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Journal articles on the topic 'Coordination chemistry of gold(I)'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Hagen, Siegbert, Ingo Pantenburg, Florian Weigend, Claudia Wickleder, and Lars Wesemann. "GoldGold Interaction—Stannaborate [SnB11H11]2 Coordination Chemistry." Angewandte Chemie International Edition 42, no. 13 (2003): 1501–5. http://dx.doi.org/10.1002/anie.200250698.

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2

Toma, Henrique E., Vitor M. Zamarion, Sergio H. Toma, and Koiti Araki. "The coordination chemistry at gold nanoparticles." Journal of the Brazilian Chemical Society 21, no. 7 (2010): 1158–76. http://dx.doi.org/10.1590/s0103-50532010000700003.

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3

Laguna, Antonio, and Mariano Laguna. "Coordination chemistry of gold(II) complexes." Coordination Chemistry Reviews 193-195 (October 1999): 837–56. http://dx.doi.org/10.1016/s0010-8545(99)00141-1.

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4

Herrera, Raquel P., and M. Concepción Gimeno. "Main Avenues in Gold Coordination Chemistry." Chemical Reviews 121, no. 14 (2021): 8311–63. http://dx.doi.org/10.1021/acs.chemrev.0c00930.

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5

Toma, Henrique E., Vitor M. Zamarion, Sergio H. Toma, and Koiti Araki. "ChemInform Abstract: The Coordination Chemistry at Gold Nanoparticles." ChemInform 42, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.201101223.

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6

Gil-Rubio, Juan, and José Vicente. "The Coordination and Supramolecular Chemistry of Gold Metalloligands." Chemistry - A European Journal 24, no. 1 (2017): 32–46. http://dx.doi.org/10.1002/chem.201703574.

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7

Wanunu, Meni, Alexander Vaskevich, Sidney R. Cohen, et al. "Branched Coordination Multilayers on Gold." Journal of the American Chemical Society 127, no. 50 (2005): 17877–87. http://dx.doi.org/10.1021/ja0556676.

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8

Wanunu, Meni, Ronit Popovitz-Biro, Hagai Cohen, Alexander Vaskevich, and Israel Rubinstein. "Coordination-Based Gold Nanoparticle Layers." Journal of the American Chemical Society 127, no. 25 (2005): 9207–15. http://dx.doi.org/10.1021/ja050016v.

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9

Vanitcha, Avassaya, Cecilia Damelincourt, Geoffrey Gontard, Nicolas Vanthuyne, Virginie Mouriès-Mansuy, and Louis Fensterbank. "Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis." Chemical Communications 52, no. 41 (2016): 6785–88. http://dx.doi.org/10.1039/c6cc02316a.

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10

López-De-Luzuriaga, José M., Annette Schier, and Hubert Schmidbaur. "Gold Coordination by 2-(Diphenylphosphanyl)aniline." Chemische Berichte 130, no. 5 (1997): 647–50. http://dx.doi.org/10.1002/cber.19971300516.

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11

Preisenberger, Max, Andreas Bauer, and Hubert Schmidbaur. "Gold Coordination by Tertiary Phosphane Sulfides." Chemische Berichte 130, no. 7 (1997): 955–58. http://dx.doi.org/10.1002/cber.19971300723.

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12

South, Clinton R, Victor Piñón, and Marcus Weck. "Erasable Coordination Polymer Multilayers on Gold." Angewandte Chemie International Edition 47, no. 8 (2008): 1425–28. http://dx.doi.org/10.1002/anie.200704418.

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13

Nahra, Fady, Kristof Van Hecke, Alan R. Kennedy, and David J. Nelson. "Coinage metal complexes of selenoureas derived from N-heterocyclic carbenes." Dalton Transactions 47, no. 31 (2018): 10671–84. http://dx.doi.org/10.1039/c8dt01506f.

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14

Langdon-Jones, Emily E., David Lloyd, Anthony J. Hayes, et al. "Alkynyl-naphthalimide Fluorophores: Gold Coordination Chemistry and Cellular Imaging Applications." Inorganic Chemistry 54, no. 13 (2015): 6606–15. http://dx.doi.org/10.1021/acs.inorgchem.5b00954.

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15

Bravo, Beatriz G., Susan L. Michelhaugh, and Manuel P. Soriaga. "Selective electrode-surface coordination chemistry: adsorbate substitutions at smooth gold." Langmuir 5, no. 4 (1989): 1092–95. http://dx.doi.org/10.1021/la00088a037.

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16

Branzi, Lorenzo, Marco Baron, Lidia Armelao, et al. "Coordination chemistry of gold with N-phosphine oxide-substituted imidazolylidenes (POxIms)." New Journal of Chemistry 43, no. 44 (2019): 17275–83. http://dx.doi.org/10.1039/c9nj04911h.

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17

Curry, Dennis, Amanda Cameron, Bruce MacDonald, et al. "Adsorption of doxorubicin on citrate-capped gold nanoparticles: insights into engineering potent chemotherapeutic delivery systems." Nanoscale 7, no. 46 (2015): 19611–19. http://dx.doi.org/10.1039/c5nr05826k.

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18

Räisänen, Minna T., Nino Runeberg, Martti Klinga, et al. "Coordination of Pyridinethiols in Gold(I) Complexes." Inorganic Chemistry 46, no. 23 (2007): 9954–60. http://dx.doi.org/10.1021/ic700453t.

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19

Fernández, Eduardo J., José M. López-de-Luzuriaga, Miguel Monge, et al. "Dithiocarbamate Ligands as Building-Blocks in the Coordination Chemistry of Gold." Inorganic Chemistry 37, no. 21 (1998): 5532–36. http://dx.doi.org/10.1021/ic971600a.

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20

Du, Jianjun, Zhenkuan Wang, Jiangli Fan, and Xiaojun Peng. "Gold nanoparticle-based colorimetric detection of mercury ion via coordination chemistry." Sensors and Actuators B: Chemical 212 (June 2015): 481–86. http://dx.doi.org/10.1016/j.snb.2015.01.110.

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21

Zhdanko, Alexander, Markus Ströbele, and Martin E. Maier. "Coordination Chemistry of Gold Catalysts in Solution: A Detailed NMR Study." Chemistry - A European Journal 18, no. 46 (2012): 14732–44. http://dx.doi.org/10.1002/chem.201201215.

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22

Mohamed, Ahmed A., Hanan E. Abdou, and John P. Fackler Jr. "Coordination chemistry of gold(II) with amidinate, thiolate and ylide ligands." Coordination Chemistry Reviews 254, no. 11-12 (2010): 1253–59. http://dx.doi.org/10.1016/j.ccr.2009.10.017.

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23

Petroski, Janet, Mei Chou, and Carol Creutz. "The coordination chemistry of gold surfaces: Formation and far-infrared spectra of alkanethiolate-capped gold nanoparticles." Journal of Organometallic Chemistry 694, no. 7-8 (2009): 1138–43. http://dx.doi.org/10.1016/j.jorganchem.2008.11.057.

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24

Grasseschi, Daniel, Rômulo A. Ando, Henrique E. Toma, and Vitor M. Zamarion. "Unraveling the nature of Turkevich gold nanoparticles: the unexpected role of the dicarboxyketone species." RSC Advances 5, no. 8 (2015): 5716–24. http://dx.doi.org/10.1039/c4ra12161a.

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25

Langdon-Jones, Emily E., and Simon J. A. Pope. "Recent developments in gold(i) coordination chemistry: luminescence properties and bioimaging opportunities." Chemical Communications 50, no. 72 (2014): 10343. http://dx.doi.org/10.1039/c4cc03259d.

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26

Xiao, Xiaoyin, Gabriel A. Montaño, Amy Allen, Komandoor E. Achyuthan, David R. Wheeler, and Susan M. Brozik. "Lipid Bilayer Templated Gold Nanoparticles Nanoring Formation Using Zirconium Ion Coordination Chemistry." Langmuir 27, no. 15 (2011): 9484–89. http://dx.doi.org/10.1021/la2014754.

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27

Selvakannan, P. R., Eddy Dumas, Frédéric Dumur, et al. "Coordination chemistry approach for the end-to-end assembly of gold nanorods." Journal of Colloid and Interface Science 349, no. 1 (2010): 93–97. http://dx.doi.org/10.1016/j.jcis.2010.05.050.

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28

Vaidya, Shefali, Oleksandra Veselska, Antonii Zhadan, et al. "Transparent and luminescent glasses of gold thiolate coordination polymers." Chemical Science 11, no. 26 (2020): 6815–23. http://dx.doi.org/10.1039/d0sc02258f.

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29

Jääskeläinen, Sirpa, Igor O. Koshevoy, Sari Suvanto, Tiina Ryhänen, and Pipsa Hirva. "Vinylimidazole coordination modes to Pt and Au metal centers." New Journal of Chemistry 44, no. 29 (2020): 12762–70. http://dx.doi.org/10.1039/d0nj00845a.

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30

Rekhroukh, Feriel, Laura Estevez, Christian Bijani, Karinne Miqueu, Abderrahmane Amgoune, and Didier Bourissou. "Coordination–Insertion of Norbornene at Gold: A Mechanistic Study." Organometallics 35, no. 7 (2016): 995–1001. http://dx.doi.org/10.1021/acs.organomet.6b00040.

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31

Nelson, David J., Fady Nahra, Scott R. Patrick, David B. Cordes, Alexandra M. Z. Slawin, and Steven P. Nolan. "Exploring the Coordination of Cyclic Selenoureas to Gold(I)." Organometallics 33, no. 13 (2014): 3640–45. http://dx.doi.org/10.1021/om500610w.

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32

Togni, Antonio. "The Molecule of the Week: A Didactic Tool for Teaching General Chemistry." CHIMIA International Journal for Chemistry 74, no. 7 (2020): 615–17. http://dx.doi.org/10.2533/chimia.2020.615.

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The molecule of the week is regularly used by the author in his first-semester course General Chemistry I (Inorganic Chemistry) to illustrate, exemplify, and deepen fundamental aspects and concepts treated in the course. Pure sulfuric acid and its autoprotolysis is used to introduce the concepts of protochemical window and superacidity. The drug Auranofin serves at showing fundamental aspects of gold redox and coordination chemistry and the widely used disinfectant trichlo- roisocyanuric acid (TCICA) exemplifies redox processes with organic compounds.

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33

Crespo, Olga, M. Concepción Gimeno, Peter G. Jones, Antonio Laguna, Mar Naranjo, and M. Dolores Villacampa. "Coordination Behaviour of Gold and Silver Towards Pyrazole Ligands." European Journal of Inorganic Chemistry 2008, no. 34 (2008): 5408–17. http://dx.doi.org/10.1002/ejic.200800578.

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34

Moav, Tamar, Anat Hatzor, Hagai Cohen, Jacqueline Libman†, Israel Rubinstein, and Abraham Shanzer. "Coordination-Based Symmetric and Asymmetric Bilayers on Gold Surfaces." Chemistry - A European Journal 4, no. 3 (1998): 502–7. http://dx.doi.org/10.1002/(sici)1521-3765(19980310)4:3<502::aid-chem502>3.0.co;2-b.

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35

Brown, Matthew L., and Daniel B. Leznoff. "Expanding uranyl dicyanoaurate coordination polymers into the second and third dimensions." Canadian Journal of Chemistry 98, no. 7 (2020): 365–72. http://dx.doi.org/10.1139/cjc-2020-0031.

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The solvothermal synthesis and characterization of a three-dimensional, interpenetrated uranyl dicyanoaurate coordination polymer, K2(UO2)2(UO2)2(Au(CN)2)2(O)2(NO3)4, from UO2(NO3)2·6H2O and KAu(CN)2 is described. The structure contains a three-dimensional (3D) lattice of planar tetranuclear uranyl–oxo–nitrate clusters connected by dicyanoaurate linkers, with the rotation of the clusters providing the increased dimensionality. The material undergoes a reversible single-crystal to single-crystal transformation on exposure to water vapour, which is taken up in the channels of the 3D system. A se

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36

Fuchs, Stefan, José M. López-de-Luzuriaga, M. Elena Olmos, Alexander Sladek, and Hubert Schmidbaur. "Gold Coordination by a Tertiary Phosphine with Three Thioether Functions." Zeitschrift für Naturforschung B 52, no. 2 (1997): 217–20. http://dx.doi.org/10.1515/znb-1997-0213.

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Abstract The reaction of tris(phenylthiomethyl)phosphine with equimolecular amounts of [AuPPh3]+[BF4]- affords the complex (tris(phenylthiomethyl)phosphine)(triphenylphosphine)- gold(I) tetrafluoroborate 1 in good yield. The X-ray diffraction analysis of this product shows an unusual conformation with the three ChLSPh arms of the phosphine folded back towards the metal atom shielding the P-Au-P′ unit. The reaction of the same substrate with Bis(tetrahydrothiophene)gold(I) perchlorate in a 1:1 molar ratio leads to the displacement of both weakly coordinated tht ligands, and a dimeric product [A

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37

Kaatz, Forrest H., Dmitry Yu Murzin, and Adhemar Bultheel. "Coordination-Dependent Kinetics in the Catalysis of Gold Nanoclusters." ACS Catalysis 11, no. 15 (2021): 9073–85. http://dx.doi.org/10.1021/acscatal.1c00892.

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38

Quek, Su Ying, Monika M. Biener, Juergen Biener, et al. "Rich Coordination Chemistry of Au Adatoms in Gold Sulfide Monolayer on Au(111)." Journal of Physical Chemistry B 110, no. 32 (2006): 15663–65. http://dx.doi.org/10.1021/jp0641379.

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39

Monkowius, Uwe, Manfred Zabel, and Hartmut Yersin. "Unprecedented coordination chemistry of a chloro(phosphine)gold(I) complex: [(Ad2BnP)2Au][AuCl2]." Inorganic Chemistry Communications 11, no. 4 (2008): 409–12. http://dx.doi.org/10.1016/j.inoche.2008.01.004.

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40

Jahnke, Mareike C., and F. Ekkehardt Hahn. "Synthesis and coordination chemistry of silver(I), gold(I) and gold(III) complexes with picoline-functionalized benzimidazolin-2-ylidene ligands." Zeitschrift für Naturforschung B 76, no. 8 (2021): 463–73. http://dx.doi.org/10.1515/znb-2021-0087.

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Abstract The reactions of N-alkyl-N′-picolyl-benzimidazolium bromides or N,N′-dipicolyl-benzimidazolium bromide with silver oxide yielded the silver dicarbene complexes of the type [Ag(NHC)2][AgBr2] 1–4 (NHC = picoline-functionalized benzimidazolin-2-ylidene). The silver complexes 1–4 have been used in carbene transfer reactions to yield the gold(I) complexes of the type [AuCl(NHC)] 5–8 in good yields. A halide exchange at the metal center of complexes 5–8 with lithium bromide yielded the gold bromide complexes 9–12. Finally, the oxidation of the gold(I) centers in complexes 9–12 with elementa

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41

Buron, Charlotte, Sihem Groni, Nathalie Ségaud, et al. "Self-assembled monolayer formation of a (N5)Fe(ii) complex on gold electrodes: electrochemical properties and coordination chemistry on a surface." Dalton Transactions 45, no. 47 (2016): 19053–61. http://dx.doi.org/10.1039/c6dt03870k.

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42

Hoy, Reinhard, Peter Lönnecke, and Evamarie Hey-Hawkins. "Selective formation of a two-dimensional coordination polymer based on a tridentate phospholane ligand and gold(i)." Dalton Transactions 47, no. 41 (2018): 14515–20. http://dx.doi.org/10.1039/c8dt03630f.

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The tridentate phosphine ligand 1,3,5-tris[(E)-(4-phospho-lano-2,6-diethyl)styryl]benzene reacts with [AuCl(tht)] independent of the stoichiometry employed with selective formation of a 2D coordination polymer (ratio 1 : 1) with gold(i) in a trigonal-planar [3 + 1] coordination geometry.

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43

Jones, Peter G., and Carsten Thöne. "Notizen: Gold Complexes with Selenium Ligands, V. Synthesis and Crystal Structure of [(Ph3PAu)2Se(p-C6F4Cl)]+SbF6-." Zeitschrift für Naturforschung B 47, no. 4 (1992): 600–602. http://dx.doi.org/10.1515/znb-1992-0425.

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The binuclear complex [(Ph3PAu)2Se(p-C6F4Cl)]+SbF6- was prepared from Ph3PAuCl and (p-C6F4Cl)2Se2 in the presence of AgSbF6. The crystal structure shows a short intramolecular gold-gold interaction, which leads to an extreme distortion in the coordination geometry at selenium.

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44

Okhrimenko, Larysa, Cynthia Cibaka Ndaya, Alexandra Fateeva, Gilles Ledoux, and Aude Demessence. "Post-synthetic functionalization and ligand exchange reactions in gold(i) phenylthiolate-based coordination polymers." New Journal of Chemistry 44, no. 41 (2020): 17970–75. http://dx.doi.org/10.1039/d0nj03833d.

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45

Ehlers, Ferdinand, Jana M. Strumberger, and Fabian Mohr. "Keto‐stabilized Arsenic Ylides and their Coordination to Gold(I)." Zeitschrift für anorganische und allgemeine Chemie 646, no. 13 (2020): 889–94. http://dx.doi.org/10.1002/zaac.202000110.

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46

Moreno-Alcántar, Guillermo, Hugo Hernández-Toledo, José Manuel Guevara-Vela, et al. "Stability and trans Influence in Fluorinated Gold(I) Coordination Compounds." European Journal of Inorganic Chemistry 2018, no. 40 (2018): 4413–20. http://dx.doi.org/10.1002/ejic.201800567.

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47

Gualco, Pauline, Maxime Mercy, Sonia Ladeira, et al. "Hypervalent Silicon Compounds by Coordination of Diphosphine-Silanes to Gold." Chemistry - A European Journal 16, no. 35 (2010): 10808–17. http://dx.doi.org/10.1002/chem.201001281.

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48

Luong, Lucy M. C., Michael M. Aristov, Alexandria V. Adams, et al. "Unsymmetrical Coordination of Bipyridine in Three-Coordinate Gold(I) Complexes." Inorganic Chemistry 59, no. 6 (2020): 4109–17. http://dx.doi.org/10.1021/acs.inorgchem.0c00138.

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49

Siemeling, Ulrich, Frauke Bretthauer, Clemens Bruhn, Tim-Patrick Fellinger, Wah-Leung Tong та Michael C. W. Chan. "Gold Nanoparticles Bearing an α-Lipoic Acid-based Ligand Shell: Synthesis, Model Complexes and Studies Concerning Phosphorescent Platinum(II)-Functionalisation". Zeitschrift für Naturforschung B 65, № 9 (2010): 1089–96. http://dx.doi.org/10.1515/znb-2010-0906.

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The surface functionalisation of gold nanoparticles (GNPs) with luminescent platinum complexes has been investigated, utilising α-lipoic acid derivatives for GNP stabilisation. Model complexes have been studied to mimic the chemisorption chemistry required to afford GNPs protected by an α-lipoic acid-based ligand shell with terminal functionalisation suitable for metal coordination, and the unambiguous binding of the cyclic disulfide moiety at a zero-valent precious metal core through oxidative addition has been confirmed by X-ray crystallography. Subsequently, gold nanoparticles bearing the α

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50

Willner, H., S. J. Rettig, J. Trotter, and F. Aubke. "The crystal and molecular structure of gold tris(fluorosulfate)." Canadian Journal of Chemistry 69, no. 3 (1991): 391–96. http://dx.doi.org/10.1139/v91-060.

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Single crystals of gold(III) tris(fluorosulfate) are obtained by recrystallization from bis(fluorosulfuryl) peroxide, S2O6F2, under O2 pressure. The crystals of [Au(SO3F)3]2 are monoclinic, a = 9.700(4), b = 9.222(2), c = 10.810(4)Å, β = 94.43(3)°, Z = 2, space group P21/a. The structure was solved by heavy atom methods and was refined by full-matrix least-squares procedures, R(F) = 0.038 and Rw(F) = 0.050 for 1491 reflections with I ≥ 3σ(I). The structure consists of centrosymmetric [Au(SO3F)3]2 dimers containing two bidentate, symmetrically bridging and four monodentate, terminal SO3F ligand

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