A mild and versatile procedure is presented for functionalization of boron chloride subphthalocyanine at the axial boron position with trimethylsilyl-protected alkyne nucleophiles in the presence of aluminum chloride. The method allows a large variety of substituents on the alkyne units, including electron-donating/withdrawing aryl groups, silyl-protected alkynyl groups, as well as ferrocenyl and azulenyl groups. In addition, ferrocene itself reacts smoothly under these conditions allowing for directly anchoring it to the boron of the subphthalocyanine.
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Gotfredsen et al. (2015) studied this question.
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