Structurally-tolerant self-assembly of zinc pyridyl porphyrins

被引：10

作者：

Bernad, Pablo L., Jr. ^{[1
]}

Guerin, Andrea J. ^{[1
]}

Haycock, Richard A. ^{[1
]}

Heath, Sarah L. ^{[1
]}

Hunter, Christopher A. ^{[1
]}

Raposo, Cesar ^{[1
]}

Rotger, Carmen ^{[1
]}

Sarson, Luke D. ^{[1
]}

Sutton, Liam R. ^{[1
]}

机构：

[1] Univ Sheffield, Dept Chem, Krebs Inst Biomol Sci, Ctr Chem Biol, Sheffield S3 7HF, S Yorkshire, England

来源：

NEW JOURNAL OF CHEMISTRY | 2008年 / 32卷 / 03期

关键词：

D O I：

10.1039/b704571a

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Zinc porphyrins equipped with pyridine ligands form macrocyclic assemblies in organic solvents. The assemblies have been characterised by (1)H NMR, UV-visible spectroscopy, X-ray crystallography and vapour pressure osmometry. The self-assembly properties of six isomeric porphyrins are relatively insensitive to the geometry of the porphyrin monomer. Changes in the internal torsion angles allow all of the porphyrins to form macrocyclic dimers but with differences in the relative orientations of the porphyrin units. The associated strain reduces the effective molarities from the value of 6 M reported previously for an 'ideal' monomer to between 0.07 and 2 M leading to dimerisation constants in the 10(5)-10(6) M(-1) range. Only one isomer has a geometry that makes dimerisation impossible without severe distortion, and this compound self-assembles to give a tetrameric macrocycle at millimolar concentrations.

引用

页码：525 / 532

页数：8

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[31] PERSPECTIVES IN SUPRAMOLECULAR CHEMISTRY - FROM MOLECULAR RECOGNITION TOWARDS MOLECULAR INFORMATION-PROCESSING AND SELF-ORGANIZATION [J].