참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetraethoxysilane | HCID 6517 | — |
| 반응물 | 1,4,8,11-Tetraazacyclotetradecane, 1,4,8,11-tetramethyl- | HCID 123502 | — |
| 반응물 | HCID 178468048 | HCID 178468048 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Tetraethoxysilane | HCID 6517 | — |
| 생성물 | Germanium monoxide | HCID 6327639 | — |
반응 단계
1.01 g tetraethylorthosilicate, 2.0 g deionized water, and 0.41 g germanium ethoxide were mixed together in a tared 23 mL Teflon liner. Then 0.42 g of 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane (Strem Chemicals) was dissolved in the mixture. The Teflon container was then capped, sealed, and placed within an 23-mL steel Parr autoclave. The autoclave was allowed to remain at room temperature for 2 days during which time the TEOS and germanium ethoxide were allowed to hydrolyze. The Teflon cup was then removed from the autoclave and 0.13 g 50% HF was added and mixed to create a white viscous gel. The ethanol (formed from the hydrolysis of the TEOS and germanium oxide) and water were allowed to evaporate within a vented hood with flowing air over the course of 3-4 days. Sufficient water was added and mixed into the gel to bring the molar ratio H2O/(Si+Ge) to 7. The liner was then capped and placed within a Parr Steel autoclave reactor. The autoclave was then fixed in a rotating spit within an oven heated at 160° C. for 10 days. The solid products were recovered from the cooled reactor by vacuum filtration and washed with copious quantities of water.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07906101B2 |
|---|
| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-8d44390428f44ba6a6ed232acbbc61e3 |
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| 출처 메모 | uspto-grants-2011_03 |
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