33401-94-4 Purity
99%
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Specification
A germole-containing π-conjugated polymer was prepared by reacting a lithiated polymer precursor with dimethylgermanium dichloride. The polymer exhibited green photoluminescence in chloroform solution and could be employed as a fluoride chemical detector.
A regioregular organometallic polymer featuring 1,4-dilithio-1,3-butadiene and 9,9-dioctylfluorene-2,7-diyl units was synthesized by reacting a tellurophene-containing polymer, which had a number-average molecular weight (Mn) of 5900 and a molecular weight distribution (Mw/Mn) of 1.9, with n-butyllithium (2.4 equivalents) at temperatures ranging from -78 to -60 °C for 3 hours.
The resulting lithiated polymer was then treated with dimethylgermanium dichloride (1.5 equivalents) at -60 °C, allowing the reaction to proceed to ambient temperature over 12 hours in tetrahydrofuran, yielding a π-conjugated polymer containing 1,1-dimethylgermole-2,5-diyl units with a 76% yield (Mn = 4400 and Mw/Mn = 1.7).
A germanium-containing polyalkylsiloxane was synthesized by polycondensation reaction using dimethylgermanium dichloride as raw material, and then a new high-permeability membrane with high selectivity for butane/methane was obtained by cross-linking with TEOS.
Synthesis of germanium-containing polyalkylsiloxane membrane
· The synthesis of 1,1,3,3,5,5-hexamethyl-1,5-dihydro-3-germyl-1,5-disilapentane was accomplished in a single reaction mixture, involving the intermediate formation of a Grignard reagent that reacts with dimethylgermanium dichloride. This method leveraged the increased reactivity of Grignard reagents derived from chloromethyl silicon compounds with the CH2-Cl bond, following a Wurtz-type reaction.
· The polycondensation reaction was employed to synthesize a new polycarbosiloxane featuring a germanium atom in the gem-position. The precursor, 1,1,3,3,5,5-hexamethyl-1,5-dihydro-3-germyl-1,5-disilapentane (I), was mixed with its ethoxy derivative (1,1,3,3,5,5-hexamethyl-1,5-diethoxy-3-germyl-1,5-disilapentane (II)), and in the presence of a catalyst (a boron complex with hexafluorobenzene), polycondensation occurred, releasing ethane and yielding products with a molecular weight between 50,000 and 15,000 g/mol.
· Dimethyltindinodecanoate was the crosslinking agent, added at a level of 0.2% by weight of the polymer. Membranes made of the produced polycarbosiloxane with the germanium atom were formulated by pouring a toluene solution on to a stainless steel mesh (mesh size 40 m). The membranes were poured, left to dry at 60 °C for 24 hours and vacuum dried at 60 °C for another 24 hours before removal of solvent. The net thickness of membranes subsequently calculated was between 70 and 80 μm.
The molecular formula of Dimethylgermanium dichloride is C2H6Cl2Ge.
The molecular weight of Dimethylgermanium dichloride is 173.60 g/mol.
The IUPAC name of Dimethylgermanium dichloride is dichloro(dimethyl)germane.
The InChI of Dimethylgermanium dichloride is InChI=1S/C2H6Cl2Ge/c1-5(2,3)4/h1-2H3.
The InChIKey of Dimethylgermanium dichloride is YQECBLVSMFAWIZ-UHFFFAOYSA-N.
The CAS number of Dimethylgermanium dichloride is 1529-48-2.
The European Community (EC) number of Dimethylgermanium dichloride is 216-216-5.
The DSSTox Substance ID of Dimethylgermanium dichloride is DTXSID30165156.
The Nikkaji Number of Dimethylgermanium dichloride is J47.005H.
Yes, Dimethylgermanium dichloride is a canonicalized compound.