A versatile and practical one-pot strategy for a greener, waste-minimized synthesis of aryloxy- and alkyloxy-substituted metallophthalocyanines <i>via</i> tandem S <sub>N</sub> Ar-cyclotetramerization

A sustainable one-pot S N Ar-cyclotetramerization reaction affords metallophthalocyanines with broad functional group tolerance, higher efficiency, and ≥90% lower E -factors than the literature values.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-12-23
DOI
https://doi.org/10.1039/d5qo01267h
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
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article

A versatile and practical one-pot strategy for a greener, waste-minimized synthesis of aryloxy- and alkyloxy-substituted metallophthalocyanines via tandem S N Ar-cyclotetramerization

Venanzio Raglione, Gloria Zanotti, Federica Palmeri, Laura Mancini
Organic Chemistry Frontiers
Porphyrin and Phthalocyanine Chemistry
article

A versatile and practical one-pot strategy for a greener, waste-minimized synthesis of aryloxy- and alkyloxy-substituted metallophthalocyanines via tandem S N Ar-cyclotetramerization

Venanzio Raglione, Gloria Zanotti, Federica Palmeri, Laura Mancini
article en

Abstract

A sustainable one-pot S N Ar-cyclotetramerization reaction affords metallophthalocyanines with broad functional group tolerance, higher efficiency, and ≥90% lower E -factors than the literature values.

Organic Chemistry FrontiersVol. 13(4)
Institute of Structure of Matter (IT), Sapienza University of Rome (IT)
Responsible consumption and production
Openalex Percentile: Top 48%
Porphyrin and Phthalocyanine Chemistry
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