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inquiryIron phthalocyanine CAS:132-16-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic interme
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Product Name: Iron phthalocyanine Synonyms: Phthalocyaninatoiron;[29H,31H-phthalocyaninato(2-)-N29,N30,N31,N32]iron;Iron(Ⅱ) phthalocyanine;Ferreousphthalocyanine;Iron(II)phthalocyanine,min.95%;Iron, 29H,31H-phthalocyaninato(2-)-.kappa.N29,.kapp
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
Conditions | Yield |
---|---|
With ammonium molybdate at 110℃; for 0.166667h; Microwave irradiation; | 90% |
Conditions | Yield |
---|---|
With ammonium molybdate at 130℃; for 0.0833333h; Microwave irradiation; | 89% |
Conditions | Yield |
---|---|
With ammonium molybdate at 120℃; for 0.166667h; Microwave irradiation; | 88% |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo{5.4.0}undec-7-ene In cellosolve=2-ethoxyethanol a mixt. of the Cu salt, phthalonitrile, and the base (molar ratio 3:10:10) was refluxed in ethyl-cellosolve for 6 h;; the ppt. was filtered off, washed with 3% HCl soln., water, and ethanol and purified by extrn. with CHCl3; IR, UV, XRD, and elem.anal.;; | 57% |
In neat (no solvent) for 0.1h; Microwave irradiation; |
Conditions | Yield |
---|---|
With 1,3-dimethyl-1H-imidazol-3-ium hydrogen carbonate; water In ethanol at 160℃; for 8h; chemoselective reaction; | 54% |
Conditions | Yield |
---|---|
With (NH4)2Mo2O7 In neat (no solvent) other Radiation; mixt. of O-phthalic anhydride, urea, metal salt and (NH4)2Mo2O7 irradiated in microwave oven at 460W for 8 min. the at 800W for 8 min, cooling to room temp.; washed (H2O, acetone, MeOH, 6M HCl), reflux with acetone, MeOH and CHCl3resp. about 12 h; elem. anal.; | 49% |
Conditions | Yield |
---|---|
In ethanol abs. ethanol; vac. sublimation; |
bis(4-methylpyridine)phthalocyaninatoiron(II)
iron(II) phthalocyanine
Conditions | Yield |
---|---|
In neat (no solvent) 180-220°C; |
bis(2-isopropylphenylisocyanide)(phthalocyaninato)iron(II)
iron(II) phthalocyanine
B
1-isocyano-2-isopropylbenzene
Conditions | Yield |
---|---|
N2 atmosphere, 220-300°C; TG/DTG/DTA monitoring; |
bis(3-methylphenylisocyanide)(phthalocyaninato)iron(II)
iron(II) phthalocyanine
B
1-isocyano-3-methylbenzene
Conditions | Yield |
---|---|
N2 atmosphere, 195-275°C; TG/DTG/DTA monitoring; |
bis(2-methylphenylisocyanide)(phthalocyaninato)iron(II)
iron(II) phthalocyanine
B
o-tolyl isocyanide
Conditions | Yield |
---|---|
N2 atmosphere, 210-285°C; TG/DTG/DTA monitoring; |
bis(4-methylphenylisocyanide)(phthalocyaninato)iron(II)
iron(II) phthalocyanine
B
4-methylphenyl isocyanide
Conditions | Yield |
---|---|
N2 atmosphere, 200-290°C; TG/DTG/DTA monitoring; |
Fe(2+)*C32H16N8(2-)*C5H4NC5H4N=Fe(C32H16N8)(C5H4NC5H4N)
iron(II) phthalocyanine
Conditions | Yield |
---|---|
byproducts: 4,4'-bipyridine; heating in N2; |
Conditions | Yield |
---|---|
With I2 In tetrahydrofuran |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With oxalic acid In pyridine byproducts: thioanisol; |
{C32H16N8FeC6H4(NC)2}(n)
iron(II) phthalocyanine
Conditions | Yield |
---|---|
byproducts: 1,4-dicyanobenzene; heating under N2-atm.; |
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran Ar; hydrolysis; 6 h; room temperature;; |
μ-oxo-bisphthalocyaninato(2-)ferrate(III)
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With N2 or Ar In dimethyl sulfoxide Kinetics; inert gas bubbled through soln.; followed spectrophotometrically; |
μ-(1,4-diazabicyclo{2.2.2}octane)-(phthalocyaninato)iron(II)
iron(II) phthalocyanine
Conditions | Yield |
---|---|
byproducts: 1,4-diazabicyclo{2.2.2}octane; heating under N2-atm.; |
(phthalocyaninato)-μ-(pyrazine)-iron(II)
iron(II) phthalocyanine
Conditions | Yield |
---|---|
byproducts: pyrazine; heating under N2-atm.; |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With CH3OH In methanol byproducts: CH2CH2, Ph2NH, CH3ONa; (Ar), to Fe-complex methanol added with stirring within 3-10 min; methanolic KOH added, chromd., filtered, washed with water, methanol and ether, IR; | |
With acetyl chloride In tetrahydrofuran byproducts: CH2CH2, MeC(O)NPh2, NaCl; (Ar), Fe-complex dissolved in THF, acetyl chloride added, methanol/pyridine added at -10°C; chromd. (Chromaton-N-Super), filtered; |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With CH2Cl2; CH3OH; CO In neat (no solvent) (inert gas); complex/CH2Cl2 treated with MeOH, stirred for 7 h under CO; filtered (vac.); elem. anal.; | 95% |
N,N,N,N,N,N-hexamethylphosphoric triamide
iron(II) phthalocyanine
Fe(C32H16N8)(CO)(OP(N(CH3)2)3)*OP(N(CH3)2)3*0.5CCl4
Conditions | Yield |
---|---|
With CO In tetrachloromethane stirred in atm. of CO at room temp. for 4 h; filtration, drying in vac. for 20 min; elem. anal.; | 94% |
iron(II) phthalocyanine
[Fe(CH3OH)(CO)(C6H4C2N2)4]
Conditions | Yield |
---|---|
With CH3OH; CO In neat (no solvent) (Ar; CO reacted with complex suspn. for 7 h with stirring; filtered, dried (vac.); elem. anal.; | 91% |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With CCl4; NH3; CO In neat (no solvent) (inert gas); complex suspn. in CCl4 treated with dry NH3, stirred for 15 h under CO; filtered, dried (vac.); elem. anal.; | 91% |
iron(II) phthalocyanine
N-trimethylsilylmethylamine
[Fe(phthalocyanine)(trimethylsilylamine)2]
Conditions | Yield |
---|---|
In tetrahydrofuran under N2; dropwise addn. of amine to soln. of iron complex in THF, stirring at room temp. for 15 min; filtration with Millipore Millex, filtrate slowly concd. under vac., oilwashed with cold hexane, filtration, drying under vac.; elem. anal.; | 90% |
In tetrahydrofuran-d8 under N2; iron complex and amine mixed in THF-d8 in NMR tube for a few min; |
3-Methylpyridine
iron(II) phthalocyanine
(phthalocyaninato)(3-picoline)2iron(II)
Conditions | Yield |
---|---|
In neat (no solvent) under N2; refluxed for 5 h; concd.; cooled to 0°C; filtered; washed (MeOH); dried (70°C); elem. anal.; UV; IR; | 87% |
iron(II) phthalocyanine
4-methoxy-benzylamine
[Fe(phthalocyanine)(p-mrthoxybenzylamine)2]
Conditions | Yield |
---|---|
In tetrahydrofuran under N2; dropwise addn. of amine to soln. of iron complex in THF, stirring at room temp. for 15 min; filtration with Millipore Millex, filtrate slowly concd. under vac., oilwashed with cold hexane, filtration, drying under vac.; elem. anal.; | 86% |
In tetrahydrofuran-d8 under N2; iron complex and amine mixed in THF-d8 in NMR tube for a few min; |
iron(II) phthalocyanine
Fe(C32H16N8)(CO)(C5H5N)*2CCl4
Conditions | Yield |
---|---|
With CO; pyridine In tetrachloromethane a suspn. of complex was stirred in atm. of CO with pyridine for 20 h; filtration, drying in vac. for 10 min; elem. anal.; | 85% |
picoline
iron(II) phthalocyanine
bis(4-methylpyridine)phthalocyaninatoiron(II)
Conditions | Yield |
---|---|
In neat (no solvent) under N2; refluxed for 5 h; concd.; cooled to 0°C; filtered; washed (MeOH); dried (70°C); elem. anal.; UV; IR; | 83% |
In chloroform Fe complex dissolved in CHCl3 soln. contained ligand; soln. stirred for 10 h at room temp.; ppt. collected by filtration, washed with hexane and dried in vac.; | 44% |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With H2O; (CH3)2CO; CO In neat (no solvent) (inert gas); complex suspended in H2O/acetone, treated with CO at room temp. for 4 h; sucked, evapd. (vac.); elem. anal.; | 82% |
Conditions | Yield |
---|---|
In benzene dry amine addn. to bezene suspension of Fe(II)-phthalocyanine, Ar atmosphere, refluxing (24 h); unreacted phthalocyanine filtered away, filtrate evapn., dry hexane addn., ppt. filtering off, vacuum drying (room temp.); | 80% |
Conditions | Yield |
---|---|
7 h at 110°C, cooling to room temp., under prepurified Ar or N2; filtered, dried in vac., elem. anal.; | 77% |
Conditions | Yield |
---|---|
With CO; CCl4 In neat (no solvent) (inert gas); complex in CCl4 treated with (C2H5)2NH under CO with stirring for 20 h; filtered, dried (vac.); elem. anal.; | 76% |
Conditions | Yield |
---|---|
In sulfolane (N2); equimolar amts; stirring at 20°C for 2 h; pouring into ice-water; centrifugation; washing (water, alcohol); drying in vac.; recrystn. (pyridine); | 75% |
diethylacetamide
iron(II) phthalocyanine
Fe(C32H16N8)(CO)((C2H5)2NCOCH3)*CH3CON(C2H5)2
Conditions | Yield |
---|---|
With CO a suspn. of complex in diethylacetamide was stirred in atm. of CO for 10 h; filtration, drying in vac.; elem. anal.; | 74% |
Conditions | Yield |
---|---|
With chromium dichloride at 80℃; for 24h; | 74% |
iron(II) phthalocyanine
1,4-diisocyano-2,3,5,6-tetramethylbenzene
(phthalocyaninato)bis(2,3,5,6-tetramethyl-1,4-diisocyanobenzene)iron(II)
Conditions | Yield |
---|---|
In chloroform exclusion of moisture and O2; 6-20 -fold excess of (CN)2C6(CH3)4, mixt. stirred for 1 h at ambient temp.; filtered, concd., addn. of n-hexane, ppt. centrifugated, dried, excess (CN)2C6(CH3)4 sublimated at 80°C under vacuum, elem.anal.; | 73% |
iron(II) phthalocyanine
hexane
1,2-dichloro-benzene
[2.2.2]cryptande
[5,6]fullerene-C70
Conditions | Yield |
---|---|
Stage #1: iron(II) phthalocyanine; sodium fluorenone; 1,2-dichloro-benzene; [2.2.2]cryptande; [5,6]fullerene-C70 at 60℃; for 4h; Stage #2: hexane | 72% |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
With (C2H5)3N; CCl4; CO In neat (no solvent) (inert gas); complex in CCl4 treated with (C2H5)3N under CO with stirring for 20 h; filtered, dried (vac.); elem. anal.; | 71% |
iron(II) phthalocyanine
Conditions | Yield |
---|---|
In xylene PcFe is added to a suspn. of TPPFeNFePc in xylene, mixt. is refluxed at 120°C under N2 with const. stirring for 8 h; mixt. is allowed to cool to room temp., xylene is sepd. by centrifugation, solid residue is washed with xylene, dried under vac. at room temp.; elem. anal.; | 65% |
iron(II) phthalocyanine
triptycene
tetramethylphosphonium bromide
(tetramethylphosphonium)∙{[Fe(I)Pc(-2)](1-)}∙triptycene
Conditions | Yield |
---|---|
Stage #1: iron(II) phthalocyanine; tetramethylphosphonium bromide With zinc In benzonitrile; 1,2-dichloro-benzene at 170 - 180℃; Stage #2: triptycene In benzonitrile; 1,2-dichloro-benzene | 65% |
iron(II) phthalocyanine
N,N,N',N'-tetrabenzyl-p-phenylenediamine
tetramethylphosphonium bromide
Conditions | Yield |
---|---|
Stage #1: iron(II) phthalocyanine; tetramethylphosphonium bromide With zinc In benzonitrile; 1,2-dichloro-benzene at 170 - 180℃; Stage #2: N,N,N'N'-tetrabenzyl-benzene-1,4-diamine In benzonitrile; 1,2-dichloro-benzene | 65% |
Conditions | Yield |
---|---|
at 190℃; for 24h; Inert atmosphere; | 64% |
iron(II) phthalocyanine
tert-butylisonitrile
bis(tert-butylisocyanide)(phthalocyaninato)iron(II)
Conditions | Yield |
---|---|
In toluene at 80℃; for 4h; Inert atmosphere; | 63.8% |
Conditions | Yield |
---|---|
With THF In tetrahydrofuran byproducts: NaCl; under Ar, suspn. of Na2(FePC)*xTHF in THF prepd. by redn. of FePc with 2.2 equivs. of (C10H8)Na, PhSCH2Cl dissolved in THF added at 0°C,stirred at room temp. for 2 h; filtered, treated with ether, crystals filtered, washed with hot ether,recrystd. from THF/ether; elem. anal.; | 62% |
iron(II) phthalocyanine
1,2-dichloro-benzene
[2.2.2]cryptande
[iron(I) phthalocyanine]-(cryptand[2,2,2])*(Na+)(o-dichlorobenzene)
Conditions | Yield |
---|---|
at 60℃; for 4h; | 56% |
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