Relevant bibliographies by topics / Gold metal complexes

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Academic literature on the topic 'Gold metal complexes'

Author: Grafiati
Published: 10 March 2023

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Journal articles on the topic "Gold metal complexes"

1

Zhou, Meng, Chenjie Zeng, Qi Li, Tatsuya Higaki, and Rongchao Jin. "Gold Nanoclusters: Bridging Gold Complexes and Plasmonic Nanoparticles in Photophysical Properties." Nanomaterials 9, no. 7 (2019): 933. http://dx.doi.org/10.3390/nano9070933.

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Recent advances in the determination of crystal structures and studies of optical properties of gold nanoclusters in the size range from tens to hundreds of gold atoms have started to reveal the grand evolution from gold complexes to nanoclusters and further to plasmonic nanoparticles. However, a detailed comparison of their photophysical properties is still lacking. Here, we compared the excited state behaviors of gold complexes, nanolcusters, and plasmonic nanoparticles, as well as small organic molecules by choosing four typical examples including the Au10 complex, Au25 nanocluster (1 nm me
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2

Kaub, Christoph, Sergei Lebedkin, Sebastian Bestgen, Ralf Köppe, Manfred M. Kappes, and Peter W. Roesky. "Defined tetranuclear coinage metal chains." Chemical Communications 53, no. 69 (2017): 9578–81. http://dx.doi.org/10.1039/c7cc04705c.

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Heterodimetallic gold/copper and gold/silver complexes were synthesized, and feature an unprecedented V-shape or linear MAu<sub>2</sub>M (M = Cu, Ag) setup in the solid state. Photoluminescence properties of the complexes strongly depend on the metal.
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Michalak and Kośnik. "Chiral N-heterocyclic Carbene Gold Complexes: Synthesis and Applications in Catalysis." Catalysts 9, no. 11 (2019): 890. http://dx.doi.org/10.3390/catal9110890.

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N-Heterocyclic carbenes have found many applications in modern metal catalysis, due to the formation of stable metal complexes, and organocatalysis. Among a myriad of N-heterocyclic carbene metal complexes, gold complexes have gained a lot of attention due to their unique propensity for the activation of carbon-carbon multiple bonds, allowing many useful transformations of alkynes, allenes, and alkenes, inaccessible by other metal complexes. The present review summarizes synthetic efforts towards the preparation of chiral N-heterocyclic gold(I) complexes exhibiting C2 and C1 symmetry, as well
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4

Dias, H. V. Rasika. "Polyfluorinated ligand-supported organometallic complexes of copper, silver, and gold." Pure and Applied Chemistry 82, no. 3 (2010): 649–56. http://dx.doi.org/10.1351/pac-con-09-10-19.

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The tris(pyrazolyl)borate [HB(3,5-(CF3)2Pz)3]− prepared using highly fluorinated 3,5-bis(trifluoromethyl)pyrazole and BH4− is an excellent supporting ligand for the stabilization of a number of rare organometallic complexes of coinage metals. For example, it has enabled the isolation of Cu(I), Ag(I), and Au(I) complexes of CO and ethylene as crystalline solids. Syntheses, spectroscopic and structural features, and properties of [HB(3,5-(CF3)2Pz)3]ML (M = Cu, Ag, Au; L = CO, C2H4) are the main focus of this discussion. Several metal adducts based on the tris(triazolyl)borate [HB(3,5-(CF3)2Tz)3]
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5

Aguado, Javier E., M. Concepción Gimeno, Peter G. Jones, and Antonio Laguna. "Unusual coordination behaviour of the ferrocenyl-terpyridine ligand with group 11 complexes." Canadian Journal of Chemistry 87, no. 1 (2009): 341–47. http://dx.doi.org/10.1139/v08-148.

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Complexes of the ligand Fcterpy (Fcterpy = 4′-ferrocenyl-2,2′:6′,2′-terpyridine) with group 11 metals display different coordination modes. The reaction with complexes [Cu(NO3)(PPh3)2] or [M(OTf)(PR3)] (OTf = trifluoromethyl sulphonate) gives the species [M(Fcterpy)(PR3)]X (M = Cu, X = PF6, PR3 = PPh3 (1); M = Ag, X = OTf, PR3 = PPh3 (2), PPh2Me (3); M = Au, X = OTf, PR3 = PPh3 (4)) in which the ligand is coordinated as a tridentate chelate to the metal. Treatment with [Cu(NCMe)4]PF6 or Ag(OTf) in 1:1 molar ratio gives the dinuclear complexes [M2(Fcterpy)2]X2 (M = Cu (5), Ag (6)), in which the
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6

Braunstein, Pierre, Michael Knorr, Antonio Tiripicchio, and Marisa Tiripicchio Camellini. "Competing metal-metal bonding in heterometallic complexes of gold and mercury. Synthesis of contrasting iron-gold-gold-iron and iron-mercury-iron complexes." Inorganic Chemistry 31, no. 18 (1992): 3685–87. http://dx.doi.org/10.1021/ic00044a002.

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7

Andrejević, Tina P., Biljana Đ. Glišić, and Miloš I. Djuran. "Amino Acids and Peptides as Versatile Ligands in the Synthesis of Antiproliferative Gold Complexes." Chemistry 2, no. 2 (2020): 203–18. http://dx.doi.org/10.3390/chemistry2020013.

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Gold complexes have been traditionally employed in medicine, and currently, some gold(I) complexes, such as auranofin, are clinically used in the treatment of rheumatoid arthritis. In the last decades, both gold(I) and gold(III) complexes with different types of ligands have gained considerable attention as potential antitumor agents, showing superior activity both in vitro and in vivo to some of the clinically used agents. The present review article summarizes the results achieved in the field of synthesis and evaluation of gold complexes with amino acids and peptides moieties for their cytot
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8

Bojan, Vilma R., José M. López-de-Luzuriaga, Elena Manso, Miguel Monge, and M. Elena Olmos. "Metal-Induced Phosphorescence in (Pentafluorophenyl)gold(III) Complexes." Organometallics 30, no. 17 (2011): 4486–89. http://dx.doi.org/10.1021/om200537w.

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9

Dahlen, Milena, Tim P. Seifert, Sergei Lebedkin, Michael T. Gamer, Manfred M. Kappes, and Peter W. Roesky. "Tetra- and hexanuclear string complexes of the coinage metals." Chemical Communications 57, no. 97 (2021): 13146–49. http://dx.doi.org/10.1039/d1cc06034a.

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10

Johnson, Alice, Isabel Marzo та M. Concepción Gimeno. "Heterobimetallic propargyl gold complexes with π-bound copper or silver with enhanced anticancer activity". Dalton Transactions 49, № 33 (2020): 11736–42. http://dx.doi.org/10.1039/d0dt02113j.

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Heterometallic propargyl gold species in which copper or silver is bound to the triple bond were prepared. The bimetallic complexes had improved activities compared to the mononuclear gold complexes, suggesting a possible synergy between the two metal centres within the cell.
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