Bibliografías temáticas / Novel Transition Metal Complexes

Literatura académica sobre el tema "Novel Transition Metal Complexes"

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Publicado: 18 de mayo de 2024

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Artículos de revistas sobre el tema "Novel Transition Metal Complexes"

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Galal, Shadia A., Amira S. Abd El-All, Khaled H. Hegab, Asmaa A. Magd-El-Din, Nabil S. Youssef y Hoda I. El-Diwani. "Novel antiviral benzofuran-transition metal complexes". European Journal of Medicinal Chemistry 45, n.º 7 (julio de 2010): 3035–46. http://dx.doi.org/10.1016/j.ejmech.2010.03.034.

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Zayed, Ehab M., Gehad G. Mohamed y Ahmed M. M. Hindy. "Transition metal complexes of novel Schiff base". Journal of Thermal Analysis and Calorimetry 120, n.º 1 (4 de septiembre de 2014): 893–903. http://dx.doi.org/10.1007/s10973-014-4061-3.

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Beldon, Patrick J., Sebastian Henke, Bartomeu Monserrat, Satoshi Tominaka, Norbert Stock y Anthony K. Cheetham. "Transition metal coordination complexes of chrysazin". CrystEngComm 18, n.º 27 (2016): 5121–29. http://dx.doi.org/10.1039/c5ce00792e.

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Eleven novel coordination compounds, composed of chrysazin (1,8-dihydroxyanthraquinone) and different first-row transition metals (Fe, Co, Ni, Cu), were synthesised and the structures determined by single-crystal X-ray diffraction.
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Bligh, S. W. Annie, Nick Choi, Donovan St C. Green, Harry R. Hudson, Catherine M. McGrath, Mary McPartlin y Max Pianka. "Transition metal complexes of dialkyl α-hydroxyiminophosphonates, a novel class of metal complexes". Polyhedron 12, n.º 23 (diciembre de 1993): 2887–90. http://dx.doi.org/10.1016/s0277-5387(00)80073-x.

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Andrade, Marta A. y Luísa M. D. R. S. Martins. "Novel Chemotherapeutic Agents - The Contribution of Scorpionates". Current Medicinal Chemistry 26, n.º 41 (8 de enero de 2020): 7452–75. http://dx.doi.org/10.2174/0929867325666180914104237.

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: The development of safe and effective chemotherapeutic agents is one of the uppermost priorities and challenges of medicinal chemistry and new transition metal complexes are being continuously designed and tested as anticancer agents. Scorpionate ligands have played a great role in coordination chemistry, since their discovery by Trofimenko in the late 1960s, with significant contributions in the fields of catalysis and bioinorganic chemistry. Scorpionate metal complexes have also shown interesting anticancer properties, and herein, the most recent (last decade) and relevant scorpionate complexes reported for application in medicinal chemistry as chemotherapeutic agents are reviewed. The current progress on the anticancer properties of transition metal complexes bearing homo- or hetero- scorpionate ligands, derived from bis- or tris-(pyrazol-1-yl)-borate or -methane moieties is highlighted.
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Anusuya, A. M., B. S. Krishna, S. B. Benaka Prasad, K. Yogesh Kumar, R. Raveesha y M. K. Prashanth. "Novel Heterocyclic Transition Metal Complexes: Synthesis, Characterization, Antimicrobial and Anticancer Activity". Asian Journal of Chemistry 33, n.º 10 (2021): 2519–24. http://dx.doi.org/10.14233/ajchem.2021.23519.

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A heterocyclic ligand, 5-(2-(4-chlorophenyl)-1H-benzo[d]imidazol-1-yl)quinolin-8-ol and its Co(II), Ni(II), Cu(II) and Zn(II) complexes were synthesized and characterized by elemental analysis and spectroscopic techniques. According to the spectral analysis, the ligand acts as a bidentate ligand and coordinating through the nitrogen and deprotonated oxygen atoms. For Cu(II) and Ni(II) complexes, spectral analysis reveals square planer geometry, whereas Co(II) and Zn(II) complexes have tetrahedral geometry. The antibacterial results show that Zn(II) complex is more effective than the other metal(II) complexes examined. The ligand and its metal complexes were tested for anticancer activity using the MTT assay with cisplatin as the reference drug against A549, MCF7, and HCT116 cancer cell lines. Results showed that the metal(II) complexes were shown to be more active than the ligand, especially Zn(II) complex being the most potent among this series.
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Office, Editorial. "The steric and electronic effects of metal-containing substituents on Fischer carbene metal clusters". Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie 28, n.º 3 (6 de septiembre de 2009): 237–60. http://dx.doi.org/10.4102/satnt.v28i3.61.

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Baklouti, Lassaad. "Novel phthalonitrile derivatives as potential compounds for extraction and complexation of metal cations". JOURNAL OF ADVANCES IN CHEMISTRY 11, n.º 10 (17 de diciembre de 2016): 3870–74. http://dx.doi.org/10.24297/jac.v11i10.2185.

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The synthesis and the binding properties of novel phthalonitrile derivatives 1-3 towards metal cations have been described in this paper. The complexation and extraction of some transition and heavy metal cations have been followed by UV-visible spectrophotometry absorption in methanol. The conductivity studies have been used in order to confirm complex’s stoichiometries. The treatment of UV spectra by digital program showed the formation of ML (with ML2 in some cases) (M=metal, L=ligand) species. Beyond the discussion of the stability profiles of complexes particular attention is paid to the selectivity towards Cu2+ in the 1st sequence of transition metal cations and towards Hg2+ in the sequence of heavy metal cations.
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Bhale, S. P., A. R. Yadav, S. U. Tekale, R. B. Nawale, R. P. Marathe, P. S. Kendrekar y R. P. Pawar. "Synthesis, Characterization and Antimicrobial Screening of Novel Hydrazide Ligand & It’s Transition Metal Complexes". Asian Journal of Chemistry 31, n.º 4 (27 de febrero de 2019): 938–42. http://dx.doi.org/10.14233/ajchem.2019.21795.

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Different transition metal complexes were synthesized from novel 3-bromo-2-[1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)ethylidene]hydrazide ligand (H2L) and characterized by spectral techniques. The synthesized ligand was found to act mono as well as di deprotonated (OH, NH) manner and stoichiometry of the ligand to metal ions was confirmed to be 1:1 in case of complex using metal chloride salts, whereas 1:2 in case of metal(II) complexes using metal acetate(II) salt. Structures of metal complexes were confirmed by IR, 1H NMR, TGA, XRD, elemental analysis and UV technique which revealed that Mn(II), Co(II), Ni(II), Cu(II) complexes were octahedral geometry and those of Cu(II), Zn(II) showed square planner and tetrahedral geometry around metal ion respectively. Furthermore H2L and its metal complexes were screened for antimicrobial activity which showed that ligand enhanced its biological activity after coordination with metal ions. In particular, Cd(II) and Mn(II) complexes exhibited excellent antifungal activity.
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Kumar, Manoj, Anita Rani, Hardeep Singh Tuli, Rajshree Khare y Vinit Parkash. "Synthesis and Spectral Investigations of Polymeric Hydrazone Schiff Base and its Transition Metal Complexes with Promising Antimicrobial, Anti-Angeogenic and DNA Photo-Cleavage Activities". Asian Journal of Chemistry 31, n.º 10 (30 de agosto de 2019): 2331–36. http://dx.doi.org/10.14233/ajchem.2019.22157.

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This report describes the synthesis and exploration of novel Schiff base ligand in the form of a polymer (heptamer) which was prepared by reaction between 3,4-diacetyl-2,5-hexanedione and hydrazine hydrate in ethanol. On further reaction of Schiff base with transition metals ions (Co and Cu) leads to formation of its transition metal complexes. The structural identification of Schiff base ligand and its transition metal complexes were characterized by classical structural techniques like FT-IR, NMR and mass spectra. The free ligand and its transition metal complexes have been screened for in vitro biological activities against various strains of bacteria and fungi. The prepared Schiff base and its metal complexes were also screened for antiangiogenic activity. The results have shown the remarkable antimicrobial and antiangiogenic activities of the Schiff base and its metal complexes.
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Tesis sobre el tema "Novel Transition Metal Complexes"

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Veighy, Clifford Robert. "Novel cyclopentadienyl transition metal complexes". Thesis, University of Southampton, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327366.

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Blunden, Ralph Benedict. "Novel early transition metal cyclopropenyl complexes". Thesis, University of Sussex, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360552.

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Dossett, David Michael. "The synthesis of novel chiral transition metal complexes". Thesis, University of Southampton, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.402060.

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Cairns, Gareth Alan. "Novel aspects of alkyne substituted transition metal complexes". Thesis, University of Bath, 1998. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242813.

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Mayo, Richard Andrew. "Transition-metal derivatives of phosphine, arsine and stibine". Thesis, University of Edinburgh, 1986. http://hdl.handle.net/1842/15303.

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Blincko, Stuart. "Novel luminescent compounds for immunoassay". Thesis, City University London, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.255249.

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Lu, Canzhong. "Novel transition metal complexes of sterically hindered silyl thiolate ligands". Thesis, University of Essex, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307857.

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Green, Simon Michael. "The synthesis and application of novel chiral transition metal complexes". Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285879.

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Yoo, Hyunsuk S. M. Massachusetts Institute of Technology. "Synthesis and mechanistic studies of novel antitumor transition metal complexes". Thesis, Massachusetts Institute of Technology, 2014. http://hdl.handle.net/1721.1/91121.

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Thesis: S.M. in Inorganic Chemistry, Massachusetts Institute of Technology, Department of Chemistry, 2014.
Cataloged from PDF version of thesis. Vita.
Includes bibliographical references.
In order to overcome side effects and drug resistance associated with conventional Pt(II) drugs, our lab has developed novel platinum complexes. One of the new platinum complexes developed in our lab is the monofunctional platinum anti-cancer compound phenanthriplatin. We have found that by binding to sulfur complexes, phenanthriplatin undergoes changes in its kinetic and cytotoxic properties. Sulfur adducts of phenanthriplatin were synthesized to study the complex roles sulfur compounds serve in the cellular action of the monofunctional compound. In addition, we have examined how Pt(IV) chemistry can be successfully applied to increase the efficacy of Pt(II) compounds. We conjugated hydrophobic chains to trans-[Pt(NH₃)₂Cl₂] (TDDP) through isocyanate couplings and successfully transformed TDDP into an active compound. We demonstrated that Pt(IV) chemistry can be applied to transform even inactive trans compounds into active complexes that can potentially be used in chemotherapy. Finally, we examined the anticancer properties of the dinuclear osmium(VI) nitrido complex [NBu₄]₂[(OsNCl₄)₂(pyz)]. We studied its cellular activity in the hope of discovering interesting and unexpected properties. We found that the compound has moderate cytotoxicity and leads to DNA damage and apoptosis.
by Hyunsuk Yoo.
S.M. in Inorganic Chemistry
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Smith, Charles J. "Transition metal complexes on novel, polydentate, water-soluble, phosphine ligands /". free to MU campus, to others for purchase, 1997. http://wwwlib.umi.com/cr/mo/fullcit?p9841335.

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Libros sobre el tema "Novel Transition Metal Complexes"

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Nishibayashi, Yoshiaki, ed. Transition Metal-Dinitrogen Complexes. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527344260.

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Kreißl, F. R., ed. Transition Metal Carbyne Complexes. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1666-4.

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Yam, Vivian W. W., ed. Photofunctional Transition Metal Complexes. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-36810-6.

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R, Kreissl F. y North Atlantic Treaty Organization. Scientific Affairs Division., eds. Transition metal carbyne complexes. Dordrecht: Kluwer Academic, 1993.

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W, Yam Vivian W. y Balch Alan L, eds. Photofunctional transition metal complexes. Berlin: Springer Verlag, 2007.

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Qiu, Zaozao. Late Transition Metal-Carboryne Complexes. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-24361-5.

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Molecular orbitals of transition metal complexes. Oxford: Oxford University Press, 2005.

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Kettle, Sidney. The theory of transition metal complexes. London: Royal Society of Chemistry. Educational Techniques Group Trust, 1994.

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Baiada, Anthony. Novel tricoordinate univalent coinage metal complexes. London: NELP, 1986.

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Hartt, Virginia. Spectroelectrochemical studies of some transition metal complexes. Birmingham: University of Birmingham, 2002.

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Capítulos de libros sobre el tema "Novel Transition Metal Complexes"

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Fischer, H., C. Troll y J. Schleu. "Novel Cyclizations Involving Cationic Carbyne Complexes". En Transition Metal Carbyne Complexes, 79–84. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1666-4_9.

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Yeung, Margaret Ching-Lam y Vivian Wing-Wah Yam. "Molecular Design of Novel Classes of Luminescent Transition Metal Complexes and Their Use in Sensing, Biolabeling, and Cell Imaging". En Luminescent and Photoactive Transition Metal Complexes as Biomolecular Probes and Cellular Reagents, 109–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/430_2014_172.

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Hidai, Masanobu y Yasushi Mizobe. "Toward Novel Organic Synthesis on Multimetallic Centers: Synthesis and Reactivities of Polynuclear Transition-Metal—Sulfur Complexes". En ACS Symposium Series, 310–23. Washington, DC: American Chemical Society, 1996. http://dx.doi.org/10.1021/bk-1996-0653.ch019.

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Hendrickson, David N., David M. Adams, Chi-Cheng Wu y Sheila M. J. Aubin. "Bistable Transition Metal Complexes". En Magnetism: A Supramolecular Function, 357–82. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-015-8707-5_19.

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Atwood, David A. "(II) Transition Metal Complexes". En Inorganic Reactions and Methods, 176. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch169.

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Harrod, John F. y Bruce Arndtsen. "Transition Metal Hydride Complexes". En Inorganic Reactions and Methods, 337–41. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch238.

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Huang, Xin y Zhengyang Lin. "Transition Metal Catalyzed Borations". En Catalysis by Metal Complexes, 189–212. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/0-306-47718-1_8.

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Baranoff, Etienne, Francesco Barigelletti, Sylvestre Bonnet, Jean-Paul Collin, Lucia Flamigni, Pierre Mobian y Jean-Pierre Sauvage. "From Photoinduced Charge Separation to Light-driven Molecular Machines". En Photofunctional Transition Metal Complexes, 41–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/430_037.

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Kume, Shoko y Hiroshi Nishihara. "Metal-based Photoswitches Derived from Photoisomerization". En Photofunctional Transition Metal Complexes, 79–112. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/430_2006_038.

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Contakes, Stephen M., Yen Hoang Le Nguyen, Harry B. Gray, Edith C. Glazer, Anna-Maria Hays y David B. Goodin. "Conjugates of Heme-Thiolate Enzymes with Photoactive Metal-Diimine Wires". En Photofunctional Transition Metal Complexes, 177–203. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/430_2006_039.

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Actas de conferencias sobre el tema "Novel Transition Metal Complexes"

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York, William D., D. Keith Walters y James H. Leylek. "A Novel Transition-Sensitive Conjugate Methodology Applied to Turbine Vane Heat Transfer". En ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-41555.

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A documented numerical methodology for conjugate heat transfer was employed to predict the metal temperature of an internally-cooled gas turbine vane at realistic operating conditions. The conjugate heat transfer approach involves the simultaneous solution of the flow field (convection) and the conduction within the metal vane, allowing a solution of the complete heat transfer problem in a single simulation. This technique means better accuracy and faster turn-around time than the typical industry practice of multiple, decoupled solutions. In the present simulations, the solid and fluid zones were coupled by energy conservation at the interfaces. In the fluid zones, the Reynoldsaveraged Navier-Stokes equations were closed with a three-equation, eddy-viscosity model, developed in-house and previously documented, with the capability to predict laminar-to-turbulent boundary-layer transition. The single-point model is fully-predictive for transition and requires no problem-dependent user inputs. For comparison, a simulation was also run with a commercially available Realizable k-ε turbulence model. A high-quality, unstructured gird was employed in both cases. Numerical predictions for midspan temperature on the airfoil surface are compared to data from an open-literature experiment with the same geometry and operating conditions. The new model captured transition of the initially laminar boundary layer to a turbulent boundary layer on the suction surface. The results with the new model show excellent agreement with measured data for surface temperature over the majority of the airfoil surface. The new model showed a marked improvement over the Realizable k-ε model in all regions where laminar boundary layers exist, highlighting the importance of accurately modeling transition in turbomachinery heat transfer simulations.
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Lee, Taewoo, Christian Reich, Christopher M. Laperle, Xiaodi Li, Margaret Grant, Christoph G. Rose-Petruck y Frank Benesch-Lee. "Ultrafast XAFS of transition metal complexes". En International Conference on Ultrafast Phenomena. Washington, D.C.: OSA, 2006. http://dx.doi.org/10.1364/up.2006.wd4.

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Acharya, Sunil, Rhushik Matroja, Mohammad Elyyan Elyyan, Henri De Charnace’ y Yi Zhang. "Novel Design Optimization for Additive Manufactured Components". En Offshore Technology Conference. OTC, 2021. http://dx.doi.org/10.4043/30956-ms.

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Abstract In the last 10 years, Metal Additive Manufacturing (AM) has matured substantially [1,2]. The evolution of metal powder-bed AM now, facilitates production-quality parts to be manufactured. Additive manufacturing has specially attracted attention for its ability to manufacture parts with complex shapes that are cost-ineffective or impossible to manufacture with traditional technologies. For Oil and Gas industry, this ability to manufacture complex shapes offers unprecedented opportunity to redesign and optimize wide ranging components from cutting heads, heat exchangers [3], pumping and filtration equipment to drill motors, inline static-mixers and flanges. as well as advantages over traditional manufacturing techniques. The present work shows how optimization and simulation tools are valuable in rapid development of more efficient and light-weighted components that take advantage of the 3D printing process. Additive Manufacturing, while promising offers its own challenges related to process parameter optimization and part distortions. So, testing new paradigm-shifting design becomes time consuming and expensive trial and error process. Computational methods for optimization and physics simulation reduce the risk of testing new designs concepts and make the transition to new products efficient and inexpensive. Conventional design and design-optimization techniques typically do not apply for AM part design. The flexibility of AM in generating complex shapes implies a lesser number of components and implicit savings in assembly. Also, the possibility of latticed structures allows for reduced components through consolidation. The ability to incorporate these structures broadens the design criteria to achieve previously unforeseen possibilities. After arriving at the part design, the "print design" needs to be addressed. The AM process involves large thermal transients, phase change and non-linear material properties potentially leading to distortions and residual stresses in the finished component. Process simulation is valuable in estimating stresses generated in components, distortion, and adequacy of the support design. The presentation illustrates the simulation methodologies in design, multi-physics and process optimization for a drill-head geometry.
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Slinker, Jason, Dan Bernards, Samuel Flores-Torres, Stefan Bernhard, Paul L. Houston, Héctor D. Abruña y George G. Malliaras. "Light emitting diodes from transition metal complexes". En Frontiers in Optics. Washington, D.C.: OSA, 2003. http://dx.doi.org/10.1364/fio.2003.wnn2.

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Latouche, Camille, Vincenzo Barone y Julien Bloino. "ANHARMONIC VIBRATIONAL SPECTROSCOPY ON METAL TRANSITION COMPLEXES". En 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.rc08.

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Xu, Wenying, James N. Demas y Benjamin A. DeGraff, Jr. "Highly luminescent transition metal complexes as sensors". En OE/LASE '94, editado por James A. Harrington, David M. Harris, Abraham Katzir y Fred P. Milanovich. SPIE, 1994. http://dx.doi.org/10.1117/12.180739.

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Gu, Xun, Yoshiyuki Kikuchi, Toshihisa Nozawa y Seiji Samukawa. "A novel metallic complex reaction etching for transition metal and magnetic material by low-temperature and damage-free neutral beam process for non-volatile MRAM device applications". En 2014 IEEE Symposium on VLSI Technology. IEEE, 2014. http://dx.doi.org/10.1109/vlsit.2014.6894362.

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Tsakalakos, Loucas, Lauraine Denault, Michael Larsen, Mohamed Rahmane, Yan Gao, Joleyn Balch y Paul Wilson. "Mo2C Nanowires and Ribbons on Si via Two-Step Vapor Phase Growth". En ASME 2004 3rd Integrated Nanosystems Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/nano2004-46098.

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Transition metal carbides are an interesting class of electronic materials owing to their high electrical conductivity at room temperature, which is only slightly lower than that of their constituent transition metal elements. For example, the room temperature electrical resistivity of bulk Mo2C is ∼70 μΩ-cm compared to that of Mo (4.85 μΩ-cm), whereas that of NbC is ∼50 μΩ-cm as compared to 15.2 μΩ-cm for Nb. Indeed, the temperature dependent resistivity of many transition metal carbides suggests metallic-like conduction. Furthermore, certain transition metal carbides are known to become superconducting, with transition temperatures ranging from 1.15 °K for TiC1−x to 14 °K for NbC. [1] They are also able to withstand high temperatures and are chemically stable. Initial synthesis of metal carbide nanorods was demonstrated using the carbon nanotube (CNT) confined reaction mechanism by Lieber and co-workers [2] and subsequent superconducting behavior was shown by Fukunaga et al. [3]. Vapor-liquid-solid growth was employed by Johnson et al. [4] to synthesize micron-sized carbide whiskers. Here, we have successfully synthesized Mo2C nanorods and ribbons on Si substrates using a novel two-step catalytic approach, which allows for synthesis of such high temperature nanostructures at manufacturable temperatures (≤ 1000 °C) and time scales (≤ 60 min). In the first step we utilize a catalytic vapor phase process to grow Mo and/or molybdenum oxide nanostructures, which are subsequently carburized in situ to form the desired Mo2C nanostructures. Unlike true VLS growth of carbides, in which high temperature (≤ 1100–1200 °C) is required to adequately dissolve carbon into the catalyst particles, our strategy is to react the nanostructures along their entire length with a carbon vapor source after creating the oxide/metal nanostructures, which for Mo2C can be achieved at relatively low temperatures. (≤ 1000 °C). The nanorods and ribbons are polycrystalline, with a mean grain size of 20–50 nm and 50–150 nm, respectively. We hypothesize that the growth mechanism is a complex mixture of VLS, VSS, and auto-catalytic growth, in which molten catalyst nanoparticles enter a three phase region once the metal precursor is supplied. The growth then presumably continues via a vapor-solid-solid process and is possible assisted by the presence of various molybdenum oxide species on the surface. Initial single nanowire electrical measurements yield a higher resistivity than in the bulk, which is attributed to the fine grain sizes and/or the presence of an oxide layer. A discussion of the growth mechanism will be presented along with issues relating to single nanowire device fabrication and control of nanowire orientation.
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Malliaras, George G. "Light Emitting Devices from Ionic Transition Metal Complexes". En Frontiers in Optics. Washington, D.C.: OSA, 2005. http://dx.doi.org/10.1364/fio.2005.smb3.

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Chi-Chiu, Ko, Han Jingqi, Cheng Shun-Cheung y Ng Chi-On. "SSpectroscopic study on luminescent mechanochromic transition metal complexes". En Asian Spectroscopy Conference 2020. Institute of Advanced Studies, Nanyang Technological University, 2020. http://dx.doi.org/10.32655/asc_8-10_dec2020.13.

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Informes sobre el tema "Novel Transition Metal Complexes"

1

Hartwig, John. Chemistry of Complexes with Transition Metal Heteroatom Bonds Novel Insertion Chemistry and XH Bond Activation. Office of Scientific and Technical Information (OSTI), febrero de 2012. http://dx.doi.org/10.2172/1035516.

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White, Carter James. Selenophene transition metal complexes. Office of Scientific and Technical Information (OSTI), julio de 1994. http://dx.doi.org/10.2172/10190649.

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Sharp, P. R. Late transition metal oxo and imido complexes. Office of Scientific and Technical Information (OSTI), diciembre de 1992. http://dx.doi.org/10.2172/7017245.

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Sharp, P. R. Late transition metal. mu. -oxo and. mu. -imido complexes. Office of Scientific and Technical Information (OSTI), enero de 1990. http://dx.doi.org/10.2172/6332549.

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Sharp, P. Late transition metal. mu. -oxo and. mu. -imido complexes. Office of Scientific and Technical Information (OSTI), enero de 1990. http://dx.doi.org/10.2172/7003275.

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Norton, Jack. The Activation of Hydrogen by First-Row Transition-Metal Complexes. Office of Scientific and Technical Information (OSTI), marzo de 2020. http://dx.doi.org/10.2172/1604425.

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Du, Guodong. Group 4 Metalloporphyrin diolato Complexes and Catalytic Application of Metalloporphyrins and Related Transition Metal Complexes. Office of Scientific and Technical Information (OSTI), enero de 2003. http://dx.doi.org/10.2172/835301.

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8

Krishnan Balasubramanian. Electronic Structure of Transition Metal Clusters, Actinide Complexes and Their Reactivities. Office of Scientific and Technical Information (OSTI), julio de 2009. http://dx.doi.org/10.2172/959347.

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Meyer, T. J. Excited state processes in transition metal complexes: Redox splitting in soluble polymers. Office of Scientific and Technical Information (OSTI), marzo de 1992. http://dx.doi.org/10.2172/5573491.

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Meyer, T. J. y J. M. Papanikolas. Excited State Processes in Transition Metal Complexes, Redox Splitting in Soluble Polymers. Office of Scientific and Technical Information (OSTI), agosto de 2002. http://dx.doi.org/10.2172/830013.

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