関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Octadecyldimethylchlorosilane | HCID 87738 | — |
| 反応物 | HCID 178526211 | HCID 178526211 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine | HCID 137226509 | — |
反応手順
In analogy to a procedure by Wheeler et.al., J. Am. Chem. Soc. 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 fast 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05358940 |
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| 出典データセット | uspto-grants-1994_10 |
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| ORD ID | ord-877c980e1c9d4a3bb90424c6a8b25e4d |
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| 出典メモ | uspto-grants-1994_10 |
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