Synthesis p. 406 - 409 (1986)
Update date:2022-09-26
Topics:
Greenberg, Shafrira
Marcuccio, Sebastian M.
Leznoff, Clifford C.
Tomer, Kenneth B.
The diiminoisoindolines obtained from 4-neopentoxyphthalonitrile and bis<3,4-dicyanophenyl> ether gave, in a mixed condensation reaction, binuclear and trinuclear phthalocyanines covalently linked by one atom oxy bridges with the dimer predominating.The underivatized 4-neopentoxyphthalonitrile condensed with the diiminoisoindoline of bis<3,4-dicyanophenyl> ether in a cross reaction to give the same dimer and trimeric phthalocyanines but the trimer predominated in this reaction.A cobalt derivative of bis-2-<9,16,23-trineopentoxyphthalocyaninyl> ether, the binuclearphthalocyanine, was prepared.All phthalocyanines exhibited parent ions in their fast atom bombardment mass spectra.
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Doi:10.1007/BF00515002
(1986)Doi:10.1021/op900178d
(2009)Doi:10.1021/ja01488a016
(1960)Doi:10.1016/S0022-328X(00)89361-4
(1976)Doi:10.1016/0022-328X(89)85114-9
(1989)Doi:10.1007/BF00763779
(1986)
