ChemicalBook--->CAS DataBase List--->28923-39-9

28923-39-9

28923-39-9 Structure

28923-39-9 Structure
IdentificationBack Directory
[Name]

NICKEL(II) BROMIDE ETHYLENE GLYCOL DIMETHYL ETHER COMPLEX
[CAS]

28923-39-9
[Synonyms]

ether compL
(II) bromide ethyL
NICKEL(II) BROMIDE ETHYLE
dibromonickel,1,2-dimethoxyethane
(1,2-Dimethoxyethane)nickel dibromide
1,2-Dimethoxyethane - dibromonickel (1:1)
Nickel,dibromo[1,2-di(methoxy-kO)ethane]-
NICKEL(II)BROMIDE,DIMETHOXYETHANEADDUCT,MIN.97%
nickel(ii) bromide ethylene glycol dimethyl ether
Nickel(II) bromide, dimethoxyethane adduct, min. 97%
NICKEL(II) BROMIDE ETHYLENE GLYCOL DIMETHYL ETHER COMPLEX
Nickel(II) broMide ethylene glycol diMethyl ether coMplex 97%
[Molecular Formula]

C4H10Br2NiO2
[MDL Number]

MFCD00013480
[MOL File]

28923-39-9.mol
[Molecular Weight]

308.62
Questions And AnswerBack Directory
[Synthesis]

100 g, 771.6 mmol NiCl2 was dissolved in a mixture of 300 mL methanol and 50 mL trimethyl orthoformate and stirred under reflux overnight. After the reaction, unreacted NiCl2 was removed by filtration, and 80% of the solution was removed under reduced pressure to obtain a green gel. This gel was dissolved in a minimal amount of methanol, and 300 mL DME was added. The solution was refluxed and stirred overnight. The yellow powder precipitate of [NiCl2(DME)] was separated by filtration through a conduit. The powder was washed with pentane and dried under a nitrogen stream. Orange powder ethylene glycol dimethyl ether nickel bromide was given, yield: 135.0 g, 80%. The synthetic route is shown in Figure 2.


Synthetic Route of NICKEL(II) BROMIDE ETHYLENE GLYCOL DIMETHYL ETHER COMPLEX

Figure: Synthetic Route of NICKEL(II) BROMIDE ETHYLENE GLYCOL DIMETHYL ETHER COMPLEX

Chemical PropertiesBack Directory
[Melting point ]

186-188 °C
[Fp ]

124 °F
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Methanol (Slightly), Water (Slightly)
[form ]

Powder
[color ]

peachy
[Sensitive ]

moisture sensitive
[Stability:]

Moisture Sensitive
[Major Application]

battery precursors
catalysts
material synthesis precursor
[InChI]

InChI=1S/C4H10O2.2BrH.Ni/c1-5-3-4-6-2;;;/h3-4H2,1-2H3;2*1H;/q;;;+2/p-2
[InChIKey]

VHSVJTYBTJCDFL-UHFFFAOYSA-L
[SMILES]

C(COC)OC.[Ni](Br)Br
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS02,GHS07,GHS08,GHS09
[Signal word ]

Danger
[Hazard statements ]

H228-H317-H332-H334-H341-H351-H361f-H372-H410
[Precautionary statements ]

P210-P273-P280-P302+P352-P304+P340+P312-P308+P313
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-20/21/22-36/37/38
[Safety Statements ]

16-22-26-36/37/39-45
[RIDADR ]

UN 1325 4.1/PG 2
[WGK Germany ]

3
[HazardClass ]

4.1
[Storage Class]

4.1B - Flammable solid hazardous materials
[Hazard Classifications]

Acute Tox. 4 Inhalation
Aquatic Acute 1
Aquatic Chronic 1
Carc. 2 Inhalation
Flam. Sol. 1
Muta. 2
Repr. 2
Resp. Sens. 1
Skin Sens. 1
STOT RE 1 Inhalation
Hazard InformationBack Directory
[Uses]

Nickel(II) bromide ethylene glycol dimethyl ether complex is a nickel based catalyst that is used in the preparation of poly(3-hexylthiophene) (P3HT) Kumada catalyst transfer polymerization. It facilitates good control over the molecular weight of the conjugating polymer.
[reaction suitability]

reagent type: catalyst
core: nickel
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