Inorganic chemistry

Novel Pathway to Synthesize Unsymmetrical 2, 3, 9, 10, 16, 17, 23-heptakis (alkoxyl)-24-mono (dimethylaminoalkoxyl) phthalocyanines

Z Bai, Y Gao, P Zhu, Y Bian, J Jiang

Index: Bai, Zhaopin; Gao, Yingning; Zhu, Peihua; Bian, Yongzhong; Jiang, Jianzhuang Inorganic Chemistry, 2010 , vol. 49, # 19 p. 9005 - 9011

Full Text: HTML

Citation Number: 13

Abstract

A new pathway by means of transetherification during the cyclic tetramerization of 4, 5-di (alkoxyl) phthalonitrile has been developed for the synthesis of a series of novel unsymmetrical 2, 3, 9, 10, 16, 17, 23-heptakis (alkoxyl)-24-mono (dimethylaminoalkoxyl) phthalocyanines M {Pc (OR) 7 (OR′)}(M= 2H, Cu)[R= C4H9, C5H11, C8H17; R′= C2H4, CH (CH3) CH2].

Related Articles:

An efficient two-step synthesis of metal-free phthalocyanines using a Zn (II) template

[Alzeer, Jawad; Roth, Phillipe J. C.; Luedtke, Nathan W. Chemical Communications, 2009 , # 15 p. 1970 - 1971]

Evidence of an ordered columnar mesophase in peripherally octa??n??alkoxy??substituted phthalocyanines

[Pol, J. F. van der; Neeleman, E.; Zwikker, J. W.; Nolte, R. J. M.; Drenth, W. Recueil des Travaux Chimiques des Pays-Bas, 1988 , vol. 107, p. 615 - 620]

More Articles...