2816-54-8

Usage

Uses

Used in Organic Synthesis:
Triisopropylchlorogermane is used as a reagent in the synthesis of various organogermanium compounds, contributing to the development of new materials and chemical entities.
Used in Organic Reactions:
It serves as a catalyst in organic reactions, facilitating the conversion of reactants to products and enhancing the efficiency of the processes.
Used in Organic Chemistry Research:
Triisopropylchlorogermane is employed as a reagent in research settings, aiding chemists in understanding the properties and reactivity of organogermanium compounds.
Used in the Semiconductor Industry:
In the production of electronic devices, triisopropylchlorogermane is used as a precursor for the deposition of germanium-containing thin films, which are essential for the performance of semiconductors.
Used in Electronic Device Manufacturing:
Triisopropylchlorogermane plays a crucial role in the semiconductor industry, where it is used to create germanium-based thin films that are integral to the construction and functionality of electronic devices. Proper handling and storage of this chemical are imperative to prevent potential hazards.

InChI:InChI=1/C9H21ClGe/c1-7(2)11(10,8(3)4)9(5)6/h7-9H,1-6H3

Upstream product

• 920-39-8 isopropylmagnesium bromide 
• 10038-98-9 germaniumtetrachloride 
• 24004-54-4 bis(triisopropylgermyl)mercury 
• 59274-04-3 1-triisopropylgermyloxy-2-(triisopropylgermylmercurioxy)-3,5-di-tert-butylbenzene 
• 100-56-1 phenylmercury(II) chloride 
• 7647-01-0 hydrogenchloride 
• 1068-55-9 isopropylmagnesium chloride 

Downstream Products

• 171089-40-0 2,2-diphenyl-1,1,1,3,3,3-hexa-i-propyltrigermane 
• 996-69-0 Triisopropylgerman 
• 1394357-99-3 2-(3,5-dimethylphenyl)-6-(triisopropylgermyl)quinoline 
• 1031401-83-8 Pr(i)3GeGePh₃ 
• 3383-21-9 3,5-di-tert-butyl-o-benzoquinone 
• 59274-07-6 diisopropy(3,5-di-tert-butyl-o-phenylenedioxy)germane 
• 7647-14-5 sodium chloride 

Relevant academic research and scientific papers

A series of isopropyl-substituted oligogermanes Pri3Ge(GePh2)nGePri3 (n = 0-3) featuring a luminescent and dichroic pentagermane Pri3Ge(GePh2)3GePri3

The series of oligogermanes Pri3Ge(GePh2)nGePri3 (n = 0, 2; n = 1, 3; n = 2, 4; n = 3, 5) were prepared by the hydrogermolysis reaction. All four species were characterized by NMR (1H and 13C) and UV/visible spectroscopy as well by cyclic voltammetry and differential pulse voltammetry. The oligogermanes exhibited a successive red shift in their absorbance maxima as the length of the Ge-Ge chain was increased, and these molecules also became easier to oxidize as the chain length was increased. The X-ray crystal structures of 4 and 5 as well as the trigermane HPh2GeGePh2GePh2H (6) were determined. The pentagermane 5 was shown to be dichroic in the solid state due to the packing of the individual molecules in a columnar fashion in the crystal. Pentagermane 5 is also luminescent in solution, exhibiting an emission maximum at 380 nm. The physical properties of 5, like the hexagermane Pri3Ge(GePh)4GePri3, mimic the properties of the larger polygermane systems.

Synthesis and characterization of germa[n]pericyclynes

The synthesis and characterization of novel pericyclynes comprising germanium atoms and acetylenes, germa[n]pericyclynes, are described. The prepared germa[4]-, [6]-, and [8]pericyclynes were compared by 13C NMR spectroscopy, X-ray crystallogra

Ethynylisopropylgermanes and their trimethylsilyl derivatives

The reaction of ethynylmagnesium bromide with chloroisopropylgermanes (i-Pr4-nGeCln, n = 1-3) was used to prepare previously unknown ethynylisopropylgermanes i-Pr4-nGe(C≡CH)n (n = 1-3). The reaction of Me3

Preparation of stable compound with O-Hg-Ge grouping

1. The first stable compound with an O-Hg-Ge grouping was obtained by the reaction of 4,6-ditert-butyl-1,2-benzoquinone with bis(triisopropylgermyl)mercury. 2. A study was made of the photodecomposition of 1-triisopropylgermyloxy-2-triisopropylgermyl-mercuroxy-3,5-di-tert-butylbenzene, and also of its reaction with hydrochloric acid and ethylmercury chloride.