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HRID 1379003생성일: 2026년 10월 26일

L-Selenocysteine → Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine

https://huagongshe.com/reaction/1379003

반응식

참여 물질

역할이름HCID투입량
반응물L-SelenocysteineHCID 25076—
반응물OctadecyldimethylchlorosilaneHCID 87738—
반응물HCID 178526211HCID 178526211—
용매PyridineHCID 1049—
생성물Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05670491
출처 데이터셋uspto-grants-1997_09
ORD IDord-19f8da6eee6249d78df90e7691d9d5d2
출처 메모uspto-grants-1997_09