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Phosphorus sesquisulfideAppearance:Pls see the Details Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Po
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sulfur
A
phosphorus sulfide
phosphorus sulfide
tetraphosphorus tetrasulphide
E
phosphorus sulfide
Conditions | Yield |
---|---|
In melt vac., 10-100 mol% S, heating (1 week, 673 K); extraction (CS2), filtn.; followed by (31)P NMR; |
sulfur
A
phosphorus sulfide
B
phosphorous trisulfide
E
phosphorus sulfide
Conditions | Yield |
---|---|
In melt vac.,; 54 mol% S, heating (573-873 K), standing (5 weeks, room temp.); extraction (CS2), filtn.; followed by (31)P NMR; | |
In melt vac.,; 54 mol% S, heating (573-873 K); extraction (CS2), filtn.; followed by (31)P NMR; |
sulfur
A
tetraphosphorus decasulfide
B
phosphorus sulfide
C
phosphorus sulfide
thionyl chloride
phosphan
A
hydrogenchloride
B
trichlorothiophosphine
D
phosphorus sulfide
E
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) room temp.;; further unidentified liquid products;; |
thionyl chloride
phosphan
A
hydrogenchloride
C
phosphorus sulfide
D
trichlorophosphate
hydrogen sulfide
phosphorus trichloride
phosphorus sulfide
Conditions | Yield |
---|---|
With 2-methylpyridine In not given byproducts: CH3C5H4NH(PS2Cl2), CH3C5H4NH(Cl); |
sulfuryl dichloride
phosphan
A
hydrogenchloride
C
phosphorus sulfide
D
trichlorophosphate
Conditions | Yield |
---|---|
With sulfur with pured and dried PH3 in vacuum; at 450°C; equilibrium reaction 3-4.5 mol S for two mol PH3; | |
With S with pured and dried PH3 in vacuum; at 450°C; equilibrium reaction 3-4.5 mol S for two mol PH3; |
Conditions | Yield |
---|---|
With sulfuryl dichloride In neat (no solvent) react. of SO2Cl2 with dry PH3; formation of HCl, P4S3, red P, POCl3 and P2O3;; | |
With thionyl chloride In neat (no solvent) react. of SOCl2 with dry PH3; formation of HCl, P4S3 and red P;; |
pyrosulfuryl chloride
A
hydrogenchloride
B
chlorosulfonic acid
D
phosphorus sulfide
E
sulfur dioxide
Conditions | Yield |
---|---|
With hydrogen phosphide In neat (no solvent) 10°C;; |
Conditions | Yield |
---|---|
In not given byproducts: HCl, SO2; |
A
tetraphosphorus decasulfide
B
phosphorus sulfide
C
phosphorus sulfide
D
tetraphosphorus nonasulfide
E
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) heating (dehydration at 500-550°C, 13-130 Pa, 10 min, open quartz ampoule), sealing of ampoule and heating again (1000-1050°C); mixt. of products not sepd.; (31)P-NMR spectroscopy; |
Conditions | Yield |
---|---|
In melt melting together P and S in a glycerine bath at 170°C;; recrystn. from CS2;; | |
With phosphoric acid In melt formation from P and S in the melt, with less than 1% H3PO4; stirring in a cast iron vessel;; distn. first at atm. pressure, then in vac.;; | |
In neat (no solvent) continuous prepn. by heating P and S at 313-318°C under CO2-atmosphere;; |
Conditions | Yield |
---|---|
In melt stoich. amts. of reagents are reacted in a quartz tube under vac.; recrystn. from CS2; |
thionyl chloride
phosphan
A
trichlorothiophosphine
B
phosphorus sulfide
C
sulfur dioxide
D
trichlorophosphate
Conditions | Yield |
---|---|
In not given react. of SOCl2 with PH3;; | |
In not given react. of SOCl2 with PH3;; |
Conditions | Yield |
---|---|
In not given react. of PH3 with SOCl2 at ambient temp.;; |
Conditions | Yield |
---|---|
In not given | |
In neat (no solvent) heating P4 with S at 165°C;; extraction with CS2 or PCl3;; | |
In further solvent(s) slow addn. of a soln. of S in αchloronaphthalene heated to 150°C to a boiling soln. of P4 in αchloronaphthalene under CO2-atmosphere; boiling for 1 h;; filtn. and washing with CCl4;; |
phosphorus
sulfur
A
tetraphosphorus decasulfide
B
phosphorus sulfide
P4S8, I
D
phosphorus sulfide
E
tetraphosphorus nonasulfide
Conditions | Yield |
---|---|
In carbon disulfide vac.; several months, room temp., light; followed by (31)P NMR; |
phosphorus
sulfur
A
phosphorus sulfide
P4S8, II
P4S7, III
Conditions | Yield |
---|---|
In carbon disulfide vac.; several months, room temp., light; followed by (31)P NMR; |
phosphorus
sulfur
A
tetraphosphorus decasulfide
B
phosphorus sulfide
C
phosphorus sulfide
D
tetraphosphorus nonasulfide
Conditions | Yield |
---|---|
In melt vac.; 15-79 mol% S, heating (363 K, 10-30 d); extraction (CS2), fitln., followed by (31)P NMR; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: P, H2S; react. of PH3 with S above 320°C (ratio: 2:3);; |
Conditions | Yield |
---|---|
In neat (no solvent) heating red P with powdered S at 100°C under CO2 atmosphere or in a evacuated react.-tube;; distn. by further heating; extraction with CS2; distn. under CO2-atmosphere;; | |
iodine In not given formation from red P and S with I2 as catalyst;; | |
In neat (no solvent) formation from red P and S at 250-330°C in a stream of CO2;; |
tetraphosphorus pentasulphide
A
phosphorus sulfide
B
phosphorus sulfide
Conditions | Yield |
---|---|
In neat (no solvent) reversible react. at higher temp.;; | |
In not given formation from P4S5 at higher temp.;; |
tetraphosphorus pentasulphide
triphenyl arsine sulfide
A
phosphorus sulfide
B
phosphorus sulfide
C
γ-P4S6
D
β-P4S8
E
α-P4S6
Conditions | Yield |
---|---|
In carbon disulfide absence of air and moisture; molar ratio P4S5:Ph3AsS=1:1, stirring for 2h; product mixt. not sepd., detd by (31)P-NMR spectroscopy; |
tetraphosphorus pentasulphide
triphenyl arsine sulfide
A
phosphorus sulfide
B
phosphorus sulfide
C
γ-P4S6
D
α-P4S6
Conditions | Yield |
---|---|
In carbon disulfide absence of air and moisture; molar ratio P4S5:Ph3AsS=0.2-1:1, stirring for 2 h; product mixt. not sepd., detd by (31)P-NMR spectroscopy; product ratio depending on educt ratio; |
tetraphosphorus pentasulphide
triphenyl arsine sulfide
A
phosphorus sulfide
B
phosphorus sulfide
C
tetraphosphorus nonasulfide
D
β-P4S8
E
α-P4S6
Conditions | Yield |
---|---|
In carbon disulfide absence of air and moisture; molar ratio P4S5:Ph3AsS=2:1, stirring for 2h; product mixt. not sepd., detd by (31)P-NMR spectroscopy; |
hydrogen sulfide
tetraphenyl phosphonium chloride
phosphorus trichloride
A
phosphorus sulfide
Conditions | Yield |
---|---|
With α-picoline In further solvent(s) byproducts: (HNC6H8)Cl; passing dry H2S in a soln. of PCl3 in 2-methylpyridine, exotherm react., cooling of mixture in H2O-bath to 20-30°C, yellow ppt.; condensation of excess 2-methylpyridine, elution of residue with CS2 (twice), isolation of P4S3 by sepn. of solvent from eluate, washing with CH2Cl2, drying in vac.; dissoln. of solid residue in CH3CN and isolation as Ph4P-salt; elem. anal.; |
hydrogen sulfide
phosphorus trichloride
A
phosphorus sulfide
phosphorus sulfide
C
phosphorus sulfide
tetraphosphorus pentasulphide
Conditions | Yield |
---|---|
With NaY zeolite vac. line; P-compd. condensation into zeolite, H2S condensation into PCl3/zeolite at liq. N2 temp. (ratio P:S=4:10), mixt. sealing, heating at 164°C; |
hydrogen sulfide
phosphorus trichloride
A
phosphorus sulfide
phosphorus sulfide
tetraphosphorus pentasulphide
Conditions | Yield |
---|---|
With NaY zeolite vac. line; P-compd. condensation into zeolite, H2S condensation into PCl3/zeolite at liq. N2 temp. (ratio P:S=4:3 or 4:5), mixt. sealing, heating at 100°C; |
hydrogen sulfide
phosphorus trichloride
A
phosphorus sulfide
B
phosphorus sulfide
Conditions | Yield |
---|---|
With NaY zeolite vac. line; P-compd. condensation into zeolite, H2S condensation into PCl3/zeolite at liq. N2 temp. (ratio P:S=4:5), mixt. sealing, heating at 100°C; |
Conditions | Yield |
---|---|
In carbon disulfide; dichloromethane Ag(CH2Cl2)Al(pftb)4 and P4S3 in CS2-CH2Cl2 were stirred overnight at room temp.; suspn. was filtered, filtrate was concd. and stored at 0°C; elem.anal.; | 90% |
Conditions | Yield |
---|---|
In carbon disulfide (N2); P4S3 in CS2 was added to soln. of BBr3 in CS2 at room temp.; cooled to -78°C; filtered; dried in vac. at room temp.; | 88% |
phosphorus sulfide
[Re(1,1,1-tris(diphenylphosphanylmethyl)ethane)(CO)2]triflate
Conditions | Yield |
---|---|
In dichloromethane CH2Cl2 soln. of Re-complex was brought to reflux, soln. of P4S3 in CH2Cl2 was added for 20 min, refluxed for 30 min under stirring; concd. under vac., hexane was added, filtered under N2, washed with light petroleum ether, dried under N2; | 81% |
phosphorus sulfide
boron triiodide
tetraphosphorus trisulfide boron triiodide
Conditions | Yield |
---|---|
In carbon disulfide (N2); P4S3 (1 equiv.) in CS2 was added to soln. of BI3 (1 equiv.) in CS2at room temp.; suspn. was stirred for 15 min; filtered; washed (CS2); dried in vac. at room temp.; | 81% |
Conditions | Yield |
---|---|
In toluene; acetonitrile under N2, by Schlenk technique; CuBr soln. in MeCN layered over P4S3 in toluene for 7 d; washed with CH2Cl2/CH3CN; dried in vac.; detd. by XRD and MAS NMR; elem.anal.; | 80% |
phosphorus sulfide
copper(I) bromide
triethylphosphine
CuBr(P4S3)(PEt3)2
Conditions | Yield |
---|---|
In toluene; acetonitrile N2; Cu compd. and phosphane in MeCN added to toluene soln. of P4S3 (0.454:1.135:0.454 molar ratio), stirred for 12 h at room temp.; evapd., dissolved (toluene), crystd. (-20°C), elem. anal.; | 80% |
Conditions | Yield |
---|---|
In toluene; acetonitrile N2; Cu compd. and phosphane in MeCN added to toluene soln. of P4S3 (0.454:1.135:0.454 molar ratio), stirred for 12 h at room temp.; evapd., dissolved (toluene), crystd. (-20°C), elem. anal.; | 80% |
copper(l) iodide
phosphorus sulfide
triethylphosphine
CuI(P4S3)(PEt3)2
Conditions | Yield |
---|---|
In toluene; acetonitrile N2; Cu compd. and phosphane in MeCN added to toluene soln. of P4S3 (0.454:1.135:0.454 molar ratio), stirred for 12 h at room temp.; evapd., dissolved (toluene), crystd. (-20°C), elem. anal.; | 80% |
phosphorus sulfide
tungsten pentacarbonyl tetrahydrofuran
W(CO)5(P4S3)
Conditions | Yield |
---|---|
In tetrahydrofuran under N2 by Schlenk technique; P4S3 added to soln. of W(CO)5(THF) (1.36:2.045 mol) in THF; stirred at room temp. for 20 h; evapd.; product washed (toluene, 3 times); elem. anal.; | 78% |
Conditions | Yield |
---|---|
In carbon disulfide AgAl(hfip)4 and P4S3 in CS2 were stirred overnight at room temp.; suspn. was filtered, filtrate was concd. and stored at -30°C; elem. anal.; | 77% |
phosphorus sulfide
sodium tetraphenyl borate
(η5-pentamethylcyclopentadienyl)ruthenium(II)[(1-diphenylarsanyl-2-diphenylphosphanyl)ethylene](η1-tetraphosphorus trisulfide) tetraphenylborate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: Cl(-); (Ar), Ru complex in THF added to P4S3 in THF, treated with NaBPh4, stirred at room temp. for 2 h; slowly dissolved in ethanol/light petroleum 1:1, crystd., elem. anal.; | 70% |
phosphorus sulfide
(η5-pentamethylcyclopentadienyl)ruthenium(II)chloro[cis-1,2-bis(diphenylphosphanyl)ethylene]
sodium tetraphenyl borate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: Cl(-); (Ar), Ru complex in THF added to P4S3 in THF, treated with NaBPh4, stirred at room temp. for 2 h; slowly dissolved in ethanol/light petroleum 1:1, crystd., elem. anal.; | 68% |
phosphorus sulfide
B
cyclopentadienylchromiumtricarbonyl hydride
Conditions | Yield |
---|---|
In toluene N2 or Ar-atmosphere; stirring (room temp., 13 d); filtering, chromy. (SiO2, n-hexane, n-hexane / toluene = 1 : 2, n-hexane), crystn. on concg. (-28°C), recrystn. (THF / hexane, -30°C, several d); elem. anal.; | A 66% B 19% C 2% D 12.7% |
phosphorus sulfide
Conditions | Yield |
---|---|
In toluene 13 d at room temp.; chromy. (silica gel, toluene/hexane 7:3); | A 8% B 66% |
phosphorus sulfide
sodium tetraphenyl borate
(η5-pentamethylcyclopentadienyl)ruthenium(II)[bis(diphenylphosphanyl)methane](η1-tetraphosphorus trisulfide) tetraphenylborate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: Cl(-); (Ar), Ru complex in THF added to P4S3 in THF, treated with NaBPh4, stirred at room temp. for 2 h; slowly dissolved in ethanol/light petroleum 1:1, crystd., elem. anal.; | 65% |
phosphorus sulfide
sodium tetraphenyl borate
(η5-pentamethylcyclopentadienyl)ruthenium(II)[bis(diphenylphosphanyl)ethane](η1-tetraphosphorus trisulfide) tetraphenylborate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: Cl(-); (Ar), Ru complex in THF added to P4S3 in THF, treated with NaBPh4, stirred at room temp. for 2 h; slowly dissolved in ethanol/light petroleum 1:1, crystd., elem. anal.; | 65% |
phosphorus sulfide
[CpFeCl(dppe)]
silver trifluoromethanesulfonate
[(η5-C5H5)Fe(1,2-(diphenylphosphino)ethane)(η1-P(basal)-tetraphosphorus trisulfide)] triflate
Conditions | Yield |
---|---|
In tetrahydrofuran; dichloromethane (N2); slurry of Fe compd., AgOTf and P4S3 in CH2Cl2/THF stirred for 4 h; mixt. filtered, filtrate evapd. under vac., residue washed with toluene and n-hexane, dried; elem. anal.; | 60% |
Conditions | Yield |
---|---|
In tetrahydrofuran; dichloromethane (N2); slurry of Fe compd., AgOTf, and P4S3 in CH2Cl2/THF stirred for 4 h; mixt. filtered, filtrate evapd. under vac., residue washed with toluene and n-hexane, dried; elem. anal.; | 60% |
phosphorus sulfide
Conditions | Yield |
---|---|
With isoprene In toluene N2 or Ar-atmosphere; stirring (room temp., 9 d); filtering, concg., chromy. (SiO2, n-hexane, n-hexane / toluene = 9 : 1, 8 : 2, 7 : 3, 1 : 1, toluene, ether), evapn.; | A 58.9% B 2.5% C 5.3% D 4.4% |
phosphorus sulfide
(Cr(η5-C5H5)(CO)2)2Se
B
cyclopentadienylchromiumtricarbonyl hydride
Conditions | Yield |
---|---|
In toluene N2-atmosphere; stirring (room temp., 6 d), filtering; chromy. (SiO2, n-hexane / toluene); | A 6.4% B 5% C 51.5% D 1% E 15.5% |
phosphorus sulfide
silver tetrakis([2,2,2-trifluoro-1,1-bis(trifluoromethyl)ethyl]oxy)aluminate
Conditions | Yield |
---|---|
Stage #1: phosphorus sulfide; silver tetrakis([2,2,2-trifluoro-1,1-bis(trifluoromethyl)ethyl]oxy)aluminate In dichloromethane at 20℃; Inert atmosphere; Stage #2: dicarbonylcyclopentadienylbromoiron(II) In dichloromethane for 32h; Inert atmosphere; | 50% |
phosphorus sulfide
[2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine]
Conditions | Yield |
---|---|
With ethanol In tetrahydrofuran; ethanol; benzene under N2, solm. of P4S3 in benzene added to soln. obtained by mixing Nisalt in ethanol and triphos in THF, refluxed for 2 h; concd. under N2, crystals filtered off, dried in vac., recrystd. from acetone and ethanol; elem. anal.; | 45% |
sulfur
phosphorus sulfide
Conditions | Yield |
---|---|
In water P4S3 was added to an aq. soln. of Na2S*9H2O and S8 under stirring (temp. increase to about 50°C); the soln. was heated at 80 °C for 45 min and H2O added; after cooling to room temp. pptn. by addn. of ethanol;; isolation of S2O6(4-): recrystn. of the ppt. from a small amt. of hot H2O; isolation of S3P7O(5-) from filtrate: addn. of EtOH, stirring for 15-20 min, decantation, repeated pptn. from aq. Ca(Ac)2/NH4NO3 soln. with EtOH; elem. anal.;; | A 40% B n/a |
di-μ-chloro-bis(1,5-cyclooctadiene)dirhodium
phosphorus sulfide
[2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine]
{(triphos)Rh(P3S3)}*C6H6
Conditions | Yield |
---|---|
In tetrahydrofuran; butan-1-ol; benzene N2-atmosphere; refluxing (5 h); concn. of hot soln. (crystn.); | 35% |
In not given | |
In tetrahydrofuran; benzene P4S3 (2 mmol) in benzene (50 ml) was added to a mixture of triphos (2 mmol) in THF (20 ml) and {RhCl(cod)}2 (1 mmol) in THF (50 ml) under nitrogen, reflux for 1 h, addition of 40 ml warm 1-butanol; filtration, refluxing filtrate overnight;; crystals washed with ethanol and light petroleum (bp 40-70 ° C), recrystn. from benzene and CH2Cl2, elem. anal.;; | 35-40 |
phosphorus sulfide
phosphorus sulfide
Conditions | Yield |
---|---|
With I2 In carbon disulfide byproducts: PI3; react. of iodine in CS2 with P4S3;; | 34% |
With iodine In not given byproducts: PI3; react. of P4S3 with iodine;; | |
With I2 In not given byproducts: PI3; react. of P4S3 with iodine;; | |
With S In not given |
phosphorus sulfide
A
cyclopentadienylchromiumtricarbonyl hydride
Conditions | Yield |
---|---|
In toluene N2 or Ar-atmosphere; stirring (room temp., 24 h, 60°C, 18 h); filtering, concg., chromy. (SiO2, n-hexane / toluene = 4 : 1, 3 : 1, 1 :1, toluene / ether = 1 : 1), evapn.; | A 34% B 14% C 10% D 30% |
phosphorus sulfide
silver tetrakis([2,2,2-trifluoro-1,1-bis(trifluoromethyl)ethyl]oxy)aluminate
Conditions | Yield |
---|---|
Stage #1: phosphorus sulfide; silver tetrakis([2,2,2-trifluoro-1,1-bis(trifluoromethyl)ethyl]oxy)aluminate In dichloromethane at 20℃; Inert atmosphere; Stage #2: (η5-C5H5)Fe(CO)PPh3Br In dichloromethane for 28h; Inert atmosphere; | 34% |
cobalt(II) tetrafluoroborate hexahydrate
phosphorus sulfide
[2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine]
Conditions | Yield |
---|---|
With benzene In tetrahydrofuran; ethanol; benzene P4S3 dissolved in benzene was added to soln. of Co(BF4)2*6H2O in EtOH and ligand in THF, soln. was refluxed under N2 for 1 h; concd. under N2; | 30% |
With benzene In ethanol; benzene under N2 atm. warm soln. P4S3 in benzene added to soln. Co(BF4)2*6H2O in ethanol and toome in benzene, soln. refluxed overnight; ethanol added, soln. concd., complex collected, washed with ethanol-benzene (1:1) and light petroleum (b.p. 40-70°C) and dried, recrystd. from CH2Cl2 and benzene; elem. anal.; |
Conditions | Yield |
---|---|
In toluene Inert atmosphere; Schlenk technique; Glovebox; Reflux; | 30% |
phosphorus sulfide
B
cyclopentadienylchromiumtricarbonyl hydride
Conditions | Yield |
---|---|
In toluene N2 or Ar-atmosphere; stirring (60°C, 3 d); filtering, concg., chromy. (SiO2, n-hexane, n-hexane / toluene = 9 : 1, 8 : 2, 7 : 3, 1 : 1, toluene, ether), evapn.; | A 22.2% B 3% C 1% D 0.4% E 6.8% |
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