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Journal articles on the topic 'Gold compounds'

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Published: 4 June 2021
Last updated: 28 July 2024

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1

Parish, R. V., and Stephanie M. Cottrill. "Medicinal gold compounds." Gold Bulletin 20, no. 1-2 (March 1987): 3–12. http://dx.doi.org/10.1007/bf03214653.

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2

Steggerda, J. J. "Platinum-Gold Cluster Compounds." Comments on Inorganic Chemistry 11, no. 2-3 (December 1990): 113–29. http://dx.doi.org/10.1080/02603599008035821.

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3

Baukova, T. V., L. G. Kuz'mina, A. V. Churakov, N. A. Oleinikova, and P. V. Petrovskii. "Hypercoordinated gold (i) compounds." Russian Chemical Bulletin 47, no. 2 (February 1998): 343–48. http://dx.doi.org/10.1007/bf02498963.

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4

Rapson, W. S. "Intermetallic compounds of gold." Gold Bulletin 29, no. 4 (December 1996): 141–42. http://dx.doi.org/10.1007/bf03214750.

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5

Baukova, T. V., L. G. Kuzmina, and A. V. Churakov. "Hypercoordinated gold(I) compounds." Russian Chemical Bulletin 46, no. 12 (December 1997): 2127–29. http://dx.doi.org/10.1007/bf02495267.

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6

Baukova, T. V., L. G. Kuz'mina, N. A. Oleinikova, and D. A. Lemenovskii. "Hypercoordinated gold(i) compounds." Russian Chemical Bulletin 44, no. 10 (October 1995): 1952–54. http://dx.doi.org/10.1007/bf00707234.

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7

Fackler, John P., Zerihun Assefa, Jennifer M. Forward, and Richard J. Staples. "Excited States of Gold(I) Compounds, Luminescence and Gold-Gold Bonding." Metal-Based Drugs 1, no. 5-6 (January 1, 1994): 459–66. http://dx.doi.org/10.1155/mbd.1994.459.

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It has long been established by Khan that the superoxide anion, O2-, generates singlet oxygen, O21Δg, during dismutation. Auranofin, gold-phosphine thiols, β-Carotene, and metal-sulfur compounds can rapidly quench singlet O2. The quenching of the O21Δg, which exists at 7752 cm-1 above the ground state triplet, may be due to the direct interaction of the singlet O2 with gold(I) or may require special ligands such as those containing sulfur coordinated to the metal. Thus we have been examining the excited state behavior of gold(I) species and the mechanisms for luminescence. Luminescence is observed under various conditions, with visible emission ranging from blue to red depending on the ligands coordinated to gold(I). Triplet state emission can be found from mononuclear three coordinate Au(I) species, including species which display this behavior in aqueous solution. A description is given of the luminescent three coordinate TPA (triazaphosphaadamantane) and TPPTS (triphenylphosphine-trisulfonate) complexes, the first examples of water soluble luminescent species of gold(I).
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8

Sutton, Blaine M. "Gold compounds for rheumatoid arthritis." Gold Bulletin 19, no. 1 (March 1986): 15–16. http://dx.doi.org/10.1007/bf03214639.

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9

JONES, G., and P. M. BROOKS. "INJECTABLE GOLD COMPOUNDS: AN OVERVIEW." Rheumatology 35, no. 11 (November 1, 1995): 1154–58. http://dx.doi.org/10.1093/rheumatology/35.11.1154.

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10

Baukova, T. V., N. A. Oleinikova, D. A. Lemenovskii, and L. G. Kuz'mina. "Hypercoordinated compounds of gold(I)." Russian Chemical Bulletin 43, no. 4 (April 1994): 681–88. http://dx.doi.org/10.1007/bf00699848.

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11

Baukova, T. V., V. P. Dyadchenko, N. A. Oleinikova, D. A. Lemenovskii, and L. G. Kuz'mina. "Compounds of hypercoordinated gold(i)." Russian Chemical Bulletin 43, no. 6 (June 1994): 1063–68. http://dx.doi.org/10.1007/bf01558082.

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12

Schwerdtfeger, Peter, Michael Dolg, W. H. Eugen Schwarz, Graham A. Bowmaker, and Peter D. W. Boyd. "Relativistic effects in gold chemistry. I. Diatomic gold compounds." Journal of Chemical Physics 91, no. 3 (August 1989): 1762–74. http://dx.doi.org/10.1063/1.457082.

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13

Schwerdtfeger, Peter, Peter D. W. Boyd, Stephane Brienne, and Anthony K. Burrell. "Relativistic effects in gold chemistry. 4. Gold(III) and gold(V) compounds." Inorganic Chemistry 31, no. 16 (August 1992): 3411–22. http://dx.doi.org/10.1021/ic00042a016.

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14

Goldermann, R., H. C. Schuppe, E. Gleichmann, P. Kind, H. Merk, R. Rau, and G. Goerz. "Adverse immune reactions to gold in rheumatoid arthritis: lack of skin reactivity." Acta Dermato-Venereologica 73, no. 3 (June 1, 1993): 220–22. http://dx.doi.org/10.2340/0001555573220222.

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Adverse immune reactions develop in up to 30% of patients treated with gold compounds. However, sensitization to gold(I) drugs is rarely demonstrated by in vivo or in vitro testing. Recent data from a mouse model provides evidence that gold(I) is oxidized to gold(III) before T cells are sensitized. To study the diagnostic value of skin tests, patch testing with various gold compounds / including gold(I) and gold(III) / was performed in 50 patients with rheumatoid arthritis treated with gold(I) drugs. Positive patch test reactions to either gold(I) or gold(III) compounds were not detected. In contrast, the lymphocyte transformation test (LTT) revealed a gold(III)/induced response in one of the 7 patients being tested. We conclude that patch testing fails to indicate T cell sensitization to gold(I) drugs in rheumatoid arthritis patients. The in vitro response to gold(III) obtained by LTT supports the hypothesis that biooxidation of gold(I) compounds may play a crucial role for sensitization.
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15

Moore, Laila S., R. V. (‘Dick’) Parish, Scott S. D. Brown, and Ian D. Salter. "Gold-197 Mössbauer spectra of some gold–ruthenium cluster compounds." J. Chem. Soc., Dalton Trans., no. 10 (1987): 2333–36. http://dx.doi.org/10.1039/dt9870002333.

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16

Hainfeld, J. F., R. D. Powell, F. R. Furuya, and J. S. Wall. "Gold Cluster Crystals." Microscopy and Microanalysis 6, S2 (August 2000): 326–27. http://dx.doi.org/10.1017/s1431927600034127.

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Gold clusters are gold compounds with a core of gold atoms and organic groups covalently bound to the surface gold atoms. An example is undecagold, Au11(P(C6H5)3)7, whose structure was solved by x-ray crystallography using 3-dimensional crystals. These differ from colloidal gold, which are suspensions of metal particles, usually formed by metal ion reduction; although the particles may be approximately the same size, they vary due to the statistical process of formation. Gold clusters are compounds with a definite formula, and should all be perfectly identical. However, it is known that there is a family of stable gold cluster compounds, such as Au6, Au11, Au13, AU55, Au67, etc. In a given preparation of gold clusters, there is usually some mixture of these, thus leading to some size variation. Methods such as gel filtration column chromatography and ultrafiltration can be used to separate most of these species, so that relatively pure preparations may be achieved.
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17

Schmidbaur, Hubert, Gabriele Weidenhiller, Aref A. M. Aly, Oliver Steigelmann, and Gerhard Müller. "Gold(I)-Komplexe sekundärer Phosphine / Gold(I) Complexes of Secondary Phosphines." Zeitschrift für Naturforschung B 44, no. 12 (December 1, 1989): 1503–8. http://dx.doi.org/10.1515/znb-1989-1206.

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Gold(I) complexes with secondary phosphines R2PH (la—d) of the type R2PH · AuCl (2a—d) have been obtained in good yield from reactions of (carbonyl)chlorogold(I) and the corresponding ligand in diethylether. Both compounds 2a, b bearing aromatic substituents with R = 2,4,6-trimethylphenyl (mesityl) and 2-methylphenyl (o-tolyl), and compounds 2c, d with the bulky alkyl substituents R = t-butyl and R = cyclohexyl, resp., are air-stable crystalline solids. — The coordination compounds have been characterized by NMR and IR data, and — in the cases of 2b and 2c — by single crystal X-ray diffraction studies. Crystals of these two compounds are both monoclinic, space group P21/c with four formula units (Z = 4). The analysis shows independent monomers for compound 2c with no intermolecular Au···Au contacts. Molecules of 2b are arranged in centrosymmetrical dimers (head to tail) with an Au···Au distance of 3.56 Å and a dihedral angle P—Au—Au′—P′ of 180°. (This structural study is as yet incomplete and suffers from an unsatisfactory data set for 2b.) It appears that intermolecular contacts are largely controlled by steric effects.
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18

Robinson, J. M., T. Takizawa, and D. D. Vandré. "Gold Cluster Compounds are Useful Immunoprobes." Microscopy and Microanalysis 6, S2 (August 2000): 328–29. http://dx.doi.org/10.1017/s1431927600034139.

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Immunocytochemistry generally refers to methods directed toward obtaining information on the in situ distribution of antigens in cells and tissues. Immunocytochemical methods can be applied at either the light or electron microscope levels, or both in concert. The detection of antibody recognition of an antigen (i.e., localization of an antigen) relies upon a reporter system. At the light microscope level, enzymes (e.g., horseradish peroxidase) or fluorochromes are the most widely used reporters in immunocytochemistry. At the electron microscope level, particulate probes (e.g., colloidal gold) are the most widely used reporters. However, enzymes and even fluorochromes can be used at the EM level.In this abstract, we discuss our use of gold cluster immunoprobes as the reporter system in both light and electron microscope level immuncytochemistry. These gold cluster immunoprobes, are commercially known as NanogoldTM (NG). These probes are very small with a diameter of 1.4-nm.
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19

Gabbiani, Chiara, Angela Casini, and Luigi Messori. "Gold(III) compounds as anticancer drugs." Gold Bulletin 40, no. 1 (March 2007): 73–81. http://dx.doi.org/10.1007/bf03215296.

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20

Fonteh, Pascaline N., Frankline K. Keter, and Debra Meyer. "HIV therapeutic possibilities of gold compounds." BioMetals 23, no. 2 (February 3, 2010): 185–96. http://dx.doi.org/10.1007/s10534-010-9293-5.

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21

Parish, R. V. "Structure and bonding in gold compounds." Hyperfine Interactions 40, no. 1-4 (February 1988): 159–69. http://dx.doi.org/10.1007/bf02049087.

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22

Wei, Fang, Chuanling Song, Yudao Ma, Ling Zhou, Chen-Ho Tung, and Zhenghu Xu. "Gold carbene chemistry from diazo compounds." Science Bulletin 60, no. 17 (September 2015): 1479–92. http://dx.doi.org/10.1007/s11434-015-0874-0.

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23

MIYACHI, Y., A. YOSHIOKA, S. IMAMURA, and Y. NIWA. "Anti-oxidant effects of gold compounds." British Journal of Dermatology 116, no. 1 (January 1987): 39–46. http://dx.doi.org/10.1111/j.1365-2133.1987.tb05789.x.

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24

Gallego, M. Luz, Alejandro Guijarro, Oscar Castillo, Teodor Parella, Ruben Mas-Balleste, and Felix Zamora. "Nuclearity control in gold dithiocarboxylato compounds." CrystEngComm 12, no. 8 (2010): 2332. http://dx.doi.org/10.1039/c001150a.

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25

Hiller, Wolfgang, and Christian Erich Zybill. "ChemInform Abstract: Gold and Its Compounds." ChemInform 30, no. 27 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.199927264.

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26

Vollenbroek, F. A., J. W. A. van der Velden, J. J. Bour, and J. M. Trooster. "Mössbauer investigation of gold cluster compounds." Recueil des Travaux Chimiques des Pays-Bas 100, no. 10 (September 2, 2010): 375–77. http://dx.doi.org/10.1002/recl.19811001007.

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27

MINGOS, D. M. P., and M. J. WATSON. "ChemInform Abstract: Heteronuclear Gold Cluster Compounds." ChemInform 25, no. 41 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199441257.

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28

Houbrechts, Stephan, Carlo Boutton, Koen Clays, André Persoons, Ian R. Whittall, Raina H. Naulty, Marie P. Cifuentes, and Mark G. Humphrey. "Novel Organometallic Compounds for Nonlinear Optics." Journal of Nonlinear Optical Physics & Materials 07, no. 01 (March 1998): 113–20. http://dx.doi.org/10.1142/s0218863598000090.

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Hyper-Rayleigh scattering is used to investigate the nonlinear optical properties of novel metal (ruthenium, nickel and gold) σ-arylacetylide complexes. The influence of the organometallic donor group and conjugating bridge on the quadratic hyperpolarizability is studied. For all organic ligands, the addition of the metal (donor) group is shown to increase the static hyperpolarizability by a factor of 2, 4 and 7 for gold, nickel and ruthenium complexes, respectively. Moreover, replacement of phenyl with a heterocyclic ring is demonstrated to enlarge the hyperpolarizability in the case of gold and ruthenium compounds.
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29

Cirri, Damiano, Andrea Geri, Lara Massai, Michele Mannelli, Tania Gamberi, Francesca Magherini, Matteo Becatti, Chiara Gabbiani, Alessandro Pratesi, and Luigi Messori. "Chemical Modification of Auranofin Yields a New Family of Anticancer Drug Candidates: The Gold(I) Phosphite Analogues." Molecules 28, no. 3 (January 20, 2023): 1050. http://dx.doi.org/10.3390/molecules28031050.

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A panel of four novel gold(I) complexes, inspired by the clinically established gold drug auranofin (1-Thio-β-D-glucopyranosatotriethylphosphine gold-2,3,4,6-tetraacetate), was prepared and characterized. All these compounds feature the replacement of the triethylphosphine ligand of the parent compound auranofin with a trimethylphosphite ligand. The linear coordination around the gold(I) center is completed by Cl−, Br−, I− or by the thioglucose tetraacetate ligand (SAtg). The in-solution behavior of these gold compounds as well as their interactions with some representative model proteins were comparatively analyzed through 31PNMR and ESI-MS measurements. Notably, all panel compounds turned out to be stable in aqueous media, but significant differences with respect to auranofin were disclosed in their interactions with a few leading proteins. In addition, the cytotoxic effects produced by the panel compounds toward A2780, A2780R and SKOV-3 ovarian cancer cells were quantitated and found to be in the low micromolar range, since the IC50 of all compounds was found to be between 1 μM and 10 μM. Notably, these novel gold complexes showed large and similar inhibition capabilities towards the key enzyme thioredoxin reductase, again comparable to those of auranofin. The implications of these results for the discovery of new and effective gold-based anticancer agents are discussed.
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30

Hainfeld, James F. "Gold Covalently Bound to Antibodies." Microscopy and Microanalysis 1, no. 2 (June 1995): 87–92. http://dx.doi.org/10.1017/s1431927695110879.

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A new class of gold immunoprobes has been developed with substantially different characteristics from the usual colloidal gold probes. Instead of chunks of gold metal (colloidal gold) just adsorbed to immunoglobulins by ionic or hydrophobic interactions, well-defined gold compounds are covalently attached to antibodies. Gold, along with several other metals, is known to form organo-cluster compounds with multiple metal atoms. The first gold cluster immunoprobe developed was undecagold (Au11), containing 11 gold atoms in an 0.8-nm sphere (Figure 1), covalently attached to Fab′ antibody fragments (Hainfeld, 1987). A more recent development has been the synthesis of a larger 1.4-nm gold cluster (Hainfeld et al, 1991; Hainfeld and Furuya, 1992).
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31

SCHWERDTFEGER, P., P. D. W. BOYD, S. BRIENNE, and A. K. BURRELL. "ChemInform Abstract: Relativistic Effects in Gold Chemistry. Part 4. Gold(III) and Gold(V) Compounds." ChemInform 23, no. 45 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199245001.

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32

Fonseca, Custódia, and Manuel Aureliano. "Biological Activity of Gold Compounds against Viruses and Parasitosis: A Systematic Review." BioChem 2, no. 2 (May 14, 2022): 145–59. http://dx.doi.org/10.3390/biochem2020010.

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In this contribution, we provide an overview of gold compound applications against viruses or parasites during recent years. The special properties of gold have been the subject of intense investigation in recent years, which has led to the development of its chemistry with the synthesis of new compounds and the study of its applicability in various areas such as catalysis, materials, nanotechnology and medicine. Herein, thirteen gold articles with applications in several viruses, such as hepatitis C virus (HCV), influenza A virus (H1N1), vesicular stomatitis virus (VSV), coronavirus (SARS-CoV and SARS-CoV-2), Dengue virus, and several parasites such as Plasmodium sp., Leishmania sp., Tripanossoma sp., Brugia sp., Schistosoma sp., Onchocerca sp., Acanthamoeba sp., and Trichomonas sp. are described. Gold compounds with anti-viral activity include gold nanoparticles with the ligands mercaptoundecanosulfonate, 1-octanethiol and aldoses and gold complexes with phosphine and carbene ligands. All of the gold compounds with anti-parasitic activity reported are gold complexes of the carbene type. Auranofin is a gold drug already used against rheumatoid arthritis, and it has also been tested against virus and parasites.
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33

Fereidoonnezhad, Masood, and Salar Nosrati. "Antimicrobial Activity of Diphenyl Pyridine Phosphine Gold(I)-thiolate Compounds and their Molecular Docking With Thioredoxin Reductase Enzyme." Jundishapur journal of Medical Sciences 21, no. 2 (June 1, 2022): 218–32. http://dx.doi.org/10.32598/jsmj.21.2.2231.

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Background and Objectives Despite several studies and abundant efforts to control microbial agents, humans have not yet been able to eliminate these agents. Recent studies have shown that gold(I) compounds are promising candidates for making antimicrobial drugs. The interest in gold-based drugs is increasing day by day. Inhibition of the thioredoxin reductase (TrxR) enzyme is the most important biological target for antimicrobial gold(I) compounds. Subjects and Methods In this study, the antimicrobial properties of five diphenyl pyridine phosphine gold(I)-thiolate compounds against gram-positive bacteria (P. aeruginosa, E. coli), gram-negative bacteria (S. aureus, B. subtilis), a fungus (C. albicans), and a yeast (S. cerevisiae) were evaluated. The molecular docking studies were carried out using AutoDock 4.2 to find the best compound in the active site of the TrxR enzyme (PDB ID: 4CBQ). Results The gold(I) compounds had a minimum inhibitory concentration (MIC) value ranged from 3 to 100 μg/mL. The most active compound was Au3 which had a MIC of 3.89, 3.15, 4.36, 5.44, 6.13, and 8.37 μg/mL against P. aeruginosa, E. coli, S. aureus, B. subtilis, C. albicans and S. cerevisiae, respectively. Conclusion The gold(I) compounds act better on gram-negative bacteria and yeast strains compared to auranofin as antirheumatic drug. These compounds, especially the Au3, are potentially valuable for the control of antimicrobial agents.
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34

Shi, Min, and Qiang Wang. "Synthesis of Cyclic and Heterocyclic Compounds via Gold-Catalyzed Reactions." Synlett 28, no. 17 (July 27, 2017): 2230–40. http://dx.doi.org/10.1055/s-0036-1590827.

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This account outlines the latest advances from our group in the field of gold catalysis. A variety of cyclic and heterocyclic compounds, containing different sized skeletons, are synthesized selectively by fine-tuning the substrates, catalysts, and ligands. Au(I)/Au(III) redox catalysis is applied in our latest work through adding external oxidation. The reaction mechanisms are discussed in detail. Moreover, the photoredox catalytic process is also introduced briefly, which opens avenues for the development of new strategies in gold chemistry.1 Introduction2 Gold-Catalyzed Cycloisomerization of Enynes3 Gold-Catalyzed Intramolecular Cyclization of Propargylic Ester Substrates4 Gold-Catalyzed C(sp3)–H Functionalizations5 The Au(I)/Au(III) Redox Catalytic Cycle6 Conclusion
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35

Wu, Zhen Dong. "Preparation of Gold Nanoparticles by Using Cholesteryl Compounds." Applied Mechanics and Materials 368-370 (August 2013): 795–98. http://dx.doi.org/10.4028/www.scientific.net/amm.368-370.795.

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Gold nanoparticles were synthesized by two bolaform cholesteryl imide derivatives with different lengths of ethyleneamine spacers at a liquid-liquid interface. By stirring the aqueous solution containing AuCl4- ions with the chloroform solution of bolaform amphiphile, AuCl4- ions were transferred into the organic phase and reduced to gold nanoparticles. Spectral and morphological measurements indicated that both bolaform amphiphiles could serve as both capping and reducing agents. Different gold nanostructures could be obtained depending on the different spacers and the molar ratios of amphiphile to AuCl4- ions.
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36

Graabaek, P. M., and S. M. Pedersen. "Effect of two gold compounds on lysosomes." Annals of the Rheumatic Diseases 47, no. 6 (June 1, 1988): 509–14. http://dx.doi.org/10.1136/ard.47.6.509.

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37

Blakey, Idriss, Zul Merican, Llewellyn Rintoul, Ya-Mi Chuang, Kevin S. Jack, and Aaron S. Micallef. "Interactions of iodoperfluorobenzene compounds with gold nanoparticles." Physical Chemistry Chemical Physics 14, no. 10 (2012): 3604. http://dx.doi.org/10.1039/c2cp23809h.

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38

Li, Huanrong, Zhiping Li, and Zhangjie Shi. "Gold-catalyzed benzylic oxidation to carbonyl compounds." Tetrahedron 65, no. 9 (February 2009): 1856–58. http://dx.doi.org/10.1016/j.tet.2008.12.055.

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39

Palade, P., F. E. Wagner, A. D. Jianu, and G. Filoti. "Electronic properties of gold–aluminium intermetallic compounds." Journal of Alloys and Compounds 353, no. 1-2 (April 2003): 23–32. http://dx.doi.org/10.1016/s0925-8388(02)01203-3.

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40

Jones, Peter G. "X-ray structural investigations of gold compounds." Gold Bulletin 19, no. 2 (June 1986): 46–57. http://dx.doi.org/10.1007/bf03214643.

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41

Mills, Andrew, Anne Lepre, Brian R. C. Theobald, Elizabeth Slade, and Barry A. Murrer. "Luminescent gold compounds in optical oxygen sensors." Gold Bulletin 31, no. 2 (June 1998): 68–70. http://dx.doi.org/10.1007/bf03214763.

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42

Oroz, Miguel Monge, Annette Schier, and Hubert Schmidbaur. "(Tnmethylphosphine)(triphenylsilyl)gold(I) and Related Compounds." Zeitschrift für Naturforschung B 54, no. 1 (January 1, 1999): 26–29. http://dx.doi.org/10.1515/znb-1999-0108.

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Mononuclear coordination compounds of the type (R3P)AuSiR′3 with R = R’ = Ph and R = Me, R′ = Ph have been obtained from reactions of the corresponding halide complexes (R3P)AuCl with the silyllithium reagent LiSiPh3. The fully phenylated species undergoes ligand redistribution in solution to give homoleptic ionic species. (Me3P)AuSiPh3 is less susceptible to this process and crystallizes from solutions as the heteroleptic complex. The crystal structure of this compound has been determined by X-ray diffraction. In the crystal lattice the molecules are not associated.
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43

Schmidbaur, Hubert. "Ludwig Mond Lecture. High-carat gold compounds." Chemical Society Reviews 24, no. 6 (1995): 391. http://dx.doi.org/10.1039/cs9952400391.

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44

Medved, A. "Spectra and structure correlations of gold compounds." Journal of Molecular Structure 299 (October 1993): 177–83. http://dx.doi.org/10.1016/0022-2860(93)80292-4.

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45

Adokoh, Christian K. "Therapeutic potential of dithiocarbamate supported gold compounds." RSC Advances 10, no. 5 (2020): 2975–88. http://dx.doi.org/10.1039/c9ra09682e.

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46

Fricker, Simon P. "Medicinal chemistry and pharmacology of gold compounds." Transition Metal Chemistry 21, no. 4 (August 1996): 377–83. http://dx.doi.org/10.1007/bf00139037.

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47

Al-Majid, Abdullah M., Sammer Yousuf, M. Iqbal Choudhary, Fady Nahra, and Steven P. Nolan. "Gold-NHC complexes as potent bioactive compounds." ChemistrySelect 1, no. 1 (January 2016): 76–80. http://dx.doi.org/10.1002/slct.201600009.

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48

Larsson, Sven. "Superconductivity in Copper, Silver, and Gold Compounds." Chemistry - A European Journal 10, no. 21 (November 5, 2004): 5276–83. http://dx.doi.org/10.1002/chem.200400017.

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49

Moreno-Mañas, M., R. Pleixats, and M. Tristany. "Gold nanoparticles entrapped in heavily fluorinated compounds." Journal of Fluorine Chemistry 126, no. 9-10 (October 2005): 1435–38. http://dx.doi.org/10.1016/j.jfluchem.2005.08.009.

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50

Mohr, Fabian. "The chemistry of gold-fluoro compounds: A continuing challenge for gold chemists." Gold Bulletin 37, no. 3-4 (September 2004): 164–69. http://dx.doi.org/10.1007/bf03215208.

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