Gotowe bibliografie tematyczne / Metal complexes

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Gotowa bibliografia na temat „Metal complexes”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 12 kwietnia 2025

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Artykuły w czasopismach na temat "Metal complexes"

Nabeshima, Tatsuya, Yusuke Chiba, Takashi Nakamura i Ryota Matsuoka. "Synthesis and Functions of Oligomeric and Multidentate Dipyrrin Derivatives and their Complexes". Synlett 31, nr 17 (24.07.2020): 1663–80. http://dx.doi.org/10.1055/s-0040-1707155.

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The dipyrrin–metal complexes and especially the boron complex 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) have recently attracted considerable attention because of their interesting properties and possible applications. We have developed two unique and useful ways to extend versatility and usefulness of the dipyrrin complexes. The first one is the linear and macrocyclic oligomerization of the BODIPY units. These arrangements of the B–F moieties of the oligomerized BODIPY units provide sophisticated functions, such as unique recognition ability toward cationic guest, associated with changes in the photophysical properties by utilizing unprecedented interactions between the B–F and a cationic species. The second one is introduction of additional ligating moieties into the dipyrrin skeleton. The multidentate N2Ox dipyrrin ligands thus obtained form a variety of complexes with 13 and 14 group elements, which are difficult to synthesize using the original N2 dipyrrin derivatives. Interestingly, these unique complexes exhibit novel structures, properties, and functions such as guest recognition, stimuli-responsive structural conversion, switching of the optical properties, excellent stability of the neutral radicals, etc. We believe that these multifunctional dipyrrin complexes will advance the basic chemistry of the dipyrrin complexes and develop their applications in the materials and medicinal chemistry fields.1 Introduction2 Linear Oligomers of Boron–Dipyrrin Complexes3 Cyclic Oligomers of Boron–Dipyrrin Complexes4 A Cyclic Oligomer of Zinc–Dipyrrin Complexes5 Group 13 Element Complexes of N2Ox Dipyrrins6 Chiral N2 and N2Ox Dipyrrin Complexes7 Group 14 Element Complexes of N2O2 Dipyrrins8 Other N2O2 Dipyrrin Complexes with Unique Properties and Functions9 Conclusion

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Sethi, Pooja, Rajshree Khare i Renuka Choudhary. "Complexes of Pyrimidine Thiones: Mechanochemical Synthesis and Biological Evaluation". Asian Journal of Chemistry 32, nr 10 (2020): 2594–600. http://dx.doi.org/10.14233/ajchem.2020.22813.

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A new series of metal complexes with 1-(2-methylphenyl)-4,4,6-trimethyl pyrimidine-2-thione (2-HL1) and 1-(4-methylphenyl)-4,4,6-trimethyl pyrimidine-2-thione (4-HL2) ligands, [M(mppt)2(H2O)n] (M(II) = Cu, Mn, Co; n = 2 and M(II) = Ni, Zn; n = 0) have been synthesized using mechanochemical protocol. The complexes have been framed as [M(mppt)2(H2O)n] due to 1:2 (metal:ligand) nature of these metal complexs. Structures have been further confirmed on the basis of elemental analysis, Magnetic susceptibility measurements, electronic, infrared, far infrared, proton NMR, Mass spectral moment and thermogravimetric analysis studies. The infrared spectral data suggested that ligand behaves as a bidentate, coordinating through – N (endocyclic) and – S (exocyclic) donor atoms. All the compounds have also been screened for antibacterial and DNA photocleavage potential. Ligands complexed with Mn and Ni metals have shown the effect of substitution on their biological potentials. It was found that substitution at 4th or para position makes the ligand and its metal complexes have better antibacterial and DNA photocleaving agents.

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Medjidov, A. A., R. H. Ismayilov, P. A. Fatullayeva i D. B. Tagiyev. "REACTIVITY OF METAL COMPLEXES WITH RADICALS". Azerbaijan Chemical Journal, nr 1 (10.02.2025): 5–24. https://doi.org/10.32737/0005-2531-2025-1-5-24.

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This review presents the results of studies on the reactivity of metal complexes with short-lived radicals (primarily peroxyl radicals) and metal complexes (mainly Cu(II) ions) with chelating nitroxide radicals. The reactions of newly synthesized paramagnetic ligands – Schiff bases derived from ortho-hydroxyaromatic aldehydes and two nitroxide radicals, 2,2,5,5-tetramethyl-3-amino-pyrrolidine-1-oxide and 2,2,6,6-tetramethyl-piperidine-4-amino-1-oxide – are discussed. It has been shown that in the derivative of the five-membered pyrrolidine radical, the radical center becomes part of the coordination sphere of the Cu(II) ion and is reduced to hydroxylamine. Ultimately, this leads to the formation of binuclear complexes with strong antiferromagnetic interactions between the Cu(II) ions. At room temperature, the resulting binuclear complexes interact with chloroform to abstract HCl and, with pyridine in the presence of oxygen, form paramagnetic mononuclear Cu(II) complexes. Separate sections of the review are devoted to catalytic oxidation reactions of alcohols and other substrates using metal complexes with nitroxide radicals (mainly TEMPO) as catalysts. Additionally, the catalytic reactions of metal complexes with phenoxyl radicals, which serve as biochemical models of the enzyme galactose oxidase, are discussed

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Prema. S, Prema S., i Leema Rose. A. "Metal Complexes of Phenyl Glycine-O-Carboxylic Acid: Preparation, Characterization, Electrochemical and Biological Properties". Oriental Journal Of Chemistry 38, nr 3 (30.06.2022): 698–708. http://dx.doi.org/10.13005/ojc/380321.

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Metal complexes are the effective therapeutic compound and it became more emerging field in the drug discovery and delivery. A novel ligand phenyl-glycine -o- carboxylic acid was synthesized and further complexed with the metal (II) chlorides. The synthesized metal complexes was interpreted by FT-IR spectroscopy, Ultra Violet- visible, 1H-NMR, molar conductance, magnetic susceptibility and thermogravimetric study. The electrochemical properties of the ligand and its complexes were inquired in DMF. Antibacterial and fungal activities of the phenyl-glycine -o- carboxylic acid (ligand) and metal complexes were analyzed by three fungal and four bacteria pathogens. The ligand has no activity against Aspergillus terreus, but nickel, copper and cobalt chloride complexes showed good activity against Aspergillus terreus. On anti-bacterial activity compare to ligands and other metal (II) complexes the cobalt (II) complex revealed greater inhibition effect on selected bacteria.

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Irfandi, Rizal, Indah Raya, Ahyar Ahmad, Ahmad Fudholi, Hasnah Natsir, Desy Kartina, Harningsih Karim, Santi Santi i Subakir Salnus. "Review on Anticancer Activity of Essential Metal Dithiocarbamate Complexes". Indonesian Journal of Chemistry 22, nr 6 (8.08.2022): 1722. http://dx.doi.org/10.22146/ijc.73738.

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The importance of essential metal ions and their metal complexes in the creation of prospective medical therapies has long been recognized. In chemistry, molecular biology, and medicinal fields; the interaction of metal complexes with DNA has been a subject of study. The dithiocarbamate essential metal complex is described extensively in the literature for its various benefits and advantages. With proper use of ligands, it is proven to increase the cytotoxic activity of metal complexes against cancer cells. Some researches have shown significant progress regarding the biological activities of the dithiocarbamate essential metal complex as antimicrobial, antioxidant, and anticancer agents. Metal complexes form complexes with dithiocarbamate ligands with unique structural variations. In this study, we presented an overview of the cytotoxic effects of some dithiocarbamate essential metal complexes on cancer cells, as well as fresh approaches to the design of essential metal-based therapeutics containing dithiocarbamate and molecular targets in cancer therapy. This review may provide an update on recent developments in the medicinal use of essential metals with dithiocarbamate ligands, carried out to identify recent relevant literature. Finally, we predict that the essential metal complexed with dithiocarbamate can be a new breakthrough in the future development of cancer drugs.

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Sridhar, M., P. Ramesh, K. Laxma Reddy, S. Durga, P. Muralidhar Reddy i A. Krishnam Raju. "Synthesis, Spectral Characterization and Biological, DNA Binding, Molecular Docking and ADMET Studies of a New Benzyl (Z)-N’-((E)- 3-Ethoxy-2-Hydroxybenzylidene) Carbamohydrazonothioate and Its Co (II), Ni (II), Cu (II) and Zn (II) Metal Complexes Derived From S-Benzyl Thiosemicabazide-Salicylaldehyde." INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 14, nr 03 (25.09.2024): 1469–78. http://dx.doi.org/10.25258/ijddt.14.3.30.

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This study presents the synthesis, characterization, and biological evaluation of metal complexes derived from benzyl carbamohydrazonothioate. The ligand was synthesized through a condensation reaction and subsequently complexed with various metal ions, including Cu(II), Ni(II), Co(II), and Zn(II). The resulting metal complexes were characterized using a range of spectroscopic techniques, including FT-IR, UV-Vis, and NMR spectroscopy, confirming the successful coordination of the metal ions with the ligand. The structural elucidation was further supported by elemental analysis and molar conductance measurements. The biological activities of the synthesized complexes were evaluated for their antibacterial, antifungal, and antioxidant properties. The results indicated that the metal complexes exhibited enhanced biological activities compared to the free ligand, suggesting their potential as effective antimicrobial and antioxidant agents. This study highlights the significance of metal complexation in enhancing the biological efficacy of organic ligands.

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Sumrra, Sajjad Hussain, Muhammad Ibrahim, Sabahat Ambreen, Muhammad Imran, Muhammad Danish i Fouzia Sultana Rehmani. "Synthesis, Spectral Characterization, and Biological Evaluation of Transition Metal Complexes of Bidentate N, O Donor Schiff Bases". Bioinorganic Chemistry and Applications 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/812924.

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New series of three bidentate N, O donor type Schiff bases(L1)–(L3)were prepared by using ethylene-1,2-diamine with 5-methyl furfural, 2-anisaldehyde, and 2-hydroxybenzaldehyde in an equimolar ratio. These ligands were further complexed with Co(II), Cu(II), Ni(II), and Zn(II) metals to produce their new metal complexes having an octahedral geometry. These compounds were characterized on the basis of their physical, spectral, and analytical data. Elemental analysis and spectral data of the uncomplexed ligands and their metal(II) complexes were found to be in good agreement with their structures, indicating high purity of all the compounds. All ligands and their metal complexes were screened for antimicrobial activity. The results of antimicrobial activity indicated that metal complexes have significantly higher activity than corresponding ligands. This higher activity might be due to chelation process which reduces the polarity of metal ion by coordinating with ligands.

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Iqbal, Pervez, i Kiran Aftab. "Study of Complexation Behaviour of Lignite Extracted Humic Acid with Some Divalent Cations". Engineering Science Letter 2, nr 03 (9.10.2023): 99–104. http://dx.doi.org/10.56741/esl.v2i03.431.

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In biogeochemical cycles, humic substances are natural electron shuttles in transforming nutrients and environmental pollutants. Humic acid complexes with macro and micronutrient metals are eco-friendly organo-mineral fertilisers. This study prepared and characterised lignite-extracted humic acid-metal (Fe, Mg, Zn) complexes. The proximate analysis exhibited the moisture, volatile matter, ash and fixed carbon contents of extracted humic acid of 02.61%, 17.31%, 57.18% and 22.90%, respectively. The percentage of metal ions in humic acid complexes ranges from 3.5-7.25%. The FTIR analysis of coal-extracted humic acids-metal complexes showed Zn, Mg and Fe ions complexed in a bidentate manner predominantly with the carboxylic acid moiety of humic acid. Thermal gravimetric analysis indicated a higher value of humic acid decomposition than their metal complexes. The thermal stability observed order is HA- Zn >HA-Fe>HA- Mg. The X-ray diffraction pattern pointed toward the noncrystalline nature of humic acid and their respective complexes due to having few intense and small diffuse peaks in the 2θ range from 0 to 80°. Hence, the humic acid-metals complexes increase the soil humic content and the availability of essential nutrients that enhance the loam's biotic action.

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NOMURA, Mitsushiro, Satoshi HORIKOSHI i Masatsugu KAJITANI. "Metal Dithiolene Complexes". Journal of the Japan Society of Colour Material 82, nr 7 (2009): 296–305. http://dx.doi.org/10.4011/shikizai.82.296.

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Trachevskii, V. V., S. V. Zimina i E. P. Rodina. "Thiosulfate metal complexes". Russian Journal of Coordination Chemistry 34, nr 9 (wrzesień 2008): 664–69. http://dx.doi.org/10.1134/s1070328408090066.

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Rozprawy doktorskie na temat "Metal complexes"

Brayshaw, Simon Keith. "Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes". University of Western Australia. School of Biomedical and Chemical Sciences, 2004. http://theses.library.uwa.edu.au/adt-WU2005.0017.

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This thesis is comprised of two parts. The first part describes the synthesis of cyclopentadienyltungsten complexes containing a pendant alkyne group (I), and the subsequent photo-induced intramolecular coordination of the alkyne, forming complexes such as II. Compounds containing intramolecularly coordinated alkynes are rare, and this is the first example using cyclopentadiene as the core ligand. The second part describes the synthesis and structural characterisation of a number of novel metal complexes containing N-heterocyclic carbene ligands, some containing particular functionality for taylored applications. New methods were used to form complexes of rhodium, iridium, silver and gold (eg. III, IV). Structural and spectroscopic properties of the complexes were correlated with electronic characteristics of the ancillary ligands. A number of rhodium and iridium complexes (eg. IV) derived from imidazolium-linked cyclophanes were synthesised and structurally characterised. Complexes of N-heterocyclic carbenes with pendant ionic groups were synthesised, and a preliminary examination of their catalytic activity in water was performed. N-Heterocyclic carbenes complexes containing an electron withdrawing nitro group were synthesised and the effect of the nitro group on metal-ligand bonding was examined.

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Barron, Andrew Ross. "Transition metal aluminohydride complexes". Thesis, Imperial College London, 1986. http://hdl.handle.net/10044/1/37935.

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Alem, Nassreen. "Zeolite encapsulated metal complexes". Thesis, University of Reading, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239055.

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Jasim, Naseralla. "Transition metal bifluoride complexes". Thesis, University of York, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323538.

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Ho, Kin-ying. "Synthesis, characterization and spectroscopic properties of d6 and d10 metal complexes with pyridyl amine ligands /". Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20667905.

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Jones, Simon C. "Metal-metal coupling in bi- and multimetallic systems : organometallic pentalene and group 14-bridged cyclopentadienyl complexes of transition metals". Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270635.

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Humphrey, Elizabeth Rebecca. "Tris(pyrazolyl)borate metal complexes : new ligands and metal-metal interactions". Thesis, University of Bristol, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340301.

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Zhao, Ningfeng Eichhorn David M. "Cyano-substituted polypyrazolylborate metal complexes". Diss., Click here for available full-text of this thesis, 2005. http://library.wichita.edu/digitallibrary/etd/2005/d019.pdf.

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Thesis (Ph.D.)--Wichita State University, College of Liberal Arts and Sciences, Dept. of Chemistry.
"December 2005." Title from PDF title page (viewed on February 8, 2007). Thesis adviser: David Eichhorn. Includes bibliographic references (leaves 123-128).

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Rao, Sumitrananda N. R. "Novel adsorbents using metal complexes". Thesis, Georgia Institute of Technology, 1993. http://hdl.handle.net/1853/10200.

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Felsher, Dave. "Electrowinning of metal - DETA complexes". Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33329.

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Sludges formed by lime treatment of acidic mine effluents are a widespread environmental hazard. One treatment option is to recover the toxic and potentially valuable contained metals. A method has been reported to selectively recover the metals by leaching with a complexing agent, diethylenetriamine (DETA). In this thesis a novel method has been developed to recover metals from the metal---DETA complexes by direct electrowinning. Copper was studied initially as a test system due to the relative ease with which it is recovered in conventional sulphate electrowinning. The main industrial interest, and hence the main focus of the work, is in the nickel---DETA system. For both metals, initially batch tests were run to determine acceptable electrowinning conditions. These were followed by recycle tests to simulate a potential process flowsheet. In the nickel-DETA system the effects of pH, nickel concentration, temperature, and DETA to nickel ratio on current efficiency were determined.
Recycle tests for copper showed that a steady DETA concentration was achieved after ca. six hours. In the case of nickel, the system seemed to continually deteriorate. A pH range of 4.6 to 4.8 maximized the current efficiency, due to a competition between hydrogen formation at low pH and increased complex stability at high pH. Both increasing Ni concentration and temperature increased the current efficiency, while increasing the DETA to nickel ratio lowered it.

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Książki na temat "Metal complexes"

Tomasik, Piotr. Pyridine-metal complexes. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. New York: Wiley, 1985.

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Hartley, F. R. Supported Metal Complexes. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5247-8.

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Voloshin, Yan, Irina Belaya i Roland Krämer. Cage Metal Complexes. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56420-3.

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Ciardelli, F., E. Tsuchida i D. Wöhrle, red. Macromolecule-Metal Complexes. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-60986-2.

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Tomasik, Piotr. Pyridine-metal complexes. Redaktorzy Ratajewicz Zbigniew, Newkome George R i Strekowski Lucjan. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Redaktorzy Ratajewicz Zbigniew, Newkome George R i Strekowski Lucjan. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Redaktorzy Ratajewicz Zbigniew, Newkome George R i Strekowski Lucjan. New York: Wiley, 1985.

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F, Ciardelli, Tsuchida E. 1930- i Wöhrle Dieter 1939-, red. Macromolecule-metal complexes. Berlin: Springer, 1996.

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Tomasik, Piotr. Pyridine-metal complexes. Redaktorzy Ratajewicz Zbigniew, Newkome George R i Strekowski Lucjan. New York: Wiley, 1985.

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Części książek na temat "Metal complexes"

Farrell, Nicholas. "Metals, Metal Complexes, and Radiation". W Transition Metal Complexes as Drugs and Chemotherapeutic Agents, 183–207. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-011-7568-5_9.

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Chaloner, Penny A., Miguel A. Esteruelas, Ferenc Joó i Luis A. Oro. "Supported Metal Complexes". W Catalysis by Metal Complexes, 241–53. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-017-1791-5_6.

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Markó, L., J. Takács, Kenton H. Whitmire, B. A. Matrana i H. D. Kaesz. "Trinuclear Metal Complexes". W Inorganic Syntheses, 243–46. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132579.ch42.

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Govindrajan, Subbiah, i Singanahally T. Aruna. "Hydrazinium Metal Complexes". W Inorganic Hydrazine Derivatives, 171–218. Chichester, United Kingdom: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch05.

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Ingraham, Llyod L., i Damon L. Meyer. "Metal-Dioxygen Complexes". W Biochemistry of Dioxygen, 113–20. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2475-1_8.

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Mishra, Munmaya, i Biao Duan. "Polymer Metal Complexes". W The Essential Handbook of Polymer Terms and Attributes, 168–69. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003161318-164.

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Hoffman, M. Z. "Of Metal Complexes". W Inorganic Reactions and Methods, 276–77. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145302.ch110.

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Gates, B. C. "Supported Metal Complexes". W Inorganic Reactions and Methods, 36–39. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch18.

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Rây, Priyadaranjan, i W. Conard Fernelius. "Metal Biguanide Complexes". W Inorganic Syntheses, 65–68. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132371.ch19.

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Wani, Mohmmad Younus, i Manzoor Ahmad Malik. "Anticancer Metal Complexes". W Gold and its Complexes in Anticancer Chemotherapy, 35–39. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6314-4_4.

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Streszczenia konferencji na temat "Metal complexes"

Arikawa, Yasuhiro, Kenichiro Omoto, Eri Sakuda, Keisuke Umakoshi i Motoki Yamada. "Reductive Conversion of Small Molecules on Transition Metal Complexes". W 2024 13th International Conference on Renewable Energy Research and Applications (ICRERA), 1444–46. IEEE, 2024. https://doi.org/10.1109/icrera62673.2024.10815323.

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Brewer, Karen J., Shawn Swavey, Rodd L. Williams, Zhenglai Fang i Elizabeth R. Bullock. "Designing mixed-metal supramolecular complexes". W Complex Adaptive Structures, redaktor William B. Spillman, Jr. SPIE, 2001. http://dx.doi.org/10.1117/12.446777.

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Lee, Taewoo, Christian Reich, Christopher M. Laperle, Xiaodi Li, Margaret Grant, Christoph G. Rose-Petruck i Frank Benesch-Lee. "Ultrafast XAFS of transition metal complexes". W International Conference on Ultrafast Phenomena. Washington, D.C.: OSA, 2006. http://dx.doi.org/10.1364/up.2006.wd4.

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Fukaya, Toshio, Masagi Mizuno, Shigeo Murata i Akihiro Mito. "THG properties of metal-dithiolene complexes". W OE/LASE '92, redaktorzy Robert A. Fisher i John F. Reintjes. SPIE, 1992. http://dx.doi.org/10.1117/12.58089.

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Hulubei, C., E. Hamciuc, M. Bruma i M. Ignat. "Polymer blends containing maleimide-metal complexes". W 2008 International Semiconductor Conference. IEEE, 2008. http://dx.doi.org/10.1109/smicnd.2008.4703401.

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Al-Khaykanee, Mohsin K., Faeq A. Al-Temimei, A. A. Al-Jobory, Dhay Ali Sabur i Hamid I. Abbood. "Thermoelectric properties of platinum metal complexes". W THE 7TH INTERNATIONAL CONFERENCE ON APPLIED SCIENCE AND TECHNOLOGY (ICAST 2019). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5123090.

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Singh, Nidhi, Satya, Kulsum Hashmi, Sakshi Gupta i Seema Joshi. "Cytotoxic Activity of Metal Nanoparticle Complexes". W ASEC 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/asec2023-15242.

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MOISEEV, ILYA I. "METAL COMPLEX CATALYSIS OF OXIDATION REACTIONS: CATALYSIS WITH PALLADIUM COMPLEXES". W Proceedings of the NIOK (Netherlands Institute for Catalysis Research) Course on Catalytic Oxidation. WORLD SCIENTIFIC, 1995. http://dx.doi.org/10.1142/9789814503884_0010.

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Swavey, Shawn, Rodd L. Williams, Zhenglai Fang, Matthew Milkevitch i Karen J. Brewer. "DNA binding of supramolecular mixed-metal complexes". W Complex Adaptive Structures, redaktor William B. Spillman, Jr. SPIE, 2001. http://dx.doi.org/10.1117/12.446779.

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Slinker, Jason, Dan Bernards, Samuel Flores-Torres, Stefan Bernhard, Paul L. Houston, Héctor D. Abruña i George G. Malliaras. "Light emitting diodes from transition metal complexes". W Frontiers in Optics. Washington, D.C.: OSA, 2003. http://dx.doi.org/10.1364/fio.2003.wnn2.

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Raporty organizacyjne na temat "Metal complexes"

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

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Cotton, F. A., i S. C. Haefner. Metal-metal multiply bonded complexes of technetium. Final report. Office of Scientific and Technical Information (OSTI), marzec 1995. http://dx.doi.org/10.2172/434856.

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Lawson, Chris M., i Gary M. Gray. New Metal Organic Nonlinear Optical Complexes. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2000. http://dx.doi.org/10.21236/ada391105.

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

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Fujita, Etsuko. Photoreduction of CO{sub 2} using metal complexes. Office of Scientific and Technical Information (OSTI), kwiecień 1996. http://dx.doi.org/10.2172/211478.

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Crosby, G. A. Investigations of charge-separation processes in metal complexes. Office of Scientific and Technical Information (OSTI), luty 1991. http://dx.doi.org/10.2172/5943145.

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Theopold, K. H. [Oxidation catalysis with tris(pyrazolyl)borate metal complexes]. Office of Scientific and Technical Information (OSTI), styczeń 1993. http://dx.doi.org/10.2172/6487292.

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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), styczeń 2003. http://dx.doi.org/10.2172/835301.

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

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Rubin, Yves F. Total Synthesis of Buckminsterfullerene (C60) and Endohedral Metal Complexes. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1997. http://dx.doi.org/10.21236/ada328578.

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