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Relevant bibliographies by topics / Organometallic compounds

Academic literature on the topic 'Organometallic compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 July 2024

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Journal articles on the topic "Organometallic compounds"

1

Polosan, Silviu, Iulia Corina Ciobotaru, and Claudiu Constantin Ciobotaru. "Organometallic Coatings for Electroluminescence Applications." Coatings 10, no. 3 (March 17, 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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Dong, Zhi-Bing, and Jin-Quan Chen. "Recent Progress in Utilization of Functionalized Organometallic Reagents in Cross Coupling Reactions and Nucleophilic Additions." Synthesis 52, no. 24 (November 4, 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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Sutton, Derek. "Organometallic diazo compounds." Chemical Reviews 93, no. 3 (May 1993): 995–1022. http://dx.doi.org/10.1021/cr00019a008.

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Gasser, Gilles, Ingo Ott, and Nils Metzler-Nolte. "Organometallic Anticancer Compounds." Journal of Medicinal Chemistry 54, no. 1 (January 13, 2011): 3–25. http://dx.doi.org/10.1021/jm100020w.

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Carr, G. E., R. D. Chambers, T. F. Holmes, and D. G. Parker. "Polyfluoroaryl organometallic compounds." Journal of Organometallic Chemistry 325, no. 1-2 (May 1987): 13–23. http://dx.doi.org/10.1016/0022-328x(87)80383-2.

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Asaad, Noora, Ahmed Z. M. AL-Bassam, and Sahar S. M. Alabdullah. "Uses of organometallic compounds in chemical processes." International Journal of Research in Engineering and Innovation 06, no. 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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Gadd, G. M. "Microbial formation and transformation of organometallic and organometalloid compounds." FEMS Microbiology Reviews 11, no. 4 (August 1993): 297–316. http://dx.doi.org/10.1111/j.1574-6976.1993.tb00003.x.

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Kwofie, Samuel K., Emmanuel Broni, Bismark Dankwa, Kweku S. Enninful, Joshua Teye, Cedar R. Davidson, Josephine B. Nimely, et al. "Review of Atypical Organometallic Compounds as Antimalarial Drugs." Journal of Chemistry 2020 (May 20, 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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Lappert, Michael F. "Organometallic intramolecular-coordination compounds." Journal of Organometallic Chemistry 319, no. 3 (January 1987): C60. http://dx.doi.org/10.1016/s0022-328x(00)99620-7.

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Eaborn, Colin. "Dictionary of organometallic compounds." Journal of Organometallic Chemistry 286, no. 3 (May 1985): c51—c52. http://dx.doi.org/10.1016/0022-328x(85)80060-7.

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Dissertations / Theses on the topic "Organometallic compounds"

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Williams, Michael Lloyd. "New aspects of organometallic chemistry /." Title page, contents and abstract only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09phw725.pdf.

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Wu, Jingcun. "Photoelectron spectroscopy of organometallic compounds." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq28691.pdf.

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Martin, Jeffrey Thomas. "Organometallic nitrosyl hydrides of tungsten." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/27449.

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Although hydrides of metal carbonyls are widely known, the number of hydrides in the related family of metal nitrosyls is extremely small. The preparation of a series of nitrosyl hydrides from the treatment of [CpW(NO)I₂]₂ (Cp=ƞ⁵-C₅H₅) with Na[H₂Al(OCH₂CH₂OCH₃)₂] is described. The addition of one or two equivalents of the aluminum reagent results in the formation of [CpW(NO)IH]₂ or [CpW(NO)H₂]₂ respectively. The reaction of [CpW(NO)IH]₂ with a Lewis base (L=P(OPh)₃, P(OMe)₃, PPh₃ or PMe₃) gives the monometallic CpW(NO)IHL, while [CpW(NO)H₂]₂ reacts with P(OPh)₃ or P(OMe)₃ to yield [CpW(NO)HL]₂ which undergoes further reaction to give CpW(NO)H₂L. Proton NMR spectroscopy shows that all bimetallic species contain bridging hydride ligands and are therefore best, formulated as [CpW(NO)1]₂(µ-H)₂, [CpW(NO)H]₂(µ-H)₂ and [CpW(NO)L]₂(µ-H)₂. The ¹H NMR spectrum of [CpW(NO)H]₂(µ-H)₂ shows that there is no hydride ligand exchange on the NMR time scale and that ¹jH(terminal)W ≃ ¹jH(bridging)w > ²jHW. From this finding, it is possible to develop new criteria for assessing the static or fluxional nature of hydride ligands for several families of organotungsten hydrides (Cp₂W, CpW(CO)₃, W(CO)₃ and CpW(NO)x (x=l or 2)). Within each family, the magnitude of ¹JHW strongly reflects the type of metal hydride bonding, i.e. [Formula Omitted] and suggests that bridge bonding involves all the atoms in the bridge and therefore the "fused" notation is introduced. Treatment of CpW(NO)(CH₂SiMe₃)₂ with low pressures of H₂ (60-80 psig) in the presence of Lewis bases (L=P(0Ph)₃, PMePh₂) gives the unusually stable alkyl hydride compounds CpW(NO)(H)(CH₂SiMe₃)L. This chemistry is then extended to the Cp* (Cp*=ƞ⁵ -C₅Me₅) analogues, including the preparation of the appropriate starting materials. Upon thermolysis of Cp*W(NO)(H)(CH₂SiMe₃)(PMe₃) in C₆H₆, the intermolecular C-H activation product Cp*W(N0)(H)(C₆H₅)(PMe₃) is cleanly formed. However, intermolecular activation of CH₄, C₆H₁₂ or n-C₆H₁₄ does not occur under similar experimental conditions. Hydrogenolysis of Cp*W(NO)(CH₂SiMe₃)₂ at high pressures (≃920 psig) with no Lewis base present results in the formation of isolable [Cp*W(NO)H]₂(µ-H)₂ and [Cp*W(N0)H](µ-H)₂[Cp*W(N0)(CH₂SiMe₃)]. The latter is a new example of the rare class of dinuclear alkyl hydride complexes. Proton NMR spin tickling experiments on this compound allow the complete assignment of all couplings in the spectrum and show that ¹jH(terminal)W' ¹JH(bridging)W and ²jHW have the same sign.
Science, Faculty of
Chemistry, Department of
Graduate

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Watkin, John Graham. "Low-valent organometallic compounds of niobium." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236173.

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Tooze, R. P. "Organometallic compounds of platinum group metals." Thesis, Imperial College London, 1985. http://hdl.handle.net/10044/1/37880.

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Callahan, Ryan Patrick. "The synthesis of perfluorinated compounds by direct fluorination organometallic compounds and carboranes /." Access restricted to users with UT Austin EID Full text (PDF) from UMI/Dissertation Abstracts International, 2001. http://wwwlib.umi.com/cr/utexas/fullcit?p3036160.

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Tagg, Woo Chiat, and n/a. "Novel fluorescent organometallic materials." University of Otago. Department of Chemistry, 2009. http://adt.otago.ac.nz./public/adt-NZDU20090430.133100.

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This thesis describes the synthesis and properties of some extended donor-acceptor dyads with the donor being a ferrocenyl moiety and a fluorescent naphthalimide group as the acceptor. Two series of extended ferrocenyl-naphthalimide dyads were prepared in reasonable yield depending on the synthetic route. The first are a series of three ferrocenyl-CH=CH-spacer-C[triple bond]C-naphthalimide dyads in which the spacers are phenyl, biphenyl and anthryl and the second are a series of three ferrocenyl-C[triple bond]C-spacer-C[triple bond]C-naphthalimide dyads in which the spacers are 2,2� -bithiophene, 2,5-dimethoxybenzene and tetrafluorobenzene groups. The molecular structures of some compounds have been determined by X-ray diffraction although with many challenges because of the extensive [pi]-[pi] stacking of molecules that leads to ready aggregation in the solid state, particularly for the ferrocenyl-CH=CH-spacer-C[triple bond]C-naphthalimide dyads, in which the naphthalimide bears a methyl head group. In order to reduce the [pi]-[pi] stacking effect between the molecules and also to produce chiral molecules for the potential nonlinear optical applications, a chiral α-methylbenzylamine was introduced as the head group of naphthalimide for the ferrocenyl-C[triple bond]C-spacer-C[triple bond]C-naphthalimide dyads. The resulting comounds successfully gave crystals of sufficient quality for X-ray structural investigation. While the oxidative electrochemistry of the ferrocenyl compound in the two series of dyads was largely predictable (E� ~ 0.55 V for ferrocenyl-CH=CH- and ~ 0.72 V for ferrocenyl-C[triple bond]C-), the presence of spacers in the dyads appeared to afford stability to the reduced naphthalimide species. This was exhibited by the appearance of chemically reversible one-electron reduction processes for each of the compounds investigated. Similar unusual chemical reversibility was also shown by the spacer-C[triple bond]C-naphthalimide precursor systems. For the ferrocenyl-CH=CH-spacer-C[triple bond]C-naphthalimide dyads, the oxidation and reduction potentials closely resembled those of the simple ferrocenyl-CH=CH-spacer systems. This suggested that augmentation of the simple ferrocenyl-CH=CH-phenyl, -biphenyl and -anthryl systems with an alkyne linked naphthalimide unit showed little influence on the oxidation of the ferrocenyl moiety or the reduction of the naphthalimide unit. However, for the ferrocenyl-C[triple bond]C-spacer-C[triple bond]C-naphthalimide dyads, the oxidation and reduction potentials are influenced by the inductive effects of the spacers. While an anodic shift was observed for the dyad with the electron-withdrawing spacer tetrafluorobenzene, a cathodic shift was displayed for the dyads with the electron-donating spacers 2,2�-bithiophene and 2,5-dimethoxybenzene compared to that in the simple ferrocenyl-C[triple bond]C-naphthalimide system. The spectroscopic properties of the ferrocenyl-CH=CH-spacer-C[triple bond]C-naphthalimide dyads showed that interpolation of the aromatic spacers does not interfere with the internal charge separation. Oxidation of the ferrocenyl moiety resulted in bleaching of the metal-to-ligand charge transfer band at ~ 500 nm and the growth of a new band in the near infrared region at ~ 1000 nm. This new band can be assigned to a ligand-to-metal charge transfer transition, where the ferrocenium now acts as an acceptor to the naphthalimide donor. For the ferrocenyl-C[triple bond]C-spacer-C[triple bond]C-naphthalimide dyads, the spectroscopic properties showed that the mutually electron-withdrawing tetrafluorobenzene and naphthalimide units had little interaction despite their connection by a conductive alkyne link. In contrast, the dyads containing the electron-donating 2,2�-bithiophene and 2,5-dimethoxybenzene showed some degree of interaction between the spacer and the naphthalimide fragments. This was evidenced by the appearance of a broad absorption band in the range 410 - 440 nm, which is associated with an orbital that is delocalised between the spacer and the naphthalimide fragments. Again, the roles of donor and acceptor were reversed on oxidation of the ferrocenyl moiety. This resulted in the growth of a new near infrared band at ~750 mn for the dyad containing the tetrafluorobenzene spacer and at ~ 1000 nm for the dyads with 2,2�-bithiophene and 2,5 -dimethoxybenzene spacers. The ferrocenyl unit went from being a net donor to ferrocenium, which was acting as an acceptor, with the tetrafluorobenzene spacer adopting the donor role more reluctantly than the delocalised 2,2�-bithiophene-C[triple bond]C-naphthalimide and 2,5-dimethoxybenzene-C[triple bond]C-naphthalimide moieties. 1,3,5-Tri- and 1,2,4,5-tetra-substituted benzene cores were also used as spacers for the preparation of extended arrays of ferrocenyl-naphthalimide dyads. Utilisation of the 1,3,5 -tri-substituted benzene core enabled the core to be embellished in three directions, resulting in Y-motif extended arrays containing either one ferrocenyl unit [(ethenylferrocenyl)-C₆H₃-(C[triple bond]C-C₆H₅)₂] or one naphthalimide moiety [(4-piperidino-N-propargyl-naphthalimide)-C₆H₃-(Br)₂]. With the 1,2,4,5-tetra-substituted benzene core, the extension of the core was possible in four directions and gave extended arrays in an X-motif. Again, these systems contained either ferrocenyl units [bis(alkoxyferrocenyl)-C₆H₂-(C[triple bond]C-C₆H₅)₂] or naphthalimide moieties [(tetrakis-naphthalimide)-C₆H₂]. Attempts to incorporate both ferrocenyl and naphthalimide fragments into the X- or Y-motif extended arrays were unsuccessful. By adding C₂Co₂(CO)₆dppm across the triple bonds of two of the four alkyne groups in the X-motif naphthalimide system [(tetrakis-naphthalimide)-C₆H₂], it was possible to incorporate two oxidisable C₂Co₂(CO)₄dppm cluster units into the molecule. The electrochemistry of the resulting system showed two discrete oxidation processes, suggesting the possibility of some interaction between the dicobalt cluster redox centres.

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Yonchev, Raycho. "Permeation of organometallic compounds through phspholipid membranes." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=979680972.

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Lawrence, Heather Bunting Elizabeth. "Organometallic compounds with non-linear optical properties." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.276835.

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Rafferty, Karen. "Novel organometallic compounds as potential antitumour agents." Thesis, University of Leeds, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.487773.

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Books on the topic "Organometallic compounds"

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1938-, King R. B., and Eisch John J. 1930-, eds. Organometallic syntheses. Amsterdam: Elsevier Science, 1986.

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Macintyre, J. E., D. J. Cardin, S. A. Cotton, R. J. Cross, M. Green, P. G. Harrison, G. R. Knox, et al., eds. Dictionary of Organometallic Compounds. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4615-6844-5.

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Macintyre, J. E., ed. Dictionary of Organometallic Compounds. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4615-6847-6.

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Macintyre, J. E., F. M. Daniel, D. J. Cardin, S. A. Cotton, R. J. Cross, A. G. Davies, R. S. Edmundson, et al., eds. Dictionary of Organometallic Compounds. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-4966-3.

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MacIntyre, Jane E. Dictionary of Organometallic Compounds. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-6848-7.

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Smith, K., ed. Organometallic Compounds of Boron. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-3069-9.

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Walton, D. R. M., ed. Organometallic Compounds of Silicon. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7166-1.

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Knox, G. R., ed. Organometallic Compounds of Iron. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7168-5.

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Hall, Chapman and, ed. Dictionary of organometallic compounds. 2nd ed. London: Chapman and Hall, 1995.

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1958-, Macintyre J., ed. Dictionary of organometallic compounds. London: Chapman & Hall, 1990.

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Book chapters on the topic "Organometallic compounds"

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Vančik, Hrvoj. "Organometallic Compounds." In Aromatic C-nitroso Compounds, 121–40. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6337-1_4.

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Paulus, Wilfried. "Organometallic Compounds." In Microbicides for the Protection of Materials, 401–17. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2118-7_19.

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Paulus, Wilfried. "Organometallic compounds." In Directory of Microbicides for the Protection of Materials, 733–45. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/1-4020-2818-0_42.

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Gevers, E. Ch Th. "Organometallic Compounds." In Mass Spectrometry in Environmental Sciences, 353–65. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2361-7_16.

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Burton, Donald J., and Long Lu. "Fluorinated Organometallic Compounds." In Organofluorine Chemistry, 45–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/3-540-69197-9_2.

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Lee, W. D. "From Organometallic Compounds." In Inorganic Reactions and Methods, 424–25. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145173.ch293.

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Norman, A. D. "In Organometallic Compounds." In Inorganic Reactions and Methods, 120–24. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch93.

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Norman, A. D. "From Organometallic Compounds." In Inorganic Reactions and Methods, 126–29. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch96.

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Lindsell, W. E. "With Organometallic Compounds." In Inorganic Reactions and Methods, 273–75. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145241.ch164.

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Omae, Iwao. "Organometallic Intramolecular-Coordination Compounds." In Cyclometalation Reactions, 23–31. Tokyo: Springer Japan, 2013. http://dx.doi.org/10.1007/978-4-431-54604-7_4.

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Conference papers on the topic "Organometallic compounds"

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Shensky, William M., Jianmin Shi, Michael J. Ferry, and Timothy M. Pritchett. "Tricycloquinazoline-Based Organometallic Compounds for Optical Switching." In CLEO: Science and Innovations. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/cleo_si.2015.sm2g.8.

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Diaz-Garcia, Maria A., Fernando Agullo-Lopez, M. G. Hutchings, P. F. Gordon, and Francois Kajzar. "Third-order hyperpolarizabilities of soluble organometallic compounds." In SPIE's 1994 International Symposium on Optics, Imaging, and Instrumentation, edited by Gustaaf R. Moehlmann. SPIE, 1994. http://dx.doi.org/10.1117/12.187518.

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Aamoum, A., S. Taboukhat, Y. El Kouari, A. Zawadzka, A. Andrushchak, and B. Sahraoui. "Optical Properties of Some Selected Organometallic Compounds." In 2023 23rd International Conference on Transparent Optical Networks (ICTON). IEEE, 2023. http://dx.doi.org/10.1109/icton59386.2023.10207187.

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Heck, Jürgen, Marc H. Prosenc, Timo Meyer-Friedrichsen, Jan Holtmann, Edyta Walczuk, Markus Dede, Tony Farrell, et al. "Structure-property relationship in organometallic compounds regarding SHG." In Photonic Devices + Applications, edited by Jean-Michel Nunzi. SPIE, 2007. http://dx.doi.org/10.1117/12.736166.

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Fernández-Figueiras, Adolfo, Fátima Lucio, Paula Munín, Francisco Reigosa, Jose Vila, Maria Pereira, and Paula Polo. "SYNTHESIS OF IMINOPHOSPHORANES AS LIGANDS FOR ORGANOMETALLIC COMPOUNDS." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a016.

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Tagmatarchis, Nikos, and Kosmas Prassides. "Synthesis and characterization of organometallic compounds of fullerene derivatives." In ELECTRONIC PROPERTIES OF NOVEL MATERIALS--SCIENCE AND TECHNOLOGY OF MOLECULAR NANOSTRUCTURES. ASCE, 1999. http://dx.doi.org/10.1063/1.59779.

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Tutt, Lee W., Stephen W. McCahon, and Marvin B. Klein. "Optimization of optical limiting properties of organometallic cluster compounds." In Orlando '90, 16-20 April, edited by Rudolf Hartmann, M. J. Soileau, and Vijay K. Varadan. SPIE, 1990. http://dx.doi.org/10.1117/12.21681.

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Costuas, Karine. "Molecular switches in carbon-rich organometallic compounds: Theoretical aspects." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2010 (ICCMSE-2010). AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4906720.

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Ryder, D. F., and J. H. Fernstermacher. "Processing and characterization of hexagonal ferrite thin-film from organometallic compounds." In International Magnetics Conference. IEEE, 1989. http://dx.doi.org/10.1109/intmag.1989.689928.

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G. Teixeira, Ricardo, Dimas C. Belisario, Ana Isabel Tomaz, Maria Helena Garcia, Chiara Riganti, and Andreia Valente. "Ruthenium organometallic compounds as ABC drug efflux-targeted agents and collateral sensitizers." In 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07439.

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Reports on the topic "Organometallic compounds"

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Casey, C. P. Organometallic chemistry of bimetallic compounds. Office of Scientific and Technical Information (OSTI), July 1991. http://dx.doi.org/10.2172/5977032.

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Casey, C. P. Organometallic chemistry of bimetallic compounds. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/7047078.

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Casey, C. Organometallic chemistry of bimetallic compounds. Office of Scientific and Technical Information (OSTI), August 1990. http://dx.doi.org/10.2172/6619707.

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Casey, C. P. Organometallic chemistry of bimetallic compounds. [Annual report]. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/10187589.

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Casey, C. P. Organometallic chemistry of bimetallic compounds. Annual progress report. Office of Scientific and Technical Information (OSTI), July 1993. http://dx.doi.org/10.2172/10192817.

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Casey, C. P. Organometallic chemistry of bimetallic compounds. Final progress report. Office of Scientific and Technical Information (OSTI), July 1991. http://dx.doi.org/10.2172/10110610.

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Casey, C. P. Organometallic chemistry of bimetallic compounds. Progress report, January 1992--July 1995. Office of Scientific and Technical Information (OSTI), July 1994. http://dx.doi.org/10.2172/10106407.

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Cowley, Alan H. Reactions of Organometallic Compounds with Phosphorus (V) Esters and Related Species. Fort Belvoir, VA: Defense Technical Information Center, November 1987. http://dx.doi.org/10.21236/ada190893.

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Larsen, C. A., R. W. Gedridge, Li Jr., Stringfellow S. H., and G. B. Decomposition Mechanisms of Antimony Source Compounds for Organometallic Vapor-Phase Epitaxy. Fort Belvoir, VA: Defense Technical Information Center, December 1990. http://dx.doi.org/10.21236/ada237644.

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Mingos, D. M. Design of Non-Linear Optical Materials Based on Co-ordination and Organometallic Compounds. Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada252046.

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