4.5 Article

Synthesis and Supramolecular Properties of a Novel Octaphosphonate Porphyrin

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2009, Issue 24, Pages 4128-4134

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200900589

Keywords

Porphyrinods; Self-assembly; Supramolecular chemistry; Nitrogen heterocycles; Nanostructures; Electron microscopy

Funding

  1. Australian Research Council [DP0878220]
  2. Council for Scientific and Industrial Research (CSIR), India [01(2283)/08/EMR-II]
  3. Australian Research Council [DP0878220] Funding Source: Australian Research Council

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Two complementary routes were developed for preparing novel octaphosphonate porphyrins. The use of protected/deprotected phosphonate-substituted precursors in the rational synthesis gave an overall yield 16%. A more streamlined synthetic path gave 21% overall yield of the target molecule. Octaphosphonate porphyrin possesses promising properties in supramolecular aggregate formation with cyclam. Cofacial reversible self-assembly of a meso-substituted octaphosphonate porphyrin with cyclam yields micrometer-long nanowires with a height of about 1-1.5 nm. The resulting wires were characterized by UV/Vis absorption, emission and atomic force microscopy and transmission electron microscopy. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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