Stabilisation of small mono- and bimetallic gold-silver nanoparticles by calix[8]arene derivatives

Similar documents
Supporting Information for

An Efficient Total Synthesis and Absolute Configuration. Determination of Varitriol

Supporting Information. Application of the Curtius rearrangement to the synthesis of 1'- aminoferrocene-1-carboxylic acid derivatives

Facile Multistep Synthesis of Isotruxene and Isotruxenone

Supporting Information for Sonogashira Hagihara reactions of halogenated glycals. Experimental procedures, analytical data and NMR spectra

Drastically Decreased Reactivity of Thiols and Disulfides Complexed by Cucurbit[6]uril

Supplementary Information (Manuscript C005066K)

Electronic Supplementary Information

Block: Synthesis, Aggregation-Induced Emission, Two-Photon. Absorption, Light Refraction, and Explosive Detection

Stereoselective Synthesis of a Topologically Chiral Molecule: The Trefoil Knot

Supporting Information for

Supporting Information. (1S,8aS)-octahydroindolizidin-1-ol.

The First Asymmetric Total Syntheses and. Determination of Absolute Configurations of. Xestodecalactones B and C

Supporting Information. for. Synthetic routes to [Au(NHC)(OH)] (NHC = N- heterocyclic carbene) complexes

Electronic Supplementary Information (ESI)

Triazabicyclodecene: an Effective Isotope. Exchange Catalyst in CDCl 3

Supporting Information

A supramolecular approach for fabrication of photo- responsive block-controllable supramolecular polymers

Supplementary Materials

Synthesis and characterization of innovative well-defined difluorophosphonylated-(co)polymers by RAFT polymerization

Synthesis of borinic acids and borinate adducts using diisopropylaminoborane

Supporting Information

Appendix A. Supplementary Information. Design, synthesis and photophysical properties of 8-hydroxyquinoline-functionalized

Straightforward Synthesis of Enantiopure (R)- and (S)-trifluoroalaninol

Supporting Text Synthesis of (2 S ,3 S )-2,3-bis(3-bromophenoxy)butane (3). Synthesis of (2 S ,3 S

Supporting Information

Synthesis of Glaucogenin D, a Structurally Unique. Disecopregnane Steroid with Potential Antiviral Activity

Supporting Information

Supplementary Figure S1 X-ray crystallographic structure of (C)-(-)-6. (a) ORTEP drawing of (C)-(-)-6 at probability ellipsoids of 50%: tope view.

Supporting information. Enantioselective synthesis of 2-methyl indoline by palladium catalysed asymmetric C(sp 3 )-H activation/cyclisation.

with EDCI (5.73 g, 30.0 mmol) for 10 min. Bromoethylamine hydrobromide (6.15

Electronic Supplementary Material

Supplementary Material

SUPPLEMENTARY INFORMATION

Supporting Information for

How to build and race a fast nanocar Synthesis Information

Supplementary Note 1 : Chemical synthesis of (E/Z)-4,8-dimethylnona-2,7-dien-4-ol (4)

Supporting Information

first step towards nano-optics at surface.

Introduction 1. DSC scan 5-bromo-2-aminopyridine..3. DSC scan 5-bromo-2-nitropyridine...4

Tetrahydrofuran (THF) was distilled from benzophenone ketyl radical under an argon

Babak Karimi* and Majid Vafaeezadeh

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2003

Supporting Information For:

1G (bottom) with the phase-transition temperatures in C and associated enthalpy changes (in

Photooxidations of 2-(γ,ε-dihydroxyalkyl) furans in Water: Synthesis of DE-Bicycles of the Pectenotoxins

Synthesis and nucleophilic aromatic substitution of 3- fluoro-5-nitro-1-(pentafluorosulfanyl)benzene

Synthesis of Trifluoromethylated Naphthoquinones via Copper-Catalyzed. Cascade Trifluoromethylation/Cyclization of. 2-(3-Arylpropioloyl)benzaldehydes

Supporting Information

All solvents and reagents were used as obtained. 1H NMR spectra were recorded with a Varian

Supporting Material. 2-Oxo-tetrahydro-1,8-naphthyridine-Based Protein Farnesyltransferase Inhibitors as Antimalarials

Effect of Conjugation and Aromaticity of 3,6 Di-substituted Carbazole On Triplet Energy

Supporting Information. Enantioselective Organocatalyzed Henry Reaction with Fluoromethyl Ketones

Supplementary Table 1. Small molecule screening data

Chia-Shing Wu, Huai-An Lu, Chiao-Pei Chen, Tzung-Fang Guo and Yun Chen*

Halogen halogen interactions in diiodo-xylenes

Supporting Information. A rapid and efficient synthetic route to terminal. arylacetylenes by tetrabutylammonium hydroxide- and

SUPPLEMENTARY INFORMATION

Red Color CPL Emission of Chiral 1,2-DACH-based Polymers via. Chiral Transfer of the Conjugated Chain Backbone Structure

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2002

Enantioselectivity switch in copper-catalyzed conjugate addition. reaction under influence of a chiral N-heterocyclic carbene-silver complex

Supporting Information

Synthesis of fluorophosphonylated acyclic nucleotide analogues via Copper (I)- catalyzed Huisgen 1-3 dipolar cycloaddition

Supporting Information

Supporting Information

hydroxyanthraquinones related to proisocrinins

Electronic Supplementary Information. ligands for efficient organic light-emitting diodes (OLEDs)

Selective Reduction of Carboxylic acids to Aldehydes Catalyzed by B(C 6 F 5 ) 3

Synthesis of hydrophilic monomer, 1,4-dibromo-2,5-di[4-(2,2- dimethylpropoxysulfonyl)phenyl]butoxybenzene (Scheme 1).

Supporting Information. Rh (III)-Catalyzed Meta-C H Olefination Directed by a Nitrile Template

Compound Number. Synthetic Procedure

Supporting Information

A Mild, Catalytic and Highly Selective Method for the Oxidation of α,β- Enones to 1,4-Enediones. Jin-Quan Yu, a and E. J.

Supplementary Figure 2. Full power on times. Histogram showing on times of bursts with 100 pm 1, 100 pm 2 and 1 nm Et 3 N at full laser power.

Synthesis of Secondary and Tertiary Amine- Containing MOFs: C-N Bond Cleavage during MOF Synthesis

N-[2-(dimethylamino)ethyl]-1,8-naphthalimide Derivatives as Photoinitiators under LEDs

Supporting Information

SYNTHESIS OF A 3-THIOMANNOSIDE

Reduction-free synthesis of stable acetylide cobalamins. Table of Contents. General information. Preparation of compound 1

Aminoacid Based Chiral N-Amidothioureas. Acetate Anion. Binding Induced Chirality Transfer

Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-

2017 Reaction of cinnamic acid chloride with ammonia to cinnamic acid amide

Influence of photo-isomerisation on host-guest interaction in poly(azocalix[4]arene)s

Electronic Supplementary Information. Highly Efficient Deep-Blue Emitting Organic Light Emitting Diode Based on the

Discovery of 3-substituted 1H-indole-2-carboxylic Acid Derivatives as a Novel Class of CysLT 1 Selective Antagonists

Supporting Information for

Supporting Information

Practical Synthesis of -oxo benzo[d]thiazol sulfones: Scope and Limitations

Silver-catalyzed decarboxylative acylfluorination of styrenes in aqueous media

Supporting Information

Chiral Sila[1]ferrocenophanes

Supplementary Information

Supporting Information

Supporting Information (SI) Revealing the Conformational. Preferences of Proteinogenic Glutamic Acid. Derivatives in Solution by 1 H NMR

Recent applications of click chemistry for the functionalization of gold nanoparticles and their conversion to glyco-gold nanoparticles

Supporting Information. Cells. Mian Wang, Yanglei Yuan, Hongmei Wang* and Zhaohai Qin*

SBA-15-functionalized sulfonic acid confined acidic ionic liquid: a powerful and water-tolerant catalyst for solvent-free esterifications

Supporting Information for Synthesis of C(3) Benzofuran Derived Bis-Aryl Quaternary Centers: Approaches to Diazonamide A

Synthesis and Use of QCy7-derived Modular Probes for Detection and. Imaging of Biologically Relevant Analytes. Supplementary Methods

New Efficient Delayed-Action Catalysts Based on Guanidine Templates for Polyurethane Synthesis

Transcription:

Electronic Supplementary Material (ESI) for New Journal of Chemistry. This journal is The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 208 Supplementary Information Stabilisation of small mono- and bimetallic gold-silver nanoparticles by calix[8]arene derivatives Priyanka Ray, a,b Marie Clément, a,b Cyril Martini, b Ibrahim Abdellah, b Patricia Beaunier, c Jose-Juis Rodriguez-Lopes, d Vincent Huc, b Hynd Remita a and Isabelle Lampre *a a Laboratoire de Chimie Physique, Univ Paris-Sud UMR 8000 CNRS, Université Paris-Saclay, 9405 Orsay cedex, France b Institut de Chimie Moléculaire et des Matériaux d Orsay, Univ Paris-Sud UMR 882 CNRS, Université Paris-Saclay, 9405 Orsay cedex, France c Sorbonne Université, CNRS, Laboratoire de Réactivité de Surface, UMR 797, F-75005 Paris cedex 05 (France) d Advanced Materials Departement, IPYCIT, A.C., 7826 San Luis Potosi, Mexico. Synthesis of the octa(hydroxy)-octa(mercaptobutoxy)calix[8]arene 5 2. H-NMR spectrum of calix[8]arene 5 3. Synthesis of the monomer 4-(4-mercaptobutoxy)phenol 4. Characterisation of silver nanoparticles stabilised by calix[8]arenes 5 5. Characterisation of gold nanoparticles stabilised by calix[8]arenes 5 6. Characterisation of gold-silver nanoparticles stabilised by calix[8]arenes 5

. Synthesis of the octa(hydroxy)-octa(mercaptobutoxy)calix[8]arene 5 Scheme S. Synthetic route toward the octa(hydroxy)-octa(mercapto)butoxycalix[8]arene 5. p-octa(benzyloxy)-octa(chlorobutoxy)calix[8]arène 2: To a solution of (42.3 g, 24.9 mmol, equiv.) in anhydrous DMF (64 ml) was added -bromo-4- chlorobutane (92.3 ml,.7 mol, 67 equiv.). The mixture was stirred and heated to 40 C under argon. NaH (9.57 g, 0.4 mol, 6 equiv.) was carefully introduced in 3 times over 6 h and the reaction mixture was stirred for 8 h under argon at 40 C. Then the mixture was cooled down and MeOH were added to the mixture to neutralize NaH excess (around 50 ml). The suspension was filtered through celite with CH2Cl2. The filtrate was stirred for h with MeOH (500 ml). The suspension was filtered after one night and washed with MeOH. The residue was purified by column chromatography (SiO 2, toluene/ch 2Cl 2, gradient from 0 to 80 % CH2Cl2). The compound 2 was obtained as a white powder in 78.3 % yield (47.25 g, 9.5 mmol). 2

H NMR (250 MHz, CDCl 3, ppm): δ 7.5 (m, 40H, Ha), 6.50 (s, 6H, Hc), 4.69 (s, 6H, Hb), 3.89 (s, 6H, Hd), 3.56 (m, 6H, He), 3.47 (t, 6H, 3 J(H e,h h)=6.4 Hz, Hh),.74 (m, 6H, Hf),.64 (m, 6H, Hg). 3 C NMR (300 MHz, DMSO-d 6, ppm): δ 53.8, 48.5, 36.7, 34.3, 28.0, 27.4, 4.4, 72.0, 68.9, 44.9, 30.5, 29.5, 28.8, 27.0. m/z (ESI, CH 2Cl 2-isopropanol, positive mode): 2439.85 [M+Na] + (calc. = 246.36). p-octa(hydroxy)-octa(chlorobutoxy)calix[8]arène 3: To a suspension of 2 (4 g,.65 mmol, equiv.) in THF (70 ml) and EtOH (70 ml) in a two-necked flask equipped with a reflux condenser were added cyclohexene (45 ml, 0.44 mol, 300 equiv.) and Pearlman s catalyst Pd(OH) 2/C (20 % Pd, 2.64 g, 8.80 mmol, equiv.) at room temperature (rt). The mixture was stirred overnight under argon at 75 C. The mixture was cooled down and filtered through celite and washed with THF. The solvent was removed under reduced pressure at 40 C. A yellowish oil was obtained and stirred in 200 ml pentane overnight. The mixture was filtered and the residual solid washed with pentane. The solid residue was washed with Et 2O for 2 h (2 x 00 ml). The solution was filtered and the residual solid was washed with Et2O and dried under vacuum. The product 3 was obtained as a white powder in 98 % yield (2.75 g,.6 mmol). H NMR (300 MHz, DMSO-d6, ppm): δ 8.85 (s, 8H, Ha), 6.30 (s, 6H, Hc), 3.79 (s, 6H, Hb), 3.55 (m, 32H, He/Hf),.80 (m, 6H, Hd),.70 (m, 6H, Hg). 3 C NMR (300 MHz, DMSO-d6, ppm): δ 53.72, 48.28, 35.20, 5.96, 73.6, 67.96, 46.7, 30.07, 28.3. m/z ESI (THF-isopropanol, negative mode): 695.48 [M-H] + (calc. = 696.48). p-octa(hydroxy)-octa(thioacetanobutoxy)calix[8]arène 4: To a solution of 3 (2 g,.8 mmol, equiv.) in DMSO (40 ml) was added potassium thioacetate (.34 g,.8 mmol, 0 equiv.) at rt. The mixture was stirred overnight at rt under argon. The solution was diluted with water (450 ml) and placed for h at -5 C. Then, the solution was stirred for 2 h at rt. The solution was filtered and the solid was washed with water and dried under vacuum. The crude residue was purified by column chromatography (SiO2, MeOH/CH 2Cl 2 gradient from 2 to 3 % MeOH). The product 4 is obtained as white powder in 78 % yield (.85 g, 0.92 mmol). 3

H NMR (250 MHz, DMSO-d 6, ppm): δ 8.75 (s, 8H, Ha), 6.26 (s, 6H, Hb), 3.79 (s, 6H, Hc), 3.57 (t, 6H, Hd), 2.84 (t, 3 J (Hg,Hh)=6.4 Hz, 6H, Hg), 2.27 (s, 24H, Hh),.67 (m, 32H, He/Hf). 3 C NMR (300 MHz, DMSO-d 6, ppm): δ 95.97, 53.64, 48.28, 35.7, 5.89, 73.40, 3.32, 29.77, 29.27, 26.97. m/z (ESI, THF-isopropanol, positive mode): 2039.65 [M+Na] + (calc. = 206.66). m/z (ESI, THF-isopropanol, negative mode): 205.65 [M-H] + (calc. = 206.66). IR (KBr, cm - ): 3200 (vs, O-H stretching); 3024, 2938, 2867 (s, C-H stretching); 689, 665 (vs, C=O stretching); 597, 455 (vs, aromatic breathing); 204 (vs, C-O stretching). p-octa(hydroxy)-octa(mercaptobutoxy)calix[8]arène 5: To a degassed solution of compound 4 (0.40 g, 0.98 mmol, equiv.) in dry THF (5 ml) was added a degassed solution of Na (0.274 g,.88 mmol, 60 equiv.) in dry MeOH (5 ml). The mixture was stirred for h at rt. To the mixture was added dropwise an aqueous solution of HCl ( M) until a ph of was reached. The residue was extracted with CH 2Cl 2 (3 x 00 ml). The organic layer was dried over MgSO4 and filtered with CH2Cl2. The solvent was removed under vacuum. The residue was resolubilised under argon in a mixture of CHCl 3/MeOH/H 2O (30/4/0.5 ml) and tri-n-butylphosphine (586 µl, 2.38 mmol, 2 equiv.) was added. The mixture was stirred for 30 min at rt. Pentane (200 ml) was fed upon stirring for 5 min. The mixture was filtered and the solid was dried under vacuum. The product 5 was obtained as a white powder in 9 % yield (0.8 g, 0.475 mmol). H NMR (360 MHz, CDCl 3/MeOD: 80:20, ppm): δ 6.6 (s, 6H, Hb), 3.80 (s, 6H, Hc), 3.58 (bs, 6H, Hd), 2.43 (t, 6H, Hg),.68 (bs, 32H, 6He/6Hf). H NMR (360 MHz, DMSO-d 6, ppm): δ 8.82 (s, 8H, Ha), 6.28 (s, 6H, Hb), 3.79 (s, 6H, Hc), 3.55 (brt, 6H, Hd), 2.45 (dt, 3 J(Hg,Hh)= 7.3 Hz, 6H, Hg), 2.06 (s, 8H, Hh),.67 (bs, 32H, He/Hf). 3 C NMR (300 MHz, CDCl 3/MeOD: 80/20, ppm): δ 52.26 (Cd), 48.39 (Ca), 35.7 (Cc), 5.30 (Cb), 73.9 (Cf), 30.85 (Cg), 29.93 (Ce), 29.7 (Ch), 24.52 (Ci). m/z (ESI, THF-MeOH, positive mode): 680.57 [M+H] +, 703.54 [M+Na] +, 78.54 [M+K] + (calc. = 680.57). m/z (ESI, THF-MeOH, negative mode): 679.57 [M-H] + (calc. = 680.57). IR (KBr, cm - ): 3293 (vs, O-H stretching); 2935, 2867 (s, C-H stretching); 256 (w, S-H stretching); 598, 456 (vs, aromatic breathing); 205, 006 (vs, C-O stretching); 86 (s, aromatic C-H stretching). 4

2. H-NMR spectrum of calix[8]arene 5 Hb OHa Hb Hc O He He Hd Hd Hc Hf Hf 8 Hg Hg SHh Protons Ha Hb Hc Hd He Hf Hg Hh δ (ppm) 8.82 6.28 3.79 3.55.67.67 2.43 2.06 Figure S. H-RMN spectrum of calix[8]arene 5 in d6-dmso, recorded at 360 MHz and 25 C.. The symmetry and high flexibility allow the recording of well-resolved, symmetrical and narrow signals. The integration of all signals gives a multiple of 8. It is to be noted that the signal at 2.43 ppm, attributed to the protons Hg located on carbon atom in α position of the sulfur atom, corresponds to a splitted triplet due to the coupling between these protons and the proton Hh on the sulfur atom ( 3 J(Hg,Hh)= 7,34 Hz). 5

3. Synthesis of the monomer 4-(4-mercaptobutoxy)phenol Scheme 2. Synthetic route toward the monomer 6 -(benzyloxy)-4-(4-chlorobutoxy)benzene 9 A solution of 0 (0 g, 50 mmol) in -Bromo-4-chlorobutane (37 ml) and anhydrous DMF (4 ml) was placed under argon and stirred at 40 C. NaH (4 g, 00 mmol) was carefully introduced in small fractions over 6 h and the reaction mixture was heated overnight at 50 C. The middle was condensed at 70 C under reduced pressure and precipitated with pentane (500 ml). The suspension was placed overnight at 0 C and filtered (2.46 g, η=86 %). H NMR (CDCl3, ppm): 7.45-7.3 (m, 5H), 6.92-6.80 (m, 4H), 5.02 (s, 2H), 3.94 (t, 2H), 3.62 (t, 2H),.94 (m, 4H). m/z (ESI, THF-EtOH, positive mode): 33.09 [M+Na + ]. 4-(4-chlorobutoxy)phenol 8 A suspension of 9 (8 g, 27.5 mmol) and Pd(OH) 2/C (20 % Pd, 3 g) in cyclohexene (90 ml) and THF (300 ml) was placed under argon and refluxed overnight. The suspension was then filtered over celite, condensed under reduced pressure and precipitated in pentane (200 ml). The white powder was filtrated and dried under vacuum (5.32 g, 2.65 mmol, η=96 %). 6

H NMR (CDCl 3, ppm): 6.77 (s br, 4H), 5.29 (s vbr, H), 3.94 (t, 2H), 3.6 (t, 2H),.94 (m, 4H). m/z (ESI, THF-EtOH, negative mode): 99.05 ([M-H + ]. S-4-(4-hydroxyphenoxy)butyl ethanethioate 7 A solution of 8 (4 g, 9.9 mmol) and potassium thioacetate (2.5 g, 2.9 mmol) in DMSO (34 ml) was heated overnight at 30 C. A solution of brine was added and the middle was extracted twice with DCM (50 ml). After evaporating DCM, the residue was recrystallized in heptane and filtered to afford a white powder (4.2 g, 7. mmol, η=86 %). H NMR (CDCl 3, ppm): 6.75 (s, 4H), 3.89 (t, 2H), 2.93 (t, 2H), 2.33 (s, 3H),.79 (m, 4H). m/z (ESI, THF-EtOH, negative mode): 239.07 ([M-H + ]. 4-(4-mercaptobutoxy)phenol 6 A suspension of MeONa in anhydrous MeOH (Na: 2.30 g, 00 mmol; MeOH: 5 ml) under argon was added to a solution of compound 2 (3 g, 2.5 mmol) in anhydrous THF (40 ml) under argon. The reaction mixture was stirred 30 min and treated with sonicated HCl M (00 ml), then extracted with DCM (3 50mL). The combined organic phases were dried over MgSO 4 and condensed under reduced pressure at room temperature. The product was recrystallized in heptane (300 ml) and filtrated to afford needles (2.25 g,.36 mmol, η=92 %). H NMR (CDCl 3, ppm): 6.76 (s, 2H 2+2H 3), 5.09 (s vbr, H ), 3.9 (t, 2H 4), 2.60 (q, 2H 7),.83 (m, 2H 5 + 2H 6),.39 (t, H8). 3 C NMR (CDCl 3, ppm): 53.35 (C d), 49.85 (C a), 6.42 (C c), 6.06 (C b), 68.46 (C e), 30.90 (C f), 28.37 (C g), 24.7 (Ch). m/z (ESI, THF-EtOH, negative mode): 97.07 [M-H + ]. 7

4. Characterisation of silver nanoparticles stabilised by calix[8]arenes 5 Effect of Ag + /calix ratio 20 Number of particles 5 0 5 50 nm Number of particles Number of particles 0 45 30 5 0 80 60 40 20 0 0 2 4 6 8 0 2 4 Diameter (nm) Figure S2. TEM micrographs and size distribution of silver nanoparticles obtained by total γ-reduction of ethanolic solutions containing 5 0-5 M calix[8]arene 5 and different concentrations of AgClO 4 : (top) 0-3 M (dose 440 Gy), (middle) 7.5 0-4 M (dose 080 Gy), (bottom) 5 0-4 M (dose 720 Gy). The scale is the same for the three micrographs. 8

4. Characterisation of silver nanoparticles stabilised by calix[8]arenes 5 Effect of silver salts Figure S3. TEM micrographs and size distribution of silver nanoparticles obtained by total γ-reduction (dose 720 Gy) of ethanolic solutions containing 5 0-5 M calix[8]arene 5 and 5 0-4 M silver salt : (top) AgPF 6, (middle) AgOTf, (bottom) AgBF 4. 9

5. Characterisation of gold nanoparticles stabilised by calix[8]arenes 5 Figure S4. (a) TEM micrographs and (b) size distribution of gold nanoparticles obtained by total γ-reduction (dose 260 Gy) of ethanolic solutions containing 5 0-5 M calix[8]arene 5 and 5 0-4 M HAuCl 4. 0

6. Characterisation of gold-silver nanoparticles stabilised by calix[8]arenes 5 Effect of silver salt Figure S5. TEM micrographs and size distribution of gold-silver nanoparticles obtained by total γ-reduction (dose 440 Gy) of ethanolic solutions containing 5 0-5 M calix[8]arene 5, 2.5 0-4 M HAuCl 4 and 2.5 0-4 M silver salt : (top) AgPF 6, (middle) AgOTf, (bottom) AgClO 4.

6. Characterisation of gold-silver nanoparticles stabilised by calix[8]arenes 5 XPS analysis Figure S6. XPS spectrum of gold-silver nanoparticles obtained by total γ-reduction (dose 440 Gy) of ethanolic solutions containing 5 0-5 M calix[8]arene 5, 2.5 0-4 M HAuCl 4 and 2.5 0-4 M AgClO 4 2

6. Characterisation of gold-silver nanoparticles stabilised by calix[8]arenes 5 EDX analysis Figure S7. EDX spectra of gold-silver nanoparticles obtained by total γ-reduction (dose 440 Gy) of ethanolic solutions containing 5 0-5 M calix[8]arene 5, 2.5 0-4 M HAuCl 4 and 2.5 0-4 M AgBF 4 Table S. Element quantification for the bimetallic nanoparticles in Figure S7 (a) (b) Element Atomic percentage Sulphur 22.08 29.4 Gold 57.8 22.02 Silver 20.74 48.57 3