Conditions | Yield |
---|---|
In neat (no solvent) allowed to stand in the dark for 64 h at ambient temp.; identified spectroscopically; | A n/a B 102 % C 91% |
In benzene 30 min at 7°C, allowed to warm to 17°C, after 1 h allowed to procced at room temp., reaction time: 170 d; followed by (1)H-NMR; |
Conditions | Yield |
---|---|
In hydrogen bromide according to T.S. Piper, M.K. Wilson, J. Inorg. Nucl. Chem., 4, 22 (1957) and J.E.Griffiths, Inorg. Chem., 2, 375 (1963); collected into -134°C trap, purified by passing through a columnwith silica gel and mol. sieve 5A at -30 °C, detd. by chromy. and mass spectrometric analysis; | 90% |
chlorogermane
bis(difluorophosphino) sulphide
A
germane
B
difluoro(germylthio)phosphine
C
chlorodifluorophosphine
D
difluorophosphine sulfide
Conditions | Yield |
---|---|
mixt. was warmed to 209 K for 2 h; examined by NMR, sepd. by fractional condensation; | A <1 B 87% C n/a D <1 |
tetracarbonylgermyliron(1-)
chlorotrimethylgermane
A
germane
tetracarbonyl(trimethylgermyl)germyliron
C
[Fe2(μ-GeH2)2(CO)8]
D
trimethylgermane
Conditions | Yield |
---|---|
In diethyl ether under N2, 30 min; pumping for 3 h at diffusion pump vacuum, extn. (cyclohexane): ((Fe(CO)4(GeH2))2); | A n/a B 23% C 58% D n/a |
Conditions | Yield |
---|---|
In solid matrix byproducts: LiCl, AlCl3; distilling gaseous GeCl4 in vac. on solid matrix of LiAlH4 in ether (cooled with liq. N2), heating to room temp.;; fractional condensation at -111.9 °C;; | 27.7% |
In solid matrix byproducts: LiCl, AlCl3; distilling gaseous GeCl4 in vac. on solid matrix of LiAlH4 in ether (cooled with liq. N2), heating to room temp.;; fractional condensation at -111.9 °C;; | 27.7% |
Conditions | Yield |
---|---|
In solid byproducts: Ge, LiI; mechanically acivated interaction in vac. vibrating ball mill, accordingto: V. V. Volkov, K. G. Myakishev, I. I. Gorbacheva, Izv. Sib. Otd. Aka d. Nauk SSSR, Ser. Khim. Nauk, 5 (1983) No. 12, p. 79; monitored by volumetric anal., IR spectroscopy, chem. anal.; | A 1% B n/a |
Conditions | Yield |
---|---|
In hydrogen bromide in dild. aq. HBr soln.; | |
In hydrogen bromide aq. HBr; in dild. aq. HBr soln.; |
Conditions | Yield |
---|---|
byproducts: H2O; | |
byproducts: H2O; |
Conditions | Yield |
---|---|
byproducts: H2O; | |
byproducts: H2O; |
Conditions | Yield |
---|---|
In tetrahydrofuran | |
In water | |
In water |
Conditions | Yield |
---|---|
In gas byproducts: ethane, ethene; Irradiation (UV/VIS); laser-induced photolytic chemical vapour deposition (LPCVD) of (C2H5)GeH3 (2.5 kPa) at 193 nm and deposition of Ge on a reactor NaCl window;; IR and energy-dispersive X-ray spectroscopy; further byproducts;; |
Conditions | Yield |
---|---|
In gas byproducts: ethane, ethene; Irradiation (UV/VIS); laser-induced photolytic chemical vapour deposition (LPCVD) of (C2H5)2GeH2 (2.7 kPa) at 193 nm and deposition of Ge on a reactor NaCl window;; IR and energy-dispersive X-ray spectroscopy;; |
tetracarbonylgermyl(methylgermyl)iron
A
germane
B
germanium dihydride dichloride
{Fe(CO)4(GeH3)(Ge(CH3)ClH)}
D
methylgermyl chloride
E
methylgermane
Conditions | Yield |
---|---|
With CCl4 In benzene under N2, 3-80 days; detn. by (1)H-NMR; |
tetracarbonylgermyl(methylgermyl)iron
A
germane
B
{Fe(CO)4(GeH3)H}
C
{Fe(CO)4(Ge(CH3)ClH)H}
D
methylgermyl chloride
Conditions | Yield |
---|---|
In benzene under N2, 84 days; detn. by (1)H-NMR; |
tetracarbonylgermyl(methylgermyl)iron
A
germane
B
[Fe2(μ-GeH2)2(CO)8]
C
{(Fe(CO)4(GeH3))2(Ge(CH3)H)}
D
methylgermane
Conditions | Yield |
---|---|
In benzene 2 y in a sealed NMR tube at room temp.; detn. by (1)H-NMR; |
tetracarbonylgermyl(methylgermyl)iron
A
germane
B
[Fe2(μ-GeH2)2(CO)8]
C
[Fe(CO)4(Ge(CH3)H)]2
D
{(Fe(CO)4)2(Ge(CH3)2)(Ge(CH3)H)}
E
methylgermane
Conditions | Yield |
---|---|
In neat (no solvent) 122 d in the dark, sealed tube; detn. by IR-spectroscopy; |
tetrachlorosilane
tetracarbonylgermyl(methylgermyl)iron
A
germane
{Fe(CO)4(GeH3)(Ge(CH3)ClH)}
C
methylgermyl chloride
D
methylgermane
Conditions | Yield |
---|---|
In benzene under N2, 47 and 91 days; detn. by (1)H-NMR; |
methanol
A
germane
B
digermane
C
trigermane
D
digermyl ether
E
methoxygermane
Conditions | Yield |
---|---|
In Dimethyl ether byproducts: (CH3)3NHBr; MeOH was added to Me3N*GeH3Br*Me2O in Me2O, mixt. was warmed to -63°C for 4-5 h; volatiles were removed in vac., sepd. by low temp. high-vac. distn.; | A <1 B <1 C <1 D <1 E 55-62 |
Conditions | Yield |
---|---|
With aluminium trichloride; sodium chloride In melt byproducts: Al, H2, LiCl; dissolution of LiH in a AlCl3/NaCl melt, introduction of GeCl4 and H2; | 0% |
With potassium chloride; lithium chloride; sodium chloride In melt byproducts: Ge; LiH dissolved in the dried LiCl-NaCl-KCl melt (400°C), introduction of H2 and GeCl4; |
Conditions | Yield |
---|---|
In sulfuric acid using 3 - 4 n H2SO4;; drying the gas with CaCl or P2O5; passing through aq. KOH (50 %); condensing with liquid air;; | |
In sulfuric acid aq. H2SO4; using 3 - 4 n H2SO4;; drying the gas with CaCl or P2O5; passing through aq. KOH (50 %); condensing with liquid air;; |
Conditions | Yield |
---|---|
methane In neat (no solvent) Electric Arc; using Ge electrodes; very small losses;; product is impured with organic compounds;; | |
methane In neat (no solvent) Electric Arc; using Ge electrodes; very small losses;; product is impured with organic compounds;; |
Conditions | Yield |
---|---|
In sulfuric acid adding Zn to sulfuric soln. of Ge;; | |
In sulfuric acid aq. H2SO4; adding Zn to sulfuric soln. of Ge;; |
Conditions | Yield |
---|---|
In sulfuric acid adding Na Hg alloy to a sulfuric soln. of Ge;; | |
In sulfuric acid aq. H2SO4; adding Na Hg alloy to a sulfuric soln. of Ge;; |
Conditions | Yield |
---|---|
In water Electrolysis; using Ge as the cathode and H3PO4 (50 %) as the electrolyte; slow reaction;; | |
In water Electrolysis; using Ge as the cathode and H3PO4 (50 %) as the electrolyte; slow reaction;; |
Conditions | Yield |
---|---|
In solid matrix byproducts: Ge2H4, Ge2H6, GeH3(1-); (Ar or Ne); laser ablated germanium atoms; 3.5 K; IR; | |
In neat (no solvent) co-depositon laser-ablated Ge with H2 at 3.5 K; other products - Ge2H4, Ge2H6, GeH3(1-); identified by IR spectroscopy; |
Conditions | Yield |
---|---|
In neat (no solvent) co-depositon laser-ablated Ge with H2 at 3.5 K; other products - GeH, GeH2, GeH3, Ge2H2; identified by IR spectroscopy; |
Conditions | Yield |
---|---|
With 27 glow discharge, low yield; | |
With 27 glow discharge, low yield; |
germane
germyl
Conditions | Yield |
---|---|
With Cl byproducts: HCl; | 100% |
With F byproducts: HF; | 100% |
Conditions | Yield |
---|---|
germane introducing to evac. reaction vessel (clean or with walls coatedbeforehand by layer of germanium powder) to pressure 0.6-3.0 at, decomp n. initiation by spark discharge, germanium powder deposition on reaction vessel walls; monitoring by pressure measů powder melting in high vac. resistancefurnace; mass spectrometric anal.; | A 99% B n/a |
Kinetics; other Radiation; shock tube; GeH4 was diluted with Ar; T = 1200-1500 K; p ca. 150 kPa; AAS; | |
In gaseous matrix Kinetics; the surface of the reactors are coated with KCl and MgO, the temp. is varied between 420 and 670 K; |
Conditions | Yield |
---|---|
In hexane byproducts: CO, H2; GeH4 and Co2(CO)8 in 1:1 molar ratio were reacted for 21 days in dry hexane in sealed ampules at room temp.; ampule was opened onto a vac. line and volatiles (H2, CO) were removed,residue was recrystd. from CH2Cl2/hexane; IR; | 90% |
Conditions | Yield |
---|---|
With carbon dioxide In gas gas phase ion-molecule reaction; 20 eV impact; GeH4/CO2 (1/25); 5*E-7 torr; under FTMS conditions; FTMS; CIMS; | A 75% B 25% |
Conditions | Yield |
---|---|
In acetonitrile byproducts: Me2NH; (N2); Schlenk technique; GeH4 was condensed into soln. of Ge compd. in MeCN at 77 K; warmed to room temp.; heated at 85°C for 18 h; evapd. (vac.); elem. anal.; | 74% |
Conditions | Yield |
---|---|
With carbon monoxide In gas gas phase ion-molecule reaction; 20 eV electron beam; GeH4/CO mixture (1/25) at 5*E-7 torr; in FTMS cell; disappearance of CO(1+) in less than 100 ms; Fourier transform mass spectroscopy (FTMS); chemical ionization mass spectroscopy (CIMS); | A 65% B 15% C 20% |
With carbon monoxide In gas byproducts: GeC; gas phase ion-molecule reaction; GeH4/CO ratio 1/10; total pressure >1 torr; under chemical ionization conditions; CIMS; |
germane
molybdenum(carbonyl)(dpe)2
Conditions | Yield |
---|---|
In benzene Ar; condensing 1 equiv. of GeH4 onto frozen benzene soln. of Mo complex,warming to room temp.; taking the soln. off, washing the solid with toluene, hexane (twice): elem. anal.; | 49% |
hydrogenchloride
germane
A
chlorogermane
B
germanium dihydride dichloride
Conditions | Yield |
---|---|
With AlCl3 congealing of the products; pumping H2 out; fractionating; transition temp.: -135 - -120 °C (GeH4), -120 - -90 °C (HCl), -83 - -78 °C (H3GeCl) and -61 - -52 °C (H2GeCl2);; | A 14% B 48% |
With AlCl3 congealing of the products; pumping H2 out; fractionating; transition temp.: -135 - -120 °C (GeH4), -120 - -90 °C (HCl), -83 - -78 °C (H3GeCl) and -61 - -52 °C (H2GeCl2);; | A 48% B 14% |
In neat (no solvent) reaction of GeH4 with HCl-gas over AlCl3;; product mixt. obtained, sepn. by fractional distillation;; | |
In neat (no solvent) reaction of GeH4 with HCl-gas over AlCl3;; product mixt. obtained, sepn. by fractional distillation;; |
germane
diiron nonacarbonyl
iron pentacarbonyl
B
triiron dodecarbonyl
C
Ge{Fe2(CO)8}2
Conditions | Yield |
---|---|
In hexane byproducts: hydrogen, carbon monoxide; in an evacuated vessel(temp.77K) the reaction mixture was warmed in the closed ampoule to room temp., then at 65°C for 15 minutes, the soln. was brown-yellow and little solid Fe2(CO)9 remained; incondensible gases and Fe(CO)5 was removed, residue was chromd. (pentane) on silica gel to give, in order of elution, green Fe3(CO)12, yellow Ge(Fe2(CO)8)2 (recryst. from pentane red crystals), two minor unidentified products and orange Ge2Fe6(CO)23; | A n/a B n/a C 43% D 10% |
In hexane addn. of the reaction mixture in an evacuated vessel(77K), reaction at 50°C for 8d; incondensible gases and Fe(CO)5 was removed, residue was chromd. (pentane) on silica gel to give, in order of eluation, green Fe3(CO)12, yellow Ge(Fe2(CO)8)2 and orange Ge2Fe6(CO)23; | A n/a B n/a C 19% D n/a |
In hexane byproducts: hydrogen, carbon monoxide; addn. of the reaction mixture in an evacuated vessel(77K), reaction at 30°C for 10d; incondensible gases and Fe(CO)5 was removed, residue was chromd. (pentane) on silica gel to give, in order of eluation, green Fe3(CO)12, yellow Ge(Fe2(CO)8)2 and orange Ge2Fe6(CO)23; | A n/a B n/a C 10% D n/a |
In hexane byproducts: hydrogen, carbon monoxide; addn. of the reaction mixture in an evacuated vessel(77K), reaction at 25°C for 10d; incondensible gases and Fe(CO)5was removed, residue was chromd. (pentane) on silica gel to give, in order of eluation, green Fe3(CO)12, yellow Ge(fe2(CO)8)2 and orange Ge2Fe6(CO)23; | A n/a B n/a C 5% D n/a |
germane
digermane
Conditions | Yield |
---|---|
In gas byproducts: H2, Ge; Electrochem. Process; silent electric discharge (SED) at -78°C for 1,5 h; according toS.D. Gokhale, J.E. Drake, W.L. Jolly, J. Inorg. Nucl. Chem., 27, 1911 (1965); detd. by gas chromy.; | 42% |
Conditions | Yield |
---|---|
In diethyl ether complex suspn. at -196°C condensed with GeH4, reacted for 1 h at20°C; filtered off, washed with ether, recrystd. (CH2Cl2/ether, cooling); elem. anal.; | 39% |
germane
iron pentacarbonyl
cyclopentadienyl iron(II) dicarbonyl dimer
A
Ge{Fe2(CO)8}2
Conditions | Yield |
---|---|
In petroleum ether vac.; petroleum ether (bp. 100-130°C), heating (150°C, 160 min); removal of volatiles, sepn. of Ge(Fe2(CO)8)2 with extn. (pentane), extn. (CH2Cl2); | A 25% B 35% |
Conditions | Yield |
---|---|
In acetonitrile (N2) GeH4 was condensed at 77 K, Ph3GeCH2CN in MeCN was added, allowed to warm to room temp. and heated at 85°C for 5 days; volatiles were removed in vacuo, residue was washed with hexane and dried in vacuo; elem. anal.; | 32% |
Conditions | Yield |
---|---|
byproducts: water; GeH4 and F3CNO react in an evacuated glass ampoule at 120°C to water and N-trifluoromethylgermaimine.; Isolation at -96°C, separation by a trap-to-trap fractionation as white solid.; | 25% |
dicobalt octacarbonyl
germane
A
Ge2Co6(CO)20
Conditions | Yield |
---|---|
In hexane byproducts: CO, H2; GeH4 and Co2(CO)8 (1:1 or 2:1) were reacted for 14 weeks in dry hexane in sealed ampules at room temp.; ampule was opened onto a vac. line and volatiles (H2, CO) were removed,residue was recrystd. from CH2Cl2/hexane; | A 20% B n/a |
Conditions | Yield |
---|---|
In hexane byproducts: CO, H2; react. of GeH4 and Fe2(CO)9 in hexane at 68°C; preparative chromy. on silica with petroleum spirit-CH2Cl2 as eluent; | A <1 B 1-2 C 7% D 35-45 |
Molecular Structure:
Molecular Formula: H4Ge
Molecular Weight: 76.6718
IUPAC Name: Germane
Synonyms of Germane (CAS NO.7782-65-2): EINECS 231-961-6 ; Germanium hydride ; Germanium tetrahydride ; Monogermane ; Germane [UN2192] [Poison gas] ; UN2192
CAS NO: 7782-65-2
Classification Code: TWA (0.2 ppm)
Melting point: -165°C
Boiling Point: -88°C
Density: 1,53 g/cm3
Merck: 13,4418
Germane (CAS NO.7782-65-2) is used in the semiconductor industry for the epitaxial growth of germanium by MOVPE or chemical beam epitaxy.[5] Organogermanium precursors (e.g. isobutylgermane, alkylgermanium trichlorides, and dimethylaminogermanium trichloride) have been examined as less hazardous liquid alternatives to germane for deposition of Ge-containing films by MOVPE.[6]
A typical synthesis involved the reaction of Na2GeO3 with sodium borohydride.
Na2GeO3 + NaBH4 + H2O → GeH4 + 2 NaOH + NaBO2
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LC50 | inhalation | 1380mg/m3 (1380mg/m3) | BEHAVIORAL: EXCITEMENT BEHAVIORAL: ATAXIA BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(2), Pg. 56, 1974. |
mouse | LD50 | oral | 1250mg/kg (1250mg/kg) | BEHAVIORAL: EXCITEMENT BEHAVIORAL: ATAXIA BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(2), Pg. 56, 1974. |
Reported in EPA TSCA Inventory.
Hazard Codes of Germane (CAS NO.7782-65-2): FT
Risk Statements: 17-21/22-23
R17: Spontaneously flammable in air.
R21/22: Harmful in contact with skin and if swallowed.
R23: Toxic by inhalation.
Safety Statements: 16-24-26-36/37/39-45
S16: Keep away from sources of ignition.
S24: Avoid contact with skin.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection.
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: 2192
RTECS: LY4900000
TSCA: Yes
HazardClass: 2.3
Poison by inhalation. Moderately toxic by ingestion. A hemolytic gas. Ignites spontaneously in air. Incompatible with Br2. See also HYDRIDES, GERMANIUM COMPOUNDS, and GERMANIUM.
ACGIH TLV: TWA 0.2 ppm
DOT Classification: 2.3; Label: Poison Gas, Flammable Gas
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View