참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | L-Selenocysteine | HCID 25076 | — |
| 반응물 | Octadecyldimethylchlorosilane | HCID 87738 | — |
| 반응물 | HCID 178526211 | HCID 178526211 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine | HCID 137226509 | — |
반응 단계
[In analogy to a procedure by Wheeler et. al., J. Am. Chem. Sec. 106, 7404 (1984)] 3.3 g (9.5 mmol) of dimethyl-octadecyl-chlorosilane and 0.5 g (0.8 mmol) of dihydroxygermanium-phthalocyanine in 50 ml of pyridine are stirred for 2 hours at 50°. The solution is cooled and filtered using a suction filter. The solvent is removed in vacuo, and 250 ml of hexane are added to the residue. The resulting precipitate is filtered off with suction and washed first with hexane, then in portions with 200 ml of acetone/water (1:1). The residue is dried overnight under a high vacuum, then extracted with toluene in a Soxhlet, freed of solvent and dried, yielding bis(dimethyl-octadecyl-siloxy)germanium-phthalocyanine; NMR (pyridine-d5): δ=9.8-9.9 (m, 8H); 8.3-8.5 (m,8H): aromatic H's; 0.75-1.46 (various m's); 0.45(m); -0.03 (m); -0.88 (m); -1.91 (m); -2.48 (m, 4×CH3 : silyl side chains) ppm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05670491 |
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| 출처 데이터셋 | uspto-grants-1997_09 |
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| ORD ID | ord-19f8da6eee6249d78df90e7691d9d5d2 |
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| 출처 메모 | uspto-grants-1997_09 |
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