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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293063Generated: October 25, 2026

Octadecyldimethylchlorosilane → Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine

https://huagongshe.com/reaction/2293063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctadecyldimethylchlorosilaneHCID 87738—
ReactantHCID 178526211HCID 178526211—
SolventPyridineHCID 1049—
ProductBis(dimethyl-octadecyl-siloxy)germanium phthalocyanineHCID 137226509—

Reaction Steps

[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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686439
Source datasetuspto-grants-1997_11
ORD IDord-3fa59259dee8400f8fe09fa55377eceb
Source noteuspto-grants-1997_11