Conditions | Yield |
---|---|
In neat (no solvent) fast and complete react. of Rb vapour and elec. activated N2 at 60-70°C;; | |
In neat (no solvent) react. of elec. activated nitrogen with Rb (drops); formation of Rb3N by decompn. of RbN3;; small amt. of Rb3N;; | |
In neat (no solvent) react. of activated nitrogen with Rb mirror;; |
Conditions | Yield |
---|---|
In water ion-exchange procedure; volune reduction (353 K), pptn. on EtOH addn.; | |
With Ionenaustauscher III(OH(1-)) In water loading anion exchange resin with N3(1-) ions using column technique and0.1 N aq. soln. of NaN3, passing aq. soln. of RbCl through the column; evapn. in vac.; X-ray diffraction anal.; |
Conditions | Yield |
---|---|
In water NaN3 treated in acidic cation-exchange resin column; HN3 eluate dripped in Rb2CO3 soln. with rate of 5 mL/min; water evapd.; detd. by Raman spectroscopy; | |
In water mixt. of Rb2CO3 and NaN3 in water; pptn. of RbN3, filtration, washing with 70% ethanol, recrystn., drying in exsiccator over CaCl2 and in vac.; | |
With acidic cation exchanger In water ion-exchange method; |
Conditions | Yield |
---|---|
In water recrystn.;; |
Conditions | Yield |
---|---|
In neat (no solvent) on weak heating with dry N2;; mixt. of RbN3 and RbNH2 obtained;; | |
In neat (no solvent) on weak heating with dry N2;; mixt. of RbN3 and RbNH2 obtained;; |
Conditions | Yield |
---|---|
In neat (no solvent) react. of elec. activated nitrogen with Rb (drops);; | |
In neat (no solvent) react. of elec. activated nitrogen with Rb (drops);; |
Conditions | Yield |
---|---|
In water solns. mixed in 1:1 mol. ratio; filtered, recrystd.; |
Conditions | Yield |
---|---|
In water introduction of pure HN3 in a soln. of Rb2CO3 in a Pt-vessel; evapn.;; drying at 80°C; specially pure;; | |
In water introduction of pure HN3 in a soln. of Rb2CO3 in a Pt-vessel; evapn.;; drying at 80°C; specially pure;; | |
In water aq. HN3 was reacted with Rb2CO3; |
Conditions | Yield |
---|---|
In ammonia aq. NH3; |
Conditions | Yield |
---|---|
In water react. of RbOH and HN3 in weakly acidic soln.; evapn.;; | |
In water react. of RbOH and HN3 in weakly acidic soln.; evapn.;; | |
In diethyl ether react. of hydroxide with HN3 dissolved in Et2O; recrystn. from small amt. of H2O at 80°C; |
Conditions | Yield |
---|---|
In water byproducts: CO2; to aq. NaN3 soln. aq. H2SO4 added; liberated HN3 distd. into aq. RbCO3 soln.; evapn.; recrystn. from EtOH; vac. dried at 150°C; |
rubidium azide
Conditions | Yield |
---|---|
In neat (no solvent) thermal decompn., quartz tube, vac. app.; preheating for 12 h to 200°C, heating to 395°C (decompn. temp.), 0.1 mmHg (max.), several days;; distn.; blue-green residue contains silicate, undecomposed azide, and about 80% nitride;; | 60% |
In neat (no solvent) byproducts: N2; heating of RbN3 in a vessel of quartz at 395°C and high vac.; sometimes the decompn. take place only after hours;; | |
In neat (no solvent) byproducts: N2, Rb3N; decompn. of RbN3; distn. of Rb;; the residue contains essentially Rb3N;; |
rubidium azide
nitrogen
Conditions | Yield |
---|---|
tendency to explode of explosion; decompn. start at 260°C; continuous evolution of N2 at 310°C; product pure; |
Conditions | Yield |
---|---|
In neat (no solvent) decompn. of RbN3;; separation of Rb by sublimation;; | |
In neat (no solvent) decompn. of RbN3;; separation of Rb by sublimation;; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: N2; RbN3:RbNO3:Mn2O3 molar ratio was 5:1:3, grinding, pressing (1E5 N), drying (1E-3 mbar, 130 °C, 12 h), heating under Ar flow: 25/260 °C (100 k/h), 260/380 °C (5 k/h), 380/600 °C (20 K/h), annealing at 600 °C for 30 h; |
Conditions | Yield |
---|---|
In water react. of CS2 and RbN3 in H2O; addn. of ethanol at <0°C;; crystn. from soln.;; | |
In water |
Conditions | Yield |
---|---|
In water dissolving freshly prepared, moisted Cu(N3)2 in hot, concd. RbN3 soln.; cooling;; pptn.; washing with cold water and methanol; drying at ambient temp.;; | |
In ethanol on dissolving Cu(N3)2 in the concd. soln. of the azide;; | |
In water dissolving freshly prepared, moisted Cu(N3)2 in hot, concd. RbN3 soln.; cooling;; pptn.; washing with cold water and methanol; drying at ambient temp.;; |
Conditions | Yield |
---|---|
In water crystn. from concd. aq. equimolar soln. in desiccator under Ar over CaCl2 within 4 wk;; drying over P2O5 in oil pump vac.; product is not free from educts (X-ray);; | |
In melt react. in melt at 320-340°C (<15 min);; partial decompn. of azide (X-ray);; |
Conditions | Yield |
---|---|
In neat (no solvent) heated to 300°C for 30 min, then at 500°C at 0.5 mTorr;; |
rubidium azide
fullerene-C60
Conditions | Yield |
---|---|
In neat (no solvent) heating stoichiometric amts. of C60 and alkali metal azide to its decompn. temp. under dynamic vac.; cooling to room temp.; | |
In not given soln. mixed and evapn., thermal decompn. of RbN3; |
cesium azide
rubidium azide
fullerene-C60
Conditions | Yield |
---|---|
In neat (no solvent) heating stoichiometric amts. of C60 and alkali metal azides to their decompn. temp. under dynamic vac.; cooling to room temp.; |
cesium azide
rubidium azide
fullerene-C60
Conditions | Yield |
---|---|
In neat (no solvent) heating stoichiometric amts. of C60 and alkali metal azides to their decompn. temp. under dynamic vac.; cooling to room temp.; |
cesium azide
rubidium azide
fullerene-C60
Conditions | Yield |
---|---|
In neat (no solvent) heating stoichiometric amts. of C60 and alkali metal azides to their decompn. temp. under dynamic vac.; cooling to room temp.; |
cesium azide
rubidium azide
fullerene-C60
Conditions | Yield |
---|---|
In neat (no solvent) heating stoichiometric amts. of C60 and alkali metal azides to their decompn. temp. under dynamic vac.; cooling to room temp.; |
cesium azide
rubidium azide
fullerene-C60
Conditions | Yield |
---|---|
In neat (no solvent) heating stoichiometric amts. of C60 and alkali metal azides to their decompn. temp. under dynamic vac.; cooling to room temp.; |
The MF of RUBIDIUM AZIDE(22756-36-1): N3Rb
The MW of RUBIDIUM AZIDE(22756-36-1): 127.4879
RUBIDIUM AZIDE(22756-36-1) is a colorless needle or flake crystals, it is easy deliquescent and soluble in water.
RUBIDIUM AZIDE(22756-36-1) in vacuum heating is decomposed into metal Rb and nitriding Rb and release nitrogen.
The Structure of RUBIDIUM AZIDE(22756-36-1):
1. | orl-rat LD50:70 mg/kg | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0571920 . | ||
2. | orl-mus LD50:59 mg/kg | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0571920 . |
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