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Germylene, methylphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53572-89-7

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53572-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53572-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53572-89:
(7*5)+(6*3)+(5*5)+(4*7)+(3*2)+(2*8)+(1*9)=137
137 % 10 = 7
So 53572-89-7 is a valid CAS Registry Number.

53572-89-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name poly(methylphenylgermylene)

1.2 Other means of identification

Product number -
Other names MePhGe

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53572-89-7 SDS

53572-89-7Relevant academic research and scientific papers

Electrochemical synthesis of polygermanes

Okano,Takeda,Toriumi,Hamano

, p. 659 - 666 (2008/10/08)

Five dialkyl-substituted and three phenyl substituted polygermanes were electrochemically synthesized. Among them, dibutyl-, dipentyl-, and dihexyl-substituted polygermanes gave the best synthetic results, i.e., relatively high yields (25-45%), high curre

Catalytic synthesis of poly(arylmethylgermanes) by demethanative coupling: A mild route to σ-conjugated polymers

Katz, Sandra M.,Reichl, Jennifer A.,Berry, Donald H.

, p. 9844 - 9849 (2007/10/03)

A variety of poly(arylmethylgermanes) have been synthesized from aryldimethylgermanes in high yield via mild catalytic demethanative coupling using tetrakis(trimethylphosphine)dimethylruthenium as a convenient catalyst precursor. Polymerizations of germanes Me2GeArH (At = phenyl, p-tolyl, p- fluoro, p-trifluorotolyl, p-anisyl, and m-xylyl) proceed in neat monomer at room temperature. Catalyst removal can be effected by treatment of the reaction mixture with air, which gives polymer yields between 70% and 100%. Alternatively, separation of the catalyst by precipitation of the polymers from THF solution with methanol gives lower yields, but of somewhat higher molecular weight material. The new polygermanes are characterized by 1H NMR and by gel permeation chromatography (GPC) using both polystyrene standards and light scattering methods. Molecular weights calculated by polystyrene analysis fall in the ranges of M(w) = 3 x 103 to 7 x 103 and M(n) = 2 x 103 to 6 x 103. Values obtained from light scattering are approximately 60% and 82% higher, respectively, resulting in M(w) measured by SEC/LS in the range 5 x 103 to 1 x 104, with M(w)/M(n) ~ 1.3. The absorption spectra of the polygermanes exhibit λ(max) in the range 326-338 nm. Comparison of the properties of poly(phenylmethylgermane) prepared by catalytic demethanative coupling and Wurtz coupling of MePhGeCl2 with sodium revealed no significant differences.

Synthesis, absorption characteristics and some reactions of polygermanes

Mochida, Kunio,Chiba, Hiromi

, p. 45 - 54 (2007/10/02)

A number of high molecular weight polygermanes were prepared by an improvement on Wurtz coupling reactions of dichlorogermanes and sodium metal, and by a method using diiodogermylene and Grignard reagents (or organolithiums).Most of the polygermanes thus prepared showed a narrow molecular distribution containing molecular weights 103-104.In solution, the polygermanes showed characteristic electronic absorption bands at 300-350 nm and were strongly thermochromic for alkyl-substituted derivatives.Photolysis of the polygermanes proceeded by both contraction of the chain with loss of diorganogermylenes and homolytic scission of the germanium-germanium ? bond. Key words: Germanium; Polygermane; Photochemistry

Laser flash photolysis of polygermanes. Generation of germylenes and polygermyl radicals

Mochida, Kunio,Kimijima, Kohichi,Chiba, Hiromi,Wakasa, Masanobu,Hayashi, Hisaharu

, p. 404 - 406 (2008/10/08)

Laser flash photolysis of polygermanes involves both Ge-Ge bond homolysis to give polygermyl radicals and extrusion of germylenes.

Electronic absorption spectra of diorganogermylenes in matrices: Formation of diorganogermylene complexes with heteroatom-containing substrates

Ando, Wataru,Itoh, Hiroyuki,Tsumuraya, Takeshi

, p. 2759 - 2766 (2008/10/08)

Diorganogermylenes were generated in hydrocarbon matrices at 77 K by the photolysis of 7-germanorbornadienes 1a-e or bis(trimethylsilyl)germanes 2a-g. The germylenes show electronic absorption bands at 420-558 nm. The germylenes react with heteroatom-containing substrates (R2O, R2S, R3P, R3N, RCl, and ROH) to form adducts, which show characteristic absorption bands at shorter wavelengths than those of germylenes.

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