markus R. Keitsch, Jörg Demtschuk i Gary A. Molander. "Organometallic compounds of the lanthanides". Journal of Organometallic Chemistry 582, nr 1 (czerwiec 1999): 70–82. http://dx.doi.org/10.1016/s0022-328x(98)01188-7.

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28

Burton, Donald J. "Organometallic approaches to organofluorine compounds". Journal of Fluorine Chemistry 45, nr 1 (październik 1989): 83. http://dx.doi.org/10.1016/s0022-1139(00)84455-3.

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29

Hamilton, E. I. "Organometallic compounds in the environment". Marine Pollution Bulletin 18, nr 5 (maj 1987): 253. http://dx.doi.org/10.1016/0025-326x(87)90472-3.

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30

Birch, Arthur J., Brian Chauncy, Lawrence F. Kelly i David J. Thompson. "Organometallic compounds in organic synthesis". Journal of Organometallic Chemistry 286, nr 1 (kwiecień 1985): 37–46. http://dx.doi.org/10.1016/0022-328x(85)87233-8.

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31

Fitzmaurice, Neil J., W. Roy Jackson i Patrick Perlmutter. "The stereochemistry of organometallic compounds". Journal of Organometallic Chemistry 285, nr 1-3 (kwiecień 1985): 375–81. http://dx.doi.org/10.1016/0022-328x(85)87381-2.

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32

Eaborn, Colin. "Organometallic compounds and living organisms". Journal of Organometallic Chemistry 286, nr 2 (maj 1985): c36—c37. http://dx.doi.org/10.1016/0022-328x(85)88017-7.

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33

Fakhr, A., Y. Mugnier, B. Gautheron i E. Laviron. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 302, nr 1 (marzec 1986): C7—C9. http://dx.doi.org/10.1016/0022-328x(86)80070-5.

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34

Moriarty, F. "Organometallic compounds in the environment". Environmental Pollution 44, nr 1 (1987): 81. http://dx.doi.org/10.1016/0269-7491(87)90132-1.

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35

Ciobotaru, Iulia Corina, Silviu Polosan i Constantin Claudiu Ciobotaru. "Organometallic compounds for photovoltaic applications". Inorganica Chimica Acta 483 (listopad 2018): 448–53. http://dx.doi.org/10.1016/j.ica.2018.08.042.

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36

Bellama, Jon. "Organometallic Compounds in the Environment". Organometallics 6, nr 4 (1.04.1987): 903–4. http://dx.doi.org/10.1021/om00147a606.

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37

Koch, L., A. Fakhr, Y. Mugnier, L. Roullier, C. Moise i E. Laviron. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 314, nr 1-2 (październik 1986): C17—C20. http://dx.doi.org/10.1016/0022-328x(86)80372-2.

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38

Jagannatha Swamy, S., i Herbert Schumann. "Organometallic compounds of the lanthanides". Journal of Organometallic Chemistry 334, nr 1-2 (listopad 1987): 1–7. http://dx.doi.org/10.1016/0022-328x(87)80036-0.

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39

Fakhr, A., Y. Mugnier, E. Laviron i J. Mofidi. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 346, nr 3 (czerwiec 1988): C49—C52. http://dx.doi.org/10.1016/0022-328x(88)80145-1.

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40

Schumann, Herbert, Ilse Albrecht, Michael Gallagher, Ekkehardt Hahn, Christine Muchmore i Joachim Pickardt. "Organometallic compounds of the lanthanides". Journal of Organometallic Chemistry 349, nr 1-2 (lipiec 1988): 103–15. http://dx.doi.org/10.1016/0022-328x(88)80441-8.

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41

Reeb, P., i Y. Mugnier. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 339, nr 1-2 (styczeń 1988): 89–96. http://dx.doi.org/10.1016/0022-328x(88)80528-x.

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42

Nabaoui, H., Y. Mugnier, A. Fakhr, E. Laviron, J. Mofidi, A. Antiñolo, F. A. Jalon, M. Fajardo i A. Otero. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 362, nr 1-2 (luty 1989): C8—C10. http://dx.doi.org/10.1016/0022-328x(89)85300-8.

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43

Da Rold, A., Y. Mugnier, R. Broussier, B. Gautheron i E. Laviron. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 362, nr 3 (maj 1989): C27—C30. http://dx.doi.org/10.1016/0022-328x(89)87263-8.

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44

Eisch, John J., Stephen R. Sexsmith i Kenneth C. Fichter. "Organometallic compounds of Group III". Journal of Organometallic Chemistry 382, nr 1-2 (luty 1990): 273–93. http://dx.doi.org/10.1016/0022-328x(90)85232-n.

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45

Mourad, Y., Y. Mugnier, H. J. Breunig i M. Ateş. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 398, nr 1-2 (listopad 1990): 85–90. http://dx.doi.org/10.1016/0022-328x(90)87006-y.

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46

Anastasiou, Despina, i W. Roy Jackson. "The stereochemistry of organometallic compounds". Journal of Organometallic Chemistry 413, nr 1-3 (sierpień 1991): 399–410. http://dx.doi.org/10.1016/0022-328x(91)80065-r.

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47

Roullier, L., D. Lucas, Y. Mugnier, A. Antiñolo, M. Fajardo i A. Otero. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 412, nr 3 (lipiec 1991): 353–62. http://dx.doi.org/10.1016/0022-328x(91)86079-6.

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48

Chollet, H., D. Lucas, Y. Mugnier, A. Antiñolo, A. Otero i M. Fajardo. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 441, nr 1 (grudzień 1992): 45–49. http://dx.doi.org/10.1016/0022-328x(92)80189-5.

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49

Lucas, Dominique, Hervé Chollet, Yves Mugnier, Antonio Antiñolo, Antonio Otero i Mariano Fajardo. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 426, nr 1 (kwiecień 1992): C4—C7. http://dx.doi.org/10.1016/0022-328x(92)83170-m.

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50

Lucas, D., Y. Mugnier, A. Antinolo, A. Otero i M. Fajardo. "Electrochemical studies on organometallic compounds". Journal of Organometallic Chemistry 435, nr 3 (wrzesień 1992): C3—C7. http://dx.doi.org/10.1016/0022-328x(92)83407-9.

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