Academic literature on the topic 'Metal complexes Metal complexes Ligands'

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Journal articles on the topic "Metal complexes Metal complexes Ligands"

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Sethi, Pooja, Rajshree Khare, and Renuka Choudhary. "Complexes of Pyrimidine Thiones: Mechanochemical Synthesis and Biological Evaluation." Asian Journal of Chemistry 32, no. 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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Sumrra, Sajjad Hussain, Muhammad Ibrahim, Sabahat Ambreen, Muhammad Imran, Muhammad Danish, and 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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Pierpont, Cortlandt G., and Attia S. Attia. "Spin Coupling Interactions in Transition Metal Complexes Containing Radical o-Semiquinone Ligands. A Review." Collection of Czechoslovak Chemical Communications 66, no. 1 (2001): 33–51. http://dx.doi.org/10.1135/cccc20010033.

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Transition metal complexes ofo-semiquinone (SQ) ligands have been studied extensively over the past 25 years. A particularly interesting aspect of this coordination chemistry concerns magnetic interactions between paramagnetic metal ions and the radical anionic ligands. In this review we begin with a survey of relatively simple complexes consisting of a paramagnetic metal ion chelated by a single SQ ligand. Recent studies have revealed the importance of SQ-SQ coupling through diamagnetic metals, and complexes of this class are described in the second section of the review. Both interactions combine to account for the often complicated magnetic properties of complexes containing multiple SQ ligands chelated to a paramagnetic metal ion. Research on these complexes is surveyed in the third section with a concluding look toward polymeric SQ complexes. A review with 51 references.
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Salassa, Giovanni, and Alessio Terenzi. "Metal Complexes of Oxadiazole Ligands: An Overview." International Journal of Molecular Sciences 20, no. 14 (July 16, 2019): 3483. http://dx.doi.org/10.3390/ijms20143483.

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Oxadizoles are heterocyclic ring systems that find application in different scientific disciplines, from medicinal chemistry to optoelectronics. Coordination with metals (especially the transition ones) proved to enhance the intrinsic characteristics of these organic ligands and many metal complexes of oxadiazoles showed attractive characteristics for different research fields. In this review, we provide a general overview on different metal complexes and polymers containing oxadiazole moieties, reporting the principal synthetic approaches adopted for their preparation and showing the variety of applications they found in the last 40 years.
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Mustapha, Abdullahi, John Reglinski, and Alan R. Kennedy. "Metal complexes as potential ligands: The deprotonation of aminephenolate metal complexes." Inorganic Chemistry Communications 13, no. 4 (April 2010): 464–67. http://dx.doi.org/10.1016/j.inoche.2010.01.009.

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Garnovskii, A. D., B. I. Kharisov, L. M. Blanco, A. P. Sadimenko, A. I. Uraev, I. S. Vasilchenko, and D. A. Garnovskii. "Review: Metal Complexes as Ligands." Journal of Coordination Chemistry 55, no. 10 (January 1, 2002): 1119–34. http://dx.doi.org/10.1080/0095897021000022195.

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Buchler, Johann W., Frank M. K�nzel, Uwe Mayer, and Michaela Nawra. "Metal complexes with tetrapyrrole ligands." Fresenius' Journal of Analytical Chemistry 348, no. 5-6 (1994): 371–76. http://dx.doi.org/10.1007/bf00323137.

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Enders, Dieter, Heike Gielen, and Klaus Breuer. "Axial Chirality in Square-Planar Metal Complexes." Zeitschrift für Naturforschung B 53, no. 9 (September 1, 1998): 1035–38. http://dx.doi.org/10.1515/znb-1998-0916.

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Metal complexes with a square-planar arrangement of ligands are frequently found for the late Transition Metals. The incorporation of C1-symmetrical planar ligands (e.g. nucleophilic carbenes) in an orientation perpendicular to the square-plane of the complex leads to various isomers which are characterized by means of an axis of chirality employing the well established Cahn-Ingold-Prelog -R/S-nomenclature.
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Bruce, MI, and AH White. "Some Chemistry of Pentakis(methoxycarbonyl)cyclopentadiene, HC5(CO2Me)5, and Related Molecules." Australian Journal of Chemistry 43, no. 6 (1990): 949. http://dx.doi.org/10.1071/ch9900949.

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This article summarizes the results of investigations into the chemistry of HC5(CO2Me)5 and, in particular, of metal complexes containing the C5(CO2Me)5 ligand . As an anion, the ligand is very stable, forming air-stable, water-soluble salts with many cations with coordination to the metal atom in the solid state generally occurring through the ester carbonyl groups. Second- and third-row transition metals form complexes which retain the covalent ligand-metal bond in solution, 'harder' metals coordinating by the ester carbonyl groups, while 'softer' metals are bound to the ring carbons; a variety of behaviour is shown by the Group 11 metals. Even when the ligand is η5-bonded to the metal, ready displacement by other ligands may occur, as found with Ru (η-C5H5){η5-C5(CO2Me)5}, for example. In the rhodium system, formal replacement of CO2Me groups by hydrogen is found, as with the formation of [ Rh {η5-C5H2(CO2Me)3}2][C5(CO2Me)5]. Brief mention is made of other polysubstituted cyclopentadienyls with electron-withdrawing ligands and some related compounds, and their metal derivatives where known.
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Mamedova, Shafa Agаеvna. "METAL COMPLEX CATALYSIS." Globus 7, no. 5(62) (August 4, 2021): 31–33. http://dx.doi.org/10.52013/2658-5197-62-5-7.

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Complexes of transition metals with chiral ligands are considered as catalysts. Among metal-containing organic complexes with semiconducting properties, compounds of the porphin series occupy a special place in electrocatalytic studies. The properties of the porphyrin macrocycle, their role in catalysis, and the influence of the nature of the metal on the catalytic properties of the complex are considered.
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Dissertations / Theses on the topic "Metal complexes Metal complexes Ligands"

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Cheung, Wai Man. "Transition metal complexes with dichalcogenoimidodiphosphinate ligands /." View abstract or full-text, 2007. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202007%20CHEUNG.

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McHugh, Paul. "Oligonuclear metal complexes of compartmental ligands." Thesis, University of Sheffield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408313.

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Onyiriuka, Emmanuel C. "Pyrazolyl ligands in mixed metal complexes." Thesis, University of British Columbia, 1986. http://hdl.handle.net/2429/27178.

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The anions LMo(CO)₃⁻ (L = MeGapz₃ or MeGa(3,5-Me₂pz)₃) have been isolated as the Na⁺, Et₄N⁺ or HAsPh₃⁺ salts and the solution structures of the Na⁺ salts in THF have been defined by analysis of the v[sub CO] ir spectra. Ion-pair interaction of the LMo(CO)₃⁻ anion with Na⁺cation in THF solution is apparent from the spectroscopic evidence obtained. The MeGapz₃Mo(CO)₃ ⁻anion reacted with HCl or EtBr to give the seven-coordinate [MeGapz₃]-Mo(CO)₃R (R = H or Et) complexes. However, with Mel or PhCOCl complexes of the type [MeGapz₃]Mo(CO)₂(n₂-COR) (R = Me or Ph) were obtained. The reactions of the LMo(CO)₃⁻ ions (L = MeGapz₃ HBpz₃ or Me₂Gapz(0-CH₂CH₂NMe₂)) with a variety of transition metal halide species have yielded complexes with transition metal-transition metal bonds. The X-ray crystal structures of two such complexes [MeGapz₃]Mo(CO)₃Cu(PPh₃) and [MeGapz₃]Mo-(CO)₃Rh(PPh₃)₂ have been determined. The former complex provides a rare example of a 3:3:1, or capped octahedral structure, with a short (mean) Mo-Cu distance of 2.513(9)Å. The latter compound displays one terminal and two bridging CO ligands and a Mo-Rh distance of 2.6066(5)Å. Transition metal-group 14 (Si, Ge or Sn) element bonded complexes of the type [MeGapz₃]Mo(CO) ₃M'Y (Y = Me₃ or Ph₃, M' = Ge or Sn; Y = Me₃, M' = Si; Y = Me₂Cl, M' = Sn) have been prepared from the reaction of the MeGapz₃Mo(CO)₃anion with the appropriate organo-group 14 chloride. In all the complexes, direct Mo-M' (M' = Si, Ge or Sn) single bonds are featured. The [MeGapz₃]Mo(CO) ₃SnMe₂Cl complex shows an interesting solution behaviour in which a transition from a 3:4, or piano stool structure, to a 3:3:1, or capped octahedral arrangement, is thought to occur. The 3:3:1 structure has been demonstrated in the solid state for the [MeGapz₃]Mo(CO)₃SnPh₃ compound by means of a crystal structure determination. The 'Mo-SnPh₃' and the 'Mo-Cu' compounds discussed in this work are the first examples of such complexes incorporating either the MeGapz₃⁻, HBpz₃⁻ or C₅H₅⁻ ligands in which the 3:3:1 arrangement has been demonstrated unequivocally. The novel tridentate unsymmetric ligands Me₂GapzO(C₅H₃N)CH₂NMe₂⁻ (L[sub a]⁻) and Me₂GapzO(C₉H₆N)⁻ (L[sub q]⁻) have been prepared and numerous transition metal compounds containing these ligands synthesized. The compounds L[sub a] M(CO)₃(M = Mn or Re) are the first examples of transition metal carbonyl complexes in which both the fac and mer arrangements of the unsymmetric ligand about the central metal have been found to co-exist in solution. The square planar rhodium(I) complex, L[sub q]Rh(CO) has been shown to add Mel oxidatively, followed by facile methyl migration reaction to produce the five-coordinate Rh(III) acetyl derivative, L[sub q]Rh(COMe)I. In contrast, the reaction of L[sub a]Rh(CO) with Mel, led to the six-coordinate Rh(III) oxidative addition product, L[sub a]Rh(Me)(I)CO.
Science, Faculty of
Chemistry, Department of
Graduate
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Crofts, Rhona D. "Platinum metal complexes of macrocyclic ligands." Thesis, University of Edinburgh, 1995. http://hdl.handle.net/1842/13493.

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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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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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Stewart, Peter John. "Metal-ligand multiply bonded complexes supported by amidinate ligands." Thesis, University of Nottingham, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243747.

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Dubberley, Stuart R. "New calix[4]arene metal complexes." Thesis, University of Oxford, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365290.

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Lam, Chong Ho. "Metal complexes containing oxygen tripod ligands : models of metal oxides /." View Abstract or Full-Text, 2003. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202003%20LAMC.

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Thesis (Ph. D.)--Hong Kong University of Science and Technology, 2003.
Includes bibliographical references (leaves 275-290). Also available in electronic version. Access restricted to campus users.
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Landman, Marile. "Synthesis of metal complexes with thiophene ligands." Thesis, Access to E-Thesis, 2000. http://upetd.up.ac.za/thesis/available/etd-12042006-143722/.

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Books on the topic "Metal complexes Metal complexes Ligands"

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Buchler, J. W., ed. Metal Complexes with Tetrapyrrole Ligands II. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/3-540-52899-7.

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Buchler, Johann Walter, ed. Metal Complexes with Tetrapyrrole Ligands I. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/bfb0036788.

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Lane, H. P. Transition metal complexes of group fifteen donor ligands. Manchester: UMIST, 1994.

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Chauvin, Remi, and Yves Canac, eds. Transition Metal Complexes of Neutral eta1-Carbon Ligands. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-04722-0.

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Kühl, Olaf. Functionalised N-heterocyclic carbene complexes. Hoboken, N.J: Wiley, 2009.

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Kühl, Olaf. Functionalised N-heterocyclic carbene complexes. Chichester, U.K: Wiley, 2010.

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Functionalised N-heterocyclic carbene complexes. Hoboken, N.J: Wiley, 2009.

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Kühl, Olaf. Functionalised N-heterocyclic carbene complexes. Hoboken, N.J: Wiley, 2009.

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Transition metal complexes of neutral [Eta]1-carbon ligands. Heidelberg: Springer Verlag, 2010.

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Hawkins, Ian Michael. New transition metal complexes containing phosphine and sulphur ligands. Norwich: University of East Anglia, 1988.

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Book chapters on the topic "Metal complexes Metal complexes Ligands"

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Martell, Arthur E., and Robert D. Hancock. "Chelating Ligands." In Metal Complexes in Aqueous Solutions, 63–95. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1486-6_3.

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Guerchais, Véronique, and Hubert Le Bozec. "Metal Complexes Featuring Photochromic Ligands." In Topics in Organometallic Chemistry, 171–225. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01866-4_6.

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McGuinness, David S. "Cr Complexes of Nitrogen Donor Ligands for Olefin Oligomerisation and Polymerisation." In Catalysis by Metal Complexes, 1–26. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3815-9_1.

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Mayr, A. "The Role of Nucleophiles and Electrophiles in Coupling Reactions of Alkylidyne Ligands." In Transition Metal Carbyne Complexes, 219–30. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1666-4_25.

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Lungwitz, B., and A. C. Filippou. "Electron-Rich Tungsten Aminocarbyne Complexes with Cp* Ligands Synthesis and Protonation Reactions." In Transition Metal Carbyne Complexes, 249–54. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1666-4_28.

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Trifonov, Alexander A. "Rare-Earth Metal Complexes Supported by Nitrogen-Containing Ligands in Olefin Polymerization." In Catalysis by Metal Complexes, 119–52. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3815-9_3.

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Dzhardimalieva, Gulzhian I., and Igor E. Uflyand. "Metal Complexes with Polymer Chelating Ligands." In Chemistry of Polymeric Metal Chelates, 199–366. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-56024-3_3.

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Yamada, Jun-ichi, and Toyonari Sugimoto. "TTFs as Ligands of Metal Complexes." In TTF Chemistry, 155–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-10630-3_7.

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Cotton, F. A., and C. M. Lukehart. "Transition Metal Complexes Containing Carbenoid Ligands." In Progress in Inorganic Chemistry, 487–613. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166178.ch3.

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Liu, Chen-Wei, and J. Derek Woollins. "Metal Complexes Containing P-Se Ligands." In Selenium and Tellurium Chemistry, 303–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-20699-3_13.

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Conference papers on the topic "Metal complexes Metal complexes Ligands"

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Ayadi, A., K. El Korchi, D. Guichaoua, S. Taboukhat, and A. El-Ghayoury. "Azo-Based Ligands and Metal Complexes for NLO Applications." In 2019 21st International Conference on Transparent Optical Networks (ICTON). IEEE, 2019. http://dx.doi.org/10.1109/icton.2019.8840333.

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Palopoli, Stephen F., and Thomas B. Brill. "Synthesis And Thermolysis Of Metal Complexes Containing Energetic Ligands." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by Joseph Flanagan. SPIE, 1988. http://dx.doi.org/10.1117/12.943744.

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Sahraoui, Bouchta, Konstantinos Iliopoulos, and Abdelkrim El-Ghayoury. "NLO investigations of electroactive ligands and of their electroactive metal complexes." In 2013 15th International Conference on Transparent Optical Networks (ICTON). IEEE, 2013. http://dx.doi.org/10.1109/icton.2013.6602961.

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Gale, David C., Gary M. Gray, and Christopher M. Lawson. "Nonlinear optical properties of metal-organic complexes with phosphorous-donor ligands." In Optical Science, Engineering and Instrumentation '97, edited by Christopher M. Lawson. SPIE, 1997. http://dx.doi.org/10.1117/12.284168.

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Gude, Lourdes, Katerina Duskova, Sara Sierra, María-José Fernández, and Antonio Lorente. "Synthesis of 2,2'-bipyridine metal complexes as potential G-quadruplex DNA ligands." In XVth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112330.

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Cannizzo, Andrea, Franziska Frei, Thomas Feurer, Ahmad Odeh, Frank van Mourik, Majed Chergui, Davide Espa, et al. "Ultrafast Electronic Relaxations in Metal Mixed-Ligand Dithiolene Complexes." In International Conference on Ultrafast Structural Dynamics. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/icusd.2012.im3d.4.

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Morris, J. B., and M. V. Johnston. "Multiphoton ioniztion of metal β-diketonates and metal tetraphenylporphyrin complexes: Ligand dissociation vs. molecular ionization." In AIP Conference Proceedings Volume 146. AIP, 1986. http://dx.doi.org/10.1063/1.35926.

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Tobysheva, P. D., L. A. Khamidullina, I. S. Puzyrev, and A. V. Pestov. "Biological activity of complexes based on polycarbonyl ligands: assessment of the mode of action using molecular docking." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.249.

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Avramenko, Valentin, Vitaly Mayorov, Dmitry Marinin, Alexander Mironenko, Marina Palamarchuk, and Valentin Sergienko. "Macroporous Catalysts for Hydrothermal Oxidation of Metallorganic Complexes at Liquid Radioactive Waste Treatment." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40186.

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One of the main problems of liquid radioactive waste (LRW) management is concerned with treatment of decontamination waters containing organic ligands. The organic ligands like oxalic, citric and ethylenediaminetetraacetic acids form stable complexes with radionuclides which puts restrictions on application of many technologies of LRW management. One of the ways of destruction of metallorganic complexes consists in using the catalytic oxidation. However, the heterophase catalytic oxidation is rather problematic due to formation of metal oxides on the catalyst surface and calmatation of meso- and micropores. A possible solution of the above problem can be found in synthesis of macroporous catalysts for oxidation having a regular macroporous structure. The present paper describes the template synthesis of macroporous metalloxide catalysts performed with using siloxane-acrylate microemulsions as templates. The method for impregnation of precious metals (PM) particles into the template, which enables one to produce PM nanoparticles of a specific size and immobilize them in the porous structure of the synthesized metalloxide catalysts, is presented. A possible mechanism of the synthesis of macroporous catalysts is suggested and the comparison of the electronic and photon-correlation spectroscopy results obtained at different stages of catalysts synthesis was conducted.
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Dhindsa, Ajaib S., Allan E. Underhill, Stephen N. Oliver, and Stephen V. Kershaw. "Third-order NLO properties of metal complexes containing delocalized oxygen or sulphur donor ligands and mixed oxygen and sulphur donor ligands." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Carl M. Lampert, Satyen K. Deb, and Claes-Goeran Granqvist. SPIE, 1995. http://dx.doi.org/10.1117/12.217353.

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Reports on the topic "Metal complexes Metal complexes Ligands"

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Rakowski-DuBois, Mary C. Aspects of C-H Activation in Metal Complexes Containing Sulfur Ligands. Office of Scientific and Technical Information (OSTI), October 2004. http://dx.doi.org/10.2172/833244.

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Reynolds, Michael. Transition Metal Complexes of Cr, Mo, W and Mn Containing η1(S)-2,5-Dimethylthiophene, Benzothiophene and Dibenzothiophene Ligands. Office of Scientific and Technical Information (OSTI), September 2000. http://dx.doi.org/10.2172/764616.

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Burns, C. J., D. S. J. Arney, R. C. Schnabel, B. P. Warner, B. E. Bursten, J. C. Green, and T. J. Marks. Metal-ligand ``multiple`` bonding: Revelations in the electronic structure of complexes of high-valent f-elements. Office of Scientific and Technical Information (OSTI), July 1997. http://dx.doi.org/10.2172/505372.

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Kubas, G. J., J. Eckert, and X. L. Luo. Binding of hydrocarbons and other extremely weak ligands to transition metal complexes that coordinate hydrogen: Investigation of cis-interactions and delocalized bonding involving sigma bonds. Office of Scientific and Technical Information (OSTI), July 1997. http://dx.doi.org/10.2172/505275.

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

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

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

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Davis, Benjamin. REDOX FLOW BATTERY HAVING METAL-LIGAND COMPLEX. Office of Scientific and Technical Information (OSTI), December 2020. http://dx.doi.org/10.2172/1739916.

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Sharp, P. R. Late transition metal oxo and imido complexes. Office of Scientific and Technical Information (OSTI), December 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), April 1996. http://dx.doi.org/10.2172/211478.

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