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Ruthenium 3 chloride hydrate

Manufactured by Merck Group
Sourced in Sweden, Singapore

Ruthenium(III) chloride hydrate is a chemical compound with the formula RuCl3•xH2O, where x is typically between 3 and 4. It is a dark red-brown, crystalline solid that is soluble in water and organic solvents. Ruthenium(III) chloride hydrate is commonly used as a precursor for the synthesis of other ruthenium compounds and as a catalyst in various chemical reactions.

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15 protocols using ruthenium 3 chloride hydrate

1

Synthesis of Fe-Based Nanomaterials

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For this study, we used FeCl3 (97%), poly(vinyl alcohol) (PVA, Mw 9000), dodecyl trimethylammonium bromide (DTAB, ≥ 98%), pyrrole (98%), and NaBH4 (≥ 98%) from Aldrich Chemical Company (St. Louis, MI, USA) and used each as purchased. Ruthenium (III) chloride hydrate (99.98%) was acquired from Aldrich Chemical Company, as well. Ammonium persulfate (APS, 98%) and pyrrole-3-carboxylic acid were obtained from Sigma-Aldrich and Acros Organics (Geel, Belgium). Sodium hydroxide (NaOH, 95%) and hydrochloric acid (HCl, 35~37%) were purchased from Samchun Pure Chemical Company (Seoul, Korea).
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2

Electrochemical Synthesis of Transition Metal Complexes

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CC was purchased from Vetec and all the chemicals used were of reagent grade or comparable purity. Methanol, dichloromethane and ether were distilled prior to use. All the aqueous solutions were prepared with ultra-pure water (ASTM type I, 18 MΩ cm of resistivity). Ruthenium(III) chloride hydrate, 1,4-bis(diphenylphosphino)butane (dppb), chloroauric acidH [AuCl4], tetrabutylammonium hexafluorophosphate (TBAH) and cobalt (II) acetate salt were purchased from Aldrich and they were used as received. Acetate buffer solutions (HAc-NaAc, 0.1 mol l−1) with different pH values were prepared by mixing 0.1 mol l−1 of acetic acid (HAc) and 0.1 mol l−1 of sodium acetate (NaAc) and the pH was adjusted by NaOH or HCl. Purified argon atmosphere was used in all procedures described to remove the dissolved oxygen.
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3

Preparation of Ruthenium and Cobalt Complexes

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All solvents and chemicals were of reagent-grade quality, obtained commercially and used without further purification, unless otherwise noted. Ruthenium(iii) chloride hydrate, ammonium hexafluorophosphate, n-butyllithium solution (2.7 M in heptane), n-pentane, and tetrahydrofuran were purchased from Aldrich Chemicals. The chemicals, such as 4,7-dimethyl-1,10-phenanthroline (Me2phen), silver sulphate, lead dioxide, and cobalt(ii) chloride, were purchased from Alfa Aesar. 2,2′-Bipyridine, 1,2,3,4,5-pentamethylcyclopentadiene, and TiIV(O)(tpyp) (tpyp = 5,10,15,20-tetra(4-pyridyl)porphyrinato anion) were obtained from Tokyo Chemical Industry Co., Ltd. Sc(NO3)3·4H2O was supplied by Mitsuwa Chemicals Co., Ltd. 18O2 gas (98% 18O-enriched) was purchased from ICON Services Inc. (Summit, NJ. USA). The purification of water (18.2 MΩ cm) was performed with a Milli-Q system (Millipore, Direct-Q 3 UV). Acetonitrile was dried according to published procedures and distilled prior to use.30 The cobalt(iii) starting complex, [CoIII(Cp*)(bpy)(H2O)]2+ (1, Cp* = η5-pentamethylcyclopenta-dienyl and bpy = 2,2-bipyridine), and the tris(4,7-dimethyl-1,10-phenanthroline)ruthenium(ii) complex, [RuII(Me2phen)3]2+, were prepared according to the published methods.25 ,31
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4

Synthesis and Characterization of Ruthenium(III) Complexes

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Ruthenium(III)-chloride
hydrate, 1,10-phenanthroline, sodium hydroxide, silver tetrafluoroborate,
salicylaldehyde, 5-chlorosalicylaldehyde, 3,5-chlorosalicylaldehyde,
5-bromosalicylaldehyde, 3,5-bromosalicylaldehyde, 3-bromo-5-chlorosalicylaldehyde,
3,5-diiodosalicylaldehyde, 4-(diethylamino)salicylaldehyde, 5-nitrosalicylaldehyde,
4-methoxysalicylaldehyde, 5-methoxysalicylaldehyde, 4-methylsalicylaldehyde,
5-methylsalicylaldehyde were obtained from Sigma-Aldrich and used
without any further purification. The solvents obtained from the same
commercial source, however, were subjected to a distillation process
before being used for the synthesis of the complexes. cis-Ru(phen)2Cl2 was prepared according to literature procedures.23 (link) FT-IR spectra were recorded using KBr pellets
on a JASCO FT/IR-6300 spectrometer (4000–400 cm–1). Elemental analyses were carried out using both the LECO’s
CHNS-932 and PerkinElmer 7300 DV elemental analyzer. NMR spectra were
recorded in quartz NMR tube by means of Bruker high resolution Avance
NEO 4500 (500 MHz) and Bruker Avance III HD 400 MHz spectrometer and
using DMSO-d6 as a solvent at 295 K.
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5

Synthesis of Metallic Nanoparticles

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Solution-based syntheses were carried out using 99.99% hydrogen tetrachloroaurate(III) trihydrate (Alfa Aesar), 99.9999% silver nitrate (Sigma-Aldrich), 99.99% copper (II) nitrate trihydrate (Sigma-Aldrich), 99.99% potassium tetrachloroplatinate(II) (Sigma-Aldrich), 99.999% sodium tetrachloropalladate(II) (Sigma-Aldrich), 99.98% ruthenium(III) chloride hydrate (Sigma-Aldrich), 99.98% hydrogen hexachloroiridate(IV) hydrate (Sigma-Aldrich), 99.98% sodium hexachlororhodate(III) (Sigma-Aldrich), and 100% isopropyl alcohol (Honeywell). Solutions for catalysis were prepared using 4-NP (Fluka), NaBH4 (Fluka), and DI water with a resistivity of 18.2 MΩ cm1. All chemicals were used as received.
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6

Synthesis and Characterization of Ru(II) Complexes

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Ruthenium(III) chloride hydrate, lithium chloride, 2,2 ′ -bipyridyl, silver tetrafluoroborate, triethylamine, 5-bromosalicylaldehyde, 3,5-dibromosalicylaldehyde, 5-chlorosalicylaldehyde, 3,5dichlorosalicylaldehyde, and 3-bromo-5-chlorosalicylaldehyde were purchased from Sigma-Aldrich and used without purification. Ru(bpy) 2 Cl 2 was prepared according to the literature procedure. [53] [54] [55] The commercial solvents were distilled and then used for the preparation of ligands and complexes. The FT-IR spectrum was recorded on a JASCO, FT/IR-6300 spectrometer (4000-400 cm -1 ) in KBr pellets. Elemental analysis was performed on Leco, CHNS-932 and PerkinElmer 7300 DV elemental analyzers. 1 H-and 13 C-NMR spectra for the Ru(II) complexes were recorded on a Bruker Avance III 400 spectrometer using DMSO as the solvent at 20 °C.
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7

Synthesis of Ruthenium-Based Compounds

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Sodium nitrate (≥99%), ruthenium (III) chloride hydrate (ruthenium content, 40.00 to 49.00%), and ruthenium (IV) oxide (≥99.9%) were purchased from Sigma-Aldrich without further purification. Sodium perrhenate (99%) was purchased from Alfa Aesar, Australia. 18O Water (18O, 97%+) was purchased from Novachem, Australia.
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8

Synthesis of Ruthenium Nanoparticles

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Ammonium heptamolybdate (AHM, (NH4)6Mo7O24·4H2O), ruthenium (III) chloride hydrate (RuCl3, Ru 38–40%), poly(vinyl-pyrrolidone) (PVP, 55 kDa), and ethylene glycol (EG, >99%) were all purchased from Sigma Aldrich (Stockholm, Sweden). Ethanol, absolute (EtOH, ≥99.8%) was obtained from VWR (Stockholm, Sweden). A MilliQ reference water purification system (Merck Millipore, Burlington, MA, USA) was used for deionized (DI) water.
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9

Ruthenium(III) Chloride Hydrate Catalyzed Reactions

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Ruthenium(III) chloride hydrate (RuCl3·xH2O, MW: 207.43), morin
hydrate [(2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one)],
nitrobenzene (≥99.0%), and CDCl3 were obtained from
Sigma-Aldrich. All other reagents required for this study were of
AR grade and used as obtained. All of the solvents used were distilled
and dried before the actual use. Triple-distilled water was used throughout
the experiment.
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10

Synthesis of Rhodium and Ruthenium Nanoparticles

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Rhodium (III) chloride hydrate (RhCl3·xH2O, Rh 38.5%–45.5%), Ruthenium (III) chloride hydrate (RuCl3·xH2O, Ru 38%–40%), Ethylene glycol (>99%), and Poly (vinyl pyrrolidone) (PVP, average MW = 55 kDa, 10 kDa) were obtained from Sigma Aldrich. Hydrochloric acid, Sodium hydroxide and solvents including acetone, ethanol of analytical grade were obtained from Sigma Aldrich. All chemicals were used without further purification.
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