The Synthesis of Monometallated and Unsymmetrically Substituted Binuclear Phthalocyanines and a Pentanuclear Phthalocyanine by Solution and Polymer Support Methods

Abstract

Binuclear phthalocyanines in which two different phthalocyanine nuclei are covalently linked through five-atom bridges, derived from 2-ethyl-2- methylpropan-1,3-diol are prepared. In the examples, one phthalocyanine ring is always substituted with neopentoxy substituents, while the other phthalocyanine ring is unsubstituted or contains a tert-butyl substituents or a neopentoxy substituted copper phthalocyanine, constituting a biculear phthalocyanine in which only one ring is metallated. The precursor, 2-(2-hydroxymethyl-2- methylbutoxy)-9,16,23-trineopentoxyphthalocyanine41 was prepared in solution and also by solid phase methods, using polymer-bound trityl chloride derived from a 1% divinylbenzene-co-styrene co-polymer. Keywords: Phthalocyanine, Binuclear, Pentanuclear, Polymer support.

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Document Details

Document Type
Technical Report
Publication Date
Aug 03, 1990
Accession Number
ADA225363

Entities

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  • Alfred Beverley Philip Lever
  • B. Khouw
  • C. C. Leznoff
  • P. I. Svirskaya
  • P. Seymour
  • R. L. Cerny

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  • University of York

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