Generation of Nanostructures by the Aggregation of Porphyrin Derivatives with Long Alkane Chain in Mix-SolventReport as inadecuate

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Journal of Nanomaterials - Volume 2007 2007, Article ID 47234, 8 pages

Research Article Central Salt and Marine Chemicals Research Institute, Bhavnagar, Gujarat 364002, India

Received 8 February 2007; Revised 20 May 2007; Accepted 31 July 2007

Academic Editor: Michael S. Wong

Copyright © 2007 Amrita Ghosh et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Controlled aggregation of tetrakis-4-hexadecyl oxy-phenyl porphyrin and its copperII-complex was studied in mix-solvent system at room temperature. Structure of the aggregates was characterized by scanning electron microscopy SEM, transmission electron microscopy TEM, powder X-ray diffraction XRD, and UV-visible spectroscopy. TEM results indicated the formation of organized nanostructures from the porphyrin derivative and its corresponding copperII-complex. XRD results showed that the bulk and nanostructured free porphyrin derivatives had the similar crystalline morphology. UV-visible-NIR spectroscopic data showed broad red-shifted Soret band, indicating JJ aggregation among the monomer units. Conjugate effect of lateral π-π interaction among the tetrapyrrole cores and hydrophobic interaction among the long alkane chains substituted in the peripheral phenyl rings is believed to lead to the organized nanostructures. Effect of solvent ratio on the aggregate structure is also revealed.

Author: Amrita Ghosh, T. Selvamani, D. Amilan Jose, Amitava Das, and I. Mukhopadhyay



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