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Relevant bibliographies by topics / Transition metal complexes. Phosphorescence

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Academic literature on the topic 'Transition metal complexes. Phosphorescence'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Transition metal complexes. Phosphorescence"

1

Chia, Y. Y., and M. G. Tay. "An insight into fluorescent transition metal complexes." Dalton Trans. 43, no. 35 (2014): 13159–68. http://dx.doi.org/10.1039/c4dt01098a.

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Three types of fluorescent emissions were found in the transition metal complexes namely pure fluorescence, thermal activated delayed fluorescence and fluorescence-phosphorescence dual emissions. The characteristics of these fluorescent emissions are reviewed in this perspective.

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Sathish, Veerasamy, Arumugam Ramdass, Pounraj Thanasekaran, Kuang-Lieh Lu, and Seenivasan Rajagopal. "Aggregation-induced phosphorescence enhancement (AIPE) based on transition metal complexes—An overview." Journal of Photochemistry and Photobiology C: Photochemistry Reviews 23 (June 2015): 25–44. http://dx.doi.org/10.1016/j.jphotochemrev.2015.04.001.

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Wang, Junsi, Yue Lu, Niamh McGoldrick, Caishun Zhang, Wenbo Yang, Jianzhang Zhao, and Sylvia M. Draper. "Dual phosphorescent dinuclear transition metal complexes, and their application as triplet photosensitizers for TTA upconversion and photodynamic therapy." Journal of Materials Chemistry C 4, no. 25 (2016): 6131–39. http://dx.doi.org/10.1039/c6tc01926a.

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Wang, Bei-Bei, Huiping Zuo, John Mack, Poulomi Majumdar, Tebello Nyokong, Kin Shing Chan, and Zhen Shen. "Optical properties and electronic structures of axially-ligated group 9 porphyrins." Journal of Porphyrins and Phthalocyanines 19, no. 08 (August 2015): 973–82. http://dx.doi.org/10.1142/s108842461550073x.

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A series of group 9 metal tetra-(p-tolyl)-porphyrin ( M(ttp) , M = Co(II) , Rh(III) , Ir(III)) complexes with axial phenyl substituents have been synthesized and characterized. An aryl bromide cleavage reaction of transition metal complexes was used to prepare the complexes from Co(ttp) , Rh(ttp) Cl and Ir(ttp)COCl , respectively. Magnetic circular dichroism (MCD) spectroscopy and TD-DFT calculations have been used to study trends in the optical spectra and electronic structures. The effect of introducing different para-substituents on the phenyl substituents was examined. During fluorescence emission studies, phosphorescence was observed for the Ir(III) complexes in the near infrared (NIR) region.

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Li, Zhi-Feng, Xiao-Ping Yang, Hui-Xue Li, and Guo-Fang Zuo. "Phosphorescent Modulation of Metallophilic Clusters and Recognition of Solvents through a Flexible Host-Guest Assembly: A Theoretical Investigation." Nanomaterials 8, no. 9 (September 2, 2018): 685. http://dx.doi.org/10.3390/nano8090685.

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MP2 (Second order approximation of Møller–Plesset perturbation theory) and DFT/TD-DFT (Density functional theory/Time-dependent_density_functional_theory) investigations have been performed on metallophilic nanomaterials of host clusters [Au(NHC)2]+⋅⋅⋅[M(CN)2]−⋅⋅⋅[Au(NHC)2]+ (NHC = N-heterocyclic carbene, M = Au, Ag) with high phosphorescence. The phosphorescence quantum yield order of clusters in the experiments was evidenced by their order of μS1/ΔES1−T1 values ( μ S 1 : S0 → S1 transition dipole, ∆ E S 1 − T 1 : splitting energy between the lowest-lying singlet S1 and the triplet excited state T1 states). The systematic variation of the guest solvents (S1: CH3OH, S2: CH3CH2OH, S3: H2O) are employed not only to illuminate their effect on the metallophilic interaction and phosphorescence but also as the probes to investigate the recognized capacity of the hosts. The simulations revealed that the metallophilic interactions are mainly electrostatic and the guests can subtly modulate the geometries, especially metallophilic Au⋅⋅⋅M distances of the hosts through mutual hydrogen bond interactions. The phosphorescence spectra of hosts are predicted to be blue-shifted under polar solvent and the excitation from HOMO (highest occupied molecular orbital) to LUMO (lowest unoccupied molecular orbital) was found to be responsible for the 3MLCT (triplet metal-to-ligand charge transfer) characters in the hosts and host-guest complexes. The results of investigation can be introduced as the clues for the design of promising blue-emitting phosphorescent and functional materials.

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Liang, Ai-Hua, Fu-Quan Bai, Jian Wang, Jian-Bo Ma, and Hong-Xing Zhang. "Theoretical Studies on Phosphorescent Materials: The Conjugation-Extended PtII Complexes." Australian Journal of Chemistry 67, no. 10 (2014): 1522. http://dx.doi.org/10.1071/ch14032.

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A theoretical study on the PtII complex A based on a dimesitylboron (BMes2)-functionalized [Pt(C^N)(acac)] (C^N = 2-phenyl-pyridyl, acac = acetylaceton) complex, as well as three conjugation-extended analogues of the methylimidazole (C*) ligand BMes2-[Pt(C^C*)(acac)] complexes B–D is performed. Their theoretical geometries, electronic structures, emission properties, and the radiative decay rate constants (kr) were also investigated. The energy differences between the two highest occupied orbitals with dominant Pt d-orbital components (Δddocc) of D both at the ground and excited states are the smallest of all. Compared with B, the charge transfer in D possesses a marked trend towards the extended conjugated group, while C changed inconspicuously. The lowest-lying absorptions and the phosphorescence of them can be described as a mixed metal-to-ligand charge transfer (MLCT)/intra-ligand π→π* charge transfer (ILCT) and 3MLCT/3ILCT, respectively. The variation of charge transfer properties induced by extended conjugation and the radiative decay rate constants (kr) calculated revealed that D is a more efficient blue phosphorescence material with a 497 nm emission transition.

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Li, Kai, Yong Chen, Jian Wang, and Chuluo Yang. "Diverse emission properties of transition metal complexes beyond exclusive single phosphorescence and their wide applications." Coordination Chemistry Reviews 433 (April 2021): 213755. http://dx.doi.org/10.1016/j.ccr.2020.213755.

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Chen, Hsing-Yi, Cheng-Han Yang, Yun Chi, Yi-Ming Cheng, Yu-Shan Yeh, Pi-Tai Chou, Hsi-Ying Hsieh, Chao-Shiuan Liu, Shie-Ming Peng, and Gene-Hsiang Lee. "Room-temperature NIR phosphorescence of new iridium (III) complexes with ligands derived from benzoquinoxaline." Canadian Journal of Chemistry 84, no. 2 (February 1, 2006): 309–18. http://dx.doi.org/10.1139/v05-253.

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A new series of new iridium (III) complexes (15) bearing ligands derived from benzoquinoxaline were designed and synthesized. X-ray structural analyses of 1 reveal a distorted octahedral geometry around the Ir atom in which the pyrazolate chelate is located opposite to the cis-oriented carbon donor atoms of benzoquinoxaline, while the benzoquinoxaline ligands adopt an eclipse configuration and their coordinated nitrogen atoms and carbon adopt trans- and cis-orientation, respectively. Complexes 15 exhibit moderate NIR phosphorescence with peak maxima located at around 910930 nm. As supported by the TDDFT approach, the transition mainly involves benzoquinoxaline 3ππ* intraligand charge transfer (ILCT) and metal (Ir) to benzoquinoxaline charge transfer (MLCT) of which the spectroscopy and dynamics of relaxation have been thoroughly investigated. The relatively weak NIR emission can be tentatively rationalized by the low energy gap of which the radiationless deactivation may be governed by nearly temperature-independent, weak-bonding motions in combination with a minor channel incorporating small torsional motions associated with phenyl ring in the benzoquinoxaline sites.Key words: phosphorescence, NIR, iridium, benzoquinoxaline, isoquinoline, bipyridine, pyrazolate, acetylacetonate.

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Wang, Xue-Mei, Jia-Yan Qiang, Ai-Quan Jia, Bihai Tong, and Qian-Feng Zhang. "Syntheses, crystal structures and phosphorescence properties of cyclometalated iridium(III) bis(pyridylbenzaldehyde) complexes with dithiolate ligands." Zeitschrift für Naturforschung B 72, no. 12 (December 20, 2017): 941–46. http://dx.doi.org/10.1515/znb-2017-0105.

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AbstractThe synthesis of three neutral bis-cyclometalated iridium(III) complexes [Ir(pba)2(S^S)] (pbaH=4-(2-pyridyl)benzaldehyde; S^S=Et2NCS2− (1), iPrOCS2− (2), (nPrO)2PS2− (3)) from [{Ir(μ-Cl)(pba)2}2] and the corresponding sodium or potassium dithiolates in methanol-dichloromethane is described. The composition of complexes 1–3 is discussed on the basis of 1H NMR, 13C NMR, IR, and mass spectroscopy, and the crystal structures of 1 and 3 were determined by X-ray crystallography. The absorption and emission spectra show that the [Ir(pba)2(S^S)] complexes may be effective candidates as green-emitting phosphorescent materials. The stability of the three cyclometalated iridium(III) complexes towards different transition metal ions was also investigated in acetonitrile-water solvent.

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Connell, Timothy U., and Paul S. Donnelly. "Labelling proteins and peptides with phosphorescent d6 transition metal complexes." Coordination Chemistry Reviews 375 (November 2018): 267–84. http://dx.doi.org/10.1016/j.ccr.2017.12.001.

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Dissertations / Theses on the topic "Transition metal complexes. Phosphorescence"

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Carlson, William Brenden. "The design, synthesis, characterization, and application of phosphorescent metal complexes /." Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/8548.

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Sinha, Pankaj. "Phosphorescent Emissions of Coinage Metal-Phosphine Complexes: Theory and Photophysics." Thesis, University of North Texas, 2009. https://digital.library.unt.edu/ark:/67531/metadc12200/.

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The major topics discussed are all relevant to the bright phosphorescent emissions of coinage metal complexes (Cu(I), Ag(I) and Au(I)) with an explanation of the theoretical background, computational results and ongoing work on the application in materials and optoelectronic devices. Density functional computations have been performed on the majority of the discussed complexes and determined that the most significant distortion that occurs in Au(I)-phosphine complexes is a near and beyond a T-shape within the P-Au-P angle when the complexes are photoexcited to the lowest phosphorescent excited state. The large distortion is experimentally qualified with the large Stokes' shift that occurs between the excitation and emission spectra and can be as large as 18 000 cm-1 for the neutral Au(I) complexes. The excited state distortion has been thoroughly investigated and it is determined that not only is it pertinent to the efficient luminescence but also for the tunability in the emission. The factors that affect tunability have been determined to be electronics, sterics, rigidity of solution and temperature. The luminescent shifts determined from varying these parameters have been described systematically and have revealed emission colors that span the entire visible spectrum. These astounding features that have been discovered within studies of coinage metal phosphorescent complexes are an asset to applications ranging from materials development to electronics.

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Sinha, Pankaj Omary Mohammad A. "Phosphorescent emissions of coinage metal-phosphine complexes theory and photophysics /." [Denton, Tex.] : University of North Texas, 2009. http://digital.library.unt.edu/ark:/67531/metadc12200.

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Hedley, Gordon J. "Ultrafast photophysics of iridium complexes." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/1981.

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This thesis presents ultrafast photophysical measurements on a number of phosphorescent iridium complexes and establishes relationships between the relaxation rates and the vibrational properties of the material. When ultrafast luminescence is measured on the peak of the phosphorescence spectrum and on its red-side, 230 fs and 3 ps decay time constants were observed in all materials studied, and this was attributed to population redistribution amongst the three electronic substates of the lowest triplet metal-ligand charge transfer (MLCT) state. The observation of luminescence at higher values of energy embodied ultrafast dissipation of excess energy by intramolecular vibrational redistribution (IVR) and it was found that the dissipation channels and rate of IVR could be modified by chemical modification of the emitting molecule. This was tested in two ways. Firstly by adding electronically inactive dendrons to the core, an increase in the preference for dissipation of excess energy by IVR rather than by picosecond cooling to the solvent molecules was found, but this did not change the rate of IVR. The second method of testing was by fusing a phenyl moiety directly onto the ligand, this both increased the rate of IVR and also the preference for dissipation by it rather than by picosecond cooling. Fluorescence was recorded in an iridium complex for the first time and a decay time constant of 65 fs was found, thus allowing a direct observation of intersystem crossing (ISC) to be made. In a deep red emitting iridium complex internal conversion (IC) and ISC were observed and the factors controlling their time constants deduced. IC was found to occur by dissipation of excess energy by IVR. The rate of IC was found to be dependent on the amount of vibrational energy stored in the molecule, with IC fast (< 45 fs) when < 0.6 eV of energy is stored and slower (~ 70 fs) when the value is > 0.6 eV. The rate of ISC agreed with these findings, indicating that the very process of ISC may be thought of as closely analogous to that of IC given the strongly spin-mixed nature of the singlet and triplet MLCT states.

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Sinha, Pankaj Omary Mohammad A. "A computational investigation of the photophysical, electronic and bonding properties of exciplex-forming Van Der Waals System." [Denton, Tex.] : University of North Texas, 2007. http://digital.library.unt.edu/permalink/meta-dc-5121.

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Liu, Shuang Ph D. Massachusetts Institute of Technology. "Design and synthesis of cyclometalated transition metal complexes as functional phosphorescent materials." Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/73364.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2012.
Vita. Cataloged from PDF version of thesis.
Includes bibliographical references.
Cyclometalated Ir(III) and Pt(II) compounds are among the most promising phosphorescent emitters for various applications, such as organic light emitting diodes (OLEDs), chemical sensors and bioimaging labels. This family of complexes exhibits high thermal and photo-stability, excellent quantum efficiency, and relatively short lifetime. More importantly, their luminescent properties can be fully tunable by modifying the coordinating ligands. In this thesis, a series of 2-(1,2,3-triazol-4-yl)-pyridine derivatives, referred to as the "click" ligands, are used to build phosphorescent Ir(III) and Pt(II) compounds. The robust and tolerant nature of the copper mediated 1,3-dipolar cycloaddition reactions offers great flexibility in the molecular design. Chapter 1 and Chapter 2 focus on the synthesis of heteroleptic cyclometalated Ir (III) and Pt(II) complexes by utilizing the Cu(I) triazolide intermediates generated in "click" reactions as transmetalating reagents. Ligand synthesis and metalation can be achieved in one pot under mild reaction conditions. For the Ir(III) system, the "click" ligands show switchable coordination modes, between the C, N- and N, N-chelation. These ligands act as C, N, N-bridging units to form unique zwitterionic dinuclear complexes with two cyclometalated Pt(II) units. In Chapter 3, cyclometalated Pt(II) complexes with N, N-chelating "click" ligands are synthesized. Their aggregation-induced solid-state emission is highly responsive to environmental stimuli, such as solvents, heat and mechanical force. This family of compounds represents the first thermotropic Col(h) liquid crystals with only one sidechain. Furthermore, the combined liquid crystalline and mechanochromic properties make them attractive functional materials.
by Shuang Liu.
Ph.D.

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Sinha, Pankaj. "A Computational Investigation of the Photophysical, Electronic and Bonding Properties of Exciplex-Forming Van der Waals Systems." Thesis, University of North Texas, 2007. https://digital.library.unt.edu/ark:/67531/metadc5121/.

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Calculations were performed on transition-metal complexes to (1) extrapolate the structure and bonding of the ground and phosphorescent states (2) determine the luminescence energies and (3) assist in difficult assignment of luminescent transitions. In the [Pt(SCN)4]2- complex, calculations determined that the major excited-state distortion is derived from a b2g bending mode rather than from the a1g symmetric stretching mode previously reported in the literature. Tuning of excimer formation was explained in the [Au(SCN)2]22- by interactions with the counterion. Weak bonding interactions and luminescent transitions were explained by calculation of Hg dimers, excimers and exciplexes formed with noble gases.

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

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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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Books on the topic "Transition metal complexes. Phosphorescence"

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

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

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Molecular electronic structures of transition metal complexes. Heidelberg: Springer, 2012.

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Roundhill, D. M. Photochemistry and photophysics of metal complexes. New York: Plenum Press, 1994.

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Book chapters on the topic "Transition metal complexes. Phosphorescence"

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Zhang, Kenneth Yin, Shujuan Liu, Qiang Zhao, Fuyou Li, and Wei Huang. "Phosphorescent Iridium(III) Complexes for Bioimaging." In Luminescent and Photoactive Transition Metal Complexes as Biomolecular Probes and Cellular Reagents, 131–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/430_2014_166.

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Zou, Taotao, Faan-Fung Hung, Chen Yang, and Chi-Ming Che. "Strongly Phosphorescent Transition-Metal Complexes with N-Heterocyclic Carbene Ligands as Cellular Probes." In Luminescent and Photoactive Transition Metal Complexes as Biomolecular Probes and Cellular Reagents, 181–203. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/430_2015_173.

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Baggaley, Elizabeth, Julia A. Weinstein, and J. A. Gareth Williams. "Time-Resolved Emission Imaging Microscopy Using Phosphorescent Metal Complexes: Taking FLIM and PLIM to New Lengths." In Luminescent and Photoactive Transition Metal Complexes as Biomolecular Probes and Cellular Reagents, 205–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/430_2014_168.

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Atwood, David A. "(II) Transition Metal Complexes." In 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., and Bruce Arndtsen. "Transition Metal Hydride Complexes." In 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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Hendrickson, David N., David M. Adams, Chi-Cheng Wu, and Sheila M. J. Aubin. "Bistable Transition Metal Complexes." In 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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Huang, Xin, and Zhengyang Lin. "Transition Metal Catalyzed Borations." In 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, and Jean-Pierre Sauvage. "From Photoinduced Charge Separation to Light-driven Molecular Machines." In 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, and Hiroshi Nishihara. "Metal-based Photoswitches Derived from Photoisomerization." In 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, and David B. Goodin. "Conjugates of Heme-Thiolate Enzymes with Photoactive Metal-Diimine Wires." In 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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Conference papers on the topic "Transition metal complexes. Phosphorescence"

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

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Slinker, Jason, Dan Bernards, Samuel Flores-Torres, Stefan Bernhard, Paul L. Houston, Héctor D. Abruña, and George G. Malliaras. "Light emitting diodes from transition metal complexes." In 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, and Julien Bloino. "ANHARMONIC VIBRATIONAL SPECTROSCOPY ON METAL TRANSITION COMPLEXES." In 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, and Benjamin A. DeGraff, Jr. "Highly luminescent transition metal complexes as sensors." In OE/LASE '94, edited by James A. Harrington, David M. Harris, Abraham Katzir, and Fred P. Milanovich. SPIE, 1994. http://dx.doi.org/10.1117/12.180739.

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Malliaras, George G. "Light Emitting Devices from Ionic Transition Metal Complexes." In 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, and Ng Chi-On. "SSpectroscopic study on luminescent mechanochromic transition metal complexes." In 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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Pietschnig, Rudolf, Carmen Moser, Stefan Spirk, and Sven Schäfer. "Synthesis and Structure of Transition Metal Bisalkinylselenolato Complexes." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01518.

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Demas, J. N., and B. A. DeGraff. "Design Of Transition Metal Complexes As Luminescence Probes." In OE/FIBERS '89, edited by Robert A. Lieberman and Marek T. Wlodarczyk. SPIE, 1990. http://dx.doi.org/10.1117/12.963191.

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Crosby, G. A., K. J. Jordan, and G. R. Gamble. "Designing Energy Migration Barriers Into Transition-Metal Complexes." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by E. R. Menzel. SPIE, 1988. http://dx.doi.org/10.1117/12.945458.

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Spears, Kenneth G., Liang Wang, Xinming Zhu, and Steven M. Arrivo. "Picosecond transient-IR absorption of unsaturated transition metal complexes." In OE/LASE '90, 14-19 Jan., Los Angeles, CA, edited by Keith A. Nelson. SPIE, 1990. http://dx.doi.org/10.1117/12.17906.

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Reports on the topic "Transition metal complexes. Phosphorescence"

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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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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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Sharp, P. R. Late transition metal. mu. -oxo and. mu. -imido complexes. Office of Scientific and Technical Information (OSTI), January 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), January 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), March 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), January 2003. http://dx.doi.org/10.2172/835301.

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

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

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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), March 1992. http://dx.doi.org/10.2172/5573491.

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Schmehl, Russell H. Energy, Electron Transfer and Photocatalytic Reactions of Visible Light Absorbing Transition Metal Complexes. Office of Scientific and Technical Information (OSTI), March 2016. http://dx.doi.org/10.2172/1240023.

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